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Human (GRCh37.p13)
Description

IQ motif containing GTPase activating protein 2 [Source:HGNC Symbol;Acc:6111]

Location

Chromosome 5: 75,699,074-76,003,957 forward strand.

GRCh37:CM000667.1

About this gene

This gene has 19 transcripts (splice variants) and 2 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000274364.6IQGAP2-00158441575aaENSP00000274364.6
 
Protein coding
CCDS34188D6R939 E7EWC2 Q13576
NM_001285460
NM_006633
NP_001272389
NP_006624
GENCODE basic
ENST00000379730.3IQGAP2-20155981077aaENSP00000442313.1
 
Protein coding
F5H7S7 -GENCODE basic
ENST00000505766.1IQGAP2-00342551402aaENSP00000421097.1
 
Protein coding
E7EWC2 -CDS 3' incomplete
ENST00000502745.1IQGAP2-00634041071aaENSP00000426027.1
 
Protein coding
CCDS68898J3KR91 NM_001285462
NP_001272391
GENCODE basic
ENST00000396234.3IQGAP2-00533761071aaENSP00000379535.3
 
Protein coding
CCDS68897D6R999 Q13576 NM_001285461
NP_001272390
GENCODE basic
ENST00000514350.1IQGAP2-0022617824aaENSP00000423672.1
 
Protein coding
D6R939 -CDS 3' incomplete
ENST00000514001.1IQGAP2-0041648509aaENSP00000422661.1
 
Protein coding
E9PDT6 -CDS 3' incomplete
ENST00000509074.1IQGAP2-012599167aaENSP00000425351.1
 
Protein coding
D6RDK8 -CDS 3' incomplete
ENST00000504477.1IQGAP2-007203979aaENSP00000425941.1
 
Nonsense mediated decay
H0YA28 -CDS 5' incomplete
ENST00000504254.1IQGAP2-01056260aaENSP00000423258.1
 
Nonsense mediated decay
D6R999 --
ENST00000513534.1IQGAP2-011559110aaENSP00000421319.1
 
Nonsense mediated decay
D6RGC6 --
ENST00000508410.1IQGAP2-016758No protein-
 
Processed transcript
---
ENST00000512383.1IQGAP2-013576No protein-
 
Processed transcript
---
ENST00000514579.1IQGAP2-017542No protein-
 
Processed transcript
---
ENST00000515505.1IQGAP2-009427No protein-
 
Processed transcript
---
ENST00000504815.1IQGAP2-008596No protein-
 
Retained intron
---
ENST00000512256.1IQGAP2-015583No protein-
 
Retained intron
---
ENST00000504558.1IQGAP2-014447No protein-
 
Retained intron
---
ENST00000509741.1IQGAP2-018394No protein-
 
Retained intron
---

Gene-based displays