Incidental Mutation 'IGL01977:Ltbp2'
ID 181723
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ltbp2
Ensembl Gene ENSMUSG00000002020
Gene Name latent transforming growth factor beta binding protein 2
Synonyms
Accession Numbers
Essential gene? Probably essential (E-score: 0.794) question?
Stock # IGL01977
Quality Score
Status
Chromosome 12
Chromosomal Location 84829986-84923306 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 84876973 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Aspartic acid at position 391 (N391D)
Ref Sequence ENSEMBL: ENSMUSP00000002073 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000002073] [ENSMUST00000110254] [ENSMUST00000163189]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000002073
AA Change: N391D

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000002073
Gene: ENSMUSG00000002020
AA Change: N391D

DomainStartEndE-ValueType
signal peptide 1 35 N/A INTRINSIC
low complexity region 99 108 N/A INTRINSIC
EGF 184 213 6.55e-1 SMART
low complexity region 255 275 N/A INTRINSIC
EGF 384 413 8.19e-2 SMART
low complexity region 515 526 N/A INTRINSIC
Pfam:TB 546 582 3.8e-9 PFAM
EGF_CA 606 646 8.05e-10 SMART
Pfam:TB 666 707 3.4e-17 PFAM
EGF_CA 832 874 7.18e-7 SMART
EGF_CA 875 917 1.75e-10 SMART
EGF_CA 918 957 1.53e-10 SMART
EGF_CA 958 997 3.51e-10 SMART
EGF_CA 998 1038 8.3e-12 SMART
EGF_CA 1039 1080 4.56e-9 SMART
EGF_CA 1081 1122 4.56e-9 SMART
EGF_CA 1123 1163 8.76e-11 SMART
EGF_CA 1164 1205 4.38e-11 SMART
EGF_CA 1206 1246 1.75e-10 SMART
EGF_CA 1247 1290 2.24e-8 SMART
EGF_CA 1291 1332 6.01e-9 SMART
EGF 1336 1375 1.95e1 SMART
Pfam:TB 1410 1450 1.4e-13 PFAM
EGF_CA 1473 1515 2.31e-10 SMART
EGF_CA 1516 1555 7.93e-9 SMART
Pfam:TB 1582 1623 1e-13 PFAM
low complexity region 1691 1704 N/A INTRINSIC
EGF 1724 1761 4e-5 SMART
EGF_CA 1762 1806 1.91e-11 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000110254
AA Change: N411D

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000105883
Gene: ENSMUSG00000002020
AA Change: N411D

DomainStartEndE-ValueType
low complexity region 119 128 N/A INTRINSIC
EGF 204 233 6.55e-1 SMART
low complexity region 275 295 N/A INTRINSIC
EGF 404 433 8.19e-2 SMART
low complexity region 535 546 N/A INTRINSIC
Pfam:TB 565 602 4e-8 PFAM
EGF_CA 626 666 8.05e-10 SMART
Pfam:TB 685 727 3.7e-16 PFAM
EGF_CA 852 894 7.18e-7 SMART
EGF_CA 895 934 1.53e-10 SMART
EGF_CA 935 974 3.51e-10 SMART
EGF_CA 975 1015 8.3e-12 SMART
EGF_CA 1016 1057 4.56e-9 SMART
EGF_CA 1058 1099 4.56e-9 SMART
EGF_CA 1100 1140 8.76e-11 SMART
EGF_CA 1141 1182 4.38e-11 SMART
EGF_CA 1183 1223 1.75e-10 SMART
EGF_CA 1224 1267 2.24e-8 SMART
EGF_CA 1268 1309 6.01e-9 SMART
EGF 1313 1352 1.95e1 SMART
Pfam:TB 1387 1427 1.4e-11 PFAM
EGF_CA 1450 1492 2.31e-10 SMART
EGF_CA 1493 1532 7.93e-9 SMART
Pfam:TB 1558 1600 4.6e-13 PFAM
low complexity region 1668 1681 N/A INTRINSIC
EGF 1701 1738 4e-5 SMART
EGF_CA 1739 1783 1.91e-11 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000163189
AA Change: N391D

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000127693
Gene: ENSMUSG00000002020
AA Change: N391D

DomainStartEndE-ValueType
signal peptide 1 35 N/A INTRINSIC
low complexity region 99 108 N/A INTRINSIC
EGF 184 213 6.55e-1 SMART
low complexity region 255 275 N/A INTRINSIC
EGF 384 413 8.19e-2 SMART
low complexity region 515 526 N/A INTRINSIC
