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    SPART spartin [ Homo sapiens (human) ]

    Gene ID: 23111, updated on 14-Nov-2024

    Summary

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    Official Symbol
    SPARTprovided by HGNC
    Official Full Name
    spartinprovided by HGNC
    Primary source
    HGNC:HGNC:18514
    See related
    Ensembl:ENSG00000133104 MIM:607111; AllianceGenome:HGNC:18514
    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
    SPG20; TAHCCP1
    Summary
    This gene encodes a protein containing a MIT (Microtubule Interacting and Trafficking molecule) domain, and is implicated in regulating endosomal trafficking and mitochondria function. The protein localizes to mitochondria and partially co-localizes with microtubules. Stimulation with epidermal growth factor (EGF) results in protein translocation to the plasma membrane, and the protein functions in the degradation and intracellular trafficking of EGF receptor. Multiple alternatively spliced variants, encoding the same protein, have been identified. Mutations associated with this gene cause autosomal recessive spastic paraplegia 20 (Troyer syndrome). [provided by RefSeq, Nov 2008]
    Expression
    Ubiquitous expression in ovary (RPKM 20.8), adrenal (RPKM 19.3) and 25 other tissues See more
    Orthologs
    mouse all
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    Genomic context

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    See SPART in Genome Data Viewer
    Location:
    13q13.3
    Exon count:
    15
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (36301638..36370180, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (35521139..35589682, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (36875775..36944317, complement)

    Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene CCDC169-SOHLH2 readthrough Neighboring gene spermatogenesis and oogenesis specific basic helix-loop-helix 2 Neighboring gene MPRA-validated peak2068 silencer Neighboring gene coiled-coil domain containing 169 Neighboring gene Sharpr-MPRA regulatory region 14903 Neighboring gene RNA, U6 small nuclear 71, pseudogene Neighboring gene H3K27ac hESC enhancer GRCh37_chr13:36871578-36872539 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:36872540-36873502 Neighboring gene NANOG hESC enhancer GRCh37_chr13:36887598-36888362 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:36890200-36891034 Neighboring gene H3K27ac hESC enhancer GRCh37_chr13:36891035-36891868 Neighboring gene H3K27ac hESC enhancer GRCh37_chr13:36894061-36894764 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:36895467-36896169 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:36896170-36896871 Neighboring gene Sharpr-MPRA regulatory region 3304 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5263 Neighboring gene SPART antisense RNA 1 Neighboring gene ReSE screen-validated silencer GRCh37_chr13:36962882-36963065 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5264 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5265 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5266 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr13:37011626-37012825 Neighboring gene cyclin A1 Neighboring gene H2AC histone family pseudogene 1

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • 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

