This gene encodes a member of the disco-interacting protein homolog 2 family. The protein shares strong similarity with a Drosophila protein which interacts with the transcription factor disco and is expressed in the nervous system. [provided by RefSeq, Oct 2008] See more...

Aliases for DIP2C Gene

Aliases for DIP2C Gene

  • Disco Interacting Protein 2 Homolog C 2 3 5
  • KIAA0934 2 3 4
  • Disco-Interacting Protein 2 Homolog C 3 4
  • DIP2 Homolog C 3 4
  • DIP2 Disco-Interacting Protein 2 Homolog C (Drosophila) 2
  • DIP2 Disco-Interacting Protein 2 Homolog C 3

External Ids for DIP2C Gene

Previous HGNC Symbols for DIP2C Gene

  • KIAA0934

Previous GeneCards Identifiers for DIP2C Gene

  • GC10M000312

Summaries for DIP2C Gene

Entrez Gene Summary for DIP2C Gene

  • This gene encodes a member of the disco-interacting protein homolog 2 family. The protein shares strong similarity with a Drosophila protein which interacts with the transcription factor disco and is expressed in the nervous system. [provided by RefSeq, Oct 2008]

GeneCards Summary for DIP2C Gene

DIP2C (Disco Interacting Protein 2 Homolog C) is a Protein Coding gene. Diseases associated with DIP2C include Spastic Hemiplegia and Familial Cold Autoinflammatory Syndrome 3. Gene Ontology (GO) annotations related to this gene include transcription factor binding. An important paralog of this gene is DIP2A.

Additional gene information for DIP2C Gene

No data available for CIViC Summary , UniProtKB/Swiss-Prot Summary , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , Rfam classification and piRNA Summary for DIP2C Gene

Genomics for DIP2C Gene

GeneHancer (GH) Regulatory Elements for DIP2C Gene

Promoters and enhancers for DIP2C Gene
GeneHancer (GH) Identifier GH Type GH
GH Sources Gene Association Score Total Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor
Binding Sites
Gene Targets
GH10J000687 Promoter/Enhancer 2 EPDnew Ensembl ENCODE CraniofacialAtlas dbSUPER 500.7 +0.3 328 3.3 USF1 PHF8 ZFX ZBTB10 ZBTB26 TGIF2 MXI1 ZNF341 FOXA2 POLR2A DIP2C lnc-PRR26-3 ENSG00000225140 lnc-LARP4B-3
GH10J000983 Promoter/Enhancer 2.2 EPDnew Ensembl ENCODE CraniofacialAtlas 14.1 -297.5 -297476 7.6 ZBTB40 ZNF217 EP300 CTCF SIN3A NRF1 TCF12 POLR2G SP1 PHF8 GTPBP4 LARP4B ENSG00000205740 DIP2C ZMYND11 LOC101927762 WDR37 piR-42548
GH10J001498 Enhancer 1.1 FANTOM5 ENCODE 24.2 -809.8 -809815 1.6 EP300 ZSCAN5C RBAK ZNF639 ZBTB10 ZNF623 TRIM28 ZNF662 ZNF274 ATF2 DIP2C LARP4B ADARB2-AS1 ADARB2 WDR37 HSALNG0075557 HSALNG0075552
GH10J000665 Enhancer 1 ENCODE dbSUPER 21.4 +23.6 23588 1.3 ZNF639 ZNF354C ZIC2 ZBTB10 ZNF423 TRIM28 KLF7 ZNF341 OSR2 BCL11A DIP2C ZMYND11 ENSG00000225140 ENSG00000205740 lnc-LARP4B-3 PRR26
GH10J000649 Promoter/Enhancer 1.7 EPDnew Ensembl ENCODE dbSUPER 11.5 +39.2 39223 2.5 POLR2G NCOR1 ZIC2 KDM6A ZBTB25 TGIF2 TBX3 ZSCAN9 FOXA2 NR2F2 PRR26 ENSG00000225140 DIP2C lnc-LARP4B-3
- Elite GeneHancer and/or Elite GeneHancer-gene association Download GeneHancer data from 2017 publication | Request up-to-date GeneHancer data (full dataset)

