Description

Bloom syndrome, RecQ helicase-like [Source:MGI Symbol;Acc:MGI:1328362]

Location
INSDC coordinates

chromosome:GRCm38:CM001000.2:80454993:80535119:1

Transcripts

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

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
Blm-202ENSMUST0000017031548691419 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS52281E9PZ97 NM_007550
NP_031576
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
Blm-201ENSMUST0000008131445981416 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS40000O88700 NM_001042527
NP_001035992
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

Gene-based displays