abnormal rostral-caudal body axis extension Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in or failure of the long (rostral-caudal) axis of the body to elongate normally once patterning has been established (Mammalian Phenotype Ontology, MP_0003885)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003885
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Genes

14 gene mutations causing the abnormal rostral-caudal body axis extension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
C2CD3 C2 calcium-dependent domain containing 3
CYFIP1 cytoplasmic FMR1 interacting protein 1
EPB41L5 erythrocyte membrane protein band 4.1 like 5
FGFR1 fibroblast growth factor receptor 1
MLLT4 myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 4
NCSTN nicastrin
PDPK1 3-phosphoinositide dependent protein kinase 1
PHACTR4 phosphatase and actin regulator 4
PTPN12 protein tyrosine phosphatase, non-receptor type 12
RAC1 ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1)
RDH10 retinol dehydrogenase 10 (all-trans)
SALL4 spalt-like transcription factor 4
SOX9 SRY (sex determining region Y)-box 9
YAP1 Yes-associated protein 1
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