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NUTM2G NUT family member 2G [ Homo sapiens (human) ]

Gene ID: 441457, updated on 2-Apr-2017
Official Symbol
NUTM2Gprovided by HGNC
Official Full Name
NUT family member 2Gprovided by HGNC
Primary source
HGNC:HGNC:23449
See related
Ensembl:ENSG00000188152 Vega:OTTHUMG00000020305
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
NUTMG; FAM22G
Orthologs
Location:
9q22.33
Exon count:
8
Annotation release Status Assembly Chr Location
108 current GRCh38.p7 (GCF_000001405.33) 9 NC_000009.12 (96929004..96942290)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (99691286..99704572)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene prothymosin, alpha pseudogene Neighboring gene proline-rich nuclear receptor coactivator 2-like Neighboring gene major facilitator superfamily domain containing 14C Neighboring gene yrdC N(6)-threonylcarbamoyltransferase domain containing pseudogene 2 Neighboring gene cathepsin V

  • Project title: 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 Jun 15 11:32:44 2016

Related articles in PubMed

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

Preferred Names
NUT family member 2G
Names
family with sequence similarity 22, member G
family with sequence similarity 22, pseudogene
protein FAM22G

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_001045477.2NP_001038942.1  NUT family member 2G isoform 1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript but encodes the shorter isoform (1).
    Source sequence(s)
    AL158827
    Consensus CDS
    CCDS43854.1
    UniProtKB/Swiss-Prot
    Q5VZR2
    Related
    ENSP00000346670.2, OTTHUMP00000021737, ENST00000354649.7, OTTHUMT00000053292
    Conserved Domains (1) summary
    pfam12881
    Location:14480
    NUT; NUT protein
  2. NM_001170741.1NP_001164212.1  NUT family member 2G isoform 2

    See identical proteins and their annotated locations for NP_001164212.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) uses an alternate terminal exon, compared to variant 1. The resulting isoform (2) has a longer and distinct C-terminus, compared to isoform 1.
    Source sequence(s)
    AL158827
    Consensus CDS
    CCDS55329.1
    UniProtKB/Swiss-Prot
    Q5VZR2
    Related
    ENSP00000361397.3, OTTHUMP00000021736, ENST00000372322.3, OTTHUMT00000053291
    Conserved Domains (1) summary
    pfam12881
    Location:14728
    NUT; NUT protein

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 108 details...Open this link in a new tab

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

Reference GRCh38.p7 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p7 Primary Assembly

    Range
    96929004..96942290
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate CHM1_1.1

Genomic

  1. NC_018920.2 Alternate CHM1_1.1

    Range
    99838303..99851567
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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