Human (GRCh37.p13)
Description

deleted in liver cancer 1 [Source:HGNC Symbol;Acc:2897]

Gene Synonyms

ARHGAP7, DLC-1, HP, KIAA1723, STARD12, p122-RhoGAP

Location

Chromosome 8: 12,940,870-13,373,167 reverse strand.

GRCh37:CM000670.1

About this gene

This gene has 16 transcripts (splice variants) and 9 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000276297.4DLC1-00174471528aaENSP00000276297.4
 
Protein coding
CCDS5989Q96QB1 NM_182643.2GENCODE basic
ENST00000358919.2DLC1-00243921091aaENSP00000351797.2
 
Protein coding
CCDS5990Q45XF9 Q96QB1 NM_006094.4GENCODE basic
ENST00000512044.2DLC1-00537581125aaENSP00000422595.2
 
Protein coding
E9PDZ8 -GENCODE basic
ENST00000520226.1DLC1-00835561017aaENSP00000428028.1
 
Protein coding
CCDS55201Q96QB1 NM_001164271.1GENCODE basic
ENST00000511869.1DLC1-0042451463aaENSP00000425878.1
 
Protein coding
CCDS5991Q96QB1 NM_024767.3GENCODE basic
ENST00000316609.5DLC1-0031837498aaENSP00000321034.5
 
Protein coding
Q96QB1 -GENCODE basic
ENST00000503161.2DLC1-01656248aaENSP00000429537.1
 
Protein coding
E5RI70 -CDS 3' incomplete
ENST00000517868.2DLC1-01938375aaENSP00000473289.1
 
Protein coding
--CDS 5' incomplete
ENST00000510318.1DLC1-0062028No protein-
 
Processed transcript
---
ENST00000513883.1DLC1-007920No protein-
 
Processed transcript
---
ENST00000515225.1DLC1-012582No protein-
 
Processed transcript
---
ENST00000517333.1DLC1-013575No protein-
 
Processed transcript
---
ENST00000506171.1DLC1-010560No protein-
 
Processed transcript
---
ENST00000509922.1DLC1-009455No protein-
 
Processed transcript
---
ENST00000510250.2DLC1-0171925No protein-
 
Retained intron
---
ENST00000521730.1DLC1-018485No protein-
 
Retained intron
---

Retirement notice

Human only - retirement of this view

As of Ensembl release 93 this view will no longer be available for human, because we feel that the density of known human genetic variation is too great for the display to be informative in its current form.

Other species will not be affected, as they have less variation data.

For more information about the decision and on how to find variation data for a gene, please see our blog post.