Human Gene SPOCK1 (uc003lbo.3)
  Description: Homo sapiens sparc/osteonectin, cwcv and kazal-like domains proteoglycan (testican) 1 (SPOCK1), mRNA.
RefSeq Summary (NM_004598): This gene encodes the protein core of a seminal plasma proteoglycan containing chondroitin- and heparan-sulfate chains. The protein's function is unknown, although similarity to thyropin-type cysteine protease-inhibitors suggests its function may be related to protease inhibition. [provided by RefSeq, Jul 2008].
Transcript (Including UTRs)
   Position: hg19 chr5:136,310,987-136,834,438 Size: 523,452 Total Exon Count: 10 Strand: -
Coding Region
   Position: hg19 chr5:136,314,343-136,834,247 Size: 519,905 Coding Exon Count: 10 

Page IndexSequence and LinksUniProtKB CommentsPrimersGenetic AssociationsMalaCards
CTDGene AllelesRNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein Structure
Other SpeciesGO AnnotationsmRNA DescriptionsOther NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr5:136,310,987-136,834,438)mRNA (may differ from genome)Protein (439 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaAlphaFold
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H-INVHGNCHPRDLynxMalacardsMGI
neXtProtOMIMPubMedTreefamUniProtKBWikipedia
BioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: TICN1_HUMAN
DESCRIPTION: RecName: Full=Testican-1; AltName: Full=Protein SPOCK; Flags: Precursor;
FUNCTION: May play a role in cell-cell and cell-matrix interactions. May contribute to various neuronal mechanisms in the central nervous system.
SUBCELLULAR LOCATION: Secreted, extracellular space, extracellular matrix.
PTM: Contains chondroitin sulfate and heparan sulfate O-linked oligosaccharides.
SIMILARITY: Contains 1 Kazal-like domain.
SIMILARITY: Contains 1 thyroglobulin type-1 domain.
SEQUENCE CAUTION: Sequence=BAD92938.1; Type=Erroneous initiation;

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  Genetic Association Studies of Complex Diseases and Disorders
  Genetic Association Database (archive): SPOCK1
CDC HuGE Published Literature: SPOCK1
Positive Disease Associations: Creatinine , Diabetes Mellitus
Related Studies:
  1. Creatinine
    Shih-Jen Hwang et al. BMC medical genetics 2007, A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study., BMC medical genetics. [PubMed 17903292]
    Kidney function traits and TSH are associated with SNPs on the Affymetrix GeneChip Human Mapping 100K SNP set. These data will serve as a valuable resource for replication as more SNPs associated with kidney function and endocrine traits are identified.
  2. Diabetes Mellitus
    , , . [PubMed 0]

-  MalaCards Disease Associations
  MalaCards Gene Search: SPOCK1
Diseases sorted by gene-association score: chylothorax, congenital (9), coproporphyria (5)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 119.41 RPKM in Brain - Cerebellar Hemisphere
Total median expression: 796.05 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -101.30191-0.530 Picture PostScript Text
3' UTR -818.263356-0.244 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR011992 - EF-hand-like_dom
IPR011497 - Kazal-type_dom
IPR002350 - Prot_inh_Kazal
IPR019577 - SPARC/Testican_Ca-bd-dom
IPR000716 - Thyroglobulin_1

Pfam Domains:
PF00086 - Thyroglobulin type-1 repeat
PF07648 - Kazal-type serine protease inhibitor domain
PF10591 - Secreted protein acidic and rich in cysteine Ca binding region

SCOP Domains:
47473 - EF-hand
57610 - Thyroglobulin type-1 domain
100895 - Kazal-type serine protease inhibitors

ModBase Predicted Comparative 3D Structure on Q08629
FrontTopSide
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologGenome BrowserNo orthologNo orthologNo orthologNo ortholog
Gene DetailsGene Details    
Gene SorterGene Sorter    
 RGD    
 Protein Sequence    
 Alignment    

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0004867 serine-type endopeptidase inhibitor activity
GO:0004869 cysteine-type endopeptidase inhibitor activity
GO:0005509 calcium ion binding
GO:0008191 metalloendopeptidase inhibitor activity

Biological Process:
GO:0001558 regulation of cell growth
GO:0001764 neuron migration
GO:0007155 cell adhesion
GO:0007165 signal transduction
GO:0007399 nervous system development
GO:0010812 negative regulation of cell-substrate adhesion
GO:0010951 negative regulation of endopeptidase activity
GO:0010977 negative regulation of neuron projection development
GO:0021953 central nervous system neuron differentiation
GO:0022008 neurogenesis

