CD9 (GeneID: 928) | Homo sapiens
Description: CD9 molecule [Source:HGNC Symbol;Acc:HGNC:1709]
Synonyms: MRP-1, BTCC-1, TSPAN-29, MIC3, SPAN29, DRAP-27
Other ID(s): ENSG00000010278, HGNC:1709
Protein Accession Numbers: NP_001760, ENST00000382519, ENST00000009180, NP_001317241, ENST00000382518, ENST00000536586, ENST00000382515
Statistics: gnomAD(208)
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.
ENST00000009180 ENST00000382515 ENST00000382518 ENST00000382519 ENST00000536586 NP_001317241 NP_001760


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
PF00335 Tetraspanin Tetraspanin family 10-218 CL0347 Tetraspannin Mus musculus

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Non-Small Cell Lung Carcinoma Neoplasms ; Respiratory Tract Diseases ; 0.54 0.759
Colorectal Carcinoma Neoplasms ; Digestive System Diseases ; 0.54 0.759
Colorectal Neoplasms Neoplasms ; Digestive System Diseases ; 0.54 0.759
Glioblastoma Neoplasms ; 0.54 0.759
Leukemia, Myelocytic, Acute Neoplasms ; 0.54 0.759
Liver Cirrhosis Digestive System Diseases ; 0.54 0.759
Acute Myeloid Leukemia, M1 Neoplasms ; 0.54 0.759
Embryonal Neoplasm Neoplasms ; 0.54 0.759
Neoplasms, Germ Cell and Embryonal Neoplasms ; 0.54 0.759
Nerve Degeneration Pathological Conditions, Signs and Symptoms ; 0.54 0.759
Prostatic Neoplasms Neoplasms ; Male Urogenital Diseases ; 0.54 0.759
Germ cell tumor Neoplasms ; 0.54 0.759
Neoplasms, Embryonal and Mixed Neoplasms ; 0.54 0.759
Fibrosis, Liver Digestive System Diseases ; 0.54 0.759
Giant Cell Glioblastoma Neoplasms ; 0.54 0.759
Malignant neoplasm of prostate Neoplasms ; Male Urogenital Diseases ; 0.54 0.759
Germ Cell Cancer Neoplasms ; 0.54 0.759
Cancer, Embryonal Neoplasms ; 0.54 0.759
Cancer, Embryonal and Mixed Neoplasms ; 0.54 0.759
Colorectal Cancer Neoplasms ; Digestive System Diseases ; 0.54 0.759
Glioblastoma Multiforme Neoplasms ; 0.54 0.759
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.54 0.759
NO RESULT FOUND
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