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SPANXA2 SPANX family member A2 [ Homo sapiens (human) ]

Gene ID: 728712, updated on 28-Oct-2024

Summary

Official Symbol
SPANXA2provided by HGNC
Official Full Name
SPANX family member A2provided by HGNC
Primary source
HGNC:HGNC:14328
See related
Ensembl:ENSG00000203926 MIM:300493; AllianceGenome:HGNC:14328
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
SPANX; CT11.1; CT11.3; SPANXA; SPANXC; SPANX-A; SPANX-C
Summary
Temporally regulated transcription and translation of several testis-specific genes is required to initiate the series of molecular and morphological changes in the male germ cell lineage necessary for the formation of mature spermatozoa. This gene is a member of the SPANX family of cancer/testis-associated genes, which are located in a cluster on chromosome X. The SPANX genes encode differentially expressed testis-specific proteins that localize to various subcellular compartments. This particular gene maps to chromosome X in a head-to-head orientation with SPANX family member A1 and appears to be a duplication of that locus. The protein encoded by this gene targets to the nucleus where it associates with nuclear vacuoles and the redundant nuclear envelope. Based on its association with these poorly characterized regions of the sperm nucleus, this protein provides a biochemical marker to study unique structures in spermatazoa while attempting to further define its role in spermatogenesis. [provided by RefSeq, Jul 2008]
Expression
Restricted expression toward testis (RPKM 14.3) See more
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Genomic context

See SPANXA2 in Genome Data Viewer
Location:
Xq27.2
Exon count:
2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (141589708..141590762)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (139898434..139899488)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (140677835..140678889)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene NADH:ubiquinone oxidoreductase subunit B3 pseudogene 5 Neighboring gene SPANXA2 overlapping transcript 1 Neighboring gene sperm protein associated with the nucleus, X-linked, family member A1 Neighboring gene uncharacterized LOC645188 Neighboring gene SPANX family member D

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues 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

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 spermatogenesis TAS
Traceable Author Statement
more info
PubMed 
Component Evidence Code Pubs
located_in cytoplasm IEA
Inferred from Electronic Annotation
more info
 
located_in nucleus HDA PubMed 

General protein information

Preferred Names
sperm protein associated with the nucleus on the X chromosome A
Names
Cancer/testis antigen 11.3
Cancer/testis-associated protein CTp11
Nuclear-associated protein SPAN-Xc
SPANX family member A
Sperm protein associated with the nucleus on the X chromosome C
cancer/testis antigen 11.1
nuclear-associated protein SPAN-Xa
sperm protein associated with the nucleus, X chromosome, family member A2

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.

mRNA and Protein(s)

  1. NM_145662.4NP_663695.1  sperm protein associated with the nucleus on the X chromosome A

    See identical proteins and their annotated locations for NP_663695.1

    Status: REVIEWED

    Source sequence(s)
    CB110020
    Consensus CDS
    CCDS44007.1
    UniProtKB/Swiss-Prot
    Q5JWI0, Q9NS26
    UniProtKB/TrEMBL
    A0FGV1, Q4KRI2
    Related
    ENSP00000359549.3, ENST00000370518.4
    Conserved Domains (1) summary
    pfam07458
    Location:281
    SPAN-X; Sperm protein associated with nucleus, mapped to X chromosome

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    141589708..141590762
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    139898434..139899488
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)