DAZAP2

Protein-coding gene in humans From Wikipedia, the free encyclopedia

DAZ-associated protein 2 is a protein that in humans is encoded by the DAZAP2 gene.[5][6][7]

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DAZAP2
Identifiers
AliasesDAZAP2, PRTB, DAZ associated protein 2
External IDsOMIM: 607431; MGI: 1344344; HomoloGene: 8038; GeneCards: DAZAP2; OMA:DAZAP2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_011873

RefSeq (protein)

NP_036003

Location (UCSC)Chr 12: 51.24 – 51.27 MbChr 15: 100.51 – 100.52 Mb
PubMed search[3][4]
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Function

In mammals, the Y chromosome directs the development of the testes and plays an important role in spermatogenesis. A high percentage of infertile men have deletions that map to regions of the Y chromosome. The DAZ (deleted in azoospermia) gene cluster maps to the AZFc region and is deleted in many azoospermic and severely oligospermic men. It is thought that the Y chromosomal DAZ gene cluster arose from the transposition, amplification, and pruning of the ancestral autosomal gene DAZL. This gene encodes a RNA-binding protein with two RNP motifs that was originally identified by its interaction with the infertility factors DAZ and DAZL.[7]

Interactions

DAZAP2 has been shown to interact with DAZ1.[8]

References

Further reading

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