ENAH (GeneID: 55740) | Homo sapiens
Description: ENAH, actin regulator [Source:HGNC Symbol;Acc:HGNC:18271]
Synonyms: ENA, NDPP1, MENA
Other ID(s): ENSG00000154380, HGNC:18271
Protein Accession Numbers: ENST00000366843, NP_001364412, NP_001008493, ENST00000284563, NP_001364411, ENST00000366844, NP_060682, NP_001364410
Statistics: gnomAD(469) COSMIC(521) PTM(41)
Post translational modifications (PTM) by Type
2%2%80%15%10010090908080707060605050404030302020101000
Acetylation
Methylation
Phosphorylation
Ubiquitination
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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 ENST00000366844 You are here now! NP_001008493 You are here now! NP_001364410 NP_001364411 NP_001364412 NP_060682


import_contactsClinVar Data

healinggnomAD
3%5%2%59%29%10010090908080707060605050404030302020101000
Frameshift Variant
Inframe Deletion
Inframe Insertion
Missense Variant
Protein Altering Variant
Splice Region Variant
Stop Gained
Synonymous Variant
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placePost-translational Modifications (PTMs)
2%2%80%15%10010090908080707060605050404030302020101000
Acetylation
Methylation
Phosphorylation
Ubiquitination
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blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
1%5%13%1%77%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
PF00568 WH1 WH1 domain 1-108 CL0266 PH Homo sapiens
PF08776 VASP_tetra VASP tetramerisation domain 552-587 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 ; 0.773 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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