abnormal primordial germ cell migration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the orderly movement of a primordial germ cell, a cell specialized to produce haploid gametes, from one site to another during development (Mammalian Phenotype Ontology, MP_0002982)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002982
Similar Terms
Downloads & Tools

Genes

9 gene mutations causing the abnormal primordial germ cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CXCL12 chemokine (C-X-C motif) ligand 12
CXCR4 chemokine (C-X-C motif) receptor 4
DDX4 DEAD (Asp-Glu-Ala-Asp) box polypeptide 4
FOXC1 forkhead box C1
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
KITLG KIT ligand
PRDM1 PR domain containing 1, with ZNF domain
ROR2 receptor tyrosine kinase-like orphan receptor 2
WNT5A wingless-type MMTV integration site family, member 5A