abnormal circulating fructosamine level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the concentration in the blood of total non enzymatic glycated proteins in the blood (Mammalian Phenotype Ontology, MP_0010086)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010086
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17 gene mutations causing the abnormal circulating fructosamine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AFF3 AF4/FMR2 family, member 3
AP2A2 adaptor-related protein complex 2, alpha 2 subunit
AP3S2 adaptor-related protein complex 3, sigma 2 subunit
ARID4A AT rich interactive domain 4A (RBP1-like)
ARPC1B actin related protein 2/3 complex, subunit 1B, 41kDa
COL4A5 collagen, type IV, alpha 5
CRLF3 cytokine receptor-like factor 3
DBN1 drebrin 1
GLDC glycine dehydrogenase (decarboxylating)
MAP3K1 mitogen-activated protein kinase kinase kinase 1, E3 ubiquitin protein ligase
PFN1 profilin 1
RAB5C RAB5C, member RAS oncogene family
RSBN1 round spermatid basic protein 1
SIRT4 sirtuin 4
TFF1 trefoil factor 1
TMEM189 transmembrane protein 189
USP21 ubiquitin specific peptidase 21