Description

CD14 molecule [Source:HGNC Symbol;Acc:HGNC:1628]

INSDC coordinates

chromosome:GRCh38:CM000667.2:140631728:140633701:1

About this gene

This gene has 5 transcripts (splice variants), 42 orthologues, is a member of 2 Ensembl protein families and is associated with 38 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
CD14-001ENST000003020141886375aaENSP00000304236
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS4232P08571 NM_000591
NP_000582
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 PI1APPRIS principal isoform
Glossary entry for APPRIS
APPRIS website
CD14-201ENST000004017431648375aaENSP00000385519
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS4232P08571 NM_001040021
NM_001174104
NM_001174105
NP_001035110
NP_001167575
NP_001167576
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.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS PI1APPRIS principal isoform
Glossary entry for APPRIS
APPRIS website
CD14-003ENST00000498971882213aaENSP00000426543
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D6RFL4 -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.

CD14-002ENST0000051254555655aaENSP00000425447
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D6RD81 -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.

CD14-004ENST0000051971548581aaENSP00000430884
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-E7EVL5 -CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.TSL:4

TSL4:The best supporting EST for this transcript is flagged as suspect.

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