short sternum Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Decreased inferosuperior length of the sternum. (Human Phenotype Ontology, HP_0000879)
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29 gene mutations causing the short sternum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CHUK conserved helix-loop-helix ubiquitous kinase
COL27A1 collagen, type XXVII, alpha 1
CTGF connective tissue growth factor
DCHS1 dachsous cadherin-related 1
EN1 engrailed homeobox 1
FAT4 FAT atypical cadherin 4
FGF9 fibroblast growth factor 9
FGFRL1 fibroblast growth factor receptor-like 1
GLI2 GLI family zinc finger 2
GLI3 GLI family zinc finger 3
IGF2R insulin-like growth factor 2 receptor
IMPAD1 inositol monophosphatase domain containing 1
IRF6 interferon regulatory factor 6
MKS1 Meckel syndrome, type 1
MYF5 myogenic factor 5
MYOG myogenin (myogenic factor 4)
PDS5B PDS5 cohesin associated factor B
PSEN1 presenilin 1
PSIP1 PC4 and SFRS1 interacting protein 1
PTHLH parathyroid hormone-like hormone
SIK3 SIK family kinase 3
SMARCAD1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1
SOX5 SRY (sex determining region Y)-box 5
SOX9 SRY (sex determining region Y)-box 9
SULF1 sulfatase 1
TMEM107 transmembrane protein 107
TRPS1 trichorhinophalangeal syndrome I
ZEB1 zinc finger E-box binding homeobox 1