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

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Gene: GIMAP4 ENSSSCG00000027826

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Description

GTPase, IMAP family member 4 [Source:VGNC Symbol;Acc:VGNC:88446]

Location

Primary_assembly 18: 6,429,887-6,452,966 reverse strand.

Sscrofa11.1:CM000829.5

About this gene

This gene has 2 transcripts (splice variants), 134 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000052261.3	GIMAP4-201	2018	322aa	ENSSSCP00000035566.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZV97 A0A8D0RJW6	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,
ENSSSCT00000038872.3	GIMAP4-202	2302	317aa	ENSSSCP00000040504.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UZ47 K9IVM5	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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Paralogues

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