delayed hepatic development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description late onset of the induction and/or differentiation of the liver (Mammalian Phenotype Ontology, MP_0000597)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000597
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Genes

11 gene mutations causing the delayed hepatic development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP4 bone morphogenetic protein 4
DNM1L dynamin 1-like
FAM20B family with sequence similarity 20, member B
ICMT isoprenylcysteine carboxyl methyltransferase
MEN1 multiple endocrine neoplasia I
NF1 neurofibromin 1
PEX11B peroxisomal biogenesis factor 11 beta
PTK2 protein tyrosine kinase 2
RXRA retinoid X receptor, alpha
TCEB3 transcription elongation factor B (SIII), polypeptide 3 (110kDa, elongin A)
TGFB1 transforming growth factor, beta 1