FOCAD (focadhesin)

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

Gene

• Entrez ID: 54914
• Gene name: Focadhesin
• Gene symbol: FOCAD
• Synonyms (NCBI Gene): KIAA1797, SCOLIV
• Chromosome: 9
• Chromosome location: 9p21.3

miRNA Show/Hide all (25)

miRTarBase ID	miRNA	Experiments	Reference
MIRT045267	hsa-miR-186-5p	CLASH	23622248
MIRT515824	hsa-miR-5692a	PAR-CLIP	23446348
MIRT515823	hsa-miR-1277-5p	PAR-CLIP	23446348
MIRT515822	hsa-miR-5692b	PAR-CLIP	23446348
MIRT515821	hsa-miR-5692c	PAR-CLIP	23446348
MIRT515820	hsa-miR-5011-5p	PAR-CLIP	23446348
MIRT515819	hsa-miR-3074-3p	PAR-CLIP	23446348
MIRT515818	hsa-miR-154-3p	PAR-CLIP	23446348
MIRT515817	hsa-miR-487a-3p	PAR-CLIP	23446348
MIRT515816	hsa-miR-190a-3p	PAR-CLIP	23446348
MIRT515815	hsa-miR-485-3p	PAR-CLIP	23446348
MIRT515814	hsa-miR-539-3p	PAR-CLIP	23446348
MIRT515813	hsa-miR-6083	PAR-CLIP	23446348
MIRT515824	hsa-miR-5692a	PAR-CLIP	23446348
MIRT515823	hsa-miR-1277-5p	PAR-CLIP	23446348
MIRT515822	hsa-miR-5692b	PAR-CLIP	23446348
MIRT515821	hsa-miR-5692c	PAR-CLIP	23446348
MIRT515820	hsa-miR-5011-5p	PAR-CLIP	23446348
MIRT515819	hsa-miR-3074-3p	PAR-CLIP	23446348
MIRT515818	hsa-miR-154-3p	PAR-CLIP	23446348
MIRT515817	hsa-miR-487a-3p	PAR-CLIP	23446348
MIRT515816	hsa-miR-190a-3p	PAR-CLIP	23446348
MIRT515815	hsa-miR-485-3p	PAR-CLIP	23446348
MIRT515814	hsa-miR-539-3p	PAR-CLIP	23446348
MIRT515813	hsa-miR-6083	PAR-CLIP	23446348

Gene ontology (GO) Show/Hide all (8)

GO ID	Ontology	Definition	Evidence	Reference
GO:0005515	Function	Protein binding	IPI	22427331
GO:0005737	Component	Cytoplasm	IEA
GO:0005829	Component	Cytosol	IDA
GO:0005829	Component	Cytosol	IEA
GO:0005925	Component	Focal adhesion	IDA	22427331
GO:0005925	Component	Focal adhesion	IEA
GO:0060147	Process	Regulation of post-transcriptional gene silencing	IEA
GO:0070161	Component	Anchoring junction	IEA

Other IDs

• MIM: 614606
• HGNC: 23377
• e!Ensembl: ENSG00000188352

Protein

• UniProt ID: Q5VW36
• Protein name: Focadhesin
• Protein function: Required for the maintenance of SKIC2 and SKIC3 proteostatic levels in the liver. May be involved in the regulation of RNA degradation by the exosome complex (PubMed:35864190). Potential tumor suppressor in gliomas. {ECO:0000250, ECO:0000269|Pub
• Family and domains:

  Pfam

  Accession	ID	Position in sequence	Description	Type
  PF11229	Focadhesin	1213 → 1801	Focadhesin	Family
  PF12530	DUF3730	490 → 714	Protein of unknown function (DUF3730)	Family

• Tissue specificity: TISSUE SPECIFICITY: Ubiquitous. High expression in brain followed by testis, muscle, pancreas, heart, ovary, small intestine, placenta, prostate, thymus, kidney, colon, liver, lung, spleen and leukocytes. Expression is reduced in most glioblastomas and al
• Sequence:

