Type | Description |
---|---|
Definition | solute carrier family 6 member 15 |
Date | Results | Publications |
---|---|---|
2019-12-14 10:13:00 | Fine-scale haplotype mapping of MUT, AACS, SLC6A15 and PRKCA genes indicates association with insulin resistance of metabolic syndrome and relationship with branched chain amino acid metabolism or regulation. | 30913280 |
2017-11-25 14:10:00 | We observed an association between the SLC6A15 rs1545843 and resting-state brain function of the corpus callosum, cingulum and the frontal, parietal, and temporal lobes in MDD patients, which may be involved in the pathogenesis of Major Depressive Disorder. There was no interaction between rs1545843 genotypes and disease status. | 28915082 |
2017-07-08 12:09:00 | This study provides the first evidence that, at least among Han Chinese patients with PD, AA genotype at rs1545843 in the SLC6A15 gene. | 28320136 |
2017-04-29 10:38:00 | an association between the risk allele of the SLC6A15 gene rs1545843 and the White Matter Tracts integrity of the PHC in Major Depressive Disorder patients, which is known to play an important role in the neural circuit involved in emotion processing. | 27723767 |
2013-10-19 11:38:00 | The SLC6A15 gene plays a role in adrenocorticotropic hormone (ACTH) and cortisol secretion during cognitive impairments in unipolar depression. | 22475622 |
Type | IDs |
---|---|
Synonymous | NTT73, SBAT1, V7-3, hv7-3 |
Gene |
UniProtKB-ID:
S6A15_HUMAN,
Q8IXG2_HUMAN,
Q9NW50_HUMAN
UniprotKB:
Q9H2J7,
Q8IXG2,
Q9NW50
UniParc:
UPI00000743B6,
UPI0000073283,
UPI000006DAF5,
UPI0001914B71,
UPI0000038BF2
EMBL:
AF265577,
AK022853,
BC070040,
AK294945,
AK001178,
AK291207,
AC018922,
CH471054,
AF351619,
AC128657
Ensembl:
ENSG00000072041
KO:
hsa:55117
|
Nucleutide sequences |
EMBL-CDS:
AAG41361.1,
BAF83896.1,
BAB14274.1,
EAW97389.1,
BAH11933.1,
AAH70040.1,
AAN76519.1,
BAA91536.1
Ensembl_TRS:
ENST00000552192,
ENST00000450363,
ENST00000266682
|
Protein sequencees |
Ensembl_PRO:
ENSP00000266682,
ENSP00000390706,
ENSP00000450145
RefSeq:
NP_877499.1,
XP_011536827.1,
NP_060527.2,
NP_001139807.1
|
Others |
UniRef100:
UniRef100_Q9H2J7,
UniRef100_Q8IXG2,
UniRef100_Q9NW50
UniRef90:
UniRef90_Q9H2J7,
UniRef90_Q9NW50,
UniRef90_F8WJN6
UniRef50:
UniRef50_Q9NW50,
UniRef50_Q9H2J7,
UniRef50_F8WJN6
UniGene:
Hs.44424
CCDS:
CCDS9027.1,
CCDS53816.1,
CCDS9026.1
|
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Refseq |
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