Cellosaurus HH0134 (CVCL_8X27)
| Cell line name | HH0134 |
|---|---|
| Accession | CVCL_8X27 |
| Resource Identification Initiative | To cite this cell line use: HH0134 (RRID:CVCL_8X27) |
| Comments | Part of: ECACC chromosomal abnormality collection. Population: Caucasian. Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173. |
| Disease | Fragile X syndrome (NCIt: C84717) Fragile X syndrome (ORDO: Orphanet_908) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Sex unspecified |
| Age at sampling | Fetus |
| Category | Finite cell line |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 89061429 |
| Encyclopedic resources | Wikidata; Q54887420 |
| Entry history | |
| Entry creation | 23-Feb-2016 |
| Last entry update | 29-Jun-2023 |
| Version number | 8 |