| Type | Description |
|---|---|
| Definition | solute carrier family 26 member 8 |
| Date | Results | Publications |
|---|---|---|
| 2013-07-06 10:31:00 | Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia. | 23582645 |
| 2010-09-15 22:06:00 | Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) | 20628086 |
| 2010-09-15 22:06:00 | Observational study of gene-disease association. (HuGE Navigator) | 19913121 |
| 2010-06-30 22:07:00 | Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | 20379614 |
| 2010-01-21 00:00:00 | structural defects in sperm are not caused by abnormal transcription or point mutations of the TAT1 and SEPT4 genes; however, although both proteins are expressed, they are not properly localized at sperm annulus | 19221096 |
| Type | IDs |
|---|---|
| Synonymous | SPGF3, TAT1 |
| Gene |
UniProtKB-ID:
S26A8_HUMAN,
A0A024RCV0_HUMAN
UniprotKB:
Q96RN1,
A0A024RCV0
UniParc:
UPI000022CB99,
UPI00004A3A2E,
UPI000013F0A0,
UPI00000739C0
EMBL:
Z95152,
AL133507,
AK057276,
AF314959,
AF403499,
BC025408,
CH471081,
AF331522
Ensembl:
ENSG00000112053
KO:
hsa:116369
|
| Nucleutide sequences |
EMBL-CDS:
AAO26699.1,
AAK95666.1,
BAB71408.1,
EAX03862.1,
AAL26868.1,
AAH25408.1,
EAX03866.1,
EAX03863.1
Gene_ORFName:
hCG_2001149
Ensembl_TRS:
ENST00000355574,
ENST00000490799,
ENST00000394602
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000417638,
ENSP00000347778,
ENSP00000378100
RefSeq:
XP_011512596.1,
NP_001180405.1,
XP_016865724.1,
NP_443193.1,
NP_619732.2
|
| Others |
UniRef100:
UniRef100_Q96RN1
UniRef90:
UniRef90_Q96RN1
UniRef50:
UniRef50_Q96RN1
UniGene:
Hs.435836
CCDS:
CCDS4814.1,
CCDS4813.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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