Gene table of VSX1 : visual system homeobox 1

Gene-disease associations table

Disease ID	Disease name	Source of annotation with VSX1	OMIM link	Number of associated genes	genes
614195	CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME	ClinVar, OMIM, HUMSAVAR	link to OMIM	1	VSX1
PS122000	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS	ClinVar, HUMSAVAR	link to OMIM	4	OVOL2, ZEB1, VSX1, COL8A2
PS148300	KERATOCONUS	ClinVar, OMIM, HUMSAVAR	link to OMIM	2	VSX1, ZNF469

Associated genes in ENSEMBL

Associated proteins - SwissProt Accession ID

Associated PDB IDs

Cytogenetic Band

Tandem repeats annotation

Transcription regulation as annotated in TRRUST

Associated KEGG pathways

Associated REACTOME pathways

Associated GO terms for Molecular function

GO term	GO ID	GO IC
transcription regulatory region DNA binding	GO:0044212	3.03
sequence-specific DNA binding	GO:0043565	2.79
transcription factor activity, sequence-specific DNA binding	GO:0003700	2.65
organic cyclic compound binding	GO:0097159	1.05
regulatory region DNA binding	GO:0000975	3.03
regulatory region nucleic acid binding	GO:0001067	3.03
macromolecular complex binding	GO:0044877	2.61
binding	GO:0005488	0.18
nucleic acid binding	GO:0003676	1.44
DNA binding	GO:0003677	1.92
chromatin binding	GO:0003682	3.64
heterocyclic compound binding	GO:1901363	1.06
nucleic acid binding transcription factor activity	GO:0001071	2.65