Summary
- Splice variants
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- Gene alleles
Sequence
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Comparative Genomics
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Gene: Btf3l7 ENSRNOG00000031086

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Description

basic transcription factor 3 like 7 [Source:RGD Symbol;Acc:1563931]

Gene Synonyms

LOC365426, RGD1563931

Location

Primary_assembly 1: 226,983,796-226,984,270 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 1 transcript (splice variant).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSRNOT00000042738.4	Btf3l7-201	474	No protein	-	A gene that has homology to known protein-coding genes but contain a frameshift and/or stop codon(s) which disrupts the ORF. Thought to have arisen through duplication followed by loss of function.Pseudogene	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,

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Summary

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