C1orf21 chromosome 1 open reading frame 21 [Homo sapiens (human)] - Gene

Summary

Official Symbol: C1orf21provided by HGNC
Official Full Name: chromosome 1 open reading frame 21provided by HGNC
Primary source: HGNC:HGNC:15494
See related: Ensembl:ENSG00000116667 AllianceGenome:HGNC:15494
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: PIG13
Expression: Ubiquitous expression in skin (RPKM 14.5), brain (RPKM 10.8) and 23 other tissues See more
Orthologs: mouse all
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Genomic context

Location:: 1q25.3

Exon count:: 6

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	1	NC_000001.11 (184387029..184629019)
RS_2023_10	current	T2T-CHM13v2.0 (GCF_009914755.1)	1	NC_060925.1 (183750271..183992246)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	1	NC_000001.10 (184356163..184598153)

Chromosome 1 - NC_000001.11 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Expression

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See details

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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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Submit: New GeneRIF Correction

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

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

AL033847 (e-PCR)
- UniSTS:93723

D1S1846E (e-PCR)
- UniSTS:288

AL033873 (e-PCR)
- UniSTS:93749

RH77882 (e-PCR)
- UniSTS:69186

AL009811 (e-PCR)
- UniSTS:73296

AL034231 (e-PCR)
- UniSTS:94048

G32782 (e-PCR)
- UniSTS:117362

A009Q28 (e-PCR)
- UniSTS:80791

SHGC-80787 (e-PCR)
- UniSTS:102311

SHGC-76052 (e-PCR)
- UniSTS:53960

D1S1866E (e-PCR)
- UniSTS:4046

D1S2249 (e-PCR)
- UniSTS:78549

RH26692 (e-PCR)
- UniSTS:88804

A009C04 (e-PCR)
- UniSTS:2302

G32403 (e-PCR)
- UniSTS:116990

Gene Ontology Provided by GOA

Function	Evidence Code	Pubs
enables protein binding	IPI Inferred from Physical Interaction more info	PubMed

General protein information

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Preferred Names: uncharacterized protein C1orf21

Names: cell proliferation-inducing gene 13 protein; proliferation-inducing protein 13

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.