Incidental Mutation 'R4697:Tln2'
ID 355784
Institutional Source Beutler Lab
Gene Symbol Tln2
Ensembl Gene ENSMUSG00000052698
Gene Name talin 2
Synonyms
MMRRC Submission 041947-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.216) question?
Stock # R4697 (G1)
Quality Score 225
Status Validated
Chromosome 9
Chromosomal Location 67217087-67559703 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) C to T at 67395461 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Arginine to Glutamine at position 76 (R76Q)
Ref Sequence ENSEMBL: ENSMUSP00000039633 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000039662] [ENSMUST00000040025] [ENSMUST00000213584] [ENSMUST00000215784]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000039662
AA Change: R76Q

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000035272
Gene: ENSMUSG00000052698
AA Change: R76Q

DomainStartEndE-ValueType
B41 84 316 1.29e-66 SMART
IRS 311 404 6.31e-17 SMART
Pfam:Talin_middle 494 655 3.4e-59 PFAM
Pfam:I_LWEQ 661 765 1.9e-10 PFAM
low complexity region 770 778 N/A INTRINSIC
PDB:2L7A|A 797 901 3e-44 PDB
low complexity region 902 918 N/A INTRINSIC
low complexity region 923 946 N/A INTRINSIC
internal_repeat_4 973 1033 7.18e-6 PROSPERO
internal_repeat_3 1083 1210 3.53e-6 PROSPERO
internal_repeat_4 1138 1198 7.18e-6 PROSPERO
low complexity region 1313 1325 N/A INTRINSIC
low complexity region 1330 1343 N/A INTRINSIC
internal_repeat_1 1482 1554 2.88e-9 PROSPERO
internal_repeat_2 1491 1551 2.05e-7 PROSPERO
low complexity region 1679 1690 N/A INTRINSIC
Pfam:VBS 1850 1974 2.6e-67 PFAM
internal_repeat_3 2010 2138 3.53e-6 PROSPERO
low complexity region 2309 2325 N/A INTRINSIC
low complexity region 2349 2359 N/A INTRINSIC
Pfam:I_LWEQ 2384 2531 2.5e-52 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000040025
AA Change: R76Q

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000039633
Gene: ENSMUSG00000052698
AA Change: R76Q

DomainStartEndE-ValueType
B41 84 316 1.29e-66 SMART
IRS 311 404 6.31e-17 SMART
Pfam:Talin_middle 494 655 8.5e-78 PFAM
low complexity region 674 693 N/A INTRINSIC
internal_repeat_2 703 763 2.05e-7 PROSPERO
low complexity region 770 778 N/A INTRINSIC
PDB:2L7A|A 797 901 3e-44 PDB
low complexity region 902 918 N/A INTRINSIC
low complexity region 923 946 N/A INTRINSIC
internal_repeat_4 973 1033 7.18e-6 PROSPERO
internal_repeat_3 1083 1210 3.53e-6 PROSPERO
internal_repeat_4 1138 1198 7.18e-6 PROSPERO
low complexity region 1313 1325 N/A INTRINSIC
low complexity region 1330 1343 N/A INTRINSIC
internal_repeat_1 1482 1554 2.88e-9 PROSPERO
internal_repeat_2 1491 1551 2.05e-7 PROSPERO
low complexity region 1679 1690 N/A INTRINSIC
Pfam:VBS 1850 1974 9.9e-72 PFAM
internal_repeat_3 2010 2138 3.53e-6 PROSPERO
low complexity region 2309 2325 N/A INTRINSIC
low complexity region 2349 2359 N/A INTRINSIC
Pfam:I_LWEQ 2383 2533 4.3e-51 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000213584
AA Change: R78Q

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
Predicted Effect probably damaging
Transcript: ENSMUST00000215784
