IQCC (IQ motif containing C)

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Gene miRNA Gene ontology Other IDs Protein Associated diseases Related genes Diseases linked via similar genes

Gene

• Entrez ID: 55721
• Gene name: IQ motif containing C
• Gene symbol: IQCC
• Synonyms (NCBI Gene): -
• Chromosome: 1
• Chromosome location: 1p35.2

miRNA Show/Hide all (159)

miRTarBase ID	miRNA	Experiments	Reference
MIRT024282	hsa-miR-215-5p	Microarray	19074876
MIRT026654	hsa-miR-192-5p	Microarray	19074876
MIRT1069507	hsa-let-7a	CLIP-seq
MIRT1069508	hsa-let-7b	CLIP-seq
MIRT1069509	hsa-let-7c	CLIP-seq
MIRT1069510	hsa-let-7d	CLIP-seq
MIRT1069511	hsa-let-7e	CLIP-seq
MIRT1069512	hsa-let-7f	CLIP-seq
MIRT1069513	hsa-let-7g	CLIP-seq
MIRT1069514	hsa-let-7i	CLIP-seq
MIRT1069515	hsa-miR-122	CLIP-seq
MIRT1069516	hsa-miR-1255a	CLIP-seq
MIRT1069517	hsa-miR-1255b	CLIP-seq
MIRT1069518	hsa-miR-1265	CLIP-seq
MIRT1069519	hsa-miR-1321	CLIP-seq
MIRT1069520	hsa-miR-187	CLIP-seq
MIRT1069521	hsa-miR-197	CLIP-seq
MIRT1069522	hsa-miR-2392	CLIP-seq
MIRT1069523	hsa-miR-298	CLIP-seq
MIRT1069524	hsa-miR-3135b	CLIP-seq
MIRT1069525	hsa-miR-3137	CLIP-seq
MIRT1069526	hsa-miR-3155	CLIP-seq
MIRT1069527	hsa-miR-3155b	CLIP-seq
MIRT1069528	hsa-miR-3652	CLIP-seq
MIRT1069529	hsa-miR-3663-5p	CLIP-seq
MIRT1069530	hsa-miR-3938	CLIP-seq
MIRT1069531	hsa-miR-4270	CLIP-seq
MIRT1069532	hsa-miR-4430	CLIP-seq
MIRT1069533	hsa-miR-4435	CLIP-seq
MIRT1069534	hsa-miR-4441	CLIP-seq
MIRT1069535	hsa-miR-4458	CLIP-seq
MIRT1069536	hsa-miR-4468	CLIP-seq
MIRT1069537	hsa-miR-4487	CLIP-seq
MIRT1069538	hsa-miR-4500	CLIP-seq
MIRT1069539	hsa-miR-4688	CLIP-seq
MIRT1069540	hsa-miR-4716-5p	CLIP-seq
MIRT1069541	hsa-miR-4722-5p	CLIP-seq
MIRT1069542	hsa-miR-4739	CLIP-seq
MIRT1069543	hsa-miR-4756-5p	CLIP-seq
MIRT1069544	hsa-miR-4781-3p	CLIP-seq
MIRT1069545	hsa-miR-4786-3p	CLIP-seq
MIRT1069546	hsa-miR-484	CLIP-seq
MIRT1069547	hsa-miR-486-3p	CLIP-seq
MIRT1069548	hsa-miR-5096	CLIP-seq
MIRT1069549	hsa-miR-548ac	CLIP-seq
MIRT1069550	hsa-miR-548d-3p	CLIP-seq
MIRT1069551	hsa-miR-548z	CLIP-seq
MIRT1069552	hsa-miR-579	CLIP-seq
MIRT1069553	hsa-miR-720	CLIP-seq
MIRT1069554	hsa-miR-98	CLIP-seq
MIRT1069515	hsa-miR-122	CLIP-seq
MIRT1069524	hsa-miR-3135b	CLIP-seq
MIRT1069528	hsa-miR-3652	CLIP-seq
MIRT1069532	hsa-miR-4430	CLIP-seq
MIRT1922789	hsa-miR-4642	CLIP-seq
MIRT2017087	hsa-miR-3199	CLIP-seq
MIRT2017088	hsa-miR-4421	CLIP-seq
MIRT2017089	hsa-miR-4438	CLIP-seq
MIRT2017090	hsa-miR-4740-3p	CLIP-seq
MIRT2017091	hsa-miR-501-3p	CLIP-seq
MIRT2017092	hsa-miR-502-3p	CLIP-seq
MIRT2017093	hsa-miR-5095	CLIP-seq
MIRT2017094	hsa-miR-582-3p	CLIP-seq
MIRT2017095	hsa-miR-767-5p	CLIP-seq
MIRT1069507	hsa-let-7a	CLIP-seq
MIRT1069508	hsa-let-7b	CLIP-seq
MIRT1069509	hsa-let-7c	CLIP-seq
MIRT1069510	hsa-let-7d	CLIP-seq
MIRT1069511	hsa-let-7e	CLIP-seq
MIRT1069512	hsa-let-7f	CLIP-seq
MIRT1069513	hsa-let-7g	CLIP-seq
MIRT1069514	hsa-let-7i	CLIP-seq
MIRT2249068	hsa-miR-106a	CLIP-seq
