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NA02049 DNA from Fibroblast

Description:

MANNOSIDOSIS, ALPHA B, LYSOSOMAL
MANNOSIDASE, ALPHA, CLASS 2B, MEMBER 1; MAN2B1

Affected:

No Data

Sex:

Male

Age:

39 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
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Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Lysosomal Storage Diseases
Class Disorders of Carbohydrate Metabolism
Quantity 0.050mg
Quantitation Method Please see our FAQ
Cell Type Fibroblast
Transformant Untransformed
Sample Source DNA from Fibroblast
Race White
Family Member 3
Relation to Proband father
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Arab; approximately 50% of normal alphamannosidase activity; 2 affected children; clinically unaffected father of GM02050 and 02051; donor subject is heterozygous for an A>T transversion at nucleotide 212 in exon 2 of the MAN2B1 gene ( 212A>T) resulting in the substitution of leucine for histidine at codon 71 [His71Leu (H71L)]

Characterizations

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Passage Frozen 8
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase Isoenzyme Electrophoresis
 
alpha-mannosidase According to the submitter, biochemical test results for this subject showed decreased enzyme activity. EC Number: 3.2.1.24; 50% activity.
 
Gene MAN2B1
Chromosomal Location 19cen-q12
Allelic Variant 1 609458.0001; MANNOSIDOSIS, ALPHA B, LYSOSOMAL
Identified Mutation HIS71LEU

Phenotypic Data

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Remarks Arab; approximately 50% of normal alphamannosidase activity; 2 affected children; clinically unaffected father of GM02050 and 02051; donor subject is heterozygous for an A>T transversion at nucleotide 212 in exon 2 of the MAN2B1 gene ( 212A>T) resulting in the substitution of leucine for histidine at codon 71 [His71Leu (H71L)]

Publications

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Nilssen O, Berg T, Riise HM, Ramachandran U, Evjen G, Hansen GM, Malm D, Tranebjaerg L, Tollersrud OK, alpha-Mannosidosis: functional cloning of the lysosomal alpha-mannosidase cDNA and identification of a mutation in two affected siblings. Hum Mol Genet6(5):717-26 1997
PubMed ID: 9158146

External Links

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dbSNP dbSNP ID: 10477
Gene Cards MAN2B1
Gene Ontology GO:0004559 alpha-mannosidase activity
GO:0005764 lysosome
GO:0005975 carbohydrate metabolism
GO:0006464 protein modification
GO:0006517 protein deglycosylation
GO:0016798 hydrolase activity, acting on glycosyl bonds
NCBI Gene Gene ID:4125
NCBI GTR 248500 MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA
609458 MANNOSIDASE, ALPHA, CLASS 2B, MEMBER 1; MAN2B1
OMIM 248500 MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA
609458 MANNOSIDASE, ALPHA, CLASS 2B, MEMBER 1; MAN2B1
Omim Description ALPHA-MANNOSIDASE B DEFICIENCYMANNOSIDASE, ALPHA B, LYSOSOMAL, INCLUDED; MANB, INCLUDED
  ALPHA-MANNOSIDOSIS
  LYSOSOMAL ALPHA-D-MANNOSIDASE DEFICIENCY
  MANNOSIDOSIS, ALPHA B, LYSOSOMAL

Images

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International/Commercial/For-profit:
$281.00USD
U.S. Academic/Non-profit/Government:
$139.00USD
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