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    NRM nurim [ Homo sapiens (human) ]

    Gene ID: 11270, updated on 2-Nov-2024

    Summary

    Official Symbol
    NRMprovided by HGNC
    Official Full Name
    nurimprovided by HGNC
    Primary source
    HGNC:HGNC:8003
    See related
    Ensembl:ENSG00000137404 MIM:620017; AllianceGenome:HGNC:8003
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    NRM29
    Summary
    The protein encoded by this gene contains transmembrane domains and resides within the inner nuclear membrane, where it is tightly associated with the nucleus. This protein shares homology with isoprenylcysteine carboxymethyltransferase enzymes. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]
    Expression
    Ubiquitous expression in skin (RPKM 5.3), bone marrow (RPKM 5.1) and 25 other tissues See more
    Orthologs
    NEW
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    Try the new Transcript table

    Genomic context

    See NRM in Genome Data Viewer
    Location:
    6p21.33
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (30688049..30691420, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (30552255..30555626, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (30655826..30659197, complement)

    Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene alpha tubulin acetyltransferase 1 Neighboring gene prothymosin alpha pseudogene 1 Neighboring gene chromosome 6 open reading frame 136 Neighboring gene DEAH-box helicase 16 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:30638704-30639302 Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:30640498-30641094 Neighboring gene ReSE screen-validated silencer GRCh37_chr6:30642736-30642875 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:30649761-30650650 Neighboring gene protein phosphatase 1 regulatory subunit 18 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:30650651-30651540 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:30668297-30668798 Neighboring gene ribosomal protein L7 pseudogene 4 Neighboring gene MDC1 antisense RNA 1 Neighboring gene mediator of DNA damage checkpoint 1

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables molecular_function ND
    No biological Data available
    more info
     
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in biological_process ND
    No biological Data available
    more info
     
    Component Evidence Code Pubs
    located_in membrane HDA PubMed 
    located_in nuclear envelope IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in nuclear inner membrane IEA
    Inferred from Electronic Annotation
    more info
     
    is_active_in nuclear membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in nuclear membrane IDA
    Inferred from Direct Assay
    more info
     

    General protein information

    Preferred Names
    nurim
    Names
    nuclear rim protein
    nurim (nuclear envelope membrane protein)

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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_001270707.2NP_001257636.1  nurim isoform 2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) differs in the 5' UTR and uses an alternate in-frame splice site in the coding region compared to variant 1. It encodes isoform 2 which is longer than isoform 1.
      Source sequence(s)
      AK075509, BC039865, BU159435
      UniProtKB/TrEMBL
      B3KQU6
    2. NM_001270708.2NP_001257637.1  nurim isoform 3

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) differs in the 5' and 3' UTR and uses an alternate in-frame splice site in the coding region compared to variant 1. It terminates translation at an alternate stop codon resulting in an isoform (3) that is shorter than isoform 1.
      Source sequence(s)
      AI521967, BC039865, BM917173
      UniProtKB/Swiss-Prot
      Q8IXM6
      UniProtKB/TrEMBL
      B3KQU6
      Related
      ENST00000462857.5
    3. NM_001270709.2NP_001257638.1  nurim isoform 4

      See identical proteins and their annotated locations for NP_001257638.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) differs in the 5' UTR and lacks an alternate in-frame exon in the coding region compared to variant 1. It encodes isoform 4 which is shorter than isoform 1.
      Source sequence(s)
      JQ798186
      Consensus CDS
      CCDS59498.1
      UniProtKB/Swiss-Prot
      Q8IXM6
      UniProtKB/TrEMBL
      B3KQU6
      Related
      ENSP00000365602.5, ENST00000376420.9
    4. NM_001270710.2NP_001257639.1  nurim isoform 5

      See identical proteins and their annotated locations for NP_001257639.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (5) lacks two alternate in-frame exons in the coding region compared to variant 1. The resulting isoform (5) has a distinct C-terminus, compared to isoform 1.
      Source sequence(s)
      JQ798187
      UniProtKB/Swiss-Prot
      Q8IXM6
      UniProtKB/TrEMBL
      B3KQU6
      Related
      ENST00000474864.5
    5. NM_001384369.1NP_001371298.1  nurim isoform 1

