Incidental Mutation 'R8514:Tex101'
ID 656029
Institutional Source Beutler Lab
Gene Symbol Tex101
Ensembl Gene ENSMUSG00000062773
Gene Name testis expressed gene 101
Synonyms TES101RP, 1700008H15Rik
MMRRC Submission
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R8514 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 24668007-24676675 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to A at 24668532 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Glutamine to Leucine at position 167 (Q167L)
Ref Sequence ENSEMBL: ENSMUSP00000077150 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078001] [ENSMUST00000205488] [ENSMUST00000206390]
AlphaFold Q9JMI7
Predicted Effect possibly damaging
Transcript: ENSMUST00000078001
AA Change: Q167L

PolyPhen 2 Score 0.872 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000077150
Gene: ENSMUSG00000062773
AA Change: Q167L

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 possibly damaging
Transcript: ENSMUST00000205488
AA Change: Q167L

PolyPhen 2 Score 0.872 (Sensitivity: 0.83; Specificity: 0.93)
Predicted Effect possibly damaging
Transcript: ENSMUST00000206390
AA Change: Q167L

PolyPhen 2 Score 0.872 (Sensitivity: 0.83; Specificity: 0.93)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.3%
Validation Efficiency 96% (49/51)
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: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Bcam A G 7: 19,758,541 V543A probably damaging Het
C330027C09Rik T C 16: 48,997,447 V60A possibly damaging Het
Capn1 T C 19: 5,997,824 E403G probably damaging Het
Casp12 T C 9: 5,352,735 F186L probably damaging Het
Ccdc40 A G 11: 119,230,633 Q13R unknown Het
Ckap2l G T 2: 129,285,868 A130E possibly damaging Het
Creld1 C T 6: 113,492,869 R411C probably damaging Het
Dock9 A T 14: 121,658,787 S167T probably benign Het
Emc10 G T 7: 44,493,222 Q99K probably damaging Het
Fam26f G A 10: 34,126,403 T228I possibly damaging Het
Fryl T A 5: 73,085,356 I1287L probably benign Het
Gjc3 T A 5: 137,957,510 Y171F probably damaging Het
Glrp1 GTGCTGCTGCTGCTGCTG GTGCTGCTGCTGCTG 1: 88,503,320 probably benign Het
Gm597 C T 1: 28,778,505 V149M probably damaging Het
Golga4 T C 9: 118,555,796 V662A possibly damaging Het
Gpr33 A G 12: 52,023,398 V286A probably benign Het
Htr1d A G 4: 136,443,339 E293G probably damaging Het
Ints6 A G 14: 62,695,717 V847A possibly damaging Het
Iqsec3 A G 6: 121,413,562 C317R unknown Het
Mdn1 T A 4: 32,739,857 Y3704N probably damaging Het
Micall2 C A 5: 139,716,222 R422L probably damaging Het
Mndal T C 1: 173,860,192 D492G possibly damaging Het
Myom2 C T 8: 15,125,153 P1244L possibly damaging Het
Notch1 A G 2: 26,472,169 C1025R probably damaging Het
Nthl1 G A 17: 24,634,115 V98M probably damaging Het
Olfr1145 A T 2: 87,810,710 I297F probably damaging Het
Olfr1234 T C 2: 89,363,229 I67V probably benign Het
Pank3 A G 11: 35,776,359 D101G probably null Het
Phtf2 T C 5: 20,802,032 R178G possibly damaging Het
Pitrm1 T C 13: 6,568,786 probably null Het
Platr25 T C 13: 62,700,772 Y92C probably damaging Het
Plpp1 A T 13: 112,834,928 D43V probably damaging Het
Prg4 G A 1: 150,454,645 T759I unknown Het
Pros1 A G 16: 62,910,109 T321A probably benign Het
Rad50 G A 11: 53,678,939 Q882* probably null Het
Rasa3 A C 8: 13,581,322 F533V probably benign Het
Rgs18 T A 1: 144,754,027 I165F probably damaging Het
Rtl1 C T 12: 109,593,873 V511I possibly damaging Het
Sdc3 A G 4: 130,818,761 T144A unknown Het
Slc9a9 T C 9: 94,936,365 F271L probably benign Het
Snrpa1 G A 7: 66,070,633 G195R probably benign Het
Tcerg1 T A 18: 42,564,122 D759E probably damaging Het
Tecta A G 9: 42,373,110 L893P probably damaging Het
Tnrc6a C T 7: 123,184,215 R970* probably null Het
Trmt1l T C 1: 151,453,991 S562P probably damaging Het
Ubn1 A G 16: 5,073,399 E546G probably damaging Het
Usp38 T A 8: 80,985,717 Q563L probably benign Het
Vmn1r1 C T 1: 182,157,573 V176I probably benign Het
Vmn2r1 A G 3: 64,086,521 K96R probably benign Het
Vmn2r62 A G 7: 42,764,568 V817A probably benign Het
Wdfy3 A T 5: 101,851,353 C3066S possibly damaging Het
Yeats4 T C 10: 117,215,755 E199G possibly damaging Het
Zcchc11 T A 4: 108,557,357 W44R possibly damaging Het
Other mutations in Tex101
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02313:Tex101 APN 7 24668325 missense probably damaging 1.00
IGL03007:Tex101 APN 7 24670481 splice site probably benign
IGL03357:Tex101 APN 7 24668333 missense probably damaging 0.96
R1935:Tex101 UTSW 7 24668225 missense probably benign 0.33
R1936:Tex101 UTSW 7 24668225 missense probably benign 0.33
R4632:Tex101 UTSW 7 24668368 nonsense probably null
R6109:Tex101 UTSW 7 24668313 missense possibly damaging 0.79
R7049:Tex101 UTSW 7 24668258 missense probably benign 0.03
R7276:Tex101 UTSW 7 24670404 missense probably damaging 1.00
R7860:Tex101 UTSW 7 24669765 missense probably damaging 1.00
R8092:Tex101 UTSW 7 24670353 missense probably damaging 1.00
R8435:Tex101 UTSW 7 24668366 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TCATGGCCATCAGTCTGCAG -3'
(R):5'- TCTACACAGCACAGGTAGGG -3'

Sequencing Primer
(F):5'- ATCAGTCTGCAGCCGATCGTAG -3'
(R):5'- GGAGATACAACAGCCAGGACC -3'
Posted On 2020-10-20