Incidental Mutation 'R7803:Tenm2'
ID 600627
Institutional Source Beutler Lab
Gene Symbol Tenm2
Ensembl Gene ENSMUSG00000049336
Gene Name teneurin transmembrane protein 2
Synonyms 2610040L17Rik, 9330187F13Rik, D3Bwg1534e, Ten-m2, Odz2
MMRRC Submission 045858-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.514) question?
Stock # R7803 (G1)
Quality Score 225.009
Status Validated
Chromosome 11
Chromosomal Location 36006656-37235964 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 36047116 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Serine to Threonine at position 1578 (S1578T)
Ref Sequence ENSEMBL: ENSMUSP00000052014 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057207] [ENSMUST00000102801] [ENSMUST00000163524]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000057207
AA Change: S1578T

PolyPhen 2 Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000052014
Gene: ENSMUSG00000049336
AA Change: S1578T

DomainStartEndE-ValueType
Pfam:Ten_N 10 374 4.9e-177 PFAM
transmembrane domain 375 397 N/A INTRINSIC
EGF 575 603 5.62e0 SMART
EGF_like 606 634 4.93e1 SMART
EGF 639 668 1.76e1 SMART
EGF 671 700 1.43e-1 SMART
EGF 705 735 1.2e1 SMART
EGF 738 766 9.63e0 SMART
EGF 769 797 1.25e1 SMART
EGF 800 832 1.4e0 SMART
low complexity region 1459 1475 N/A INTRINSIC
low complexity region 2219 2230 N/A INTRINSIC
Pfam:Tox-GHH 2681 2758 1.4e-34 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000102801
AA Change: S1577T

PolyPhen 2 Score 0.980 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000099865
Gene: ENSMUSG00000049336
AA Change: S1577T

DomainStartEndE-ValueType
Pfam:Ten_N 9 374 2e-186 PFAM
transmembrane domain 375 397 N/A INTRINSIC
EGF 575 603 5.62e0 SMART
EGF_like 606 634 4.93e1 SMART
EGF 639 668 1.76e1 SMART
EGF 671 700 1.43e-1 SMART
EGF 705 735 1.2e1 SMART
EGF 737 765 9.63e0 SMART
EGF 768 796 1.25e1 SMART
EGF 799 831 1.4e0 SMART
low complexity region 1458 1474 N/A INTRINSIC
low complexity region 2218 2229 N/A INTRINSIC
Pfam:Tox-GHH 2679 2757 2e-34 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000163524
AA Change: S1577T

PolyPhen 2 Score 0.980 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000129951
Gene: ENSMUSG00000049336
AA Change: S1577T

DomainStartEndE-ValueType
Pfam:Ten_N 9 374 2e-186 PFAM
transmembrane domain 375 397 N/A INTRINSIC
EGF 575 603 5.62e0 SMART
EGF_like 606 634 4.93e1 SMART
EGF 639 668 1.76e1 SMART
EGF 671 700 1.43e-1 SMART
EGF 705 735 1.2e1 SMART
EGF 737 765 9.63e0 SMART
EGF 768 796 1.25e1 SMART
EGF 799 831 1.4e0 SMART
low complexity region 1458 1474 N/A INTRINSIC
low complexity region 2218 2229 N/A INTRINSIC
Pfam:Tox-GHH 2679 2757 2e-34 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.4%
Validation Efficiency 98% (49/50)
MGI Phenotype PHENOTYPE: Mice homozygous for a null allele show abnormalities in the laterality and mapping of ipsilateral retinal projections that lead to loss of ipsilateral drive, defects in binocular vision, and impaired performance on a visual discrimination task. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acta2 C A 19: 34,243,418 (GRCm38) A297S probably benign Het
Ada A G 2: 163,735,368 (GRCm38) Y67H probably benign Het
