abnormal sternebra morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of one segments of the primordial sternum of the embryo; these segments fuse to form the body of the adult vertebrate sternum (Mammalian Phenotype Ontology, MP_0004322)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004322
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Genes

45 gene mutations causing the abnormal sternebra morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP5 bone morphogenetic protein 5
BMPR1B bone morphogenetic protein receptor, type IB
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CBX2 chromobox homolog 2
CHUK conserved helix-loop-helix ubiquitous kinase
COL27A1 collagen, type XXVII, alpha 1
CTGF connective tissue growth factor
DERL2 derlin 2
DLL3 delta-like 3 (Drosophila)
EFNB1 ephrin-B1
EN1 engrailed homeobox 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FLNB filamin B, beta
FOXC1 forkhead box C1
FRAS1 Fraser extracellular matrix complex subunit 1
GLI3 GLI family zinc finger 3
HOXA10 homeobox A10
HOXA4 homeobox A4
HOXA5 homeobox A5
HOXB2 homeobox B2
HOXB4 homeobox B4
HOXB7 homeobox B7
HOXB8 homeobox B8
HOXB9 homeobox B9
HOXC4 homeobox C4
HOXC8 homeobox C8
HSPB11 heat shock protein family B (small), member 11
IFT27 intraflagellar transport 27
KAT2A K(lysine) acetyltransferase 2A
KMT2A lysine (K)-specific methyltransferase 2A
MYOG myogenin (myogenic factor 4)
PAX1 paired box 1
RPL38 ribosomal protein L38
RPS7 ribosomal protein S7
SOX11 SRY (sex determining region Y)-box 11
SOX9 SRY (sex determining region Y)-box 9
SSBP3 single stranded DNA binding protein 3
SULF1 sulfatase 1
SULF2 sulfatase 2
TASP1 taspase, threonine aspartase, 1
TSHZ1 teashirt zinc finger homeobox 1
VANGL2 VANGL planar cell polarity protein 2
ZBTB16 zinc finger and BTB domain containing 16
ZEB1 zinc finger E-box binding homeobox 1