Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
122786
Gene name Gene Name - the full gene name approved by the HGNC.
FERM domain containing 6
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
FRMD6
Synonyms (NCBI Gene) Gene synonyms aliases
C14orf31, EX1, Willin, c14_5320
Chromosome Chromosome number
14
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
14q22.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT022571 hsa-miR-124-3p Microarray 18668037
MIRT027277 hsa-miR-101-3p Sequencing 20371350
MIRT070247 hsa-miR-5197-3p HITS-CLIP 23824327
MIRT644413 hsa-miR-3123 HITS-CLIP 23824327
MIRT644414 hsa-miR-141-5p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16189514, 25416956, 29892012, 31515488
GO:0005737 Component Cytoplasm IEA
GO:0005856 Component Cytoskeleton IBA 21873635
GO:0005886 Component Plasma membrane IEA
GO:0031032 Process Actomyosin structure organization IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614555 19839 ENSG00000139926
Protein
UniProt ID Q96NE9
Protein name FERM domain-containing protein 6 (Willin)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09379 FERM_N 20 82 FERM N-terminal domain Domain
PF00373 FERM_M 118 234 FERM central domain Domain
PF09380 FERM_C 239 332 FERM C-terminal PH-like domain Domain
Sequence
MNKLNFHNNRVMQDRRSVCIFLPNDESLNIIINVKILCHQLLVQVCDLLRLKDCHLFGLS
VIQNNEHVYMELSQKLYKYCPK
EWKKEASKVRQYEVTWGIDQFGPPMIIHFRVQYYVENG
RLISDRAARYYYYWHLRKQVLHSQCVLREEAYFLLAAFALQADLGNFKRNKHYGKYFEPE
AYFPSWVVSKRGKDYILKHIPNMHKDQFALTASEAHLKYIKEAVRLDDVAVHYY
RLYKDK
REIEASLTLGLTMRGIQIFQNLDEEKQLLYDFPWTNVGKLVFVGKKFEILPDGLPSARKL
IYYTGCPMRSRHLLQLLSNSHRLYMNLQPVLR
HIRKLEENEEKKQYRESYISDNLDLDMD
QLEKRSRASGSSAGSMKHKRLSRHSTASHSSSHTSGIEADTKPRDTGPEDSYSSSAIHRK
LKTCSSMTSHGSSHTSGVESGGKDRLEEDLQDDEIEMLVDDPRDLEQMNEESLEVSPDMC
IYITEDMLMSRKLNGHSGLIVKEIGSSTSSSSETVVKLRGQSTDSLPQTICRKPKTSTDR
HSLSLDDIRLYQKDFLRIAGLCQDTAQSYTFGCGHELDEEGLYCNSCLAQQCINIQDAFP
VKRTSKYFSLDLTHDEVPEFVV
Sequence length 622
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Hippo signaling pathway
Hippo signaling pathway - multiple species
 
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Metabolic syndrome Metabolic Syndrome X rs367643250, rs587777380, rs777736953 30621171
Unknown
Disease term Disease name Evidence References Source
Metabolic Syndrome Metabolic Syndrome GWAS
Ischemic Stroke Ischemic Stroke GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma Associate 36373308
Alzheimer Disease Associate 22190428
Aortic Aneurysm Thoracic Associate 34469433
Asthma Associate 22432035
Breast Neoplasms Associate 39199284
Colorectal Neoplasms Associate 27609023
Congenital myasthenic syndrome ib Associate 33721619
Drug Related Side Effects and Adverse Reactions Associate 27433923
Hypomagnesemia primary Associate 36264865
Leukemia T Cell Associate 27433923