SMDT1 single-pass membrane protein with aspartate rich tail 1 [Macaca mulatta (Rhesus monkey)] - Gene

Summary

Official Symbol: SMDT1provided by VGNC
Official Full Name: single-pass membrane protein with aspartate rich tail 1provided by VGNC
Primary source: VGNC:VGNC:77771
Locus tag: EGK_03107
See related: Ensembl:ENSMMUG00000013061
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Macaca mulatta
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Cercopithecidae; Cercopithecinae; Macaca
Also known as: C22orf32; C10H22orf32
Orthologs: human mouse all
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Genomic context

Location:: chromosome: 10

Exon count:: 3

Annotation release	Status	Assembly	Chr	Location
103	current	Mmul_10 (GCF_003339765.1)	10	NC_041763.1 (9411245..9415252, complement)
102	previous assembly	Mmul_8.0.1 (GCF_000772875.2)	10	NC_027902.1 (84184722..84188729)

Chromosome 10 - NC_041763.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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General gene information

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Gene Ontology Provided by RefSeq

Process	Evidence Code	Pubs
involved_in calcium import into the mitochondrion	IEA Inferred from Electronic Annotation more info	PubMed
involved_in mitochondrial calcium ion homeostasis	IEA Inferred from Electronic Annotation more info	PubMed

Component	Evidence Code	Pubs
located_in mitochondrial inner membrane	IEA Inferred from Electronic Annotation more info	PubMed
part_of uniplex complex	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: essential MCU regulator, mitochondrial

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.