GM20463
LCL from B-Lymphocyte
Description:
HEMOGLOBIN--BETA LOCUS; HBB
Repository
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NIGMS Human Genetic Cell Repository
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Subcollection |
Heritable Diseases |
Biopsy Source
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Peripheral vein
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Cell Type
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B-Lymphocyte
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Tissue Type
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Blood
|
Transformant
|
Epstein-Barr Virus
|
Sample Source
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LCL from B-Lymphocyte
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Race
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Black/African American
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Family Member
|
5
|
Relation to Proband
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cousin
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Confirmation
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Clinical summary/Case history
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Species
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Homo sapiens
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Common Name
|
Human
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Remarks
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IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin confirmed by LINE assay |
|
Gene |
HBB |
Chromosomal Location |
11p15.5 |
Allelic Variant 1 |
141900.0227; HEMOGLOBIN PROVIDENCE |
Identified Mutation |
LYS83ASN (c.249G>C); See Moo-Penn et al. (1976), Charache et al. (1977), and Bardakdjian et al. (1985).
|
Remarks |
Clinically healthy; hemoglobin Providence; hemoglobin electrophoresis results: HbA = 44.6%, HbA2 = 2.9%, HbF = 0%, HbS = 0%, Hb Providence = 52.5%; hemoglobin = 14.3 g/dl; MCV = 90.3; donor subject has a substitution of asparagine for lysine at codon 82 (EF6) of the HBB gene [Lys82Asn (K82N)]; mother is GM20460; maternal grandmother is GM20459.
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Gene Cards |
HBB |
Gene Ontology |
GO:0005344 oxygen transporter activity |
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GO:0005833 hemoglobin complex |
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GO:0006810 transport |
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GO:0015671 oxygen transport |
NCBI Gene |
Gene ID:3043 |
NCBI GTR |
141900 HEMOGLOBIN--BETA LOCUS; HBB |
OMIM |
141900 HEMOGLOBIN--BETA LOCUS; HBB |
Omim Description |
BETA-THALASSEMIAS, INCLUDED |
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DYSERYTHROPOIETIC ANEMIA, CONGENITAL, IRISH OR WEATHERALL TYPE, INCLUDED |
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ERYTHREMIA, BETA-GLOBIN TYPE, INCLUDED |
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HEINZ BODY ANEMIAS, BETA-GLOBIN TYPE, INCLUDED |
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HEMOGLOBIN--BETA LOCUS; HBBSICKLE CELL ANEMIA, INCLUDED |
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METHEMOGLOBINEMIA, BETA-GLOBIN TYPE, INCLUDED |
Split Ratio |
1:2 |
Temperature |
37 C |
Percent CO2 |
5% |
Medium |
Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent |
Serum |
15% fetal bovine serum Not Inactivated |
Substrate |
None specified |
Subcultivation Method |
dilution - add fresh medium |
Supplement |
- |
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