Adcy9 A G 16: 4,304,380 (GRCm38) I839T probably benign Het
Arg1 C T 10: 24,916,791 (GRCm38) V182I possibly damaging Het
Cbx7 G A 15: 79,933,823 (GRCm38) T26M unknown Het
Ceacam5 A G 7: 17,759,392 (GRCm38) Y780C probably damaging Het
Ces2h A G 8: 105,018,400 (GRCm38) M389V probably benign Het
Chst11 A T 10: 83,191,186 (GRCm38) E149V possibly damaging Het
Clstn1 T C 4: 149,631,871 (GRCm38) W265R probably damaging Het
Col4a4 A G 1: 82,489,698 (GRCm38) probably null Het
Csrp3 T G 7: 48,833,797 (GRCm38) K119T probably benign Het
Ddx39a T C 8: 83,719,600 (GRCm38) probably null Het
Ddx41 A G 13: 55,531,921 (GRCm38) I437T probably damaging Het
Eif1ad4 T A 12: 87,895,499 (GRCm38) C44S probably benign Het
Fbln5 A T 12: 101,761,818 (GRCm38) D282E probably damaging Het
Folh1 G A 7: 86,726,098 (GRCm38) T527I probably damaging Het
Gch1 T A 14: 47,188,961 (GRCm38) T103S probably benign Het
Gpr149 A G 3: 62,530,715 (GRCm38) S674P probably damaging Het
Hecw1 G T 13: 14,234,342 (GRCm38) R1127S probably benign Het
Hmcn1 A T 1: 150,770,279 (GRCm38) C723S probably benign Het
Impg2 T C 16: 56,267,150 (GRCm38) S1111P probably damaging Het
Insl3 T C 8: 71,689,340 (GRCm38) L28P probably damaging Het
Kifc1 T C 17: 33,884,740 (GRCm38) D203G probably benign Het
Kmt2d A T 15: 98,862,923 (GRCm38) S849T unknown Het
Krt33b A G 11: 100,025,258 (GRCm38) probably null Het
Lpin3 A G 2: 160,895,390 (GRCm38) D119G possibly damaging Het
Maml2 AGC AGCCGC 9: 13,621,254 (GRCm38) probably benign Het
Maml2 AGC AGCCGC 9: 13,621,275 (GRCm38) probably benign Het
Maml2 GCA GCACCA 9: 13,621,276 (GRCm38) probably benign Het
Nsun7 T A 5: 66,276,541 (GRCm38) L178* probably null Het
Or6c1b A G 10: 129,436,931 (GRCm38) N40D probably damaging Het
Or6c205 A T 10: 129,250,995 (GRCm38) I154F probably benign Het
Or8g55 A T 9: 39,874,082 (GRCm38) D269V probably benign Het
Orc6 T A 8: 85,303,408 (GRCm38) S136T possibly damaging Het
Peg10 CATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAGGATC CATC 6: 4,756,431 (GRCm38) probably benign Het
Plxnc1 A G 10: 94,943,515 (GRCm38) probably null Het
Prkdc G A 16: 15,806,096 (GRCm38) D3308N probably null Het
Rtkn2 G A 10: 67,979,813 (GRCm38) probably null Het
Sele T C 1: 164,050,694 (GRCm38) S201P possibly damaging Het
Shq1 A G 6: 100,671,045 (GRCm38) F6S probably damaging Het
Sparc A T 11: 55,409,971 (GRCm38) I5N probably damaging Het
Spata31e3 A G 13: 50,246,190 (GRCm38) V700A probably benign Het
Srm T C 4: 148,593,945 (GRCm38) I238T probably damaging Het
Stx2 C A 5: 128,993,563 (GRCm38) E97* probably null Het
Sugp2 C T 8: 70,252,072 (GRCm38) P753L probably benign Het
Tff3 T C 17: 31,129,570 (GRCm38) T3A probably benign Het
Tmem38a C T 8: 72,572,120 (GRCm38) A6V probably benign Het
Trbv16 G A 6: 41,151,995 (GRCm38) A38T not run Het
Trim30a G A 7: 104,411,397 (GRCm38) Q391* probably null Het
Ttn T G 2: 76,776,371 (GRCm38) Y18065S probably damaging Het
Ubr5 G A 15: 37,979,832 (GRCm38) A2434V probably null Het
Vmn2r24 T A 6: 123,780,479 (GRCm38) M102K probably benign Het
Vmn2r69 G T 7: 85,407,116 (GRCm38) H605N probably benign Het
Washc1 T A 17: 66,119,060 (GRCm38) M451K possibly damaging Het
Washc3 G T 10: 88,216,075 (GRCm38) probably null Het
