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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: GLIPR1 ENSG00000139278

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Description

GLI pathogenesis-related 1 [Source:HGNC Symbol;Acc:17001]

Gene Synonyms

CRISP7, GLIPR, GliPR, RTVP1

Location

Chromosome 12: 75,874,460-75,897,633 forward strand.

GRCh37:CM000674.1

About this gene

This gene has 4 transcripts (splice variants) and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000266659.3	GLIPR1-001	5877	266aa	ENSP00000266659.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS9011	P48060	NM_006851.2	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000456650.3	GLIPR1-003	714	238aa	ENSP00000391144.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding		F6VVE8	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000550491.1	GLIPR1-004	667	89aa	ENSP00000448008.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		J3QTC9	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000536703.1	GLIPR1-002	1234	148aa	ENSP00000440595.1	Nonsense mediated decay		B4E3S5	-	-

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Summary

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