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

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Gene: CHGB ENSSSCG00000039779

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Description

chromogranin B [Source:NCBI gene (formerly Entrezgene);Acc:397154]

Gene Synonyms

CGB

Location

Primary_assembly 17: 14,746,997-14,761,995 forward strand.

Sscrofa11.1:CM000828.5

About this gene

This gene has 2 transcripts (splice variants), 122 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000046816.2	CHGB-201	2690	666aa	ENSSSCP00000034002.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZQZ7	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,
ENSSSCT00000089516.2	CHGB-202	2475	625aa	ENSSSCP00000069314.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QWI8	-

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Summary

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