Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
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Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: MBNL3 ENSBTAG00000014088

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Description

muscleblind like splicing regulator 3 [Source:VGNC Symbol;Acc:VGNC:31285]

Location

Primary_assembly X: 16,210,736-16,324,815 reverse strand.

ARS-UCD1.3:CM008197.2

About this gene

This gene has 6 transcripts (splice variants), 133 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000082968.2	MBNL3-202	2295	364aa	ENSBTAP00000064746.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M4K5	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,
ENSBTAT00000070945.2	MBNL3-204	2532	359aa	ENSBTAP00000072476.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MRK1	-
ENSBTAT00000079731.2	MBNL3-205	2496	347aa	ENSBTAP00000074098.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MRK1	-
ENSBTAT00000083513.2	MBNL3-203	2130	309aa	ENSBTAP00000058680.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LP57	-
ENSBTAT00000082204.2	MBNL3-201	2111	306aa	ENSBTAP00000062121.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LXA7	-
ENSBTAT00000018746.7	MBNL3-206	1400	362aa	ENSBTAP00000018746.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1B8I9	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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