Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
165186
Gene name Gene Name - the full gene name approved by the HGNC.
TOG array regulator of axonemal microtubules 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TOGARAM2
Synonyms (NCBI Gene) Gene synonyms aliases
FAM179A
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p23.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT713404 hsa-miR-548n HITS-CLIP 19536157
MIRT713403 hsa-miR-548az-5p HITS-CLIP 19536157
MIRT713402 hsa-miR-548t-5p HITS-CLIP 19536157
MIRT713401 hsa-miR-6871-3p HITS-CLIP 19536157
MIRT713399 hsa-miR-7108-3p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000226 Process Microtubule cytoskeleton organization IBA 21873635
GO:0005815 Component Microtubule organizing center IBA 21873635
GO:0005876 Component Spindle microtubule IBA 21873635
GO:0005881 Component Cytoplasmic microtubule IBA 21873635
GO:0005929 Component Cilium IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
620949 33715 ENSG00000189350
Protein
UniProt ID Q6ZUX3
Protein name TOG array regulator of axonemal microtubules protein 2 (Crescerin-2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12348 CLASP_N 492 689 CLASP N terminal Family
Sequence
MGTRDDVPEAKVLVPVAVYCGSIPRTSAGPRVLPPGSINSSLPHGEGSLQPEPRALLNNE
EPSQLLRGLGQLGGLKLDTPSKGWQARNGHPRNLRALSLGDQPLVLLPSPESEANSVARD
TIQIKDKLKKRRLSEGLAASSRASLDPGGGPQGVPLHSTIPRATSQRLLRVPRPMPLIQS
IPTTPEASGVKEKGLDLPGSIPGPHELRPGAQEAQISWQYLHCNDEKMQKSLGAIVIPPI
PKARTVAATPSRVPGSLPSPLPPGQGVLTGLRAPRTRLARGSGPREKTPASLEPKPLASP
IRDRPAAAKKPALPFSQSAPTLTAFSFDCAREACPPLKEEDQKEIGTKIQVTISKSAREK
MQLKQMKEMELLRRLEEPRTGQELTSQCLGSQRAFMKEGLLPLRGSGTLSVPTRLSGPCR
NDVSIILRKWASRASLPSIPISRQEPRFARHASANSLPAVLTLGSPEWEEEEEMDLRACK
ELRPFSNPELGLRDALQCLNSSDWQMKEKGLVSIQRLAACHSEVLTGKLHDVCLVVTGEV
TNLRSKVSHLAISTLGDLFQALKKNMDQEAEEIARCLLQKMADTNEFIQRAAGQSLRAMV
ENVTLARSLVVLTSAGVYHRNPLIRKYAAEHLSAVLEQIGAEKLLSGTRDSTDMLVHNLV
RLAQDSNQDTRFYGRKMVNILMANTKFDA
FLKQSLPSYDLQKVMAAIKQQGIEDNDELPS
AKGRKVLRSLVVCENGLPIKEGLSCNGPRLVGLRSTLQGRGEMVEQLRELTRLLEAKDFR
SRMEGVGQLLELCKAKTELVTAHLVQVFDAFTPRLQDSNKKVNQWALESFAKMIPLLRES
LHPMLLSIIITVADNLNSKNSGIYAAAVAVLDAMVESLDNLCLLPALAGRVRFLSGRAVL
DVTDRLAVLVASVYPRKPQAVERHVLPILWHFLNTATRNGTLPGPSGNIRGVVCRLSRSL
QEHMGSRLLDFAASQPKHVLKTLQELLDSESLGGSRKATDRGVAPDSKTTGSSYPFQLD
Sequence length 1019
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Narcolepsy Narcolepsy rs104894574, rs387906655 19629137
Unknown
Disease term Disease name Evidence References Source
Mental Depression Mental Depression GWAS
Eosinophilia Eosinophilia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Personality Disorders Associate 33450964
Prostatic Neoplasms Associate 33450964