Incidental Mutation 'R6970:Tenm3'
ID 542188
Institutional Source Beutler Lab
Gene Symbol Tenm3
Ensembl Gene ENSMUSG00000031561
Gene Name teneurin transmembrane protein 3
Synonyms Ten-m3, Odz3, 2610100B16Rik
MMRRC Submission 045080-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.598) question?
Stock # R6970 (G1)
Quality Score 225.009
Status Not validated
Chromosome 8
Chromosomal Location 48227682-48843951 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) C to T at 48236439 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Asparagine at position 2038 (D2038N)
Ref Sequence ENSEMBL: ENSMUSP00000033965 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000033965] [ENSMUST00000190840]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000033965
AA Change: D2038N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000033965
Gene: ENSMUSG00000031561
AA Change: D2038N

DomainStartEndE-ValueType
Pfam:Ten_N 11 177 6.9e-91 PFAM
Pfam:Ten_N 171 308 1e-72 PFAM
transmembrane domain 309 331 N/A INTRINSIC
EGF 517 545 2.32e-1 SMART
EGF_like 548 576 4.11e1 SMART
EGF 581 610 1.69e1 SMART
EGF 613 642 1.35e-2 SMART
EGF 647 677 6.11e-1 SMART
EGF 680 708 7.95e0 SMART
EGF 711 739 1.28e1 SMART
EGF 751 783 1.64e-1 SMART
PDB:1RWL|A 1276 1511 9e-6 PDB
low complexity region 2593 2602 N/A INTRINSIC
Pfam:Tox-GHH 2631 2708 1.5e-34 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000190840
AA Change: D2022N

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000140141
Gene: ENSMUSG00000031561
AA Change: D2022N

DomainStartEndE-ValueType
Pfam:Ten_N 10 182 7.6e-77 PFAM
Pfam:Ten_N 168 308 6.6e-50 PFAM
transmembrane domain 309 331 N/A INTRINSIC
EGF 517 545 2.32e-1 SMART
EGF_like 548 576 4.11e1 SMART
EGF 581 610 1.69e1 SMART
EGF 613 642 1.35e-2 SMART
EGF 647 677 6.11e-1 SMART
EGF 680 708 7.95e0 SMART
EGF 711 739 1.28e1 SMART
EGF 751 783 1.64e-1 SMART
PDB:1RWL|A 1276 1511 9e-6 PDB
low complexity region 2593 2602 N/A INTRINSIC
Pfam:Tox-GHH 2630 2708 3.2e-35 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.2%
  • 20x: 97.2%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a large transmembrane protein that may be involved in the regulation of neuronal development. Mutation in this gene causes microphthalmia. [provided by RefSeq, Aug 2015]
PHENOTYPE: Mice homozygous for a null mutation display abnormal ipsilateral retinal ganglion cell projections and impaired performance in visually mediated behavioral tasks. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 82 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017D01Rik A G 19: 11,112,314 (GRCm38) probably null Het
2410089E03Rik T C 15: 8,187,548 (GRCm38) V750A probably benign Het
Acadsb T C 7: 131,434,315 (GRCm38) Y285H possibly damaging Het
Adam17 A G 12: 21,345,668 (GRCm38) S285P probably benign Het
Adcy10 A G 1: 165,556,916 (GRCm38) N1082S probably benign Het
Ahdc1 T A 4: 133,062,345 (GRCm38) L299Q possibly damaging Het
Ambra1 T A 2: 91,772,600 (GRCm38) probably benign Het
Arfgef1 G T 1: 10,153,679 (GRCm38) Q1465K probably damaging Het
