Human (GRCh37.p13)
Description

seizure related 6 homolog (mouse) [Source:HGNC Symbol;Acc:15955]

Location

Chromosome 17: 27,281,919-27,333,458 reverse strand.

GRCh37:CM000679.1

About this gene

This gene has 10 transcripts (splice variants) and 2 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000317338.12SEZ6-0024471994aaENSP00000312942.11
 
Protein coding
CCDS45639K7ELJ4 Q53EL9 -GENCODE basic
ENST00000360295.9SEZ6-0014306993aaENSP00000353440.9
 
Protein coding
CCDS45638H0YF95 K7ELJ4 Q53EL9
NM_178860.4GENCODE basic
ENST00000442608.3SEZ6-0123805980aaENSP00000403784.3
 
Protein coding
K7ELJ4 -GENCODE basic
ENST00000540632.2SEZ6-0033804919aaENSP00000437650.2
 
Protein coding
H0YF95 K7ELJ4 -CDS 5' incomplete
ENST00000335960.6SEZ6-2011721508aaENSP00000337407.6
 
Protein coding
C9JFF1 K7ELJ4 -GENCODE basic
ENST00000535262.1SEZ6-018807101aaENSP00000440216.1
 
Protein coding
--CDS 5' incomplete
ENST00000539265.1SEZ6-013601131aaENSP00000443589.1
 
Protein coding
--CDS 5' incomplete
ENST00000585644.1SEZ6-01757556aaENSP00000466107.1
 
Protein coding
K7ELJ4 -CDS 3' incomplete
ENST00000540419.1SEZ6-0063468454aaENSP00000440764.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000544224.2SEZ6-011807No protein-
 
Retained intron
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