CBIGi041-A-1

IPSC0054, GBA L444P (CBIGi041-A) correction

The cell line is not validated yet.

General

Cell Line

hPSCreg name CBIGi041-A-1
Cite as:
CBIGi041-A-1
Alternative name(s)
IPSC0054, GBA L444P (CBIGi041-A) correction
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines
CBIGi041-A
(IPSC0053, GBA L444P (CBIGi041-A))
Donor's gene variants:
GBA, GBA
Donor diseases:
Parkinson Disease
CBIGi042-A-1
(GBA E326K (CBIGi042-A) correction, IPSC0056)
Donor's gene variants:
GBA, GBA
Donor diseases:
Parkinson Disease
STBCi025-A
(SFC834-03-01)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
STBCi025-B
(SFC834-03-03)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
STBCi025-C
(SFC834-03-10)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
STBCi042-A
(SFC848-03-02)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
STBCi042-B
(SFC848-03-04)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
STBCi042-C
(SFC848-03-06)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
STBCi085-A
(SFC866-03-06)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
STBCi085-B
(SFC866-03-02)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
STBCi085-C
(SFC866-03-05)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
STBCi088-A
(SFC872-03-05)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
STBCi088-B
(SFC872-03-02)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
STBCi088-C
(SFC872-03-03)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
PNUSCRi001-A
(GBA PD iPSC7)
Donor's gene variants:
GBA
Donor diseases:
Parkinson Disease
PNUSCRi002-A
(GBA PD iPSC9)
Donor's gene variants:
GBA
Donor diseases:
Parkinson Disease
CBIGi042-A
(IPSC0055, GBA E326K (CBIGi042-A))
Donor's gene variants:
GBA, GBA
Donor diseases:
Parkinson Disease
CBIGi045-A
(GBA L444P(CBIGi045-A), IPSC0077)
Donor's gene variants:
GBA, GBA
Donor diseases:
Parkinson Disease
UOXFi002-A
(MK082-26)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
UOXFi002-B
(MK082-30)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
UOXFi003-A
(MK088-1)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
UOXFi003-C
(MK088-7)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
LCSBi017-A
(M1 Cl6b, #89721)
Donor's gene variants:
GBA1, GBA1, GBA1, GBA1
Donor diseases:
Parkinson Disease
DANi002-C
(GBA-002-C3)
Donor's gene variants:
GBA
Donor diseases:
Parkinson Disease
DANi003-H
(GBA-003-C8)
Donor's gene variants:
GBA
Donor diseases:
Parkinson Disease
DANi005-A
(LRRK2-GBA-005-C1)
Donor's gene variants:
GBA, LRRK2
Donor diseases:
Parkinson Disease
LCPHi001-A
Donor's gene variants:
GBA
Donor diseases:
obsolete_Parkinson's disease
STBCi084-A
(SFC871-03-12)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
STBCi084-B
(SFC871-03-04)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
STBCi084-C
(SFC871-03-09)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
CBIGi008-A
(IPSC0011, GBA T369M)
Donor's gene variants:
GBA, GBA
Donor diseases:
Parkinson Disease
CBIGi021-A
(GBA1 L324I, IPSC0027)
Donor's gene variants:
GBA, GBA
Donor diseases:
Parkinson Disease
UOXFi001-A
(MK071-1)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
UOXFi001-B
(MK071-3)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
UOXFi001-C
(MK071-5)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
UOXFi001-D
(MK071-6)
Donor's gene variants:
GBA1
Donor diseases:
Parkinson disease
LCSBi014-A
(#89739, S1 Cl19a)
Donor's gene variants:
GBA1, GBA1
Donor diseases:
Parkinson Disease
LCSBi015-A
(S2 Cl4, 89732)
Donor's gene variants:
GBA1, GBA1
Donor diseases:
Parkinson Disease
LCSBi016-A
(S3 Cl17, 90812)
Donor's gene variants:
GBA1, GBA1
Donor diseases:
Parkinson Disease
LCSBi018-A
(M2 Cl4, #90806)
Donor's gene variants:
GBA1, GBA1
Donor diseases:
Parkinson Disease
DANi006-F
(GBA-006-C6)
Donor's gene variants:
GBA
Donor diseases:
Parkinson Disease
CBIGi002-A
(2890 (GBA W378G, heterozygous), 2890, IPSC0001)
Donor's gene variants:
GBA, GBA, GBA
Donor diseases:
Parkinson Disease
DANi010-A
(GBA-010-C1)
Donor's gene variants:
GBA
Donor diseases:
Parkinson Disease
CBIGi002-A-1
(GBA W378G-correction/2890, 2890-iso, IPSC0002)
Donor's gene variants:
GBA, GBA, GBA
Donor diseases:
Parkinson Disease
CBIGi001-A-40
(IPSC0112, GBA-KO/AIW002-02)
WIBRe001-A-83
(WIBR3_GBA1_IVS2_G2E)
WIBRe001-A-84
(WIBR3_GBA1_IVS2_E10B)
LCSBi012-A-1
(RHOT1_T610A_clone62.19.37_IsogenicControl)
Donor diseases:
Parkinson Disease
LCSBi008-A-1
(delP GC13, DJ-1-delP GC13)
Donor diseases:
Parkinson Disease
Last update 30th July 2025
Notes Isogenic control for CBIGi041-A.
User feedback
No feedback available yet.