GeneHancers around DIP2C on UCSC Golden Path with GeneCards custom track

Cistromic (ChIP-Seq) regulation report from SPP (The Signaling Pathways Project) for DIP2C

Top Transcription factor binding sites by QIAGEN in the DIP2C gene promoter:
  • Bach2
  • En-1
  • FOXJ2
  • FOXJ2 (long isoform)
  • FOXO4
  • HOXA3
  • SREBP-1a
  • SREBP-1b
  • SREBP-1c
  • TGIF

Genomic Locations for DIP2C Gene

Genomic Locations for DIP2C Gene
415,500 bases
Minus strand
415,554 bases
Minus strand

Genomic View for DIP2C Gene

Genes around DIP2C on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
DIP2C Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for DIP2C Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for DIP2C Gene

Proteins for DIP2C Gene

  • Protein details for DIP2C Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Recommended name:
    Disco-interacting protein 2 homolog C
    Protein Accession:
    Secondary Accessions:
    • B4DPI5
    • Q5SS78

    Protein attributes for DIP2C Gene

    1556 amino acids
    Molecular mass:
    170767 Da
    Quaternary structure:
    No Data Available
    • Sequence=BAA76778.2; Type=Erroneous initiation; Evidence={ECO:0000305};

    Alternative splice isoforms for DIP2C Gene


neXtProt entry for DIP2C Gene

Post-translational modifications for DIP2C Gene

  • Ubiquitination at Lys257
  • Modification sites at PhosphoSitePlus

No data available for DME Specific Peptides for DIP2C Gene

Domains & Families for DIP2C Gene

Gene Families for DIP2C Gene

Human Protein Atlas (HPA):
  • Plasma proteins
  • Predicted intracellular proteins
  • Predicted membrane proteins

Protein Domains for DIP2C Gene

  • AMP-binding signature
  • DMAP1-binding

Suggested Antigen Peptide Sequences for DIP2C Gene

GenScript: Design optimal peptide antigens:
  • cDNA FLJ50825, highly similar to Disco-interacting protein 2 homolog C (B4DPI5_HUMAN)
  • Disco-interacting protein 2 homolog C (DIP2C_HUMAN)
  • DIP2C protein (Q86XV3_HUMAN)

Graphical View of Domain Structure for InterPro Entry



  • Belongs to the DIP2 family.
  • Belongs to the DIP2 family.
genes like me logo Genes that share domains with DIP2C: view

Function for DIP2C Gene

Phenotypes From GWAS Catalog for DIP2C Gene

Gene Ontology (GO) - Molecular Function for DIP2C Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0003674 molecular_function ND --
GO:0003824 catalytic activity IEA --
genes like me logo Genes that share ontologies with DIP2C: view
genes like me logo Genes that share phenotypes with DIP2C: view

Animal Model Products

CRISPR Products

Clone Products

No data available for Molecular function , Enzyme Numbers (IUBMB) , Human Phenotype Ontology , Animal Models , Transcription Factor Targets and HOMER Transcription for DIP2C Gene

Localization for DIP2C Gene

Subcellular locations from

Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for DIP2C gene
Compartment Confidence
plasma membrane 1
extracellular 1
cytoskeleton 1
mitochondrion 1
peroxisome 1
nucleus 1
cytosol 1

Subcellular locations from the

Human Protein Atlas (HPA)
  • Cytosol (2)
  • Nucleoplasm (2)
  • Vesicles (2)
See all subcellular structures

Gene Ontology (GO) - Cellular Components for DIP2C Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005575 cellular_component ND --
genes like me logo Genes that share ontologies with DIP2C: view

No data available for Subcellular locations from UniProtKB/Swiss-Prot for DIP2C Gene

Pathways & Interactions for DIP2C Gene

PathCards logo

SuperPathways for DIP2C Gene

No Data Available

Gene Ontology (GO) - Biological Process for DIP2C Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0008150 biological_process ND --
genes like me logo Genes that share ontologies with DIP2C: view

