RBM39P1 RBM39 pseudogene 1 [Homo sapiens (human)] - Gene

Summary

Official Symbol: RBM39P1provided by HGNC
Official Full Name: RBM39 pseudogene 1provided by HGNC
Primary source: HGNC:HGNC:54942
See related: Ensembl:ENSG00000214019 AllianceGenome:HGNC:54942
Gene type: pseudo
RefSeq status: INFERRED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

Location:: Xp11.3

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	X	NC_000023.11 (44029135..44031118)
RS_2023_10	current	T2T-CHM13v2.0 (GCF_009914755.1)	X	NC_060947.1 (43435402..43437385)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	X	NC_000023.10 (43888381..43890364)

Chromosome X - NC_000023.11 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Submit: New GeneRIF Correction

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Markers

AF020217 (e-PCR)
- UniSTS:75018

GDB:607650 (e-PCR)
- UniSTS:158255

REN58783 (e-PCR)
- UniSTS:383583

REN58785 (e-PCR)
- UniSTS:383585

REN58786 (e-PCR)
- UniSTS:383586

PMC24149P5 (e-PCR)
- UniSTS:272236

RH69003 (e-PCR)
- UniSTS:85360

G64616 (e-PCR)
- UniSTS:163703

NDP (e-PCR)
- UniSTS:99471

AFMa212zg1 (e-PCR)
- UniSTS:35747

G64285 (e-PCR)
- UniSTS:158667

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.