This gene encodes a member of the bicoid subfamily of the paired (PRD) homeobox family of proteins. The encoded protein acts as a transcription factor and may be autoregulatory. A similar protein in mice plays a role in craniofacial and rib cage development during embryogenesis. [provided by RefSeq, Jul 2008]
Subcellular localization of GSC (and its protein):
Gene Ontology (GO) terms for GSC:
| Interacting Gene | Interaction | Source/Score |
| Name |
|---|
| Developmental Biology |
| POU5F1 (OCT4), SOX2, NANOG repress genes related to differentiation |
| Transcriptional regulation of pluripotent stem cells |
| Disease | Score | NofPmids | NofSnps | Source |
| SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, SKELETAL ABNORMALITIES | 0.240542884 | 2 | 3 | BeFree_CLINVAR_ORPHANET |
| Craniofacial Abnormalities | 0.12 | 1 | 0 | CTD_human |
| Glioma | 0.003528744 | 13 | 0 | BeFree |
| Congenital Abnormality | 0.002909916 | 3 | 0 | BeFree_GAD |
| Glioblastoma | 0.002442977 | 9 | 0 | BeFree |
| Diabetes Mellitus, Insulin-Dependent | 0.002367032 | 1 | 0 | GAD |
| Glioblastoma Multiforme | 0.000542884 | 2 | 0 | BeFree |
| Neoplasms, Intracranial | 0.000542884 | 2 | 0 | BeFree |
| Cornelia De Lange Syndrome | 0.000271442 | 1 | 0 | BeFree |
| Liver carcinoma | 0.000271442 | 1 | 0 | BeFree |
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