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Q8IV01 (SYT12_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 79. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (5) | Third-party data text xml rdf/xml gff fasta
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Names and origin

Protein namesRecommended name:
Synaptotagmin-12
Alternative name(s):
Synaptotagmin XII
Short name=SytXII
Gene names
Name:SYT12
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length421 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Function

May be involved in Ca2+-dependent exocytosis of secretory vesicles through Ca2+ and phospholipid binding to the C2 domain or may serve as Ca2+ sensors in the process of vesicular trafficking and exocytosis By similarity.

Subunit structure

Homodimer. Can also form heterodimers By similarity.

Subcellular location

Cytoplasmic vesiclesecretory vesiclesynaptic vesicle membrane; Single-pass membrane protein By similarity.

Sequence similarities

Belongs to the synaptotagmin family.

Contains 2 C2 domains.

Ontologies

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 421421Synaptotagmin-12
PRO_0000183972

Regions

Topological domain1 – 1818Vesicular Potential
Transmembrane19 – 3921Helical; Potential
Topological domain40 – 421382Cytoplasmic Potential
Domain168 – 272105C2 1
Domain285 – 388104C2 2

Natural variations

Natural variant1701N → H.
Corresponds to variant rs11227664 [ dbSNP | Ensembl ].
VAR_034532

Sequences

Sequence LengthMass (Da)Tools
Q8IV01 [UniParc].

Last modified March 1, 2003. Version 1.
Checksum: 9E1B3ACE0023F973

FASTA42146,537
        10         20         30         40         50         60 
MAVDVAEYHL SVIKSPPGWE VGVYAAGALA LLGIAAVSLW KLWTSGSFPS PSPFPNYDYR 

        70         80         90        100        110        120 
YLQQKYGESC AEAREKRVPA WNAQRASTRG PPSRKGSLSI EDTFESISEL GPLELMGREL 

       130        140        150        160        170        180 
DLAPYGTLRK SQSADSLNSI SSVSNTFGQD FTLGQVEVSM EYDTASHTLN VAVMQGKDLL 

       190        200        210        220        230        240 
EREEASFESC FMRVSLLPDE QIVGISRIQR NAYSIFFDEK FSIPLDPTAL EEKSLRFSVF 

       250        260        270        280        290        300 
GIDEDERNVS TGVVELKLSV LDLPLQPFSG WLYLQDQNKA ADAVGEILLS LSYLPTAERL 

       310        320        330        340        350        360 
TVVVVKAKNL IWTNDKTTAD PFVKVYLLQD GRKMSKKKTA VKRDDPNPVF NEAMIFSVPA 

       370        380        390        400        410        420 
IVLQDLSLRV TVAESSSDGR GDNVGHVIIG PSASGMGTTH WNQMLATLRR PVSMWHAVRR 


N 

« Hide

References

[1]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Brain.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
BC037406 mRNA. Translation: AAH37406.1.
IPIIPI00219472.
RefSeqNP_001171351.1. NM_001177880.1.
NP_808878.1. NM_177963.3.
UniGeneHs.287636.

3D structure databases

ProteinModelPortalQ8IV01.
SMRQ8IV01. Positions 152-420.
ModBaseSearch...

Protein-protein interaction databases

STRINGQ8IV01.

PTM databases

PhosphoSiteQ8IV01.

Polymorphism databases

DMDM33151152.

Proteomic databases

PRIDEQ8IV01.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000393946; ENSP00000377520; ENSG00000173227.
GeneID91683.
KEGGhsa:91683.
UCSCuc001oju.1. human.

Organism-specific databases

CTD91683.
GeneCardsGC11P066791.
HGNCHGNC:18381. SYT12.
HPAHPA011006.
MIM606436. gene.
neXtProtNX_Q8IV01.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG05392.
HOGENOMHBG445851.
HOVERGENHBG057176.
InParanoidQ8IV01.
OMAEYHLSVI.
OrthoDBEOG4DV5MC.
PhylomeDBQ8IV01.

Gene expression databases

ArrayExpressQ8IV01.
BgeeQ8IV01.
CleanExHS_SYT12.
GenevestigatorQ8IV01.
GermOnlineENSG00000173227. Homo sapiens.

Family and domain databases

InterProIPR000008. C2_Ca-dep.
IPR008973. C2_Ca/lipid-bd_dom_CaLB.
IPR018029. C2_membr_targeting.
[Graphical view]
PfamPF00168. C2. 2 hits.
[Graphical view]
SMARTSM00239. C2. 2 hits.
[Graphical view]
SUPFAMSSF49562. C2_CaLB. 2 hits.
PROSITEPS50004. C2. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio77391.
SOURCESearch...

Entry information

Entry nameSYT12_HUMAN
AccessionPrimary (citable) accession number: Q8IV01
Entry history
Integrated into UniProtKB/Swiss-Prot: July 19, 2003
Last sequence update: March 1, 2003
Last modified: January 25, 2012
This is version 79 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

Relevant documents

Human chromosome 11

Human chromosome 11: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

MIM cross-references

Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot

SIMILARITY comments

Index of protein domains and families