MIRT2249069	hsa-miR-106b	CLIP-seq
MIRT1069515	hsa-miR-122	CLIP-seq
MIRT2249070	hsa-miR-125a-3p	CLIP-seq
MIRT1069518	hsa-miR-1265	CLIP-seq
MIRT1069519	hsa-miR-1321	CLIP-seq
MIRT2249071	hsa-miR-1343	CLIP-seq
MIRT2249072	hsa-miR-150	CLIP-seq
MIRT2249073	hsa-miR-17	CLIP-seq
MIRT2249074	hsa-miR-1976	CLIP-seq
MIRT2249075	hsa-miR-20a	CLIP-seq
MIRT2249076	hsa-miR-20b	CLIP-seq
MIRT1069522	hsa-miR-2392	CLIP-seq
MIRT2249077	hsa-miR-302a	CLIP-seq
MIRT2249078	hsa-miR-302b	CLIP-seq
MIRT2249079	hsa-miR-302c	CLIP-seq
MIRT2249080	hsa-miR-302d	CLIP-seq
MIRT2249081	hsa-miR-302e	CLIP-seq
MIRT1069524	hsa-miR-3135b	CLIP-seq
MIRT1069528	hsa-miR-3652	CLIP-seq
MIRT2249082	hsa-miR-372	CLIP-seq
MIRT2249083	hsa-miR-373	CLIP-seq
MIRT2249084	hsa-miR-3934	CLIP-seq
MIRT1069531	hsa-miR-4270	CLIP-seq
MIRT2249085	hsa-miR-4279	CLIP-seq
MIRT2017088	hsa-miR-4421	CLIP-seq
MIRT1069532	hsa-miR-4430	CLIP-seq
MIRT2017089	hsa-miR-4438	CLIP-seq
MIRT1069534	hsa-miR-4441	CLIP-seq
MIRT1069535	hsa-miR-4458	CLIP-seq
MIRT1069537	hsa-miR-4487	CLIP-seq
MIRT1069538	hsa-miR-4500	CLIP-seq
MIRT1922789	hsa-miR-4642	CLIP-seq
MIRT2249086	hsa-miR-4731-5p	CLIP-seq
MIRT1069542	hsa-miR-4739	CLIP-seq
MIRT2017090	hsa-miR-4740-3p	CLIP-seq
MIRT1069543	hsa-miR-4756-5p	CLIP-seq
MIRT2249087	hsa-miR-4757-5p	CLIP-seq
MIRT2249088	hsa-miR-498	CLIP-seq
MIRT2017093	hsa-miR-5095	CLIP-seq
MIRT2249089	hsa-miR-512-3p	CLIP-seq
MIRT2249090	hsa-miR-519d	CLIP-seq
MIRT2249091	hsa-miR-520a-3p	CLIP-seq
MIRT2249092	hsa-miR-520b	CLIP-seq
MIRT2249093	hsa-miR-520c-3p	CLIP-seq
MIRT2249094	hsa-miR-520d-3p	CLIP-seq
MIRT2249095	hsa-miR-520e	CLIP-seq
MIRT2249096	hsa-miR-520g	CLIP-seq
MIRT2249097	hsa-miR-520h	CLIP-seq
MIRT2249098	hsa-miR-552	CLIP-seq
MIRT2017094	hsa-miR-582-3p	CLIP-seq
MIRT2249099	hsa-miR-640	CLIP-seq
MIRT2249100	hsa-miR-764	CLIP-seq
MIRT2249101	hsa-miR-93	CLIP-seq
MIRT1069554	hsa-miR-98	CLIP-seq
MIRT2249071	hsa-miR-1343	CLIP-seq
MIRT2451912	hsa-miR-136	CLIP-seq
MIRT2249074	hsa-miR-1976	CLIP-seq
MIRT2249085	hsa-miR-4279	CLIP-seq
MIRT2017088	hsa-miR-4421	CLIP-seq
MIRT2249088	hsa-miR-498	CLIP-seq
MIRT2249071	hsa-miR-1343	CLIP-seq
MIRT2451912	hsa-miR-136	CLIP-seq
MIRT2249074	hsa-miR-1976	CLIP-seq
MIRT2017087	hsa-miR-3199	CLIP-seq
MIRT2249085	hsa-miR-4279	CLIP-seq
MIRT2017088	hsa-miR-4421	CLIP-seq
MIRT2017089	hsa-miR-4438	CLIP-seq
MIRT2552682	hsa-miR-4735-5p	CLIP-seq
MIRT2552683	hsa-miR-4775	CLIP-seq
MIRT2552684	hsa-miR-4794	CLIP-seq
MIRT2249088	hsa-miR-498	CLIP-seq
MIRT2017091	hsa-miR-501-3p	CLIP-seq
MIRT2017092	hsa-miR-502-3p	CLIP-seq
MIRT2017093	hsa-miR-5095	CLIP-seq
MIRT2552685	hsa-miR-590-3p	CLIP-seq
MIRT2017095	hsa-miR-767-5p	CLIP-seq
MIRT2249071	hsa-miR-1343	CLIP-seq
MIRT2451912	hsa-miR-136	CLIP-seq
MIRT2249074	hsa-miR-1976	CLIP-seq
MIRT2249085	hsa-miR-4279	CLIP-seq
MIRT2017088	hsa-miR-4421	CLIP-seq
MIRT2552682	hsa-miR-4735-5p	CLIP-seq
MIRT2552683	hsa-miR-4775	CLIP-seq
MIRT2552684	hsa-miR-4794	CLIP-seq
MIRT2249088	hsa-miR-498	CLIP-seq
MIRT2552685	hsa-miR-590-3p	CLIP-seq

