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

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Gene: ZBTB7B ENSBTAG00000021512

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Description

zinc finger and BTB domain containing 7B [Source:VGNC Symbol;Acc:VGNC:37090]

Location

Primary_assembly 3: 15,579,983-15,598,162 reverse strand.

ARS-UCD1.3:CM008170.2

About this gene

This gene has 7 transcripts (splice variants), 188 orthologues and 27 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000093459.1	ZBTB7B-203	2317	609aa	ENSBTAP00000082729.1	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,
ENSBTAT00000124762.1	ZBTB7B-202	2185	565aa	ENSBTAP00000090568.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000107811.1	ZBTB7B-207	2158	567aa	ENSBTAP00000089510.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000124706.1	ZBTB7B-201	2152	554aa	ENSBTAP00000085164.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000118831.1	ZBTB7B-205	2097	596aa	ENSBTAP00000077656.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000123960.1	ZBTB7B-206	2040	549aa	ENSBTAP00000075872.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000028669.6	ZBTB7B-204	2009	538aa	ENSBTAP00000028669.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BGW3	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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