Washc5 A T 15: 59,368,459 (GRCm38) Y112N probably damaging Het
Zbtb40 T A 4: 137,017,327 (GRCm38) T261S probably benign Het
Other mutations in Tenm2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00161:Tenm2 APN 11 36,206,899 (GRCm38) splice site probably benign
IGL00834:Tenm2 APN 11 36,024,258 (GRCm38) missense probably damaging 1.00
IGL00911:Tenm2 APN 11 36,008,733 (GRCm38) nonsense probably null
IGL00937:Tenm2 APN 11 36,024,623 (GRCm38) missense probably damaging 1.00
IGL01154:Tenm2 APN 11 36,041,544 (GRCm38) missense probably damaging 1.00
IGL01313:Tenm2 APN 11 36,024,248 (GRCm38) missense probably damaging 0.98
IGL01346:Tenm2 APN 11 36,027,405 (GRCm38) nonsense probably null
IGL01539:Tenm2 APN 11 36,106,827 (GRCm38) missense possibly damaging 0.89
IGL01629:Tenm2 APN 11 36,864,884 (GRCm38) missense probably damaging 0.98
IGL01780:Tenm2 APN 11 36,046,941 (GRCm38) missense probably benign
IGL01821:Tenm2 APN 11 36,023,883 (GRCm38) missense probably damaging 0.98
IGL01988:Tenm2 APN 11 36,027,251 (GRCm38) missense probably damaging 1.00
IGL02002:Tenm2 APN 11 36,207,095 (GRCm38) missense probably benign
IGL02449:Tenm2 APN 11 36,023,622 (GRCm38) missense probably damaging 0.99
IGL02505:Tenm2 APN 11 36,051,916 (GRCm38) nonsense probably null
IGL02649:Tenm2 APN 11 36,207,085 (GRCm38) missense possibly damaging 0.85
IGL02688:Tenm2 APN 11 36,068,458 (GRCm38) missense probably benign 0.05
IGL02801:Tenm2 APN 11 36,047,030 (GRCm38) nonsense probably null
IGL02928:Tenm2 APN 11 36,027,170 (GRCm38) missense possibly damaging 0.69
IGL02940:Tenm2 APN 11 36,041,644 (GRCm38) missense probably damaging 1.00
IGL03202:Tenm2 APN 11 36,024,548 (GRCm38) missense probably damaging 1.00
IGL03213:Tenm2 APN 11 36,023,330 (GRCm38) missense probably benign 0.05
IGL03276:Tenm2 APN 11 36,072,776 (GRCm38) missense possibly damaging 0.95
IGL03296:Tenm2 APN 11 36,052,025 (GRCm38) splice site probably null
IGL03381:Tenm2 APN 11 36,068,411 (GRCm38) missense probably benign 0.01
IGL03398:Tenm2 APN 11 36,024,543 (GRCm38) missense probably damaging 1.00
browser UTSW 11 36,046,765 (GRCm38) critical splice donor site probably null
mosaic UTSW 11 36,063,775 (GRCm38) critical splice donor site probably null
IGL02799:Tenm2 UTSW 11 36,273,408 (GRCm38) missense probably damaging 1.00
PIT4260001:Tenm2 UTSW 11 36,163,730 (GRCm38) missense probably damaging 1.00
PIT4382001:Tenm2 UTSW 11 36,063,902 (GRCm38) missense probably damaging 0.99
R0004:Tenm2 UTSW 11 36,023,357 (GRCm38) missense probably damaging 1.00
R0420:Tenm2 UTSW 11 36,207,124 (GRCm38) splice site probably benign
R0537:Tenm2 UTSW 11 36,163,730 (GRCm38) missense probably damaging 1.00
R0599:Tenm2 UTSW 11 36,024,780 (GRCm38) missense possibly damaging 0.93
R0636:Tenm2 UTSW 11 36,943,976 (GRCm38) missense probably damaging 1.00
R0693:Tenm2 UTSW 11 36,024,809 (GRCm38) missense probably damaging 1.00
R0991:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R0992:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1167:Tenm2 UTSW 11 36,864,684 (GRCm38) missense probably benign 0.30
