Description

Nance-Horan syndrome (human) [Source:MGI Symbol;Acc:MGI:2684894]

INSDC coordinates

chromosome:GRCm38:CM001013.2:161833296:162159730:1

About this gene

This gene has 2 transcripts (splice variants), 74 orthologues, 2 paralogues and is a member of 1 Ensembl protein family.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
Nhs-001ENSMUST0000008708588051647aaENSMUSP00000084319
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS72461B1AV60 NM_001290526
NP_001277455
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).
Nhs-201ENSMUST0000008156948811626aaENSMUSP00000080280
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS41201B9EJX2 NM_001081052
NP_001074521
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.

Gene-based displays