Summary
- Splice variants
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Gene: Nsmce1 ENSRNOG00000015218

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Description

NSE1 homolog, SMC5-SMC6 complex component [Source:RGD Symbol;Acc:1307760]

Gene Synonyms

LOC361645, MGC124662, RGD1307760

Location

Primary_assembly 1: 189,462,677-189,491,432 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants) and 204 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000055034.3	Nsmce1-201	1299	289aa	ENSRNOP00000051912.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JSX1	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 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,
ENSRNOT00000089464.3	Nsmce1-202	1142	274aa	ENSRNOP00000071768.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2R4J4	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,

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Summary

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