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    CEP250 centrosomal protein 250 [ Homo sapiens (human) ]

    Gene ID: 11190, updated on 5-May-2024

    Summary

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    Official Symbol
    CEP250provided by HGNC
    Official Full Name
    centrosomal protein 250provided by HGNC
    Primary source
    HGNC:HGNC:1859
    See related
    Ensembl:ENSG00000126001 MIM:609689; AllianceGenome:HGNC:1859
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    CEP2; CNAP1; C-NAP1; CRDHL2
    Summary
    This gene encodes a core centrosomal protein required for centriole-centriole cohesion during interphase of the cell cycle. The encoded protein dissociates from the centrosomes when parental centrioles separate at the beginning of mitosis. The protein associates with and is phosphorylated by NIMA-related kinase 2, which is also associated with the centrosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]
    Expression
    Ubiquitous expression in testis (RPKM 6.5), spleen (RPKM 5.2) and 24 other tissues See more
    Orthologs
    mouse all
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    Genomic context

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    Location:
    20q11.22
    Exon count:
    39
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 20 NC_000020.11 (35455165..35519280)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 20 NC_060944.1 (37175894..37240174)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (34043419..34107108)

    Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene GDF5 promoter region Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12857 Neighboring gene GDF5 antisense RNA 1 Neighboring gene growth differentiation factor 5 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 17783 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 17784 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12858 Neighboring gene microRNA 1289-1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12859 Neighboring gene CEP250 antisense RNA 1 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 17785 Neighboring gene chromosome 20 open reading frame 173 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 17786 Neighboring gene ERGIC and golgi 3 Neighboring gene ribosomal protein L36 pseudogene 4

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • Project title: HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

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    Related articles in PubMed

    1. High-throughput sequencing for the molecular diagnosis of Usher syndrome reveals 42 novel mutations and consolidates CEP250 as Usher-like disease causative. Fuster-García C, et al. Sci Rep, 2018 Nov 20. PMID 30459346, Free PMC Article
    2. CEP250 mutations associated with mild cone-rod dystrophy and sensorineural hearing loss in a Japanese family. Kubota D, et al. Ophthalmic Genet, 2018 Aug. PMID 29718797
    3. Centriole splitting caused by loss of the centrosomal linker protein C-NAP1 reduces centriolar satellite density and impedes centrosome amplification. Flanagan AM, et al. Mol Biol Cell, 2017 Mar 15. PMID 28100636, Free PMC Article
    4. Multisite phosphorylation of C-Nap1 releases it from Cep135 to trigger centrosome disjunction. Hardy T, et al. J Cell Sci, 2014 Jun 1. PMID 24695856, Free PMC Article
    5. A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndrome. Khateb S, et al. J Med Genet, 2014 Jul. PMID 24780881

    See all (82) citations in PubMed

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. Circ_0060077 Knockdown Alleviates High-Glucose-Induced Cell Apoptosis, Oxidative Stress, Inflammation and Fibrosis in HK-2 Cells via miR-145-5p/VASN Pathway.
      Title: Circ_0060077 Knockdown Alleviates High-Glucose-Induced Cell Apoptosis, Oxidative Stress, Inflammation and Fibrosis in HK-2 Cells via miR-145-5p/VASN Pathway.
    2. Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome.
      Title: Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome.
    3. Involvement of NEK2 and its interaction with NDC80 and CEP250 in hepatocellular carcinoma.
      Title: Involvement of NEK2 and its interaction with NDC80 and CEP250 in hepatocellular carcinoma.
    4. Study identified a nonsense mutation (c.562C>T, p.R188*) in CEP250 in a consanguineous family with nonsyndromic retinitis pigmentosa (RP). The disruption of Cep250 resulted in severe impairment of retinal function and significant retinal morphological alterations a novel Cep250 knockin mouse line.
      Title: Functional characterization of CEP250 variant identified in nonsyndromic retinitis pigmentosa.
    5. CEP250 mutation is associated with Usher syndrome.
      Title: High-throughput sequencing for the molecular diagnosis of Usher syndrome reveals 42 novel mutations and consolidates CEP250 as Usher-like disease causative.
    6. Our data indicate that mutations of CEP250 can cause mild cone-rod dystrophy (CRD) and early-onset sensorineural hearing loss (SNHL) in Japanese patients. Because the ophthalmological phenotypes were very mild, high-resolution retinal imaging analysis, such as AO, will be helpful in diagnosing CEP250-associated disease.
      Title: CEP250 mutations associated with mild cone-rod dystrophy and sensorineural hearing loss in a Japanese family.
    7. C-NAP1-null cells were viable and had an increased frequency of premature centriole separation, accompanied by reduced density of the centriolar satellites, with reexpression of C-NAP1 rescuing both phenotypes. Centrosome amplification induced by DNA damage or by PLK4 or CDK2 overexpression was markedly reduced in the absence of C-NAP1.
      Title: Centriole splitting caused by loss of the centrosomal linker protein C-NAP1 reduces centriolar satellite density and impedes centrosome amplification.
    8. ASPP1/2 interacted with centrosome linker protein C-Nap1. Co-depletion of ASPP1 and ASPP2 inhibited re-association of C-Nap1 with centrosome at the end of mitosis.
      Title: The tumor suppressor proteins ASPP1 and ASPP2 interact with C-Nap1 and regulate centrosome linker reassembly.
    9. multisite phosphorylation precipitates centrosome disjunction at the onset of mitosis
      Title: Multisite phosphorylation of C-Nap1 releases it from Cep135 to trigger centrosome disjunction.
    10. A homozygous nonsense CEP250 mutation, in combination with a heterozygous C2orf71 nonsense mutation, causes an atypical form of Usher syndrome, characterised by early-onset sensorineural hearing loss and a relatively mild retinitis pigmentosa.
      Title: A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndrome.
    Submit: New GeneRIF Correction See all GeneRIFs (15)

