abnormal circulating amylase level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the concentration of a group of amylolytic enzymes that cleave starch, glycogen, and related alpha-1,4-glucans in the blood (Mammalian Phenotype Ontology, MP_0008804)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008804
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48 gene mutations causing the abnormal circulating amylase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACSL4 acyl-CoA synthetase long-chain family member 4
ALDH2 aldehyde dehydrogenase 2 family (mitochondrial)
ANKRD11 ankyrin repeat domain 11
BTK Bruton agammaglobulinemia tyrosine kinase
CDH23 cadherin-related 23
CISD2 CDGSH iron sulfur domain 2
CYBA cytochrome b-245, alpha polypeptide
DFNB31 deafness, autosomal recessive 31
EIF2B5 eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
ELMO1 engulfment and cell motility 1
FBXL3 F-box and leucine-rich repeat protein 3
FHL1 four and a half LIM domains 1
GFM1 G elongation factor, mitochondrial 1
GIMAP6 GTPase, IMAP family member 6
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
GRIN2D glutamate receptor, ionotropic, N-methyl D-aspartate 2D
H6PD hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)
HBP1 HMG-box transcription factor 1
MAPK1 mitogen-activated protein kinase 1
MAPRE3 microtubule-associated protein, RP/EB family, member 3
MIB2 mindbomb E3 ubiquitin protein ligase 2
MRAP2 melanocortin 2 receptor accessory protein 2
MYBPC3 myosin binding protein C, cardiac
MYO6 myosin VI
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
OAT ornithine aminotransferase
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta
PER2 period circadian clock 2
PEX3 peroxisomal biogenesis factor 3
PHYH phytanoyl-CoA 2-hydroxylase
PITX3 paired-like homeodomain 3
RELB v-rel avian reticuloendotheliosis viral oncogene homolog B
RPRD1B regulation of nuclear pre-mRNA domain containing 1B
RUVBL1 RuvB-like AAA ATPase 1
SCIMP SLP adaptor and CSK interacting membrane protein
SECISBP2 SECIS binding protein 2
SLC38A10 solute carrier family 38, member 10
SLCO1B3 solute carrier organic anion transporter family, member 1B3
SYTL1 synaptotagmin-like 1
THRB thyroid hormone receptor, beta
TNFAIP1 tumor necrosis factor, alpha-induced protein 1 (endothelial)
TRPC3 transient receptor potential cation channel, subfamily C, member 3
TWF1 twinfilin actin binding protein 1
UBE3B ubiquitin protein ligase E3B
USH1C Usher syndrome 1C (autosomal recessive, severe)
VAMP8 vesicle-associated membrane protein 8
XDH xanthine dehydrogenase
YDJC YdjC homolog (bacterial)