Identity
HGNC
LOCATION
17p13.2
LOCUSID
ALIAS
NYD-SP20,NYDSP20
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 84690
MIM: 617673
HGNC: 30705
Ensembl: ENSG00000141255
Variants:
dbSNP: 84690
ClinVar: 84690
TCGA: ENSG00000141255
COSMIC: SPATA22
RNA/Proteins
Expression (GTEx)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35285020 | 2022 | Bi-allelic SPATA22 variants cause premature ovarian insufficiency and nonobstructive azoospermia due to meiotic arrest. | 5 |
| 36331299 | 2022 | Nuclear localization of human MEIOB requires its NLS in the OB domain and interaction with SPATA22. | 0 |
| 35285020 | 2022 | Bi-allelic SPATA22 variants cause premature ovarian insufficiency and nonobstructive azoospermia due to meiotic arrest. | 5 |
| 36331299 | 2022 | Nuclear localization of human MEIOB requires its NLS in the OB domain and interaction with SPATA22. | 0 |
| 33812231 | 2021 | The meiosis-specific MEIOB-SPATA22 complex cooperates with RPA to form a compacted mixed MEIOB/SPATA22/RPA/ssDNA complex. | 9 |
| 34392356 | 2021 | Whole-exome sequencing of consanguineous families with infertile men and women identifies homologous mutations in SPATA22 and MEIOB. | 14 |
| 33812231 | 2021 | The meiosis-specific MEIOB-SPATA22 complex cooperates with RPA to form a compacted mixed MEIOB/SPATA22/RPA/ssDNA complex. | 9 |
| 34392356 | 2021 | Whole-exome sequencing of consanguineous families with infertile men and women identifies homologous mutations in SPATA22 and MEIOB. | 14 |
| 23675907 | 2013 | Expression analysis of MND1/GAJ, SPATA22, GAPDHS and ACR genes in testicular biopsies from non-obstructive azoospermia (NOA) patients. | 10 |
| 23675907 | 2013 | Expression analysis of MND1/GAJ, SPATA22, GAPDHS and ACR genes in testicular biopsies from non-obstructive azoospermia (NOA) patients. | 10 |
| 20378615 | 2010 | Evaluation of 172 candidate polymorphisms for association with oligozoospermia or azoospermia in a large cohort of men of European descent. | 61 |
| 20378615 | 2010 | Evaluation of 172 candidate polymorphisms for association with oligozoospermia or azoospermia in a large cohort of men of European descent. | 61 |
Citation
Dessen P
SPATA22 (spermatogenesis associated 22)
Atlas Genet Cytogenet Oncol Haematol. 2013-07-01
Online version: http://atlasgeneticsoncology.org/gene/53472/spata22-(spermatogenesis-associated-22)
