Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: RSL1D1 ENSSSCG00000023984

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Description

ribosomal L1 domain containing 1 [Source:VGNC Symbol;Acc:VGNC:92477]

Location

Primary_assembly 3: 31,278,852-31,293,246 forward strand.

Sscrofa11.1:CM000814.5

About this gene

This gene has 2 transcripts (splice variants), 212 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000088939.2	RSL1D1-202	3779	493aa	ENSSSCP00000061526.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A481ARY0 A0A8D0WKZ3	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,
ENSSSCT00000023591.3	RSL1D1-201	1574	444aa	ENSSSCP00000023066.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0WIH7 I3LG73	-

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Summary

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