CD9 (GeneID: 100141395) | Macaca mulatta
Description: CD9 molecule [Source:NCBI gene;Acc:100141395]
Synonyms: Mamu-MIC1, MIC3
Other ID(s): ENSMMUG00000041840
Protein Accession Numbers: NP_001108437, XP_014991397
Statistics: ClinVar(6)
ClinVar Pathogenicity of Variations help

∙ 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.
ENST00000400322 ENST00000400325 ENST00000414473 ENST00000415525 ENST00000417899 ENST00000417943 ENST00000418465 ENST00000420259 ENST00000420744 ENST00000421350 ENST00000423443 ENST00000427477 ENST00000432479 ENST00000436191 ENST00000438928 ENST00000446505 ENST00000449934 ENST00000460798 ENST00000546529 ENST00000547609 ENST00000547767 ENST00000552236 NP_000238 NP_001170990 NP_001276081 You are here now!


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
PF00129 MHC_I Class I Histocompatibility antigen, domains alpha 1 and 2 24-200 CL0343 MHC Homo sapiens
PF07654 C1-set Immunoglobulin C1-set domain 208-289 CL0011 Ig Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Coronary Aneurysm Cardiovascular Diseases ; 0.499 0.759
Oral Submucous Fibrosis Stomatognathic Diseases ; 0.499 0.759
Liver carcinoma Neoplasms ; Digestive System Diseases ; 0.499 0.759
Familial Ménière disease N/A 0.499 0.759
NO RESULT FOUND
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