Incidental Mutation 'R5804:Tex26'
ID 448402
Institutional Source Beutler Lab
Gene Symbol Tex26
Ensembl Gene ENSMUSG00000029660
Gene Name testis expressed 26
Synonyms 4930588N13Rik
MMRRC Submission 043211-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.071) question?
Stock # R5804 (G1)
Quality Score 225
Status Not validated
Chromosome 5
Chromosomal Location 149363125-149394444 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 149386612 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Serine at position 137 (N137S)
Ref Sequence ENSEMBL: ENSMUSP00000143863 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031667] [ENSMUST00000200985] [ENSMUST00000201610] [ENSMUST00000201683] [ENSMUST00000202677] [ENSMUST00000202920]
AlphaFold Q0VB26
Predicted Effect possibly damaging
Transcript: ENSMUST00000031667
AA Change: N221S

PolyPhen 2 Score 0.920 (Sensitivity: 0.81; Specificity: 0.94)
Predicted Effect probably benign
Transcript: ENSMUST00000200985
Predicted Effect probably benign
Transcript: ENSMUST00000201610
Predicted Effect possibly damaging
Transcript: ENSMUST00000201683
AA Change: N222S

PolyPhen 2 Score 0.920 (Sensitivity: 0.81; Specificity: 0.94)
Predicted Effect probably benign
Transcript: ENSMUST00000202677
Predicted Effect possibly damaging
Transcript: ENSMUST00000202920
AA Change: N137S

PolyPhen 2 Score 0.920 (Sensitivity: 0.81; Specificity: 0.94)
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.5%
  • 20x: 95.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abat A T 16: 8,396,100 (GRCm39) R19* probably null Het
Abcb9 A G 5: 124,218,118 (GRCm39) M406T probably benign Het
Ager A G 17: 34,817,157 (GRCm39) E32G probably damaging Het
Cdk10 T A 8: 123,955,579 (GRCm39) probably null Het
Cfap97d1 A G 11: 101,881,640 (GRCm39) N112S probably damaging Het
Ctsl A T 13: 64,514,302 (GRCm39) Y259N probably damaging Het
Ctu2 T C 8: 123,207,965 (GRCm39) probably null Het
Dse T A 10: 34,029,375 (GRCm39) I572F possibly damaging Het
Flt1 A T 5: 147,517,247 (GRCm39) probably null Het
Gatm T A 2: 122,433,083 (GRCm39) Y193F probably benign Het
Gpaa1 T C 15: 76,216,826 (GRCm39) F170S probably damaging Het
Grm3 A G 5: 9,620,155 (GRCm39) L363P probably benign Het
Heatr5b G A 17: 79,138,951 (GRCm39) P64S probably damaging Het
Hfm1 A G 5: 107,026,455 (GRCm39) probably null Het
Hivep2 A C 10: 14,009,519 (GRCm39) K1725N probably benign Het
Hmcn1 A T 1: 150,550,098 (GRCm39) C2695* probably null Het
Hmgcr G A 13: 96,802,695 (GRCm39) T68M probably damaging Het
Igsf21 A T 4: 139,755,385 (GRCm39) D423E possibly damaging Het
Jag1 T C 2: 136,930,124 (GRCm39) N751S probably benign Het
Klrc2 A T 6: 129,637,436 (GRCm39) N28K possibly damaging Het
Lrrc8c A T 5: 105,727,423 (GRCm39) D29V possibly damaging Het
Mtcl1 A C 17: 66,650,132 (GRCm39) S1329A probably benign Het
Nin C T 12: 70,092,375 (GRCm39) V645I possibly damaging Het
Or4c127 T C 2: 89,833,332 (GRCm39) I194T possibly damaging Het
Or51i1 T C 7: 103,671,439 (GRCm39) I29V probably benign Het
Or8s2 T A 15: 98,276,215 (GRCm39) M259L probably benign Het
Or9g4 T A 2: 85,504,682 (GRCm39) D271V probably damaging Het
Pfpl A T 19: 12,407,027 (GRCm39) H426L probably benign Het
Poteg A G 8: 27,946,826 (GRCm39) D238G probably damaging Het
Psen1 T C 12: 83,778,474 (GRCm39) F386L probably damaging Het
Rassf9 A T 10: 102,380,905 (GRCm39) I96F probably damaging Het
Robo1 T C 16: 72,840,077 (GRCm39) probably null Het
Slc16a4 A T 3: 107,206,280 (GRCm39) M117L probably benign Het
Slc4a8 A G 15: 100,689,506 (GRCm39) N372S possibly damaging Het
Stmn4 G A 14: 66,593,748 (GRCm39) G47D probably benign Het
Ttn T A 2: 76,747,163 (GRCm39) I4629F probably benign Het
Ubash3a G A 17: 31,427,206 (GRCm39) probably null Het
Ube3d T C 9: 86,307,401 (GRCm39) I233V probably benign Het
Utrn T A 10: 12,297,369 (GRCm39) T680S probably damaging Het
Vps13d G A 4: 144,826,640 (GRCm39) T2846I probably benign Het
Zbtb22 TGGACCCGGGAC TGGACCCGGGACCCGGGAC 17: 34,137,593 (GRCm39) probably null Het
Zfp41 C T 15: 75,490,557 (GRCm39) P170S probably damaging Het
Other mutations in Tex26
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02527:Tex26 APN 5 149,380,407 (GRCm39) missense probably damaging 1.00
R0401:Tex26 UTSW 5 149,384,323 (GRCm39) missense probably benign 0.01
R2063:Tex26 UTSW 5 149,363,204 (GRCm39) missense probably damaging 0.98
R2424:Tex26 UTSW 5 149,393,913 (GRCm39) utr 3 prime probably benign
R3779:Tex26 UTSW 5 149,369,316 (GRCm39) missense probably damaging 0.96
R4361:Tex26 UTSW 5 149,384,388 (GRCm39) missense probably benign 0.01
R4434:Tex26 UTSW 5 149,376,820 (GRCm39) missense probably benign 0.08
R5791:Tex26 UTSW 5 149,363,240 (GRCm39) splice site probably null
R8898:Tex26 UTSW 5 149,380,369 (GRCm39) missense probably benign
R9007:Tex26 UTSW 5 149,376,884 (GRCm39) missense probably damaging 1.00
R9063:Tex26 UTSW 5 149,393,826 (GRCm39) missense probably damaging 1.00
R9766:Tex26 UTSW 5 149,386,642 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CTGGTCTCCTGAAAATGGCGAC -3'
(R):5'- AGCATATTCAGAAAGGCATTCGC -3'

Sequencing Primer
(F):5'- ACCACACTCGAGCCTTTGG -3'
(R):5'- CAGAAAGGCATTCGCTATCCTGATG -3'
Posted On 2016-12-15