abnormal chest morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the part of the body between the neck and the abdomen (Mammalian Phenotype Ontology, MP_0004134)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004134
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32 gene mutations causing the abnormal chest morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACAN aggrecan
ATR ATR serine/threonine kinase
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CISD2 CDGSH iron sulfur domain 2
COL1A1 collagen, type I, alpha 1
COL2A1 collagen, type II, alpha 1
CREB3L2 cAMP responsive element binding protein 3-like 2
CTGF connective tissue growth factor
DNAH11 dynein, axonemal, heavy chain 11
FBN1 fibrillin 1
FGF18 fibroblast growth factor 18
FGFR3 fibroblast growth factor receptor 3
FGFRL1 fibroblast growth factor receptor-like 1
HOXB4 homeobox B4
HSPG2 heparan sulfate proteoglycan 2
ITPK1 inositol-tetrakisphosphate 1-kinase
NCKAP1L NCK-associated protein 1-like
NF1 neurofibromin 1
NKX2-1 NK2 homeobox 1
NKX3-2 NK3 homeobox 2
NOV nephroblastoma overexpressed
PDGFA platelet-derived growth factor alpha polypeptide
PTCH1 patched 1
PTHLH parathyroid hormone-like hormone
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RIPPLY2 ripply transcriptional repressor 2
RYR1 ryanodine receptor 1 (skeletal)
SLC35D1 solute carrier family 35 (UDP-GlcA/UDP-GalNAc transporter), member D1
SOX11 SRY (sex determining region Y)-box 11
SOX5 SRY (sex determining region Y)-box 5
TBX18 T-box 18
UNCX UNC homeobox