abnormal habenula morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the group of nuclei that makes up the small eminence on the dorsomedial surface of the thalamus, just in front of the dorsal commissure on the lateral edge of the habenular trigone (Mammalian Phenotype Ontology, MP_0004082)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004082
Similar Terms
Downloads & Tools

Genes

4 gene mutations causing the abnormal habenula morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTR2 angiotensin II receptor, type 2
MYCBP2 MYC binding protein 2, E3 ubiquitin protein ligase
NRP2 neuropilin 2
SEMA3F sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F