Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Ensembl protein families
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: C19orf44 ENSSSCG00000013859

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Description

chromosome 2 C19orf44 homolog [Source:VGNC Symbol;Acc:VGNC:86004]

Location

Chromosome 2: 61,077,140-61,105,111 reverse strand.

Sscrofa11.1:CM000813.5

About this gene

This gene has 2 transcripts (splice variants) and 243 orthologues.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
C19orf44-201	ENSSSCT00000065669.2	5511	258aa	ENSSSCP00000040200.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287A8D5	-
C19orf44-202	ENSSSCT00000059218.2	2782	638aa	ENSSSCP00000037331.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UTM7 F1S9W4	<p>APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS.</p><p>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.</p>APPRIS P1,

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Summary

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Gene-based displays