Arfgef1 T C 1: 10,153,678 (GRCm38) Q1465R probably damaging Het
Atp8a1 A G 5: 67,738,462 (GRCm38) V543A probably damaging Het
BC034090 T A 1: 155,241,439 (GRCm38) D311V probably damaging Het
Blnk G T 19: 40,962,377 (GRCm38) P110Q probably damaging Het
Cc2d2a A G 5: 43,718,585 (GRCm38) E968G probably damaging Het
Ccdc14 A T 16: 34,709,533 (GRCm38) E394V probably damaging Het
Ccdc162 A T 10: 41,615,958 (GRCm38) H1086Q probably benign Het
Ccdc85b T A 19: 5,457,220 (GRCm38) I60F probably damaging Het
Ceacam20 T A 7: 19,989,977 (GRCm38) L562Q probably damaging Het
Cntrl T C 2: 35,118,137 (GRCm38) F188L probably benign Het
Dclk1 A T 3: 55,466,601 (GRCm38) probably benign Het
Ddx20 A T 3: 105,680,358 (GRCm38) L434H probably damaging Het
Ddx51 G A 5: 110,656,862 (GRCm38) V547M probably damaging Het
Dnah11 T A 12: 118,108,944 (GRCm38) Q1472L probably benign Het
Dnajb13 T C 7: 100,507,422 (GRCm38) E149G probably damaging Het
Fat4 A G 3: 38,981,775 (GRCm38) N3192S probably damaging Het
Fat4 A T 3: 38,995,971 (GRCm38) D3994V probably damaging Het
Fcgr1 C A 3: 96,284,620 (GRCm38) probably null Het
Gm11639 A G 11: 104,776,356 (GRCm38) E1422G probably benign Het
Gm12185 G A 11: 48,907,912 (GRCm38) R585* probably null Het
Gm32687 A G 10: 81,879,470 (GRCm38) H232R probably benign Het
Gm5431 G T 11: 48,888,490 (GRCm38) A535D probably damaging Het
Gm8300 G T 12: 87,516,618 (GRCm38) probably benign Het
Gm906 A T 13: 50,246,971 (GRCm38) Y440N possibly damaging Het
Jarid2 C T 13: 44,902,985 (GRCm38) P556S probably damaging Het
Map3k4 C A 17: 12,248,916 (GRCm38) G1077V probably damaging Het
Mast4 C T 13: 102,804,647 (GRCm38) V301I probably damaging Het
Mlxip A G 5: 123,445,672 (GRCm38) T433A possibly damaging Het
Mus81 G T 19: 5,485,526 (GRCm38) H199Q probably benign Het
Mylk3 G A 8: 85,359,263 (GRCm38) T54M probably damaging Het
Nalcn A G 14: 123,314,094 (GRCm38) F1034L possibly damaging Het
Nfatc1 A C 18: 80,667,013 (GRCm38) S513A probably benign Het
Ninj2 A G 6: 120,198,131 (GRCm38) I88V possibly damaging Het
Nomo1 C T 7: 46,045,967 (GRCm38) P277L probably damaging Het
Nup214 C T 2: 32,051,798 (GRCm38) S571L probably damaging Het
Olfr1469 T A 19: 13,411,428 (GRCm38) N286K probably damaging Het
Olfr461 T C 6: 40,544,656 (GRCm38) S108G probably benign Het
Olfr980 T A 9: 40,006,713 (GRCm38) M79L probably benign Het
Pcdh15 C T 10: 74,502,687 (GRCm38) P1005S probably damaging Het
Pkhd1l1 G A 15: 44,511,674 (GRCm38) A942T possibly damaging Het
Plagl1 T C 10: 13,125,116 (GRCm38) C34R probably damaging Het
Plekha2 T C 8: 25,059,264 (GRCm38) Q168R probably benign Het
Plekha6 G A 1: 133,263,818 (GRCm38) A146T probably benign Het
Plekhm3 T G 1: 64,892,753 (GRCm38) K564T possibly damaging Het
Plpp2 A G 10: 79,530,546 (GRCm38) V26A possibly damaging Het
Prdm10 T G 9: 31,329,823 (GRCm38) Y302* probably null Het
Prdm8 A G 5: 98,184,612 (GRCm38) E124G probably damaging Het
Prg4 T G 1: 150,455,906 (GRCm38) probably benign Het
Qser1 A G 2: 104,788,130 (GRCm38) V779A probably benign Het
