SPANXB2 wt Allele

Preferred Label : SPANXB2 wt Allele;

NCIt synonyms : SPANXB1; SPANX Family, Member B2 wt Allele; SPANXB; Sperm Protein Associated With the Nucleus on the X Chromosome B/F Gene; Sperm Protein Associated With the Nucleus, X-Linked, Family Member B2 Gene; SPANX; SPANXF1; Sperm Protein Associated With the Nucleus, X Chromosome, Family Member B2 Gene; Cancer/Testis Antigen Family 11, Member 2 Gene; CT11.2;

NCIt definition : Human SPANXB2 wild-type allele is located in the vicinity of Xq27.1 and is approximately 1 kb in length. This allele, which encodes sperm protein associated with the nucleus on the X chromosome B/F protein, may be involved in spermatid development.;

NCIt note : The genes for SPANXB1 and SPANXB2 are found in a head-to-head orientation on the X chromosome. (EntrezGene); HGNC has noted symbol withdrawn, see SPANXB1.;

GenBank Accession Number : NM_145664;

Details

Origin ID

C92967;

UMLS CUI

C2985366;

Automatic exact mappings (from CISMeF team)
- Spanx family, member D [OMIM gene]
- Spanx family, member b1 [OMIM gene]
- Spanx family, member e [OMIM gene]
- Sperm protein associated with the nucleus, X chromosome, family member a1 [OMIM gene]
- risarestat [MeSH Supplementary Concept]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- Xq27.1 [NCIt concept]
gene_plays_role_in_process
- Spermatogenesis [NCIt concept]

Keyword's position in hierarchy(ies) :

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