    Bibliography

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    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. Lysosomal damage sensing and lysophagy initiation by SPG20-ITCH.
      Title: Lysosomal damage sensing and lysophagy initiation by SPG20-ITCH.
    2. Spastic Paraplegia 20 and Serine/Threonine Protein Kinase 31 Expression for the Detection of Colorectal Cancer.
      Title: Spastic Paraplegia 20 and Serine/Threonine Protein Kinase 31 Expression for the Detection of Colorectal Cancer.
    3. KLF4, DAPK1 and SPG20 promoter methylation is not affected by DNMT1 silencing and hypomethylating drugs in lymphoma cells.
      Title: KLF4, DAPK1 and SPG20 promoter methylation is not affected by DNMT1 silencing and hypomethylating drugs in lymphoma cells.
    4. The novel mutation in SPART leads to a profound bioenergetic imbalance.
      Title: A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism.
    5. hypermethylation status of SPG20 gene promoter is significantly associated with intra-hepatic metastasis and contribute to HCC metastasis
      Title: Aberrant methylation status of SPG20 promoter in hepatocellular carcinoma: A potential tumor metastasis biomarker.
    6. Methylation-induced Spastic paraplegia 20 silencing facilitates gastric cancer cell proliferation by activating the EGFR/MAPK signaling pathway.
      Title: Methylation-induced silencing of SPG20 facilitates gastric cancer cell proliferation by activating the EGFR/MAPK pathway.
    7. we report the clinical findings in three brothers of a consanguineous Moroccan family, aged 24, 17, and 7 yr old, with spastic paraplegia, short stature, motor and cognitive delay, and severe intellectual disability. Targeted exon capture and sequencing showed a homozygous nonsense mutation in the SPG20 gene, c.1369C>T (p.Arg457*), in the three affected boys.
      Title: SPG20 mutation in three siblings with familial hereditary spastic paraplegia.
    8. Study identified mutation in SPG20 as the disease causing mutation for Troyer Syndrome in Turkish siblings.
      Title: Recurrent null mutation in SPG20 leads to Troyer syndrome.
    9. Up-regulation of SPG20 expression, brought about by trisomy 13 in colon cancer cells trisomy 13 amniocytes, is sufficient for the cytokinesis failure phenotype.
      Title: Chromosome mis-segregation and cytokinesis failure in trisomic human cells.
    10. hypermethylation of the spastic paraplegia-20 promoter occurred frequently in gastric cancer.
      Title: Detection of aberrant hypermethylated spastic paraplegia-20 as a potential biomarker and prognostic factor in gastric cancer.
    Submit: New GeneRIF Correction See all GeneRIFs (25)

    Phenotypes

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    Find tests for this gene in the NIH Genetic Testing Registry (GTR)

    Review eQTL and phenotype association data in this region using PheGenI

    Associated conditions

    Description Tests
    Troyer syndrome
    MedGen: C0393559 OMIM: 275900 GeneReviews: Troyer Syndrome
    		not available

    Variation

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    See Variation Viewer (GRCh37.p13)

    Pathways from PubChem

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    Interactions

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    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

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    Markers

    Homology

    Clone Names

    • KIAA0610

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables lipid binding IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    		 PubMed 
    enables ubiquitin protein ligase binding IPI
    Inferred from Physical Interaction
    more info
    		 PubMed 
    Process Evidence Code Pubs
    involved_in BMP signaling pathway IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in adipose tissue development IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in cell division IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in cell division IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    involved_in collateral sprouting in absence of injury IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in lipid catabolic process IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in lipid droplet organization IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in lipid transport IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    involved_in lipophagy IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    involved_in midbody abscission IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    involved_in negative regulation of BMP signaling pathway IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in negative regulation of collateral sprouting in absence of injury IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in neuromuscular process IEA
    Inferred from Electronic Annotation
    more info
    		  
    acts_upstream_of_or_within regulation of mitochondrial membrane potential IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    Component Evidence Code Pubs
    located_in cytoplasm IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in cytosol IDA
    Inferred from Direct Assay
    more info
    		  
    located_in intracellular membrane-bounded organelle IDA
    Inferred from Direct Assay
    more info
    		  
    located_in lipid droplet IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in midbody IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in mitochondrial outer membrane IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    is_active_in plasma membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    located_in synapse IEA
    Inferred from Electronic Annotation
    more info
    		  

    General protein information

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    Preferred Names
    spartin
    Names
    spastic paraplegia 20 (Troyer syndrome)
    trans-activated by hepatitis C virus core protein 1

    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.

