Gene: Slc25a37 ENSMUSG00000034248

Description

solute carrier family 25, member 37 [Source:MGI Symbol;Acc:MGI:1914962]

Gene Synonyms

1700020E22Rik, 4930513O14Rik, 4930526G11Rik, C330015G08Rik, Frascati, Mfrn, Mfrn1, Mscp, mitoferrin

Location

Chromosome 14: 69,479,297-69,522,561 reverse strand.

GRCm39:CM001007.3

About this gene

This gene has 7 transcripts (splice variants), 206 orthologues, 48 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000037064.5	Slc25a37-201	4174	338aa	ENSMUSP00000039990.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS27238	Q920G8-1	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, GENCODE Primary represents a minimal set that contains MANE Select, MANE Plus Clinical and Ensembl Canonical transcripts and transcripts containing any conserved exons and common alternative splicing events (including exons skips) that are absent from the MANE and Ensembl Canonical transcripts for protein-coding genes. Other biotypes will have the GENCODE Primary flag added to the Ensembl Canonical transcript and for lncRNA genes only this will be the transcripts with the longest genomic span.GENCODE Primary, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic, 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, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENSMUST00000183882.2	Slc25a37-202	342	100aa	ENSMUSP00000139178.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		J3QPY4	TSL 3: A transcript where the only support is from a single EST The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:3, 3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSMUST00000508004.1	Slc25a37-207	4711	182aa	ENSMUSP00000286367.1	Nonsense mediated decay		-	-
ENSMUST00000508003.1	Slc25a37-206	4532	182aa	ENSMUSP00000286366.1	Nonsense mediated decay		-	-
ENSMUST00000508002.1	Slc25a37-205	4502	182aa	ENSMUSP00000286365.1	Nonsense mediated decay		-	-
ENSMUST00000184914.2	Slc25a37-204	2212	182aa	ENSMUSP00000139104.2	Nonsense mediated decay		Q920G8-2	TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENSMUST00000184497.2	Slc25a37-203	5927	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,

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Gene: Slc25a37 ENSMUSG00000034248

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Gene: Slc25a37 ENSMUSG00000034248

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