SPANXB1 wt Allele

Preferred Label : SPANXB1 wt Allele;

NCIt synonyms : SPANXB; Cancer/Testis Antigen Family 11, Member 2 Gene; Sperm Protein Associated With the Nucleus, X-Linked, Family Member B1 Gene; SPANX Family, Member B1 wt Allele; Sperm Protein Associated With the Nucleus on the X Chromosome B/F Gene; SPANX-B; Sperm Protein Associated With the Nucleus, X Chromosome, Family Member B1 Gene; SPANXB2; B1; SPANXF1; CT11.2;

NCIt definition : Human SPANXB1 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 play a role in gametogenesis.;

NCIt note : The genes for SPANXB1 and SPANXB2 are found in a head-to-head orientation on the X chromosome. (EntrezGene);

GenBank Accession Number : NM_032461;

Details

Origin ID

C92965;

UMLS CUI

C2985365;

Automatic exact mappings (from CISMeF team)
- Apical segmental bronchus [FMA entity]
- Bardet-Biedl syndrome 9 [ORDO Gene]
- Membrane-spanning 4 domains, subfamily a, member 1 [OMIM gene]
- Parathyroid hormone-responsive b1 gene [OMIM gene]
- Spanx family, member b1 [OMIM gene]
- membrane spanning 4-domains A1 [ORDO Gene]
- risarestat [MeSH Supplementary Concept]
OMIM relation
- Spanx family, member b1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
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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