TEX26

testis expressed 26

Basic information

Region (hg38): 13:30932656-30975500

Previous symbols: [ "C13orf26" ]

Links

ENSG00000175664NCBI:122046HGNC:28622Uniprot:Q8N6G2AlphaFoldGenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the TEX26 gene.

  • not_specified (48 variants)
  • not_provided (2 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the TEX26 gene is commonly pathogenic or not. These statistics are base on transcript: NM_000152325.3. Only rare variants are included in the table.

In the table, we include only reliable ClinVar variants with their consequences to MANE Select, Mane Plus Clinical transcripts, or transcripts with TSL equals 1. Click the count to view the source variants.

Warning: slight differences between displayed counts and the number of variants in ClinVar may occur, primarily due to (1) the application of a different transcript and/or consequence by our variant effect predictor or (2) differences in clinical significance: we classify Benign/Likely benign variants as Likely benign and Pathogenic/Likely pathogenic variants as Likely pathogenic.

EffectPLPVUSLBBSum
synonymous
1
clinvar
1
missense
47
clinvar
2
clinvar
49
nonsense
0
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
0
Total 0 0 47 3 0
Loading clinvar variants...

GnomAD

Source: gnomAD

GeneTypeBio TypeTranscript Coding Exons Length
TEX26protein_codingprotein_codingENST00000380473 742800
pLI Probability
LOF Intolerant
pRec Probability
LOF Recessive
Individuals with
no LOFs
Individuals with
Homozygous LOFs
Individuals with
Heterozygous LOFs
Defined p
3.14e-90.1735484415696552071257470.340
Z-Score Observed Expected Observed/Expected Mutation Rate Total Possible in Transcript
Missense-1.141841451.260.000007071896
Missense in Polyphen5742.9111.3283577
Synonymous-1.416451.11.250.00000247514
Loss of Function0.3811415.60.8967.45e-7189

LoF frequencies by population

EthnicitySum of pLOFs p
African & African-American0.3970.397
Ashkenazi Jewish0.4010.399
East Asian0.3030.303
Finnish0.4020.401
European (Non-Finnish)0.3760.374
Middle Eastern0.3030.303
South Asian0.3700.368
Other0.3730.371

dbNSFP

Source: dbNSFP

Intolerance Scores

loftool
rvis_EVS
0.46
rvis_percentile_EVS
78.59

Haploinsufficiency Scores

pHI
0.0488
hipred
N
hipred_score
0.180
ghis
0.385

Essentials

essential_gene_CRISPR
N
essential_gene_CRISPR2
N
essential_gene_gene_trap
N
gene_indispensability_pred
N
gene_indispensability_score
0.114

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumHigh
CancerMediumMediumMedium

Mouse Genome Informatics

Gene name
Tex26
Phenotype

Gene ontology

Biological process
Cellular component
cytoplasm
Molecular function