Incidental Mutation 'R7049:Tex101'
ID 547482
Institutional Source Beutler Lab
Gene Symbol Tex101
Ensembl Gene ENSMUSG00000062773
Gene Name testis expressed gene 101
Synonyms 1700008H15Rik, TES101RP
MMRRC Submission 045147-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7049 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 24367437-24371475 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 24367683 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 223 (I223T)
Ref Sequence ENSEMBL: ENSMUSP00000077150 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078001] [ENSMUST00000205488] [ENSMUST00000206390]
AlphaFold Q9JMI7
Predicted Effect probably benign
Transcript: ENSMUST00000078001
AA Change: I223T

PolyPhen 2 Score 0.029 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000077150
Gene: ENSMUSG00000062773
AA Change: I223T

DomainStartEndE-ValueType
signal peptide 1 25 N/A INTRINSIC
Pfam:UPAR_LY6 141 217 3.9e-15 PFAM
low complexity region 232 246 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000205488
Predicted Effect probably benign
Transcript: ENSMUST00000206390
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.8%
Validation Efficiency 100% (46/46)
MGI Phenotype PHENOTYPE: Male mice homozygous for a knockout allele of this marker are infertile due to the failure of sperm to migrate into the oviduct. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca4 T C 3: 121,941,497 (GRCm39) V447A probably benign Het
Adam6b A G 12: 113,454,122 (GRCm39) D313G probably damaging Het
Adcy10 G T 1: 165,367,443 (GRCm39) C571F probably damaging Het
Anxa1 A G 19: 20,352,635 (GRCm39) V313A probably benign Het
Bpifb6 A T 2: 153,750,733 (GRCm39) probably null Het
Cacna1c C A 6: 118,578,124 (GRCm39) C1713F probably benign Het
Cep135 A G 5: 76,754,585 (GRCm39) N354S probably benign Het
Cers2 A G 3: 95,228,965 (GRCm39) D200G probably damaging Het
Cpne1 A G 2: 155,920,727 (GRCm39) L133P probably damaging Het
Ddhd1 A G 14: 45,840,138 (GRCm39) Y16H probably damaging Het
Depp1 T C 6: 116,629,254 (GRCm39) L199P probably damaging Het
Fastkd2 T C 1: 63,771,009 (GRCm39) F122L probably benign Het
Fastkd5 A T 2: 130,457,431 (GRCm39) D386E probably damaging Het
Gm5134 T A 10: 75,828,292 (GRCm39) C291S probably damaging Het
Gria2 T C 3: 80,596,634 (GRCm39) S811G probably damaging Het
Hcn1 C T 13: 118,111,998 (GRCm39) P654L unknown Het
Hrnr C A 3: 93,230,461 (GRCm39) S233* probably null Het
Hspa5 C T 2: 34,663,204 (GRCm39) P127L probably damaging Het
Itgal A T 7: 126,895,573 (GRCm39) probably benign Het
L3mbtl4 G T 17: 68,768,561 (GRCm39) R223L probably benign Het
Mical1 A G 10: 41,358,246 (GRCm39) R420G possibly damaging Het
Mllt6 T A 11: 97,564,637 (GRCm39) L481Q probably damaging Het
Mtdh T A 15: 34,131,311 (GRCm39) N174K probably damaging Het
Nhsl1 A G 10: 18,407,386 (GRCm39) M1507V probably damaging Het
Npm3 A T 19: 45,737,994 (GRCm39) M1K probably null Het
Or1e21 C T 11: 73,344,430 (GRCm39) G203R probably damaging Het
Pold1 A T 7: 44,190,795 (GRCm39) W290R possibly damaging Het
Prss52 C T 14: 64,350,021 (GRCm39) T216I probably damaging Het
Psme4 T C 11: 30,763,904 (GRCm39) probably null Het
Pwwp2a T A 11: 43,597,018 (GRCm39) F453I probably damaging Het
Rttn A G 18: 89,082,340 (GRCm39) N1422S probably damaging Het
Scaf4 A C 16: 90,057,075 (GRCm39) I92R unknown Het
Slc12a1 A G 2: 125,013,177 (GRCm39) K345E probably benign Het
Slc22a28 A T 19: 8,049,270 (GRCm39) N326K probably benign Het
Smgc A G 15: 91,744,576 (GRCm39) E311G possibly damaging Het
Snx7 C T 3: 117,633,680 (GRCm39) R90H possibly damaging Het
Tnik A T 3: 28,715,853 (GRCm39) K1093* probably null Het
Tnxb T G 17: 34,936,242 (GRCm39) probably null Het
Trio T C 15: 27,749,885 (GRCm39) N2272S possibly damaging Het
Tubal3 T C 13: 3,982,756 (GRCm39) Y179H probably damaging Het
Vmn2r4 C T 3: 64,296,550 (GRCm39) G745D probably benign Het
Vps9d1 A T 8: 123,973,882 (GRCm39) Y300* probably null Het
Zfp646 T A 7: 127,479,199 (GRCm39) C459S possibly damaging Het
Other mutations in Tex101
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02313:Tex101 APN 7 24,367,750 (GRCm39) missense probably damaging 1.00
IGL03007:Tex101 APN 7 24,369,906 (GRCm39) splice site probably benign
IGL03357:Tex101 APN 7 24,367,758 (GRCm39) missense probably damaging 0.96
R1935:Tex101 UTSW 7 24,367,650 (GRCm39) missense probably benign 0.33
R1936:Tex101 UTSW 7 24,367,650 (GRCm39) missense probably benign 0.33
R4632:Tex101 UTSW 7 24,367,793 (GRCm39) nonsense probably null
R6109:Tex101 UTSW 7 24,367,738 (GRCm39) missense possibly damaging 0.79
R7276:Tex101 UTSW 7 24,369,829 (GRCm39) missense probably damaging 1.00
R7860:Tex101 UTSW 7 24,369,190 (GRCm39) missense probably damaging 1.00
R8092:Tex101 UTSW 7 24,369,778 (GRCm39) missense probably damaging 1.00
R8435:Tex101 UTSW 7 24,367,791 (GRCm39) missense probably damaging 1.00
R8514:Tex101 UTSW 7 24,367,957 (GRCm39) missense possibly damaging 0.87
Predicted Primers PCR Primer
(F):5'- TCCAGTATCAGCAGGCAGAAGG -3'
(R):5'- GATCCCTCAGGTTTCTGGTG -3'

Sequencing Primer
(F):5'- GAAGGCTCCCTCCTAGGCAAAG -3'
(R):5'- TGCTCGGGGCTCTAGAG -3'
Posted On 2019-05-13