Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
114818
Gene name Gene Name - the full gene name approved by the HGNC.
Kelch like family member 29
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
KLHL29
Synonyms (NCBI Gene) Gene synonyms aliases
KBTBD9
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p24.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT440355 hsa-miR-127-5p HITS-CLIP 24374217
MIRT440355 hsa-miR-127-5p HITS-CLIP 24374217
MIRT1098381 hsa-miR-1 CLIP-seq
MIRT1098382 hsa-miR-103a CLIP-seq
MIRT1098383 hsa-miR-107 CLIP-seq
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 25036637, 28514442
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q96CT2
Protein name Kelch-like protein 29 (Kelch repeat and BTB domain-containing protein 9)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00651 BTB 319 431 BTB/POZ domain Domain
PF07707 BACK 436 538 BTB And C-terminal Kelch Domain
PF01344 Kelch_1 672 717 Kelch motif Repeat
PF01344 Kelch_1 719 765 Kelch motif Repeat
PF01344 Kelch_1 810 857 Kelch motif Repeat
Sequence
MSRHHSRFERDYRVGWDRREWSVNGTHGTTSICSVTSGAGGGTASSLSVRPGLLPLPVVP
SRLPTPATAPAPCTTGSSEAITSLVASSASAVTTKAPGISKGDSQSQGLATSIRWGQTPI
NQSTPWDTDEPPSKQMRESDNPGTGPWVTTVAAGNQPTLIAHSYGVAQPPTFSPAVNVQA
PVIGVTPSLPPHVGPQLPLMPGHYSLPQPPSQPLSSVVVNMPAQALYASPQPLAVSTLPG
VGQVARPGPTAVGNGHMAGPLLPPPPPAQPSATLPSGAPATNGPPTTDSAHGLQMLRTIG
VGKYEFTDPGHPREMLKELNQQRRAKAFTDLKIVVEGREFEVHQNVLASCSLYFKDLIQR
SVQDSGQGGREKLELVLSNLQADVLELLLEFVYTGSLVIDSANAKTLLEAASKFQFHTFC
KVCVSFLEKQL
TASNCLGVLAMAEAMQCSELYHMAKAFALQIFPEVAAQEEILSISKDDF
IAYVSNDSLNTKAEELVYETVIKWIKKDPATRTQYAAELLAVVRLPFIHPSYLLNVVD
NE
ELIKSSEACRDLVNEAKRYHMLPHARQEMQTPRTRPRLSAGVAEVIVLVGGRQMVGMTQR
SLVAVTCWNPQNNKWYPLASLPFYDREFFSVVSAGDNIYLSGGMESGVTLADVWCYMSLL
DNWNLVSRMTVPRCRHNSLVYDGKIYTLGGLGVAGNVDHVERYDTITNQWEAVAPLPKAV
HSAAATVCGGKIYVFGGVNEAGRAAGVLQSYVPQTNTWSFIESPM
IDNKYAPAVTLNGFV
FILGGAYARATTIYDPEKGNIKAGPNMNHSRQFCSAVVLDGKIYATGGIVSSEGPALGNM
EAYEPTTNTWTLLPHMP
CPVFRHGCVVIKKYIQSG
Sequence length 875
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Epilepsy Epilepsy, Generalized rs113994140, rs28937874, rs1589762127, rs104894166, rs28939075, rs2134001459, rs104894167, rs119488099, rs119488100, rs387906420, rs121917752, rs121918622, rs281865564, rs387907313, rs397514670
View all (165 more)
30531953
Hypertension Hypertensive disease rs13306026 21347282
Unknown
Disease term Disease name Evidence References Source
Coronary heart disease Coronary heart disease 21347282 ClinVar
Mental depression Major Depressive Disorder 29942085 ClinVar
Neuroticism Neuroticism GWAS
Schizophrenia Schizophrenia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Inhibit 37845393
Colorectal Neoplasms Associate 28081303
Medulloblastoma Associate 36273157
Neoplasms Associate 28081303, 36273157
Neoplasms Inhibit 37845393
Triple Negative Breast Neoplasms Associate 37845393