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- WFS1: Wolfram syndrome 1 (wolframin)
- Homo sapiens
- 1..33416
- organism | Homo sapiens
- mol_type | genomic DNA
- db_xref | taxon:9606
- chromosome | 4
- 1..33416
- gene | WFS1
- note | Derived by automated computational analysis using gene prediction method: BestRefseq.
- db_xref | GeneID:7466
- db_xref | HGNC:12762
- db_xref | HPRD:05864
- db_xref | MIM:606201
- join(1..165,7602..7838,17244..17326,19138..19282,21348..21518,22068..22148,25192..25340,30808..33416)
- gene | WFS1
- product | Wolfram syndrome 1 (wolframin), transcript variant 1
- note | Derived by automated computational analysis using gene prediction method: BestRefseq.
- db_xref | GI:224994202
- db_xref | GeneID:7466
- db_xref | HGNC:12762
- db_xref | HPRD:05864
- db_xref | MIM:606201
- join(1..165,7606..7838,17244..17326,19138..19282,21348..21518,22068..22148,25192..25340,30808..33416)
- gene | WFS1
- product | Wolfram syndrome 1 (wolframin), transcript variant 2
- note | Derived by automated computational analysis using gene prediction method: BestRefseq.
- db_xref | GI:224994204
- db_xref | GeneID:7466
- db_xref | HGNC:12762
- db_xref | HPRD:05864
- db_xref | MIM:606201
- join(7607..7838,17244..17326,19138..19282,21348..21518,22068..22148,25192..25340,30808..32619)
- gene | WFS1
- note | Derived by automated computational analysis using gene prediction method: BestRefseq.
- codon_start | 1
- transl_table | 1
- product | wolframin
- protein_id | NP_005996.2
- db_xref | GI:224994203
- db_xref | CCDS:CCDS3386.1
- db_xref | GeneID:7466
- db_xref | HGNC:12762
- db_xref | HPRD:05864
- db_xref | MIM:606201
- join(7607..7838,17244..17326,19138..19282,21348..21518,22068..22148,25192..25340,30808..32619)
- gene | WFS1
- note | Derived by automated computational analysis using gene prediction method: BestRefseq.
- codon_start | 1
- transl_table | 1
- product | wolframin
- protein_id | NP_001139325.1
- db_xref | GI:224994205
- db_xref | GeneID:7466
- db_xref | HGNC:12762
- db_xref | HPRD:05864
- db_xref | MIM:606201
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