ADAMTSL3 - ADAMTS like 3 Gene

Also Known as ADAMTSL-3

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 57188

About ADAMTSL3

Cytogenetic location: 15q25.2 Genomic coordinates (GRCh38): 15:83,654,123-84,039,842 (from NCBI)

This gene has 8 transcripts (splice variants), 193 orthologues and 25 paralogues. Broad expression in lung (RPKM 4.5), placenta (RPKM 4.0) and 24 other tissues.

Summary

Predicted to be involved in extracellular matrix organization. Located in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Apr 2022]

ADAMTSL3 Products (2)

mRNA Protein Name
NM_001301110.2 NP_001288039.1 ADAMTS-like protein 3 isoform b precursor
NM_207517.3 NP_997400.2 ADAMTS-like protein 3 isoform a precursor
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ADAMTSL3 Protein Structure

TSP_1

TSP_1: Thrombospondin type 1 domain (80 - 123)

TSP_1

TSP_1: Thrombospondin type 1 domain (425 - 452)

TSP_1

TSP_1: Thrombospondin type 1 domain (486 - 508)

TSP_1

TSP_1: Thrombospondin type 1 domain (571 - 608)

TSP_1

TSP_1: Thrombospondin type 1 domain (710 - 759)

TSP_1

TSP_1: Thrombospondin type 1 domain (766 - 801)

TSP_1

TSP_1: Thrombospondin type 1 domain (826 - 880)

Ig_2

Ig_2: Immunoglobulin domain (926 - 986)

Ig_2

Ig_2: Immunoglobulin domain (1211 - 1271)

I-set

I-set: Immunoglobulin I-set domain (1309 - 1382)

TSP_1

TSP_1: Thrombospondin type 1 domain (1431 - 1483)

TSP_1

TSP_1: Thrombospondin type 1 domain (1489 - 1527)

PLAC

PLAC: PLAC (protease and lacunin) domain (1659 - 1689)

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  • 1691 a.a.
Protein Preferred Names Protein Names

ADAMTS-like protein 3

  • a disintegrin-like and metalloprotease domain with thrombospondin type I motifs-like 3

ADAMTSL3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ADAMTSL3 P82987 KRT40 Homo sapiens Q6A162 25416956
Intra
ADAMTSL3 P82987 KRT40 Homo sapiens Q6A162 25416956
Intra
ADAMTSL3 P82987 KRTAP10-8 Homo sapiens P60410 32296183
Intra
ADAMTSL3 P82987 KRTAP10-8 Homo sapiens P60410 25416956
Intra
ADAMTSL3 P82987 KRTAP10-8 Homo sapiens P60410 32296183
Intra
ADAMTSL3 P82987 KRTAP2-3 Homo sapiens P0C7H8 25416956
Intra
ADAMTSL3 P82987 KRTAP12-3 Homo sapiens P60328 32296183
Intra
ADAMTSL3 P82987 KRTAP12-3 Homo sapiens P60328 32296183
Intra
ADAMTSL3 P82987 KRTAP1-1 Homo sapiens Q07627 32296183
Intra
ADAMTSL3 P82987 KRTAP1-1 Homo sapiens Q07627 32296183
Intra
ADAMTSL3 P82987 KRTAP1-1 Homo sapiens Q07627 32296183
Intra
ADAMTSL3 P82987 KRTAP5-7 Homo sapiens Q6L8G8 32296183
Intra
ADAMTSL3 P82987 KRTAP5-7 Homo sapiens Q6L8G8 32296183
Intra
ADAMTSL3 P82987 KRTAP5-7 Homo sapiens Q6L8G8 32296183
Intra
ADAMTSL3 P82987 KRTAP10-6 Homo sapiens P60371 32296183
Intra
ADAMTSL3 P82987 KRTAP10-6 Homo sapiens P60371 32296183
Intra
ADAMTSL3 P82987 KRTAP2-4 Homo sapiens Q9BYR9 32296183
Intra
ADAMTSL3 P82987 KRTAP2-4 Homo sapiens Q9BYR9 32296183
Intra
ADAMTSL3 P82987 KRTAP2-4 Homo sapiens Q9BYR9 32296183
Intra
ADAMTSL3 P82987 GLRX3 Homo sapiens O76003 32296183
Intra
ADAMTSL3 P82987 GLRX3 Homo sapiens O76003 32296183
Intra
ADAMTSL3 P82987 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
ADAMTSL3 P82987 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
ADAMTSL3 P82987 MDFI Homo sapiens Q99750 25416956
Intra
ADAMTSL3 P82987 MDFI Homo sapiens Q99750 32296183
Intra
ADAMTSL3 P82987 MDFI Homo sapiens Q99750 32296183
Intra
ADAMTSL3 P82987 MDFI Homo sapiens Q99750 25416956
Intra
ADAMTSL3 P82987 MDFI Homo sapiens Q99750 32296183
Intra
ADAMTSL3 P82987 KRTAP3-2 Homo sapiens Q9BYR7 32296183
Intra
ADAMTSL3 P82987 KRTAP3-2 Homo sapiens Q9BYR7 32296183
Intra
ADAMTSL3 P82987 KRTAP3-2 Homo sapiens Q9BYR7 32296183
Intra
ADAMTSL3 P82987 NOTCH2NLA Homo sapiens Q7Z3S9 25416956
Intra
ADAMTSL3 P82987 NOTCH2NLA Homo sapiens Q7Z3S9 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Radial Nerve Lesion
  • Lesion Of Radial Nerve

