Description

hydrolethalus syndrome 1 [Source:MGI Symbol;Acc:MGI:1924082]

Location
INSDC coordinates

chromosome:GRCm38:CM001002.2:35560820:35570398:1

About this gene

This gene has 2 transcripts (splice variants), 55 orthologues and is a member of 1 Ensembl protein family.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSRefSeqFlags
Hyls1-001ENSMUST000001151101973314aaENSMUSP00000110762
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS52754NM_029762
NP_084038
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.

Hyls1-002ENSMUST000001325474269No protein-
 
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.
--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.

Gene-based displays