Description

B cell leukemia/lymphoma 11B [Source:MGI Symbol;Acc:MGI:1929913]

INSDC coordinates

chromosome:GRCm38:CM001005.2:107910403:108003602:1

Transcripts

This gene has 3 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
Bcl11b-001ENSMUST000000660608111884 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS36553Q3TEG9 Q99PV8 NM_001079883
NP_001073352
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 CI1APPRIS candidate principal isoform (longest coding sequence)
Glossary entry for APPRIS
APPRIS website
Bcl11b-003ENSMUST000001098912888812 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS36552Q3TEG9 Q99PV8 NM_021399
NP_067374
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 CIAPPRIS candidate principal isoform
Glossary entry for APPRIS
APPRIS website
Bcl11b-002ENSMUST000001098872522690 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS70419Q3TEG9 Q99PV8 NM_001286343
NP_001273272
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).

Gene-based displays