Pfam:TB 545 582 4e-8 PFAM
EGF_CA 606 646 8.05e-10 SMART
Pfam:TB 665 707 3.8e-16 PFAM
EGF_CA 832 874 7.18e-7 SMART
EGF_CA 875 914 1.53e-10 SMART
EGF_CA 915 954 3.51e-10 SMART
EGF_CA 955 995 8.3e-12 SMART
EGF_CA 996 1037 4.56e-9 SMART
EGF_CA 1038 1079 4.56e-9 SMART
EGF_CA 1080 1120 8.76e-11 SMART
EGF_CA 1121 1162 4.38e-11 SMART
EGF_CA 1163 1203 1.75e-10 SMART
EGF_CA 1204 1247 2.24e-8 SMART
EGF_CA 1248 1289 6.01e-9 SMART
EGF 1293 1332 1.95e1 SMART
Pfam:TB 1367 1407 1.5e-11 PFAM
EGF_CA 1430 1472 2.31e-10 SMART
EGF_CA 1473 1512 7.93e-9 SMART
Pfam:TB 1538 1580 4.7e-13 PFAM
low complexity region 1648 1661 N/A INTRINSIC
EGF 1681 1718 4e-5 SMART
EGF_CA 1719 1763 1.91e-11 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000168699
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the family of latent transforming growth factor (TGF)-beta binding proteins (LTBP), which are extracellular matrix proteins with multi-domain structure. This protein is the largest member of the LTBP family possessing unique regions and with most similarity to the fibrillins. It has thus been suggested that it may have multiple functions: as a member of the TGF-beta latent complex, as a structural component of microfibrils, and a role in cell adhesion. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a null allele exhibit early embryonic lethality prior to E6.5. Mice homozygous for a different null allele are viable, fertile, and developmentally normal but develop lens dislocations due to ciliary zonule fragmentation. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca7 T A 10: 79,841,986 (GRCm39) S1040T probably benign Het
Adam25 T C 8: 41,208,134 (GRCm39) Y467H probably benign Het
Ank1 A G 8: 23,605,449 (GRCm39) I1061V probably benign Het
Anxa10 T C 8: 62,529,348 (GRCm39) E123G probably damaging Het
Arhgap35 G A 7: 16,297,128 (GRCm39) L646F probably damaging Het
Atp8b5 A G 4: 43,320,590 (GRCm39) probably null Het
Brap A G 5: 121,816,910 (GRCm39) probably benign Het
Carmil3 A G 14: 55,730,993 (GRCm39) T87A probably damaging Het
Ccdc172 A G 19: 58,541,309 (GRCm39) D256G possibly damaging Het
Cep350 C T 1: 155,787,714 (GRCm39) A1375T probably benign Het
Chrdl2 A T 7: 99,671,263 (GRCm39) Q127L probably benign Het
Cyp2c29 T C 19: 39,279,341 (GRCm39) probably benign Het
Ddi1 C A 9: 6,266,226 (GRCm39) V48F probably benign Het
Ddrgk1 C T 2: 130,497,166 (GRCm39) probably benign Het
Fastkd1 C T 2: 69,524,932 (GRCm39) V626I possibly damaging Het
Fgd5 A G 6: 92,001,543 (GRCm39) T755A probably benign Het
Fpgt G T 3: 154,793,655 (GRCm39) T124K probably damaging Het
Gnl2 G A 4: 124,941,405 (GRCm39) probably null Het
Got1 A T 19: 43,504,284 (GRCm39) S46T probably benign Het
Hbb-bt G T 7: 103,463,070 (GRCm39) H3N probably benign Het
Ikbke C T 1: 131,199,838 (GRCm39) probably benign Het
Il2rb A G 15: 78,365,897 (GRCm39) S467P probably benign Het
Kcnma1 A G 14: 23,580,367 (GRCm39) probably benign Het
Npr3 A T 15: 11,858,804 (GRCm39) I360N probably damaging Het
Nradd G A 9: 110,451,237 (GRCm39) P44S possibly damaging Het
Or5m10 G T 2: 85,717,711 (GRCm39) C189F probably damaging Het
Or7h8 G A 9: 20,123,755 (GRCm39) V37I possibly damaging Het
Pcdh17 A G 14: 84,770,537 (GRCm39) E1005G possibly damaging Het
Pcdhb11 A G 18: 37,555,344 (GRCm39) T225A possibly damaging Het
Pja2 T C 17: 64,604,821 (GRCm39) D454G probably benign Het
