absent tail Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description completely lacking the appendage at the caudal end of the vertebral column (Mammalian Phenotype Ontology, MP_0003456)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003456
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11 gene mutations causing the absent tail phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CYP26A1 cytochrome P450, family 26, subfamily A, polypeptide 1
GDF11 growth differentiation factor 11
MSGN1 mesogenin 1
NOG noggin
NOTO notochord homeobox
PCSK5 proprotein convertase subtilisin/kexin type 5
PTK7 protein tyrosine kinase 7 (inactive)
RPL38 ribosomal protein L38
SP8 Sp8 transcription factor
T T, brachyury homolog (mouse)
WNT3A wingless-type MMTV integration site family, member 3A