DIS3L2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 2[12]
- Cytogenetic location
- 2q37.1[15]
- Encodes
- DIS3 like 3'-5' exoribonuclease 2[10]
- Expressed in
- sural nerve, sperm, buccal mucosa cell, right uterine tube, right lobe of thyroid gland, right testis, left testis, Achilles tendon, left lobe of thyroid gland, left ovary[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- Perlman syndrome[13]
- HomoloGene ID
- 62417[3]
- Strand orientation
- forward strand[14]
🏷️ Also known as
en DIS3L2
en DIS3 like 3'-5' exoribonuclease 2
en FAM6A
en hDIS3L2
en PRLMNS
ar DIS٣L٢
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000144535
- Ensembl transcript ID
- ENST00000498319, ENST00000273009, ENST00000325385, ENST00000390005, ENST00000409401, ENST00000417808, ENST00000418143, ENST00000429283, ENST00000433430, ENST00000434477, ENST00000441279, ENST00000445090, ENST00000464554, ENST00000470087
- Entrez Gene ID
- 129563
- Exact match
- identifiers.org
- Freebase ID
- /m/011vl82z
- HGNC ID
- 28648
- HGNC gene symbol
- DIS3L2
- OMIM ID
- 614184
- RefSeq RNA ID
- NR_046477, NM_001257281, NM_001257282, NM_152383, NR_046476
- UMLS CUI
- C2239353
🔗 Connections
Expressed in 3
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
← Genetic association 1
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Summary
DIS3L2 is a gene[1].