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

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Gene: Enpp4 ENSRNOG00000010174

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Description

ectonucleotide pyrophosphatase/phosphodiesterase 4 [Source:RGD Symbol;Acc:1308689]

Gene Synonyms

LOC301261

Location

Primary_assembly 9: 24,360,272-24,396,152 forward strand.

GRCr8:CM070399.1

About this gene

This gene has 6 transcripts (splice variants), 213 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000134157.1	Enpp4-204	4978	605aa	ENSRNOP00000110540.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000172326.1	Enpp4-206	4969	571aa	ENSRNOP00000099066.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000136805.1	Enpp4-205	4879	523aa	ENSRNOP00000103183.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000124075.1	Enpp4-203	4655	540aa	ENSRNOP00000108921.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000065048.6	Enpp4-202	4638	457aa	ENSRNOP00000059215.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A2W1	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,
ENSRNOT00000045937.6	Enpp4-201	4523	471aa	ENSRNOP00000050116.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LTZ5	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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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

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

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Personal Data