Rbm39 G A 2: 156,167,584 (GRCm38) R123C probably damaging Het
Ric1 C T 19: 29,587,772 (GRCm38) P640S probably damaging Het
Rpl14 G A 9: 120,574,227 (GRCm38) probably benign Het
Rsl1d1 T A 16: 11,193,694 (GRCm38) D382V probably benign Het
Rubcn G T 16: 32,868,144 (GRCm38) probably benign Het
Sec16a G A 2: 26,430,486 (GRCm38) R1361C probably damaging Het
Slc26a11 T G 11: 119,356,972 (GRCm38) V41G probably damaging Het
Slc41a2 A G 10: 83,316,096 (GRCm38) F172L possibly damaging Het
Slc4a4 A C 5: 89,179,831 (GRCm38) Y674S probably damaging Het
Strc A C 2: 121,378,014 (GRCm38) M292R probably benign Het
Syde2 A G 3: 145,988,626 (GRCm38) T210A probably benign Het
Tcf7l2 C A 19: 55,755,048 (GRCm38) A97E probably benign Het
Tepsin G A 11: 120,095,364 (GRCm38) T168M probably damaging Het
Tex15 A T 8: 33,557,428 (GRCm38) M178L probably benign Het
Tgfbr2 T C 9: 116,110,051 (GRCm38) N236S probably damaging Het
Tnrc18 A G 5: 142,727,989 (GRCm38) V2531A probably damaging Het
Ttn T G 2: 76,895,423 (GRCm38) probably benign Het
Tubgcp3 G T 8: 12,637,000 (GRCm38) D630E probably damaging Het
Ubr4 G A 4: 139,406,528 (GRCm38) W745* probably null Het
Vmn2r115 G A 17: 23,346,015 (GRCm38) G292D probably benign Het
Vmn2r38 T A 7: 9,075,341 (GRCm38) K681* probably null Het
Xrcc6 A G 15: 82,031,174 (GRCm38) K98E probably benign Het
Zfp423 A G 8: 87,803,779 (GRCm38) V13A probably benign Het
Zfp512b A G 2: 181,586,348 (GRCm38) I5T possibly damaging Het
Zmynd8 C T 2: 165,875,750 (GRCm38) E14K probably damaging Het
Other mutations in Tenm3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00272:Tenm3 APN 8 48,417,060 (GRCm38) missense probably damaging 1.00
IGL00538:Tenm3 APN 8 48,236,025 (GRCm38) missense probably damaging 1.00
IGL00719:Tenm3 APN 8 48,279,042 (GRCm38) missense probably benign 0.39
IGL00720:Tenm3 APN 8 48,276,421 (GRCm38) missense probably damaging 0.98
IGL00870:Tenm3 APN 8 48,417,132 (GRCm38) missense probably benign 0.00
IGL00976:Tenm3 APN 8 48,256,841 (GRCm38) missense probably benign 0.14
IGL01469:Tenm3 APN 8 48,236,423 (GRCm38) missense probably damaging 1.00
IGL01508:Tenm3 APN 8 48,276,645 (GRCm38) missense probably benign 0.09
IGL01590:Tenm3 APN 8 48,228,802 (GRCm38) missense probably damaging 1.00
IGL01610:Tenm3 APN 8 48,254,477 (GRCm38) missense probably damaging 1.00
IGL01874:Tenm3 APN 8 48,236,758 (GRCm38) nonsense probably null
IGL01892:Tenm3 APN 8 48,276,396 (GRCm38) missense probably benign 0.09
IGL02098:Tenm3 APN 8 48,276,576 (GRCm38) missense possibly damaging 0.94
IGL02382:Tenm3 APN 8 48,235,476 (GRCm38) missense probably damaging 1.00
IGL02397:Tenm3 APN 8 48,236,694 (GRCm38) missense possibly damaging 0.94
IGL02475:Tenm3 APN 8 48,279,198 (GRCm38) splice site probably benign
IGL02502:Tenm3 APN 8 48,288,016 (GRCm38) missense probably damaging 1.00
IGL02508:Tenm3 APN 8 48,299,639 (GRCm38) missense probably benign 0.30
IGL02543:Tenm3 APN 8 48,298,956 (GRCm38) missense probably damaging 1.00
IGL02723:Tenm3 APN 8 48,276,903 (GRCm38) missense probably benign 0.02
