Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Btbd19 ENSRNOG00000042163

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Description

BTB domain containing 19 [Source:RGD Symbol;Acc:2320529]

Gene Synonyms

LOC100361234

Location

Primary_assembly 5: 135,834,508-135,840,903 reverse strand.

GRCr8:CM070395.1

About this gene

This gene has 3 transcripts (splice variants), 115 orthologues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000067675.5	Btbd19-201	2324	356aa	ENSRNOP00000062687.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3Z860	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,
ENSRNOT00000095182.2	Btbd19-202	2264	336aa	ENSRNOP00000082729.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZXT3	-
ENSRNOT00000096215.2	Btbd19-203	2164	286aa	ENSRNOP00000088296.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y5K1	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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Orthologues

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