increased circulating serum albumin level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002965
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Genes

19 gene mutations causing the increased circulating serum albumin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BAG3 BCL2-associated athanogene 3
CTH cystathionine gamma-lyase
DFNB31 deafness, autosomal recessive 31
DPP9 dipeptidyl-peptidase 9
FAS Fas cell surface death receptor
GHR growth hormone receptor
ITGA1 integrin, alpha 1
KCNJ9 potassium channel, inwardly rectifying subfamily J, member 9
KISS1R KISS1 receptor
KPTN kaptin (actin binding protein)
MRPL54 mitochondrial ribosomal protein L54
NDFIP2 Nedd4 family interacting protein 2
RNASE10 ribonuclease, RNase A family, 10 (non-active)
SAG S-antigen; retina and pineal gland (arrestin)
SELENBP1 selenium binding protein 1
SLC5A10 solute carrier family 5 (sodium/sugar cotransporter), member 10
STK32A serine/threonine kinase 32A
TM9SF4 transmembrane 9 superfamily protein member 4
UBE2B ubiquitin-conjugating enzyme E2B