Description

cytochrome P450, family 4, subfamily F, polypeptide 11 [Source:HGNC Symbol;Acc:HGNC:13265]

Location
INSDC coordinates

chromosome:GRCh38:CM000681.2:15912367:15934867:1

About this gene

This gene has 5 transcripts (splice variants), 69 orthologues, 16 paralogues, is a member of 1 Ensembl protein family and is associated with 162 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
CYP4F11-001ENST000004021193161524aaENSP00000384588
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS12337Q9HBI6 NM_021187
NP_067010
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.

CYP4F11-004ENST000002480412977524aaENSP00000248041
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS12337Q9HBI6 NM_001128932
NP_001122404
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.

CYP4F11-201ENST000006206142908454aaENSP00000481243
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-F8W978 -TSL:5

Transcript Support Level 5, for transcripts that are not supported at all by either an mRNA or an 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).
CYP4F11-002ENST000003267422877454aaENSP00000319859
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-F8W978 -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).
CYP4F11-003ENST000005918412531199aaENSP00000476972
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-V9GYP6 -TSL:2

Transcript Support Level 2, when transcripts are supported by multiple ESTs or by an mRNA 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.

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

Gene-based displays