short rostral-caudal axis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description length reduction or truncation of the axis that runs from the head to the tail of the body (Mammalian Phenotype Ontology, MP_0012173)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012173
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Genes

12 gene mutations causing the short rostral-caudal axis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP7 bone morphogenetic protein 7
FN1 fibronectin 1
FURIN furin (paired basic amino acid cleaving enzyme)
ITGA5 integrin, alpha 5 (fibronectin receptor, alpha polypeptide)
LMO2 LIM domain only 2 (rhombotin-like 1)
MIXL1 Mix paired-like homeobox
PPAP2B phosphatidic acid phosphatase type 2B
PSEN1 presenilin 1
TCF15 transcription factor 15 (basic helix-loop-helix)
TDGF1 teratocarcinoma-derived growth factor 1
TXNRD1 thioredoxin reductase 1
VCL vinculin