GUCY2D
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 17[12]
- Cytogenetic location
- 17p13.1[16]
- Expressed in
- mucosa of esophagus, white blood cell, monocyte, minor salivary glands, granulocyte, vagina, right lung, lymph node, prostate, primary visual cortex[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- cone-rod dystrophy 6, cone-rod dystrophy[13][14]
- HomoloGene ID
- 55442[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en CACD1
en CG-E
en CORD5
en CORD6
en CSNB1I
en CYGD
en guanylate cyclase 2D, retinal
en GUC1A4
en GUC2D
en GUCY2D
en LCA
en LCA1
en RCD2
en retGC
en RETGC-1
en ROSGC
en ROS-GC1
hu guanilát-cikláz 2D, retinal
hu retina guanilil cikláz 1
🔖 Identifiers · 12
- OpenAlex ID
- C31519591
- Ensembl gene ID
- ENSG00000132518
- Ensembl transcript ID
- ENST00000574510, ENST00000254854
- Entrez Gene ID
- 3000
- Exact match
- identifiers.org
- Freebase ID
- /m/03c3g8t
- HGNC ID
- 4689
- HGNC gene symbol
- GUCY2D
- Microsoft Academic ID (discontinued)
- 31519591
- OMIM ID
- 600179
- RefSeq RNA ID
- XM_011523816, NM_000180
- UMLS CUI
- C1415364
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