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    SYT16 synaptotagmin 16 [ Homo sapiens (human) ]

    Gene ID: 83851, updated on 10-Dec-2024

    Summary

    Official Symbol
    SYT16provided by HGNC
    Official Full Name
    synaptotagmin 16provided by HGNC
    Primary source
    HGNC:HGNC:23142
    See related
    Ensembl:ENSG00000139973 MIM:610950; AllianceGenome:HGNC:23142
    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
    SYT14L; syt14r; Strep14; CHR14SYT
    Summary
    Predicted to enable phospholipid binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Dec 2024]
    Expression
    Biased expression in brain (RPKM 5.2), prostate (RPKM 0.7) and 2 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See SYT16 in Genome Data Viewer
    Location:
    14q23.2
    Exon count:
    17
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (61812162..62112825)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (56019035..56320045)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (62278880..62579268)

    Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene HIF1A antisense RNA 3 Neighboring gene hypoxia inducible factor 1 subunit alpha Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5825 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr14:62221703-62222902 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:62223301-62223886 Neighboring gene H3K27ac hESC enhancer GRCh37_chr14:62227132-62227876 Neighboring gene H3K27ac hESC enhancer GRCh37_chr14:62227877-62228620 Neighboring gene H3K27ac hESC enhancer GRCh37_chr14:62228621-62229364 Neighboring gene H3K27ac hESC enhancer GRCh37_chr14:62229365-62230108 Neighboring gene HIF1A antisense RNA 2 Neighboring gene small nuclear RNA activating complex polypeptide 1 Neighboring gene H3K27ac hESC enhancer GRCh37_chr14:62298837-62299336 Neighboring gene cytochrome c oxidase subunit 4I1 pseudogene 1 Neighboring gene molybdenum cofactor synthesis 3 pseudogene 1 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr14:62396930-62397782 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5826 Neighboring gene NANOG hESC enhancer GRCh37_chr14:62537700-62538201 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 8503 Neighboring gene SERTA domain containing 4B, pseudogene Neighboring gene tubulin alpha 1c pseudogene Neighboring gene long intergenic non-protein coding RNA 644

    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

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    A genome-wide association study of self-rated health.
    EBI GWAS Catalog
    Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study.
    EBI GWAS Catalog
    Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age.
    EBI GWAS Catalog

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables identical protein binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables phospholipid binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 

    General protein information

    Preferred Names
    synaptotagmin-16
    Names
    chr14 synaptotagmin
    synaptotagmin 14-like protein
    synaptotagmin XIV-related protein
    synaptotagmin XVI

    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_001367650.1NP_001354579.1  synaptotagmin-16 isoform 2

      Status: VALIDATED

      Source sequence(s)
      AL137918, AL356018, AL390816
    2. NM_001367652.1NP_001354581.1  synaptotagmin-16 isoform 1

      Status: VALIDATED

      Source sequence(s)
      AL137918, AL356018, AL390816
    3. NM_001367654.1NP_001354583.1  synaptotagmin-16 isoform 3

      Status: VALIDATED

      Source sequence(s)
      AL137918, AL356018, AL390816
    4. NM_001367656.1NP_001354585.1  synaptotagmin-16 isoform 4

      Status: VALIDATED

      Source sequence(s)
      AL137918, AL356018, AL390816
      Consensus CDS
      CCDS45121.1
      UniProtKB/Swiss-Prot
      B4DZH2, B7ZL60, C9J8I3, Q17RD7, Q707N2, Q7Z441, Q8IUU0, Q9BQR8
      Related
      ENSP00000508274.1, ENST00000683842.1
      Conserved Domains (2) summary
      cd08389
      Location:350473
      C2A_Synaptotagmin-14_16; C2A domain first repeat present in Synaptotagmins 14 and 16
      cd08408
      Location:506643
      C2B_Synaptotagmin-14_16; C2 domain second repeat present in Synaptotagmins 14 and 16
    5. NM_001367657.1NP_001354586.1  synaptotagmin-16 isoform 5

      Status: VALIDATED

      Source sequence(s)
      AL137918, AL356018, AL390816
    6. NM_001367659.1NP_001354588.1  synaptotagmin-16 isoform 6

      Status: VALIDATED

      Source sequence(s)
      AL137918, AL356018, AL390816
    7. NM_001367661.1NP_001354590.1  synaptotagmin-16 isoform 4

      Status: VALIDATED

      Source sequence(s)
      AL137918, AL356018, AL390816
      Consensus CDS
      CCDS45121.1
      UniProtKB/Swiss-Prot
      B4DZH2, B7ZL60, C9J8I3, Q17RD7, Q707N2, Q7Z441, Q8IUU0, Q9BQR8
      Conserved Domains (2) summary
      cd08389
      Location:350473
      C2A_Synaptotagmin-14_16; C2A domain first repeat present in Synaptotagmins 14 and 16
      cd08408
      Location:506643
      C2B_Synaptotagmin-14_16; C2 domain second repeat present in Synaptotagmins 14 and 16
    8. NM_001367663.1NP_001354592.1  synaptotagmin-16 isoform 4

