Human Gene CUX1 (ENST00000622516.6_4) from GENCODE V47lift37
  Description: cut like homeobox 1, transcript variant 2 (from RefSeq NM_001913.5)
Gencode Transcript: ENST00000622516.6_4
Gencode Gene: ENSG00000257923.12_14
Transcript (Including UTRs)
   Position: hg19 chr7:101,459,287-101,927,250 Size: 467,964 Total Exon Count: 23 Strand: +
Coding Region
   Position: hg19 chr7:101,459,311-101,926,382 Size: 467,072 Coding Exon Count: 23 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
Gene AllelesMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsPathwaysOther NamesModel InformationMethods
Data last updated at UCSC: 2024-08-22 23:36:26

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr7:101,459,287-101,927,250)mRNA (may differ from genome)Protein (678 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaAlphaFold
BioGPSEnsemblEntrez GeneExonPrimerGeneCardsHGNC
MalacardsMGIOMIMPubMedReactomeUniProtKB
WikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: CASP_HUMAN
DESCRIPTION: RecName: Full=Protein CASP;
FUNCTION: May be involved in intra-Golgi retrograde transport.
SUBUNIT: Homodimer; disulfide-linked. Interacts with GOLGA5.
SUBCELLULAR LOCATION: Golgi apparatus membrane; Single-pass type IV membrane protein.
SIMILARITY: Belongs to the CASP family.

-  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


-  MalaCards Disease Associations
  MalaCards Gene Search: CUX1
Diseases sorted by gene-association score: fiedler's myocarditis (9), norrie disease (7), dirofilariasis (7), histidinemia (6), histidine metabolism disease (6), leiomyoma (3)

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

+  Common Gene Haplotype Alleles
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+  Microarray Expression Data
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-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR 0.00240.000 Picture PostScript Text
3' UTR -289.00868-0.333 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
IPR012955 - CASP_C

Pfam Domains:
PF08172 - CASP C terminal

ModBase Predicted Comparative 3D Structure on Q13948
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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 orthologGenome BrowserNo ortholog
Gene DetailsGene Details  Gene Details 
Gene SorterGene Sorter  Gene Sorter 
 RGDEnsembl WormBase 
    Protein Sequence 
    Alignment 

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding

Biological Process:
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0006891 intra-Golgi vesicle-mediated transport

Cellular Component:
GO:0000139 Golgi membrane
GO:0005654 nucleoplasm
GO:0005794 Golgi apparatus
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0030173 integral component of Golgi membrane


-  Descriptions from all associated GenBank mRNAs
  AK125076 - Homo sapiens cDNA FLJ43086 fis, clone BRTHA3019048, highly similar to Protein CASP.
AK303151 - Homo sapiens cDNA FLJ57247 complete cds, highly similar to Protein CASP.
AK222832 - Homo sapiens mRNA for CCAAT displacement protein isoform b variant, clone: HEP07381.
AK125097 - Homo sapiens cDNA FLJ43107 fis, clone CTONG2020108, highly similar to Protein CASP.
BC066592 - Homo sapiens cut-like homeobox 1, mRNA (cDNA clone MGC:75164 IMAGE:5740343), complete cds.
L12579 - Human alternatively spliced CUTL1 mRNA, complete cds.
AK297548 - Homo sapiens cDNA FLJ57747 complete cds, highly similar to Protein CASP.
BC012323 - Homo sapiens cDNA clone IMAGE:4550607, containing frame-shift errors.
AK122726 - Homo sapiens cDNA FLJ16230 fis, clone FEBRA2025249, highly similar to Protein CASP.
BC025422 - Homo sapiens cut-like homeobox 1, mRNA (cDNA clone IMAGE:4864729), complete cds.
AB462994 - Synthetic construct DNA, clone: pF1KB9775, Homo sapiens CUTL1 gene for cut-like homeobox 1, without stop codon, in Flexi system.
M74099 - Human displacement protein (CCAAT) mRNA.
AB075522 - Homo sapiens neuroblastoma cDNA, clone:Nbla10317, full insert sequence.
KF421948 - Homo sapiens CUX1/RET fusion (CUX1/RET fusion) mRNA, partial cds.
BC036852 - Homo sapiens mRNA similar to cut-like 1, CCAAT displacement protein (Drosophila) (cDNA clone IMAGE:5415882).
JD123985 - Sequence 105009 from Patent EP1572962.
JD226573 - Sequence 207597 from Patent EP1572962.
JD442338 - Sequence 423362 from Patent EP1572962.
JD335725 - Sequence 316749 from Patent EP1572962.
JD392070 - Sequence 373094 from Patent EP1572962.
JD465448 - Sequence 446472 from Patent EP1572962.
JD367823 - Sequence 348847 from Patent EP1572962.
JD067690 - Sequence 48714 from Patent EP1572962.
JD397594 - Sequence 378618 from Patent EP1572962.
JD123637 - Sequence 104661 from Patent EP1572962.
JD387326 - Sequence 368350 from Patent EP1572962.
JD382235 - Sequence 363259 from Patent EP1572962.
JD112797 - Sequence 93821 from Patent EP1572962.
JD228488 - Sequence 209512 from Patent EP1572962.
JD209277 - Sequence 190301 from Patent EP1572962.
JD275191 - Sequence 256215 from Patent EP1572962.

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

Protein Q13948 (Reactome details) participates in the following event(s):

R-HSA-8847544 The COG complex and CUX1 and GOLGA5 dimers contribute to intra-Golgi vesicle tethering
R-HSA-6811438 Intra-Golgi traffic
R-HSA-6811442 Intra-Golgi and retrograde Golgi-to-ER traffic
R-HSA-199991 Membrane Trafficking
R-HSA-5653656 Vesicle-mediated transport

-  Other Names for This Gene
  Alternate Gene Symbols: B3KWH3, B3KWH8, B4DZZ2, CASP_HUMAN, CUTL1, ENST00000622516.1, ENST00000622516.2, ENST00000622516.3, ENST00000622516.4, ENST00000622516.5, G3V1Z6, J3KPQ6, NM_001913, Q13948, Q53GU9, Q8TBS3, uc327uhs.1
UCSC ID: ENST00000622516.6_4
RefSeq Accession: NM_001913.5
Protein: Q13948 (aka CASP_HUMAN)

-  Gene Model Information
  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.