Incidental Mutation 'IGL00272:Tenm3'
ID 12834
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 # IGL00272
Quality Score
Status
Chromosome 8
Chromosomal Location 48227682-48843951 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) C to T at 48417060 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 233 (V233I)
Ref Sequence ENSEMBL: ENSMUSP00000033965 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000033965] [ENSMUST00000110343] [ENSMUST00000110345] [ENSMUST00000110346] [ENSMUST00000190840] [ENSMUST00000211976]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000033965
AA Change: V233I

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000033965
Gene: ENSMUSG00000031561
AA Change: V233I

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 benign
Transcript: ENSMUST00000110343
SMART Domains Protein: ENSMUSP00000105972
Gene: ENSMUSG00000031561

DomainStartEndE-ValueType
Pfam:Ten_N 1 36 2.3e-15 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000110345
SMART Domains Protein: ENSMUSP00000105974
Gene: ENSMUSG00000031561

DomainStartEndE-ValueType
Pfam:Ten_N 1 36 2.3e-15 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000110346
SMART Domains Protein: ENSMUSP00000105975
Gene: ENSMUSG00000031561

DomainStartEndE-ValueType
Pfam:Ten_N 1 36 1.1e-14 PFAM
transmembrane domain 37 59 N/A INTRINSIC
EGF 245 273 2.32e-1 SMART
EGF_like 276 304 4.11e1 SMART
EGF 309 338 1.69e1 SMART
EGF 341 370 1.35e-2 SMART
EGF 375 405 6.11e-1 SMART
EGF 408 436 7.95e0 SMART
EGF 439 467 1.28e1 SMART
Predicted Effect unknown
Transcript: ENSMUST00000190840
AA Change: V233I
SMART Domains Protein: ENSMUSP00000140141
Gene: ENSMUSG00000031561
AA Change: V233I

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
Predicted Effect probably benign
Transcript: ENSMUST00000211976
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: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700030J22Rik A G 8: 116,973,540 (GRCm38) V41A probably damaging Het
4932431P20Rik G T 7: 29,537,622 (GRCm38) noncoding transcript Het
AI481877 A G 4: 59,086,961 (GRCm38) F284L probably benign Het
Ankrd12 C T 17: 65,986,174 (GRCm38) V755I probably benign Het
Arrdc3 T C 13: 80,890,572 (GRCm38) S218P probably damaging Het
Bzw1 T C 1: 58,402,942 (GRCm38) V292A possibly damaging Het
Cers2 T C 3: 95,321,900 (GRCm38) Y228H probably damaging Het
Egf C T 3: 129,711,449 (GRCm38) M625I probably benign Het
Fbxw8 A T 5: 118,068,097 (GRCm38) H595Q probably benign Het
Fshr T A 17: 88,985,271 (GRCm38) I660F probably benign Het
Gapdh C T 6: 125,162,507 (GRCm38) V267M probably damaging Het
Ginm1 T C 10: 7,792,696 (GRCm38) probably benign Het
Gja1 A G 10: 56,388,322 (GRCm38) D259G probably benign Het
Gm21814 T A 6: 149,582,004 (GRCm38) noncoding transcript Het
Gm26870 T C 9: 3,002,340 (GRCm38) probably benign Het
Habp2 G A 19: 56,317,832 (GRCm38) C482Y probably damaging Het
Knl1 A C 2: 119,064,083 (GRCm38) N79T probably damaging Het
Lama3 G A 18: 12,491,548 (GRCm38) C1450Y probably damaging Het
Lats2 T C 14: 57,691,569 (GRCm38) T950A probably benign Het
Map2k2 T A 10: 81,121,073 (GRCm38) M95K probably damaging Het
Med12l T A 3: 59,042,336 (GRCm38) I160N probably damaging Het
Olfr1158 A T 2: 87,990,438 (GRCm38) D109V probably damaging Het
Olfr1160 A G 2: 88,006,644 (GRCm38) S45P probably damaging Het
Pes1 T C 11: 3,976,803 (GRCm38) S362P probably damaging Het
Pih1h3b A G X: 140,105,962 (GRCm38) I197V probably benign Het
Ppp6r2 G T 15: 89,285,813 (GRCm38) A844S probably benign Het
Rnf130 A G 11: 50,093,796 (GRCm38) I308V probably damaging Het
Scn11a T C 9: 119,816,603 (GRCm38) N95S probably damaging Het
Skint2 A G 4: 112,624,212 (GRCm38) T91A probably damaging Het
Smg1 A G 7: 118,198,271 (GRCm38) probably benign Het
Snapc1 A G 12: 73,968,374 (GRCm38) probably null Het
Stard10 A T 7: 101,321,966 (GRCm38) Y47F probably damaging Het
Tex14 G A 11: 87,535,643 (GRCm38) S1165N probably damaging Het
Unc5a A G 13: 54,995,820 (GRCm38) I106V probably benign Het
Vps54 T A 11: 21,277,909 (GRCm38) Y275N possibly damaging Het
Other mutations in Tenm3
AlleleSourceChrCoordTypePredicted EffectPPH Score
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
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 2012-12-06