Description |
catechol-O-methyltransferase |
solute carrier family 48 member 1 |
Image |
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No pdb structure |
Cellular Component |
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Molecular Function |
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Biological Process |
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Pathways |
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Drugs |
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Diseases |
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GWAS |
- Blood metabolite levels ( 24816252)
- Serum metabolite levels ( 23093944)
- Systolic blood pressure x alcohol consumption interaction (2df test) ( 29912962)
- Urinary metabolite levels in chronic kidney disease ( 31959995)
- Urinary metabolite modules (eigenmetabolites) in chronic kidney disease ( 31959995)
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- Asthma (adult onset) ( 31036433)
- Bipolar disorder ( 31043756)
- Chronic obstructive pulmonary disease or high blood pressure (pleiotropy) ( 30940143)
- High light scatter reticulocyte count ( 32888494)
- High light scatter reticulocyte percentage of red cells ( 32888494)
- Immature fraction of reticulocytes ( 32888494)
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Interacting Genes |
68 interacting genes:
ACE
AQP7
AVPR2
BEST2
CCL4L2
CDC27
CDC42
CNR2
CREB3L1
EMD
FAM209A
FFAR3
GET1
GJB1
GJB3
GJB4
GJB5
GLP1R
GPR152
GPR161
GPR42
HIBADH
HSD3B7
KCNK5
KRT31
KRT40
KRTAP5-9
LITAF
MFSD14B
MTNR1A
MYADML2
NIPAL4
OTOP3
PGAP2
PLPP6
REEP4
RGS2
RHBDD2
RHBDL1
S1PR3
SELENOK
SLC10A6
SLC16A7
SLC2A5
SLC35A4
SLC35F1
SLC39A1
SLC39A2
SLC48A1
SLC7A1
SLC7A8
SMIM1
THSD7A
TLCD4
TMEM100
TMEM120B
TMEM14B
TMEM14C
TMEM187
TMEM205
TMEM222
TMEM50A
TRHR
TRIP13
VAMP3
VAMP5
VKORC1
XRN2
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7 interacting genes:
APP
COMT
LAMP1
MEOX2
TMEM14B
TMEM159
UNC93A
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Entrez ID |
1312 |
55652 |
HPRD ID |
00284 |
07916 |
Ensembl ID |
ENSG00000093010
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ENSG00000211584
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Uniprot IDs |
A0A140VJG8
P21964
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Q6P1K1
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PDB IDs |
3A7E
3BWM
3BWY
4PYI
4PYJ
4PYK
4XUC
4XUD
4XUE
5LSA
6I3C
6I3D
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
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Tagcloud (Difference) ? |
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Tagcloud (Intersection) ? |
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