Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Snx19 ENSRNOG00000014719

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Description

sorting nexin 19 [Source:RGD Symbol;Acc:1309857]

Gene Synonyms

LOC315478

Location

Primary_assembly 8: 37,088,191-37,125,264 forward strand.

GRCr8:CM070398.1

About this gene

This gene has 2 transcripts (splice variants), 265 orthologues, 3 paralogues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000020041.8	Snx19-201	6051	997aa	ENSRNOP00000020041.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZXB9	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 ALT2: 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 appear to be conserved in fewer than 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 ALT2,
ENSRNOT00000097104.2	Snx19-202	4236	926aa	ENSRNOP00000089305.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ABN1	-

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Summary

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