Incidental Mutation 'R3794:Tex16'
ID 272708
Institutional Source Beutler Lab
Gene Symbol Tex16
Ensembl Gene ENSMUSG00000034555
Gene Name testis expressed gene 16
Synonyms 4933403O08Rik
MMRRC Submission 040756-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.072) question?
Stock # R3794 (G1)
Quality Score 222
Status Validated
Chromosome X
Chromosomal Location 110804655-111159053 bp(+) (GRCm39)
Type of Mutation start codon destroyed
DNA Base Change (assembly) T to G at 111150375 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Arginine at position 1 (M1R)
Ref Sequence ENSEMBL: ENSMUSP00000132926 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000132037] [ENSMUST00000152343] [ENSMUST00000164272] [ENSMUST00000207962]
AlphaFold A2RT18
Predicted Effect probably benign
Transcript: ENSMUST00000132037
Predicted Effect probably null
Transcript: ENSMUST00000152343
AA Change: M1R

PolyPhen 2 Score 0.272 (Sensitivity: 0.91; Specificity: 0.88)
Predicted Effect probably null
Transcript: ENSMUST00000164272
AA Change: M1R

PolyPhen 2 Score 0.272 (Sensitivity: 0.91; Specificity: 0.88)
Predicted Effect probably benign
Transcript: ENSMUST00000207962
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.4%
Validation Efficiency 97% (37/38)
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy6 C T 15: 98,496,824 (GRCm39) V482I probably damaging Het
Adgrv1 T A 13: 81,431,486 (GRCm39) M1L probably damaging Het
Ceacam13 A G 7: 17,747,340 (GRCm39) *264W probably null Het
Dennd5b A T 6: 149,002,715 (GRCm39) D31E possibly damaging Het
Dip2c T C 13: 9,654,597 (GRCm39) V706A probably damaging Het
Enpp3 T C 10: 24,707,630 (GRCm39) probably null Het
Exoc4 T G 6: 33,452,932 (GRCm39) V474G probably benign Het
F2rl1 A G 13: 95,649,719 (GRCm39) Y388H unknown Het
Fasl T C 1: 161,609,306 (GRCm39) R17G probably benign Het
Htr1a G A 13: 105,580,852 (GRCm39) V31M possibly damaging Het
Inpp4b T C 8: 82,759,845 (GRCm39) V445A probably damaging Het
Itih3 T C 14: 30,640,351 (GRCm39) Y319C probably damaging Het
Katnip A G 7: 125,419,261 (GRCm39) N476S probably benign Het
Kmt2d T C 15: 98,735,240 (GRCm39) probably benign Het
Mobp A T 9: 119,997,033 (GRCm39) K55* probably null Het
Ndufaf5 T A 2: 140,044,843 (GRCm39) M279K possibly damaging Het
Nlrc3 T C 16: 3,765,739 (GRCm39) I1057V probably benign Het
Or10al7 A G 17: 38,365,786 (GRCm39) Y224H probably damaging Het
Or4c112 G T 2: 88,853,770 (GRCm39) H192Q probably benign Het
Piezo2 C T 18: 63,214,864 (GRCm39) R1257Q probably damaging Het
Pigv A G 4: 133,392,502 (GRCm39) S223P possibly damaging Het
Pkdcc A G 17: 83,531,382 (GRCm39) T464A probably damaging Het
Polr2k A G 15: 36,175,193 (GRCm39) I18V probably damaging Het
Pon3 A G 6: 5,221,578 (GRCm39) Y351H probably benign Het
Rsf1 ATGGCG ATGGCGACGGTGGCG 7: 97,229,111 (GRCm39) probably benign Het
Scaf8 A G 17: 3,240,524 (GRCm39) E632G probably damaging Het
Smurf1 A G 5: 144,837,985 (GRCm39) probably null Het
Tln1 G T 4: 43,536,295 (GRCm39) A1999D probably damaging Het
Trgv5 A T 13: 19,376,694 (GRCm39) H47L probably benign Het
Ttn C T 2: 76,772,781 (GRCm39) V2405I possibly damaging Het
Vps13d G A 4: 144,812,007 (GRCm39) probably benign Het
Xrcc1 A G 7: 24,269,985 (GRCm39) T469A probably benign Het
Zfp287 G T 11: 62,605,070 (GRCm39) H612Q probably damaging Het
Zfp352 C T 4: 90,113,386 (GRCm39) H509Y probably damaging Het
Other mutations in Tex16
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01712:Tex16 APN X 111,003,451 (GRCm39) missense probably damaging 1.00
IGL02576:Tex16 APN X 111,028,653 (GRCm39) missense probably benign 0.07
IGL03261:Tex16 APN X 111,028,552 (GRCm39) missense possibly damaging 0.90
R1766:Tex16 UTSW X 111,150,782 (GRCm39) missense probably benign 0.02
R2274:Tex16 UTSW X 111,030,838 (GRCm39) missense probably damaging 0.98
R3607:Tex16 UTSW X 111,003,667 (GRCm39) missense probably damaging 1.00
R4209:Tex16 UTSW X 111,030,640 (GRCm39) missense probably benign 0.01
R4210:Tex16 UTSW X 111,030,640 (GRCm39) missense probably benign 0.01
U24488:Tex16 UTSW X 111,028,815 (GRCm39) missense probably benign 0.05
Z1176:Tex16 UTSW X 111,151,010 (GRCm39) missense probably benign 0.36
Predicted Primers PCR Primer
(F):5'- TGTGAATCCAAACTTCCAGTACAG -3'
(R):5'- ACCCAGTGAAGTGCAAAGTTG -3'

Sequencing Primer
(F):5'- CAGACGCACTCAAAATATTTCTGATG -3'
(R):5'- CAACAAGTATTGCGGTGCC -3'
Posted On 2015-03-25