Gene and Protein Information
Species	TM	AA	Chromosomal Location	Gene Symbol	Gene Name	Reference
Human	-	854	4p16.3	PDE6B	phosphodiesterase 6B
Mouse	-	856	5 53.07 cM	Pde6b	phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide
Rat	-	-	14 p22	Pde6b	phosphodiesterase 6B

Previous and Unofficial Names

phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide

Database Links
Alphafold	P35913 (Hs), P23440 (Mm)
BRENDA	3.1.4.17
CATH/Gene3D	1.10.1300.10, 3.30.450.40
ChEMBL Target	CHEMBL3430880 (Hs)
Ensembl Gene	ENSG00000133256 (Hs), ENSMUSG00000029491 (Mm), ENSRNOG00000000065 (Rn)
Entrez Gene	5158 (Hs), 18587 (Mm), 289878 (Rn)
Human Protein Atlas	ENSG00000133256 (Hs)
KEGG Enzyme	3.1.4.17
KEGG Gene	hsa:5158 (Hs), mmu:18587 (Mm), rno:289878 (Rn)
OMIM	180072 (Hs)
Pharos	P35913 (Hs)
UniProtKB	P35913 (Hs), P23440 (Mm)
Wikipedia	PDE6B (Hs)

Enzyme Reaction
EC Number: 3.1.4.17

Clinically-Relevant Mutations and Pathophysiology
Disease:  Night blindness, congenital stationary, autosomal dominant 2; CSNBAD2 Synonyms: Congenital stationary night blindness [Orphanet: ORPHA215] [Disease Ontology: DOID:0050534] Disease Ontology: DOID:0050534 OMIM: 163500 Orphanet: ORPHA215
Disease:  Retinitis pigmentosa 40; RP40 Synonyms: Retinitis pigmentosa [Orphanet: ORPHA791] [Disease Ontology: DOID:10584] Disease Ontology: DOID:10584 OMIM: 613801 Orphanet: ORPHA791