Gene Gene information from NCBI Gene database.
Entrez ID 120
Gene name Adducin 3
Gene symbol ADD3
Synonyms (NCBI Gene)
ADDLCPSQ3
Chromosome 10
Chromosome location 10q25.1-q25.2
Summary Adducins are heteromeric proteins composed of different subunits referred to as adducin alpha, beta and gamma. The three subunits are encoded by distinct genes and belong to a family of membrane skeletal proteins involved in the assembly of spectrin-actin
SNPs SNP information provided by dbSNP.
2
SNP ID Visualize variation Clinical significance Consequence
rs143966199 T>A Conflicting-interpretations-of-pathogenicity Missense variant, coding sequence variant
rs564185858 G>A Pathogenic Missense variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
321
miRTarBase ID miRNA Experiments Reference
MIRT016076 hsa-miR-374b-5p Sequencing 20371350
MIRT022859 hsa-miR-124-3p Proteomics;Microarray 18668037
MIRT030536 hsa-miR-24-3p Microarray 19748357
MIRT437436 hsa-miR-145-5p FlowLuciferase reporter assayqRT-PCRWestern blot 23814265
MIRT437436 hsa-miR-145-5p FlowLuciferase reporter assayqRT-PCRWestern blot 23814265
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
26
GO ID Ontology Definition Evidence Reference
GO:0000794 Component Condensed nuclear chromosome IEA
GO:0003779 Function Actin binding IEA
GO:0005080 Function Protein kinase C binding IEA
GO:0005200 Function Structural constituent of cytoskeleton IEA
GO:0005200 Function Structural constituent of cytoskeleton TAS 8893809
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601568 245 ENSG00000148700
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UEY8
Protein name Gamma-adducin (Adducin-like protein 70)
Protein function Membrane-cytoskeleton-associated protein that promotes the assembly of the spectrin-actin network. Plays a role in actin filament capping (PubMed:23836506). Binds to calmodulin (Probable). Involved in myogenic reactivity of the renal afferent ar
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00596 Aldolase_II 139 321 Class II Aldolase and Adducin N-terminal domain Domain
Tissue specificity TISSUE SPECIFICITY: [Isoform 1]: ubiquitously expressed. {ECO:0000269|PubMed:8893809}.; TISSUE SPECIFICITY: Cleavage fragment 1-357 is abundantly expressed in the brain of patients with Alzheimer disease (AD), but hardly detectable in age-matched control
Sequence
MSSDASQGVITTPPPPSMPHKERYFDRINENDPEYIRERNMSPDLRQDFNMMEQRKRVTQ
ILQSPAFREDLECLIQEQMKKGHNPTGLLALQQIADYIMANSFSGFSSPPLSLGMVTPIN
DLPGADTSSYVKGEKLTRCKLASLYRLVDLFGWAHLANTYISVRISKEQDHIIIIPRGLS
FSEATASNLVKVNIIGEVVDQGSTNLKIDHTGFSPHAAIYSTRPDVKCVIHIHTLATAAV
SSMKCGILPISQESLLLGDVAYYDYQGSLEEQEERIQLQKVLGPSCKVLVLRNHGVVALG
ETLEEAFHYIFNVQLACEIQV
QALAGAGGVDNLHVLDFQKYKAFTYTVAASGGGGVNMGS
HQKWKVGEIEFEGLMRTLDNLGYRTGYAYRHPLIREKPRHKSDVEIPATVTAFSFEDDTV
PLSPLKYMAQRQQREKTRWLNSPNTYMKVNVPEESRNGETSPRTKITWMKAEDSSKVSGG
TPIKIEDPNQFVPLNTNPNEVLEKRNKIREQNRYDLKTAGPQSQLLAGIVVDKPPSTMQF
EDDDHGPPAPPNPFSHLTEGELEEYKRTIERKQQGLEDAEQELLSDDASSVSQIQSQTQS
PQNVPEKLEENHELFSKSFISMEVPVMVVNGKDDMHDVEDELAKRVSRLSTSTTIENIEI
TIKSPEKIEEVLSPEGSPSKSPSKKKKKFRTPSFLKKNKKKEKVEA
Sequence length 706
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Miscellaneous transport and binding events
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
18
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cerebral palsy Likely pathogenic; Pathogenic rs564185858 RCV000234930
Cerebral palsy, spastic quadriplegic, 3 Likely pathogenic; Pathogenic rs564185858 RCV000231295
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
ADD3-related disorder Likely benign rs373955551, rs568629103, rs754743252, rs148633520, rs149170169 RCV003916638
RCV003956626
RCV003957277
RCV003975514
RCV003950808
Complex neurodevelopmental disorder with motor features Uncertain significance rs551170650, rs55763936 RCV005358090
RCV005358091
Familial cancer of breast Benign rs113052722 RCV005903618
Lung cancer Benign rs113052722 RCV005903619
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 30124448
Astrocytoma Associate 12937144
Biliary Atresia Associate 24104524, 25285724, 28902846, 29685956, 30358741, 32315284, 36114336, 37834180
Bipolar Disorder Associate 28072414
Carcinoma Non Small Cell Lung Associate 30290240
Frailty Associate 39464190
Glioblastoma Associate 12937144
Leukemia Myeloid Acute Associate 29286103
Liver Cirrhosis Associate 28902846
Lung Neoplasms Associate 33196842