increased body length Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased measure of the head and trunk (head, thorax and abdomen) in the rostral-caudal direction (Mammalian Phenotype Ontology, MP_0001257)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001257
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Genes

30 gene mutations causing the increased body length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANKRD26 ankyrin repeat domain 26
ASIP agouti signaling protein
CBX7 chromobox homolog 7
CEP19 centrosomal protein 19kDa
COL1A1 collagen, type I, alpha 1
CPE carboxypeptidase E
ESR2 estrogen receptor 2 (ER beta)
FGF21 fibroblast growth factor 21
FGL1 fibrinogen-like 1
GCG glucagon
IL1R1 interleukin 1 receptor, type I
LEP leptin
LEPR leptin receptor
LTA lymphotoxin alpha
MC4R melanocortin 4 receptor
MRAP2 melanocortin 2 receptor accessory protein 2
NGFR nerve growth factor receptor
NPR3 natriuretic peptide receptor 3
POMC proopiomelanocortin
PPP1R3A protein phosphatase 1, regulatory subunit 3A
PRLHR prolactin releasing hormone receptor
RDH16 retinol dehydrogenase 16 (all-trans)
SIM1 single-minded family bHLH transcription factor 1
SMG1 SMG1 phosphatidylinositol 3-kinase-related kinase
SOCS2 suppressor of cytokine signaling 2
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
STC2 stanniocalcin 2
TNF tumor necrosis factor
TXNDC2 thioredoxin domain containing 2 (spermatozoa)
WBP5 WW domain binding protein 5