  MSDDIRKRFEFPNSLIQSQAVGHLIAAVLKENGFSEKIHQSTNQTPALNLLWEKCCSDNV
  VVRTACCEGLVALVAQDHAEFSYVLNGILNLIPSTRNTHGLIKAIMHLLQMQALKEGQGG
  EKNIQSIYTIRNHPHPLITVLEHRPDCWPVFLQQLTAFFQQCPERLEVSCIQIMAPFLWY
  LYCEPSQLQEYAKLRLALLKVLLQPQVLCDKDQPSILEQQILQLCCDIVPCLQVKDLIQT
  TEAMMFIEEVCLSLLRHPVFWKIQLTQMSLQLLCVSEVSLKITGECSSSIHLLEHSVELL
  KEDFPVELVIIGIALLLLQTPASQQKPILNLALKLLSVTEDQKIPKSSLLLVMPILQILS
  STALEDCISVDEEGPSRQQLALNLLEMIQQECYRDDHQKLSYKLVCPVTSMYGTIFTAWR
  ILEVMTDSSAASDWLASVESLLPITAVIPAPAFLLLAHLLVEDKGQNLHQILKVTTELAQ
  ADSSQVPNLIPVLMFKLGRPLEPILYNDILYTLPKLGVHKVCIGQILRIIQLLGTTPRLR
  AVTLRLLTSLWEKQDRVYPELQRFMAVSDVPSLSVGKEVQWEKLIAKAASIRDICKQRPY
  QHGADMLAAISQVLNECTKPDQATPAALVLQGLHALCQAEVVCIRSTWNALSPKLSCDTR
  PLILKTLSELFSLVPSLTVNTTEYENFKVQVLSFLWTHTQNKDPIVANAAYRSLANFTAG
  EHTILHLPEKIRPEIPIPEELDDDEDVEDVDLSVPGSCYLKLLSLTPPLVLPALEEFFTS
  LVKQEMVNMPRGIYHSALKGGARSDQGKTVAGIPNFILKMYETNKQPGLKPGLAGGMLFC
  YDVSMYQSKDGKPLNRLMASRGRSFKQTSLALVHEVHIQLSEWHRAIFLPQAWLAYMNRA
  YHAILQGRLGELELQLKHGKEEPEEVQYKKSTAWLWVRDMLTDEITKAAAKESPVVKGNA
  LLALSSLAVVVSRHEASLSSDSDGLLEVQPNFLSMKEWVSMVLDTLLVIVDSHYQPRGQL
  LSWFYYKSYSGENTASAIARSAAATALSLLVPVFIISCKEKVEEILNMLTARLPGKPSAD
  ESQAVQIHMGLALGMFLSRLCEEKLSDISGQEMNLLLMKSLDALENCCFDTSLEYNTGCI
  LGVGLVLSLMSHSSQMQSRVHVAALLRKLSAHVDDSGSQSRTFQEVLAYTLSCVCTSAFS
  AGIIEATEAEDVMNKLRLLVENSQQTSGFALALGNIVHGLSVCGHGKAEDLGSKLLPAWI
  RIVLTEGTPTMLCLAALHGMVALVGSEGDVMQLKSEAIQTSHFQGRLNEVIRTLTQVISV
  SGVIGLQSNAVWLLGHLHLSTLSSSQSRASVPTDYSYLPESSFIGAAIGFFITGGKKGPE
  SVPPSLLKVVMKPIATVGESYQYPPVNWAALLSPLMRLNFGEEIQQLCLEIMVTQAQSSQ
  NAAALLGLWVTPPLIHSLSLNTKRYLLISAPLWIKHISDEQILGFVENLMVAVFKAASPL
  GSPELCPSALHGLSQAMKLPSPAHHLWSLLSEATGKIFDLLPNKIRRKDLELYISIAKCL
  LEMTDDDANRIAQVTKSNIEKAAFVKLYLVSQGRFPLVNLTDMLSVAVQHREKEVLAWMI
  LHSLYQARIVSHANTGVLKRMEWLLELMGYIRNVAYQSTSFHNTALDKALDFFLLIFATA
  VVAWADHTAPLLLGLSASWLPWHQENGPAGPVPSFLGRSPMHRVTLQEVLTLLPNSMALL
  LQKEPWKEQTQKFIDWLFSIMESPKEALSAQSRDLLKATLLSLRVLPEFKKKAVWTRAYG
  W

• Sequence length: 1801

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)

Causal
Phenotype Name	Clinical Significance	dbSNP ID	RCV Accession	Evidence Score
Liver disease, severe congenital	Pathogenic; Likely pathogenic	rs1161907698, rs1481004397, rs1833052702, rs200873740, rs2132603627, rs1834683448	RCV002275888 RCV002275456 RCV002275457 RCV002275458 RCV002275889 RCV003990836	★★★★★ ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)

Unknown / Other Associations Show/Hide Unknown Diseases (28)
Phenotype Name	Clinical Significance	Source	Reference	Evidence Score
Acute myeloid leukemia	Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Adrenocortical carcinoma, hereditary	Uncertain significance	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
CENTRAL NERVOUS SYSTEM CANCER	—	GWAS catalog	36810956	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Cervical cancer	Uncertain significance; Benign; Conflicting classifications of pathogenicity; Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Cholangiocarcinoma	Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Clear cell carcinoma of kidney	Uncertain significance; Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Familial cancer of breast	Benign; Uncertain significance; Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
FOCAD-related disorder	Benign; Uncertain significance; Conflicting classifications of pathogenicity; Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Gastric cancer	Benign; Uncertain significance; Conflicting classifications of pathogenicity; Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
GLIOBLASTOMA MULTIFORME	—	GWAS catalog	36810956	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
GLIOMA	—	GWAS catalog	36810956	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Hepatocellular carcinoma	Benign; Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
LIVER CIRRHOSIS	—	CTD, Disgenet CTD, Disgenet	35864190	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Lung cancer	Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Malignant tumor of esophagus	Uncertain significance; Benign; Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Malignant tumor of urinary bladder	Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Melanoma	Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
METABOLIC SYNDROME	—	GWAS catalog	39349817	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Nonpapillary renal cell carcinoma	Uncertain significance	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Ovarian cancer	Uncertain significance	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Ovarian serous cystadenocarcinoma	Uncertain significance; Benign; Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Sarcoma	Likely benign; Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA	—	GWAS catalog	35396580	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Thymoma	Uncertain significance	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS	—	GWAS catalog	30297969, 32541925, 38374256, 39349817	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Uterine carcinosarcoma	Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Uterine corpus endometrial carcinoma	Benign; Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Uveal melanoma	Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations

