asymmetric rib-sternum attachment Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description loss of bilateral symmetry in rib attachments to the sternum (Mammalian Phenotype Ontology, MP_0008146)
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28 gene mutations causing the asymmetric rib-sternum attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARID5B AT rich interactive domain 5B (MRF1-like)
BMP7 bone morphogenetic protein 7
CHUK conserved helix-loop-helix ubiquitous kinase
CSRNP1 cysteine-serine-rich nuclear protein 1
DPPA4 developmental pluripotency associated 4
EN1 engrailed homeobox 1
FSTL1 follistatin-like 1
GPC3 glypican 3
HOXA10 homeobox A10
HOXA5 homeobox A5
HOXC9 homeobox C9
HOXD3 homeobox D3
HOXD8 homeobox D8
MAP3K4 mitogen-activated protein kinase kinase kinase 4
MLLT3 myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 3
PHC2 polyhomeotic homolog 2 (Drosophila)
PTCH1 patched 1
RPL38 ribosomal protein L38
RPS7 ribosomal protein S7
SCHIP1 schwannomin interacting protein 1
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
SGPL1 sphingosine-1-phosphate lyase 1
SMARCAD1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1
SOX11 SRY (sex determining region Y)-box 11
SSBP3 single stranded DNA binding protein 3
TIPARP TCDD-inducible poly(ADP-ribose) polymerase
TRAF4 TNF receptor-associated factor 4
ZFAND5 zinc finger, AN1-type domain 5