Human Gene SPARCL1 (uc003hqs.4)
  Description: Homo sapiens SPARC-like 1 (hevin) (SPARCL1), transcript variant 2, mRNA.
Transcript (Including UTRs)
   Position: hg19 chr4:88,394,488-88,450,655 Size: 56,168 Total Exon Count: 11 Strand: -
Coding Region
   Position: hg19 chr4:88,394,927-88,420,726 Size: 25,800 Coding Exon Count: 10 

Page IndexSequence and LinksUniProtKB CommentsPrimersGenetic AssociationsCTD
Gene AllelesRNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther Species
GO AnnotationsmRNA DescriptionsPathwaysOther NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr4:88,394,488-88,450,655)mRNA (may differ from genome)Protein (664 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaAlphaFold
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H-INVHGNCHPRDLynxMGIneXtProt
OMIMPubMedReactomeTreefamUniProtKBWikipedia
BioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: SPRL1_HUMAN
DESCRIPTION: RecName: Full=SPARC-like protein 1; AltName: Full=High endothelial venule protein; Short=Hevin; AltName: Full=MAST 9; Flags: Precursor;
SUBCELLULAR LOCATION: Secreted, extracellular space, extracellular matrix (By similarity).
TISSUE SPECIFICITY: Highly expressed in lymph node, brain, heart, lung, skeletal muscle, ovary, small intestine, and colon, with lower levels in placenta, pancreas, testis, spleen, and thymus, and no expression in kidney, liver, and peripheral blood leukocytes.
PTM: N- and O-glycosylated. O-glycosylated with a core 1 or possibly core 8 glycan. Thr-398 is the preferred site to Thr-399.
SIMILARITY: Belongs to the SPARC family.
SIMILARITY: Contains 1 EF-hand domain.
SIMILARITY: Contains 1 follistatin-like domain.
SIMILARITY: Contains 1 Kazal-like domain.

-  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): SPARCL1
CDC HuGE Published Literature: SPARCL1
Positive Disease Associations: Carotid Arteries
Related Studies:
  1. Carotid Arteries
    Christopher J O'Donnell et al. BMC medical genetics 2007, Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study., BMC medical genetics. [PubMed 17903303]
    The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.

-  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: 970.46 RPKM in Artery - Aorta
Total median expression: 15624.84 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 -132.90470-0.283 Picture PostScript Text
3' UTR -85.00439-0.194 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
IPR018247 - EF_Hand_1_Ca_BS
IPR018249 - EF_HAND_2
IPR003645 - Fol_N
IPR015369 - Follistatin/Osteonectin_EGF
IPR001999 - Osteonectin_CS
IPR002350 - Prot_inh_Kazal
IPR016359 - SPARC-like_p1
IPR019577 - SPARC/Testican_Ca-bd-dom

Pfam Domains:
PF00050 - Kazal-type serine protease inhibitor domain
PF07648 - Kazal-type serine protease inhibitor domain
PF09289 - Follistatin/Osteonectin-like EGF domain
PF10591 - Secreted protein acidic and rich in cysteine Ca binding region

SCOP Domains:
47473 - EF-hand
100895 - Kazal-type serine protease inhibitors

ModBase Predicted Comparative 3D Structure on Q14515
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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 orthologNo orthologNo orthologNo orthologNo orthologNo ortholog
Gene Details     
Gene Sorter     
      
      
      

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0005509 calcium ion binding
GO:0005515 protein binding
GO:0005518 collagen binding
GO:0046872 metal ion binding
GO:0050840 extracellular matrix binding

Biological Process:
GO:0007165 signal transduction
GO:0043687 post-translational protein modification
GO:0044267 cellular protein metabolic process
GO:0048856 anatomical structure development

Cellular Component:
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005788 endoplasmic reticulum lumen


-  Descriptions from all associated GenBank mRNAs
  BC022484 - Homo sapiens cDNA clone IMAGE:4799805, containing frame-shift errors.
X82157 - H.sapiens mRNA for high endothelial venule.
AL833430 - Homo sapiens mRNA; cDNA DKFZp313N0839 (from clone DKFZp313N0839).
BC033721 - Homo sapiens SPARC-like 1 (hevin), mRNA (cDNA clone MGC:45264 IMAGE:4939390), complete cds.
X86693 - H.sapiens mRNA for hevin like protein.
BX647713 - Homo sapiens mRNA; cDNA DKFZp686F10266 (from clone DKFZp686F10266).
JD049063 - Sequence 30087 from Patent EP1572962.
AK304494 - Homo sapiens cDNA FLJ52396 complete cds, highly similar to SPARC-like protein 1 precursor.
AK316533 - Homo sapiens cDNA, FLJ79432 complete cds, highly similar to SPARC-like protein 1 precursor.
AK300956 - Homo sapiens cDNA FLJ54387 complete cds, moderately similar to SPARC-like protein 1 precursor.
JD088923 - Sequence 69947 from Patent EP1572962.
JD346126 - Sequence 327150 from Patent EP1572962.
AK298039 - Homo sapiens cDNA FLJ54278 complete cds, highly similar to SPARC-like protein 1 precursor.
JD273614 - Sequence 254638 from Patent EP1572962.
AK304628 - Homo sapiens cDNA FLJ55140 complete cds, highly similar to SPARC-like protein 1 precursor.
JD314455 - Sequence 295479 from Patent EP1572962.
JD066869 - Sequence 47893 from Patent EP1572962.
JD042179 - Sequence 23203 from Patent EP1572962.
AY513278 - Homo sapiens proliferation-inducing protein 33 (PIG33) mRNA, complete cds.
AK294335 - Homo sapiens cDNA FLJ50481 complete cds, highly similar to SPARC-like protein 1 precursor.
EU832833 - Synthetic construct Homo sapiens clone HAIB:100067862; DKFZo008G0933 SPARC-like 1 (mast9, hevin) protein (SPARCL1) gene, encodes complete protein.
GQ129224 - Synthetic construct Homo sapiens clone HAIB:100068524; DKFZo004G0934 SPARC-like 1 (mast9, hevin) protein (SPARCL1) gene, partial cds.
BC010383 - Homo sapiens SPARC-like 1 (mast9, hevin), mRNA (cDNA clone IMAGE:4272629), with apparent retained intron.
JD277569 - Sequence 258593 from Patent EP1572962.

-  Biochemical and Signaling Pathways
  Reactome (by CSHL, EBI, and GO)

Protein Q14515 (Reactome details) participates in the following event(s):

R-HSA-8952289 FAM20C phosphorylates FAM20C substrates
R-HSA-381426 Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
R-HSA-8957275 Post-translational protein phosphorylation
R-HSA-392499 Metabolism of proteins
R-HSA-597592 Post-translational protein modification

-  Other Names for This Gene
  Alternate Gene Symbols: NM_004684, NP_004675, Q14515, Q14800, SPRL1_HUMAN
UCSC ID: uc003hqs.4
RefSeq Accession: NM_004684
Protein: Q14515 (aka SPRL1_HUMAN or SPL1_HUMAN)
CCDS: CCDS3622.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_004684.4
exon count: 11CDS single in 3' UTR: no RNA size: 2956
ORF size: 1995CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 4047.00frame shift in genome: no % Coverage: 98.24
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: 0# 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.