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search submit
GM22496
LCL
from
B-Lymphocyte
Description:
PROPIONIC ACIDEMIA
Affected:
Yes
Sex:
Male
Age:
8
WK
(At Sampling)
Sample Description
Overview
Characterizations
Phenotypic Data
Publications
External Links
Culture Protocols
Overview
Repository
NIGMS Human Genetic Cell Repository
Subcollection
Heritable Diseases
Biopsy Source
Peripheral vein
Cell Type
B-Lymphocyte
Tissue Type
Blood
Transformant
Epstein-Barr Virus
Sample Source
LCL from B-Lymphocyte
Race
White
Ethnicity
Not Hispanic/Latino
Family Member
1
Family History
N
Relation to Proband
proband
Confirmation
Clinical summary/Case history
Species
Homo
sapiens
Common Name
Human
Remarks
Clinically affected; diagnosed by newborn screening; hospitalized for decreased feeding; low muscle tone, hypothermia, severe hyperammonemia and metabolic acidosis; markedly elevated propionic acid metabolites by urine organic acid analysis; no family history; on levocarnitine; donor subject is homozygous for a 14 bp deletion and a 12 bp insertion at nucleotide 1218 in exon 12 of the PCCB gene [c.1218_1231delinsTAGAGCACAGGA (c.1218del14ins12)] resulting in a frameshift and stop codon at Gly406 (Gly406fs)
Characterizations
IDENTIFICATION OF SPECIES OF ORIGIN
Species of Origin confirmed by LINE assay
Gene
PCCB
Chromosomal Location
3q21-q22
Allelic Variant 1
232050.0003
; PROPIONIC ACIDEMIA
Identified Mutation
12-BP INS, 14-BP DEL, NT1218
; Rodriguez-Pombo et al. (1998) found that the most frequent mutation causing PCCB deficiency (606054) in Spain and Latin America was an insertion/deletion of 12 bp and 14 bp, respectively, following nucleotide 1218. This mutation accounted for 31% of the alleles from Spanish patients and 47% of the alleles from Latin American patients. The ins/del caused a frameshift and a premature stop codon in the coding sequence.
Gene
PCCB
Chromosomal Location
3q21-q22
Allelic Variant 2
232050.0003
; PROPIONIC ACIDEMIA
Identified Mutation
12-BP INS, 14-BP DEL, NT1218
; Rodriguez-Pombo et al. (1998) found that the most frequent mutation causing PCCB deficiency (606054) in Spain and Latin America was an insertion/deletion of 12 bp and 14 bp, respectively, following nucleotide 1218. This mutation accounted for 31% of the alleles from Spanish patients and 47% of the alleles from Latin American patients. The ins/del caused a frameshift and a premature stop codon in the coding sequence.
Phenotypic Data
Demographic Data
Relation to Proband
proband
Age at Sampling
8 WK
Sex
Male
Hispanic or Latino/Not Hispanic or Latino
Not Hispanic/Latino
Racial Category
White
Data Elements
Clinical Element Type: Propionic Acidemia
(Baseline)
Neonatal Data
Was this child newborn screened?
yes
no
unknown
If yes, was the result prior to hospitalization
yes
no
unknown
Weight at birth in kgs
3.09
Length at birth in cm
50.17
Was child breast-fed?
yes
no
unknown
If yes, duration in months
VERY LITTLE BEFORE HOSPITALIZATION
Failure to thrive?
yes
no
unknown
Molecular/Enzyme Laboratory Test Results
Which Gene: PCCA?
yes
no
unknown
Which Gene: PCCB?
yes
no
unknown
Mutations Allele 1
C.1218DEL14INS12
Mutations Allele 2
C.1218DEL14INS12
Family History
Are there other family members with PA?
yes
no
unknown
Other affected relatives?
yes
no
unknown
Has the individual passed away?
yes
no
unknown
Clinical Evaluation
Respiratory
Apnea
yes
no
unknown
Tachypnea
yes
no
unknown
Cardiovascular
Cardiomyopathy
yes
no
unknown
Long QT?
yes
no
unknown
If yes, type
No Data
Abdominal/Gastrointestinal
Pancreatitis
chronic
acute
never noted
Kidney problems
yes
no
unknown
Liver transplant
yes
no
unknown
Port-a-cath
currently in place
not currently in place
never had one
Gut motility
normal
slow
requires medication
unknown
Reflux
yes
no
unknown
Eating by mouth
100%
Tube fed
yes
no
unknown
Are anti-emetics used for vomiting
No Data
Neurologic
Basal ganglia damage
yes
no
unknown
If yes, determined by
No Data
Seizures
yes
no
unknown
Autism spectrum disorder
yes
no
unknown
ADD/ADHD
yes
no
unknown
Optic nerve damage
yes
no
unknown
Neutropenia
chronic
acute
unknown
Anemia
yes
no
unknown
Immune deficiency
yes
no
unknown
Treated with IVIG
yes
no
unknown
Low platelets
chronic
acute
not applicable
unknown
Asthma
yes
no
unknown
Secondary hip dysplasia
yes
no
unknown
Broken bones
yes
no
unknown
Short stature
yes
no
unknown
Growth hormone treatment
yes
no
unknown
Osteoporosis
yes
no
unknown
Developmental Evaluation
IQ
known
untested
unsure
Metabolic
Is the individual biotin responsive
yes
no
unknown
Episodes of ketoacidosis
yes
no
unknown
Chronic hyperammonemia
yes
no
unknown
Is the individual currently on metabolic formula
yes
no
unknown
If yes, which ones
Is the individual taking levocarnitine
yes
no
unknown
Other supllements
Remarks
Clinically affected; diagnosed by newborn screening; hospitalized for decreased feeding; low muscle tone, hypothermia, severe hyperammonemia and metabolic acidosis; markedly elevated propionic acid metabolites by urine organic acid analysis; no family history; on levocarnitine; donor subject is homozygous for a 14 bp deletion and a 12 bp insertion at nucleotide 1218 in exon 12 of the PCCB gene [c.1218_1231delinsTAGAGCACAGGA (c.1218del14ins12)] resulting in a frameshift and stop codon at Gly406 (Gly406fs)
Publications
Yeeok Kang, Seong-Hyeuk Nam, Kyung Sun Park, Yoonjung Kim, Jong-Won Kim, Eunjung Lee, Jung Min Ko, Kyung-A Lee and Inho ParkEmail
, DeviCNV: detection and visualization of exon-level copy number variants in targeted next-generation sequencing data BMC Bioinformatics19: 2018
PubMed ID:
30326846
External Links
GEO
GEO Accession No: GSM1050455
GEO Accession No: GSM1050456
NCBI GTR
606054 PROPIONIC ACIDEMIA
OMIM
606054 PROPIONIC ACIDEMIA
Omim Description
PROPIONIC ACIDEMIA
Culture Protocols
Split Ratio
1:4
Temperature
37 C
Percent CO2
5%
Percent O2
AMBIENT
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
Commercial/For-profit:
$311.00
USD
Academic/Non-profit/Government:
$176.00
USD
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