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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: SEMG2 ENSG00000124157

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Description

semenogelin II [Source:HGNC Symbol;Acc:10743]

Gene Synonyms

SGII

Location

Chromosome 20: 43,849,941-43,853,099 forward strand.

GRCh37:CM000682.1

About this gene

This gene has 1 transcript (splice variant) and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000372769.3	SEMG2-001	2051	582aa	ENSP00000361855.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS13346	Q02383	NM_003008.2	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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