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FAM9A family with sequence similarity 9 member A [ Homo sapiens (human) ]

Gene ID: 171482, updated on 11-Jun-2021

Summary

Official Symbol
FAM9Aprovided by HGNC
Official Full Name
family with sequence similarity 9 member Aprovided by HGNC
Primary source
HGNC:HGNC:18403
See related
Ensembl:ENSG00000183304 MIM:300477
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
TEX39A
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]
Expression
Restricted expression toward testis (RPKM 1.9) See more
Orthologs
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Genomic context

See FAM9A in Genome Data Viewer
Location:
Xp22.31
Exon count:
10
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (8790795..8801383, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (8758836..8769424, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene anosmin 1 Neighboring gene dorsal inhibitory axon guidance protein pseudogene 1 Neighboring gene ANAPC15 pseudogene 1 Neighboring gene uncharacterized LOC105373125

Genomic regions, transcripts, and products

Expression

  • 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

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Homology

Clone Names

  • MGC138227, MGC142009

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
Process Evidence Code Pubs
involved_in meiotic cell cycle IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
involved_in spermatid development IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Component Evidence Code Pubs
located_in nucleolus IEA
Inferred from Electronic Annotation
more info
 
is_active_in synaptonemal complex IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 

General protein information

Preferred Names
protein FAM9A
Names
testis expressed 39A

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_016564.2 RefSeqGene

    Range
    5001..15589
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001171186.1NP_001164657.1  protein FAM9A

    See identical proteins and their annotated locations for NP_001164657.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript (1). Both variant 1 and 2 encode the same protein.
    Source sequence(s)
    AC003685, BC143805
    Consensus CDS
    CCDS14131.1
    UniProtKB/Swiss-Prot
    Q8IZU1
    Related
    ENSP00000440163.1, ENST00000543214.1
    Conserved Domains (1) summary
    pfam04803
    Location:277332
    Cor1; Cor1/Xlr/Xmr conserved region
  2. NM_174951.3NP_777611.1  protein FAM9A

    See identical proteins and their annotated locations for NP_777611.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Both variants 1 and 2 encode the same protein.
    Source sequence(s)
    AC003685, AF494343
    Consensus CDS
    CCDS14131.1
    UniProtKB/Swiss-Prot
    Q8IZU1
    Related
    ENSP00000370391.3, ENST00000381003.7
    Conserved Domains (1) summary
    pfam04803
    Location:277332
    Cor1; Cor1/Xlr/Xmr conserved region

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    8790795..8801383 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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