Incidental Mutation 'IGL02502:Tenm3'
ID 296122
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tenm3
Ensembl Gene ENSMUSG00000031561
Gene Name teneurin transmembrane protein 3
Synonyms Ten-m3, Odz3, 2610100B16Rik
Accession Numbers
Essential gene? Possibly essential (E-score: 0.598) question?
Stock # IGL02502
Quality Score
Status
Chromosome 8
Chromosomal Location 48227682-48843951 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 48288016 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 782 (E782G)
Gene Model predicted gene model for transcript(s): [ENSMUST00000033965] [ENSMUST00000190840]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000033965
AA Change: E1144G

PolyPhen 2 Score 0.960 (Sensitivity: 0.78; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000033965
Gene: ENSMUSG00000031561
AA Change: E1144G

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: ENSMUST00000129821
AA Change: E782G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000145344
Predicted Effect probably benign
Transcript: ENSMUST00000190840
AA Change: E1135G

PolyPhen 2 Score 0.321 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000140141
Gene: ENSMUSG00000031561
AA Change: E1135G

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
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: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acoxl A G 2: 128,075,884 (GRCm38) N216S probably damaging Het
Akap12 A G 10: 4,353,163 (GRCm38) D96G probably damaging Het
Akna A G 4: 63,368,203 (GRCm38) V1353A probably benign Het
Ambra1 A G 2: 91,900,532 (GRCm38) D914G probably damaging Het
Ap1s3 A G 1: 79,623,722 (GRCm38) V84A possibly damaging Het
Arhgef6 T C X: 57,280,263 (GRCm38) E282G probably damaging Het
C2cd2 G T 16: 97,876,390 (GRCm38) S378Y possibly damaging Het
Cd101 C A 3: 101,011,825 (GRCm38) A654S probably damaging Het
Cep295 A C 9: 15,350,913 (GRCm38) probably benign Het
Csn1s1 A G 5: 87,680,925 (GRCm38) I283V probably benign Het
Cst3 A G 2: 148,875,145 (GRCm38) probably benign Het
Cyp2b9 T C 7: 26,187,814 (GRCm38) probably null Het
Dffb A G 4: 153,965,616 (GRCm38) probably benign Het
Dnah10 A G 5: 124,821,287 (GRCm38) Y3711C probably damaging Het
Eif4g2 T C 7: 111,081,541 (GRCm38) S3G probably damaging Het
Erbb3 C T 10: 128,570,284 (GRCm38) R1088H probably benign Het
Evpl T C 11: 116,222,718 (GRCm38) D1382G probably damaging Het
Fam168a A G 7: 100,824,210 (GRCm38) D102G probably damaging Het
Fbxo7 A G 10: 86,033,297 (GRCm38) Y284C probably damaging Het
G6pd2 T C 5: 61,809,628 (GRCm38) Y249H probably damaging Het
Gm1123 A T 9: 99,009,390 (GRCm38) Y335* probably null Het
Gm5624 C T 14: 44,559,839 (GRCm38) probably null Het
Hectd1 A T 12: 51,797,852 (GRCm38) M536K possibly damaging Het
Ikbkg T A X: 74,443,827 (GRCm38) V334E probably benign Het
Ipo7 T C 7: 110,051,050 (GRCm38) L769P probably damaging Het
Jmjd1c A T 10: 67,225,861 (GRCm38) K1331I probably benign Het
Krt32 T C 11: 100,087,923 (GRCm38) K102E probably damaging Het
Lrrc34 A T 3: 30,645,245 (GRCm38) N20K probably benign Het
Lrrc47 A G 4: 154,016,014 (GRCm38) E349G probably benign Het
Mdn1 A G 4: 32,670,579 (GRCm38) I415V possibly damaging Het
Myh10 A G 11: 68,814,372 (GRCm38) probably null Het
Nbeal2 A G 9: 110,633,768 (GRCm38) S1376P probably damaging Het
Nfx1 T C 4: 40,976,345 (GRCm38) probably benign Het
Notch3 A T 17: 32,158,278 (GRCm38) C246* probably null Het
Nr3c2 A G 8: 77,242,514 (GRCm38) Y976C probably damaging Het
Olfr1484 A G 19: 13,585,748 (GRCm38) Y105C probably damaging Het
Olfr503 T A 7: 108,544,639 (GRCm38) M36K probably damaging Het
Olfr64 A G 7: 103,893,489 (GRCm38) V82A probably damaging Het
P2rx7 C T 5: 122,680,987 (GRCm38) R491C possibly damaging Het
Pdzd3 G A 9: 44,249,651 (GRCm38) A206V probably benign Het
Phex T A X: 157,183,827 (GRCm38) Y625F possibly damaging Het
Pkhd1 T C 1: 20,392,165 (GRCm38) D2055G probably damaging Het
Pmm2 T C 16: 8,645,363 (GRCm38) probably benign Het
Prdm15 T C 16: 97,839,339 (GRCm38) D16G probably damaging Het
Prune2 T A 19: 17,123,881 (GRCm38) C2250S probably benign Het
Rasgef1a T A 6: 118,080,482 (GRCm38) F48Y probably benign Het
Rhoq T C 17: 86,963,649 (GRCm38) V15A probably damaging Het
Rnf216 G A 5: 143,068,867 (GRCm38) A585V probably damaging Het
Sept9 T A 11: 117,290,662 (GRCm38) I96N probably damaging Het
Shprh T A 10: 11,194,357 (GRCm38) D1492E possibly damaging Het
Slc22a26 A T 19: 7,790,760 (GRCm38) probably null Het
Tek T G 4: 94,853,581 (GRCm38) probably null Het
Trmt5 A G 12: 73,281,227 (GRCm38) C401R probably benign Het
Tspear T G 10: 77,852,958 (GRCm38) probably benign Het
Ubr5 G A 15: 38,030,689 (GRCm38) T414I probably benign Het
Vcl A T 14: 21,019,385 (GRCm38) T710S probably damaging Het
Vmn2r25 A T 6: 123,839,433 (GRCm38) D396E probably damaging Het
Wtip A G 7: 34,118,669 (GRCm38) probably null Het
Zap70 A G 1: 36,778,806 (GRCm38) probably benign 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
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
R6970: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
Posted On 2015-04-16