abnormal interscapular fat pad morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the encapsulated adipose tissue located between the scapulae (Mammalian Phenotype Ontology, MP_0006320)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006320
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Genes

19 gene mutations causing the abnormal interscapular fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BRD2 bromodomain containing 2
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
GCGR glucagon receptor
GHR growth hormone receptor
GNAS GNAS complex locus
HDC histidine decarboxylase
ID2 inhibitor of DNA binding 2, dominant negative helix-loop-helix protein
LEP leptin
LIPA lipase A, lysosomal acid, cholesterol esterase
LPIN1 lipin 1
NBEA neurobeachin
NR1H4 nuclear receptor subfamily 1, group H, member 4
PLIN1 perilipin 1
PNPLA2 patatin-like phospholipase domain containing 2
PPARD peroxisome proliferator-activated receptor delta
PPARG peroxisome proliferator-activated receptor gamma
PTPN1 protein tyrosine phosphatase, non-receptor type 1
RBL1 retinoblastoma-like 1
TWIST2 twist family bHLH transcription factor 2