IGL03037:Tenm3 APN 8 48,298,878 (GRCm38) missense possibly damaging 0.90
IGL03160:Tenm3 APN 8 48,646,418 (GRCm38) missense probably benign 0.05
IGL03268:Tenm3 APN 8 48,235,523 (GRCm38) missense probably damaging 1.00
IGL02988:Tenm3 UTSW 8 48,235,346 (GRCm38) missense probably damaging 0.99
PIT4431001:Tenm3 UTSW 8 48,235,607 (GRCm38) missense probably damaging 1.00
PIT4504001:Tenm3 UTSW 8 48,293,657 (GRCm38) missense probably damaging 1.00
R0079:Tenm3 UTSW 8 48,343,345 (GRCm38) missense possibly damaging 0.90
R0121:Tenm3 UTSW 8 48,342,659 (GRCm38) missense probably damaging 0.99
R0123:Tenm3 UTSW 8 48,674,472 (GRCm38) missense probably damaging 1.00
R0134:Tenm3 UTSW 8 48,674,472 (GRCm38) missense probably damaging 1.00
R0147:Tenm3 UTSW 8 48,236,720 (GRCm38) missense probably damaging 1.00
R0148:Tenm3 UTSW 8 48,236,720 (GRCm38) missense probably damaging 1.00
R0309:Tenm3 UTSW 8 48,341,034 (GRCm38) missense probably damaging 1.00
R0322:Tenm3 UTSW 8 48,236,912 (GRCm38) splice site probably benign
R0335:Tenm3 UTSW 8 48,232,105 (GRCm38) missense probably damaging 1.00
R0355:Tenm3 UTSW 8 48,228,975 (GRCm38) missense probably damaging 1.00
R0411:Tenm3 UTSW 8 48,287,791 (GRCm38) missense possibly damaging 0.61
R0505:Tenm3 UTSW 8 48,341,160 (GRCm38) splice site probably benign
R0573:Tenm3 UTSW 8 48,674,399 (GRCm38) splice site probably benign
R0599:Tenm3 UTSW 8 48,277,710 (GRCm38) missense probably damaging 1.00
R0616:Tenm3 UTSW 8 48,276,156 (GRCm38) missense possibly damaging 0.76
R0637:Tenm3 UTSW 8 48,236,525 (GRCm38) missense probably damaging 1.00
R0726:Tenm3 UTSW 8 48,236,594 (GRCm38) missense probably damaging 1.00
R0840:Tenm3 UTSW 8 48,335,742 (GRCm38) missense probably damaging 0.99
R0981:Tenm3 UTSW 8 48,298,965 (GRCm38) missense probably damaging 1.00
R1006:Tenm3 UTSW 8 48,228,542 (GRCm38) missense probably damaging 1.00
R1199:Tenm3 UTSW 8 48,235,582 (GRCm38) missense probably damaging 0.99
R1223:Tenm3 UTSW 8 48,240,396 (GRCm38) missense possibly damaging 0.72
R1240:Tenm3 UTSW 8 48,287,893 (GRCm38) missense possibly damaging 0.74
R1394:Tenm3 UTSW 8 48,276,400 (GRCm38) missense probably benign
R1455:Tenm3 UTSW 8 48,279,048 (GRCm38) missense possibly damaging 0.87
R1459:Tenm3 UTSW 8 48,235,971 (GRCm38) missense probably damaging 1.00
R1473:Tenm3 UTSW 8 48,310,625 (GRCm38) missense probably damaging 1.00
R1501:Tenm3 UTSW 8 48,343,316 (GRCm38) missense probably damaging 0.99
R1507:Tenm3 UTSW 8 48,287,822 (GRCm38) missense probably benign 0.01
R1522:Tenm3 UTSW 8 48,395,576 (GRCm38) missense probably damaging 1.00
R1524:Tenm3 UTSW 8 48,228,981 (GRCm38) missense possibly damaging 0.92
R1553:Tenm3 UTSW 8 48,236,421 (GRCm38) missense probably damaging 1.00
R1572:Tenm3 UTSW 8 48,228,993 (GRCm38) missense possibly damaging 0.94
R1583:Tenm3 UTSW 8 48,279,074 (GRCm38) missense probably benign 0.09
R1676:Tenm3 UTSW 8 48,417,119 (GRCm38) missense possibly damaging 0.83
R1732:Tenm3 UTSW 8 48,310,634 (GRCm38) missense probably damaging 1.00
