KLHL32 (kelch like family member 32)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
114792
Gene name Gene Name - the full gene name approved by the HGNC.
Kelch like family member 32
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
KLHL32
Synonyms (NCBI Gene) Gene synonyms aliases
BKLHD5, KIAA1900, UG0030H05, dJ21F7.1
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6q16.1
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(53)
miRTarBase ID miRNA Experiments Reference
MIRT018022 hsa-miR-335-5p Microarray 18185580
MIRT445939 hsa-miR-3200-5p PAR-CLIP 22100165
MIRT445938 hsa-miR-4251 PAR-CLIP 22100165
MIRT445937 hsa-miR-4329 PAR-CLIP 22100165
MIRT445936 hsa-miR-6761-5p PAR-CLIP 22100165
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(1)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32814053
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Q96NJ5
Protein name Kelch-like protein 32 (BTB and kelch domain-containing protein 5)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00651 BTB 32 → 139 BTB/POZ domain Domain
PF07707 BACK 144 → 245 BTB And C-terminal Kelch Domain
PF01344 Kelch_1 335 → 385 Kelch motif Repeat
PF01344 Kelch_1 387 → 432 Kelch motif Repeat
PF01344 Kelch_1 483 → 530 Kelch motif Repeat
Sequence 
MPSERCLSIQEMLTGQRLCHSESHNDSVLAALNQQRSDGILCDITLIAEEQKFHAHKAVL
AACSDYFRAMFSLCMVESGADEVNLHGVTSLGLKQALEFAYTGQILLEPGVIQDVLAAGS
HLQLLELLNLCSHYLIQELNSFNYLDLYRLADLFNLTLLEKAVIDFLVKHLSELLKSRPE
EVLTLPYCLLQEVLKSDRLTSLSEEQIWQLAVRWLEHNCHYQYMDELLQYIRFGLMDVDT
LHTVALSHPLVQASETATALVNEALEYHQSIYAQPVWQTRRTKPRFQSDTLYIIGGKKRE
VCKVKELRYFNPVDQENALIAAIANWSELAPMPVGRSHHCVAVMGDFLFVAGGEVEHASG
RTCAVRTACRYDPRSNSWAEIAPMKNCREHFVLGAMEEYLYAVGGRNELRQVLPTVERYC
PKKNKWTFVQSFDRSLSCHAGYVADGLLWISGGVTNTAQYQNRLMVYEPNQNKWISRSPM
LQRRVYHSMAAVQRKLYVLGGNDLDYNNDRILVRHIDSYNIDTDQWTRCNFNLLTGQNES
GVAVHNGRIYLVGGYSIWTNEPLACIQVLDVSREGKEEVFYGPTLPFASNGIAACFLPAP
YFTCPNLQTLQVPHHRIGTI
Sequence length 620
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (2)
Unknown
Disease term Disease name Evidence References Source
Chronic obstructive pulmonary disease Chronic Obstructive Airway Disease 26634245 ClinVar
Metabolic Syndrome Metabolic Syndrome GWAS
Show/Hide Text Mining Associations (4)
Associations from Text Mining
Disease Name Relationship Type References
Autistic Disorder Associate 23253088
Language Development Disorders Associate 23253088
Obsessive Compulsive Disorder Associate 23253088
Tourette Syndrome Associate 23253088