decreased trabecular bone thickness Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description thinner than normal bone with a lattice-like or spongy structure (Mammalian Phenotype Ontology, MP_0009346)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009346
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Genes

30 gene mutations causing the decreased trabecular bone thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AKR1A1 aldo-keto reductase family 1, member A1 (aldehyde reductase)
CASP3 caspase 3, apoptosis-related cysteine peptidase
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CHSY1 chondroitin sulfate synthase 1
CISD2 CDGSH iron sulfur domain 2
CIT citron rho-interacting serine/threonine kinase
CLDN18 claudin 18
CLEC2D C-type lectin domain family 2, member D
CNOT3 CCR4-NOT transcription complex, subunit 3
CREB3L1 cAMP responsive element binding protein 3-like 1
CSF1 colony stimulating factor 1 (macrophage)
CTGF connective tissue growth factor
CTHRC1 collagen triple helix repeat containing 1
FAM20C family with sequence similarity 20, member C
ID1 inhibitor of DNA binding 1, dominant negative helix-loop-helix protein
IGHM immunoglobulin heavy constant mu
IL10 interleukin 10
IL6ST interleukin 6 signal transducer
INPP5D inositol polyphosphate-5-phosphatase, 145kDa
IRS1 insulin receptor substrate 1
MGP matrix Gla protein
NACA nascent polypeptide-associated complex alpha subunit
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
NLRP3 NLR family, pyrin domain containing 3
PRKACA protein kinase, cAMP-dependent, catalytic, alpha
RASSF2 Ras association (RalGDS/AF-6) domain family member 2
SUCO SUN domain containing ossification factor
THRB thyroid hormone receptor, beta
TRPV5 transient receptor potential cation channel, subfamily V, member 5
WWOX WW domain containing oxidoreductase