Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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: NSMCE1 ENSPTRG00000007912

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Description

NSE1 homolog, SMC5-SMC6 complex component [Source:VGNC Symbol;Acc:VGNC:5852]

Location

Chromosome 16: 26,755,386-26,798,965 reverse strand.

Pan_tro_3.0:CM000330.3

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
ENSPTRT00000014590.4	NSMCE1-201	1245	266aa	ENSPTRP00000013521.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2W514 H2QAT5	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,
ENSPTRT00000099026.1	NSMCE1-202	213	70aa	ENSPTRP00000092159.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8JMC8 A0A6D2WJ63	-

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Summary

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