Description:
GALACTOKINASE DEFICIENCY
GALACTOKINASE 1; GALK1
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Heritable Diseases |
Class |
Disorders of Carbohydrate Metabolism |
Cell Type
|
Fibroblast
|
Transformant
|
Untransformed
|
Race
|
White
|
Family Member
|
3
|
Relation to Proband
|
father
|
Confirmation
|
Clinical summary/Case history
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase Isoenzyme Electrophoresis |
|
galactokinase |
According to the submitter, biochemical test results for this subject showed decreased enzyme activity. EC Number: 2.7.1.6; 79% activity. |
|
Gene |
GALK1 |
Chromosomal Location |
17q25.1 |
Allelic Variant 1 |
604313.0001; GALACTOKINASE DEFICIENCY WITH CATARACTS |
Identified Mutation |
VAL32MET; In family GB in which the proband had galactokinase deficiency and congenital cataracts, Stambolian et al. (1995) found a single base substitution of A for G at position 94, which resulted in a val32-to-met substitution.
|
Remarks |
Passage 4 at CCR; 79% of control galactokinase activity in fibroblasts; clinically unaffected father of GM00334A |
Stambolian D, Ai Y, Sidjanin D, Nesburn K, Sathe G, Rosenberg M, Bergsma DJ, Cloning of the galactokinase cDNA and identification of mutations in two families with cataracts. Nat Genet10:307-12 1995 |
PubMed ID: 7670469 |
|
Stephenson C, Brivet M, Gautier M, Deschatrette J, Gitzelmann R, Karran P, Normal expression of thymidine kinase and O6-methylguanine-DNA methyltransferase in cultured fibroblasts from individuals with hereditary galactokinase deficiency. Biochem Genet29:135-44 1991 |
PubMed ID: 1859354 |
|
Schoen RC, Cox SH, Wagner RP, Thymidine-kinase activity of cultured cells from individuals with inherited galactokinase deficiency. Am J Hum Genet36:815-22 1984 |
PubMed ID: 6475956 |
|
Friedman TB, Yarkin RJ, Merril CR, Galactose and glucose metabolism in galactokinase deficient, galactose- 1-P-uridyl transferase deficient and normal human fibroblasts. J Cell Physiol85:569-78 1975 |
PubMed ID: 167035 |
Split Ratio |
1:3 |
Temperature |
37 C |
Percent CO2 |
5% |
Medium |
Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent |
Serum |
15% fetal bovine serum Not inactivated |
Substrate |
None specified |
Subcultivation Method |
trypsin-EDTA |
Supplement |
- |
|
|