Homo sapiens Gene: FAM9A
Summary
InnateDB Gene IDBG-42366.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FAM9A
Gene Name family with sequence similarity 9, member A
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000183304
Encoded Proteins
family with sequence similarity 9, member A
family with sequence similarity 9, member A
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary 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]
Gene Information
Type Protein coding
Genomic Location Chromosome X:8790795-8801383
Strand Reverse strand
Band p22.31
Transcripts
ENST00000381003 ENSP00000370391
ENST00000543214 ENSP00000440163
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 9 experimentally validated interaction(s) in this database.
Experimentally validated
Total 9 [view]
Protein-Protein 9 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
Cellular Component
GO:0005730 nucleolus
Orthologs
No orthologs found for this gene
Cross-References
SwissProt Q8IZU1
TrEMBL
UniProt Splice Variant
Entrez Gene 171482
UniGene Hs.382062
RefSeq NM_174951 NM_001171186
HUGO HGNC:18403
OMIM 300477
CCDS CCDS14131
HPRD 06506
IMGT
EMBL AF494343 BC112022 BC113449 BC143805
GenPept AAI12023 AAI13450 AAI43806 AAN07162
RNA Seq Atlas 171482