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ADAMTSL2 ADAMTS like 2 [ Homo sapiens (human) ]

Gene ID: 9719, updated on 3-Apr-2024

Summary

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Official Symbol
ADAMTSL2provided by HGNC
Official Full Name
ADAMTS like 2provided by HGNC
Primary source
HGNC:HGNC:14631
See related
Ensembl:ENSG00000197859 MIM:612277; AllianceGenome:HGNC:14631
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
GPHYSD1; ADAMTSL-2
Summary
This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) and ADAMTS-like protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The protein encoded by this gene lacks the protease domain, and is therefore of a member of the the ADAMTS-like protein subfamily. It is a secreted glycoprotein that binds the cell surface and extracellular matrix; it also interacts with latent transforming growth factor beta binding protein 1. Mutations in this gene have been associated with geleophysic dysplasia. [provided by RefSeq, Feb 2009]
Expression
Broad expression in kidney (RPKM 10.4), adrenal (RPKM 9.6) and 18 other tissues See more
Orthologs
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Genomic context

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Location:
9q34.2
Exon count:
20
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (133532164..133575519)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (145746173..145789503)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (136397286..136440641)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC102723855 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:136374104-136374823 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136377760-136378446 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136385034-136385534 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136395091-136395596 Neighboring gene myomaker, myoblast fusion factor Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20464 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136398691-136399232 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:136399233-136399772 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:136399773-136400314 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136400855-136401396 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136401937-136402476 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136404277-136405008 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136405742-136406473 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136407445-136407945 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136410411-136411066 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136420460-136420962 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136420963-136421464 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136421967-136422468 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136436438-136437078 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136442732-136443347 Neighboring gene uncharacterized LOC124902296 Neighboring gene family with sequence similarity 163 member B Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:136457531-136458030 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136480627-136481226 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:136502750-136503485 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:136519605-136520404 Neighboring gene dopamine beta-hydroxylase Neighboring gene DBH antisense RNA 1

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

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Related articles in PubMed

  1. Al-Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2-Related Disorders. Batkovskyte D, et al. J Bone Miner Res, 2023 May. PMID 36896612
  2. ADAMTSL2 protein and a soluble biomarker signature identify at-risk non-alcoholic steatohepatitis and fibrosis in adults with NAFLD. Corey KE, et al. J Hepatol, 2022 Jan. PMID 34600973, Free PMC Article
  3. ADAMTSL2 gene variant in patients with features of autosomal dominant connective tissue disorders. Steinle J, et al. Am J Med Genet A, 2021 Mar. PMID 33369194, Free PMC Article
  4. A chinese boy with geleophysic dysplasia caused by compound heterozygous mutations in ADAMTSL2. Li D, et al. Eur J Med Genet, 2017 Dec. PMID 28917829
  5. Systematic data-querying of large pediatric biorepository identifies novel Ehlers-Danlos Syndrome variant. Desai A, et al. BMC Musculoskelet Disord, 2016 Feb 16. PMID 26879370, Free PMC Article

See all (24) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Secreted ADAMTS-like 2 promotes myoblast differentiation by potentiating WNT signaling.
    Title: Secreted ADAMTS-like 2 promotes myoblast differentiation by potentiating WNT signaling.
  2. Al-Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2-Related Disorders.
    Title: Al-Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2-Related Disorders.
  3. The relationship of ADAMTSL2 and LRPAP1 gene methylation level with rheumatoid arthritis activity.
    Title: The relationship of ADAMTSL2 and LRPAP1 gene methylation level with rheumatoid arthritis activity.
  4. ADAMTSL2 protein and a soluble biomarker signature identify at-risk non-alcoholic steatohepatitis and fibrosis in adults with NAFLD.
    Title: ADAMTSL2 protein and a soluble biomarker signature identify at-risk non-alcoholic steatohepatitis and fibrosis in adults with NAFLD.
  5. Aberrant interaction between mutated ADAMTSL2 and LTBP4 is associated with adolescent idiopathic scoliosis.
    Title: Aberrant interaction between mutated ADAMTSL2 and LTBP4 is associated with adolescent idiopathic scoliosis.
  6. The extracellular matrix glycoprotein ADAMTSL2 is increased in heart failure and inhibits TGFbeta signalling in cardiac fibroblasts.
    Title: The extracellular matrix glycoprotein ADAMTSL2 is increased in heart failure and inhibits TGFβ signalling in cardiac fibroblasts.
  7. ADAMTSL2 gene variant in patients with features of autosomal dominant connective tissue disorders.
    Title: ADAMTSL2 gene variant in patients with features of autosomal dominant connective tissue disorders.
  8. Findings postulate that abnormal fibrillin microfibril assembly is the general molecular basis of geleophysic dysplasia, and the specific role of ADAMTSL2 may be to inhibit microfibril assembly, whether it be assembly of FBN2 fibrils in the embryonic period or FBN1 fibrils in tendons during the postnatal period.
    Title: Limb- and tendon-specific Adamtsl2 deletion identifies a role for ADAMTSL2 in tendon growth in a mouse model for geleophysic dysplasia.
  9. Upon investigating the interaction between LOX and ADAMTSL2 we found that the absence or inhibition of Lox affected ADAMTSL2 molecular forms and reduced its tissue levels. Thus, ADAMTSL2 stability and inter-molecular complexes may depend on the activity of lysyl oxidases.
    Title: Interactions between lysyl oxidases and ADAMTS proteins suggest a novel crosstalk between two extracellular matrix families.
  10. CpG-specific DNA methylation of ADAMTSL2 and BTN3A2 at rheumatoid arthritis diagnosis can serve as a marker of treatment response.
    Title: CpG-specific methylation at rheumatoid arthritis diagnosis as a marker of treatment response.
Submit: New GeneRIF Correction See all GeneRIFs (15)

