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C9orf47 chromosome 9 open reading frame 47 [ Homo sapiens (human) ]

Gene ID: 286223, discontinued on 13-Aug-2021

Summary

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Official Symbol
C9orf47provided by HGNC
Official Full Name
chromosome 9 open reading frame 47provided by HGNC
Primary source
HGNC:HGNC:23669
Gene type
protein coding
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
C9orf108; bA791O21.3
Expression
Broad expression in adrenal (RPKM 1.0), prostate (RPKM 0.6) and 21 other tissues See more
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Genomic context

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Location:
9q22.1
Annotation release Status Assembly Chr Location
109.20210514 latest, but not current GRCh38.p13 (GCF_000001405.39) 9 NC_000009.12 (88990863..88996142)

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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GeneRIFs: Gene References Into Functions

Phenotypes

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

EBI GWAS Catalog

Description
Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial.
EBI GWAS Catalog

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh38)

Genotypes

General gene information

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Clone Names

  • FLJ37523

General protein information

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Names
chromosome 9 open reading frame 47
uncharacterized protein C9orf47
Nucleotide Protein
Heading Accession and Version

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