CSMCi001-A-1

CS011iMEN1-n4.Homo5, CS011MEN1-n4.HomoMut5

General

Cell Line

hPSCreg name CSMCi001-A-1
Cite as:
CSMCi001-A-1 (RRID:CVCL_D0DN)
Alternative name(s)
CS011iMEN1-n4.Homo5, CS011MEN1-n4.HomoMut5
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines No similar lines found.
Last update 13th April 2023
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Provider

Generator Cedars Sinai Medical Center, (CSMC)

External Databases

BioSamples SAMEA112648669
Cellosaurus CVCL_D0DN
Wikidata Q123030973

General Information

Publications
* 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 female

Phenotype and Disease related information (Donor)

Diseases A disease was diagnosed.
The donor is a carrier of a disease-associated mutation and affected.
Synonyms
  • multiple endocrine adenomatosis
  • MEA type 1
  • MEA type I
  • MEN1
  • MEN1 multiple endocrine neoplasia
  • MEN1 syndrome
  • Wermer syndrome
  • Wermer's syndrome
  • men 1
  • men type 1
  • men type I
  • multiple endocrine adenomatosis type 1
  • multiple endocrine adenomatosis type I
  • multiple endocrine adenomatosis, type I
  • multiple endocrine neoplasia 1
  • multiple endocrine neoplasia caused by mutation in MEN1
  • multiple endocrine neoplasia type 1
  • multiple endocrine neoplasia type 1 syndrome
  • multiple endocrine neoplasia type I
  • multiple endocrine neoplasia, type I
  • MEA 1
  • MEN1 somatic mutations
  • endocrine adenomatosis multiple
  • endocrine adenomatosis, multiple
  • multiple endocrine neoplasia, type 1
show more synonyms

External Databases (Donor)

BioSamples SAMEA112648427

Ethics

Also have a look at the ethics information for the parental line CSMCi001-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 CSMCi001-A.

Reprogramming method

Vector type None

Vector free reprogramming

Other

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

Culture Conditions

Medium mTeSR™ Plus

Characterisation

No characterisation data could be found for this subclone. Please open parental cell line CSMCi001-A .

Genotyping

Karyotyping (Cell Line)

Other Genotyping (Cell Line)

Genetic Modification

Disease/phenotype related modifications
Synonyms
  • multiple endocrine adenomatosis
  • MEA type 1
  • MEA type I
  • MEN1
  • MEN1 multiple endocrine neoplasia
  • MEN1 syndrome
  • Wermer syndrome
  • Wermer's syndrome
  • men 1
  • men type 1
  • men type I
  • multiple endocrine adenomatosis type 1
  • multiple endocrine adenomatosis type I
  • multiple endocrine adenomatosis, type I
  • multiple endocrine neoplasia 1
  • multiple endocrine neoplasia caused by mutation in MEN1
  • multiple endocrine neoplasia type 1
  • multiple endocrine neoplasia type 1 syndrome
  • multiple endocrine neoplasia type I
  • multiple endocrine neoplasia, type I
  • MEA 1
  • MEN1 somatic mutations
  • endocrine adenomatosis multiple
  • endocrine adenomatosis, multiple
  • multiple endocrine neoplasia, type 1
show more synonyms
Genetic modifications
MEN1 (target)
Isogenic modification
11q13
Homozygous
Mutated
Genetic modifications not related to a disease