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
External references
Supporting evidence
ID History
- Gene history

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Gene: Zfp777 ENSRNOG00000033639

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Description

zinc finger protein 777 [Source:RGD Symbol;Acc:1566056]

Gene Synonyms

LOC502764, RGD1566056, Znf777

Location

Primary_assembly 4: 78,347,315-78,373,357 reverse strand.

GRCr8:CM070394.1

About this gene

This gene has 2 transcripts (splice variants), 122 orthologues and 56 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000113218.2	Zfp777-202	3624	999aa	ENSRNOP00000079994.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZP65	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,
ENSRNOT00000038517.5	Zfp777-201	3207	860aa	ENSRNOP00000034825.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LV17	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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Gene tree

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