Cellosaurus RCMGi011-A (CVCL_C9H9)
Cell line name | RCMGi011-A |
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Synonyms | P10L1 |
Accession | CVCL_C9H9 |
Resource Identification Initiative | To cite this cell line use: RCMGi011-A (RRID:CVCL_C9H9) |
Comments | From: Research Centre for Medical Genetics; Moscow; Russia. Population: Caucasian; Russian. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
Sequence variations |
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Disease | Deafness, autosomal recessive 12 (NCIt: C201586) Mucopolysaccharidosis type IVB (NCIt: C84902) Autosomal recessive non-syndromic sensorineural deafness type DFNB (ORDO: Orphanet_90636) Mucopolysaccharidosis type 4B (ORDO: Orphanet_309310) |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
Originate from same individual | CVCL_C9HA ! RCMGi011-B |
Sex of cell | Male |
Age at sampling | 9Y |
Category | Induced pluripotent stem cell |
Publications | PubMed=37643494; DOI=10.1016/j.scr.2023.103183 |
Cross-references | |
Cell line databases/resources | hPSCreg; RCMGi011-A |
Biological sample resources | BioSamples; SAMEA112696500 |
Encyclopedic resources | Wikidata; Q123033340 |
Entry history | |
Entry creation | 05-Oct-2023 |
Last entry update | 30-Jan-2024 |
Version number | 2 |