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

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Gene: FAM110D ENSBTAG00000013131

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Description

family with sequence similarity 110 member D [Source:VGNC Symbol;Acc:VGNC:54426]

Location

Primary_assembly 2: 126,935,591-126,939,832 reverse strand.

ARS-UCD2.0:CM008169.2

About this gene

This gene has 3 transcripts (splice variants), 178 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000017456.6	FAM110D-202	1771	304aa	ENSBTAP00000017456.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A452DIM8	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 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,
ENSBTAT00000129758.1	FAM110D-201	1382	270aa	ENSBTAP00000096535.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6H7I7	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,
ENSBTAT00000095511.1	FAM110D-203	1358	270aa	ENSBTAP00000076641.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6H7I7	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,

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Summary

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