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    A430005L14Rik RIKEN cDNA A430005L14 gene [ Mus musculus (house mouse) ]

    Gene ID: 97159, updated on 9-Dec-2024

    Summary

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    Official Symbol
    A430005L14Rikprovided by MGI
    Official Full Name
    RIKEN cDNA A430005L14 geneprovided by MGI
    Primary source
    MGI:MGI:2140680
    See related
    Ensembl:ENSMUSG00000047613 AllianceGenome:MGI:2140680
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Mus musculus
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus
    Summary
    Predicted to be located in nucleoplasm. Orthologous to human C1orf174 (chromosome 1 open reading frame 174). [provided by Alliance of Genome Resources, Dec 2024]
    Expression
    Ubiquitous expression in testis adult (RPKM 28.6), CNS E11.5 (RPKM 19.4) and 28 other tissues See more
    Orthologs
    human all
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    Genomic context

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    See A430005L14Rik in Genome Data Viewer
    Location:
    4 E2; 4 83.78 cM
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    RS_2024_02 current GRCm39 (GCF_000001635.27) 4 NC_000070.7 (154041694..154046382)
    108.20200622 previous assembly GRCm38.p6 (GCF_000001635.26) 4 NC_000070.6 (153957237..153961925)

    Chromosome 4 - NC_000070.7Genomic Context describing neighboring genes Neighboring gene STARR-seq mESC enhancer starr_12225 Neighboring gene predicted gene, 25880 Neighboring gene cDNA sequence BC039966 Neighboring gene STARR-positive B cell enhancer ABC_E6293 Neighboring gene DNA fragmentation factor, beta subunit Neighboring gene centrosomal protein 104 Neighboring gene predicted gene, 31566

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    Related articles in PubMed

    1. Functional analysis of candidate genes from genome-wide association studies of hearing. Ingham NJ, et al. Hear Res, 2020 Mar 1. PMID 31927188, Free PMC Article
    2. Targeting a complex transcriptome: the construction of the mouse full-length cDNA encyclopedia. Carninci P, et al. Genome Res, 2003 Jun. PMID 12819125, Free PMC Article
    3. Mouse screen reveals multiple new genes underlying mouse and human hearing loss. Ingham NJ, et al. PLoS Biol, 2019 Apr. PMID 30973865, Free PMC Article
    4. Large-scale cDNA analysis reveals phased gene expression patterns during preimplantation mouse development. Ko MS, et al. Development, 2000 Apr. PMID 10725249
    5. Libraries enriched for alternatively spliced exons reveal splicing patterns in melanocytes and melanomas. Watahiki A, et al. Nat Methods, 2004 Dec. PMID 15782199

    See all (19) citations in PubMed

    GeneRIFs: Gene References Into Functions

    Variation

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    Alleles

    Alleles of this type are documented at Mouse Genome Informatics  (MGI)
    • Targeted (1) 

    General gene information

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    Markers

    Homology

    Gene Ontology Provided by MGI

    Function Evidence Code Pubs
    enables molecular_function ND
    No biological Data available
    more info
    		  
    Process Evidence Code Pubs
    involved_in biological_process ND
    No biological Data available
    more info
    		  
    Component Evidence Code Pubs
    located_in nucleoplasm IEA
    Inferred from Electronic Annotation
    more info
    		  
    located_in nucleoplasm ISO
    Inferred from Sequence Orthology
    more info
    		  

    General protein information

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    Preferred Names
    UPF0688 protein C1orf174 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.

    mRNA and Protein(s)

    1. NM_001163019.1 → NP_001156491.1  UPF0688 protein C1orf174 homolog isoform 2

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) lacks an alternate in-frame exon compared to variant 1. The resulting isoform (2) has the same N- and C-termini but is shorter compared to isoform 1.
      Source sequence(s)
      AK039812, BC052148, BE994111, BY781135
      Consensus CDS
      CCDS51395.1
      UniProtKB/TrEMBL
      A0A0A0MQL2, E9PUH0
      Related
      ENSMUSP00000101270.3, ENSMUST00000105645.9
      Conserved Domains (1) summary
      pfam15772
      Location:6 → 184
      UPF0688; UPF0688 family

    2. NM_175287.4 → NP_780496.2  UPF0688 protein C1orf174 homolog isoform 1

      See identical proteins and their annotated locations for NP_780496.2

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (1).
      Source sequence(s)
      AK039812, BC052148, BE994111
      Consensus CDS
      CCDS19003.1
      UniProtKB/Swiss-Prot
      A2AM12, Q80WR5, Q8CA21
      Related
      ENSMUSP00000054638.3, ENSMUST00000058393.9
      Conserved Domains (1) summary
      pfam15772
      Location:6 → 222
      UPF0688; UPF0688 family

    RefSeqs of Annotated Genomes: GCF_000001635.27-RS_2024_02

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCm39 C57BL/6J

    Genomic

    1. NC_000070.7 Reference GRCm39 C57BL/6J

      Range
      154041694..154046382
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein Strain
    Heading Accession and Version
    Protein Accession Links
    GenPept Link UniProtKB Link
    Q80WR5.1 GenPept UniProtKB/Swiss-Prot:Q80WR5

    Gene LinkOut

    The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

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