Pon3 T C 6: 5,221,670 (GRCm39) Y320C probably damaging Het
Prl2a1 A G 13: 27,990,261 (GRCm39) D70G probably damaging Het
Proc T A 18: 32,260,472 (GRCm39) T218S probably benign Het
Proz G T 8: 13,116,913 (GRCm39) G155V probably damaging Het
Rab11fip3 T C 17: 26,286,977 (GRCm39) E392G possibly damaging Het
Rab3gap2 C T 1: 184,999,220 (GRCm39) R976* probably null Het
Shisa2 G A 14: 59,867,435 (GRCm39) C229Y probably damaging Het
Slc2a5 T C 4: 150,226,675 (GRCm39) V379A probably damaging Het
Slc31a2 A T 4: 62,214,197 (GRCm39) K47N probably damaging Het
Sult2a6 G A 7: 13,987,411 (GRCm39) T88I probably benign Het
Tbc1d14 T C 5: 36,662,381 (GRCm39) Y302C probably damaging Het
Thumpd3 C A 6: 113,036,927 (GRCm39) N275K possibly damaging Het
Tnks2 T C 19: 36,849,990 (GRCm39) probably null Het
Tube1 G A 10: 39,011,041 (GRCm39) probably benign Het
Umodl1 T A 17: 31,192,742 (GRCm39) Y290N probably damaging Het
Usp34 G A 11: 23,402,661 (GRCm39) E726K probably damaging Het
Vmn2r84 T A 10: 130,229,935 (GRCm39) D59V probably benign Het
Vps11 T A 9: 44,267,516 (GRCm39) probably benign Het
Wdr19 T C 5: 65,385,912 (GRCm39) Y631H probably benign Het
Wdr62 G A 7: 29,957,526 (GRCm39) H88Y probably damaging Het
Wdr93 A T 7: 79,402,253 (GRCm39) N184I probably damaging Het
Wnk4 T A 11: 101,156,240 (GRCm39) F473Y probably damaging Het
Zbtb16 A G 9: 48,568,483 (GRCm39) W661R probably damaging Het
Other mutations in Ltbp2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00471:Ltbp2 APN 12 84,837,838 (GRCm39) missense probably damaging 1.00
IGL00938:Ltbp2 APN 12 84,878,573 (GRCm39) missense probably benign 0.03
IGL01397:Ltbp2 APN 12 84,837,042 (GRCm39) missense probably damaging 1.00
IGL01570:Ltbp2 APN 12 84,840,807 (GRCm39) missense probably benign 0.05
IGL01631:Ltbp2 APN 12 84,855,920 (GRCm39) critical splice donor site probably null
IGL01662:Ltbp2 APN 12 84,856,020 (GRCm39) missense probably benign 0.00
IGL01728:Ltbp2 APN 12 84,837,783 (GRCm39) missense probably damaging 0.99
IGL01839:Ltbp2 APN 12 84,840,432 (GRCm39) missense possibly damaging 0.48
IGL01946:Ltbp2 APN 12 84,877,522 (GRCm39) missense probably damaging 1.00
IGL02220:Ltbp2 APN 12 84,876,083 (GRCm39) missense possibly damaging 0.93
IGL02340:Ltbp2 APN 12 84,839,729 (GRCm39) critical splice donor site probably null
IGL02430:Ltbp2 APN 12 84,846,175 (GRCm39) missense probably damaging 1.00
IGL02492:Ltbp2 APN 12 84,856,439 (GRCm39) missense probably damaging 1.00
IGL02517:Ltbp2 APN 12 84,832,091 (GRCm39) missense probably benign 0.42
IGL02794:Ltbp2 APN 12 84,838,709 (GRCm39) missense probably damaging 1.00
deft UTSW 12 84,900,686 (GRCm39) missense probably damaging 0.98
masterful UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
practiced UTSW 12 84,856,122 (GRCm39) missense probably damaging 1.00
R0045:Ltbp2 UTSW 12 84,860,062 (GRCm39) missense probably damaging 1.00
R0045:Ltbp2 UTSW 12 84,856,361 (GRCm39) missense probably damaging 1.00
R0091:Ltbp2 UTSW 12 84,840,507 (GRCm39) missense probably damaging 1.00
R0094:Ltbp2 UTSW 12 84,846,200 (GRCm39) missense probably damaging 1.00
R0166:Ltbp2 UTSW 12 84,833,132 (GRCm39) missense probably benign 0.28
R0265:Ltbp2 UTSW 12 84,832,743 (GRCm39) splice site probably null
R0394:Ltbp2 UTSW 12 84,853,198 (GRCm39) splice site probably benign
