Gene: C1h19orf18 ENSRNOG00000019280

Description

similar to human chromosome 19 open reading frame 18 [Source:RGD Symbol;Acc:1595996]

Gene Synonyms

AABR07002093.1, LOC691722

Location

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 66 orthologues and is associated with 1 phenotype.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000096365.2	C1h19orf18-202	1112	227aa	ENSRNOP00000081660.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZTD7	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 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,
ENSRNOT00000026074.6	C1h19orf18-201	578	176aa	ENSRNOP00000026074.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4ADP8	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,

Strains

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.