AA Change: R78Q

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
Meta Mutation Damage Score 0.2693 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.5%
Validation Efficiency 96% (75/78)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein related to talin 1, a cytoskeletal protein that plays a significant role in the assembly of actin filaments and in spreading and migration of various cell types, including fibroblasts and osteoclasts. This protein has a different pattern of expression compared to talin 1 but, like talin 1, is thought to associate with unique transmembrane receptors to form novel linkages between extracellular matrices and the actin cytoskeleton. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit abnormal muscle morphology. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9030624J02Rik T A 7: 118,791,448 (GRCm38) I455N probably damaging Het
A2m T C 6: 121,638,284 (GRCm38) M1T probably null Het
Aatf T A 11: 84,449,138 (GRCm38) D449V probably damaging Het
Acbd3 T A 1: 180,721,944 (GRCm38) probably benign Het
BC005561 A G 5: 104,522,240 (GRCm38) K1543E probably benign Het
Bicc1 T A 10: 70,953,484 (GRCm38) I366F possibly damaging Het
Ccdc74a T C 16: 17,649,749 (GRCm38) S184P possibly damaging Het
Cntn4 T C 6: 106,525,485 (GRCm38) V401A probably damaging Het
Cux2 T C 5: 121,873,753 (GRCm38) T540A probably damaging Het
Disp2 G T 2: 118,791,684 (GRCm38) E966* probably null Het
Dpp7 A G 2: 25,354,919 (GRCm38) Y209H probably benign Het
Dstyk T A 1: 132,449,487 (GRCm38) F277Y probably damaging Het
Dtx1 A T 5: 120,694,408 (GRCm38) probably null Het
Ear-ps2 G A 14: 44,047,060 (GRCm38) noncoding transcript Het
Ednra T C 8: 77,664,995 (GRCm38) H422R probably benign Het
Erlec1 T A 11: 30,952,640 (GRCm38) I67F probably benign Het
Fam161b G A 12: 84,348,558 (GRCm38) probably benign Het
Gata5 A T 2: 180,327,379 (GRCm38) C345* probably null Het
Glmp T C 3: 88,328,274 (GRCm38) V47A probably damaging Het
Gm9762 T A 3: 78,966,550 (GRCm38) noncoding transcript Het
Gnas A T 2: 174,298,080 (GRCm38) D14V probably damaging Het
Gnl3 T C 14: 31,017,329 (GRCm38) S53G probably damaging Het
Grhl3 C T 4: 135,548,466 (GRCm38) V527M probably damaging Het
Hoxd10 T A 2: 74,694,187 (GRCm38) L281* probably null Het
Kif16b T G 2: 142,690,694 (GRCm38) Y1175S probably benign Het
Kif2b A G 11: 91,576,846 (GRCm38) S204P probably benign Het
Klhl40 T A 9: 121,778,734 (GRCm38) I320N probably damaging Het
Ksr2 G A 5: 117,708,147 (GRCm38) R693Q probably damaging Het
Mis12 A G 11: 71,025,326 (GRCm38) K62E possibly damaging Het
Mlc1 A G 15: 88,974,777 (GRCm38) C102R probably damaging Het
Muc5b T C 7: 141,857,361 (GRCm38) I1348T unknown Het
Myh7b A G 2: 155,629,322 (GRCm38) E1130G probably damaging Het
Nat8f4 T C 6: 85,901,386 (GRCm38) T52A probably benign Het
Nxpe2 C A 9: 48,320,521 (GRCm38) V379L probably benign Het
Olfr1231 C A 2: 89,302,902 (GRCm38) S230I possibly damaging Het
Olfr1231 T A 2: 89,302,903 (GRCm38) S230C probably damaging Het
Olfr1448 C T 19: 12,919,934 (GRCm38) C125Y probably damaging Het
