decreased rib number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A developmental anomaly with absence of one or more ribs. (Human Phenotype Ontology, HP_0000921)
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41 gene mutations causing the decreased rib number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AXIN1 axin 1
BMP4 bone morphogenetic protein 4
BMP5 bone morphogenetic protein 5
BMP7 bone morphogenetic protein 7
BMPER BMP binding endothelial regulator
BMPR2 bone morphogenetic protein receptor, type II (serine/threonine kinase)
CBX2 chromobox homolog 2
CDX1 caudal type homeobox 1
DLL3 delta-like 3 (Drosophila)
EN1 engrailed homeobox 1
FOXC2 forkhead box C2
FST follistatin
HES7 hes family bHLH transcription factor 7
HOXA11 homeobox A11
HOXB6 homeobox B6
HOXB7 homeobox B7
HOXC10 homeobox C10
KMT2A lysine (K)-specific methyltransferase 2A
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
MAP3K4 mitogen-activated protein kinase kinase kinase 4
MDFI MyoD family inhibitor
MLLT3 myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 3
MSGN1 mesogenin 1
NACC1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing
NDC1 NDC1 transmembrane nucleoporin
PDS5B PDS5 cohesin associated factor B
PPP5C protein phosphatase 5, catalytic subunit
PSEN1 presenilin 1
PSIP1 PC4 and SFRS1 interacting protein 1
PTCH1 patched 1
RIPPLY2 ripply transcriptional repressor 2
SHH sonic hedgehog
SLC25A30 solute carrier family 25, member 30
TCF15 transcription factor 15 (basic helix-loop-helix)
TERT telomerase reverse transcriptase
UNCX UNC homeobox
VANGL2 VANGL planar cell polarity protein 2
WDR35 WD repeat domain 35
WFIKKN1 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1
ZC3HC1 zinc finger, C3HC-type containing 1
ZIC3 Zic family member 3