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

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Gene: Armcx4 ENSRNOG00000043128

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Description

armadillo repeat containing, X-linked 4 [Source:RGD Symbol;Acc:2325053]

Gene Synonyms

LOC100359678

Location

Primary_assembly X: 102,153,800-102,164,633 forward strand.

GRCr8:CM070411.1

About this gene

This gene has 5 transcripts (splice variants), 153 orthologues and 10 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000105118.2	Armcx4-202	8976	2372aa	ENSRNOP00000082317.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZMH4	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,
ENSRNOT00000106559.2	Armcx4-203	8880	2372aa	ENSRNOP00000078017.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZMH4	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,
ENSRNOT00000040476.7	Armcx4-201	8107	2364aa	ENSRNOP00000051224.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZV39	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,
ENSRNOT00000116704.2	Armcx4-204	8081	2372aa	ENSRNOP00000079216.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZMH4	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,
ENSRNOT00000117978.2	Armcx4-205	7497	2314aa	ENSRNOP00000085816.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZMH4	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,

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Summary

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