Gene Gene information from NCBI Gene database.
Entrez ID 1780
Gene name Dynein cytoplasmic 1 intermediate chain 1
Gene symbol DYNC1I1
Synonyms (NCBI Gene)
DNCI1DNCIC1
Chromosome 7
Chromosome location 7q21.3
miRNA miRNA information provided by mirtarbase database.
13
miRTarBase ID miRNA Experiments Reference
MIRT016726 hsa-miR-335-5p Microarray 18185580
MIRT948807 hsa-miR-155 CLIP-seq
MIRT948808 hsa-miR-3160-5p CLIP-seq
MIRT948809 hsa-miR-3671 CLIP-seq
MIRT948810 hsa-miR-4729 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
32
GO ID Ontology Definition Evidence Reference
GO:0000775 Component Chromosome, centromeric region IEA
GO:0000776 Component Kinetochore IDA 19229290
GO:0000776 Component Kinetochore IEA
GO:0000922 Component Spindle pole IDA 19229290
GO:0000922 Component Spindle pole IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603772 2963 ENSG00000158560
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O14576
Protein name Cytoplasmic dynein 1 intermediate chain 1 (Cytoplasmic dynein intermediate chain 1) (Dynein intermediate chain 1, cytosolic) (DH IC-1)
Protein function Acts as one of several non-catalytic accessory components of the cytoplasmic dynein 1 complex that are thought to be involved in linking dynein to cargos and to adapter proteins that regulate dynein function. Cytoplasmic dynein 1 acts as a motor
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF11540 Dynein_IC2 143 173 Cytoplasmic dynein 1 intermediate chain 2 Family
PF00400 WD40 476 518 WD domain, G-beta repeat Repeat
Sequence
MSDKSDLKAELERKKQRLAQIREEKKRKEEERKKKEADMQQKKEPVQDDSDLDRKRRETE
ALLQSIGISPEPPLVQPLHFLTWDTCYFHYLVPTPMSPSSKSVSTPSEAGSQDSGDLGPL
TRTLQWDTDPSVLQLQSDSELGRRLHKLGVSKVTQVDFLPREVVSYSKETQTPLATHQSE
EDEEDEEMVESKVGQDSELENQDKKQEVKEAPPRELTEEEKQQILHSEEFLIFFDRTIRV
IERALAEDSDIFFDYSGRELEEKDGDVQAGANLSFNRQFYDEHWSKHRVVTCMDWSLQYP
ELMVASYNNNEDAPHEPDGVALVWNMKFKKTTPEYVFHCQSSVMSVCFARFHPNLVVGGT
YSGQIVLWDNRSHRRTPVQRTPLSAAAHTHPVYCVNVVGTQNAHNLITVSTDGKMCSWSL
DMLSTPQESMELVYNKSKPVAVTGMAFPTGDVNNFVVGSEEGTVYTACRHGSKAGIGEVF
EGHQGPVTGINCHMAVGPIDFSHLFVTSSFDWTVKLWT
TKHNKPLYSFEDNADYVYDVMW
SPVHPALFACVDGMGRLDLWNLNNDTEVPTASVAIEGASALNRVRWAQAGKEVAVGDSEG
RIWVYDVGELAVPHNDEWTRFARTLVEIRANRADSEEEGTVELSA
Sequence length 645
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Phagosome
Motor proteins
Vasopressin-regulated water reabsorption
Salmonella infection
  Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal
MHC class II antigen presentation
Separation of Sister Chromatids
Resolution of Sister Chromatid Cohesion
HSP90 chaperone cycle for steroid hormone receptors (SHR)
RHO GTPases Activate Formins
COPI-mediated anterograde transport
COPI-independent Golgi-to-ER retrograde traffic
Mitotic Prometaphase
HCMV Early Events
Aggrephagy
EML4 and NUDC in mitotic spindle formation
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
20
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Adrenocortical carcinoma, hereditary Benign rs3757697 RCV005914506
Colorectal cancer Benign rs3757697 RCV005914509
DYNC1I1-related disorder Likely benign; Benign rs147587226, rs78122113, rs76250658, rs376956482, rs867286355, rs185004446, rs550636387, rs145885345, rs370341645, rs41278809, rs42082, rs139485962, rs35314029, rs117676704 RCV003923696
RCV003978544
RCV003933453
RCV003950895
RCV003961740
RCV003931411
RCV003956889
RCV003954729
RCV003946812
RCV003972702
RCV003972703
RCV003960761
RCV003968008
RCV003923057
Hepatocellular carcinoma Benign rs42082 RCV005898239
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 21767414, 34679093
Ectrodactyly Associate 25231166, 27291887
Glioblastoma Associate 32513296
Hearing Loss Associate 25231166, 27291887
Mitral Valve Prolapse Associate 27291887
Neoplasm Metastasis Stimulate 31605449
Paranoid Personality Disorder Associate 27291887
Spasms Infantile Associate 35830182
Stomach Neoplasms Associate 31605449