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Gene: FAM9A (family with sequence similarity 9 member A) Homo sapiens
Symbol: FAM9A
Name: family with sequence similarity 9 member A
Description: This gene is a member of a gene family which arose through duplication on the X chromosome. The encoded protein may be a nuclear protein that is localized to the nucleolus, and has some similarity to a synaptonemal complex protein. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Aug 2011]
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: family with sequence similarity 9, member A; MGC138227; MGC142009; testis expressed 39A; TEX39A
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Human AssemblyChrPosition (strand)SourceGenome Browsers
GRCh38X8,790,795 - 8,801,383 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X8,758,836 - 8,769,424 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X8,718,836 - 8,729,424 (-)NCBINCBI36hg18NCBI36
Build 34X8,568,571 - 8,579,160NCBI
CeleraX12,936,488 - 12,947,076 (-)NCBI
Cytogenetic MapXp22.31NCBI
HuRefX6,585,910 - 6,596,701 (-)NCBIHuRef
CHM1_1X8,790,092 - 8,800,619 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)

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


Comparative Map Data
miRNA Target Status


Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
More on FAM9A
Alliance Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1348978
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-09-12
Status: ACTIVE


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