Description |
solute carrier family 14 member 1 (Kidd blood group) |
core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1 |
Image |
|
No pdb structure |
GO Annotations |
Cellular Component |
|
|
Molecular Function |
|
|
Biological Process |
|
|
Pathways |
|
|
Drugs |
|
|
Diseases |
|
|
GWAS |
|
- Aspartate aminotransferase levels ( 33547301)
- Blood protein levels ( 29875488)
- Chronic obstructive pulmonary disease or high blood pressure (pleiotropy) ( 30940143)
- Coronary artery disease ( 29212778)
- Daytime sleep phenotypes ( 27126917)
- Diastolic blood pressure ( 30224653)
- Erosive tooth wear (severe vs non-severe) ( 29898447)
- FEV1 ( 30804560)
- Lung function (FEV1/FVC) ( 28166213 30804560)
- Medication use (agents acting on the renin-angiotensin system) ( 31015401)
- Multiple sclerosis (severity) ( 19010793)
- Night sleep phenotypes ( 27126917)
- Peak expiratory flow ( 30804560)
- Refractive error ( 32231278)
- Serum galactose-deficient IgA1 levels ( 28187132)
- Serum galactose-deficient IgA1 levels in IgA nephropathy ( 33593824)
- Smooth-surface caries ( 24556642)
- Systolic blood pressure ( 26969751)
- Visceral adipose tissue adjusted for BMI ( 22589738)
|
Interacting Genes |
11 interacting genes:
BTN2A2
C1GALT1
FIS1
GIMAP1
MIP
RTP2
SNORC
STRIT1
THSD7B
TMEM97
TMIE
|
32 interacting genes:
ANKS6
ARL13B
C1GALT1C1
CD79A
CPLX4
ELOVL4
FAM209A
FAM210B
GJA8
GJB1
GJB5
GPR101
GPR151
GPR42
GPRC5D
GPX8
GSDME
LEPROT
LEUTX
LHFPL5
MUC1
PIGP
RETREG3
SLC14A1
SLC1A1
SLC7A14
STX1A
TMEM14B
TMEM237
TMEM52B
TRAF6
XRN1
|
Entrez ID |
6563 |
56913 |
HPRD ID |
00195 |
16631 |
Ensembl ID |
ENSG00000141469
|
ENSG00000106392
|
Uniprot IDs |
B4DFJ8
B4DHU3
F5GWS2
G0W2N5
Q13336
|
A0A024RA32
Q9NS00
|
PDB IDs |
6QD5
|
|
Enriched GO Terms of Interacting Partners? |
|
|
Tagcloud ? |
|
|
Tagcloud (Difference) ? |
|
|
Tagcloud (Intersection) ? |
|