Gene Gene information from NCBI Gene database.
Entrez ID 10863
Gene name ADAM metallopeptidase domain 28
Gene symbol ADAM28
Synonyms (NCBI Gene)
ADAM 28MDC-LMDCLeMDC IIeMDCII
Chromosome 8
Chromosome location 8p21.2
Summary This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes
miRNA miRNA information provided by mirtarbase database.
33
miRTarBase ID miRNA Experiments Reference
MIRT531705 hsa-miR-3914 PAR-CLIP 22012620
MIRT531704 hsa-miR-4717-3p PAR-CLIP 22012620
MIRT531703 hsa-miR-3913-3p PAR-CLIP 22012620
MIRT531702 hsa-miR-130a-5p PAR-CLIP 22012620
MIRT531701 hsa-miR-23a-3p PAR-CLIP 22012620
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
20
GO ID Ontology Definition Evidence Reference
GO:0004222 Function Metalloendopeptidase activity IBA
GO:0004222 Function Metalloendopeptidase activity IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005576 Component Extracellular region IEA
GO:0005739 Component Mitochondrion IDA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
606188 206 ENSG00000042980
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UKQ2
Protein name Disintegrin and metalloproteinase domain-containing protein 28 (ADAM 28) (EC 3.4.24.-) (Epididymal metalloproteinase-like, disintegrin-like, and cysteine-rich protein II) (eMDC II) (Metalloproteinase-like, disintegrin-like, and cysteine-rich protein L) (M
Protein function May play a role in the adhesive and proteolytic events that occur during lymphocyte emigration or may function in ectodomain shedding of lymphocyte surface target proteins, such as FASL and CD40L. May be involved in sperm maturation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01562 Pep_M12B_propep 29 156 Reprolysin family propeptide Family
PF01421 Reprolysin 204 399 Reprolysin (M12B) family zinc metalloprotease Domain
PF00200 Disintegrin 416 488 Disintegrin Domain
PF08516 ADAM_CR 493 591 ADAM cysteine-rich Family
Tissue specificity TISSUE SPECIFICITY: Expressed predominantly in secondary lymphoid tissues, such as lymph node, spleen, small intestine, stomach, colon, appendix and trachea. The lymphocyte population is responsible for expression of this protein in these tissues. Isoform
Sequence
Sequence length 775
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Hereditary spastic paraplegia Affects rs201643797 RCV001376690
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 22514692
Colorectal Neoplasms Associate 23527725, 30840270
Diabetes Mellitus Type 2 Associate 23010875
Inflammation Associate 23010875
Leukemia Lymphocytic Chronic B Cell Associate 27111430
Lymphoma Associate 34166375
Metabolic Syndrome Associate 23010875
Multiple Myeloma Associate 40665393
Neoplasms Associate 23527725, 27462861, 27749584, 31602160
Neoplasms Stimulate 29776401