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    SNX12 sorting nexin 12 [ Homo sapiens (human) ]

    Gene ID: 29934, updated on 10-Dec-2024

    Summary

    Official Symbol
    SNX12provided by HGNC
    Official Full Name
    sorting nexin 12provided by HGNC
    Primary source
    HGNC:HGNC:14976
    See related
    Ensembl:ENSG00000147164 MIM:300883; AllianceGenome:HGNC:14976
    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
    Summary
    This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members. A similar protein in mouse may be involved in regulating the neurite outgrowth. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]
    Expression
    Ubiquitous expression in kidney (RPKM 19.5), thyroid (RPKM 17.8) and 25 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See SNX12 in Genome Data Viewer
    Location:
    Xq13.1
    Exon count:
    7
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (71059247..71073426, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (69493335..69507559, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (70279097..70293276, complement)

    Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene RNA, U1 small nuclear 56, pseudogene Neighboring gene suppressor of cytokine signaling 5 pseudogene 4 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29734 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29735 Neighboring gene ReSE screen-validated silencer GRCh37_chrX:70288147-70288340 Neighboring gene Sharpr-MPRA regulatory region 4327 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:70320272-70320882 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29736 Neighboring gene forkhead box O4 Neighboring gene chromosome X open reading frame 65

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Clone Names

    • FLJ22128, MGC118982, MGC118983

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables enzyme binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables phosphatidylinositol binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables phosphatidylinositol-3-phosphate binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in early endosome IDA
    Inferred from Direct Assay
    more info
    PubMed 
    is_active_in early endosome membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    part_of retromer complex IBA
    Inferred from Biological aspect of Ancestor
    more info
     

    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_001256185.2NP_001243114.1  sorting nexin-12 isoform 1

      See identical proteins and their annotated locations for NP_001243114.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1). Both variants 1 and 2 encode the same isoform (1).
      Source sequence(s)
      AL590764, BC024301, DA736880
      Consensus CDS
      CCDS14405.1
      UniProtKB/Swiss-Prot
      F8W8K5, Q8WUG9, Q9UMY4
      UniProtKB/TrEMBL
      A0A087X0R6, Q3SYF1
      Related
      ENSP00000481314.1, ENST00000622277.4
      Conserved Domains (1) summary
      cd07294
      Location:27158
      PX_SNX12; The phosphoinositide binding Phox Homology domain of Sorting Nexin 12
    2. NM_001256186.2NP_001243115.1  sorting nexin-12 isoform 2

      See identical proteins and their annotated locations for NP_001243115.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) has multiple coding region differences, compared to variant 1, one of which results in a frameshift. The resulting protein (isoform 2) has a distinct C-terminus and is shorter than isoform 1.
      Source sequence(s)
      AL590764, BC024301, DA847821
      Conserved Domains (1) summary
      cl02563
      Location:2783
      PX_domain; The Phox Homology domain, a phosphoinositide binding module
    3. NM_001256187.2NP_001243116.1  sorting nexin-12 isoform 3

      See identical proteins and their annotated locations for NP_001243116.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) lacks an exon in the coding region which results in a frameshift, compared to variant 1. The resulting protein (isoform 3) has a distinct C-terminus, compared to isoform 1.
      Source sequence(s)
      AL590764, BC024301, DB251077
      Conserved Domains (1) summary
      cl02563
      Location:2787
      PX_domain; The Phox Homology domain, a phosphoinositide binding module
    4. NM_001256188.2NP_001243117.1  sorting nexin-12 isoform 4

      See identical proteins and their annotated locations for NP_001243117.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (5) uses an alternate in-frame splice site in the 5' coding region, compared to variant 1. This results in a shorter protein (isoform 4), compared to isoform 1.
      Source sequence(s)
      AL590764, BC024301, DA439434
      Consensus CDS
      CCDS59169.1
      UniProtKB/TrEMBL
      A0A087X0R6
      Related
      ENSP00000276105.3, ENST00000276105.3
      Conserved Domains (1) summary
      cl02563
      Location:27154
      PX_domain; The Phox Homology domain, a phosphoinositide binding module
    5. NM_013346.4NP_037478.2  sorting nexin-12 isoform 1

      See identical proteins and their annotated locations for NP_037478.2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) differs in the 5' UTR and represents use of an alternate promoter, compared to variant 1. Both variants 1 and 2 encode the same isoform (1).
      Source sequence(s)
      AL590764, BC024301, BC103847
      Consensus CDS
      CCDS14405.1
      UniProtKB/Swiss-Prot
      F8W8K5, Q8WUG9, Q9UMY4
      UniProtKB/TrEMBL
      A0A087X0R6, Q3SYF1
      Related
      ENSP00000363392.3, ENST00000374274.8
      Conserved Domains (1) summary
      cd07294
      Location:27158
      PX_SNX12; The phosphoinositide binding Phox Homology domain of Sorting Nexin 12

    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_000023.11 Reference GRCh38.p14 Primary Assembly

      Range
      71059247..71073426 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_047442038.1XP_047297994.1  sorting nexin-12 isoform X1

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060947.1 Alternate T2T-CHM13v2.0

      Range
      69493335..69507559 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)