ADAMTSL3 (ADAMTS like 3)

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

Gene

• Entrez ID: 57188
• Gene name: ADAMTS like 3
• Gene symbol: ADAMTSL3
• Synonyms (NCBI Gene): ADAMTSL-3
• Chromosome: 15
• Chromosome location: 15q25.2

miRNA Show/Hide all (28)

miRTarBase ID	miRNA	Experiments	Reference
MIRT766860	hsa-miR-101	CLIP-seq
MIRT766861	hsa-miR-1272	CLIP-seq
MIRT766862	hsa-miR-144	CLIP-seq
MIRT766863	hsa-miR-199a-3p	CLIP-seq
MIRT766864	hsa-miR-199b-3p	CLIP-seq
MIRT766865	hsa-miR-3129-5p	CLIP-seq
MIRT766866	hsa-miR-3130-5p	CLIP-seq
MIRT766867	hsa-miR-4272	CLIP-seq
MIRT766868	hsa-miR-4473	CLIP-seq
MIRT766869	hsa-miR-4482	CLIP-seq
MIRT766870	hsa-miR-512-3p	CLIP-seq
MIRT766871	hsa-miR-516a-5p	CLIP-seq
MIRT766872	hsa-miR-520f	CLIP-seq
MIRT1925914	hsa-miR-214	CLIP-seq
MIRT1925915	hsa-miR-3153	CLIP-seq
MIRT1925916	hsa-miR-3177-5p	CLIP-seq
MIRT1925917	hsa-miR-3619-5p	CLIP-seq
MIRT1925918	hsa-miR-3665	CLIP-seq
MIRT1925919	hsa-miR-3667-5p	CLIP-seq
MIRT1925920	hsa-miR-3934	CLIP-seq
MIRT1925921	hsa-miR-4329	CLIP-seq
MIRT1925922	hsa-miR-4438	CLIP-seq
MIRT1925923	hsa-miR-4514	CLIP-seq
MIRT1925924	hsa-miR-4692	CLIP-seq
MIRT1925925	hsa-miR-4786-5p	CLIP-seq
MIRT1925926	hsa-miR-5095	CLIP-seq
MIRT1925927	hsa-miR-761	CLIP-seq
MIRT1925928	hsa-miR-769-5p	CLIP-seq

Gene ontology (GO)

GO ID	Ontology	Definition	Evidence	Reference
GO:0005515	Function	Protein binding	IPI	25416956, 32296183
GO:0005576	Component	Extracellular region	IEA
GO:0030198	Process	Extracellular matrix organization	IEA
GO:0031012	Component	Extracellular matrix	IBA

Other IDs

• MIM: 609199
• HGNC: 14633
• e!Ensembl: ENSG00000156218

Protein

• UniProt ID: P82987
• Protein name: ADAMTS-like protein 3 (ADAMTSL-3) (Punctin-2)
• Family and domains:

  Pfam

  Accession	ID	Position in sequence	Description	Type
  PF07679	I-set	1307 → 1384	Immunoglobulin I-set domain	Domain
  PF08686	PLAC	1659 → 1689	PLAC (protease and lacunin) domain	Domain
  PF19030	TSP1_ADAMTS	707 → 759		Domain
  PF19030	TSP1_ADAMTS	422 → 479		Domain
  PF19030	TSP1_ADAMTS	763 → 819		Domain
  PF19030	TSP1_ADAMTS	568 → 625		Domain
  PF19030	TSP1_ADAMTS	1487 → 1544		Domain
  PF19030	TSP1_ADAMTS	1601 → 1655		Domain
  PF19030	TSP1_ADAMTS	482 → 534		Domain
  PF19030	TSP1_ADAMTS	1428 → 1483		Domain
  PF19030	TSP1_ADAMTS	648 → 703		Domain
  PF19030	TSP1_ADAMTS	824 → 880		Domain
  PF19030	TSP1_ADAMTS	343 → 401		Domain
  PF00090	TSP_1	79 → 123	Thrombospondin type 1 domain	Domain

• Tissue specificity: TISSUE SPECIFICITY: Expressed in epithelial cells of the colon, fallopian tube, skin, breast, prostate, epididymis, liver, pancreatic islets and bile ducts, as well as by vascular endothelial cells, smooth muscle cells, fibroblasts, cortical and ganglioni
• Sequence:

