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GM14817 LCL from B-Lymphocyte

Description:

CLEFT LIP/PALATE - ECTODERMAL DYSPLASIA SYNDROME; CLPED1
POLIOVIRUS RECEPTOR-LIKE 1; PVRL1

Affected:

Yes

Sex:

Male

Age:

24 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Class Disorders of Connective Tissue, Muscle, and Bone
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race White
Ethnicity HISPANIC
Family Member 1
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Sparse, short brittle hair; hypodontia and anodontia; scanty eyebrows and lower lashes; triangular facies; anteverted pinnae; cleft lip and soft palate; abnormal scalp; hyperkeratosis; cutaneous syndactyly of hands; see GM14818 Fibroblast; donor subject is homozygous for a G>A transition in exon 3 of the PVRL1 gene (TGG>TAG) resulting in the substitution of a termination signal for tryptophan at codon 185 [Trp185Ter (W185X)] and truncation of the MECTIN-1 protein

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis
 
Gene PVRL1
Chromosomal Location 11q23-q24
Allelic Variant 1 600644.0001; ECTODERMAL DYSPLASIA, MARGARITA ISLAND TYPE
Identified Mutation TRP185TER
 
Gene PVRL1
Chromosomal Location 11q23-q24
Allelic Variant 2 600644.0001; ECTODERMAL DYSPLASIA, MARGARITA ISLAND TYPE
Identified Mutation TRP185TER

Phenotypic Data

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Remarks Sparse, short brittle hair; hypodontia and anodontia; scanty eyebrows and lower lashes; triangular facies; anteverted pinnae; cleft lip and soft palate; abnormal scalp; hyperkeratosis; cutaneous syndactyly of hands; see GM14818 Fibroblast; donor subject is homozygous for a G>A transition in exon 3 of the PVRL1 gene (TGG>TAG) resulting in the substitution of a termination signal for tryptophan at codon 185 [Trp185Ter (W185X)] and truncation of the MECTIN-1 protein

Publications

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Suzuki K, Hu D, Bustos T, Zlotogora J, Richieri-Costa A, Helms JA, Spritz RA, Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia. Nat Genet25(4):427-30 2000
PubMed ID: 10932188
 
Bustos T, Simosa V, Pinto-Cisternas J, Abramovits W, Jolay L, Rodriguez L, Fernandez L, Ramela M, Autosomal recessive ectodermal dysplasia: I. An undescribed dysplasia/malformation syndrome. Am J Med Genet41:398-404 1991
PubMed ID: 1776626

External Links

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dbSNP dbSNP ID: 20556
Gene Cards NECTIN1
PVRL1
Gene Ontology GO:0005515 protein binding
GO:0005912 adherens junction
GO:0006955 immune response
GO:0015026 coreceptor activity
GO:0016021 integral to membrane
GO:0016337 cell-cell adhesion
GO:0046718 viral entry
NCBI Gene Gene ID:5818
NCBI GTR 225060 CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1
600644 NECTIN 1; NECTIN1
OMIM 225060 CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1
600644 NECTIN 1; NECTIN1
Omim Description ECTODERMAL DYSPLASIA, MARGARITA ISLAND TYPE
  ECTODERMAL DYSPLASIA, TYPE 4; ED4

Culture Protocols

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Split Ratio 1:3
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 -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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