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LCA5L lebercilin LCA5 like [ Macaca mulatta (Rhesus monkey) ]

Gene ID: 715569, updated on 5-Mar-2024

Summary

Official Symbol
LCA5Lprovided by VGNC
Official Full Name
lebercilin LCA5 likeprovided by VGNC
Primary source
VGNC:VGNC:74039
See related
Ensembl:ENSMMUG00000010407
Gene type
protein coding
RefSeq status
PROVISIONAL
Organism
Macaca mulatta
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Cercopithecidae; Cercopithecinae; Macaca
Orthologs
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Genomic context

See LCA5L in Genome Data Viewer
Location:
chromosome: 3
Exon count:
14
Annotation release Status Assembly Chr Location
103 current Mmul_10 (GCF_003339765.1) 3 NC_041756.1 (7168226..7212117)
102 previous assembly Mmul_8.0.1 (GCF_000772875.2) 3 NC_027895.1 (7235813..7279672)

Chromosome 3 - NC_041756.1Genomic Context describing neighboring genes Neighboring gene beta-1,3-galactosyltransferase 5 Neighboring gene myosin light polypeptide 6-like Neighboring gene SH3 domain binding glutamate rich protein Neighboring gene uncharacterized LOC114676804 Neighboring gene guided entry of tail-anchored proteins factor 1 Neighboring gene small nucleolar RNA U13 Neighboring gene high mobility group nucleosome binding domain 1

Genomic regions, transcripts, and products

General gene information

Markers

Gene Ontology Provided by RefSeq

Process Evidence Code Pubs
involved_in intraciliary transport IEA
Inferred from Electronic Annotation
more info
PubMed 
Component Evidence Code Pubs
located_in axoneme IEA
Inferred from Electronic Annotation
more info
PubMed 

General protein information

Preferred Names
lebercilin-like protein
Names
LCA5L, lebercilin like

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.

mRNA and Protein(s)

  1. NM_001194409.2NP_001181338.1  lebercilin-like protein

    See identical proteins and their annotated locations for NP_001181338.1

    Status: PROVISIONAL

    Source sequence(s)
    QNVO02000307
    UniProtKB/TrEMBL
    F7D2V2, G7MMR9
    Related
    ENSMMUP00000062773.1, ENSMMUT00000084400.1
    Conserved Domains (1) summary
    pfam15619
    Location:146325
    Lebercilin; Ciliary protein causing Leber congenital amaurosis disease

RefSeqs of Annotated Genomes: Macaca mulatta Annotation Release 103 details...Open this link in a new tab

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

Reference Mmul_10 Primary Assembly

Genomic

  1. NC_041756.1 Reference Mmul_10 Primary Assembly

    Range
    7168226..7212117
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_028845058.1XP_028700891.1  lebercilin-like protein isoform X5

  2. XM_028845051.1XP_028700884.1  lebercilin-like protein isoform X1

    UniProtKB/TrEMBL
    G7MMR9
    Conserved Domains (1) summary
    pfam15619
    Location:195374
    Lebercilin; Ciliary protein causing Leber congenital amaurosis disease
  3. XM_015132856.2XP_014988342.1  lebercilin-like protein isoform X1

    UniProtKB/TrEMBL
    G7MMR9
    Conserved Domains (1) summary
    pfam15619
    Location:195374
    Lebercilin; Ciliary protein causing Leber congenital amaurosis disease
  4. XM_028845054.1XP_028700887.1  lebercilin-like protein isoform X1

    UniProtKB/TrEMBL
    G7MMR9
    Conserved Domains (1) summary
    pfam15619
    Location:195374
    Lebercilin; Ciliary protein causing Leber congenital amaurosis disease
  5. XM_028845052.1XP_028700885.1  lebercilin-like protein isoform X1

    UniProtKB/TrEMBL
    G7MMR9
    Conserved Domains (1) summary
    pfam15619
    Location:195374
    Lebercilin; Ciliary protein causing Leber congenital amaurosis disease
  6. XM_028845053.1XP_028700886.1  lebercilin-like protein isoform X1

    UniProtKB/TrEMBL
    G7MMR9
    Conserved Domains (1) summary
    pfam15619
    Location:195374
    Lebercilin; Ciliary protein causing Leber congenital amaurosis disease
  7. XM_028845050.1XP_028700883.1  lebercilin-like protein isoform X1

    UniProtKB/TrEMBL
    G7MMR9
    Conserved Domains (1) summary
    pfam15619
    Location:195374
    Lebercilin; Ciliary protein causing Leber congenital amaurosis disease
  8. XM_015132864.2XP_014988350.1  lebercilin-like protein isoform X1

    UniProtKB/TrEMBL
    G7MMR9
    Conserved Domains (1) summary
    pfam15619
    Location:195374
    Lebercilin; Ciliary protein causing Leber congenital amaurosis disease
  9. XM_015132855.2XP_014988341.1  lebercilin-like protein isoform X1

    UniProtKB/TrEMBL
    G7MMR9
    Conserved Domains (1) summary
    pfam15619
    Location:195374
    Lebercilin; Ciliary protein causing Leber congenital amaurosis disease
  10. XM_028845049.1XP_028700882.1  lebercilin-like protein isoform X1

    UniProtKB/TrEMBL
    G7MMR9
    Conserved Domains (1) summary
    pfam15619
    Location:195374
    Lebercilin; Ciliary protein causing Leber congenital amaurosis disease
  11. XM_015132866.2XP_014988352.1  lebercilin-like protein isoform X2

    UniProtKB/TrEMBL
    F7D2V2, G7MMR9
    Conserved Domains (1) summary
    pfam15619
    Location:146325
    Lebercilin; Ciliary protein causing Leber congenital amaurosis disease
  12. XM_028845055.1XP_028700888.1  lebercilin-like protein isoform X2

    UniProtKB/TrEMBL
    F7D2V2, G7MMR9
    Related
    ENSMMUP00000064113.1, ENSMMUT00000104372.1
    Conserved Domains (1) summary
    pfam15619
    Location:146325
    Lebercilin; Ciliary protein causing Leber congenital amaurosis disease
  13. XM_028845056.1XP_028700889.1  lebercilin-like protein isoform X3

    UniProtKB/TrEMBL
    G7MMR9
    Conserved Domains (1) summary
    pfam15619
    Location:44223
    Lebercilin; Ciliary protein causing Leber congenital amaurosis disease
  14. XM_028845057.1XP_028700890.1  lebercilin-like protein isoform X4

    UniProtKB/TrEMBL
    G7MMR9
    Conserved Domains (1) summary
    pfam15619
    Location:16195
    Lebercilin; Ciliary protein causing Leber congenital amaurosis disease