C9h6orf141 similar to human chromosome 6 open reading frame 141 [Rattus norvegicus (Norway rat)] - Gene

Summary

Official Symbol: C9h6orf141provided by RGD
Official Full Name: similar to human chromosome 6 open reading frame 141provided by RGD
Primary source: RGD:1588829
See related: EnsemblRapid:ENSRNOG00000048967 AllianceGenome:RGD:1588829
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Rattus norvegicus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Rattus
Summary: Predicted to act upstream of or within blastocyst hatching. Orthologous to human C6orf141 (chromosome 6 open reading frame 141). [provided by Alliance of Genome Resources, Dec 2024]
Expression: Biased expression in Spleen (RPKM 9.0), Uterus (RPKM 6.1) and 8 other tissues See more
Orthologs: human mouse all
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Genomic context

Location:: 9q13

Exon count:: 2

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCr8 (GCF_036323735.1)	9	NC_086027.1 (27521466..27525644)
RS_2023_06	previous assembly	mRatBN7.2 (GCF_015227675.2)	9	NC_051344.1 (20024916..20029094)
106	previous assembly	Rnor_6.0 (GCF_000001895.5)	9	NC_005108.4 (23420654..23424832)

Chromosome 9 - NC_086027.1 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

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General gene information

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Gene Ontology Provided by RGD

Process	Evidence Code	Pubs
acts_upstream_of_or_within blastocyst hatching	ISO Inferred from Sequence Orthology more info

General protein information

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Preferred Names: uncharacterized protein C6orf141 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.