Description

lipase, endothelial [Source:HGNC Symbol;Acc:HGNC:6623]

Synonyms

EDL

Location
INSDC coordinates

chromosome:GRCh38:CM000680.2:49560699:49599182:1

Transcripts



This gene has 7 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
LIPG-001ENST0000026129210441500 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS11938A0A024R2B5 J3KTN7 LIPG-001
Q9Y5X9
NM_006033
NP_006024
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 PIAPPRIS principal isoform [01-09-2014]
Glossary entry for APPRIS
APPRIS website
LIPG-004ENST000005776282323390 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-J3KTN7 J3QQQ0 LIPG-004
-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.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
LIPG-002ENST000004272241760426 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-B4DTR8 J3KTN7 LIPG-002
-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.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
LIPG-003ENST000005800361453354 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-J3KTN7 LIPG-003 Q9Y5X9
-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).
LIPG-006ENST0000058308350524 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-J3KTN7 LIPG-006 -CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.TSL:3

TSL3:The only support for this transcript is from a single EST.

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.

LIPG-005ENST000006232773548No protein
 
TEC
-LIPG-005 -
LIPG-007ENST00000579750565188 aa
 
Non stop decay
-J3KTN7 LIPG-007 -CDS 5' incomplete5' truncation in transcript evidence prevents annotation of the start 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