Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9920
Gene name Gene Name - the full gene name approved by the HGNC.
Kelch repeat and BTB domain containing 11
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
KBTBD11
Synonyms (NCBI Gene) Gene synonyms aliases
KLHDC7C
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8p23.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT016377 hsa-miR-193b-3p Microarray 20304954
MIRT024631 hsa-miR-215-5p Microarray 19074876
MIRT026418 hsa-miR-192-5p Microarray 19074876
MIRT714300 hsa-miR-128-3p HITS-CLIP 19536157
MIRT714299 hsa-miR-216a-3p HITS-CLIP 19536157
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
618794 29104 ENSG00000176595
Protein
UniProt ID O94819
Protein name Kelch repeat and BTB domain-containing protein 11 (Chronic myelogenous leukemia-associated protein) (Kelch domain-containing protein 7B)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00651 BTB 138 231 BTB/POZ domain Domain
PF01344 Kelch_1 348 399 Kelch motif Repeat
PF01344 Kelch_1 401 442 Kelch motif Repeat
Sequence
MEHAVAPCVLYPGTEPGAAGESESEGAASPAQTPCSLGASLCFSSGEESPPQSLASAAEG
AATSPPSSGGPRVVERQWEAGSAGAASPEELASPEERACPEEPAAPSPEPRVWLEDPASP
EEPGEPAPVPPGFGAVYGEPDLVLEVSGRRLRAHKAVLAARSDYFRARASRDVLRVQGVS
LTALRLLLADAYSGRMAGVRPDNVAEVVAGARRLQLPGAAQRATDAVGPQL
SLANCYEVL
SAAKRQRLNELRDAAYCFMSDHYLEVLREPAVFGRLSGAERDLLLRRRLRAGRAHLLAAA
LGPAGERAGSRPQSPSGDADARGDAAVYCFHAAAGEWRELTRLPEGAPARGCGLCVLYNY
LFVAGGVAPAGPDGRARPSDQVFCYNPATDSWSAVRPLR
QARSQLRLLALDGHLYAVGGE
CLLSVERYDPRADRWAPVAPLP
RGAFAVAHEATTCHGEIYVSGGSLFYRLLKYDPRRDEW
QECPCSSSRERSADMVALDGFIYRFDLSGSRGEAQAAGPSGVSVSRYHCLAKQWSPCVAP
LRLPGGPTGLQPFRCAALDGAIYCVSRAGTWRFQPAREGEAGGDAGQGGGFEALGAPLDV
RGVLIPFALSLPEKPPRGEQGAP
Sequence length 623
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Cervical Cancer Cervical cancer N/A N/A GWAS
Colorectal Cancer Colorectal cancer N/A N/A GWAS
Dementia Dementia N/A N/A GWAS
Mental Depression Clinical depression N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinogenesis Associate 29267898
Colorectal Neoplasms Associate 29267898
Neoplasms Inhibit 29267898