CLDN19
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 1[11]
- Cytogenetic location
- 1p34.2[14]
- Encodes
- Claudin 19[9]
- Expressed in
- trigeminal ganglion, spinal ganglia, retinal pigment epithelium, renal medulla, tibial nerve, vena cava, epithelium of nasopharynx, body of tongue, ventral tegmental area, trachea[15][16][17][18][19][20][21][22][23][24]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- renal hypomagnesemia 5 with ocular involvement[12]
- HomoloGene ID
- 17528[3]
- Strand orientation
- reverse strand[13]
🏷️ Also known as
en claudin 19
en CLDN19
en HOMG5
ar CLDN١٩
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000164007
- Ensembl transcript ID
- ENST00000539749, ENST00000296387, ENST00000372539
- Entrez Gene ID
- 149461
- Exact match
- identifiers.org
- Freebase ID
- /m/03hm16t
- HGNC ID
- 2040
- HGNC gene symbol
- CLDN19
- OMIM ID
- 610036
- RefSeq RNA ID
- NM_148960, NM_001123395, NM_001185117
- UMLS CUI
- C1413468
🔗 Connections
Expressed in 8
Chromosome 1
Found in taxon 1
Instance of 1
Press Enter · cited answer in seconds