Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: fam110b ENSDARG00000088073

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Description

family with sequence similarity 110 member B [Source:NCBI gene (formerly Entrezgene);Acc:573995]

Location

Chromosome 2: 22,208,404-22,286,828 reverse strand.

GRCz11:CM002886.2

About this gene

This gene has 2 transcripts (splice variants), 182 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000168653.2	fam110b-202	2701	397aa	ENSDARP00000138309.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1R180	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,
ENSDART00000127810.3	fam110b-201	2620	397aa	ENSDARP00000104632.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1R180	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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