2310065F04Rik RIKEN cDNA 2310065F04 gene [Mus musculus (house mouse)] - Gene

Summary

Official Symbol: 2310065F04Rikprovided by MGI
Official Full Name: RIKEN cDNA 2310065F04 geneprovided by MGI
Primary source: MGI:MGI:1921434
See related: Ensembl:ENSMUSG00000087410 AllianceGenome:MGI:1921434
Gene type: ncRNA
RefSeq status: VALIDATED
Organism: Mus musculus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus
Also known as: linc-Myh
Summary: Is expressed in hindlimb muscle; nervous system; neural retina; and skeletal muscle tissue. [provided by Alliance of Genome Resources, Apr 2022]
Expression: Biased expression in mammary gland adult (RPKM 3.0) and testis adult (RPKM 0.4) See more
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Genomic context

Location:: 11 B3; 11 40.59 cM

Exon count:: 5

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCm39 (GCF_000001635.27)	11	NC_000077.7 (67003287..67010906, complement)
108.20200622	previous assembly	GRCm38.p6 (GCF_000001635.26)	11	NC_000077.6 (67112461..67120080, complement)

Chromosome 11 - NC_000077.7 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Expression

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See details

Project title: Mouse ENCODE transcriptome data
Description: RNA profiling data sets generated by the Mouse ENCODE project.
BioProject: PRJNA66167
Publication: PMID 25409824
Analysis date: n/a

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Linc-MYH configures INO80 to regulate muscle stem cell numbers and skeletal muscle hypertrophy.
Title: Linc-MYH configures INO80 to regulate muscle stem cell numbers and skeletal muscle hypertrophy.

Submit: New GeneRIF Correction

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.