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GM16866 Fibroblast from Skin, Arm

Description:

PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A

Affected:

Yes

Sex:

Female

Age:

14 FW (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 Other Disorders of Known Biochemistry
Biopsy Source Arm
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Sample Source Fibroblast from Skin, Arm
Race White
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Clinically affected; complementation group 8; culture set up from skin biopsy taken from the inner forearm; transverse palmar creases; large anterior fontanelle; hypotonia; failure to thrive; developmental delay; jaundice; broad nasal bridge; bilateral hypergyration; asymmetric cranium with plagiocephaly; small ears; supraorbital ridge hypoplasia; narrow palpebral fissures; 5th nail hypoplasia; bilateral nail hypoplasia on big toe; renal cortical cysts; hepatic fibrosis and bile stasis; patent ductus arteriosus; affected older sister; deficient peroxisomal plasmalogen synthesis enzymes; elevated very long chain fatty acids. No detectable level of PEX26 mRNA.

Characterizations

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Passage Frozen 14
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase,Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis
 

Phenotypic Data

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Remarks Clinically affected; complementation group 8; culture set up from skin biopsy taken from the inner forearm; transverse palmar creases; large anterior fontanelle; hypotonia; failure to thrive; developmental delay; jaundice; broad nasal bridge; bilateral hypergyration; asymmetric cranium with plagiocephaly; small ears; supraorbital ridge hypoplasia; narrow palpebral fissures; 5th nail hypoplasia; bilateral nail hypoplasia on big toe; renal cortical cysts; hepatic fibrosis and bile stasis; patent ductus arteriosus; affected older sister; deficient peroxisomal plasmalogen synthesis enzymes; elevated very long chain fatty acids. No detectable level of PEX26 mRNA.

Publications

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Pierre M.Jean Beltran, Katelyn C.Cook, Yutaka Hashimoto, Cyril Galitzine, Laura A. Murray, Olga Vitek, Ileana M. Cristea, Infection-Induced Peroxisome Biogenesis Is a Metabolic Strategy for Herpesvirus Replication Cell Host and Microbe24:526-541 2018
PubMed ID: 30269970
 
Matsumoto N, Tamura S, Furuki S, Miyata N, Moser A, Shimozawa N, Moser HW, Suzuki Y, Kondo N, Fujiki Y, Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation. Am J Hum Genet73(2):233-46 2003
PubMed ID: 12851857

External Links

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dbSNP dbSNP ID: 14959
NCBI GTR 614872 PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A
OMIM 614872 PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A

Culture Protocols

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Passage Frozen 14
Split Ratio 1:4
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 -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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