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

Configure this page

Share this page

Bookmark this page

.

Gene: Fam110c ENSRNOG00000005660

.

Description

family with sequence similarity 110, member C [Source:RGD Symbol;Acc:1564713]

Gene Synonyms

LOC500638

Location

Primary_assembly 6: 53,352,870-53,401,117 forward strand.

GRCr8:CM070396.1

About this gene

This gene has 3 transcripts (splice variants), 170 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000168352.1	Fam110c-203	4339	384aa	ENSRNOP00000104159.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000125199.1	Fam110c-202	7107	326aa	ENSRNOP00000099942.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HB40 Q5RKJ0	-
ENSRNOT00000007466.6	Fam110c-201	4764	326aa	ENSRNOP00000007466.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2Q3A6 A6HB40 Q5RKJ0	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,

.

Summary

.

.