Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
57055
Gene name Gene Name - the full gene name approved by the HGNC.
Deleted in azoospermia 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DAZ2
Synonyms (NCBI Gene) Gene synonyms aliases
pDP1678
Chromosome Chromosome number
Y
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Yq11.223
Summary Summary of gene provided in NCBI Entrez Gene.
This gene is a member of the DAZ gene family and is a candidate for the human Y-chromosomal azoospermia factor (AZF). Its expression is restricted to premeiotic germ cells, particularly in spermatogonia. It encodes an RNA-binding protein that is important
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT923348 hsa-miR-1270 CLIP-seq
MIRT923349 hsa-miR-203 CLIP-seq
MIRT923350 hsa-miR-3140-5p CLIP-seq
MIRT923351 hsa-miR-3682-5p CLIP-seq
MIRT923352 hsa-miR-3923 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding TAS 7670487
GO:0003730 Function MRNA 3'-UTR binding IBA 21873635
GO:0005515 Function Protein binding IPI 10857750
GO:0005634 Component Nucleus IEA
GO:0005737 Component Cytoplasm IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
400026 15964 ENSG00000205944
Protein
UniProt ID Q13117
Protein name Deleted in azoospermia protein 2
Protein function RNA-binding protein that plays an essential role in spermatogenesis. May act by binding to the 3'-UTR of mRNAs and regulating their translation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00076 RRM_1 42 109 RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) Domain
PF18872 Daz 170 190 Daz repeat Repeat
PF18872 Daz 194 214 Daz repeat Repeat
PF18872 Daz 218 238 Daz repeat Repeat
PF18872 Daz 242 262 Daz repeat Repeat
PF18872 Daz 266 286 Daz repeat Repeat
PF18872 Daz 290 310 Daz repeat Repeat
PF18872 Daz 314 334 Daz repeat Repeat
PF18872 Daz 338 358 Daz repeat Repeat
PF18872 Daz 362 382 Daz repeat Repeat
PF18872 Daz 386 406 Daz repeat Repeat
PF18872 Daz 410 430 Daz repeat Repeat
PF18872 Daz 434 454 Daz repeat Repeat
PF18872 Daz 458 478 Daz repeat Repeat
PF18872 Daz 482 502 Daz repeat Repeat
PF18872 Daz 506 526 Daz repeat Repeat
Tissue specificity TISSUE SPECIFICITY: Testis specific. {ECO:0000269|PubMed:10936047}.
Sequence
Sequence length 558
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Azoospermia Azoospermia rs200969445, rs144567652, rs765353898
Cryptorchidism Cryptorchidism rs121912555, rs104894697, rs104894698, rs398122886
Non-obstructive azoospermia Non-obstructive azoospermia rs587777872, rs879253743, rs1600840291, rs1600877766, rs753462162, rs1588618614, rs1602684496, rs377712900
Oligospermia Oligospermia rs1602125411, rs377712900
Associations from Text Mining
Disease Name Relationship Type References
Infertility Male Associate 15744033, 37365340
Sertoli Cell Only Syndrome Associate 20823911
Spermatogenic Failure Nonobstructive Y Linked Associate 15744033, 16580401