R1177:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1178:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1179:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1180:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1181:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1193:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1194:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1195:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1195:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1195:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1259:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1265:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1267:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1268:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1269:Tenm2 UTSW 11 36,008,358 (GRCm38) missense possibly damaging 0.64
R1270:Tenm2 UTSW 11 36,041,659 (GRCm38) missense probably damaging 1.00
R1272:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1273:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1311:Tenm2 UTSW 11 36,068,594 (GRCm38) splice site probably benign
R1374:Tenm2 UTSW 11 36,008,454 (GRCm38) missense probably benign 0.00
R1542:Tenm2 UTSW 11 36,300,220 (GRCm38) missense probably damaging 0.99
R1573:Tenm2 UTSW 11 36,047,069 (GRCm38) missense probably damaging 1.00
R1579:Tenm2 UTSW 11 36,106,783 (GRCm38) missense probably damaging 1.00
R1697:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1722:Tenm2 UTSW 11 36,008,103 (GRCm38) missense probably damaging 1.00
R1756:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1793:Tenm2 UTSW 11 36,023,382 (GRCm38) missense probably damaging 0.99
R1950:Tenm2 UTSW 11 36,063,177 (GRCm38) missense possibly damaging 0.94
R1954:Tenm2 UTSW 11 36,047,547 (GRCm38) missense possibly damaging 0.87
R2025:Tenm2 UTSW 11 36,047,264 (GRCm38) nonsense probably null
R2117:Tenm2 UTSW 11 36,024,854 (GRCm38) missense probably damaging 1.00
R2244:Tenm2 UTSW 11 36,864,862 (GRCm38) missense probably damaging 0.98
R2298:Tenm2 UTSW 11 36,046,777 (GRCm38) missense possibly damaging 0.62
R2432:Tenm2 UTSW 11 36,027,191 (GRCm38) missense probably damaging 1.00
R3014:Tenm2 UTSW 11 36,023,973 (GRCm38) missense probably damaging 1.00
R3115:Tenm2 UTSW 11 36,023,366 (GRCm38) missense probably damaging 1.00
R3684:Tenm2 UTSW 11 36,051,817 (GRCm38) missense probably benign 0.00
R3685:Tenm2 UTSW 11 36,051,817 (GRCm38) missense probably benign 0.00
R3705:Tenm2 UTSW 11 36,068,326 (GRCm38) missense probably damaging 0.97
R3820:Tenm2 UTSW 11 36,024,320 (GRCm38) missense probably damaging 0.98
R3821:Tenm2 UTSW 11 36,024,320 (GRCm38) missense probably damaging 0.98
R3822:Tenm2 UTSW 11 36,024,320 (GRCm38) missense probably damaging 0.98
R3844:Tenm2 UTSW 11 36,047,538 (GRCm38) missense probably damaging 0.98
R3878:Tenm2 UTSW 11 36,139,574 (GRCm38) critical splice donor site probably null
R4019:Tenm2 UTSW 11 36,047,074 (GRCm38) missense probably benign 0.04
R4062:Tenm2 UTSW 11 36,008,655 (GRCm38) missense probably damaging 1.00
R4367:Tenm2 UTSW 11 36,027,398 (GRCm38) missense probably benign
R4395:Tenm2 UTSW 11 36,024,624 (GRCm38) missense probably benign 0.23
R4508:Tenm2 UTSW 11 36,008,345 (GRCm38) missense possibly damaging 0.82
