Gene Gene information from NCBI Gene database.
Entrez ID 163782
Gene name KN motif and ankyrin repeat domains 4
Gene symbol KANK4
Synonyms (NCBI Gene)
ANKRD38dJ1078M7.1
Chromosome 1
Chromosome location 1p31.3
miRNA miRNA information provided by mirtarbase database.
308
miRTarBase ID miRNA Experiments Reference
MIRT616260 hsa-miR-129-5p HITS-CLIP 23824327
MIRT628088 hsa-miR-3936 HITS-CLIP 23824327
MIRT616259 hsa-miR-6085 HITS-CLIP 23824327
MIRT616258 hsa-miR-6813-5p HITS-CLIP 23824327
MIRT616257 hsa-miR-3119 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IDA 25961457
GO:0005737 Component Cytoplasm IEA
GO:0005829 Component Cytosol IDA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
614612 27263 ENSG00000132854
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5T7N3
Protein name KN motif and ankyrin repeat domain-containing protein 4 (Ankyrin repeat domain-containing protein 38)
Protein function May be involved in the control of cytoskeleton formation by regulating actin polymerization.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12075 KN_motif 24 62 KN motif Motif
PF00023 Ank 823 856 Ankyrin repeat Repeat
PF13857 Ank_5 915 970 Repeat
Tissue specificity TISSUE SPECIFICITY: Strongly expressed in colon, liver, lung, skeletal muscle and kidney. {ECO:0000269|PubMed:17996375}.
Sequence
MEKTDAKDQSSQGDEEKDPPKSHPYSVETPYGFHLDLDFLKYVDDIEKGNTIKRIPIHRR
AK
QAKFSTLPRNFSLPDSGARPPAAPPLQNWSPVVPREASLGTQEQNQSPPLGNAPQAST
SRSEVSYHRKALLAEATRQLEAAEPEDAELTFGSGRPQLLRASSMPATLLHSRASEEPGL
SLGPPAPPALPPLQGEGSVCDGTFEPAEGLAGFHSSSPRASTRIPELVQEGAEPPEGVVK
VPNHLPLPGPPFSFQNVLVVLEDKEDEHNAREAEVLFTPGSPTPSPPPLPSPIPENELLL
EEIELNISEIPPPPPVEVDMRSIGIRVTEESLGLARVDPGSISSLKQQVSALEGELSGRT
EELAQVRTALQQQEEEIKAREQRIRELEFTVAQLEGQFHQENAKDTQGQTDVMVNTDPVH
GLLTRESCDKGIEVNLLGSMESESWGHRGEENGLLWGPDGHKQGNQSPAERVLLPQLSLP
QGPEQVLTSSVHSFLSTELRIEEAGTEQEGGPQGGTRGAGGFLWGSDRKTPPAGREETSS
NLPGKEHPGRPPSSPTDATIGQYVKKIQELLQEQWNCLEHGYPELASAIKQPASKLSSIQ
SQLLSSLNLLLSAYSAQAHPPKEPPASSSSPPVEISPSTSLKSIMKKKDYGFRAGGNGTK
KNLQFVGVNGGYETTSSEETSGEDSTPEDLSDSEAEKKCDGPDHKHVKDAHLTCEAGQGI
PEGTCHAAQESGPGEEVPHSKAERYKPSEEFLNACRALSQHLPETGTTTDQLLRQSLNTI
SQEWFRVSSRKSSSPAVVASYLHEVQPHSPHFLKLLVNLADHNGNTALHYSVSHSNFSIV
KLLLETGVCNVDHQNK
AGYTAVMITPLASAETNEDMAVVWKLLREGNVNIQATQGGQTAL
MLGVSHDREDMVQALLSCQADVNLQDHDGSSALMVACHHGNVDLVRLLLAHPACDSSLTD
KAGRTALSIA
LKSPTHMEIAGLLRAHAEQGRSLGL
Sequence length 995
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
52
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Benign rs140001310 RCV005916833
Cervical cancer Benign rs115190866 RCV005914602
Colon adenocarcinoma Benign rs115190866 RCV005914601
Colorectal cancer Benign rs115190866 RCV005914603
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Arthritis Rheumatoid Associate 24397353
Fuchs' Endothelial Dystrophy Associate 28358029
Lymphatic Metastasis Associate 38211648
Osteoarthritis Associate 24397353
Pancreatic Neoplasms Associate 37036756