Olfr1465 A T 19: 13,313,717 (GRCm38) D189E probably benign Het
Olfr288 G A 15: 98,186,868 (GRCm38) R310W probably damaging Het
Pcdhga7 A T 18: 37,717,208 (GRCm38) Y756F probably damaging Het
Pcsk6 T A 7: 65,959,241 (GRCm38) Y284N probably damaging Het
Pdcd11 T C 19: 47,126,347 (GRCm38) V1367A possibly damaging Het
Postn T A 3: 54,375,071 (GRCm38) N484K probably damaging Het
Prkd3 C T 17: 78,961,171 (GRCm38) V572I probably benign Het
Qser1 T C 2: 104,787,183 (GRCm38) S1005G probably benign Het
Radil G T 5: 142,486,801 (GRCm38) D951E probably benign Het
Ripk1 C T 13: 34,027,942 (GRCm38) R352* probably null Het
Sacs T C 14: 61,212,747 (GRCm38) F4081L probably benign Het
Sbf1 A G 15: 89,315,085 (GRCm38) V11A possibly damaging Het
Sgip1 T A 4: 102,934,587 (GRCm38) F536I probably damaging Het
Slc45a1 A G 4: 150,638,284 (GRCm38) L381P probably damaging Het
Smarcad1 C T 6: 65,052,641 (GRCm38) P71L probably benign Het
Spns1 T A 7: 126,377,037 (GRCm38) D14V probably damaging Het
Sv2c T A 13: 95,986,018 (GRCm38) I417F possibly damaging Het
Tas2r113 T A 6: 132,893,516 (GRCm38) M169K probably benign Het
Tgm1 A T 14: 55,705,681 (GRCm38) N567K probably benign Het
Trpm6 T C 19: 18,853,791 (GRCm38) V1340A probably benign Het
Tspan18 A T 2: 93,312,030 (GRCm38) probably null Het
Txndc11 C T 16: 11,084,314 (GRCm38) V679I probably damaging Het
Usf1 G T 1: 171,416,964 (GRCm38) G144V possibly damaging Het
Vmn1r59 T C 7: 5,454,452 (GRCm38) Y103C probably damaging Het
Vmn2r23 A T 6: 123,741,826 (GRCm38) I713F probably damaging Het
Vmn2r79 A T 7: 87,037,960 (GRCm38) I850F probably damaging Het
Wdr90 C T 17: 25,855,363 (GRCm38) R676H probably benign Het
Zfp867 G A 11: 59,463,661 (GRCm38) R281W probably damaging Het
Zfp939 T C 7: 39,472,942 (GRCm38) noncoding transcript Het
Other mutations in Tln2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00468:Tln2 APN 9 67,344,187 (GRCm38) missense possibly damaging 0.59
IGL01110:Tln2 APN 9 67,250,582 (GRCm38) nonsense probably null
IGL01112:Tln2 APN 9 67,311,811 (GRCm38) missense probably damaging 1.00
IGL01307:Tln2 APN 9 67,395,467 (GRCm38) missense probably benign 0.25
IGL01374:Tln2 APN 9 67,261,923 (GRCm38) missense probably damaging 1.00
IGL01625:Tln2 APN 9 67,370,623 (GRCm38) missense probably damaging 1.00
IGL01865:Tln2 APN 9 67,250,614 (GRCm38) nonsense probably null
IGL01999:Tln2 APN 9 67,392,505 (GRCm38) missense possibly damaging 0.81
IGL02002:Tln2 APN 9 67,356,698 (GRCm38) missense probably damaging 0.98
IGL02005:Tln2 APN 9 67,392,505 (GRCm38) missense possibly damaging 0.81
IGL02015:Tln2 APN 9 67,361,439 (GRCm38) splice site probably benign
IGL02368:Tln2 APN 9 67,240,810 (GRCm38) splice site probably benign
IGL02444:Tln2 APN 9 67,258,592 (GRCm38) splice site probably benign
IGL02646:Tln2 APN 9 67,255,996 (GRCm38) missense probably benign 0.43
IGL02744:Tln2 APN 9 67,229,376 (GRCm38) nonsense probably null
IGL02869:Tln2 APN 9 67,221,525 (GRCm38) splice site probably benign
IGL02930:Tln2 APN 9 67,393,662 (GRCm38) nonsense probably null
