SNRNP200
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 2[14]
- Cytogenetic location
- 2q11.2[17]
- Expressed in
- ventricular zone, embryo, epithelium of nasopharynx, ganglionic eminence, nasal epithelium, urethra, parotid gland, pylorus, nipple, tibia[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[13]
- Genetic association
- retinitis pigmentosa 33[15]
- HomoloGene ID
- 5859[3]
- Strand orientation
- reverse strand[16]
🏷️ Also known as
en ASCC3L1
en BRR2
en HELIC2
en RP33
en small nuclear ribonucleoprotein U5 subunit 200
en SNRNP200
en U5-200KD
🔖 Identifiers · 11
- Image (Wikimedia Commons)
- Protein ASCC3L1 PDB 2q0z.png ↗
- Ensembl gene ID
- ENSG00000144028
- Ensembl transcript ID
- ENST00000497539, ENST00000323853, ENST00000429650, ENST00000480242, ENST00000480615, ENST00000480835, ENST00000484372, ENST00000493271, ENST00000652267
- Entrez Gene ID
- 23020
- Exact match
- identifiers.org
- Freebase ID
- /m/03gxf5r
- HGNC ID
- 30859
- HGNC gene symbol
- SNRNP200
- OMIM ID
- 601664
- RefSeq RNA ID
- NM_014014
- UMLS CUI
- C1540207
🔗 Connections
Expressed in 7
Chromosome 1
Found in taxon 1
Instance of 1
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