No data available for Pathways by source and SIGNOR curated interactions for DIP2C Gene

Drugs & Compounds for DIP2C Gene

No Compound Related Data Available

Transcripts for DIP2C Gene

mRNA/cDNA for DIP2C Gene

13 NCBI additional mRNA sequence :
5 Ensembl transcripts including schematic representations, and UCSC links to gene/alias where relevant :

CRISPR Products

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for DIP2C Gene

No ASD Table

Relevant External Links for DIP2C Gene

GeneLoc Exon Structure for

Expression for DIP2C Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and SAGE for DIP2C Gene

Protein differential expression in normal tissues from HIPED for DIP2C Gene

This gene is overexpressed in Spinal cord (50.6).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, MaxQB, and MOPED for DIP2C Gene

Transcriptomic regulation report from SPP (The Signaling Pathways Project) for DIP2C

SOURCE GeneReport for Unigene cluster for DIP2C Gene:


Evidence on tissue expression from TISSUES for DIP2C Gene

  • Nervous system(4.7)
  • Kidney(4.3)
  • Liver(4.1)
  • Skin(2)
genes like me logo Genes that share expression patterns with DIP2C: view

No data available for mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , mRNA differential expression in normal tissues , Protein tissue co-expression partners , mRNA Expression by UniProt/SwissProt and Phenotype-based relationships between genes and organs from Gene ORGANizer for DIP2C Gene

Orthologs for DIP2C Gene

This gene was present in the common ancestor of animals and fungi.

Orthologs for DIP2C Gene

Organism Taxonomy Gene Similarity Type Details
(Pan troglodytes)
Mammalia DIP2C 31 30
  • 97.6 (n)
(Monodelphis domestica)
Mammalia DIP2C 31
  • 97 (a)
(Ornithorhynchus anatinus)
Mammalia DIP2C 31
  • 96 (a)
(Canis familiaris)
Mammalia DIP2C 31
  • 95 (a)
LOC610591 30
  • 87.38 (n)
(Bos Taurus)
Mammalia DIP2C 31 30
  • 88.22 (n)
(Rattus norvegicus)
Mammalia Dip2c 30
  • 87.19 (n)
(Mus musculus)
Mammalia Dip2c 17 31 30
  • 87.17 (n)
(Gallus gallus)
Aves DIP2C 31 30
  • 80.96 (n)
(Anolis carolinensis)
Reptilia DIP2C 31
  • 93 (a)
tropical clawed frog
(Silurana tropicalis)
Amphibia dip2c 30
  • 79.6 (n)
(Danio rerio)
Actinopterygii dip2c 31 30
  • 79.26 (n)
fruit fly
(Drosophila melanogaster)
Insecta DIP2 31 30
  • 57.91 (n)
African malaria mosquito
(Anopheles gambiae)
Insecta AgaP_AGAP011333 30
  • 32.14 (n)
(Caenorhabditis elegans)
Secernentea F28B3.1 31 30
  • 54.8 (n)
baker's yeast
(Saccharomyces cerevisiae)
Saccharomycetes -- 31
  • 19 (a)
sea squirt
(Ciona savignyi)
Ascidiacea CSA.49 31
  • 54 (a)
Species where no ortholog for DIP2C was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Ashbya gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African clawed frog (Xenopus laevis)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • fission yeast (Schizosaccharomyces pombe)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • K. lactis yeast (Kluyveromyces lactis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rainbow trout (Oncorhynchus mykiss)
  • rice (Oryza sativa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • thale cress (Arabidopsis thaliana)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • wheat (Triticum aestivum)

Evolution for DIP2C Gene

Gene Tree for DIP2C (if available)
Gene Tree for DIP2C (if available)
Evolutionary constrained regions (ECRs) for DIP2C: view image

Paralogs for DIP2C Gene

Paralogs for DIP2C Gene

(4) SIMAP similar genes for DIP2C Gene using alignment to 7 proteins:

