| Type | Description |
|---|---|
| Definition | TSPY like 1 |
| Date | Results | Publications |
|---|---|---|
| 2018-09-08 11:09:00 | The expression of spermatogenic phenotypes of TSPY1 defects is independent of variations in TSPYL1 and TSPYL5 in the Han Chinese population. | 28847364 |
| 2015-11-14 10:46:00 | Results show that mutations and polymorphisms in the TSPYL1 gene were not associated with sudden infant death syndrome in a cohort of 165 deceased Swiss infants. | 25449952 |
| 2012-03-17 10:31:00 | Mutations in the TSPYL1 gene do not seem to play a major role in the pathogenesis of idiopathic male infertility, and mutation screening of the TSPYL1 gene can currently not be recommended in routine diagnostics of idiopathic male infertility. | 22137496 |
| 2010-01-21 00:00:00 | The chromatin remodeling factor TSPYL1 had a very similar pattern of expression with an incremental increase in HPFH and decreased expression in deltabeta-thalassemia. | 16952470 |
| 2010-01-21 00:00:00 | Mutations in TSPYL1 may contribute to anomalies of testicular development/function. | 19463995 |
| Type | IDs |
|---|---|
| Synonymous | TSPYL |
| Gene |
UniProtKB-ID:
TSYL1_HUMAN
UniprotKB:
Q9H0U9
UniParc:
UPI000006EE16
EMBL:
AL136629,
AL050331,
BC048969,
CH471051,
AF042181
Ensembl:
ENSG00000189241
KO:
hsa:7259
|
| Nucleutide sequences |
EMBL-CDS:
EAW48232.1,
AAC62384.1,
CAB66564.1,
AAH48969.1
Ensembl_TRS:
ENST00000368608,
ENST00000652202
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000498597,
ENSP00000357597
RefSeq:
NP_003300.1
|
| Others |
UniRef100:
UniRef100_Q9H0U9
UniRef90:
UniRef90_Q9H0U9
UniRef50:
UniRef50_Q9H0U9
UniGene:
Hs.458358,
Hs.744978
CCDS:
CCDS34518.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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