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GM04489 Fibroblast from Skin, Arm

Description:

XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC
XPC COMPLEX SUBUNIT, DNA DAMAGE RECOGNITION AND REPAIR FACTOR; XPC

Affected:

Yes

Sex:

Female

Age:

7 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 Repair Defective and Chromosomal Instability Syndromes
Biopsy Source Arm
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Sample Source Fibroblast from Skin, Arm
Race Black/African American
Family Member 1
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks XP25BE; freckling; photophobia; eye lesions; see GM04490 Lymphoid; donor subject is homozygous for a 2 bp deletion in intron 11 of the XPC gene (IVS11-1_IVS11-2delAG)and a 2 bp insertion between -6 and -7 (IVS11-6_IVS11-7insCC) leading to three alternately spliced XPC mRNA isoforms: one with exon 12 skipped, one with the deletion of 44 bp at the 5' end of exon 12, and one with retention of intron 11

Characterizations

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Passage Frozen 2
 
Gene XPC
Chromosomal Location 3p25
Allelic Variant 1 skipped ex 12; XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
Identified Mutation IVS11-1_IVS11-2delAG; IVS11-6_IVS11-7insCC
 
Gene XPC
Chromosomal Location 3p25
Allelic Variant 2 skipped ex 12; XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
Identified Mutation IVS11-1_IVS11-2delAG; IVS11-6_IVS11-7insCC

Phenotypic Data

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Remarks XP25BE; freckling; photophobia; eye lesions; see GM04490 Lymphoid; donor subject is homozygous for a 2 bp deletion in intron 11 of the XPC gene (IVS11-1_IVS11-2delAG)and a 2 bp insertion between -6 and -7 (IVS11-6_IVS11-7insCC) leading to three alternately spliced XPC mRNA isoforms: one with exon 12 skipped, one with the deletion of 44 bp at the 5' end of exon 12, and one with retention of intron 11

Publications

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Khan SG, Oh KS, Shahlavi T, Ueda T, Busch DB, Inui H, Emmert S, Imoto K, Muniz-Medina V, Baker CC, Digiovanna JJ, Schmidt D, Khadavi A, Metin A, Gozukara E, Slor H, Sarasin A, Kraemer KH, Reduced XPC DNA repair gene mRNA levels in clinically normal arents of xeroderma pigmentosum patients. Carcinogenesis27(1):84-94 2005
PubMed ID: 16081512

External Links

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Gene Cards XPC
Gene Ontology GO:0003684 damaged DNA binding
GO:0003697 single-stranded DNA binding
GO:0005634 nucleus
GO:0006289 nucleotide-excision repair
NCBI Gene Gene ID:7508
NCBI GTR 278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC
613208 XPC COMPLEX SUBUNIT, DNA DAMAGE RECOGNITION AND REPAIR FACTOR; XPC
OMIM 278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC
613208 XPC COMPLEX SUBUNIT, DNA DAMAGE RECOGNITION AND REPAIR FACTOR; XPC
Omim Description XERODERMA PIGMENTOSUM III; XP3
  XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC
  XP, GROUP C
  XPCC

Culture Protocols

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Passage Frozen 2
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 20% fetal bovine serum Not inactivated
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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