Smim13 small integral membrane protein 13 [Rattus norvegicus (Norway rat)] - Gene

Summary

Official Symbol: Smim13provided by RGD
Official Full Name: small integral membrane protein 13provided by RGD
Primary source: RGD:1591023
See related: EnsemblRapid:ENSRNOG00000073728 AllianceGenome:RGD:1591023
Gene type: protein coding
RefSeq status: VALIDATED
Organism: Rattus norvegicus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Rattus
Also known as: RGD1566043
Summary: Predicted to be located in membrane. Orthologous to human SMIM13 (small integral membrane protein 13). [provided by Alliance of Genome Resources, Dec 2024]
Expression: Biased expression in Testes (RPKM 231.0), Brain (RPKM 131.3) and 9 other tissues See more
Orthologs: human mouse all
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Genomic context

Location:: 17p12

Exon count:: 2

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCr8 (GCF_036323735.1)	17	NC_086035.1 (23703414..23721457, complement)
RS_2023_06	previous assembly	mRatBN7.2 (GCF_015227675.2)	17	NC_051352.1 (23497662..23515705, complement)
106	previous assembly	Rnor_6.0 (GCF_000001895.5)	17	NC_005116.4 (21334989..21353252, complement)

Chromosome 17 - NC_086035.1 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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Markers

RH138588 (e-PCR)
- UniSTS:220675

RH134225 (e-PCR)
- UniSTS:217507

Gene Ontology Provided by RGD

Component	Evidence Code	Pubs
located_in membrane	IEA Inferred from Electronic Annotation more info

General protein information

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Preferred Names: small integral membrane protein 13

Names: UPF0766 protein C6orf228 homolog; rCG44158

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.