Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Nrp1 ENSRNOG00000010744

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Description

neuropilin 1 [Source:RGD Symbol;Acc:621588]

Gene Synonyms

Nrp

Location

Primary_assembly 19: 73,256,557-73,411,702 forward strand.

GRCr8:CM070409.1

About this gene

This gene has 4 transcripts (splice variants), 259 orthologues, 36 paralogues and is associated with 15 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000014492.7	Nrp1-201	3839	923aa	ENSRNOP00000014492.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9QWJ9	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, 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,
ENSRNOT00000080465.3	Nrp1-202	5528	915aa	ENSRNOP00000075034.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2R9S2	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,
ENSRNOT00000114861.2	Nrp1-204	5282	899aa	ENSRNOP00000085705.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A3Y3	-
ENSRNOT00000108605.2	Nrp1-203	3727	905aa	ENSRNOP00000082340.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZTD9	-

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Summary

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