  MASWTSPWWVLIGMVFMHSPLPQTTAEKSPGAYFLPEFALSPQGSFLEDTTGEQFLTYRY
  DDQTSRNTRSDEDKDGNWDAWGDWSDCSRTCGGGASYSLRRCLTGRNCEGQNIRYKTCSN
  HDCPPDAEDFRAQQCSAYNDVQYQGHYYEWLPRYNDPAAPCALKCHAQGQNLVVELAPKV
  LDGTRCNTDSLDMCISGICQAVGCDRQLGSNAKEDNCGVCAGDGSTCRLVRGQSKSHVSP
  EKREENVIAVPLGSRSVRITVKGPAHLFIESKTLQGSKGEHSFNSPGVFLVENTTVEFQR
  GSERQTFKIPGPLMADFIFKTRYTAAKDSVVQFFFYQPISHQWRQTDFFPCTVTCGGGYQ
  LNSAECVDIRLKRVVPDHYCHYYPENVKPKPKLKECSMDPCPSSDGFKEIMPYDHFQPLP
  RWEHNPWTACSVSCGGGIQRRSFVCVEESMHGEILQVEEWKCMYAPKPKVMQTCNLFDCP
  KWIAMEWSQCTVTCGRGLRYRVVLCINHRGEHVGGCNPQLKLHIKEECVIPIPCYKPKEK
  SPVEAKLPWLKQAQELEETRIATEEPTFIPEPWSACSTTCGPGVQVREVKCRVLLTFTQT
  ETELPEEECEGPKLPTERPCLLEACDESPASRELDIPLPEDSETTYDWEYAGFTPCTATC
  VGGHQEAIAVCLHIQTQQTVNDSLCDMVHRPPAMSQACNTEPCPPRWHVGSWGPCSATCG
  VGIQTRDVYCLHPGETPAPPEECRDEKPHALQACNQFDCPPGWHIEEWQQCSRTCGGGTQ
  NRRVTCRQLLTDGSFLNLSDELCQGPKASSHKSCARTDCPPHLAVGDWSKCSVSCGVGIQ
  RRKQVCQRLAAKGRRIPLSEMMCRDLPGLPLVRSCQMPECSKIKSEMKTKLGEQGPQILS
  VQRVYIQTREEKRINLTIGSRAYLLPNTSVIIKCPVRRFQKSLIQWEKDGRCLQNSKRLG
  ITKSGSLKIHGLAAPDIGVYRCIAGSAQETVVLKLIGTDNRLIARPALREPMREYPGMDH
  SEANSLGVTWHKMRQMWNNKNDLYLDDDHISNQPFLRALLGHCSNSAGSTNSWELKNKQF
  EAAVKQGAYSMDTAQFDELIRNMSQLMETGEVSDDLASQLIYQLVAELAKAQPTHMQWRG
  IQEETPPAAQLRGETGSVSQSSHAKNSGKLTFKPKGPVLMRQSQPPSISFNKTINSRIGN
  TVYITKRTEVINILCDLITPSEATYTWTKDGTLLQPSVKIILDGTGKIQIQNPTRKEQGI
  YECSVANHLGSDVESSSVLYAEAPVILSVERNITKPEHNHLSVVVGGIVEAALGANVTIR
  CPVKGVPQPNITWLKRGGSLSGNVSLLFNGSLLLQNVSLENEGTYVCIATNALGKAVATS
  VLHLLERRWPESRIVFLQGHKKYILQATNTRTNSNDPTGEPPPQEPFWEPGNWSHCSATC
  GHLGARIQRPQCVMANGQEVSEALCDHLQKPLAGFEPCNIRDCPARWFTSVWSQCSVSCG
  EGYHSRQVTCKRTKANGTVQVVSPRACAPKDRPLGRKPCFGHPCVQWEPGNRCPGRCMGR
  AVRMQQRHTACQHNSSDSNCDDRKRPTLRRNCTSGACDVCWHTGPWKPCTAACGRGFQSR
  KVDCIHTRSCKPVAKRHCVQKKKPISWRHCLGPSCDRDCTDTTHYCMFVKHLNLCSLDRY
  KQRCCQSCQEG

• Sequence length: 1691

Pathways

Reactome Pathway

Defective B3GALTL causes Peters-plus syndrome (PpS)