    Phenotypes

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    Find tests for this gene in the NIH Genetic Testing Registry (GTR)

    Review eQTL and phenotype association data in this region using PheGenI

    Associated conditions

    Description Tests
    Cone-rod dystrophy and hearing loss 2
    MedGen: C5193051 OMIM: 618358 GeneReviews: Not available
    		Compare labs

    EBI GWAS Catalog

    Description
    A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci.
    EBI GWAS Catalog
    Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
    EBI GWAS Catalog
    Many sequence variants affecting diversity of adult human height.
    EBI GWAS Catalog
    Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci.
    EBI GWAS Catalog

    Variation

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    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    Genotypes

    Pathways from PubChem

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    Interactions

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    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

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    Markers

    Homology

    Clone Names

    • MGC88542

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    		 PubMed 
    enables protein domain specific binding IPI
    Inferred from Physical Interaction
    more info
    		 PubMed 
    Process Evidence Code Pubs
    involved_in centriole-centriole cohesion IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    involved_in cilium assembly IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in cilium assembly IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    involved_in detection of light stimulus involved in visual perception ISS
    Inferred from Sequence or Structural Similarity
    more info
    		  
    involved_in mitotic cell cycle IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    involved_in non-motile cilium assembly IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    involved_in positive regulation of protein localization to centrosome IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    involved_in protein localization IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    involved_in protein localization to centrosome IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    involved_in protein localization to organelle IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    involved_in regulation of centriole-centriole cohesion IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    Component Evidence Code Pubs
    is_active_in centriole IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    colocalizes_with centriole IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in centriole IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    is_active_in centrosome IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    located_in centrosome IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in ciliary basal body ISS
    Inferred from Sequence or Structural Similarity
    more info
    		  
    located_in cytosol TAS
    Traceable Author Statement
    more info
    		  
    located_in extracellular exosome HDA PubMed 
    located_in microtubule organizing center NAS
    Non-traceable Author Statement
    more info
    		 PubMed 
    located_in perinuclear region of cytoplasm IEA
    Inferred from Electronic Annotation
    more info
    		  
    located_in photoreceptor inner segment ISS
    Inferred from Sequence or Structural Similarity
    more info
    		  
    located_in photoreceptor outer segment ISS
    Inferred from Sequence or Structural Similarity
    more info
    		  
    part_of protein-containing complex IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 

    General protein information

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    Preferred Names
    centrosome-associated protein CEP250
    Names
    250 kDa centrosomal protein
    centrosomal Nek2-associated protein 1

    NCBI Reference Sequences (RefSeq)

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    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    Genomic

    1. NG_051604.2 RefSeqGene

      Range
      5435..69117
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001318219.1 → NP_001305148.1  centrosome-associated protein CEP250 isoform 2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) contains a distinct 5' UTR and lacks an in-frame portion of the 5' coding region, compared to variant 1. The resulting isoform (2) has a shorter N-terminus, compared to isoform 1.
      Source sequence(s)
      AF049105, AW083819, BC144706, FO393401
      UniProtKB/Swiss-Prot
      Q9BV73
      Conserved Domains (1) summary
      TIGR02168
      Location:158 → 920
      SMC_prok_B; chromosome segregation protein SMC, common bacterial type

