Cell line name |
XPHM1WI |
Synonyms |
GM01632; GM-1632; GM1632 |
Accession |
CVCL_1F08 |
Resource Identification Initiative |
To cite this cell line use: XPHM1WI (RRID:CVCL_1F08) |
Comments |
Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
Sequence variations |
- Mutation; HGNC; HGNC:12814; XPA; Simple; p.Gln185His (c.555G>C); ClinVar=VCV000550646; Zygosity=Heterozygous; Note=Also produces mis-splicing (Coriell=GM01632).
|
Species of origin |
Homo sapiens (Human)
(NCBI Taxonomy: 9606) |
Originate from same individual |
CVCL_1F23 ! XPHM1WI LCL |
Sex of cell |
Female |
Age at sampling |
25Y |
Category |
Finite cell line |
Publications | DOI=10.5962/bhl.title.4090 Coriell L.L., Greene A.E. The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 4th edition. October 1977. (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977) CLPUB00447 Mulivor R.A., Suchy S.F. 1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992. (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992) PubMed=9671271; DOI=10.1002/(SICI)1098-1004(1998)12:2<103::AID-HUMU5>3.0.CO;2-6 States J.C., McDuffie E.R., Myrand S.P., McDowell M.L., Cleaver J.E. Distribution of mutations in the human xeroderma pigmentosum group A gene and their relationships to the functional regions of the DNA damage recognition protein. Hum. Mutat. 12:103-113(1998) |
Cross-references |
Cell line collections (Providers) |
Coriell; GM01632
|
Cell line databases/resources |
CLO; CLO_0031496
|
Biological sample resources |
BioSample; SAMN00806997
|
Encyclopedic resources |
Wikidata; Q54836967
|
Entry history |
Entry creation | 08-Jul-2015 |
Last entry update | 19-Dec-2024 |
Version number | 17 |
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