Gene ontology (GO)

GO ID	Ontology	Definition	Evidence	Reference
GO:0005515	Function	Protein binding	IPI	32296183, 33961781

Other IDs

• MIM: HGNC
• HGNC: N/A
• e!Ensembl: HGNC

Protein

• UniProt ID: Q4KMZ1
• Protein name: IQ domain-containing protein C
• Sequence:

  MEPELLVRKVSALQACVRGFLVRRQFQSLRAEYEAIVREVEGDLGTLQWTEGRIPRPRFL
  PEKAKSHQTWKAGDRVANPEQGLWNHFPCEESEGEATWEEMVLKKSGESSANQGSLCRDH
  SSWLQMKQNRKPSQEKTRDTTRMENPEATDQRLPHSQPQLQELQYHRSHLAMELLWLQQA
  INSRKEYLLLKQTLRSPEAGPIREEPRVFLEHGEQACERDQSQPSAPLEDQSYRDRTTGE
  LEQEDDSCHRVKSPHRSPGSLATTQKNIAGAKCREPCYSKSGPPSSIPSNSQALGDRLTK
  GPDDGRQTFGGTCLLQMKILEDQTPRGLKPRNHCPRKSRTQLSALYEDSNIKEMSPRKLD
  HKEPDCRTVRTQELGLSEDHIIWDGTLGGPEHSVLDLWRTKPPKGQAPTDRSSRDGTSNE
  PSHEGQKKQRTIPWRSKSPEILSSTKAGCTGEEQWRGRPWKTEPPG

