Uromodulin

AltitudeomicsDB
Protein Official symbol UMOD
Aliases UMOD
Chromosomal Location 16
Length 640
Uniprot ID P07911
EC number None
Protein family Information(Pfam) PF12947;PF07645;PF00100;
PDB id 4WRN;
InterPro ID IPR001881;IPR013032;IPR000742;IPR000152;IPR018097;IPR024731;IPR009030;IPR001507;IPR017977;
dbSNP rs121917768 rs28934584 rs780462125 rs1555487621 rs121917769 rs121917770 rs28934582 rs28934583 rs28934583 rs1447458978 rs886043751 rs121917771 rs121917772 rs121917773 rs1555487318 rs55772253

Protein Protein Interaction

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AltitudeomicsDB
Protein 1 Protein 2 Combine Score
UMOD B4GALNT2 0.947
Gene Ontology Semantic Similarity
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# 7369 (UMOD) 124872 (B4GALNT2)
7369 (UMOD) 1.00 0.08
124872 (B4GALNT2) 0.08 1.00
Association with High Altitude
Protein Official symbol Source Organism Tissue of Expression Level of hypoxia Altitude Duration of experiment Level of expression Fold change Experiment details geographical location ethnicity of the patients Control group Control (Fold change) Reference (PMID)
UMOD Human Urine - 5400 m 5 day downregulated - MALDI-TOF/TOF of petides Himalayas Italians - Males and females residing < 500 m above sea level 22146998
UMOD Human Urine - 5400 m 5 day downregulated - MALDI-TOF/TOF of petides Himalayas Italians - Males and females residing < 500 m above sea level 22146999
UMOD Human Urine - 3500 m 3 day downregulated - MALDI-TOF/TOF of petides Himalayas Italians - Males and females residing < 500 m above sea level 22146999
UMOD Human Urine - 3500 m 3 day downregulated - MALDI-TOF/TOF of petides Himalayas Italians - Males and females residing < 500 m above sea level 22146998
Association with TF
TF TF Entrez Gene Gene Entrez Type PMID Database
HNF1B 6928 UMOD 7369 Repression 23836662 TRUSST
Association with miRNA
miRTarBase ID miRNA Species (miRNA) Protein Official Symbol Human Entrez ID Species (Target Gene) Experiments Support Type References (PMID)
Gene Ontology
ID GO ID GO Term GO Type
7369 GO:0072218 metanephric ascending thin limb development GOTERM_BP_DIRECT
7369 GO:0007159 leukocyte cell-cell adhesion GOTERM_BP_DIRECT
7369 GO:0031225 anchored component of membrane GOTERM_CC_DIRECT
7369 GO:0072233 metanephric thick ascending limb development GOTERM_BP_DIRECT
7369 GO:0072221 metanephric distal convoluted tubule development GOTERM_BP_DIRECT
7369 GO:0007588 excretion GOTERM_BP_DIRECT
7369 GO:0005509 calcium ion binding GOTERM_MF_DIRECT
7369 GO:0006968 cellular defense response GOTERM_BP_DIRECT
7369 GO:0016021 integral component of membrane GOTERM_CC_DIRECT
7369 GO:0016324 apical plasma membrane GOTERM_CC_DIRECT
7369 GO:0070062 extracellular exosome GOTERM_CC_DIRECT
7369 GO:0008285 negative regulation of cell proliferation GOTERM_BP_DIRECT
7369 GO:0019898 extrinsic component of membrane GOTERM_CC_DIRECT
7369 GO:0048878 chemical homeostasis GOTERM_BP_DIRECT
7369 GO:1990266 neutrophil migration GOTERM_BP_DIRECT
7369 GO:0000922 spindle pole GOTERM_CC_DIRECT
7369 GO:0072372 primary cilium GOTERM_CC_DIRECT
7369 GO:0005578 proteinaceous extracellular matrix GOTERM_CC_DIRECT
7369 GO:0016323 basolateral plasma membrane GOTERM_CC_DIRECT
7369 GO:0007157 heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules GOTERM_BP_DIRECT
7369 GO:2000021 regulation of ion homeostasis GOTERM_BP_DIRECT
7369 GO:0019864 calcium channel inhibitor activity GOTERM_MF_DIRECT
7369 GO:0005929 cilium GOTERM_CC_DIRECT
7369 GO:0005201 extracellular matrix structural constituent GOTERM_MF_DIRECT
7369 GO:0005576 extracellular region GOTERM_CC_DIRECT
7369 GO:0060170 ciliary membrane GOTERM_CC_DIRECT
Pathways
Human Entrez ID KEGG ID KEGG Term
Association with Disease
Protein Official Symbol Human Entrez ID Disease Name Disease Id Disease Semantic Type Semantic score DSI DPI Disease Type
UMOD 7369 Hypertensive disease C0020538 Disease or Syndrome 0.5 0.6 0.517 group
UMOD 7369 Kidney Diseases C0022658 Disease or Syndrome 0.7 0.6 0.517 group
UMOD 7369 Familial juvenile gout C0268113 Disease or Syndrome 1 0.6 0.517 disease
UMOD 7369 Medullary Cystic Kidney Disease Type 2 C1859040 Disease or Syndrome 0.78 0.6 0.517 disease
UMOD 7369 Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria C1835934 Disease or Syndrome 0.6 0.6 0.517 disease
UMOD 7369 Cystic Kidney Diseases C1691228 Disease or Syndrome 0.34 0.6 0.517 group
UMOD 7369 Cakut C1968949 Disease or Syndrome 0.3 0.6 0.517 disease
UMOD 7369 Ciliopathies C4277690 Congenital Abnormality 0.3 0.6 0.517 group
Association with Drug
Protein Official Symbol Human Entrez ID drug_claim_primary_name drug_name drug_chembl_id interaction_types
UMOD 7369 LYMPHOKINES None None None
UMOD 7369 VITAMIN A RETINOL CHEMBL986 None