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Human (GRCh38.p14)
Description

bridging integrator 3 [Source:HGNC Symbol;Acc:HGNC:1054]

Location

Chromosome 8: 22,620,418-22,669,148 reverse strand.

GRCh38:CM000670.2

About this gene

This gene has 11 transcripts (splice variants), 201 orthologues and 3 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000276416.11BIN3-2011836253aaENSP00000276416.6
 
Protein coding
CCDS47825Q9NQY0-1 NM_018688.6MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000519513.5BIN3-2051431199aaENSP00000430423.1
 
Protein coding
Q9NQY0-2 -GENCODE BasicTSL:2
ENST00000399977.8BIN3-2021340205aaENSP00000382859.4
 
Protein coding
CCDS87587H7BYV6 -GENCODE PrimaryGENCODE BasicTSL:2
ENST00000520292.1BIN3-207775149aaENSP00000429660.1
 
Protein coding
E5RHU4 -GENCODE BasicTSL:5
ENST00000522268.1BIN3-21032127aaENSP00000428768.1
 
Protein coding
E5RGB5 -GENCODE PrimaryGENCODE BasicTSL:5
ENST00000522687.5BIN3-21165963aaENSP00000430546.1
 
Nonsense mediated decay
E5RJI6 -TSL:5
ENST00000519335.5BIN3-204893No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000519863.5BIN3-206803No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000520489.5BIN3-2083589No protein-
 
Retained intron
--TSL:2
ENST00000521140.1BIN3-209591No protein-
 
Retained intron
--TSL:5
ENST00000518366.1BIN3-203470No protein-
 
Retained intron
--TSL:3