      Status: VALIDATED

      Source sequence(s)
      AL137918, AL356018, AL390816
      Consensus CDS
      CCDS45121.1
      UniProtKB/Swiss-Prot
      B4DZH2, B7ZL60, C9J8I3, Q17RD7, Q707N2, Q7Z441, Q8IUU0, Q9BQR8
      Conserved Domains (2) summary
      cd08389
      Location:350473
      C2A_Synaptotagmin-14_16; C2A domain first repeat present in Synaptotagmins 14 and 16
      cd08408
      Location:506643
      C2B_Synaptotagmin-14_16; C2 domain second repeat present in Synaptotagmins 14 and 16
    9. NM_001387087.1NP_001374016.1  synaptotagmin-16 isoform 4

      Status: VALIDATED

      Description
      Transcript Variant: This variant (10), as well as variants 4, 7, and 9, encodes isoform 4.
      Source sequence(s)
      AL137918, AL356018, AL390816
      Consensus CDS
      CCDS45121.1
      UniProtKB/Swiss-Prot
      B4DZH2, B7ZL60, C9J8I3, Q17RD7, Q707N2, Q7Z441, Q8IUU0, Q9BQR8
      Conserved Domains (2) summary
      cd08389
      Location:350473
      C2A_Synaptotagmin-14_16; C2A domain first repeat present in Synaptotagmins 14 and 16
      cd08408
      Location:506643
      C2B_Synaptotagmin-14_16; C2 domain second repeat present in Synaptotagmins 14 and 16
    10. NM_001387088.1NP_001374017.1  synaptotagmin-16 isoform 7

      Status: VALIDATED

      Source sequence(s)
      AL137918, AL356018, AL390816
      Conserved Domains (2) summary
      cd08389
      Location:350473
      C2A_Synaptotagmin-14_16; C2A domain first repeat present in Synaptotagmins 14 and 16
      cl14603
      Location:506541
      C2; C2 domain

    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_000014.9 Reference GRCh38.p14 Primary Assembly

      Range
      61812162..62112825
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_017021697.3XP_016877186.1  synaptotagmin-16 isoform X5

    2. XM_047431804.1XP_047287760.1  synaptotagmin-16 isoform X3

    3. XM_024449730.2XP_024305498.1  synaptotagmin-16 isoform X7

      Conserved Domains (2) summary
      cd08389
      Location:44167
      C2A_Synaptotagmin-14_16; C2A domain first repeat present in Synaptotagmins 14 and 16
      cd08408
      Location:200337
      C2B_Synaptotagmin-14_16; C2 domain second repeat present in Synaptotagmins 14 and 16
    4. XM_024449729.2XP_024305497.1  synaptotagmin-16 isoform X7

      Conserved Domains (2) summary
      cd08389
      Location:44167
      C2A_Synaptotagmin-14_16; C2A domain first repeat present in Synaptotagmins 14 and 16
      cd08408
      Location:200337
      C2B_Synaptotagmin-14_16; C2 domain second repeat present in Synaptotagmins 14 and 16
    5. XM_047431802.1XP_047287758.1  synaptotagmin-16 isoform X1

      UniProtKB/Swiss-Prot
      B4DZH2, B7ZL60, C9J8I3, Q17RD7, Q707N2, Q7Z441, Q8IUU0, Q9BQR8
    6. XM_047431803.1XP_047287759.1  synaptotagmin-16 isoform X1

      UniProtKB/Swiss-Prot
      B4DZH2, B7ZL60, C9J8I3, Q17RD7, Q707N2, Q7Z441, Q8IUU0, Q9BQR8
    7. XM_024449726.2XP_024305494.1  synaptotagmin-16 isoform X2

      Conserved Domains (2) summary
      cd08389
      Location:350473
      C2A_Synaptotagmin-14_16; C2A domain first repeat present in Synaptotagmins 14 and 16
      cl14603
      Location:506541
      C2; C2 domain
    8. XM_011537227.2XP_011535529.2  synaptotagmin-16 isoform X4

    9. XM_011537229.3XP_011535531.1  synaptotagmin-16 isoform X6

      Conserved Domains (2) summary
      cd08389
      Location:129252
      C2A_Synaptotagmin-14_16; C2A domain first repeat present in Synaptotagmins 14 and 16
      cd08408
      Location:285422
      C2B_Synaptotagmin-14_16; C2 domain second repeat present in Synaptotagmins 14 and 16

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060938.1 Alternate T2T-CHM13v2.0

      Range
      56019035..56320045
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054376801.1XP_054232776.1  synaptotagmin-16 isoform X5

    2. XM_054376799.1XP_054232774.1  synaptotagmin-16 isoform X3

    3. XM_054376804.1XP_054232779.1  synaptotagmin-16 isoform X7

    4. XM_054376803.1XP_054232778.1  synaptotagmin-16 isoform X7

    5. XM_054376796.1XP_054232771.1  synaptotagmin-16 isoform X1

      UniProtKB/Swiss-Prot
      B4DZH2, B7ZL60, C9J8I3, Q17RD7, Q707N2, Q7Z441, Q8IUU0, Q9BQR8
    6. XM_054376797.1XP_054232772.1  synaptotagmin-16 isoform X1

      UniProtKB/Swiss-Prot
      B4DZH2, B7ZL60, C9J8I3, Q17RD7, Q707N2, Q7Z441, Q8IUU0, Q9BQR8
    7. XM_054376798.1XP_054232773.1  synaptotagmin-16 isoform X2

    8. XM_054376800.1XP_054232775.1  synaptotagmin-16 isoform X4

    9. XM_054376802.1XP_054232777.1  synaptotagmin-16 isoform X6

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_031914.2: Suppressed sequence

      Description
      NM_031914.2: This RefSeq has been removed because currently there is insufficient support for the transcript and protein.