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Gene: FAM47A (family with sequence similarity 47 member A) Homo sapiens
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Symbol: FAM47A
Name: family with sequence similarity 47 member A
Description: ASSOCIATED WITH autistic disorder; Malformations of Cortical Development, Group II; Neurodevelopmental Disorders; INTERACTS WITH valproic acid
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: family with sequence similarity 47, member A; hypothetical protein LOC158724; MGC27003
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblX34,129,756 - 34,132,314 (-)Ensembl
GRCh38X34,129,752 - 34,132,330 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X34,147,869 - 34,150,447 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X34,057,794 - 34,060,349 (-)NCBINCBI36hg18NCBI36
Build 34X33,907,533 - 33,910,085NCBI
CeleraX38,275,096 - 38,277,674 (-)NCBI
Cytogenetic MapXp21.1NCBI
HuRefX31,885,862 - 31,888,440 (-)NCBIHuRef
CHM1_1X34,178,212 - 34,180,790 (-)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

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM47A
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1347430
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-12-25
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.