Description

lysophosphatidic acid receptor 1 [Source:MGI Symbol;Acc:MGI:108429]

Location
INSDC coordinates

chromosome:GRCm38:CM000997.2:58435255:58553898:1

About this gene

This gene has 8 transcripts (splice variants), 67 orthologues, 12 paralogues and is a member of 4 Ensembl protein families.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
Lpar1-002ENSMUST000001075713543364aaENSMUSP00000103197
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS18212A2AMI9 A2AMJ0 A2AMJ1
P61793 Q544V2
-TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

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 PI3APPRIS candidate principal isoform (earliest CCDS)
Glossary entry for APPRIS
APPRIS website
Lpar1-001ENSMUST000000550183512364aaENSMUSP00000052581
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS18212A2AMI9 A2AMJ0 A2AMJ1
P61793 Q544V2
NM_172989
NP_766577
TSL:1

TSL1: All splice junctions of the transcript 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 PI3APPRIS candidate principal isoform (earliest CCDS)
Glossary entry for APPRIS
APPRIS website
Lpar1-004ENSMUST000001075743437364aaENSMUSP00000103200
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS18212A2AMI9 A2AMJ0 A2AMJ1
P61793 Q544V2
-TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

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 PI3APPRIS candidate principal isoform (earliest CCDS)
Glossary entry for APPRIS
APPRIS website
Lpar1-003ENSMUST000001075753421364aaENSMUSP00000103201
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS18212A2AMI9 A2AMJ0 A2AMJ1
P61793 Q544V2
NM_010336
NP_034466
TSL:1

TSL1: All splice junctions of the transcript 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 PI3APPRIS candidate principal isoform (earliest CCDS)
Glossary entry for APPRIS
APPRIS website
Lpar1-005ENSMUST000001075703244346aaENSMUSP00000103196
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS71391P61793 NM_001290486
NP_001277415
TSL:1

TSL1: All splice junctions of the transcript 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 ALT1APPRIS candidate principal isoform that is conserved in at least three tested non-primate species
Glossary entry for APPRIS
APPRIS website
Lpar1-008ENSMUST0000015517051475aaENSMUSP00000121440
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-A2AMI9 A2AMJ0 A2AMJ1
-CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

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.

Lpar1-006ENSMUST0000014735445456aaENSMUSP00000123694
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-A2AMJ0 A2AMJ1 -CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.TSL:2

TSL2: The best supporting mRNA is flagged as suspect or the support is from multiple ESTs.

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.

Lpar1-007ENSMUST0000014536133545aaENSMUSP00000116856
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-A2AMJ1 -CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.TSL:2

TSL2: The best supporting mRNA is flagged as suspect or the support is from multiple ESTs.

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.

Gene-based displays