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Cellosaurus ZIPi015-K (CVCL_UD58)

[Text version]
Cell line name ZIPi015-K
Synonyms AS_ID; ZIP15
Accession CVCL_UD58
Resource Identification Initiative To cite this cell line use: ZIPi015-K (RRID:CVCL_UD58)
Comments From: Zentrum fur Integrative Psychiatrie; Kiel; Germany.
Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Angelman syndrome (NCIt: C75462)
Angelman syndrome (ORDO: Orphanet_72)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_A8GQ ! ZIPi015-A
CVCL_A8GR ! ZIPi015-B
CVCL_A8GS ! ZIPi015-C
CVCL_A8GT ! ZIPi015-D
CVCL_A8GU ! ZIPi015-E
CVCL_A8GV ! ZIPi015-F
CVCL_A8GW ! ZIPi015-G
CVCL_A8GX ! ZIPi015-H
CVCL_A8GY ! ZIPi015-I
CVCL_A8GZ ! ZIPi015-J
Sex of cell Female
Age at sampling 12Y
Category Induced pluripotent stem cell
Publications

PubMed=30296670; DOI=10.1016/j.scr.2018.09.015
Neureiter A., Brandl B., Hiber M., Tandon R., Muller F.-J., Steenpass L.
Generation of an iPSC line of a patient with Angelman syndrome due to an imprinting defect.
Stem Cell Res. 33:20-24(2018)

Cross-references
Cell line databases/resources hPSCreg; ZIPi015-K
Encyclopedic resources Wikidata; Q98136517
Entry history
Entry creation13-Nov-2018
Last entry update29-Jun-2023
Version number7