FXYD6 (GeneID: 53826) | Homo sapiens
Description: FXYD domain containing ion transport regulator 6 [Source:HGNC Symbol;Acc:HGNC:4030]
Synonyms:
Other ID(s): ENSG00000137726, HGNC:4030
Protein Accession Numbers: ENST00000527429, NP_001158303, ENST00000524656, ENST00000540359, ENST00000529335, NP_001158308, ENST00000526014, ENST00000584394, ENST00000539526, NP_071286, ENST00000260282, ENST00000527717, NP_001158304, ENST00000524841, ENST00000584230, ENST00000530956, NP_001158309
Statistics: gnomAD(581) COSMIC(1028) PTM(2)
Post translational modifications (PTM) by Type

∙ 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.
ENST00000260282 You are here now! ENST00000524656 You are here now! ENST00000524841 ENST00000526014 You are here now! ENST00000527429 ENST00000527717 You are here now! ENST00000529335 ENST00000530956 You are here now! ENST00000539526 You are here now! ENST00000540359 You are here now! ENST00000584230 ENST00000584394 NP_001158303 You are here now! NP_001158304 You are here now! NP_001158308 You are here now! NP_001158309 You are here now! NP_071286 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
PF02038 ATP1G1_PLM_MAT8 ATP1G1/PLM/MAT8 family 25-72 Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Leukemia, Myelocytic, Acute Neoplasms ; 0.785 0.138
Liver Cirrhosis, Experimental Digestive System Diseases ; 0.785 0.138
Acute Myeloid Leukemia, M1 Neoplasms ; 0.785 0.138
Schizophrenia Mental Disorders ; 0.785 0.138
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.785 0.138
NO RESULT FOUND
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