Human (GRCh38.p14)
Description

importin 7 [Source:HGNC Symbol;Acc:HGNC:9852]

Gene Synonyms

IMP7, RANBP7

Location

Chromosome 11: 9,384,626-9,448,127 forward strand.

GRCh38:CM000673.2

About this gene

This gene has 11 transcripts (splice variants), 216 orthologues and 4 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000379719.8IPO7-20161621038aaENSP00000369042.3
 
Protein coding
CCDS31425O95373 NM_006391.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000877280.1IPO7-20952131008aaENSP00000547339.1
 
Protein coding
--GENCODE Basic
ENST00000877281.1IPO7-2103596584aaENSP00000547340.1
 
Protein coding
--GENCODE Basic
ENST00000970585.1IPO7-21133611027aaENSP00000640644.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000527431.1IPO7-202607130aaENSP00000435235.1
 
Protein coding
E9PLB2 -TSL:4CDS 3' incomplete
ENST00000630083.1IPO7-20819564aaENSP00000486575.1
 
Protein coding
E9PLJ0 -GENCODE BasicTSL:5
ENST00000533233.1IPO7-20657864aaENSP00000433313.1
 
Nonsense mediated decay
E9PLJ0 -TSL:4
ENST00000533680.1IPO7-207639No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000528833.1IPO7-203355No protein-
 
Retained intron
--TSL:5
ENST00000530037.1IPO7-204347No protein-
 
Retained intron
--TSL:2
ENST00000531235.1IPO7-205283No protein-
 
Retained intron
--TSL:3