neurohypophyseal diabetes insipidus Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_12388)
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Genes

52 genes co-occuring with the disease neurohypophyseal diabetes insipidus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
AVP arginine vasopressin 2.9018
NPTX2 neuronal pentraxin II 1.9811
AQP2 aquaporin 2 (collecting duct) 1.71499
AVPR2 arginine vasopressin receptor 2 1.63993
UBOX5 U-box domain containing 5 1.51018
OXT oxytocin/neurophysin I prepropeptide 1.30357
POMC proopiomelanocortin 1.28916
ZFPL1 zinc finger protein-like 1 1.03872
CRH corticotropin releasing hormone 1.02692
CLCNKA chloride channel, voltage-sensitive Ka 1.02144
WFS1 Wolfram syndrome 1 (wolframin) 0.906086
GHRH growth hormone releasing hormone 0.876148
PRL prolactin 0.792541
PCSK1 proprotein convertase subtilisin/kexin type 1 0.763902
TRH thyrotropin-releasing hormone 0.728143
REN renin 0.619051
ILVBL ilvB (bacterial acetolactate synthase)-like 0.613183
CLCNKB chloride channel, voltage-sensitive Kb 0.607714
AVPR1A arginine vasopressin receptor 1A 0.60147
ARHGAP4 Rho GTPase activating protein 4 0.588612
AQP3 aquaporin 3 (Gill blood group) 0.536957
HIRA histone cell cycle regulator 0.526518
LHX4 LIM homeobox 4 0.51534
IGF1 insulin-like growth factor 1 (somatomedin C) 0.510728
INS insulin 0.491597
NPS neuropeptide S 0.471846
GLI2 GLI family zinc finger 2 0.461639
CA10 carbonic anhydrase X 0.456732
FNDC3A fibronectin type III domain containing 3A 0.429642
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone) 0.42214
CUTA cutA divalent cation tolerance homolog (E. coli) 0.41465
NPTN neuroplastin 0.412779
L1CAM L1 cell adhesion molecule 0.392257
ZIC2 Zic family member 2 0.379256
PIK3C3 phosphatidylinositol 3-kinase, catalytic subunit type 3 0.378885
C5ORF38 chromosome 5 open reading frame 38 0.377773
SOX3 SRY (sex determining region Y)-box 3 0.374809
C2 complement component 2 0.366301
BSND barttin CLCNK-type chloride channel accessory beta subunit 0.360395
HESX1 HESX homeobox 1 0.351555
CYS1 cystin 1 0.337608
NPPA natriuretic peptide A 0.313552
SLC17A7 solute carrier family 17 (vesicular glutamate transporter), member 7 0.309928
DHX9 DEAH (Asp-Glu-Ala-His) box helicase 9 0.301254
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1 0.265849
RPN1 ribophorin I 0.206248
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1 0.195183
TRPV4 transient receptor potential cation channel, subfamily V, member 4 0.193285
APEH acylaminoacyl-peptide hydrolase 0.189244
HADHA hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit 0.182086
ADCY2 adenylate cyclase 2 (brain) 0.171785
GLO1 glyoxalase I 0.169571