    Genomic

    1. NG_011559.2 RefSeqGene

      Range
      28787..73543
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001142294.2 → NP_001135766.1  spartin

      See identical proteins and their annotated locations for NP_001135766.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) differs in the 5' UTR, compared to variant 1. Variants 1, 2, 3, and 4 encode the same protein.
      Source sequence(s)
      AK057764, AL139377, BC047083, BU622545, DA347686
      Consensus CDS
      CCDS9356.1
      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9, A8K6Q9
      Related
      ENSP00000347314.4, ENST00000355182.8
      Conserved Domains (2) summary
      cd02679
      Location:16 → 95
      MIT_spastin; MIT: domain contained within Microtubule Interacting and Trafficking molecules. This MIT domain sub-family is found in the AAA protein spastin, a probable ATPase involved in the assembly or function of nuclear protein complexes; spastins might also be ...
      pfam06911
      Location:427 → 611
      Senescence; Senescence-associated protein

    2. NM_001142295.2 → NP_001135767.1  spartin

      See identical proteins and their annotated locations for NP_001135767.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) differs in the 5' UTR, compared to variant 1. Variants 1, 2, 3, and 4 encode the same protein.
      Source sequence(s)
      AL139377
      Consensus CDS
      CCDS9356.1
      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9, A8K6Q9
      Related
      ENSP00000414147.1, ENST00000451493.5
      Conserved Domains (2) summary
      cd02679
      Location:16 → 95
      MIT_spastin; MIT: domain contained within Microtubule Interacting and Trafficking molecules. This MIT domain sub-family is found in the AAA protein spastin, a probable ATPase involved in the assembly or function of nuclear protein complexes; spastins might also be ...
      pfam06911
      Location:427 → 611
      Senescence; Senescence-associated protein

    3. NM_001142296.2 → NP_001135768.1  spartin

      See identical proteins and their annotated locations for NP_001135768.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) differs in the 5' UTR, compared to variant 1. Variants 1, 2, 3, and 4 encode the same protein.
      Source sequence(s)
      AL139377, BC026284, BU622545
      Consensus CDS
      CCDS9356.1
      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9, A8K6Q9
      Related
      ENSP00000473599.1, ENST00000494062.2
      Conserved Domains (2) summary
      cd02679
      Location:16 → 95
      MIT_spastin; MIT: domain contained within Microtubule Interacting and Trafficking molecules. This MIT domain sub-family is found in the AAA protein spastin, a probable ATPase involved in the assembly or function of nuclear protein complexes; spastins might also be ...
      pfam06911
      Location:427 → 611
      Senescence; Senescence-associated protein

    4. NM_015087.5 → NP_055902.1  spartin

      See identical proteins and their annotated locations for NP_055902.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the longest transcript. Variants 1, 2, 3, and 4 encode the same protein.
      Source sequence(s)
      AB011182, AL139377, BU622545, DA710623
      Consensus CDS
      CCDS9356.1
      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9, A8K6Q9
      Related
      ENSP00000406061.2, ENST00000438666.7
      Conserved Domains (2) summary
      cd02679
      Location:16 → 95
      MIT_spastin; MIT: domain contained within Microtubule Interacting and Trafficking molecules. This MIT domain sub-family is found in the AAA protein spastin, a probable ATPase involved in the assembly or function of nuclear protein complexes; spastins might also be ...
      pfam06911
      Location:427 → 611
      Senescence; Senescence-associated protein

    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_000013.11 Reference GRCh38.p14 Primary Assembly

      Range
      36301638..36370180 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_005266314.4 → XP_005266371.1  spartin isoform X1

      See identical proteins and their annotated locations for XP_005266371.1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9, A8K6Q9
      Conserved Domains (2) summary
      cd02679
      Location:16 → 95
      MIT_spastin; MIT: domain contained within Microtubule Interacting and Trafficking molecules. This MIT domain sub-family is found in the AAA protein spastin, a probable ATPase involved in the assembly or function of nuclear protein complexes; spastins might also be ...
      pfam06911
      Location:427 → 611
      Senescence; Senescence-associated protein

    2. XM_047430211.1 → XP_047286167.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    3. XM_011535012.3 → XP_011533314.1  spartin isoform X1