    2. NM_007186.6 → NP_009117.2  centrosome-associated protein CEP250 isoform 1

      See identical proteins and their annotated locations for NP_009117.2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) encodes the longer isoform (1).
      Source sequence(s)
      FO393401
      Consensus CDS
      CCDS13255.1
      UniProtKB/Swiss-Prot
      E1P5Q3, O14812, O60588, Q9BV73, Q9H450
      UniProtKB/TrEMBL
      A0A9L9PXX3
      Related
      ENSP00000380661.1, ENST00000397527.6
      Conserved Domains (4) summary
      COG1196
      Location:252 → 1057
      Smc; Chromosome segregation ATPase [Cell cycle control, cell division, chromosome partitioning]
      TIGR02168
      Location:790 → 1552
      SMC_prok_B; chromosome segregation protein SMC, common bacterial type
      TIGR04376
      Location:604 → 709
      TIGR04376; TIGR04376 family protein
      pfam15035
      Location:40 → 215
      Rootletin; Ciliary rootlet component, centrosome cohesion

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000020.11 Reference GRCh38.p14 Primary Assembly

      Range
      35455165..35519280
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_006723691.2 → XP_006723754.1  centrosome-associated protein CEP250 isoform X1

      See identical proteins and their annotated locations for XP_006723754.1

      UniProtKB/Swiss-Prot
      E1P5Q3, O14812, O60588, Q9BV73, Q9H450
      UniProtKB/TrEMBL
      A0A9L9PXX3
      Conserved Domains (4) summary
      COG1196
      Location:252 → 1057
      Smc; Chromosome segregation ATPase [Cell cycle control, cell division, chromosome partitioning]
      TIGR02168
      Location:790 → 1552
      SMC_prok_B; chromosome segregation protein SMC, common bacterial type
      TIGR04376
      Location:604 → 709
      TIGR04376; TIGR04376 family protein
      pfam15035
      Location:40 → 215
      Rootletin; Ciliary rootlet component, centrosome cohesion

    2. XM_047439854.1 → XP_047295810.1  centrosome-associated protein CEP250 isoform X2

    3. XM_005260262.5 → XP_005260319.1  centrosome-associated protein CEP250 isoform X1

      See identical proteins and their annotated locations for XP_005260319.1

      UniProtKB/Swiss-Prot
      E1P5Q3, O14812, O60588, Q9BV73, Q9H450
      UniProtKB/TrEMBL
      A0A9L9PXX3
      Conserved Domains (4) summary
      COG1196
      Location:252 → 1057
      Smc; Chromosome segregation ATPase [Cell cycle control, cell division, chromosome partitioning]
      TIGR02168
      Location:790 → 1552
      SMC_prok_B; chromosome segregation protein SMC, common bacterial type
      TIGR04376
      Location:604 → 709
      TIGR04376; TIGR04376 family protein
      pfam15035
      Location:40 → 215
      Rootletin; Ciliary rootlet component, centrosome cohesion

    4. XM_005260264.5 → XP_005260321.1  centrosome-associated protein CEP250 isoform X4

      UniProtKB/TrEMBL
      A0A9L9PXX3
      Conserved Domains (3) summary
      COG1196
      Location:241 → 980
      Smc; Chromosome segregation ATPase [Cell cycle control, cell division, chromosome partitioning]
      TIGR02168
      Location:713 → 1475
      SMC_prok_B; chromosome segregation protein SMC, common bacterial type
      pfam15035
      Location:40 → 215
      Rootletin; Ciliary rootlet component, centrosome cohesion

    5. XM_047439862.1 → XP_047295818.1  centrosome-associated protein CEP250 isoform X7

    6. XM_006723692.5 → XP_006723755.1  centrosome-associated protein CEP250 isoform X1

      See identical proteins and their annotated locations for XP_006723755.1

      UniProtKB/Swiss-Prot
      E1P5Q3, O14812, O60588, Q9BV73, Q9H450
      UniProtKB/TrEMBL
      A0A9L9PXX3
      Conserved Domains (4) summary
      COG1196
      Location:252 → 1057
      Smc; Chromosome segregation ATPase [Cell cycle control, cell division, chromosome partitioning]
      TIGR02168
      Location:790 → 1552
      SMC_prok_B; chromosome segregation protein SMC, common bacterial type
      TIGR04376
      Location:604 → 709
      TIGR04376; TIGR04376 family protein
      pfam15035
      Location:40 → 215
      Rootletin; Ciliary rootlet component, centrosome cohesion

