Human (GRCh38.p14)
Description

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

Gene Synonyms

BSN2, FLJ20043

Location

Chromosome 9: 16,409,503-16,870,843 reverse strand.

GRCh38:CM000671.2

About this gene

This gene has 16 transcripts (splice variants), 130 orthologues, 1 paralogue and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000380672.9BNC2-203128081099aaENSP00000370047.3
 
Protein coding
CCDS6482Q6ZN30-1 NM_017637.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:2
ENST00000545497.5BNC2-2103750729aaENSP00000444640.2
 
Protein coding
F5H586 -GENCODE basicTSL:1
ENST00000418777.5BNC2-2053673860aaENSP00000408370.1
 
Protein coding
H0Y6W5 -TSL:5CDS 5' incomplete
ENST00000700553.1BNC2-21534491011aaENSP00000515060.1
 
Protein coding
A0A8V8TPU4 -CDS 5' incomplete
ENST00000380667.6BNC2-20233611032aaENSP00000370042.1
 
Protein coding
B1APH0 -GENCODE basicAPPRIS ALT2TSL:5
ENST00000411752.5BNC2-2042106327aaENSP00000392212.1
 
Protein coding
H0Y4J1 -TSL:1CDS 5' incomplete
ENST00000380666.6BNC2-2011211294aaENSP00000370041.3
 
Protein coding
A0A1B0GX98 -TSL:5CDS 3' incomplete
ENST00000603713.5BNC2-2121008245aaENSP00000474045.1
 
Protein coding
Q06HB9 -TSL:1CDS 3' incomplete
ENST00000471301.3BNC2-20774543aaENSP00000474832.1
 
Protein coding
S4R3X5 -GENCODE basicTSL:3
ENST00000486514.5BNC2-209688164aaENSP00000474647.1
 
Protein coding
S4R3R8 -TSL:2CDS 3' incomplete
ENST00000617779.1BNC2-21468740aaENSP00000482793.1
 
Protein coding
Q06HC7 -TSL:1CDS 3' incomplete
ENST00000468187.6BNC2-206662109aaENSP00000474468.1
 
Protein coding
S4R3K9 -TSL:3CDS 5' incomplete
ENST00000613349.4BNC2-21356140aaENSP00000477717.1
 
Protein coding
Q06HC7 -TSL:1CDS 3' incomplete
ENST00000603313.5BNC2-211545121aaENSP00000473935.1
 
Protein coding
S4R351 -TSL:4CDS 3' incomplete
ENST00000700554.1BNC2-21627686aaENSP00000515061.1
 
Protein coding
Q06HB5 -CDS 5' incomplete
ENST00000484726.5BNC2-2084841903aaENSP00000431516.1
 
Nonsense mediated decay
Q6ZN30-2 -TSL:5