| Cell line name |
GM00081 |
|---|
| Synonyms |
GM-81 |
|---|
| Accession |
CVCL_9Q86 |
|---|
| Resource Identification Initiative |
To cite this cell line use: GM00081 (RRID:CVCL_9Q86) |
|---|
| Comments |
Population: Caucasian.
Cell type: Fibroblast; CL=CL_0000057. |
|---|
| Sequence variations |
|
|---|
| Species of origin |
Homo sapiens (Human)
(NCBI Taxonomy: 9606) |
|---|
| Sex of cell |
Male |
|---|
| Age at sampling |
23Y |
|---|
| 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=16465621; DOI=10.1086/500849; PMCID=PMC1380288
Kudo M., Brem M.S., Canfield W.M.
Mucolipidosis II (I-cell disease) and mucolipidosis IIIA (classical pseudo-Hurler polydystrophy) are caused by mutations in the GlcNAc-phosphotransferase alpha/beta-subunits precursor gene.
Am. J. Hum. Genet. 78:451-463(2006) |
|---|
| Cross-references |
|---|
| Cell line collections (Providers) |
Coriell; GM00081
|
|---|
| Cell line databases/resources |
CLO; CLO_0025150
|
|---|
| Encyclopedic resources |
Wikidata; Q54836022
|
|---|
| Entry history |
|---|
| Entry creation | 23-Feb-2016 |
|---|
| Last entry update | 19-Dec-2024 |
|---|
| Version number | 12 |
|---|