    7. XM_047439859.1 → XP_047295815.1  centrosome-associated protein CEP250 isoform X4

    8. XM_006723690.5 → XP_006723753.1  centrosome-associated protein CEP250 isoform X1

      See identical proteins and their annotated locations for XP_006723753.1

      UniProtKB/Swiss-Prot
      E1P5Q3, O14812, O60588, Q9BV73, Q9H450
      UniProtKB/TrEMBL
      A0A9L9PXX3
      Conserved Domains (4) summary
      COG1196
      Location:252 → 1057
      Smc; Chromosome segregation ATPase [Cell cycle control, cell division, chromosome partitioning]
      TIGR02168
      Location:790 → 1552
      SMC_prok_B; chromosome segregation protein SMC, common bacterial type
      TIGR04376
      Location:604 → 709
      TIGR04376; TIGR04376 family protein
      pfam15035
      Location:40 → 215
      Rootletin; Ciliary rootlet component, centrosome cohesion

    9. XM_047439853.1 → XP_047295809.1  centrosome-associated protein CEP250 isoform X2

    10. XM_047439857.1 → XP_047295813.1  centrosome-associated protein CEP250 isoform X4

    11. XM_006723693.5 → XP_006723756.1  centrosome-associated protein CEP250 isoform X1

      See identical proteins and their annotated locations for XP_006723756.1

      UniProtKB/Swiss-Prot
      E1P5Q3, O14812, O60588, Q9BV73, Q9H450
      UniProtKB/TrEMBL
      A0A9L9PXX3
      Conserved Domains (4) summary
      COG1196
      Location:252 → 1057
      Smc; Chromosome segregation ATPase [Cell cycle control, cell division, chromosome partitioning]
      TIGR02168
      Location:790 → 1552
      SMC_prok_B; chromosome segregation protein SMC, common bacterial type
      TIGR04376
      Location:604 → 709
      TIGR04376; TIGR04376 family protein
      pfam15035
      Location:40 → 215
      Rootletin; Ciliary rootlet component, centrosome cohesion

    12. XM_047439860.1 → XP_047295816.1  centrosome-associated protein CEP250 isoform X4

    13. XM_005260263.5 → XP_005260320.1  centrosome-associated protein CEP250 isoform X3

      UniProtKB/TrEMBL
      A0A9L9PXZ7
      Conserved Domains (4) summary
      COG1196
      Location:252 → 1057
      Smc; Chromosome segregation ATPase [Cell cycle control, cell division, chromosome partitioning]
      TIGR02168
      Location:790 → 1552
      SMC_prok_B; chromosome segregation protein SMC, common bacterial type
      TIGR04376
      Location:604 → 709
      TIGR04376; TIGR04376 family protein
      pfam15035
      Location:40 → 215
      Rootletin; Ciliary rootlet component, centrosome cohesion

    14. XM_047439863.1 → XP_047295819.1  centrosome-associated protein CEP250 isoform X9

    15. XM_017027617.2 → XP_016883106.1  centrosome-associated protein CEP250 isoform X6

      UniProtKB/TrEMBL
      A0A9L9PXD2, A0A9L9PXZ7
      Related
      ENSP00000516578.1, ENST00000706830.1

    16. XM_047439856.1 → XP_047295812.1  centrosome-associated protein CEP250 isoform X3

    17. XM_047439861.1 → XP_047295817.1  centrosome-associated protein CEP250 isoform X5

    18. XM_047439864.1 → XP_047295820.1  centrosome-associated protein CEP250 isoform X13

    19. XM_047439858.1 → XP_047295814.1  centrosome-associated protein CEP250 isoform X4

    20. XM_047439855.1 → XP_047295811.1  centrosome-associated protein CEP250 isoform X3

      Related
      ENSP00000516577.1, ENST00000706829.1

    21. XM_011528518.4 → XP_011526820.1  centrosome-associated protein CEP250 isoform X8

      UniProtKB/TrEMBL
      A0A9L9PXX3
      Conserved Domains (4) summary
      COG1196
      Location:129 → 934
      Smc; Chromosome segregation ATPase [Cell cycle control, cell division, chromosome partitioning]
      TIGR02168
      Location:667 → 1429
      SMC_prok_B; chromosome segregation protein SMC, common bacterial type
      TIGR04376
      Location:481 → 586
      TIGR04376; TIGR04376 family protein
      pfam15035
      Location:1 → 92
      Rootletin; Ciliary rootlet component, centrosome cohesion

