ADAM10 (GeneID: 102) | Homo sapiens
Description: ADAM metallopeptidase domain 10 [Source:HGNC Symbol;Acc:HGNC:188]
Synonyms: kuz, CD156c, AD10, HsT18717, ADM, RAK, CDw156, AD18
Other ID(s): ENSG00000137845, HGNC:188
Protein Accession Numbers: ENST00000402627, ENST00000260408.3, NP_001101, ENST00000558004, ENST00000396140, ENST00000260408, ENST00000561288, ENST00000439637, ENST00000396136, NP_001307499, ENST00000559053
Statistics: gnomAD(43) COSMIC(439)
gnomAD Variants By Annotation

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000260408 ENST00000396136 ENST00000396140 ENST00000402627 ENST00000439637 ENST00000558004 ENST00000559053 ENST00000561288 NP_001101 NP_001307499


import_contactsClinVar Data
Variation ID filter_list Allele ID filter_list RS Number filter_list Variant Type filter_list Record filter_list Alteration filter_list Clinicial Sig. filter_list Last Update filter_list Phenotypes filter_list Cytogenetic filter_list Review Status filter_list RCV Acc.N. filter_list

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
NO DOMAINS EXIST

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Malignant neoplasm of breast Neoplasms ; Skin and Connective Tissue Diseases ; 0.552 0.724
Reticulate acropigmentation of Kitamura Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Skin and Connective Tissue Diseases ; 0.552 0.724
Breast Carcinoma Neoplasms ; Skin and Connective Tissue Diseases ; 0.552 0.724
Mammary Neoplasms, Human Neoplasms ; Skin and Connective Tissue Diseases ; 0.552 0.724
Stage IV Skin Melanoma N/A 0.552 0.724
Mammary Neoplasms Neoplasms ; Skin and Connective Tissue Diseases ; 0.552 0.724
dowling-degos disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Skin and Connective Tissue Diseases ; 0.552 0.724
ALZHEIMER DISEASE 18 N/A 0.552 0.724
NO RESULT FOUND
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