R4534:Tenm2 UTSW 11 36,063,104 (GRCm38) missense possibly damaging 0.64
R4539:Tenm2 UTSW 11 36,046,780 (GRCm38) missense probably damaging 1.00
R4644:Tenm2 UTSW 11 36,047,136 (GRCm38) missense probably benign 0.00
R4661:Tenm2 UTSW 11 36,024,448 (GRCm38) missense probably damaging 0.99
R4669:Tenm2 UTSW 11 36,010,487 (GRCm38) missense probably damaging 1.00
R4687:Tenm2 UTSW 11 36,049,097 (GRCm38) missense probably benign
R4711:Tenm2 UTSW 11 36,300,212 (GRCm38) missense probably damaging 0.98
R4816:Tenm2 UTSW 11 36,027,290 (GRCm38) missense probably damaging 1.00
R4843:Tenm2 UTSW 11 36,024,020 (GRCm38) missense probably damaging 1.00
R4850:Tenm2 UTSW 11 36,023,488 (GRCm38) nonsense probably null
R4870:Tenm2 UTSW 11 36,078,569 (GRCm38) missense probably damaging 1.00
R5058:Tenm2 UTSW 11 36,207,080 (GRCm38) missense possibly damaging 0.80
R5071:Tenm2 UTSW 11 36,068,381 (GRCm38) missense probably damaging 0.99
R5073:Tenm2 UTSW 11 36,068,381 (GRCm38) missense probably damaging 0.99
R5074:Tenm2 UTSW 11 36,068,381 (GRCm38) missense probably damaging 0.99
R5081:Tenm2 UTSW 11 36,024,633 (GRCm38) missense possibly damaging 0.95
R5093:Tenm2 UTSW 11 36,944,162 (GRCm38) missense probably damaging 1.00
R5170:Tenm2 UTSW 11 36,024,806 (GRCm38) missense probably damaging 0.98
R5253:Tenm2 UTSW 11 36,047,201 (GRCm38) nonsense probably null
R5343:Tenm2 UTSW 11 36,069,503 (GRCm38) missense probably benign 0.00
R5493:Tenm2 UTSW 11 36,864,676 (GRCm38) missense probably benign 0.01
R5600:Tenm2 UTSW 11 36,163,714 (GRCm38) splice site probably null
R5677:Tenm2 UTSW 11 36,141,683 (GRCm38) missense probably damaging 0.98
R5703:Tenm2 UTSW 11 36,023,799 (GRCm38) missense probably benign 0.34
R5707:Tenm2 UTSW 11 36,047,182 (GRCm38) missense possibly damaging 0.79
R6026:Tenm2 UTSW 11 36,072,729 (GRCm38) critical splice donor site probably null
R6063:Tenm2 UTSW 11 36,163,717 (GRCm38) critical splice donor site probably null
R6086:Tenm2 UTSW 11 36,008,646 (GRCm38) missense possibly damaging 0.64
R6151:Tenm2 UTSW 11 36,008,783 (GRCm38) missense probably damaging 1.00
R6169:Tenm2 UTSW 11 36,139,690 (GRCm38) missense probably damaging 0.99
R6193:Tenm2 UTSW 11 36,046,794 (GRCm38) missense probably damaging 1.00
R6405:Tenm2 UTSW 11 36,864,859 (GRCm38) missense probably benign 0.44
R6477:Tenm2 UTSW 11 36,010,507 (GRCm38) critical splice acceptor site probably null
R6607:Tenm2 UTSW 11 36,063,775 (GRCm38) critical splice donor site probably null
R6668:Tenm2 UTSW 11 36,046,765 (GRCm38) critical splice donor site probably null
R6825:Tenm2 UTSW 11 36,046,884 (GRCm38) missense probably benign 0.02
R6885:Tenm2 UTSW 11 36,023,580 (GRCm38) missense possibly damaging 0.95
R7017:Tenm2 UTSW 11 36,171,409 (GRCm38) missense probably damaging 0.98
R7115:Tenm2 UTSW 11 36,163,817 (GRCm38) missense probably damaging 0.99
R7153:Tenm2 UTSW 11 36,024,182 (GRCm38) missense probably damaging 0.98
R7173:Tenm2 UTSW 11 36,041,551 (GRCm38) missense probably damaging 0.99
R7199:Tenm2 UTSW 11 36,171,436 (GRCm38) missense probably damaging 1.00
R7205:Tenm2 UTSW 11 36,049,129 (GRCm38) missense probably damaging 0.99
R7250:Tenm2 UTSW 11 36,072,798 (GRCm38) missense probably damaging 1.00