Associations from Text Mining Show/Hide Text Mining Associations (14)
Disease Name	Disease (Merged)	Source	PMID	Relationship Type	Evidence Score
Astrocytoma	Astrocytoma	BEFREE	31473790		★☆☆☆☆ Found in Text Mining only
Astrocytoma	Astrocytoma	Pubtator	31473790	Inhibit	★☆☆☆☆ Found in Text Mining only
Breast Neoplasms	Breast neoplasm	Pubtator	22362584	Associate	★☆☆☆☆ Found in Text Mining only
Colonic Neoplasms	Colonic neoplasm	Pubtator	25712196	Associate	★☆☆☆☆ Found in Text Mining only
Colorectal Carcinoma	Colorectal Cancer	BEFREE	25712196		★☆☆☆☆ Found in Text Mining only
Colorectal Neoplasms	Colorectal neoplasm	Pubtator	25712196, 36184622	Associate	★☆☆☆☆ Found in Text Mining only
Glioblastoma	Glioblastoma	BEFREE	22427331		★☆☆☆☆ Found in Text Mining only
Glioblastoma Multiforme	Glioblastoma	BEFREE	22427331		★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Glioma	Glioma	BEFREE	22427331		★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Glioma	Glioma	Pubtator	31473790	Inhibit	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Hypertension	Hypertension	Pubtator	22479346	Associate	★☆☆☆☆ Found in Text Mining only
Intestinal Polyposis	Intestinal polyposis	Pubtator	25712196	Associate	★☆☆☆☆ Found in Text Mining only
Neoplasms	Neoplasms	BEFREE	22427331, 25712196, 31473790		★☆☆☆☆ Found in Text Mining only
Triple Negative Breast Neoplasms	Triple negative breast cancer	Pubtator	34685504	Associate	★☆☆☆☆ Found in Text Mining only

Related Genes

Sort by: Blended Diseases Pathways Evidence source

ST8SIA1 2 shared diseasesLiver cirrhosis, Liver disease 1 shared evidence sourceDisgenet (Liver disease) Related via 2 shared diseases including Liver cirrhosis, Liver disease — evidence mostly Disgenet. KHDRBS3 2 shared diseasesLiver cirrhosis, Liver disease Related via 2 shared diseases including Liver cirrhosis, Liver disease. MTARC1 2 shared diseasesLiver cirrhosis, Liver disease Related via 2 shared diseases including Liver cirrhosis, Liver disease. TM6SF2 2 shared diseasesLiver cirrhosis, Liver disease 2 shared evidence sourcesCTD (Liver cirrhosis), Disgenet (Liver cirrhosis) Related via 2 shared diseases including Liver cirrhosis, Liver disease — evidence mostly CTD. HKDC1 2 shared diseasesLiver cirrhosis, Liver disease Related via 2 shared diseases including Liver cirrhosis, Liver disease.

Related Gene	Shared Diseases	Shared Disease Names	Shared Pathways	Shared Pathway Names	Shared Evidence Sources	Shared Evidence Names
ST8SIA1	2	["Liver cirrhosis","Liver disease"]	0	[]	1	["Disgenet (Liver disease)"]
KHDRBS3	2	["Liver cirrhosis","Liver disease"]	0	[]	0	[]
MTARC1	2	["Liver cirrhosis","Liver disease"]	0	[]	0	[]
TM6SF2	2	["Liver cirrhosis","Liver disease"]	0	[]	2	["CTD (Liver cirrhosis)","Disgenet (Liver cirrhosis)"]
HKDC1	2	["Liver cirrhosis","Liver disease"]	0	[]	0	[]

Diseases Linked via Similar Genes

Nonalcoholic fatty liver disease Linked via 4 of 5 related genesST8SIA1, KHDRBS3, MTARC1, TM6SF2 Major depressive disorder Linked via 2 of 5 related genesST8SIA1, KHDRBS3 Myocardial infarction Linked via 2 of 5 related genesKHDRBS3, TM6SF2 Attention deficit hyperactivity disorder Linked via 1 of 5 related genesST8SIA1 Dementia Linked via 1 of 5 related genesST8SIA1

Disease	Linked Via (Gene Count)	Linked Via (Gene Names)
Nonalcoholic fatty liver disease	4	["ST8SIA1","KHDRBS3","MTARC1","TM6SF2"]
Major depressive disorder	2	["ST8SIA1","KHDRBS3"]
Myocardial infarction	2	["KHDRBS3","TM6SF2"]
Attention deficit hyperactivity disorder	1	["ST8SIA1"]
Dementia	1	["ST8SIA1"]