Gene Details | GeDiPNet - Complete Gene Info, Disease Associations & Pathways

Gene Gene information from NCBI Gene database. Gene SNPs miRNA Gene ontology Other IDs Protein Pathways Associated diseases
Entrez ID	1781
Gene name	Dynein cytoplasmic 1 intermediate chain 2
Gene symbol	DYNC1I2
Synonyms (NCBI Gene)	DIC74DNCI2IC2NEDMIBA
Chromosome	2
Chromosome location	2q31.1
Summary	This gene encodes a member of the dynein intermediate chain family. The encoded protein is a non-catalytic component of the cytoplasmic dynein 1 complex, which acts as a retrograde microtubule motor to transport organelles and vesicles. A pseudogene of th

Show/Hide all (3)

SNP ID	Visualize variation	Clinical significance	Consequence
rs752940799	A>G	Pathogenic	Coding sequence variant, missense variant
rs1574594051	G>A	Pathogenic	Splice donor variant
rs1574596084	C>T	Pathogenic	Stop gained, coding sequence variant

Show/Hide all (87)

miRTarBase ID	miRNA	Experiments	Reference
MIRT036037	hsa-miR-1301-3p	CLASH	23622248
MIRT704094	hsa-miR-3129-3p	HITS-CLIP	23313552
MIRT704093	hsa-miR-5583-5p	HITS-CLIP	23313552
MIRT704092	hsa-miR-496	HITS-CLIP	23313552
MIRT704091	hsa-miR-4789-5p	HITS-CLIP	23313552
MIRT704090	hsa-miR-3924	HITS-CLIP	23313552
MIRT704094	hsa-miR-3129-3p	HITS-CLIP	23313552
MIRT704093	hsa-miR-5583-5p	HITS-CLIP	23313552
MIRT704092	hsa-miR-496	HITS-CLIP	23313552
MIRT704091	hsa-miR-4789-5p	HITS-CLIP	23313552
MIRT704090	hsa-miR-3924	HITS-CLIP	23313552
MIRT948812	hsa-miR-146a	CLIP-seq
MIRT948813	hsa-miR-146b-5p	CLIP-seq
MIRT948814	hsa-miR-298	CLIP-seq
MIRT948815	hsa-miR-3115	CLIP-seq
MIRT948816	hsa-miR-3132	CLIP-seq
MIRT948817	hsa-miR-3174	CLIP-seq
MIRT948818	hsa-miR-3662	CLIP-seq
MIRT948819	hsa-miR-410	CLIP-seq
MIRT948820	hsa-miR-425	CLIP-seq
MIRT948821	hsa-miR-4471	CLIP-seq
MIRT948822	hsa-miR-4679	CLIP-seq
MIRT948823	hsa-miR-4719	CLIP-seq
MIRT948824	hsa-miR-4742-3p	CLIP-seq
MIRT948825	hsa-miR-568	CLIP-seq
MIRT948826	hsa-miR-589	CLIP-seq
MIRT948827	hsa-miR-642b	CLIP-seq
MIRT948828	hsa-miR-921	CLIP-seq
MIRT1548100	hsa-miR-3173-3p	CLIP-seq
MIRT1548101	hsa-miR-4428	CLIP-seq
MIRT1548102	hsa-miR-4521	CLIP-seq
MIRT1548103	hsa-miR-4802-3p	CLIP-seq
MIRT1548104	hsa-miR-490-5p	CLIP-seq
MIRT1548105	hsa-miR-586	CLIP-seq
MIRT1981178	hsa-miR-1266	CLIP-seq
MIRT1981179	hsa-miR-142-5p	CLIP-seq
MIRT1981180	hsa-miR-340	CLIP-seq
MIRT1981181	hsa-miR-3653	CLIP-seq
MIRT1981182	hsa-miR-3658	CLIP-seq
MIRT1981183	hsa-miR-3664-3p	CLIP-seq
MIRT948819	hsa-miR-410	CLIP-seq
MIRT1981184	hsa-miR-4474-5p	CLIP-seq
MIRT1981185	hsa-miR-4475	CLIP-seq
MIRT1981186	hsa-miR-4511	CLIP-seq
MIRT1981187	hsa-miR-4518	CLIP-seq
MIRT948823	hsa-miR-4719	CLIP-seq
MIRT948824	hsa-miR-4742-3p	CLIP-seq
MIRT1981188	hsa-miR-548b-3p	CLIP-seq
MIRT948825	hsa-miR-568	CLIP-seq
MIRT948827	hsa-miR-642b	CLIP-seq
MIRT948823	hsa-miR-4719	CLIP-seq
MIRT948827	hsa-miR-642b	CLIP-seq
MIRT2216252	hsa-miR-656	CLIP-seq
MIRT1548103	hsa-miR-4802-3p	CLIP-seq
MIRT1548104	hsa-miR-490-5p	CLIP-seq
MIRT1981178	hsa-miR-1266	CLIP-seq
MIRT2520233	hsa-miR-1273d	CLIP-seq
MIRT1981179	hsa-miR-142-5p	CLIP-seq
MIRT2520234	hsa-miR-299-5p	CLIP-seq
MIRT1981180	hsa-miR-340	CLIP-seq
MIRT1981183	hsa-miR-3664-3p	CLIP-seq
MIRT948819	hsa-miR-410	CLIP-seq
MIRT1981184	hsa-miR-4474-5p	CLIP-seq
MIRT1981185	hsa-miR-4475	CLIP-seq
MIRT1981187	hsa-miR-4518	CLIP-seq
MIRT948823	hsa-miR-4719	CLIP-seq
MIRT2520235	hsa-miR-4729	CLIP-seq
MIRT2520236	hsa-miR-502-5p	CLIP-seq
MIRT2520237	hsa-miR-513a-3p	CLIP-seq
MIRT948827	hsa-miR-642b	CLIP-seq
MIRT2520238	hsa-miR-944	CLIP-seq
MIRT1981178	hsa-miR-1266	CLIP-seq
MIRT2520233	hsa-miR-1273d	CLIP-seq
MIRT1981179	hsa-miR-142-5p	CLIP-seq
MIRT2520234	hsa-miR-299-5p	CLIP-seq
MIRT1981180	hsa-miR-340	CLIP-seq
MIRT1981183	hsa-miR-3664-3p	CLIP-seq
MIRT948819	hsa-miR-410	CLIP-seq
MIRT1981184	hsa-miR-4474-5p	CLIP-seq
MIRT1981185	hsa-miR-4475	CLIP-seq
MIRT1981187	hsa-miR-4518	CLIP-seq
MIRT948823	hsa-miR-4719	CLIP-seq
MIRT2520235	hsa-miR-4729	CLIP-seq
MIRT2520236	hsa-miR-502-5p	CLIP-seq
MIRT2520237	hsa-miR-513a-3p	CLIP-seq
MIRT948827	hsa-miR-642b	CLIP-seq
MIRT2520238	hsa-miR-944	CLIP-seq