IGL03100:Tln2 APN 9 67,295,737 (GRCm38) missense probably damaging 1.00
IGL03326:Tln2 APN 9 67,334,257 (GRCm38) missense possibly damaging 0.67
Harrier UTSW 9 67,330,552 (GRCm38) nonsense probably null
Marsh UTSW 9 67,272,654 (GRCm38) missense probably benign 0.19
BB008:Tln2 UTSW 9 67,258,460 (GRCm38) critical splice donor site probably null
BB018:Tln2 UTSW 9 67,258,460 (GRCm38) critical splice donor site probably null
R0047:Tln2 UTSW 9 67,240,672 (GRCm38) splice site probably benign
R0047:Tln2 UTSW 9 67,240,672 (GRCm38) splice site probably benign
R0107:Tln2 UTSW 9 67,370,706 (GRCm38) missense probably damaging 1.00
R0494:Tln2 UTSW 9 67,355,197 (GRCm38) missense probably benign 0.22
R0884:Tln2 UTSW 9 67,370,733 (GRCm38) missense probably damaging 1.00
R0947:Tln2 UTSW 9 67,295,813 (GRCm38) missense probably benign 0.08
R0989:Tln2 UTSW 9 67,229,454 (GRCm38) missense probably damaging 1.00
R1195:Tln2 UTSW 9 67,258,566 (GRCm38) missense probably damaging 0.96
R1195:Tln2 UTSW 9 67,258,566 (GRCm38) missense probably damaging 0.96
R1195:Tln2 UTSW 9 67,258,566 (GRCm38) missense probably damaging 0.96
R1486:Tln2 UTSW 9 67,311,839 (GRCm38) missense probably damaging 1.00
R1527:Tln2 UTSW 9 67,272,668 (GRCm38) missense possibly damaging 0.95
R1584:Tln2 UTSW 9 67,296,414 (GRCm38) missense probably damaging 1.00
R1636:Tln2 UTSW 9 67,306,532 (GRCm38) missense probably damaging 1.00
R1656:Tln2 UTSW 9 67,227,107 (GRCm38) missense possibly damaging 0.81
R1707:Tln2 UTSW 9 67,375,807 (GRCm38) missense probably benign 0.00
R1749:Tln2 UTSW 9 67,286,514 (GRCm38) missense probably benign 0.01
R1751:Tln2 UTSW 9 67,286,514 (GRCm38) missense probably benign 0.01
R1761:Tln2 UTSW 9 67,286,514 (GRCm38) missense probably benign 0.01
R1767:Tln2 UTSW 9 67,286,514 (GRCm38) missense probably benign 0.01
R1815:Tln2 UTSW 9 67,229,423 (GRCm38) missense probably damaging 1.00
R1840:Tln2 UTSW 9 67,342,043 (GRCm38) missense probably damaging 1.00
R1847:Tln2 UTSW 9 67,362,687 (GRCm38) nonsense probably null
R1964:Tln2 UTSW 9 67,342,135 (GRCm38) missense probably benign 0.00
R1968:Tln2 UTSW 9 67,255,901 (GRCm38) missense probably damaging 1.00
R2036:Tln2 UTSW 9 67,272,704 (GRCm38) missense possibly damaging 0.76
R2038:Tln2 UTSW 9 67,397,653 (GRCm38) start codon destroyed probably benign 0.01
R2152:Tln2 UTSW 9 67,302,560 (GRCm38) missense probably damaging 1.00
R2153:Tln2 UTSW 9 67,302,560 (GRCm38) missense probably damaging 1.00
R2154:Tln2 UTSW 9 67,302,560 (GRCm38) missense probably damaging 1.00
R2191:Tln2 UTSW 9 67,355,221 (GRCm38) missense probably damaging 1.00
R2192:Tln2 UTSW 9 67,355,221 (GRCm38) missense probably damaging 1.00
R2201:Tln2 UTSW 9 67,375,757 (GRCm38) missense probably damaging 1.00
R3116:Tln2 UTSW 9 67,355,139 (GRCm38) missense probably benign 0.10
R3151:Tln2 UTSW 9 67,330,547 (GRCm38) critical splice donor site probably null
R3795:Tln2 UTSW 9 67,255,915 (GRCm38) missense probably damaging 0.97
R3953:Tln2 UTSW 9 67,370,629 (GRCm38) missense probably damaging 1.00
R4450:Tln2 UTSW 9 67,344,065 (GRCm38) critical splice donor site probably null