• Sequence length: 466

Associated diseases

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
Phenotype Name	Clinical Significance	Source	Reference	Evidence Score
POLYCYSTIC OVARY SYNDROME	—	CTD, Disgenet CTD, Disgenet	21411543	★★☆☆☆ Found in Text Mining + Unknown/Other Associations

Associations from Text Mining
Disease Name	Disease (Merged)	Source	PMID	Relationship Type	Evidence Score
Breast Carcinoma	Breast Carcinoma	BEFREE	30281209		★☆☆☆☆ Found in Text Mining only
Malignant neoplasm of breast	Breast Cancer	BEFREE	30281209		★☆☆☆☆ Found in Text Mining only
Polycystic Ovary Syndrome	Polycystic Ovary Syndrome	CTD_human_DG	21411543		★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Sclerocystic Ovaries	Sclerocystic Ovaries	CTD_human_DG	21411543		★☆☆☆☆ Found in Text Mining only

Related Genes

Sort by: Blended Diseases Pathways Evidence source

ARHGAP30 1 shared diseasePolycystic ovary syndrome 2 shared evidence sourcesCTD (Polycystic ovary syndrome), Disgenet (Polycystic ovary syndrome) Related via 1 shared disease including Polycystic ovary syndrome — evidence mostly CTD. CARMIL3 1 shared diseasePolycystic ovary syndrome 2 shared evidence sourcesCTD (Polycystic ovary syndrome), Disgenet (Polycystic ovary syndrome) Related via 1 shared disease including Polycystic ovary syndrome — evidence mostly CTD. DACT3 1 shared diseasePolycystic ovary syndrome 2 shared evidence sourcesCTD (Polycystic ovary syndrome), Disgenet (Polycystic ovary syndrome) Related via 1 shared disease including Polycystic ovary syndrome — evidence mostly CTD. DCBLD2 1 shared diseasePolycystic ovary syndrome 2 shared evidence sourcesCTD (Polycystic ovary syndrome), Disgenet (Polycystic ovary syndrome) Related via 1 shared disease including Polycystic ovary syndrome — evidence mostly CTD. ELAVL3 1 shared diseasePolycystic ovary syndrome 2 shared evidence sourcesCTD (Polycystic ovary syndrome), Disgenet (Polycystic ovary syndrome) Related via 1 shared disease including Polycystic ovary syndrome — evidence mostly CTD.

Related Gene	Shared Diseases	Shared Disease Names	Shared Pathways	Shared Pathway Names	Shared Evidence Sources	Shared Evidence Names
ARHGAP30	1	["Polycystic ovary syndrome"]	0	[]	2	["CTD (Polycystic ovary syndrome)","Disgenet (Polycystic ovary syndrome)"]
CARMIL3	1	["Polycystic ovary syndrome"]	0	[]	2	["CTD (Polycystic ovary syndrome)","Disgenet (Polycystic ovary syndrome)"]
DACT3	1	["Polycystic ovary syndrome"]	0	[]	2	["CTD (Polycystic ovary syndrome)","Disgenet (Polycystic ovary syndrome)"]
DCBLD2	1	["Polycystic ovary syndrome"]	0	[]	2	["CTD (Polycystic ovary syndrome)","Disgenet (Polycystic ovary syndrome)"]
ELAVL3	1	["Polycystic ovary syndrome"]	0	[]	2	["CTD (Polycystic ovary syndrome)","Disgenet (Polycystic ovary syndrome)"]

Diseases Linked via Similar Genes

Intellectual developmental disorder Linked via 1 of 5 related genesDACT3 Stomach neoplasms Linked via 1 of 5 related genesDCBLD2 Alzheimer disease Linked via 1 of 5 related genesELAVL3 Oligodendroglioma Linked via 1 of 5 related genesELAVL3

Disease	Linked Via (Gene Count)	Linked Via (Gene Names)
Intellectual developmental disorder	1	["DACT3"]
Stomach neoplasms	1	["DCBLD2"]
Alzheimer disease	1	["ELAVL3"]
Oligodendroglioma	1	["ELAVL3"]