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Gene: FAM47C (family with sequence similarity 47 member C) Homo sapiens
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Symbol: FAM47C
Name: family with sequence similarity 47 member C
Description: This gene encodes a product belonging to a family of proteins with unknown function. The coding sequence of this family member includes several tandemly repeated regions. [provided by RefSeq, Sep 2011]
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: family with sequence similarity 47, member C; putative protein FAM47C
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X37,008,359 - 37,011,666 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X37,026,432 - 37,029,739 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X36,936,391 - 36,939,660 (+)NCBINCBI36hg18NCBI36
CeleraX41,150,900 - 41,154,207 (+)NCBI
Cytogenetic MapXp21.1NCBI
HuRefX34,812,733 - 34,813,039 (+)NCBIHuRef
CHM1_1X37,057,508 - 37,060,815 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM47C
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1605768
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2019-06-18
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.