      Status: REVIEWED

      Source sequence(s)
      AL662797
      Consensus CDS
      CCDS4686.1
      UniProtKB/Swiss-Prot
      B0S7R0, B0S7R1, I3XIE2, I3XIE3, Q5JP57, Q5JP58, Q5JP59, Q5JP60, Q8IXM6, Q8WU45, Q9BSX3, Q9UN92
      UniProtKB/TrEMBL
      A0A1U9X845, B3KQU6
      Related
      ENSP00000365603.5, ENST00000376421.7
    6. NM_007243.3NP_009174.1  nurim isoform 1

      See identical proteins and their annotated locations for NP_009174.1

      Status: REVIEWED

      Source sequence(s)
      AL662797
      Consensus CDS
      CCDS4686.1
      UniProtKB/Swiss-Prot
      B0S7R0, B0S7R1, I3XIE2, I3XIE3, Q5JP57, Q5JP58, Q5JP59, Q5JP60, Q8IXM6, Q8WU45, Q9BSX3, Q9UN92
      UniProtKB/TrEMBL
      A0A1U9X845, B3KQU6
      Related
      ENSP00000259953.4, ENST00000259953.8

    RNA

    1. NR_073065.2 RNA Sequence

      Status: REVIEWED

      Description
      Transcript Variant: This variant (7) uses an alternate splice site compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AI521967, BC039865, BM847576
      Related
      ENST00000470733.1
    2. NR_073066.2 RNA Sequence

      Status: REVIEWED

      Description
      Transcript Variant: This variant (8) lacks an alternate internal exon compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AI521967, AK075509, AK298152
      Related
      ENST00000482141.5
    3. NR_073072.2 RNA Sequence

      Status: REVIEWED

      Source sequence(s)
      AL662797
      Related
      ENST00000444096.5

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000006.12 Reference GRCh38.p14 Primary Assembly

      Range
      30688049..30691420 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_047418138.1XP_047274094.1  nurim isoform X2

    2. XM_017010224.3XP_016865713.1  nurim isoform X1

      UniProtKB/TrEMBL
      B4DP16

    Reference GRCh38.p14 ALT_REF_LOCI_1

    Genomic

    1. NT_167244.2 Reference GRCh38.p14 ALT_REF_LOCI_1

      Range
      2017556..2020927 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054328446.1XP_054184421.1  nurim isoform X2

    2. XM_054328445.1XP_054184420.1  nurim isoform X1

    Reference GRCh38.p14 ALT_REF_LOCI_2

    Genomic

    1. NT_113891.3 Reference GRCh38.p14 ALT_REF_LOCI_2

      Range
      2167793..2171164 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054329730.1XP_054185705.1  nurim isoform X2

    2. XM_054329729.1XP_054185704.1  nurim isoform X1

    Reference GRCh38.p14 ALT_REF_LOCI_3

    Genomic

    1. NT_167245.2 Reference GRCh38.p14 ALT_REF_LOCI_3

      Range
      1943903..1947274 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054330228.1XP_054186203.1  nurim isoform X2

    2. XM_054330227.1XP_054186202.1  nurim isoform X1

    Reference GRCh38.p14 ALT_REF_LOCI_4

    Genomic

    1. NT_167246.2 Reference GRCh38.p14 ALT_REF_LOCI_4

      Range
      1998302..2001673 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054330516.1XP_054186491.1  nurim isoform X2

    2. XM_054330515.1XP_054186490.1  nurim isoform X1

    Reference GRCh38.p14 ALT_REF_LOCI_5

    Genomic

    1. NT_167247.2 Reference GRCh38.p14 ALT_REF_LOCI_5

      Range
      2032126..2035497 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054330763.1XP_054186738.1  nurim isoform X2

    2. XM_054330762.1XP_054186737.1  nurim isoform X1

    Reference GRCh38.p14 ALT_REF_LOCI_6

    Genomic

    1. NT_167248.2 Reference GRCh38.p14 ALT_REF_LOCI_6

      Range
      1943163..1946534 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054331000.1XP_054186975.1  nurim isoform X2

    2. XM_054330999.1XP_054186974.1  nurim isoform X1

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060930.1 Alternate T2T-CHM13v2.0

      Range
      30552255..30555626 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054354141.1XP_054210116.1  nurim isoform X2

    2. XM_054354140.1XP_054210115.1  nurim isoform X1