Human (GRCh37.p13)
Description

seizure threshold 2 homolog (mouse) [Source:HGNC Symbol;Acc:29040]

Gene Synonyms

C1orf84, EIEE18, FLJ10387, FLJ34502, KIAA0467, RP11-506B15.1, RP11-506B15.3, SZT2A, SZT2B

Location

Chromosome 1: 43,855,553-43,918,321 forward strand.

GRCh37:CM000663.1

About this gene

This gene has 11 transcripts (splice variants) and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000562955.1SZT2-004122813375aaENSP00000457168.1
 
Protein coding
CCDS30694Q5T011 NM_015284.3GENCODE basic
ENST00000372442.1SZT2-202102172533aaENSP00000361519.1
 
Protein coding
Q5T011 -GENCODE basic
ENST00000310739.4SZT2-2011196180aaENSP00000312234.4
 
Protein coding
E2QRB6 -GENCODE basic
ENST00000372450.4SZT2-0021191178aaENSP00000361528.4
 
Protein coding
Q5T011 -GENCODE basic
ENST00000406439.2SZT2-0032133168aaENSP00000386070.2
 
Nonsense mediated decay
Q5T011 --
ENST00000471177.1SZT2-008574No protein-
 
Processed transcript
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ENST00000460536.1SZT2-0094286No protein-
 
Retained intron
---
ENST00000470139.1SZT2-0054098No protein-
 
Retained intron
---
ENST00000357658.3SZT2-0011623No protein-
 
Retained intron
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ENST00000478140.1SZT2-006543No protein-
 
Retained intron
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ENST00000470897.1SZT2-007466No protein-
 
Retained intron
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