small hippocampus Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of the deep lying structure of the cerebrum involved with memory storage and spatial navigation (Mammalian Phenotype Ontology, MP_0008283)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008283
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Genes

25 gene mutations causing the small hippocampus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AK8 adenylate kinase 8
ARL4D ADP-ribosylation factor-like 4D
ARL6 ADP-ribosylation factor-like 6
BBS1 Bardet-Biedl syndrome 1
BBS2 Bardet-Biedl syndrome 2
BBS4 Bardet-Biedl syndrome 4
BDNF brain-derived neurotrophic factor
CDK5RAP2 CDK5 regulatory subunit associated protein 2
CHD7 chromodomain helicase DNA binding protein 7
CLCN3 chloride channel, voltage-sensitive 3
CPLX2 complexin 2
EFHC1 EF-hand domain (C-terminal) containing 1
FOXG1 forkhead box G1
HSF2 heat shock transcription factor 2
LRRTM1 leucine rich repeat transmembrane neuronal 1
MBOAT7 membrane bound O-acyltransferase domain containing 7
MKKS McKusick-Kaufman syndrome
OTX1 orthodenticle homeobox 1
PPP1R9B protein phosphatase 1, regulatory subunit 9B
RPS7 ribosomal protein S7
SOX11 SRY (sex determining region Y)-box 11
UBE3B ubiquitin protein ligase E3B
USP14 ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase)
ZBTB18 zinc finger and BTB domain containing 18
ZDHHC17 zinc finger, DHHC-type containing 17