Human (GRCh37.p13)
Description

basonuclin 2 [Source:HGNC Symbol;Acc:30988]

Gene Synonyms

BSN2, FLJ20043

Location

Chromosome 9: 16,409,501-16,870,841 reverse strand.

GRCh37:CM000671.1

About this gene

This gene has 12 transcripts (splice variants), 1 paralogue and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000380672.4BNC2-008128441099aaENSP00000370047.3
 
Protein coding
CCDS6482D3DRJ1 Q06HB9 Q06HC2
Q06HC7 Q6ZN30 S4R351
NM_017637.5GENCODE basic
ENST00000418777.1BNC2-0093673860aaENSP00000408370.1
 
Protein coding
H0Y6W5 Q06HB9 Q06HC2
Q06HC7 S4R351
-CDS 5' incomplete
ENST00000380667.2BNC2-01033611032aaENSP00000370042.1
 
Protein coding
B1APH0 D3DRJ1 -GENCODE basic
ENST00000545497.1BNC2-20230151004aaENSP00000444640.1
 
Protein coding
D3DRJ1 F5H586 -GENCODE basic
ENST00000380666.2BNC2-2012852903aaENSP00000370041.2
 
Protein coding
Q06HB9 Q06HC2 Q06HC7
Q6ZN30 S4R351
-GENCODE basic
ENST00000411752.1BNC2-0052106327aaENSP00000392212.1
 
Protein coding
H0Y4J1 -CDS 5' incomplete
ENST00000603713.1BNC2-0111008245aaENSP00000474045.1
 
Protein coding
Q06HB9 Q06HC7 S4R351
-CDS 3' incomplete
ENST00000471301.2BNC2-00374543aaENSP00000474832.1
 
Protein coding
S4R3X5 -GENCODE basic
ENST00000486514.1BNC2-007688164aaENSP00000474647.1
 
Protein coding
Q06HC7 S4R351 S4R3R8
-CDS 3' incomplete
ENST00000468187.2BNC2-002662109aaENSP00000474468.1
 
Protein coding
Q06HC7 S4R3K9 -CDS 5' incomplete
ENST00000603313.1BNC2-012545121aaENSP00000473935.1
 
Protein coding
Q06HC7 S4R351 -CDS 3' incomplete
ENST00000484726.1BNC2-0014841903aaENSP00000431516.1
 
Nonsense mediated decay
Q06HB9 Q06HC2 Q06HC7
Q6ZN30 S4R351
--