  • Radial Nerve Lesions

  • Radial Neuropathy

  • Radial Nerve Mononeuritis

Geleophysic Dysplasia
  • Geleophysic Dwarfism

  • Gphysd

Isolated Ectopia Lentis
  • Familial Ectopia Lentis

  • Ectopia Lentis

  • Ectopia Lentis Syndrome

  • Lens Subluxation

  • Iel

  • Congenital Ectopia Lentis

  • Subluxation Of Lens

  • Ectopia Lentis, Isolated

  • Ectopia Lentis Isolated

Ehlers-Danlos Syndrome, Dermatosparaxis Type
  • Dermatosparaxis

  • EDSDERMS

  • Ehlers-Danlos Syndrome, Type Vii, Autosomal Recessive

  • Eds Viic

  • Eds7c

  • Ehlers-Danlos Syndrome Dermatosparaxis Type

  • Dermatosparaxis Ehlers-Danlos Syndrome

  • Dermatosparaxis Eds

  • Ehlers-Danlos Syndrome Type 7c

  • Deds

  • Human Dermatosparaxis Eds Viic

  • Ehlers-Danlos Syndrome 7c

  • Ehlers-Danlos Syndrome, Type Viic

Weill-Marchesani Syndrome
  • Gemss Syndrome

  • Spherophakia-Brachymorphia Syndrome

  • Marchesani-Weill Syndrome

  • Wms

  • Congenital Mesodermal Dystrophy

  • Mesodermal Dysmorphodystrophy, Congenital

  • Spherophakia Brachymorphia Syndrome

  • Mesodermal Dysmorphodystrophy Congenital

  • Wm Syndrome

  • Brachydactyly-Spherophakia Syndrome

  • Brachymorphy With Spherophakia Syndrome

  • Congenital Mesodermal Dysmorphodystrophy

  • Marchesani Syndrome

  • Weill-Marchesani Syndrome, Autosomal Recessive

  • Weill-Marchesani Syndrome, Autosomal Dominant

Peters-Plus Syndrome
  • Krause-Kivlin Syndrome

  • Peters Plus Syndrome

  • Peters Anomaly

  • Irido-Corneo-Trabecular Dysgenesis

  • PTRPLS

  • Peters Anomaly With Short-Limb Dwarfism

  • Peters Anomaly-Short Limb Dwarfism Syndrome

  • Peters Anomaly With Short Limb Dwarfism

  • Peters Congenital Glaucoma

  • Krause-Van Schooneveld-Kivlin Syndrome

  • Peters' Plus Syndrome

  • Peters'-Plus Syndrome

  • Anomaly Peters

Radial Neuropathy
Acromicric Dysplasia
  • ACMICD

  • Acromicric Skeletal Dysplasia

  • Dysplasia, Acromicric

Winchester Syndrome
  • WNCHRS

  • Winchester Disease

  • Winchester-Grossman Syndrome

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus ADAMTSL3 RGD RGD:1305155
Macaca mulatta ADAMTSL3 VGNC VGNC:69400
Felis catus ADAMTSL3 VGNC VGNC:59601
Bos taurus ADAMTSL3 VGNC VGNC:58360
Canis familiaris ADAMTSL3 VGNC VGNC:54916
Mus musculus ADAMTSL3 MGD MGI:3028499
Others ADAMTSL3 NCBI