Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss 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

Configure this page

Share this page

Bookmark this page

.

Gene: fd19B FBgn0031086

.

Description

forkhead domain 19B

Gene Synonyms

fd19B

Location

Primary_assembly X: 20,091,428-20,092,408 reverse strand.

BDGP6.54:AE014298.5

About this gene

This gene has 1 transcript (splice variant), 33 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0070032	fd19B-RA	981	260aa	FBpp0070031	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B4F604 B4F605 B4F607 B4F608 B4F611 C0MLX8 C0MLX9 C0MLY1 Q0IGQ1 Q9W5X5	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 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,

.

Summary

.

.