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Lin9 lin-9 DREAM MuvB core complex component [ Mus musculus (house mouse) ]

Gene ID: 72568, updated on 27-Nov-2024

Summary

Official Symbol
Lin9provided by MGI
Official Full Name
lin-9 DREAM MuvB core complex componentprovided by MGI
Primary source
MGI:MGI:1919818
See related
Ensembl:ENSMUSG00000058729 AllianceGenome:MGI:1919818
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
Also known as
TGS; Bara; TGS1; Lin-9; mLin-9; 2700022J23Rik
Summary
Predicted to enable DNA binding activity. Predicted to be involved in regulation of cell cycle and regulation of transcription by RNA polymerase II. Predicted to be part of transcription repressor complex. Predicted to be active in nucleoplasm. Is expressed in telencephalon ventricular layer. Orthologous to human LIN9 (lin-9 DREAM MuvB core complex component). [provided by Alliance of Genome Resources, Nov 2024]
Expression
Broad expression in CNS E11.5 (RPKM 4.0), placenta adult (RPKM 3.7) and 26 other tissues See more
Orthologs
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Genomic context

See Lin9 in Genome Data Viewer
Location:
1 H4; 1 84.46 cM
Exon count:
16
Annotation release Status Assembly Chr Location
RS_2024_02 current GRCm39 (GCF_000001635.27) 1 NC_000067.7 (180468715..180518252)
108.20200622 previous assembly GRCm38.p6 (GCF_000001635.26) 1 NC_000067.6 (180641150..180690687)

Chromosome 1 - NC_000067.7Genomic Context describing neighboring genes Neighboring gene poly (ADP-ribose) polymerase family, member 1 Neighboring gene microRNA 6904 Neighboring gene STARR-seq mESC enhancer starr_03209 Neighboring gene predicted gene, 53485 Neighboring gene Mix paired-like homeobox Neighboring gene acyl-Coenzyme A binding domain containing 3

Genomic regions, transcripts, and products

Expression

  • 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

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Variation

Alleles

Alleles of this type are documented at Mouse Genome Informatics  (MGI)
  • Endonuclease-mediated (3) 
  • Gene trapped (1) 
  • Targeted (4)  1 citation

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Gene Ontology Provided by MGI

Function Evidence Code Pubs
enables DNA binding IBA
Inferred from Biological aspect of Ancestor
more info
 
Process Evidence Code Pubs
involved_in DNA biosynthetic process IEA
Inferred from Electronic Annotation
more info
 
involved_in DNA-templated transcription IEA
Inferred from Electronic Annotation
more info
 
involved_in regulation of cell cycle IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in regulation of transcription by RNA polymerase II IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in reproductive process IBA
Inferred from Biological aspect of Ancestor
more info
 
Component Evidence Code Pubs
is_active_in nucleoplasm IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in nucleoplasm IEA
Inferred from Electronic Annotation
more info
 
located_in nucleoplasm ISO
Inferred from Sequence Orthology
more info
 
part_of transcription repressor complex IEA
Inferred from Electronic Annotation
more info
 

General protein information

Preferred Names
protein lin-9 homolog
Names
TUDOR gene similar 1 protein
lin-9 homolog
type I interferon receptor beta chain-associated protein

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_001103182.3NP_001096652.3  protein lin-9 homolog

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript and encodes the functional protein.
    Source sequence(s)
    AC167020
    Consensus CDS
    CCDS48468.2
    UniProtKB/Swiss-Prot
    Q5TKA0, Q8C735, Q8C9D8
    Related
    ENSMUSP00000141331.3, ENSMUST00000192561.6
    Conserved Domains (1) summary
    pfam06584
    Location:127231
    DIRP

RNA

  1. NR_120498.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) uses an alternate splice site at an internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AC167020, BC088992
    Related
    ENSMUST00000193892.6

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_000067.7 Reference GRCm39 C57BL/6J

    Range
    180468715..180518252
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_006496988.3XP_006497051.1  protein lin-9 homolog isoform X1

    See identical proteins and their annotated locations for XP_006497051.1

    UniProtKB/TrEMBL
    A0A0A6YVZ7
    Conserved Domains (1) summary
    pfam06584
    Location:75179
    DIRP
  2. XM_006496987.1XP_006497050.1  protein lin-9 homolog isoform X1

    See identical proteins and their annotated locations for XP_006497050.1

    UniProtKB/TrEMBL
    A0A0A6YVZ7
    Conserved Domains (1) summary
    pfam06584
    Location:75179
    DIRP

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_175186.4: Suppressed sequence

    Description
    NM_175186.4: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.