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

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Gene: ZBTB18 ENSBTAG00000000385

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Description

zinc finger and BTB domain containing 18 [Source:VGNC Symbol;Acc:VGNC:37063]

Location

Primary_assembly 16: 33,149,464-33,158,383 reverse strand.

ARS-UCD2.0:CM008183.2

About this gene

This gene has 5 transcripts (splice variants), 199 orthologues and 37 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000000497.6	ZBTB18-203	3853	531aa	ENSBTAP00000000497.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A140T829	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 ALT1: 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 is conserved in at least 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 ALT1,
ENSBTAT00000121793.1	ZBTB18-201	4177	522aa	ENSBTAP00000099022.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0JN76	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,
ENSBTAT00000091501.1	ZBTB18-202	3905	522aa	ENSBTAP00000078776.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0JN76	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,
ENSBTAT00000076393.3	ZBTB18-204	906	227aa	ENSBTAP00000069945.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1NED1	-
ENSBTAT00000134543.1	ZBTB18-205	171	56aa	ENSBTAP00000076298.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S2G3	-

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Summary

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