Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- 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: Zbtb21 ENSRNOG00000001623

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Description

zinc finger and BTB domain containing 21 [Source:RGD Symbol;Acc:1310841]

Gene Synonyms

LOC304056, Zfp295, Znf295

Location

Primary_assembly 11: 50,781,099-50,796,560 reverse strand.

GRCr8:CM070401.1

About this gene

This gene has 5 transcripts (splice variants), 197 orthologues and 25 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000116969.2	Zbtb21-203	5876	1082aa	ENSRNOP00000079938.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZPL5	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,
ENSRNOT00000143371.1	Zbtb21-205	7082	1054aa	ENSRNOP00000104239.1	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,
ENSRNOT00000102067.2	Zbtb21-202	6280	1054aa	ENSRNOP00000076506.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y585	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,
ENSRNOT00000041177.7	Zbtb21-201	5288	886aa	ENSRNOP00000049174.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZVF2	-
ENSRNOT00000130609.1	Zbtb21-204	2433	408aa	ENSRNOP00000103395.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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