      See identical proteins and their annotated locations for XP_011533314.1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9, A8K6Q9
      Conserved Domains (2) summary
      cd02679
      Location:16 → 95
      MIT_spastin; MIT: domain contained within Microtubule Interacting and Trafficking molecules. This MIT domain sub-family is found in the AAA protein spastin, a probable ATPase involved in the assembly or function of nuclear protein complexes; spastins might also be ...
      pfam06911
      Location:427 → 611
      Senescence; Senescence-associated protein

    4. XM_005266313.6 → XP_005266370.1  spartin isoform X1

      See identical proteins and their annotated locations for XP_005266370.1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9, A8K6Q9
      Conserved Domains (2) summary
      cd02679
      Location:16 → 95
      MIT_spastin; MIT: domain contained within Microtubule Interacting and Trafficking molecules. This MIT domain sub-family is found in the AAA protein spastin, a probable ATPase involved in the assembly or function of nuclear protein complexes; spastins might also be ...
      pfam06911
      Location:427 → 611
      Senescence; Senescence-associated protein

    5. XM_047430213.1 → XP_047286169.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    6. XM_024449334.2 → XP_024305102.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9, A8K6Q9
      Conserved Domains (2) summary
      cd02679
      Location:16 → 95
      MIT_spastin; MIT: domain contained within Microtubule Interacting and Trafficking molecules. This MIT domain sub-family is found in the AAA protein spastin, a probable ATPase involved in the assembly or function of nuclear protein complexes; spastins might also be ...
      pfam06911
      Location:427 → 611
      Senescence; Senescence-associated protein

    7. XM_047430210.1 → XP_047286166.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    8. XM_005266317.4 → XP_005266374.1  spartin isoform X1

      See identical proteins and their annotated locations for XP_005266374.1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9, A8K6Q9
      Conserved Domains (2) summary
      cd02679
      Location:16 → 95
      MIT_spastin; MIT: domain contained within Microtubule Interacting and Trafficking molecules. This MIT domain sub-family is found in the AAA protein spastin, a probable ATPase involved in the assembly or function of nuclear protein complexes; spastins might also be ...
      pfam06911
      Location:427 → 611
      Senescence; Senescence-associated protein

    9. XM_005266315.4 → XP_005266372.1  spartin isoform X1

      See identical proteins and their annotated locations for XP_005266372.1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9, A8K6Q9
      Conserved Domains (2) summary
      cd02679
      Location:16 → 95
      MIT_spastin; MIT: domain contained within Microtubule Interacting and Trafficking molecules. This MIT domain sub-family is found in the AAA protein spastin, a probable ATPase involved in the assembly or function of nuclear protein complexes; spastins might also be ...
      pfam06911
      Location:427 → 611
      Senescence; Senescence-associated protein

    10. XM_047430209.1 → XP_047286165.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    11. XM_047430212.1 → XP_047286168.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    RNA

    1. XR_007063671.1 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060937.1 Alternate T2T-CHM13v2.0

      Range
      35521139..35589682 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054374304.1 → XP_054230279.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    2. XM_054374298.1 → XP_054230273.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    3. XM_054374308.1 → XP_054230283.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    4. XM_054374309.1 → XP_054230284.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    5. XM_054374301.1 → XP_054230276.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    6. XM_054374300.1 → XP_054230275.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    7. XM_054374307.1 → XP_054230282.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    8. XM_054374302.1 → XP_054230277.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    9. XM_054374306.1 → XP_054230281.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    10. XM_054374299.1 → XP_054230274.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    11. XM_054374305.1 → XP_054230280.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    12. XM_054374303.1 → XP_054230278.1  spartin isoform X1

      UniProtKB/Swiss-Prot
      O60349, Q86Y67, Q8N0X7, Q9H1T2, Q9H1T3
      UniProtKB/TrEMBL
      A0A024RDV9

    RNA

    1. XR_008488749.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version
    Protein Accession Links
    GenPept Link UniProtKB Link
    Q8N0X7.1 GenPept UniProtKB/Swiss-Prot:Q8N0X7

    Gene LinkOut

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

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