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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Rcc1l ENSRNOG00000001483

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Description

RCC1 like [Source:RGD Symbol;Acc:1307558]

Gene Synonyms

LOC360796, Wbscr16

Location

Primary_assembly 12: 28,180,154-28,215,151 forward strand.

GRCr8:CM070402.1

About this gene

This gene has 2 transcripts (splice variants), 207 orthologues, 9 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000136900.1	Rcc1l-202	2446	463aa	ENSRNOP00000110821.1	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,
ENSRNOT00000002032.7	Rcc1l-201	2262	461aa	ENSRNOP00000002032.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J0K7 D4AE90	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,

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Summary

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