O-glycosylation of TSR domain-containing proteins

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 Show/Hide Unknown Diseases (23)
Phenotype Name	Clinical Significance	Source	Reference	Evidence Score
ASTHMA	—	GWAS catalog	32296059, 34103634, 36344522	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Cervical cancer	Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Cholangiocarcinoma	Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
CHRONIC OBSTRUCTIVE PULMONARY DISEASE	—	GWAS catalog	30804561, 33909500, 37069358	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Colon adenocarcinoma	Uncertain significance; Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
DEVELOPMENTAL DYSPLASIA OF THE HIP	—	GWAS catalog	36902448	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
DRY EYE SYNDROME	—	GWAS catalog	38767906	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Familial cancer of breast	Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Gastric cancer	Uncertain significance	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
INFLAMMATORY BOWEL DISEASE	—	GWAS catalog	38102678	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Lung adenocarcinoma	Uncertain significance	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Lung cancer	Benign; Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Malignant lymphoma, large B-cell, diffuse	Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
OSTEOARTHRITIS, HIP	—	GWAS catalog	40205036	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
OSTEOARTHRITIS, KNEE	—	GWAS catalog	40205036	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
PEPTIC ULCER DISEASE	—	GWAS catalog	38102678	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
RESPIRATORY SYSTEM DISEASE	—	GWAS catalog	30595370, 38965376	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Sarcoma	Benign; Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA	—	Disgenet, GWAS catalog Disgenet, GWAS catalog	25056061, 26198764, 28991256, 30285260	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
SCOLIOSIS	—	GWAS catalog	30019117	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Squamous cell carcinoma	Uncertain significance	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Thyroid cancer, nonmedullary, 1	Likely benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS	—	GWAS catalog	32541925	★★☆☆☆ Found in Text Mining + Unknown/Other Associations

Associations from Text Mining Show/Hide Text Mining Associations (24)
Disease Name	Disease (Merged)	Source	PMID	Relationship Type	Evidence Score
Chronic Obstructive Airway Disease	Chronic Obstructive Pulmonary Disease	GWASCAT_DG	30804561		★☆☆☆☆ Found in Text Mining only
Colon Carcinoma	Colon Carcinoma	BEFREE	17597111		★☆☆☆☆ Found in Text Mining only
Colorectal Carcinoma	Colorectal Cancer	BEFREE	17597111		★☆☆☆☆ Found in Text Mining only
Colorectal Carcinoma	Colorectal Cancer	UNIPROT_DG			★☆☆☆☆ Found in Text Mining only
Colorectal Neoplasms	Colorectal Neoplasms	BEFREE	17597111		★☆☆☆☆ Found in Text Mining only
Colorectal Neoplasms	Colorectal Neoplasms	LHGDN	17597111		★☆☆☆☆ Found in Text Mining only
Colorectal Neoplasms	Colorectal neoplasm	Pubtator	28865443	Associate	★☆☆☆☆ Found in Text Mining only
Diabetes	Diabetes	BEFREE	29162515		★☆☆☆☆ Found in Text Mining only
Diabetes Mellitus	Diabetes Mellitus	BEFREE	29162515		★☆☆☆☆ Found in Text Mining only
Diabetes Mellitus Type 2	Diabetes mellitus, type 2	Pubtator	34390125	Associate	★☆☆☆☆ Found in Text Mining only
Glaucoma, Primary Open Angle	Glaucoma	BEFREE	18474779		★☆☆☆☆ Found in Text Mining only
Heart Diseases	Heart Diseases	BEFREE	24793337		★☆☆☆☆ Found in Text Mining only
Malignant Neoplasms	Malignant Neoplasm	BEFREE	17597111		★☆☆☆☆ Found in Text Mining only
Malignant tumor of colon	Colonic Neoplasms	BEFREE	17597111		★☆☆☆☆ Found in Text Mining only
Meningioma	Meningioma	BEFREE	28193203		★☆☆☆☆ Found in Text Mining only
Narcolepsy	Narcolepsy	GWASDB_DG	19629137		★☆☆☆☆ Found in Text Mining only
Neoplasms	Neoplasms	BEFREE	17597111		★☆☆☆☆ Found in Text Mining only
Periodontitis	Periodontitis	Pubtator	36927684	Associate	★☆☆☆☆ Found in Text Mining only
Respiratory Tract Diseases	Respiratory Tract Diseases	GWASCAT_DG	30595370		★☆☆☆☆ Found in Text Mining only
Schizophrenia	Schizophrenia	GWASDB_DG	19197363		★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Schizophrenia	Schizophrenia	PSYGENET_DG	21239144		★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Schizophrenia	Schizophrenia	BEFREE	21239144		★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Schizophrenia	Schizophrenia	GWASCAT_DG	25056061, 26198764, 28991256, 30285260		★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Skin Neoplasms	Skin Neoplasms	BEFREE	17597111		★☆☆☆☆ Found in Text Mining only

