CXorf51A chromosome X open reading frame 51A [Homo sapiens (human)] - Gene

Summary

Official Symbol: CXorf51Aprovided by HGNC
Official Full Name: chromosome X open reading frame 51Aprovided by HGNC
Primary source: HGNC:HGNC:30533
See related: Ensembl:ENSG00000224440 AllianceGenome:HGNC:30533
Gene type: protein coding
RefSeq status: VALIDATED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: CXorf51; CXorf51B
Expression: Restricted expression toward testis (RPKM 27.8) See more
Orthologs: all
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Genomic context

Location:: Xq27.3

Exon count:: 2

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	X	NC_000023.11 (146814106..146814744, complement)
RS_2023_10	current	T2T-CHM13v2.0 (GCF_009914755.1)	X	NC_060947.1 (145073947..145074585, complement)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	X	NC_000023.10 (145895624..145896262, complement)

Chromosome X - NC_000023.11 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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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 variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Interactions

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Products	Interactant	Other Gene	Complex	Source	Pubs	Description

General gene information

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Markers

DXS8306 (e-PCR)
- UniSTS:99706

SHGC-100327 (e-PCR)
- UniSTS:185026

General protein information

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Preferred Names: uncharacterized protein CXorf51A

Names: Uncharacterized protein CXorf51B

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.