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: Serinc1 ENSRNOG00000029360

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Description

serine incorporator 1 [Source:RGD Symbol;Acc:727843]

Gene Synonyms

LRRGT00191, Tde1l, Tde2

Location

Primary_assembly 20: 37,396,497-37,443,124 reverse strand.

GRCr8:CM070410.1

About this gene

This gene has 2 transcripts (splice variants), 178 orthologues and 16 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000074379.4	Serinc1-202	6383	1687aa	ENSRNOP00000064593.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0R5C9	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 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,
ENSRNOT00000001066.8	Serinc1-201	2763	453aa	ENSRNOP00000001066.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6K4C4 Q7TNK0	-

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Summary

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