R4685:Tln2 UTSW 9 67,302,572 (GRCm38) missense probably damaging 1.00
R4688:Tln2 UTSW 9 67,397,653 (GRCm38) start codon destroyed probably benign 0.01
R4696:Tln2 UTSW 9 67,395,461 (GRCm38) missense probably damaging 1.00
R4700:Tln2 UTSW 9 67,346,527 (GRCm38) missense probably benign 0.03
R4701:Tln2 UTSW 9 67,346,527 (GRCm38) missense probably benign 0.03
R4741:Tln2 UTSW 9 67,386,555 (GRCm38) critical splice donor site probably null
R4806:Tln2 UTSW 9 67,331,733 (GRCm38) missense probably benign 0.29
R4807:Tln2 UTSW 9 67,331,733 (GRCm38) missense probably benign 0.29
R4808:Tln2 UTSW 9 67,331,733 (GRCm38) missense probably benign 0.29
R4967:Tln2 UTSW 9 67,355,125 (GRCm38) missense probably damaging 0.97
R5061:Tln2 UTSW 9 67,354,468 (GRCm38) missense probably benign
R5092:Tln2 UTSW 9 67,256,028 (GRCm38) missense probably benign 0.13
R5093:Tln2 UTSW 9 67,334,314 (GRCm38) missense probably benign 0.44
R5126:Tln2 UTSW 9 67,258,535 (GRCm38) missense probably damaging 1.00
R5204:Tln2 UTSW 9 67,354,482 (GRCm38) missense probably benign 0.00
R5236:Tln2 UTSW 9 67,365,923 (GRCm38) missense probably damaging 0.99
R5287:Tln2 UTSW 9 67,242,359 (GRCm38) missense probably damaging 1.00
R5568:Tln2 UTSW 9 67,311,865 (GRCm38) missense probably damaging 1.00
R5571:Tln2 UTSW 9 67,334,320 (GRCm38) missense possibly damaging 0.88
R5642:Tln2 UTSW 9 67,296,358 (GRCm38) missense probably benign 0.01
R5711:Tln2 UTSW 9 67,392,547 (GRCm38) missense probably benign 0.00
R5776:Tln2 UTSW 9 67,258,250 (GRCm38) missense probably damaging 1.00
R5791:Tln2 UTSW 9 67,386,605 (GRCm38) missense probably damaging 0.98
R5866:Tln2 UTSW 9 67,266,868 (GRCm38) missense probably damaging 1.00
R5888:Tln2 UTSW 9 67,229,403 (GRCm38) missense probably damaging 1.00
R5902:Tln2 UTSW 9 67,362,717 (GRCm38) missense probably benign 0.02
R6106:Tln2 UTSW 9 67,323,020 (GRCm38) missense probably damaging 0.99
R6175:Tln2 UTSW 9 67,224,081 (GRCm38) missense probably damaging 1.00
R6385:Tln2 UTSW 9 67,278,129 (GRCm38) missense probably benign 0.45
R6430:Tln2 UTSW 9 67,272,665 (GRCm38) missense probably damaging 1.00
R6441:Tln2 UTSW 9 67,272,689 (GRCm38) missense probably damaging 1.00
R6738:Tln2 UTSW 9 67,386,664 (GRCm38) missense possibly damaging 0.91
R6776:Tln2 UTSW 9 67,262,905 (GRCm38) missense probably damaging 1.00
R6794:Tln2 UTSW 9 67,286,558 (GRCm38) missense probably benign 0.07
R6850:Tln2 UTSW 9 67,258,535 (GRCm38) missense probably damaging 1.00
R6907:Tln2 UTSW 9 67,397,635 (GRCm38) missense probably damaging 0.98
R6909:Tln2 UTSW 9 67,392,532 (GRCm38) missense probably damaging 0.97
R6951:Tln2 UTSW 9 67,258,485 (GRCm38) missense probably damaging 0.97
R7015:Tln2 UTSW 9 67,362,647 (GRCm38) missense possibly damaging 0.55
R7051:Tln2 UTSW 9 67,346,417 (GRCm38) missense probably benign 0.00
R7246:Tln2 UTSW 9 67,262,979 (GRCm38) missense probably damaging 1.00
R7292:Tln2 UTSW 9 67,346,461 (GRCm38) missense probably benign
R7753:Tln2 UTSW 9 67,395,473 (GRCm38) missense probably damaging 1.00
R7868:Tln2 UTSW 9 67,348,226 (GRCm38) missense probably damaging 1.00
