Description

notochord homeobox [Source:HGNC Symbol;Acc:HGNC:31839]

Location
INSDC coordinates

chromosome:GRCh38:CM000664.2:73202258:73212513:1

About this gene

This gene has 1 transcript (splice variant), 54 orthologues, 4 paralogues, is a member of 1 Ensembl protein family and is associated with 15 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
NOTO-001ENST000003984682749251aaENSP00000381486
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS46335A8MTQ0 NM_001134462
NP_001127934
TSL:2

Transcript Support Level 2, when transcripts are supported by multiple ESTs or by an mRNA flagged as suspect.

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