Login to share your feedback, experiences or results with the research community.

Provider

Generator Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
Distributors
Derivation country Canada

External Databases

BioSamples SAMEA117982038

General Information

* Is the cell line readily obtainable for third parties?
Yes
Research use: allowed
Clinical use: not allowed
Commercial use: not allowed
Subclone of

Donor Information

General Donor Information

Sex male

Phenotype and Disease related information (Donor)

Diseases A disease was diagnosed.
Synonyms
  • Parkinson Disease
  • Parkinson's disease
  • Parkinson's Disease
Genetic variants
GBA (target)
NM_000157.4:c.1448T>C

External Databases (Donor)

BioSamples SAMEA117982037

Ethics

Also have a look at the ethics information for the parental line CBIGi041-A .
For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used?

hIPSC Derivation

General

The source cell information can be found in the parental cell line CBIGi041-A.
Passage number reprogrammed P14

Reprogramming method

Vector type Non-integrating
Vector Episomal
Genes
Is reprogramming vector detectable?
Unknown
Methods used
Immunostaining

Vector free reprogramming

Other

Derived under xeno-free conditions
Unknown
Derived under GMP?
Unknown
Available as clinical grade?
Unknown

Culture Conditions

Surface coating Matrigel/Geltrex
Passage method Enzyme-free cell dissociation
Gentle Cell Dissociation Reagent
O2 Concentration 21 %
CO2 Concentration 5 %
Medium mTeSR™ 1
Has Rock inhibitor (Y27632) been used at passage previously with this cell line?
Yes
Has Rock inhibitor (Y27632) been used at cryo previously with this cell line?
No
Has Rock inhibitor (Y27632) been used at thaw previously with this cell line?
Yes

Characterisation

Analysis of Undifferentiated Cells
Marker Expressed Immunostaining RT-PCR Flow Cytometry Enzymatic Assay Expression Profiles
NANOG
Yes
TRA 1-60
Yes
SSEA-4
Yes
POU5F1 (OCT-4)
Yes

Microbiology / Virus Screening

HIV 1 Negative
HIV 2 Negative
Hepatitis B Negative
Hepatitis C Negative
Mycoplasma Negative

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
Normal 46, XY
Passage number: P14
Karyotyping method: G-Banding

Other Genotyping (Cell Line)

Genetic Modification

Disease/phenotype related modifications
Synonyms
  • Parkinson Disease
  • Parkinson's disease
  • Parkinson's Disease
Genetic modifications
GBA (target)
Isogenic modification
1q22
After CRISPR/Cas9 editing, Sanger sequencing confirms that the wt codon CTC has replaced the mutant codon CCG, correcting the missense mutation L444P.
Repaired