    22. XM_011528519.3 → XP_011526821.1  centrosome-associated protein CEP250 isoform X10

      UniProtKB/TrEMBL
      A0A9L9PXX3
      Conserved Domains (3) summary
      COG1196
      Location:50 → 855
      Smc; Chromosome segregation ATPase [Cell cycle control, cell division, chromosome partitioning]
      TIGR02168
      Location:588 → 1350
      SMC_prok_B; chromosome segregation protein SMC, common bacterial type
      TIGR04376
      Location:402 → 507
      TIGR04376; TIGR04376 family protein

    23. XM_017027618.2 → XP_016883107.1  centrosome-associated protein CEP250 isoform X11

      UniProtKB/TrEMBL
      A0A9L9PXX3

    24. XM_017027619.2 → XP_016883108.1  centrosome-associated protein CEP250 isoform X12

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060944.1 Alternate T2T-CHM13v2.0

      Range
      37175894..37240174
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054322887.1 → XP_054178862.1  centrosome-associated protein CEP250 isoform X1

      UniProtKB/Swiss-Prot
      E1P5Q3, O14812, O60588, Q9BV73, Q9H450

    2. XM_054322894.1 → XP_054178869.1  centrosome-associated protein CEP250 isoform X3

    3. XM_054322906.1 → XP_054178881.1  centrosome-associated protein CEP250 isoform X9

    4. XM_054322903.1 → XP_054178878.1  centrosome-associated protein CEP250 isoform X6

      UniProtKB/TrEMBL
      A0A9L9PXD2

    5. XM_054322910.1 → XP_054178885.1  centrosome-associated protein CEP250 isoform X13

    6. XM_054322901.1 → XP_054178876.1  centrosome-associated protein CEP250 isoform X4

    7. XM_054322891.1 → XP_054178866.1  centrosome-associated protein CEP250 isoform X1

      UniProtKB/Swiss-Prot
      E1P5Q3, O14812, O60588, Q9BV73, Q9H450

    8. XM_054322890.1 → XP_054178865.1  centrosome-associated protein CEP250 isoform X1

      UniProtKB/Swiss-Prot
      E1P5Q3, O14812, O60588, Q9BV73, Q9H450

    9. XM_054322902.1 → XP_054178877.1  centrosome-associated protein CEP250 isoform X5

    10. XM_054322892.1 → XP_054178867.1  centrosome-associated protein CEP250 isoform X2

    11. XM_054322897.1 → XP_054178872.1  centrosome-associated protein CEP250 isoform X4

    12. XM_054322904.1 → XP_054178879.1  centrosome-associated protein CEP250 isoform X7

    13. XM_054322896.1 → XP_054178871.1  centrosome-associated protein CEP250 isoform X3

    14. XM_054322899.1 → XP_054178874.1  centrosome-associated protein CEP250 isoform X4

    15. XM_054322889.1 → XP_054178864.1  centrosome-associated protein CEP250 isoform X1

      UniProtKB/Swiss-Prot
      E1P5Q3, O14812, O60588, Q9BV73, Q9H450

    16. XM_054322900.1 → XP_054178875.1  centrosome-associated protein CEP250 isoform X4

    17. XM_054322888.1 → XP_054178863.1  centrosome-associated protein CEP250 isoform X1

      UniProtKB/Swiss-Prot
      E1P5Q3, O14812, O60588, Q9BV73, Q9H450

    18. XM_054322893.1 → XP_054178868.1  centrosome-associated protein CEP250 isoform X2

    19. XM_054322895.1 → XP_054178870.1  centrosome-associated protein CEP250 isoform X3

    20. XM_054322898.1 → XP_054178873.1  centrosome-associated protein CEP250 isoform X4

    21. XM_054322905.1 → XP_054178880.1  centrosome-associated protein CEP250 isoform X8

    22. XM_054322907.1 → XP_054178882.1  centrosome-associated protein CEP250 isoform X10

    23. XM_054322908.1 → XP_054178883.1  centrosome-associated protein CEP250 isoform X11

    24. XM_054322909.1 → XP_054178884.1  centrosome-associated protein CEP250 isoform X12

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001035518.1: Suppressed sequence

      Description
      NM_001035518.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
    Nucleotide Protein
    Heading Accession and Version
    Protein Accession Links
    GenPept Link UniProtKB Link
    Q9BV73.2 GenPept UniProtKB/Swiss-Prot:Q9BV73

    Gene LinkOut

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