Gene Gene information from NCBI Gene database.
Entrez ID 83473
Gene name Katanin catalytic subunit A1 like 2
Gene symbol KATNAL2
Synonyms (NCBI Gene)
-
Chromosome 18
Chromosome location 18q21.1
miRNA miRNA information provided by mirtarbase database.
36
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
25
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
614697 25387 ENSG00000167216
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
47
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Likely benign rs117367547 RCV005901847
Familial cancer of breast Benign rs139560400 RCV005931848
Gastric cancer Benign rs139560400, rs144819676 RCV005931851
RCV005901835
KATNAL2-related autism Uncertain significance rs1569106508 RCV004799389
Associations from Text MiningDisease 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