R0535:Ltbp2 UTSW 12 84,837,826 (GRCm39) missense probably damaging 1.00
R0535:Ltbp2 UTSW 12 84,831,632 (GRCm39) missense probably damaging 1.00
R1465:Ltbp2 UTSW 12 84,860,074 (GRCm39) missense probably damaging 1.00
R1465:Ltbp2 UTSW 12 84,860,074 (GRCm39) missense probably damaging 1.00
R1513:Ltbp2 UTSW 12 84,838,718 (GRCm39) missense probably damaging 1.00
R1858:Ltbp2 UTSW 12 84,877,555 (GRCm39) nonsense probably null
R1880:Ltbp2 UTSW 12 84,876,045 (GRCm39) missense probably benign 0.45
R1894:Ltbp2 UTSW 12 84,834,735 (GRCm39) missense probably damaging 1.00
R1900:Ltbp2 UTSW 12 84,877,432 (GRCm39) missense probably damaging 1.00
R1903:Ltbp2 UTSW 12 84,876,879 (GRCm39) missense probably benign 0.01
R1912:Ltbp2 UTSW 12 84,832,637 (GRCm39) missense probably damaging 0.98
R1993:Ltbp2 UTSW 12 84,855,220 (GRCm39) critical splice acceptor site probably null
R1995:Ltbp2 UTSW 12 84,855,220 (GRCm39) critical splice acceptor site probably null
R2069:Ltbp2 UTSW 12 84,840,507 (GRCm39) missense probably damaging 1.00
R2126:Ltbp2 UTSW 12 84,832,483 (GRCm39) splice site probably null
R2139:Ltbp2 UTSW 12 84,862,753 (GRCm39) missense probably damaging 1.00
R2341:Ltbp2 UTSW 12 84,855,937 (GRCm39) missense probably benign 0.08
R2511:Ltbp2 UTSW 12 84,851,183 (GRCm39) splice site probably null
R3737:Ltbp2 UTSW 12 84,851,248 (GRCm39) missense probably damaging 1.00
R3738:Ltbp2 UTSW 12 84,851,248 (GRCm39) missense probably damaging 1.00
R3739:Ltbp2 UTSW 12 84,851,248 (GRCm39) missense probably damaging 1.00
R3889:Ltbp2 UTSW 12 84,831,681 (GRCm39) unclassified probably benign
R4034:Ltbp2 UTSW 12 84,851,248 (GRCm39) missense probably damaging 1.00
R4542:Ltbp2 UTSW 12 84,878,593 (GRCm39) nonsense probably null
R4621:Ltbp2 UTSW 12 84,856,122 (GRCm39) missense probably damaging 1.00
R4623:Ltbp2 UTSW 12 84,856,122 (GRCm39) missense probably damaging 1.00
R4831:Ltbp2 UTSW 12 84,840,414 (GRCm39) missense possibly damaging 0.55
R5080:Ltbp2 UTSW 12 84,850,638 (GRCm39) missense probably damaging 1.00
R5116:Ltbp2 UTSW 12 84,856,511 (GRCm39) missense probably damaging 1.00
R5351:Ltbp2 UTSW 12 84,837,132 (GRCm39) missense possibly damaging 0.95
R5445:Ltbp2 UTSW 12 84,856,428 (GRCm39) missense probably null 1.00
R5608:Ltbp2 UTSW 12 84,834,238 (GRCm39) splice site probably null
R5784:Ltbp2 UTSW 12 84,915,513 (GRCm39) missense probably damaging 1.00
R5838:Ltbp2 UTSW 12 84,835,875 (GRCm39) missense probably benign 0.16
R5859:Ltbp2 UTSW 12 84,840,837 (GRCm39) missense possibly damaging 0.52
R6004:Ltbp2 UTSW 12 84,922,923 (GRCm39) missense probably benign 0.00
R6028:Ltbp2 UTSW 12 84,831,626 (GRCm39) missense probably damaging 1.00
R6347:Ltbp2 UTSW 12 84,900,686 (GRCm39) missense probably damaging 0.98
R6615:Ltbp2 UTSW 12 84,860,091 (GRCm39) missense probably damaging 1.00
R6636:Ltbp2 UTSW 12 84,922,612 (GRCm39) missense probably benign 0.00
R6637:Ltbp2 UTSW 12 84,922,612 (GRCm39) missense probably benign 0.00
R6755:Ltbp2 UTSW 12 84,841,847 (GRCm39) missense probably damaging 1.00
R6759:Ltbp2 UTSW 12 84,834,184 (GRCm39) missense probably damaging 0.99
R6806:Ltbp2 UTSW 12 84,856,012 (GRCm39) missense possibly damaging 0.74
R6968:Ltbp2 UTSW 12 84,835,857 (GRCm39) critical splice donor site probably null
R7084:Ltbp2 UTSW 12 84,915,459 (GRCm39) missense probably damaging 1.00
R7250:Ltbp2 UTSW 12 84,834,166 (GRCm39) nonsense probably null
