Human (GRCh37.p13)
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.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000266659.3GLIPR1-0015877266aa
 
Protein coding
CCDS9011P48060 NM_006851.2Ensembl CanonicalGENCODE Basic
ENST00000456650.3GLIPR1-003714238aa
 
Protein coding
F6VVE8 -CDS 3' incomplete
ENST00000550491.1GLIPR1-00466789aa
 
Protein coding
J3QTC9 -CDS 3' incomplete
ENST00000536703.1GLIPR1-0021234148aa
 
Nonsense mediated decay
B4E3S5 --
Name

GLIPR1 (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: P48060

CCDS

This gene is a member of the Human CCDS set: CCDS9011.1

Ensembl version

ENSG00000139278.5

Other assemblies

This gene maps to 75,480,680-75,503,853 in GRCh38 coordinates.

Gene type

Protein coding

Annotation method

Annotation for this gene includes both automatic annotation from Ensembl and Havana manual curation, see article.

Alternative genes

This gene corresponds to the following database identifiers:

Havana gene:
OTTHUMG00000169757 (version 1)

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