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Gene Gene information from NCBI Gene database.
Entrez ID 347688
Gene name Tubulin beta 8 class VIII
Gene symbol TUBB8
Synonyms (NCBI Gene)
OOMDOOMD2OZEMA2bA631M21.2
Chromosome 10
Chromosome location 10p15.3
Summary The protein encoded by this gene represents the primary beta-tubulin subunit of oocytes and the early embryo. Defects in this gene, which is primate-specific, are a cause of oocyte maturation defect 2 and infertility. [provided by RefSeq, Mar 2016]
SNPs SNP information provided by dbSNP.
12 Show/Hide all (12)
SNP ID Visualize variation Clinical significance Consequence
rs782246853 C>-,CC Pathogenic Coding sequence variant, intron variant, frameshift variant
rs782269374 C>T Likely-pathogenic Coding sequence variant, missense variant
rs869025271 A>G Pathogenic Coding sequence variant, missense variant
rs869025272 C>T Pathogenic Coding sequence variant, missense variant
rs869025273 C>T Pathogenic Coding sequence variant, intron variant, upstream transcript variant, genic upstream transcript variant, missense variant
miRNA miRNA information provided by mirtarbase database.
28 Show/Hide all (28)
miRTarBase ID miRNA Experiments Reference
MIRT517366 hsa-miR-5680 PAR-CLIP 20371350
MIRT517365 hsa-miR-8060 PAR-CLIP 20371350
MIRT517364 hsa-miR-3185 PAR-CLIP 20371350
MIRT517363 hsa-miR-4253 PAR-CLIP 20371350
MIRT517362 hsa-miR-6862-5p PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
26 Show/Hide all (26)
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0000226 Process Microtubule cytoskeleton organization IBA
GO:0000278 Process Mitotic cell cycle IBA
GO:0001556 Process Oocyte maturation IMP 26789871
GO:0003924 Function GTPase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616768 20773 ENSG00000261456
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q3ZCM7
Protein name Tubulin beta-8 chain (Tubulin beta 8 class VIII)
Protein function Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers. Microtubules grow by the addition of GTP-tubulin dimers to the microtubule en
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00091 Tubulin 3 → 212 Tubulin/FtsZ family, GTPase domain Domain
PF03953 Tubulin_C 261 → 383 Tubulin C-terminal domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed at a high level in oocytes, at different stages of development. {ECO:0000269|PubMed:26789871}.
Sequence
Sequence length 444
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
KEGG Pathway Reactome Pathway
Phagosome Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane
Gap junction MHC class II antigen presentation
Motor proteins Separation of Sister Chromatids
Alzheimer disease Resolution of Sister Chromatid Cohesion
Parkinson disease HSP90 chaperone cycle for steroid hormone receptors (SHR)
Amyotrophic lateral sclerosis Recruitment of NuMA to mitotic centrosomes
Huntington disease Recycling pathway of L1
Prion disease Cilium Assembly
Pathways of neurodegeneration - multiple diseases RHO GTPases activate IQGAPs
Pathogenic Escherichia coli infection RHO GTPases Activate Formins
Salmonella infection COPI-mediated anterograde transport
  COPI-dependent Golgi-to-ER retrograde traffic
  COPI-independent Golgi-to-ER retrograde traffic
  Mitotic Prometaphase
  The role of GTSE1 in G2/M progression after G2 checkpoint
  Carboxyterminal post-translational modifications of tubulin
  HCMV Early Events
  Aggrephagy
  EML4 and NUDC in mitotic spindle formation
  Sealing of the nuclear envelope (NE) by ESCRT-III
  Kinesins
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
15
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Inherited oocyte maturation defect Likely pathogenic rs782269374 RCV000856582
★★★★★
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ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Oocyte maturation defect 2 Pathogenic; Likely pathogenic rs869025271, rs869025272, rs869025273, rs869025611, rs869025612, rs869025610, rs869025609, rs1057520306, rs1057520307, rs782246853, rs1588270347, rs782269374, rs1834346707, rs1834347552, rs1834348631
View all (22 more)
RCV000207100
RCV000207225
RCV000207037
RCV000208778
RCV000208765
View all (32 more)
★★★★★
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Show/Hide Unknown Diseases (13)
Phenotype Name Clinical Significance Source Reference Evidence Score
Aplasia/Hypoplasia of the phalanges of the 4th toe not provided ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CIC-rearranged sarcoma not provided ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Familial cancer of breast Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Female infertility Uncertain significance ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
FEMALE INFERTILITY DUE TO OOCYTE MEIOTIC ARREST — Orphanet 26789871
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (10)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Carcinoma Embryonal Embryonal carcinoma Pubtator 36735156 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Carcinoma Squamous Cell Squamous cell carcinoma Pubtator 39237897 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Congenital Abnormalities Congenital abnormalities Pubtator 38007525 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Developmental Disabilities Developmental disability Pubtator 38007525 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Female infertility due to oocyte meiotic arrest Female infertility Orphanet
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Infertility Infertility Pubtator 29704226, 32063091, 36197634, 37904145, 38007525 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Infertility Female Female infertility Pubtator 30297906, 32524331, 36197634, 36735156, 38007525 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
OOCYTE MATURATION DEFECT 2 Oocyte Maturation Defect UNIPROT_DG 26789871, 27273344
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ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
OOCYTE MATURATION DEFECT 2 Oocyte Maturation Defect CTD_human_DG
★★★★★
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
OOCYTE MATURATION DEFECT 2 Oocyte Maturation Defect CLINVAR_DG
★★★★★
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)