Related Genes

Sort by: Blended Diseases Pathways Evidence source

FCER1G 2 shared diseasesPeptic ulcer disease, Respiratory system disease 2 shared evidence sourcesGWAS catalog (Peptic ulcer disease), GWAS catalog (Respiratory system disease) Related via 2 shared diseases including Peptic ulcer disease, Respiratory system disease — evidence mostly GWAS catalog. THSD7A 1 shared diseaseDry eye syndrome 2 shared pathwaysDefective B3GALTL causes Peters-plus syndrome (PpS), O-glycosylation of TSR domain-containing proteins 1 shared evidence sourceGWAS catalog (Dry eye syndrome) Related via 2 shared pathways including Defective B3GALTL causes Peters-plus syndrome (PpS), O-glycosylation of TSR domain-containing proteins — evidence mostly GWAS catalog. TSPAN14 2 shared diseasesPeptic ulcer disease, Respiratory system disease 2 shared evidence sourcesGWAS catalog (Peptic ulcer disease), GWAS catalog (Respiratory system disease) Related via 2 shared diseases including Peptic ulcer disease, Respiratory system disease — evidence mostly GWAS catalog. SPON2 2 shared pathwaysDefective B3GALTL causes Peters-plus syndrome (PpS), O-glycosylation of TSR domain-containing proteins Related via 2 shared pathways including Defective B3GALTL causes Peters-plus syndrome (PpS), O-glycosylation of TSR domain-containing proteins. SPON1 2 shared pathwaysDefective B3GALTL causes Peters-plus syndrome (PpS), O-glycosylation of TSR domain-containing proteins Related via 2 shared pathways including Defective B3GALTL causes Peters-plus syndrome (PpS), O-glycosylation of TSR domain-containing proteins.

Related Gene	Shared Diseases	Shared Disease Names	Shared Pathways	Shared Pathway Names	Shared Evidence Sources	Shared Evidence Names
FCER1G	2	["Peptic ulcer disease","Respiratory system disease"]	0	[]	2	["GWAS catalog (Peptic ulcer disease)","GWAS catalog (Respiratory system disease)"]
THSD7A	1	["Dry eye syndrome"]	2	["Defective B3GALTL causes Peters-plus syndrome (PpS)","O-glycosylation of TSR domain-containing proteins"]	1	["GWAS catalog (Dry eye syndrome)"]
TSPAN14	2	["Peptic ulcer disease","Respiratory system disease"]	0	[]	2	["GWAS catalog (Peptic ulcer disease)","GWAS catalog (Respiratory system disease)"]
SPON2	0	[]	2	["Defective B3GALTL causes Peters-plus syndrome (PpS)","O-glycosylation of TSR domain-containing proteins"]	0	[]
SPON1	0	[]	2	["Defective B3GALTL causes Peters-plus syndrome (PpS)","O-glycosylation of TSR domain-containing proteins"]	0	[]

Diseases Linked via Similar Genes

Alzheimer disease Linked via 4 of 5 related genesFCER1G, THSD7A, TSPAN14, SPON1 Coronary artery disease Linked via 2 of 5 related genesTHSD7A, TSPAN14 Crohn disease Linked via 2 of 5 related genesTHSD7A, TSPAN14 Ulcerative colitis Linked via 2 of 5 related genesTHSD7A, TSPAN14 Atrial fibrillation Linked via 2 of 5 related genesTSPAN14, SPON1

Disease	Linked Via (Gene Count)	Linked Via (Gene Names)
Alzheimer disease	4	["FCER1G","THSD7A","TSPAN14","SPON1"]
Coronary artery disease	2	["THSD7A","TSPAN14"]
Crohn disease	2	["THSD7A","TSPAN14"]
Ulcerative colitis	2	["THSD7A","TSPAN14"]
Atrial fibrillation	2	["TSPAN14","SPON1"]