Show/Hide all (20)

GO ID	Ontology	Definition	Evidence	Reference
GO:0003777	Function	Microtubule motor activity	NAS	8522607
GO:0005515	Function	Protein binding	IPI	16189514, 24986880, 25416956, 31515488, 32296183, 33961781, 35271311
GO:0005737	Component	Cytoplasm	IEA
GO:0005737	Component	Cytoplasm	NAS	8522607
GO:0005813	Component	Centrosome	IDA	21399614
GO:0005829	Component	Cytosol	TAS
GO:0005856	Component	Cytoskeleton	IEA
GO:0005868	Component	Cytoplasmic dynein complex	IBA
GO:0005868	Component	Cytoplasmic dynein complex	IEA
GO:0005868	Component	Cytoplasmic dynein complex	IPI	24986880
GO:0005874	Component	Microtubule	IDA	21525035
GO:0005874	Component	Microtubule	IEA
GO:0007018	Process	Microtubule-based movement	IEA
GO:0007018	Process	Microtubule-based movement	NAS	8522607
GO:0010970	Process	Transport along microtubule	IBA
GO:0030286	Component	Dynein complex	IEA
GO:0031982	Component	Vesicle	IDA	20682791
GO:0032388	Process	Positive regulation of intracellular transport	NAS	33957056
GO:0045503	Function	Dynein light chain binding	IBA
GO:0045504	Function	Dynein heavy chain binding	IBA

MIM	HGNC	e!Ensembl
603331	2964	ENSG00000077380

Q13409

Protein name

Cytoplasmic dynein 1 intermediate chain 2 (Cytoplasmic dynein intermediate chain 2) (Dynein intermediate chain 2, cytosolic) (DH IC-2)

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 (PubMed:31079899). Cytoplasmic dynein

PDB

5JPW , 6F1T , 6F1U , 6F1Z , 6F38 , 6F3A , 7Z8F , 7Z8I , 7Z8J , 7Z8K , 8PQW , 8PQZ , 8PR0 , 8PR1 , 8PR2 , 8PR3 , 8PTK

Family and domains

Pfam

Accession	ID	Position in sequence	Description	Type
PF11540	Dynein_IC2	133 → 163	Cytoplasmic dynein 1 intermediate chain 2	Family
PF00400	WD40	468 → 510	WD domain, G-beta repeat	Repeat