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Associated conditions

Description Tests
Geleophysic dysplasia 1
MedGen: C3278147 OMIM: 231050 GeneReviews: Geleophysic Dysplasia
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Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

Pathways from PubChem

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Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

Homology

Clone Names

  • FLJ45164, KIAA0605

Gene Ontology Provided by GOA

Function Evidence Code Pubs
NOT enables metalloendopeptidase activity IBA
Inferred from Biological aspect of Ancestor
more info
  
enables microfibril binding IEA
Inferred from Electronic Annotation
more info
  
enables protein binding IPI
Inferred from Physical Interaction
more info
 PubMed 
Process Evidence Code Pubs
involved_in extracellular matrix organization IEA
Inferred from Electronic Annotation
more info
  
involved_in lobar bronchus epithelium development IEA
Inferred from Electronic Annotation
more info
  
involved_in negative regulation of transforming growth factor beta receptor signaling pathway IMP
Inferred from Mutant Phenotype
more info
 PubMed 
Component Evidence Code Pubs
is_active_in extracellular matrix IBA
Inferred from Biological aspect of Ancestor
more info
  
located_in extracellular region IEA
Inferred from Electronic Annotation
more info
  

General protein information

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Preferred Names
ADAMTS-like protein 2

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_009931.1 RefSeqGene

    Range
    7541..48356
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001145320.2 → NP_001138792.1  ADAMTS-like protein 2 precursor

    See identical proteins and their annotated locations for NP_001138792.1

    Status: REVIEWED

    Source sequence(s)
    BX324209, BX629352, BX649571
    Consensus CDS
    CCDS6976.1
    UniProtKB/Swiss-Prot
    B1B0D5, O60345, Q86TH1
    UniProtKB/TrEMBL
    B1B0D4
    Related
    ENSP00000346478.4, ENST00000354484.8
    Conserved Domains (3) summary
    smart00209
    Location:50 → 106
    TSP1; Thrombospondin type 1 repeats
    pfam05986
    Location:216 → 330
    ADAM_spacer1; ADAM-TS Spacer 1
    pfam08686
    Location:916 → 947
    PLAC; PLAC (protease and lacunin) domain

  2. NM_014694.4 → NP_055509.2  ADAMTS-like protein 2 precursor

    See identical proteins and their annotated locations for NP_055509.2

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) represents the shorter transcript. Variants 1 and 2 encode the same protein.
    Source sequence(s)
    BC050544, BX324209, BX629352
    Consensus CDS
    CCDS6976.1
    UniProtKB/Swiss-Prot
    B1B0D5, O60345, Q86TH1
    UniProtKB/TrEMBL
    B1B0D4
    Related
    ENSP00000498961.2, ENST00000651351.2
    Conserved Domains (3) summary
    smart00209
    Location:50 → 106
    TSP1; Thrombospondin type 1 repeats
    pfam05986
    Location:216 → 330
    ADAM_spacer1; ADAM-TS Spacer 1
    pfam08686
    Location:916 → 947
    PLAC; PLAC (protease and lacunin) domain

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    133532164..133575519
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_011519241.3 → XP_011517543.2  ADAMTS-like protein 2 isoform X1

    UniProtKB/TrEMBL
    B1B0D4

  2. XM_005272239.3 → XP_005272296.1  ADAMTS-like protein 2 isoform X4

    See identical proteins and their annotated locations for XP_005272296.1

    UniProtKB/Swiss-Prot
    B1B0D5, O60345, Q86TH1
    UniProtKB/TrEMBL
    B1B0D4
    Conserved Domains (3) summary
    smart00209
    Location:50 → 106
    TSP1; Thrombospondin type 1 repeats
    pfam05986
    Location:216 → 330
    ADAM_spacer1; ADAM-TS Spacer 1
    pfam08686
    Location:916 → 947
    PLAC; PLAC (protease and lacunin) domain

  3. XM_011519242.4 → XP_011517544.1  ADAMTS-like protein 2 isoform X2

    UniProtKB/TrEMBL
    B1B0D4
    Conserved Domains (3) summary
    smart00209
    Location:881 → 930
    TSP1; Thrombospondin type 1 repeats
    pfam05986
    Location:238 → 352
    ADAM_spacer1; ADAM-TS Spacer 1
    pfam08686
    Location:938 → 969
    PLAC; PLAC (protease and lacunin) domain

  4. XM_005272238.4 → XP_005272295.1  ADAMTS-like protein 2 isoform X3

    Conserved Domains (3) summary
    smart00209
    Location:869 → 918
    TSP1; Thrombospondin type 1 repeats
    pfam05986
    Location:226 → 340
    ADAM_spacer1; ADAM-TS Spacer 1
    pfam08686
    Location:926 → 957
    PLAC; PLAC (protease and lacunin) domain

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    145746173..145789503
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_054364285.1 → XP_054220260.1  ADAMTS-like protein 2 isoform X1

  2. XM_054364288.1 → XP_054220263.1  ADAMTS-like protein 2 isoform X4

    UniProtKB/Swiss-Prot
    B1B0D5, O60345, Q86TH1

  3. XM_054364286.1 → XP_054220261.1  ADAMTS-like protein 2 isoform X2

  4. XM_054364287.1 → XP_054220262.1  ADAMTS-like protein 2 isoform X3

Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
Q86TH1.1 GenPept UniProtKB/Swiss-Prot:Q86TH1

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