Gene Gene information from NCBI Gene database.
Entrez ID 55773
Gene name TBC1 domain family member 23
Gene symbol TBC1D23
Synonyms (NCBI Gene)
NS4ATP1PCH11
Chromosome 3
Chromosome location 3q12.1-q12.2
SNPs SNP information provided by dbSNP.
3
SNP ID Visualize variation Clinical significance Consequence
rs1553730885 T>AA Pathogenic Frameshift variant, coding sequence variant
rs1553731603 G>A Pathogenic Splice donor variant
rs1553731605 T>A Pathogenic Splice donor variant
miRNA miRNA information provided by mirtarbase database.
204
miRTarBase ID miRNA Experiments Reference
MIRT1412767 hsa-miR-3684 CLIP-seq
MIRT1412768 hsa-miR-4503 CLIP-seq
MIRT1412769 hsa-miR-1207-5p CLIP-seq
MIRT1412770 hsa-miR-190 CLIP-seq
MIRT1412771 hsa-miR-190b CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
21
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 29084197, 32296183, 32814053
GO:0005794 Component Golgi apparatus IDA
GO:0005794 Component Golgi apparatus IEA
GO:0005802 Component Trans-Golgi network IBA
GO:0005802 Component Trans-Golgi network IDA 28823706, 29084197, 29426865
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617687 25622 ENSG00000036054
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NUY8
Protein name TBC1 domain family member 23 (HCV non-structural protein 4A-transactivated protein 1)
Protein function Putative Rab GTPase-activating protein which plays a role in vesicular trafficking (PubMed:28823707). Involved in endosome-to-Golgi trafficking. Acts as a bridging protein by binding simultaneously to golgins, including GOLGA1 and GOLGA4, locate
PDB 6JL7 , 6JM5 , 8JJ9 , 8QQF
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00566 RabGAP-TBC 47 246 Rab-GTPase-TBC domain Family
PF00581 Rhodanese 323 440 Rhodanese-like domain Domain
Tissue specificity TISSUE SPECIFICITY: Isoform 1: Widely expressed, including in fetal adult brain (corpus callosum, pons, cerebellum), spinal cord, heart, skeletal muscle, thymus and bone marrow, and at lower levels in spleen. Hardly detected in liver, kidney, colon and te
Sequence
MAEGEDVPPLPTSSGDGWEKDLEEALEAGGCDLETLRNIIQGRPLPADLRAKVWKIALNV
AGKGDSLASWDGILDLPEQNTIHKDCLQFIDQLSVPEEKAAELLLDIESVITFYCKSRNI
KYSTSLSWIHLLKPLVHLQLPRSDLYNCFYAIMNKYIPRDCSQKGRPFHLFRLLIQYHEP
ELCSYLDTKKITPDSYALNWLGSLFACYCSTEVTQAIWDGYLQQADPFFIYFLMLIILVN
AKEVIL
TQESDSKEEVIKFLENTPSSLNIEDIEDLFSLAQYYCSKTPASFRKDNHHLFGS
TLLGIKDDDADLSQALCLAISVSEILQANQLQGEGVRFFVVDCRPAEQYNAGHLSTAFHL
DSDLMLQNPSEFAQSVKSLLEAQKQSIESGSIAGGEHLCFMGSGREEEDMYMNMVLAHFL
QKNKEYVSIASGGFMALQQH
LADINVDGPENGYGHWIASTSGSRSSINSVDGESPNGSSD
RGMKSLVNKMTVALKTKSVNVREKVISFIENTSTPVDRMSFNLPWPDRSCTERHVSSSDR
VGKPYRGVKPVFSIGDEEEYDTDEIDSSSMSDDDRKEVVNIQTWINKPDVKHHFPCKEVK
ESGHMFPSHLLVTATHMYCLREIVSRKGLAYIQSRQALNSVVKITSKKKHPELITFKYGN
SSASGIEILAIERYLIPNAGDATKAIKQQIMKVLDALES
Sequence length 699
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
40
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Pontocerebellar hypoplasia, type 11 Likely pathogenic; Pathogenic rs1354130291, rs2148863572, rs2148861371, rs2472195074, rs1553730872, rs1553730885, rs1553731605, rs1553731603, rs773150360 RCV001785049
RCV001785050
RCV001783847
RCV003229782
RCV000508996
RCV000508999
RCV000508992
RCV000508997
RCV000509001
RCV001196964
RCV005630906
Pontoneocerebellar hypoplasia Pathogenic rs1553730872, rs1553730885, rs1553731605 RCV000515777
RCV000515789
RCV000515797
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Lung cancer Benign rs150469892 RCV005911594
TBC1D23-related disorder Uncertain significance; Likely benign; Benign rs375470588, rs540028785, rs111649998, rs199619948, rs200926398, rs146856935, rs561632705, rs535337346, rs199967519, rs148623930, rs768581587 RCV003392831
RCV003908942
RCV003923958
RCV003924027
RCV003894338
RCV003974182
RCV003974283
RCV003961665
RCV003939320
RCV003924692
RCV003966770
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Non Small Cell Lung Stimulate 34363324
Neoplasm Metastasis Associate 34363324
Neoplasms Associate 34363324
Pontocerebellar Hypoplasia Type 2 Associate 36076253