Cellosaurus Lis39_FXS8N (CVCL_Y365)
Cell line name | Lis39_FXS8N |
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Synonyms | Lis39_FXS_8_N; LIS39; LIS2 |
Accession | CVCL_Y365 |
Resource Identification Initiative | To cite this cell line use: Lis39_FXS8N (RRID:CVCL_Y365) |
Comments | From: Tel-Aviv Sourasky Medical Center; Tel-Aviv; Israel. Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-15-0319. Omics: Genomics; ChIP-seq; H3K27ac. Omics: Genomics; ChIP-seq; H3K27me3. Omics: Genomics; ChIP-seq; H3K4me1. Omics: Genomics; ChIP-seq; H3K4me3. Omics: Genomics; ChIP-seq; H3K9me3. Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358. Cell type: Embryonic stem cell; CL=CL_0002322. |
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 | Blastocyst stage |
Category | Embryonic stem cell |
Publications | PubMed=24172903; DOI=10.1038/nature12745 |
Cross-references | |
Cell line databases/resources | NIHhESC; NIHhESC-15-0319 |
Encyclopedic resources | Wikidata; Q54902626 |
Gene expression databases | GEO; GSM1571895
GEO; GSM1571896 GEO; GSM1571897 GEO; GSM1571898 GEO; GSM1571899 GEO; GSM1571900 GEO; GSM1571901 GEO; GSM1571902 GEO; GSM1571903 GEO; GSM1571904 GEO; GSM1571905 GEO; GSM1571906 |
Entry history | |
Entry creation | 07-Nov-2014 |
Last entry update | 10-Apr-2025 |
Version number | 12 |