Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: Mitf ENSRNOG00000008658

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Description

melanocyte inducing transcription factor [Source:RGD Symbol;Acc:3092]

Location

Primary_assembly 4: 131,965,714-132,177,790 forward strand.

GRCr8:CM070394.1

About this gene

This gene has 5 transcripts (splice variants), 276 orthologues, 3 paralogues and is associated with 26 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000051121.6	Mitf-201	4937	525aa	ENSRNOP00000044350.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2ULS4	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 ALT1: 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 is conserved in at least 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 ALT1,
ENSRNOT00000083127.3	Mitf-202	4933	510aa	ENSRNOP00000073565.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K5U8	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4,
ENSRNOT00000171312.1	Mitf-205	4839	501aa	ENSRNOP00000100525.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000094478.2	Mitf-203	4716	419aa	ENSRNOP00000084182.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZYC4 A6IBG2	-
ENSRNOT00000128180.1	Mitf-204	1830	416aa	ENSRNOP00000100348.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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