|
1041
|
|
|
Carboxyl ester lipase |
BAL, BSDL, BSSL, CELL, CEase, FAP, FAPP, LIPA, MODY8 |
Hyperinsulinemic hypoglycemia, Pancreatic hypoplasia, Diabetes mellitus, Exocrine pancreatic insufficiency, Hepatocellular adenoma, Hyperglycemia, Hypoinsulinemia, Kidney disease, Mason type diabetes, Hypoglycemia, Obesity, Pancreatitis, Renal cyst, Retinal diseases |
|
1042
|
|
|
Solute carrier family 19 member 2 |
TC1, THMD1, THT1, THTR1, TRMA |
Anemia, Anorexia, Atrial septal defect, Cone-rod dystrophy, Congestive heart failure, Diabetes mellitus, Dwarfism, Hearing loss, Nystagmus, Optic atrophy, Retinal dystrophy, Sideroblastic anemia, Stroke, Thiamine responsive megaloblastic anemia syndrome, Ventricular septal defect |
|
1043
|
|
|
Interferon induced protein 44 |
MTAP44, TLDC5, p44 |
|
|
1044
|
|
|
B3GALT1 antisense RNA 1 |
- |
|
|
1045
|
|
|
Olfactomedin 4 |
GC1, GW112, OLM4, OlfD, UNQ362, bA209J19.1, hGC-1, hOLfD, pDP4 |
|
|
1046
|
|
|
C-X-C motif chemokine ligand 13 |
ANGIE, ANGIE2, BCA-1, BCA1, BLC, BLR1L, SCYB13 |
|
|
1047
|
|
|
ARF guanine nucleotide exchange factor 2 |
BIG2, PVNH2, dJ1164I10.1 |
Aortic aneurysm, Aortic valve insufficiency, Breast cancer, Developmental delay, Epilepsy, Gastroesophageal reflux disease, Hydrocephalus, Hypoplasia of corpus callosum, Mental retardation, Patent ductus arteriosus, Periventricular heterotopia, Periventricular nodular heterotopia, Scoliosis |
|
1048
|
|
|
ARF guanine nucleotide exchange factor 1 |
ARFGEP1, BIG1, DEDISB, P200 |
|
|
1049
|
|
|
A-kinase anchoring protein 3 |
AKAP 110, AKAP110, CT82, FSP95, HEL159, PRKA3, SOB1, SPGF82 |
|
|
1050
|
|
|
Solute carrier family 34 member 2 |
NAPI-3B, NAPI-IIb, NPTIIb, NaPi2b, PULAM |
|