R1768:Tenm3 UTSW 8 48,232,104 (GRCm38) missense probably damaging 1.00
R1777:Tenm3 UTSW 8 48,417,179 (GRCm38) missense probably benign 0.05
R1793:Tenm3 UTSW 8 48,674,544 (GRCm38) missense probably damaging 0.98
R1801:Tenm3 UTSW 8 48,276,256 (GRCm38) missense probably benign 0.39
R1863:Tenm3 UTSW 8 48,276,346 (GRCm38) missense probably benign 0.20
R1898:Tenm3 UTSW 8 48,310,761 (GRCm38) missense probably damaging 1.00
R1971:Tenm3 UTSW 8 48,236,313 (GRCm38) missense probably damaging 1.00
R1972:Tenm3 UTSW 8 48,228,591 (GRCm38) missense probably damaging 1.00
R1996:Tenm3 UTSW 8 48,228,668 (GRCm38) missense probably damaging 1.00
R2061:Tenm3 UTSW 8 48,342,256 (GRCm38) critical splice donor site probably null
R2109:Tenm3 UTSW 8 48,343,349 (GRCm38) missense possibly damaging 0.94
R2124:Tenm3 UTSW 8 48,417,006 (GRCm38) critical splice donor site probably null
R2190:Tenm3 UTSW 8 48,395,544 (GRCm38) missense probably damaging 1.00
R2204:Tenm3 UTSW 8 48,674,550 (GRCm38) missense probably benign 0.17
R2233:Tenm3 UTSW 8 48,276,169 (GRCm38) missense probably benign 0.04
R2234:Tenm3 UTSW 8 48,276,169 (GRCm38) missense probably benign 0.04
R2235:Tenm3 UTSW 8 48,276,169 (GRCm38) missense probably benign 0.04
R2237:Tenm3 UTSW 8 48,342,337 (GRCm38) missense probably damaging 1.00
R2418:Tenm3 UTSW 8 48,276,658 (GRCm38) missense possibly damaging 0.87
R2419:Tenm3 UTSW 8 48,276,658 (GRCm38) missense possibly damaging 0.87
R2435:Tenm3 UTSW 8 48,287,953 (GRCm38) missense probably damaging 1.00
R2483:Tenm3 UTSW 8 48,240,270 (GRCm38) missense probably damaging 0.99
R3406:Tenm3 UTSW 8 48,228,555 (GRCm38) missense probably damaging 1.00
R3724:Tenm3 UTSW 8 48,277,746 (GRCm38) missense probably damaging 0.97
R4009:Tenm3 UTSW 8 48,349,223 (GRCm38) missense probably damaging 1.00
R4210:Tenm3 UTSW 8 48,349,404 (GRCm38) missense probably damaging 1.00
R4293:Tenm3 UTSW 8 48,395,658 (GRCm38) missense probably damaging 1.00
R4656:Tenm3 UTSW 8 48,293,726 (GRCm38) missense probably damaging 1.00
R4663:Tenm3 UTSW 8 48,235,970 (GRCm38) missense probably damaging 1.00
R4835:Tenm3 UTSW 8 48,313,236 (GRCm38) critical splice donor site probably null
R4851:Tenm3 UTSW 8 48,310,621 (GRCm38) critical splice donor site probably null
R4867:Tenm3 UTSW 8 48,235,821 (GRCm38) missense probably damaging 1.00
R4892:Tenm3 UTSW 8 48,276,861 (GRCm38) missense probably damaging 0.99
R4895:Tenm3 UTSW 8 48,300,971 (GRCm38) missense probably damaging 1.00
R4962:Tenm3 UTSW 8 48,278,961 (GRCm38) nonsense probably null
R4995:Tenm3 UTSW 8 48,229,137 (GRCm38) missense possibly damaging 0.87
R4996:Tenm3 UTSW 8 48,235,826 (GRCm38) missense probably damaging 0.97
R5091:Tenm3 UTSW 8 48,342,308 (GRCm38) missense probably benign 0.14
R5228:Tenm3 UTSW 8 48,236,355 (GRCm38) missense probably damaging 1.00
R5253:Tenm3 UTSW 8 48,229,198 (GRCm38) missense possibly damaging 0.92
R5260:Tenm3 UTSW 8 48,236,855 (GRCm38) missense probably damaging 1.00
R5363:Tenm3 UTSW 8 48,287,831 (GRCm38) missense possibly damaging 0.55
R5414:Tenm3 UTSW 8 48,236,355 (GRCm38) missense probably damaging 1.00
