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Gene: Nrn1 ENSRNOG00000050767

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Description

neuritin 1 [Source:RGD Symbol;Acc:621586]

Gene Synonyms

MGC105351, Nrn

Location

Primary_assembly 17: 28,334,616-28,344,354 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 3 transcripts (splice variants), 205 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000154275.1	Nrn1-203	1649	214aa	ENSRNOP00000112822.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000073967.3	Nrn1-201	1618	142aa	ENSRNOP00000066878.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RBE5	APPRIS ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1,
ENSRNOT00000116839.2	Nrn1-202	1469	157aa	ENSRNOP00000082569.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	O08957	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data