Cellular Component:
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005737 cytoplasm
GO:0014069 postsynaptic density
GO:0016528 sarcoplasm
GO:0031594 neuromuscular junction
GO:0033268 node of Ranvier


-  Descriptions from all associated GenBank mRNAs
  BC030691 - Homo sapiens sparc/osteonectin, cwcv and kazal-like domains proteoglycan (testican) 1, mRNA (cDNA clone MGC:26308 IMAGE:4821322), complete cds.
AF231124 - Homo sapiens testican-1 mRNA, complete cds.
X73608 - H.sapiens mRNA for testican.
AK094489 - Homo sapiens cDNA FLJ37170 fis, clone BRACE2027896, highly similar to Testican-1 precursor.
AB209701 - Homo sapiens mRNA for sparc/osteonectin, cwcv and kazal-like domains proteoglycan precursor variant protein.
DQ890914 - Synthetic construct clone IMAGE:100003544; FLH167057.01X; RZPDo839G1088D sparc/osteonectin, cwcv and kazal-like domains proteoglycan (testican) 1 (SPOCK1) gene, encodes complete protein.
DQ894065 - Synthetic construct Homo sapiens clone IMAGE:100008525; FLH167053.01L; RZPDo839G1087D sparc/osteonectin, cwcv and kazal-like domains proteoglycan (testican) 1 (SPOCK1) gene, encodes complete protein.
KJ897596 - Synthetic construct Homo sapiens clone ccsbBroadEn_06990 SPOCK1 gene, encodes complete protein.
AB463280 - Synthetic construct DNA, clone: pF1KB7272, Homo sapiens SPOCK1 gene for sparc/osteonectin, cwcv and kazal-like domains proteoglycan (testican) 1, without stop codon, in Flexi system.
JD134358 - Sequence 115382 from Patent EP1572962.
JD094379 - Sequence 75403 from Patent EP1572962.
JD556116 - Sequence 537140 from Patent EP1572962.
JD532762 - Sequence 513786 from Patent EP1572962.
JD297642 - Sequence 278666 from Patent EP1572962.
JD516206 - Sequence 497230 from Patent EP1572962.
JD152620 - Sequence 133644 from Patent EP1572962.
JD297971 - Sequence 278995 from Patent EP1572962.
JD124289 - Sequence 105313 from Patent EP1572962.
JD243425 - Sequence 224449 from Patent EP1572962.
JD486601 - Sequence 467625 from Patent EP1572962.
JD503803 - Sequence 484827 from Patent EP1572962.
JD059179 - Sequence 40203 from Patent EP1572962.
JD510540 - Sequence 491564 from Patent EP1572962.
JD164248 - Sequence 145272 from Patent EP1572962.
JD483292 - Sequence 464316 from Patent EP1572962.
JD396673 - Sequence 377697 from Patent EP1572962.
JD520797 - Sequence 501821 from Patent EP1572962.
JD165850 - Sequence 146874 from Patent EP1572962.
JD181747 - Sequence 162771 from Patent EP1572962.
JD060992 - Sequence 42016 from Patent EP1572962.
JD330347 - Sequence 311371 from Patent EP1572962.
JD454992 - Sequence 436016 from Patent EP1572962.
JD182038 - Sequence 163062 from Patent EP1572962.
JD429070 - Sequence 410094 from Patent EP1572962.
JD109294 - Sequence 90318 from Patent EP1572962.
JD403893 - Sequence 384917 from Patent EP1572962.
JD359524 - Sequence 340548 from Patent EP1572962.
JD049449 - Sequence 30473 from Patent EP1572962.
JD362310 - Sequence 343334 from Patent EP1572962.
JD352164 - Sequence 333188 from Patent EP1572962.

-  Other Names for This Gene
  Alternate Gene Symbols: AK094489, B3KSW3, NM_004598, NP_004589, Q08629, Q59EW0, Q8N630, Q9UCL8, SPOCK, TIC1, TICN1, TICN1_HUMAN
UCSC ID: uc003lbo.3
RefSeq Accession: NM_004598
Protein: Q08629 (aka TICN1_HUMAN)
CCDS: CCDS4191.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: AK094489.1
exon count: 10CDS single in 3' UTR: no RNA size: 1954
ORF size: 1320CDS single in intron: no Alignment % ID: 99.95
txCdsPredict score: 2646.50frame shift in genome: no % Coverage: 99.95
has start codon: yes stop codon in genome: no # of Alignments: 1
has end codon: yes retained intron: no # AT/AC introns 0
selenocysteine: no end bleed into intron: 191# strange splices: 0
Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.