Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
83473
Gene name Gene Name - the full gene name approved by the HGNC.
Katanin catalytic subunit A1 like 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
KATNAL2
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
18
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
18q21.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1079191 hsa-miR-1206 CLIP-seq
MIRT1079192 hsa-miR-1207-3p CLIP-seq
MIRT1079193 hsa-miR-1276 CLIP-seq
MIRT1079194 hsa-miR-1285 CLIP-seq
MIRT1079195 hsa-miR-1289 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0000212 Process Meiotic spindle organization IBA
GO:0000922 Component Spindle pole IDA 26929214
GO:0000922 Component Spindle pole IEA
GO:0005515 Function Protein binding IPI 25910212, 32296183
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614697 25387 ENSG00000167216
Protein
UniProt ID Q8IYT4
Protein name Katanin p60 ATPase-containing subunit A-like 2 (Katanin p60 subunit A-like 2) (EC 5.6.1.1) (p60 katanin-like 2)
Protein function Severs microtubules in vitro in an ATP-dependent manner. This activity may promote rapid reorganization of cellular microtubule arrays.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08513 LisH 27 53 LisH Domain
PF00004 AAA 290 422 ATPase family associated with various cellular activities (AAA) Domain
PF17862 AAA_lid_3 450 497 AAA+ lid domain Domain
Sequence
MELSYQTLKFTHQAREACEMRTEARRKNLLILISHYLTQEGYIDTANALEQETKLGLRRF
EVCDNIDLETILMEYESYYFVKFQKYPKIVKKSSDTAENNLPQRSRGKTRRMMNDSCQNL
PKINQQRPRSKTTAGKTGDTKSLNKEHPNQEVVDNTRLESANFGLHISRIRKDSGEENAH
PRRGQIIDFQGLLTDAIKGATSELALNTFDHNPDPSERLLKPLSAFIGMNSEMRELAAVV
SRDIYLHNPNIKWNDIIGLDAAKQLVKEAVVYPIRYPQLFTGILSPWKGLLLYGPPGTGK
TLLAKAVATECKTTFFNISASTIVSKWRGDSEKLVRVLFELARYHAPSTIFLDELESVMS
QRGTASGGEHEGSLRMKTELLVQMDGLARSEDLVFVLAASNLPWELDCAMLRRLEKRILV
DL
PSREARQAMIYHWLPPVSKSRALELHTELEYSVLSQETEGYSGSDIKLVCREAAMRPV
RKIFDALENHQSESSDL
PRIQLDIVTTADFLDVLTHTKPSAKNLAQRYSDWQREFESV
Sequence length 538
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
Dementia Dementia N/A N/A GWAS
Neurodevelopmental Disorders complex neurodevelopmental disorder N/A N/A GenCC
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Autism Spectrum Disorder Associate 22495311
Autistic Disorder Associate 22495311
Carcinogenesis Associate 23018867
Carcinoma Ovarian Epithelial Associate 33482905
Mouth Diseases Associate 23018867
Radiation induced meningioma Associate 21364586
Restless Legs Syndrome Associate 22929029