Enah (GeneID: 360891) | Rattus norvegicus
Description: ENAH, actin regulator [Source:RGD Symbol;Acc:1307666]
Synonyms:
Other ID(s): ENSRNOG00000031934
Protein Accession Numbers: XP_017454343, XP_017454351, XP_006250462, XP_017454348, XP_017454345, XP_017454342, XP_017454350, XP_006250455, XP_017454347, XP_017454344, XP_006250463, XP_017454349, NP_001012150, XP_017454346
Statistics: ClinVar(2) gnomAD(452) COSMIC(503)
ClinVar Pathogenicity of Variations help
100%10010090908080707060605050404030302020101000
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∙ 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.
ENST00000284563 ENST00000366843 You are here now! ENST00000366844 NP_001008493 NP_001364410 NP_001364411 NP_001364412 NP_060682 You are here now!


import_contactsClinVar Data

healinggnomAD
2%5%2%58%30%10010090908080707060605050404030302020101000
Frameshift Variant
Inframe Deletion
Inframe Insertion
Missense Variant
Protein Altering Variant
Splice Region Variant
Stop Gained
Synonymous Variant
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blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
1%1%1%5%14%1%75%10010090908080707060605050404030302020101000
Deletion - Frameshift
Deletion - In Frame
Insertion - Frameshift
Insertion - In Frame
Substitution - Coding Silent
Substitution - Missense
Substitution - Nonsense
Unknown
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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
Leukemia, Myelocytic, Acute Neoplasms ; 0.773 0.172
Acute Myeloid Leukemia, M1 Neoplasms ; 0.773 0.172
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.773 0.172
NO RESULT FOUND
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Classification of Clinicial Significance of ClinVar Data
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