R7931:Tln2 UTSW 9 67,258,460 (GRCm38) critical splice donor site probably null
R8023:Tln2 UTSW 9 67,224,064 (GRCm38) missense probably damaging 1.00
R8081:Tln2 UTSW 9 67,356,747 (GRCm38) missense probably damaging 1.00
R8164:Tln2 UTSW 9 67,319,420 (GRCm38) missense probably benign 0.31
R8192:Tln2 UTSW 9 67,346,529 (GRCm38) nonsense probably null
R8495:Tln2 UTSW 9 67,354,467 (GRCm38) missense probably benign 0.01
R8734:Tln2 UTSW 9 67,272,654 (GRCm38) missense probably benign 0.19
R8739:Tln2 UTSW 9 67,258,273 (GRCm38) missense probably damaging 1.00
R8757:Tln2 UTSW 9 67,367,218 (GRCm38) missense probably damaging 1.00
R8759:Tln2 UTSW 9 67,367,218 (GRCm38) missense probably damaging 1.00
R8770:Tln2 UTSW 9 67,323,022 (GRCm38) missense probably benign
R8781:Tln2 UTSW 9 67,255,951 (GRCm38) missense probably damaging 1.00
R8812:Tln2 UTSW 9 67,221,411 (GRCm38) missense possibly damaging 0.75
R8814:Tln2 UTSW 9 67,221,411 (GRCm38) missense possibly damaging 0.75
R8816:Tln2 UTSW 9 67,221,517 (GRCm38) missense probably damaging 1.00
R8816:Tln2 UTSW 9 67,221,411 (GRCm38) missense possibly damaging 0.75
R8833:Tln2 UTSW 9 67,221,411 (GRCm38) missense possibly damaging 0.75
R8835:Tln2 UTSW 9 67,397,693 (GRCm38) splice site probably benign
R8837:Tln2 UTSW 9 67,250,584 (GRCm38) missense probably damaging 0.99
R8843:Tln2 UTSW 9 67,395,545 (GRCm38) missense probably damaging 1.00
R8864:Tln2 UTSW 9 67,330,552 (GRCm38) nonsense probably null
R8867:Tln2 UTSW 9 67,330,550 (GRCm38) missense probably damaging 0.98
R8921:Tln2 UTSW 9 67,266,823 (GRCm38) missense probably damaging 0.99
R9080:Tln2 UTSW 9 67,346,561 (GRCm38) missense probably damaging 1.00
R9083:Tln2 UTSW 9 67,362,645 (GRCm38) missense probably damaging 0.96
R9150:Tln2 UTSW 9 67,221,496 (GRCm38) missense probably damaging 1.00
R9287:Tln2 UTSW 9 67,370,698 (GRCm38) missense probably benign 0.20
R9330:Tln2 UTSW 9 67,321,931 (GRCm38) missense possibly damaging 0.61
R9343:Tln2 UTSW 9 67,323,071 (GRCm38) missense probably benign 0.10
R9355:Tln2 UTSW 9 67,355,247 (GRCm38) missense possibly damaging 0.46
R9383:Tln2 UTSW 9 67,370,761 (GRCm38) missense probably benign 0.17
R9386:Tln2 UTSW 9 67,365,967 (GRCm38) missense possibly damaging 0.78
R9407:Tln2 UTSW 9 67,229,450 (GRCm38) missense probably damaging 1.00
R9483:Tln2 UTSW 9 67,392,487 (GRCm38) missense probably damaging 1.00
R9523:Tln2 UTSW 9 67,258,484 (GRCm38) missense probably damaging 0.99
R9642:Tln2 UTSW 9 67,250,544 (GRCm38) missense probably benign 0.02
R9703:Tln2 UTSW 9 67,386,656 (GRCm38) missense probably damaging 1.00
X0027:Tln2 UTSW 9 67,376,853 (GRCm38) missense probably damaging 1.00
X0064:Tln2 UTSW 9 67,348,138 (GRCm38) missense probably damaging 1.00
X0067:Tln2 UTSW 9 67,370,691 (GRCm38) missense probably damaging 1.00
Z1176:Tln2 UTSW 9 67,346,485 (GRCm38) missense possibly damaging 0.46
Predicted Primers PCR Primer
(F):5'- TTCCATAGGTAGCTCCCCAG -3'
(R):5'- GTGATGGACAGTATCGTCCTCC -3'

Sequencing Primer
(F):5'- TGGCACCAAGACTGTTTAGC -3'
(R):5'- GATGGACAGTATCGTCCTCCTTTCTG -3'
Posted On 2015-10-21