Description

nescient helix loop helix 2 [Source:HGNC Symbol;Acc:HGNC:7818]

Synonyms

bHLHa34, HEN2, NSCL2

INSDC coordinates

chromosome:GRCh38:CM000663.2:115836377:115843917:1

About this gene

This gene has 3 transcripts (splice variants), 46 orthologues, 10 paralogues, is a member of 1 Ensembl protein family and is associated with 15 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
NHLH2-001ENST000003695067226135aaENSP00000358519
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS885A0A024R0I7 Q02577 -TSL:NA

Transcript Support Level Not Analysed. Pseudogenes, single exon transcripts, HLA, T-cell receptor and Ig transcripts are not analysed and therefore not given any of the TSL categories.

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.

NHLH2-002ENST000003202382512135aaENSP00000322087
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS885A0A024R0I7 Q02577 NM_001111061
NM_005599
NP_001104531
NP_005590
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.

NHLH2-003ENST00000429731855107aaENSP00000405062
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-A6PVY9 -CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.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