  • F6XJ20_HUMAN
  • H0Y5A8_HUMAN
  • H0Y7Q3_HUMAN
  • Q86XV3_HUMAN
genes like me logo Genes that share paralogs with DIP2C: view

Variants for DIP2C Gene

Sequence variations, with clinical significance, from ClinVar and Humsavar, with links to dbSNP for DIP2C Gene

SNP ID Clinical significance and condition Chr 10 pos Variation AA Info Type
708364 Benign: not provided 423,038(-) G/T INTRON_VARIANT
716929 Benign: not provided 384,556(-) G/A SYNONYMOUS_VARIANT
716930 Benign: not provided 389,982(-) G/C INTRON_VARIANT
722390 Benign: not provided 399,211(-) C/G SYNONYMOUS_VARIANT
724891 Benign: not provided 423,020(-) G/A SYNONYMOUS_VARIANT

Additional dbSNP identifiers (rs#s) for DIP2C Gene

Structural Variations from Database of Genomic Variants (DGV) for DIP2C Gene

Variant ID Type Subtype PubMed ID
dgv118n67 CNV gain 20364138
dgv11n6 CNV deletion 16902084
dgv26e215 CNV deletion 23714750
dgv329n106 CNV deletion 24896259
dgv330n106 CNV deletion 24896259
dgv331n106 CNV deletion 24896259
dgv332n106 CNV duplication 24896259
dgv339e59 CNV duplication 20981092
dgv340e59 CNV duplication 20981092
dgv341e59 CNV duplication 20981092
dgv651n100 CNV gain 25217958
dgv652n100 CNV gain 25217958
dgv653n100 CNV gain 25217958
dgv68e201 CNV deletion 23290073
dgv69e201 CNV deletion 23290073
dgv924n54 CNV gain 21841781
esv1024446 CNV insertion 17803354
esv1103672 CNV deletion 17803354
esv1111279 CNV insertion 17803354
esv1139005 CNV insertion 17803354
esv1191119 CNV insertion 17803354
esv1255045 CNV deletion 17803354
esv1320039 CNV deletion 17803354
esv1344682 CNV insertion 17803354
esv1366852 CNV deletion 17803354
esv1374087 CNV deletion 17803354
esv1403517 CNV deletion 17803354
esv1439616 CNV insertion 17803354
esv1450884 CNV insertion 17803354
esv1514144 CNV insertion 17803354
esv1547088 CNV insertion 17803354
esv1558074 CNV deletion 17803354
esv1664973 CNV insertion 17803354
esv1678258 CNV insertion 17803354
esv1755649 CNV deletion 17803354
esv1922448 CNV deletion 18987734
esv2016393 CNV deletion 18987734
esv2037768 CNV deletion 18987734
esv21741 CNV gain 19812545
esv2242829 CNV deletion 18987734
esv2276553 CNV deletion 18987734
esv22803 CNV loss 19812545
esv2328251 CNV deletion 18987734
esv2341391 CNV deletion 18987734
esv2467819 CNV insertion 19546169
esv24994 CNV loss 19812545
esv2500904 CNV deletion 19546169
esv2537541 CNV insertion 19546169
esv25478 CNV gain+loss 19812545
esv2572990 CNV deletion 19546169
esv2594246 CNV deletion 19546169
esv26085 CNV gain 19812545
esv2638964 CNV deletion 19546169
esv2650676 CNV insertion 19546169
esv2659464 CNV deletion 23128226
esv2660097 CNV deletion 23128226
esv2663036 CNV deletion 23128226
esv2664614 CNV deletion 23128226
esv2665059 CNV deletion 23128226
esv2666164 CNV deletion 23128226
esv2667724 CNV deletion 23128226
esv2675490 CNV deletion 23128226
esv2678056 CNV deletion 23128226
esv2728339 CNV deletion 23290073
esv2728350 CNV deletion 23290073
esv2728363 CNV deletion 23290073
esv2728385 CNV deletion 23290073
esv2728396 CNV deletion 23290073
esv2728407 CNV deletion 23290073
esv2728418 CNV deletion 23290073
esv2728429 CNV deletion 23290073
esv2728440 CNV deletion 23290073
esv2728451 CNV deletion 23290073
esv2728462 CNV deletion 23290073
esv2728474 CNV deletion 23290073
esv2728485 CNV deletion 23290073
esv2728496 CNV deletion 23290073
esv2728507 CNV deletion 23290073
esv2728518 CNV deletion 23290073
esv2728529 CNV deletion 23290073
esv2728540 CNV deletion 23290073
esv2728551 CNV deletion 23290073
esv2728562 CNV deletion 23290073
esv2728573 CNV deletion 23290073
esv2728585 CNV deletion 23290073
esv2728596 CNV deletion 23290073
esv2728607 CNV deletion 23290073
esv2728618 CNV deletion 23290073
esv2728629 CNV deletion 23290073
esv2728640 CNV deletion 23290073
esv2728651 CNV deletion 23290073
esv2728673 CNV deletion 23290073
