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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 Show/Hide all (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 Show/Hide all (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
PF00400 WD40 476 → 518 WD domain, G-beta repeat Repeat
PF11540 Dynein_IC2 143 → 173 Cytoplasmic dynein 1 intermediate chain 2 Family
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 Pathway Reactome Pathway
Phagosome Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal
Motor proteins MHC class II antigen presentation
Vasopressin-regulated water reabsorption Separation of Sister Chromatids
Salmonella infection 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 (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
18
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Show/Hide Unknown Diseases (18)
Phenotype Name Clinical Significance Source Reference Evidence Score
Adrenocortical carcinoma, hereditary Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ALZHEIMER'S DISEASE NEUROPATHOLOGIC CHANGE — GWAS catalog 25188341
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ASTROCYTOMA — GWAS catalog 36810956
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Colorectal cancer Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DEMENTIA — GWAS catalog 25188341
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (21)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 21767414, 34679093 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Classical Lissencephaly Lissencephaly BEFREE 28734834
★★★★★
★☆☆☆☆
Found in Text Mining only
Congenital Foot Deformity Congenital deformity of foot BEFREE 24459211, 25231166
★★★★★
★☆☆☆☆
Found in Text Mining only
Degenerative polyarthritis Arthritis GWASCAT_DG 30664745
★★★★★
★☆☆☆☆
Found in Text Mining only
Ectrodactyly Ectrodactyly Pubtator 25231166, 27291887 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Glioblastoma Glioblastoma BEFREE 30250299
★★★★★
★☆☆☆☆
Found in Text Mining only
Glioblastoma Glioblastoma Pubtator 32513296 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Glioblastoma Multiforme Glioblastoma BEFREE 30250299
★★★★★
★☆☆☆☆
Found in Text Mining only
Hearing Loss Hearing loss Pubtator 25231166, 27291887 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of stomach Stomach Neoplasms BEFREE 31249807, 31605449
★★★★★
★☆☆☆☆
Found in Text Mining only