Gene: NOTCH2NLR ENSG00000286106

Description

notch 2 N-terminal like R [Source:HGNC Symbol;Acc:HGNC:53925]

Location

Chromosome 1: 120,723,912-120,794,851 forward strand.

GRCh38:CM000663.2

View alleles of this gene on alternative sequences

About this gene

This gene has 2 transcripts (splice variants), 1 gene allele, 121 orthologues, 7 paralogues and is associated with 1 phenotype.

Transcripts

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Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000624419.3	NOTCH2NLR-201	2089	274aa	ENSP00000485259.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS91030	A0A096LNW5	NM_001396072.1	The Matched Annotation from NCBI and EMBL-EBI is a collaboration between Ensembl/GENCODE and RefSeq. The MANE Select is a default transcript per human gene that is representative of biology, well-supported, expressed and highly-conserved. This transcript set matches GRCh38 and is 100% identical between RefSeq and Ensembl/GENCODE for 5' UTR, CDS, splicing and 3'UTR.MANE Select, A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL 5: A transcript where no single transcript supports the model structure. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:5,
ENST00000690847.1	NOTCH2NLR-202	1403	312aa	ENSP00000509634.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A8I5KY86	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

Gene: NOTCH2NLR ENSG00000286106

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Gene: NOTCH2NLR ENSG00000286106

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