R5427:Tenm3 UTSW 8 48,236,564 (GRCm38) missense probably damaging 1.00
R5431:Tenm3 UTSW 8 48,367,377 (GRCm38) nonsense probably null
R5566:Tenm3 UTSW 8 48,279,006 (GRCm38) missense probably damaging 1.00
R5579:Tenm3 UTSW 8 48,236,764 (GRCm38) missense probably damaging 1.00
R5656:Tenm3 UTSW 8 48,228,762 (GRCm38) missense probably damaging 1.00
R5931:Tenm3 UTSW 8 48,646,498 (GRCm38) missense probably benign 0.00
R5959:Tenm3 UTSW 8 48,646,447 (GRCm38) nonsense probably null
R5965:Tenm3 UTSW 8 48,228,508 (GRCm38) nonsense probably null
R6062:Tenm3 UTSW 8 48,343,406 (GRCm38) missense possibly damaging 0.46
R6151:Tenm3 UTSW 8 48,395,573 (GRCm38) missense probably damaging 1.00
R6157:Tenm3 UTSW 8 48,298,808 (GRCm38) missense probably damaging 0.96
R6167:Tenm3 UTSW 8 48,254,622 (GRCm38) missense possibly damaging 0.46
R6217:Tenm3 UTSW 8 48,293,665 (GRCm38) missense probably damaging 0.99
R6233:Tenm3 UTSW 8 48,417,059 (GRCm38) missense probably damaging 1.00
R6270:Tenm3 UTSW 8 48,367,394 (GRCm38) missense probably damaging 0.98
R6329:Tenm3 UTSW 8 48,276,849 (GRCm38) missense probably damaging 0.99
R6466:Tenm3 UTSW 8 48,236,063 (GRCm38) missense probably damaging 0.97
R6515:Tenm3 UTSW 8 48,417,222 (GRCm38) missense probably benign
R6516:Tenm3 UTSW 8 48,417,222 (GRCm38) missense probably benign
R6747:Tenm3 UTSW 8 48,343,243 (GRCm38) missense probably damaging 1.00
R6782:Tenm3 UTSW 8 48,646,256 (GRCm38) critical splice donor site probably null
R6788:Tenm3 UTSW 8 48,674,493 (GRCm38) missense probably damaging 1.00
R6823:Tenm3 UTSW 8 48,256,837 (GRCm38) missense probably damaging 0.99
R6846:Tenm3 UTSW 8 48,276,738 (GRCm38) missense probably benign 0.39
R6913:Tenm3 UTSW 8 48,298,937 (GRCm38) missense probably damaging 0.99
R6941:Tenm3 UTSW 8 48,674,416 (GRCm38) missense probably damaging 0.99
R6950:Tenm3 UTSW 8 48,240,479 (GRCm38) nonsense probably null
R6968:Tenm3 UTSW 8 48,236,439 (GRCm38) missense probably damaging 1.00
R6993:Tenm3 UTSW 8 48,236,439 (GRCm38) missense probably damaging 1.00
R7003:Tenm3 UTSW 8 48,240,444 (GRCm38) missense probably damaging 1.00
R7125:Tenm3 UTSW 8 48,674,553 (GRCm38) missense probably benign 0.00
R7140:Tenm3 UTSW 8 48,292,236 (GRCm38) missense probably damaging 1.00
R7222:Tenm3 UTSW 8 48,300,969 (GRCm38) missense probably damaging 1.00
R7232:Tenm3 UTSW 8 48,235,935 (GRCm38) missense probably damaging 1.00
R7336:Tenm3 UTSW 8 48,236,177 (GRCm38) missense possibly damaging 0.93
R7417:Tenm3 UTSW 8 48,236,183 (GRCm38) missense probably damaging 1.00
R7526:Tenm3 UTSW 8 48,287,812 (GRCm38) missense probably damaging 0.96
R7527:Tenm3 UTSW 8 48,276,600 (GRCm38) missense possibly damaging 0.60
R7616:Tenm3 UTSW 8 48,341,049 (GRCm38) missense possibly damaging 0.56
R7662:Tenm3 UTSW 8 48,335,727 (GRCm38) missense probably benign 0.27
R7734:Tenm3 UTSW 8 48,646,333 (GRCm38) missense probably damaging 1.00
R7802:Tenm3 UTSW 8 48,236,465 (GRCm38) missense probably damaging 1.00
R7812:Tenm3 UTSW 8 48,276,300 (GRCm38) missense probably benign 0.01