R7290:Tenm2 UTSW 11 36,023,471 (GRCm38) missense probably damaging 1.00
R7366:Tenm2 UTSW 11 36,069,414 (GRCm38) missense probably benign 0.09
R7432:Tenm2 UTSW 11 36,864,941 (GRCm38) missense probably benign
R7504:Tenm2 UTSW 11 36,139,743 (GRCm38) missense probably damaging 1.00
R7513:Tenm2 UTSW 11 36,051,900 (GRCm38) missense probably benign 0.34
R7523:Tenm2 UTSW 11 36,078,581 (GRCm38) splice site probably null
R7527:Tenm2 UTSW 11 36,206,976 (GRCm38) missense probably damaging 1.00
R7648:Tenm2 UTSW 11 36,106,736 (GRCm38) missense probably damaging 1.00
R7653:Tenm2 UTSW 11 36,047,347 (GRCm38) missense probably benign 0.09
R7717:Tenm2 UTSW 11 36,864,935 (GRCm38) missense probably damaging 0.97
R7739:Tenm2 UTSW 11 36,069,561 (GRCm38) missense possibly damaging 0.50
R7762:Tenm2 UTSW 11 36,023,306 (GRCm38) missense possibly damaging 0.74
R7786:Tenm2 UTSW 11 36,010,449 (GRCm38) missense probably damaging 0.99
R7834:Tenm2 UTSW 11 36,024,854 (GRCm38) missense probably damaging 1.00
R7838:Tenm2 UTSW 11 36,106,799 (GRCm38) missense probably benign 0.02
R8073:Tenm2 UTSW 11 36,139,644 (GRCm38) missense possibly damaging 0.56
R8076:Tenm2 UTSW 11 36,027,221 (GRCm38) missense probably benign 0.23
R8109:Tenm2 UTSW 11 36,008,310 (GRCm38) missense probably benign
R8306:Tenm2 UTSW 11 36,069,369 (GRCm38) missense possibly damaging 0.52
R8352:Tenm2 UTSW 11 36,023,601 (GRCm38) missense probably damaging 0.98
R8452:Tenm2 UTSW 11 36,023,601 (GRCm38) missense probably damaging 0.98
R8864:Tenm2 UTSW 11 36,027,195 (GRCm38) missense possibly damaging 0.95
R8880:Tenm2 UTSW 11 36,051,961 (GRCm38) missense probably damaging 0.99
R8943:Tenm2 UTSW 11 36,944,034 (GRCm38) missense probably damaging 0.98
R8969:Tenm2 UTSW 11 36,051,861 (GRCm38) missense probably damaging 0.99
R9168:Tenm2 UTSW 11 36,039,895 (GRCm38) missense probably damaging 1.00
R9279:Tenm2 UTSW 11 36,068,476 (GRCm38) missense probably benign 0.00
R9294:Tenm2 UTSW 11 36,024,500 (GRCm38) missense probably damaging 0.98
R9320:Tenm2 UTSW 11 36,023,647 (GRCm38) missense probably damaging 0.99
R9373:Tenm2 UTSW 11 36,039,886 (GRCm38) missense probably damaging 1.00
R9408:Tenm2 UTSW 11 36,069,419 (GRCm38) missense probably damaging 1.00
R9410:Tenm2 UTSW 11 36,141,569 (GRCm38) missense probably damaging 0.99
R9454:Tenm2 UTSW 11 36,221,459 (GRCm38) missense probably benign
R9489:Tenm2 UTSW 11 36,943,964 (GRCm38) missense probably damaging 0.99
R9711:Tenm2 UTSW 11 36,024,514 (GRCm38) missense probably damaging 0.99
RF021:Tenm2 UTSW 11 36,024,203 (GRCm38) missense possibly damaging 0.95
X0018:Tenm2 UTSW 11 36,024,200 (GRCm38) missense probably damaging 1.00
X0063:Tenm2 UTSW 11 36,024,730 (GRCm38) missense probably benign
Z1088:Tenm2 UTSW 11 36,273,267 (GRCm38) missense probably damaging 1.00
Z1177:Tenm2 UTSW 11 36,385,130 (GRCm38) missense probably benign 0.01
Z1177:Tenm2 UTSW 11 36,300,335 (GRCm38) missense probably damaging 0.98
Z1177:Tenm2 UTSW 11 36,008,234 (GRCm38) missense possibly damaging 0.95
Predicted Primers PCR Primer
(F):5'- CCCACGGTAAGGGTGATAATCTG -3'
(R):5'- ATCTGCTACTCGGGAGATGAC -3'

Sequencing Primer
(F):5'- TCTGATTATCAGGCATGAGCAG -3'
(R):5'- TACTCGGGAGATGACGCTTAC -3'
Posted On 2019-11-26