Cellosaurus WG3760 (CVCL_B4DZ)
Cell line name | WG3760 |
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Accession | CVCL_B4DZ |
Resource Identification Initiative | To cite this cell line use: WG3760 (RRID:CVCL_B4DZ) |
Comments | From: Montreal Children's Hospital cell repository; Montreal; Canada. Population: Hispanic. Miscellaneous: Cell line no longer available. Caution: MMUT c.1846C>T mutation indicated incorrectly as being causative of p.Pro649Leu in CelloPub=CLPUB00669 and PubMed=27233228 (personal communication of Rosenblatt, David S.). Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
Sequence variations |
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Disease | Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency (NCIt: C148366) Vitamin B12-unresponsive methylmalonic acidemia (ORDO: Orphanet_27) |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
Age at sampling | 7Y |
Category | Finite cell line |
Publications | PubMed=27233228; DOI=10.1016/j.ymgme.2016.05.014 CLPUB00669 |
Cross-references | |
Encyclopedic resources | Wikidata; Q110434382 |
Entry history | |
Entry creation | 16-Dec-2021 |
Last entry update | 19-Dec-2024 |
Version number | 6 |