Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
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  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: C16h19orf44 ENSRNOG00000023700

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Description

similar to human chromosome 19 open reading frame 44 [Source:RGD Symbol;Acc:1311847]

Gene Synonyms

LOC290615, RGD1311847

Location

Primary_assembly 16: 17,414,045-17,430,183 reverse strand.

GRCr8:CM070406.1

About this gene

This gene has 3 transcripts (splice variants) and 177 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000030617.5	C16h19orf44-201	2432	621aa	ENSRNOP00000032342.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2UKS5	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,
ENSRNOT00000146354.1	C16h19orf44-202	2782	573aa	ENSRNOP00000111014.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000152029.1	C16h19orf44-203	2190	587aa	ENSRNOP00000107929.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Orthologues

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