Human (GRCh37.p13)
Description

basigin (Ok blood group) [Source:HGNC Symbol;Acc:1116]

Gene Synonyms

5F7, CD147, EMMPRIN, M6, OK, TCSF

Location

Chromosome 19: 571,297-583,493 forward strand.

GRCh37:CM000681.1

About this gene

This gene has 12 transcripts (splice variants), 2 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000333511.3BSG-0011974385aaENSP00000333769.3
 
Protein coding
CCDS12033P35613 R4GMX5 R4GN83
NM_001728.3GENCODE basic
ENST00000545507.2BSG-0061767176aaENSP00000473664.1
 
Protein coding
CCDS58635P35613 R4GMX5 R4GN83
NM_198590.2GENCODE basic
ENST00000346916.4BSG-0021618205aaENSP00000344707.3
 
Protein coding
CCDS12032P35613 R4GMX5 R4GN83
NM_198591.2GENCODE basic
ENST00000353555.4BSG-0031616269aaENSP00000343809.4
 
Protein coding
CCDS12034B4DY23 P35613 Q54A51
R4GMX5 R4GN83
NM_198589.2GENCODE basic
ENST00000573784.1BSG-00855984aaENSP00000473393.1
 
Protein coding
R4GMX5 R4GN83 -CDS 3' incomplete
ENST00000573216.1BSG-007545160aaENSP00000458665.1
 
Protein coding
I3L192 R4GN83 -CDS 3' incomplete
ENST00000576984.1BSG-01053652aaENSP00000473528.1
 
Protein coding
R4GN83 -CDS 3' incomplete
ENST00000574970.1BSG-009567No protein-
 
Processed transcript
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ENST00000571735.1BSG-0052143No protein-
 
Retained intron
---
ENST00000576925.2BSG-011610No protein-
 
Retained intron
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ENST00000572899.1BSG-012580No protein-
 
Retained intron
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ENST00000590218.1BSG-013545No protein-
 
Retained intron
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