esv2728696 CNV deletion 23290073
esv2728707 CNV deletion 23290073
esv2728718 CNV deletion 23290073
esv2728729 CNV deletion 23290073
esv2728740 CNV deletion 23290073
esv2728751 CNV deletion 23290073
esv2728762 CNV deletion 23290073
esv2728773 CNV deletion 23290073
esv28009 CNV loss 19812545
esv28717 CNV gain 19812545
esv29290 CNV gain+loss 19812545
esv29656 CNV gain 19812545
esv3265495 CNV deletion 24192839
esv3305983 CNV mobile element insertion 20981092
esv3335198 CNV insertion 20981092
esv3416 CNV loss 18987735
esv3545686 CNV deletion 23714750
esv3545694 CNV deletion 23714750
esv3545695 CNV deletion 23714750
esv3545701 CNV deletion 23714750
esv3576016 CNV gain 25503493
esv3622078 CNV loss 21293372
esv3622079 CNV loss 21293372
esv3622080 CNV loss 21293372
esv3622081 CNV gain 21293372
esv3891734 CNV gain 25118596
esv4124 CNV loss 18987735
esv7892 CNV loss 19470904
esv9223 CNV loss 19470904
esv990983 CNV deletion 20482838
esv997336 CNV deletion 20482838
esv998813 CNV insertion 20482838
nsv1035990 CNV loss 25217958
nsv1044267 CNV gain 25217958
nsv1068258 CNV deletion 25765185
nsv1068259 CNV deletion 25765185
nsv1068260 CNV deletion 25765185
nsv1068654 CNV deletion 25765185
nsv1068655 CNV deletion 25765185
nsv1069002 CNV deletion 25765185
nsv1069435 CNV deletion 25765185
nsv1069436 CNV deletion 25765185
nsv1069437 CNV deletion 25765185
nsv1069438 CNV deletion 25765185
nsv1077314 CNV duplication 25765185
nsv1077315 CNV duplication 25765185
nsv1111021 CNV tandem duplication 24896259
nsv1112570 CNV deletion 24896259
nsv1113237 CNV deletion 24896259
nsv1113238 CNV deletion 24896259
nsv1115384 CNV duplication 24896259
nsv1119411 CNV insertion 24896259
nsv1119774 CNV deletion 24896259
nsv1119775 CNV deletion 24896259
nsv1120209 CNV tandem duplication 24896259
nsv1120210 CNV tandem duplication 24896259
nsv1121799 CNV deletion 24896259
nsv1121800 CNV deletion 24896259
nsv1121801 CNV deletion 24896259
nsv1124608 CNV duplication 24896259
nsv1126238 CNV deletion 24896259
nsv1128633 CNV duplication 24896259
nsv1129142 CNV insertion 24896259
nsv1129484 CNV tandem duplication 24896259
nsv1129485 CNV tandem duplication 24896259
nsv1132327 CNV duplication 24896259
nsv1140113 CNV insertion 24896259
nsv1140441 CNV tandem duplication 24896259
nsv1142085 CNV tandem duplication 24896259
nsv1143486 CNV deletion 24896259
nsv1145420 CNV deletion 24896259
nsv1145870 CNV deletion 26484159
nsv1146199 CNV duplication 26484159
nsv1146678 CNV insertion 26484159
nsv1148829 CNV insertion 26484159
nsv1152052 CNV duplication 26484159
nsv24219 CNV deletion 16902084
nsv25193 CNV deletion 16902084
nsv25268 CNV deletion 16902084
nsv466693 CNV gain 19166990
nsv466695 CNV gain 19166990
nsv466696 CNV gain 19166990
nsv477039 CNV novel sequence insertion 20440878
nsv509339 CNV insertion 20534489
nsv511462 CNV loss 21212237
nsv512134 CNV loss 21212237
nsv519746 CNV loss 19592680
nsv520943 CNV loss 19592680
nsv524243 CNV loss 19592680
nsv527312 CNV loss 19592680
nsv528733 CNV gain 19592680
nsv5487 CNV insertion 18451855
nsv549750 CNV gain 21841781
nsv549751 CNV gain 21841781
nsv549752 CNV loss 21841781
nsv549753 CNV gain 21841781
nsv549754 CNV loss 21841781
nsv549755 CNV loss 21841781
nsv549756 CNV gain 21841781
nsv549757 CNV loss 21841781
nsv549758 CNV loss 21841781
nsv549759 CNV loss 21841781
nsv549762 CNV loss 21841781
nsv549763 CNV gain 21841781
nsv549764 CNV loss 21841781
nsv549765 CNV gain 21841781
nsv818740 CNV gain 17921354
nsv819504 CNV gain 19587683
nsv820645 CNV deletion 20802225
nsv831765 CNV loss 17160897
nsv951221 CNV deletion 24416366
nsv951222 CNV deletion 24416366
nsv951223 CNV deletion 24416366
nsv951224 CNV deletion 24416366
nsv951225 CNV deletion 24416366
nsv951226 CNV deletion 24416366
nsv957667 CNV deletion 24416366
nsv975789 CNV duplication 23825009

