Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
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: Dok7 ENSRNOG00000022419

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Description

docking protein 7 [Source:RGD Symbol;Acc:1566416]

Gene Synonyms

LOC305448, RGD1566416

Location

Primary_assembly 14: 79,891,367-79,932,252 reverse strand.

GRCr8:CM070404.1

About this gene

This gene has 5 transcripts (splice variants), 243 orthologues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000035385.6	Dok7-201	2593	598aa	ENSRNOP00000036262.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZDW9	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,
ENSRNOT00000136750.1	Dok7-204	2870	481aa	ENSRNOP00000104998.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000118992.2	Dok7-203	2812	492aa	ENSRNOP00000096459.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GLL7	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,
ENSRNOT00000098833.2	Dok7-202	2336	360aa	ENSRNOP00000083030.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZVQ6	-
ENSRNOT00000161564.1	Dok7-205	1879	522aa	ENSRNOP00000112374.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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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Summary

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