R7843:Tenm3 UTSW 8 48,229,111 (GRCm38) nonsense probably null
R7951:Tenm3 UTSW 8 48,310,703 (GRCm38) missense possibly damaging 0.86
R8293:Tenm3 UTSW 8 48,367,422 (GRCm38) missense possibly damaging 0.91
R8336:Tenm3 UTSW 8 48,293,773 (GRCm38) missense probably damaging 1.00
R8351:Tenm3 UTSW 8 48,287,872 (GRCm38) missense probably damaging 0.96
R8387:Tenm3 UTSW 8 48,287,848 (GRCm38) missense probably damaging 0.98
R8414:Tenm3 UTSW 8 48,293,509 (GRCm38) missense probably damaging 1.00
R8451:Tenm3 UTSW 8 48,287,872 (GRCm38) missense probably damaging 0.96
R8465:Tenm3 UTSW 8 48,229,181 (GRCm38) missense probably damaging 1.00
R8528:Tenm3 UTSW 8 48,342,633 (GRCm38) missense probably damaging 1.00
R8717:Tenm3 UTSW 8 48,299,645 (GRCm38) missense possibly damaging 0.77
R8734:Tenm3 UTSW 8 48,349,356 (GRCm38) missense probably benign 0.16
R8781:Tenm3 UTSW 8 48,342,449 (GRCm38) frame shift probably null
R8820:Tenm3 UTSW 8 48,310,724 (GRCm38) missense probably damaging 0.96
R8821:Tenm3 UTSW 8 48,276,382 (GRCm38) missense
R8831:Tenm3 UTSW 8 48,276,382 (GRCm38) missense
R8853:Tenm3 UTSW 8 48,342,347 (GRCm38) missense probably damaging 1.00
R8900:Tenm3 UTSW 8 48,236,402 (GRCm38) missense probably damaging 1.00
R8931:Tenm3 UTSW 8 48,235,602 (GRCm38) missense probably damaging 1.00
R8933:Tenm3 UTSW 8 48,279,060 (GRCm38) missense possibly damaging 0.53
R8989:Tenm3 UTSW 8 48,235,348 (GRCm38) nonsense probably null
R8998:Tenm3 UTSW 8 48,276,687 (GRCm38) missense probably damaging 1.00
R9008:Tenm3 UTSW 8 48,342,653 (GRCm38) missense probably damaging 0.98
R9017:Tenm3 UTSW 8 48,254,633 (GRCm38) missense probably damaging 0.99
R9101:Tenm3 UTSW 8 48,292,151 (GRCm38) missense probably damaging 1.00
R9108:Tenm3 UTSW 8 48,313,236 (GRCm38) critical splice donor site probably null
R9142:Tenm3 UTSW 8 48,335,513 (GRCm38) missense unknown
R9231:Tenm3 UTSW 8 48,236,196 (GRCm38) missense probably damaging 1.00
R9309:Tenm3 UTSW 8 48,298,937 (GRCm38) missense probably damaging 0.99
R9310:Tenm3 UTSW 8 48,555,900 (GRCm38) unclassified probably benign
R9336:Tenm3 UTSW 8 48,417,080 (GRCm38) missense probably damaging 1.00
R9373:Tenm3 UTSW 8 48,299,655 (GRCm38) missense probably damaging 1.00
R9393:Tenm3 UTSW 8 48,674,524 (GRCm38) missense probably damaging 0.99
R9509:Tenm3 UTSW 8 48,313,257 (GRCm38) nonsense probably null
R9575:Tenm3 UTSW 8 48,235,761 (GRCm38) missense possibly damaging 0.94
R9698:Tenm3 UTSW 8 48,236,211 (GRCm38) missense probably damaging 1.00
R9722:Tenm3 UTSW 8 48,300,814 (GRCm38) missense probably benign 0.00
R9788:Tenm3 UTSW 8 48,335,561 (GRCm38) missense probably benign 0.02
X0010:Tenm3 UTSW 8 48,287,829 (GRCm38) missense probably damaging 0.98
X0025:Tenm3 UTSW 8 48,236,477 (GRCm38) missense probably damaging 1.00
Z1177:Tenm3 UTSW 8 48,276,780 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GCCCATGAGCATCAAAGTGC -3'
(R):5'- AGAAGGCAGACCAGGCTATC -3'

Sequencing Primer
(F):5'- GCTTTGTATAAGTCATCACGGCCG -3'
(R):5'- TACGACAGCACAAGAGTCAGTTTTAC -3'
Posted On 2018-11-28