ID   HUES6 SOX11 ES.HET2
AC   CVCL_E6ID
SY   ES.HET2
RX   PubMed=31035284;
CC   Knockout cell: Method=CRISPR/Cas9; HGNC; HGNC:11191; SOX11 (Note=1 of 2 alleles).
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
DI   NCIt; C35321; Coffin-Siris syndrome
DI   ORDO; Orphanet_1465; Coffin-Siris syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_B194 ! HUES 6
SX   Female
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 10-04-25; Last updated: 10-04-25; Version: 1
//
RX   PubMed=31035284; DOI=10.1093/hmg/ddz089;
RA   Turan S., Boerstler T., Kavyanifar A., Loskarn S., Reis A., Winner B.,
RA   Lie D.C.-C.;
RT   "A novel human stem cell model for Coffin-Siris syndrome-like syndrome
RT   reveals the importance of SOX11 dosage for neuronal differentiation
RT   and survival.";
RL   Hum. Mol. Genet. 28:2589-2599(2019).
//