Description

hypermethylated in cancer 2 [Source:MGI Symbol;Acc:MGI:1929869]

Location
INSDC coordinates

chromosome:GRCm38:CM001009.2:17233572:17263430:1

About this gene

This gene has 2 transcripts (splice variants), 51 orthologues, 1 paralogue and is a member of 1 Ensembl protein family.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
Hic2-001ENSMUST000000901906354619aaENSMUSP00000087656
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS27999Q9JLZ6 NM_178922
NP_849253
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
Hic2-002ENSMUST000001156982765566aaENSMUSP00000111362
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-Q9JLZ6 -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