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

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Gene: ZRANB3 ENSBTAG00000026842

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Description

zinc finger RANBP2-type containing 3 [Source:VGNC Symbol;Acc:VGNC:37373]

Location

Primary_assembly 2: 61,800,646-62,108,563 forward strand.

ARS-UCD2.0:CM008169.2

About this gene

This gene has 5 transcripts (splice variants), 196 orthologues and 30 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000038374.7	ZRANB3-205	3466	1052aa	ENSBTAP00000038188.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	K7DXW5	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,
ENSBTAT00000082650.3	ZRANB3-201	5778	1030aa	ENSBTAP00000059308.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LVH6	-
ENSBTAT00000073311.3	ZRANB3-202	5718	1010aa	ENSBTAP00000062570.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LYC7 E1BB03	-
ENSBTAT00000072233.3	ZRANB3-203	5703	1005aa	ENSBTAP00000074134.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MUB4	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,
ENSBTAT00000082407.3	ZRANB3-204	5685	999aa	ENSBTAP00000067396.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MAW7	-

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Summary

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