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GM28577 iPSC from Fibroblast

Description:

RETT SYNDROME, CONGENITAL VARIANT
FORKHEAD BOX G1; FOXG1

Affected:

Yes

Sex:

Female

Age:

2 YR (At Sampling)

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

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
FOXG1
PIGI Consented Sample
Protocols Protocol PDF
Biopsy Source Skin
Cell Type Stem cell
Cell Subtype Induced pluripotent stem cell
Transformant Reprogrammed (Sendai)
Sample Source iPSC from Fibroblast
Race More than one race
Ethnicity Not Hispanic/Latino
Ethnicity Indian (50%) / German (25%) / British (25%)
Country of Origin ITALY
Family Member 1
Family History N
Relation to Proband proband
Confirmation Molecular characterization before cell line submission to CCR
ISCN 46,XX[20]
Species Homo sapiens
Common Name Human
Remarks Externally reprogrammed from parental line GM27300 (fibroblast); clinically affected; onset of symptoms at 6 months of age; diagnosed by a geneticist at 9 months of age; gross motor delay; infantile /epileptic spasms; management includes: physical therapy, occupational therapy, and speech language therapy; heterozygous c.670G>A (p.Gly224Ser) variant found in FOXG1 gene; medications include adrenocorticotropic hormone (ACTH); LCL is GM27325; mother is GM27326. Researchers purchasing hiPSCs from the NIGMS Repository are responsible for any limited use label licenses (LULLs) applicable to the cell line purchased. The applicable LULL to this line is Sendai-CytoTune.

Characterizations

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Passage Frozen 15
 
Induced Pluripotent Stem Cell The frozen cell line submitted to the Repository was recovered and expanded. The expanded line was evaluated for viability surface antigen expression and alkaline phosphatase activity. Pluripotency was assessed via embryoid body (EB) formation. Steady-state mRNA expression patterns of undifferentiated iPSC and EBs were determined via real-time PCR. Characterization data are included in the Certificate of Analysis.
 
Gene FOXG1
Chromosomal Location 14q12
Allelic Variant 1 ; RETT SYNDROME, CONGENITAL VARIANT
Identified Mutation c.670G>A, p.Gly224Ser

Phenotypic Data

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Remarks Externally reprogrammed from parental line GM27300 (fibroblast); clinically affected; onset of symptoms at 6 months of age; diagnosed by a geneticist at 9 months of age; gross motor delay; infantile /epileptic spasms; management includes: physical therapy, occupational therapy, and speech language therapy; heterozygous c.670G>A (p.Gly224Ser) variant found in FOXG1 gene; medications include adrenocorticotropic hormone (ACTH); LCL is GM27325; mother is GM27326. Researchers purchasing hiPSCs from the NIGMS Repository are responsible for any limited use label licenses (LULLs) applicable to the cell line purchased. The applicable LULL to this line is Sendai-CytoTune.

External Links

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Gene Cards FOXG1
Gene Ontology GO:0003700 transcription factor activity
GO:0005634 nucleus
GO:0006355 regulation of transcription, DNA-dependent
GO:0007420 brain development
GO:0009653 morphogenesis
NCBI Gene Gene ID:2290
NCBI GTR 164874 FORKHEAD BOX G1; FOXG1
613454 RETT SYNDROME, CONGENITAL VARIANT
OMIM 164874 FORKHEAD BOX G1; FOXG1
613454 RETT SYNDROME, CONGENITAL VARIANT

Culture Protocols

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Passage Frozen 15
Split Ratio 1:6
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
Medium mTeSR1
Serum none
Substrate Matrigel
Supplement -
Pricing
International/Commercial/For-profit:
$1,789.00USD
U.S. Academic/Non-profit/Government:
$1,110.00USD
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How to Order
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Related Products
Same Subject
  • GM27300 - Fibroblast
  • GM27325 - B-Lymphocyte
Same Family
  • 3424
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