Description

neurotensin receptor 1 [Source:MGI Symbol;Acc:MGI:97386]

INSDC coordinates

chromosome:GRCm38:CM000995.2:180499976:180544980:1

About this gene

This gene has 2 transcripts (splice variants), 56 orthologues, 7 paralogues and is a member of 1 Ensembl protein family.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
Ntsr1-001ENSMUST000000290843917424aaENSMUSP00000029084
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS17177A2ACT4 O88319 NM_018766
NP_061236
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Ntsr1-201ENSMUST000001704482594424aaENSMUSP00000127548
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS17177A2ACT4 O88319 -TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Gene-based displays