Sequence

MSDKSELKAELERKKQRLAQIREEKKRKEEERKKKETDQKKEAVAPVQEESDLEKKRREA
EALLQSMGLTPESPIVFSEYWVPPPMSPSSKSVSTPSEAGSQDSGDGAVGSRTLHWDTDP
SVLQLHSDSDLGRGPIKLGMAKITQVDFPPREIVTYTKETQTPVMAQPKEDEEEDDDVVA
PKPPIEPEEEKTLKKDEENDSKAPPHELTEEEKQQILHSEEFLSFFDHSTRIVERALSEQ
INIFFDYSGRDLEDKEGEIQAGAKLSLNRQFFDERWSKHRVVSCLDWSSQYPELLVASYN
NNEDAPHEPDGVALVWNMKYKKTTPEYVFHCQSAVMSATFAKFHPNLVVGGTYSGQIVLW
DNRSNKRTPVQRTPLSAAAHTHPVYCVNVVGTQNAHNLISISTDGKICSWSLDMLSHPQD
SMELVHKQSKAVAVTSMSFPVGDVNNFVVGSEEGSVYTACRHGSKAGISEMFEGHQGPIT
GIHCHAAVGAVDFSHLFVTSSFDWTVKLWTTKNNKPLYSFEDNADYVYDVMWSPTHPALF
ACVDGMGRLDLWNLNNDTEVPTASISVEGNPALNRVRWTHSGREIAVGDSEGQIVIYDVG
EQIAVPRNDEWARFGRTLAEINANRADAEEEAATRIPA

Sequence length

638

Interactions

View interactions

	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 Regulation of PLK1 Activity at G2/M Transition HSP90 chaperone cycle for steroid hormone receptors (SHR) Loss of Nlp from mitotic centrosomes Recruitment of mitotic centrosome proteins and complexes Loss of proteins required for interphase microtubule organization from the centrosome Recruitment of NuMA to mitotic centrosomes Anchoring of the basal body to the plasma membrane RHO GTPases Activate Formins COPI-mediated anterograde transport COPI-independent Golgi-to-ER retrograde traffic Mitotic Prometaphase AURKA Activation by TPX2 HCMV Early Events Aggrephagy EML4 and NUDC in mitotic spindle formation

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)

Show/Hide Causal Diseases (2)

Phenotype Name	Clinical Significance	dbSNP ID	RCV Accession	Evidence Score
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Neurodevelopmental disorder with microcephaly and structural brain anomalies	Likely pathogenic; Pathogenic	rs2105689812, rs1574594051, rs752940799, rs1574596084	RCV001781012 RCV000786848 RCV000786849 RCV000786850	★★★★★ ★★★★☆ ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies	Pathogenic	rs752940799, rs1574596084	RCV001254719 RCV001254720	★★★★★ ★★★★☆ ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)

Show/Hide Unknown Diseases (13)

Phenotype Name	Clinical Significance	Source	Evidence Score
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.
Acute myeloid leukemia	Benign	ClinVar	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
DYNC1I2-related disorder	Benign; Likely benign	ClinVar	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
EYE DISEASE	—	GWAS catalog	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Familial cancer of breast	Benign	ClinVar	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Hepatocellular carcinoma	Benign	ClinVar	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Lung cancer	Benign	ClinVar	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Malignant lymphoma, large B-cell, diffuse	Benign	ClinVar	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Nonpapillary renal cell carcinoma	Benign	ClinVar	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Ovarian serous cystadenocarcinoma	Benign	ClinVar	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
PROSTATE CANCER	—	GWAS catalog	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
PROSTATE CARCINOMA	—	GWAS catalog	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA	—	GWAS catalog	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Uterine corpus endometrial carcinoma	Benign	ClinVar	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations

Show/Hide Text Mining Associations (18)

Disease Name	Disease (Merged)	Source	PMID	Relationship Type	Evidence Score
Associations from Text Mining Disease associations identified through text mining
Attention deficit hyperactivity disorder	Attention Deficit Hyperactivity Disorder	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Cerebral atrophy	Cerebral Atrophy	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Clumsiness - motor delay	Motor delay	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Dwarfism	Dwarfism	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Dysarthria	Dysarthria	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Ear Diseases	Ear disease	Pubtator	25898929	Associate	★★★★★ ★☆☆☆☆ Found in Text Mining only
Endometrial Neoplasms	Endometrial neoplasm	Pubtator	32412912	Associate	★★★★★ ★☆☆☆☆ Found in Text Mining only
Endometrioid carcinoma ovary	Ovarian endometrioid carcinoma	BEFREE	28264438, 30326146		★★★★★ ★☆☆☆☆ Found in Text Mining only
Exophthalmos	Proptosis	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Global developmental delay	Developmental Delay	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Hepatoblastoma	Hepatoblastoma	Pubtator	28160403	Associate	★★★★★ ★☆☆☆☆ Found in Text Mining only
Hyperinsulinism	Hyperinsulinism	Pubtator	39382384	Associate	★★★★★ ★☆☆☆☆ Found in Text Mining only
Intellectual Disability	Mental retardation	BEFREE	31079899		★★★★★ ★☆☆☆☆ Found in Text Mining only
Intellectual Disability	Mental retardation	GENOMICS_ENGLAND_DG	31079899		★★★★★ ★☆☆☆☆ Found in Text Mining only
Microcephaly	Microcephaly	GENOMICS_ENGLAND_DG	31079899		★★★★★ ★☆☆☆☆ Found in Text Mining only
Microcephaly	Microcephaly	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Severe intellectual disability	Mental retardation	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Wilms Tumor	Wilms tumor	Pubtator	28699632	Associate	★★★★★ ★☆☆☆☆ Found in Text Mining only

DYNC1I2 (dynein cytoplasmic 1 intermediate chain 2)