Variation tolerance for DIP2C Gene

Residual Variation Intolerance Score: 0.157% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 1.72; 32.71% of all genes are more intolerant (likely to be disease-causing)

Additional Variant Information for DIP2C Gene

Human Gene Mutation Database (HGMD)
SNPedia medical, phenotypic, and genealogical associations of SNPs for

SNP Genotyping and Copy Number Assay Products

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for DIP2C Gene

Disorders for DIP2C Gene

MalaCards: The human disease database

(3) MalaCards diseases for DIP2C Gene - From: DISEASES

Disorder Aliases PubMed IDs
spastic hemiplegia
  • congenital hemiplegia
familial cold autoinflammatory syndrome 3
  • fcas3
spastic cerebral palsy
  • palsy, cerebral, spastic
- elite association - COSMIC cancer census association via MalaCards
Search DIP2C in MalaCards View complete list of genes associated with diseases

Additional Disease Information for DIP2C

Genetic Association Database
Human Genome Epidemiology Navigator
ATLAS of Genetics and Cytogenetics in Oncology and Haematology
genes like me logo Genes that share disorders with DIP2C: view

No data available for UniProtKB/Swiss-Prot and Genatlas for DIP2C Gene

Publications for DIP2C Gene

  1. Genome-wide association study of Alzheimer's disease with psychotic symptoms. (PMID: 22005930) Hollingworth P … Williams J (Molecular psychiatry 2012) 3 41 54
  2. Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. (PMID: 20379614) Rose JE … Uhl GR (Molecular medicine (Cambridge, Mass.) 2010) 3 41 54
  3. Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study. (PMID: 20628086) Bailey SD … DREAM investigators (Diabetes care 2010) 3 41 54
  4. Association of genetic variants with hemorrhagic stroke in Japanese individuals. (PMID: 20198315) Yoshida T … Yamada Y (International journal of molecular medicine 2010) 3 41 54
  5. Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals. (PMID: 19851296) Oguri M … Yamada Y (American journal of hypertension 2010) 3 41 54

Products for DIP2C Gene

Sources for DIP2C Gene