C8h3orf62 similar to human chromosome 3 open reading frame 62 [Rattus norvegicus (Norway rat)] - Gene

Summary

Official Symbol: C8h3orf62provided by RGD
Official Full Name: similar to human chromosome 3 open reading frame 62provided by RGD
Primary source: RGD:1589651
See related: EnsemblRapid:ENSRNOG00000046155 AllianceGenome:RGD:1589651
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
Summary: Predicted to be involved in spermatogenesis. Orthologous to human C3orf62 (chromosome 3 open reading frame 62). [provided by Alliance of Genome Resources, Dec 2024]
Expression: Biased expression in Testes (RPKM 459.1) and Kidney (RPKM 16.2) See more
Orthologs: human mouse all
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Genomic context

Location:: 8q32

Exon count:: 4

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCr8 (GCF_036323735.1)	8	NC_086026.1 (117958583..117963137)
RS_2023_06	previous assembly	mRatBN7.2 (GCF_015227675.2)	8	NC_051343.1 (109080032..109084588)
106	previous assembly	Rnor_6.0 (GCF_000001895.5)	8	NC_005107.4 (117170620..117175235)

Chromosome 8 - NC_086026.1 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 RGD

Process	Evidence Code	Pubs
involved_in spermatogenesis	ISO Inferred from Sequence Orthology more info

General protein information

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Preferred Names: uncharacterized protein C3orf62 homolog

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.