Description

Bardet-Biedl syndrome 12 (human) [Source:MGI Symbol;Acc:MGI:2686651]

Location
INSDC coordinates

chromosome:GRCm38:CM000996.2:37312554:37321453:1

Transcripts

This gene has 2 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
Bbs12-001ENSMUST000000579752433708 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS38417Q5SUD9 Z4YKQ3 NM_001008502
NP_001008502
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).APPRIS PIAPPRIS principal isoform
Glossary entry for APPRIS
APPRIS website
Bbs12-002ENSMUST000001081212348593 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS57209Z4YKQ3 NM_001255992
NP_001242921
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