Human Gene CCIN (uc003zzb.4)
  Description: Homo sapiens calicin (CCIN), mRNA.
RefSeq Summary (NM_005893): The protein encoded by this gene is a basic protein of the sperm head cytoskeleton. This protein contains kelch repeats and a BTB/POZ domain and is necessary for normal morphology during sperm differentiation. This gene is intronless. [provided by RefSeq, Jul 2008].
Transcript (Including UTRs)
   Position: hg19 chr9:36,169,389-36,171,331 Size: 1,943 Total Exon Count: 1 Strand: +
Coding Region
   Position: hg19 chr9:36,169,500-36,171,266 Size: 1,767 Coding Exon Count: 1 

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 (chr9:36,169,389-36,171,331)mRNA (may differ from genome)Protein (588 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
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MGIneXtProtOMIMPubMedTreefamUniProtKB
BioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: CALI_HUMAN
DESCRIPTION: RecName: Full=Calicin;
FUNCTION: Possible morphogenetic cytoskeletal element in spermiogenic differentiation.
SUBCELLULAR LOCATION: Cytoplasm, cytoskeleton, perinuclear theca, calyx. Note=Sperm head cytoskeletal structure tightly associated to the nucleus.
TISSUE SPECIFICITY: Testis. Not detectable or shows a drastically altered pattern of arrangement in the heads of malformed spermatozoa.
SIMILARITY: Contains 1 BACK (BTB/Kelch associated) domain.
SIMILARITY: Contains 1 BTB (POZ) domain.
SIMILARITY: Contains 6 Kelch repeats.

-  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): CCIN
CDC HuGE Published Literature: CCIN
Positive Disease Associations: smoking cessation
Related Studies:
  1. smoking cessation
    Uhl ,et al. Pharmacogenomics 2010, Genome-wide association for smoking cessation success: participants in the Patch in Practice trial of nicotine replacement , Pharmacogenomics 2010 11- 3 : 357-67. [PubMed 20235792]

-  MalaCards Disease Associations
  MalaCards Gene Search: CCIN
Diseases sorted by gene-association score: pelvic varices (2)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene

+  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: 85.53 RPKM in Testis
Total median expression: 90.08 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 -21.90111-0.197 Picture PostScript Text
3' UTR -7.0065-0.108 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
IPR011705 - BACK
IPR000210 - BTB/POZ-like
IPR011333 - BTB/POZ_fold
IPR013069 - BTB_POZ
IPR015915 - Kelch-typ_b-propeller
IPR006652 - Kelch_1

Pfam Domains:
PF00651 - BTB/POZ domain
PF01344 - Kelch motif
PF07707 - BTB And C-terminal Kelch
PF13415 - Galactose oxidase, central domain
PF13418 - Galactose oxidase, central domain
PF13964 - Kelch motif

SCOP Domains:
50965 - Galactose oxidase, central domain
54695 - POZ domain

ModBase Predicted Comparative 3D Structure on Q13939
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-  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:0003779 actin binding
GO:0004842 ubiquitin-protein transferase activity

Biological Process:
GO:0007275 multicellular organism development
GO:0007283 spermatogenesis
GO:0016567 protein ubiquitination
GO:0030154 cell differentiation

Cellular Component:
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005856 cytoskeleton
GO:0015629 actin cytoskeleton
GO:0031463 Cul3-RING ubiquitin ligase complex
GO:0033150 cytoskeletal calyx


-  Descriptions from all associated GenBank mRNAs
  AK313763 - Homo sapiens cDNA, FLJ94364, highly similar to Homo sapiens calicin (CCIN), mRNA.
HM005688 - Homo sapiens clone HTL-T-65n testis tissue sperm-binding protein Li 65n mRNA, complete cds.
AF333334 - Homo sapiens calicin mRNA, complete cds.
BC019251 - Homo sapiens calicin, mRNA (cDNA clone MGC:26974 IMAGE:4825221), complete cds.
JD048235 - Sequence 29259 from Patent EP1572962.
JD423736 - Sequence 404760 from Patent EP1572962.
JD423737 - Sequence 404761 from Patent EP1572962.
JD518688 - Sequence 499712 from Patent EP1572962.
JD513826 - Sequence 494850 from Patent EP1572962.
DQ893980 - Synthetic construct Homo sapiens clone IMAGE:100008440; FLH166256.01L; RZPDo839E0785D calicin (CCIN) gene, encodes complete protein.
DQ893982 - Synthetic construct Homo sapiens clone IMAGE:100008442; FLH263631.01L; RZPDo839E0985D calicin (CCIN) gene, encodes complete protein.
EU176505 - Synthetic construct Homo sapiens clone IMAGE:100011585; FLH263632.01L; RZPDo839G04253D calicin (CCIN) gene, encodes complete protein.
DQ890826 - Synthetic construct clone IMAGE:100003456; FLH166260.01X; RZPDo839E0786D calicin (CCIN) gene, encodes complete protein.
Z46967 - H.sapiens mRNA for calicin (partial).
JD556520 - Sequence 537544 from Patent EP1572962.

-  Other Names for This Gene
  Alternate Gene Symbols: CALI_HUMAN, NM_005893, NP_005884, Q13939, Q9BXG7
UCSC ID: uc003zzb.4
RefSeq Accession: NM_005893
Protein: Q13939 (aka CALI_HUMAN)
CCDS: CCDS6599.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_005893.2
exon count: 1CDS single in 3' UTR: no RNA size: 1956
ORF size: 1767CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 3733.00frame shift in genome: no % Coverage: 99.34
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.