Cellosaurus HAX1W44X-iPSC (CVCL_A4HL)
| Cell line name | HAX1W44X-iPSC | ||
|---|---|---|---|
| Accession | CVCL_A4HL | ||
| Resource Identification Initiative | To cite this cell line use: HAX1W44X-iPSC (RRID:CVCL_A4HL) | ||
| Comments | Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. | ||
| Sequence variations |
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| Disease | Severe congenital neutropenia type 3, autosomal recessive (NCIt: C166153) Kostmann syndrome (ORDO: Orphanet_99749) | ||
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) | ||
| Hierarchy | Children:
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| Category | Induced pluripotent stem cell | ||
| Publications | PubMed=29296734; DOI=10.1182/bloodadvances.2016003798; PMCID=PMC5737589 | ||
| Cross-references | |||
| Cell line databases/resources | SKIP; SKIP003023 | ||
| Encyclopedic resources | Wikidata; Q105507550 | ||
| Entry history | |||
| Entry creation | 12-Jan-2021 | ||
| Last entry update | 19-Dec-2024 | ||
| Version number | 6 | ||