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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	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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