GTPBP10

protein-coding

GTP binding protein 10

Gene summary

Small G proteins, such as GTPBP10, act as molecular switches that play crucial roles in the regulation of fundamental cellular processes such as protein synthesis, nuclear transport, membrane trafficking, and signal transduction (Hirano et al., 2006 [PubMed 17054726]).[supplied by OMIM, Mar 2008]

MANE transcript

NM_033107.4

Inheritance

—

ClinVar variants

U:56B:2

Top phenotype

—

gnomAD constraint

pLI —, LoF o/e 0.39

Max pathogenic AF

—

Genomic locus

chr7:90,335,223-90,391,453

External References & Databases

Transcript & Mutation Effects

hg38 • Region Span ~56.2 kb
Loading mutation effect viewer...

GenCC Phenotypes & Disease Associations

Curated gene-disease validity assertions and inheritance patterns

No GenCC data available for this gene.

ClinVar Associated Diseases & Phenotypes

Reported disease conditions connected to GTPBP10 variants in ClinVar

1 Conditions Cataloged
not specifiedTotal: 48

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript NM_033107.4. Only rare variants are included.

We include only reliable ClinVar variants with their consequences to MANE Select, MANE Plus Clinical transcripts, or transcripts with TSL equal to 1. Click a count to filter the variants table below.

Slight differences between displayed counts and ClinVar may occur due to a different transcript/consequence chosen by our variant effect predictor, or because we classify Benign/Likely benign as Likely benign and Pathogenic/Likely pathogenic as Likely pathogenic.

EffectPLPVUSLBBSum
synonymous
1
clinvar
1
missense
48
clinvar
2
clinvar
50
nonsense
2
clinvar
2
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
5
clinvar
5
Total00562058
Loading ClinVar variants...

Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 4 of 30 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
NM_033107.4RefSeqNP_149098.210MANE Select
ENST00000222511.11EnsemblENSP00000222511.710MANE Select
NM_001042717.3RefSeqNP_001036182.18Standard
ENST00000257659.12EnsemblENSP00000257659.88Standard

Gene Ontology (GO) Annotations & Pathways

Biological processes, molecular functions, cellular components and pathways

Biological Process

  • ribosome biogenesis

Molecular Function

  • RNA binding
  • protein binding
  • GTP binding

Cellular Component

  • chromosome
  • nucleolus

gnomAD Constraint

Source: gnomAD

Gene type
protein_coding
Transcript type
protein_coding
Transcript
ENST00000222511
Coding exons
10
Length
56233
Individuals with no LoFs
125704
Homozygous LoFs
0
Heterozygous LoFs
43
Defined
125747
p
0.000171
Z-ScoreObservedExpectedObserved/ExpectedMutation RateTotal Possible
Missense0.2061891970.9590.000009332535
Missense (PolyPhen)7077.4480.90384936
Synonymous0.1116667.20.9830.00000328724
Loss of Function2.37717.80.3948.47e-7249

Population LoF Frequency

PopulationCAFp-valueStatus
African0.000250.00025rare
Latino/Admixed American0.000160.00014rare
Ashkenazi Jewish00.0absent
East Asian0.000610.00060rare
Finnish0.0000940.000092rare
European (Non-Finnish)0.000170.00017rare
South Asian0.0000330.000033rare
Other0.000170.00016rare

dbNSFP Gene Annotations

Source: dbNSFP

Function
FUNCTION: May be involved in the ribosome maturation process. Complements an ObgE(CgtA) function in E.coli ribosome maturation. Plays a role of GTPase in vitro. When missing, disorganization of the nucleolar architecture is observed. {ECO:0000269|PubMed:17054726}.;

Recessive Scores

pRec
0.0979

Intolerance Scores

LoFtool
0.850
RVIS EVS
1.08
RVIS percentile EVS
91.81

Essentials

Essential (CRISPR)
N
Essential (CRISPR2)
S
Essential (gene trap)
E
Indispensability pred.
E
Indispensability score
0.564

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumMedium
CancerMediumMediumMedium
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