R7374:Ltbp2 UTSW 12 84,876,949 (GRCm39) missense probably damaging 1.00
R7501:Ltbp2 UTSW 12 84,877,419 (GRCm39) missense probably damaging 1.00
R7523:Ltbp2 UTSW 12 84,837,808 (GRCm39) missense probably benign 0.00
R7754:Ltbp2 UTSW 12 84,860,012 (GRCm39) critical splice donor site probably null
R7827:Ltbp2 UTSW 12 84,836,655 (GRCm39) missense probably benign 0.19
R8042:Ltbp2 UTSW 12 84,838,673 (GRCm39) missense probably damaging 0.99
R8110:Ltbp2 UTSW 12 84,850,676 (GRCm39) nonsense probably null
R8411:Ltbp2 UTSW 12 84,833,187 (GRCm39) missense probably damaging 1.00
R8688:Ltbp2 UTSW 12 84,850,578 (GRCm39) missense probably benign 0.20
R8711:Ltbp2 UTSW 12 84,900,515 (GRCm39) missense probably benign 0.00
R8712:Ltbp2 UTSW 12 84,853,124 (GRCm39) missense probably benign 0.08
R8893:Ltbp2 UTSW 12 84,875,316 (GRCm39) missense probably damaging 1.00
R8978:Ltbp2 UTSW 12 84,834,164 (GRCm39) missense probably benign 0.00
R9016:Ltbp2 UTSW 12 84,856,467 (GRCm39) missense probably benign 0.02
R9123:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9129:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9132:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9144:Ltbp2 UTSW 12 84,856,426 (GRCm39) missense probably damaging 1.00
R9150:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9152:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9156:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9157:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9158:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9159:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9160:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9199:Ltbp2 UTSW 12 84,832,750 (GRCm39) missense probably benign 0.09
R9212:Ltbp2 UTSW 12 84,839,824 (GRCm39) missense probably damaging 1.00
R9275:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9276:Ltbp2 UTSW 12 84,876,885 (GRCm39) missense possibly damaging 0.79
R9276:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9278:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9279:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9280:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9281:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9312:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9313:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9331:Ltbp2 UTSW 12 84,922,965 (GRCm39) missense probably benign
R9355:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9375:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9377:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9378:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9450:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9457:Ltbp2 UTSW 12 84,835,927 (GRCm39) missense probably benign 0.19
R9486:Ltbp2 UTSW 12 84,878,648 (GRCm39) missense possibly damaging 0.49
R9505:Ltbp2 UTSW 12 84,900,638 (GRCm39) missense probably damaging 1.00
R9512:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9581:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9582:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9645:Ltbp2 UTSW 12 84,837,864 (GRCm39) missense probably benign 0.00
R9747:Ltbp2 UTSW 12 84,915,515 (GRCm39) missense probably damaging 1.00
R9792:Ltbp2 UTSW 12 84,876,128 (GRCm39) missense probably damaging 0.99
R9795:Ltbp2 UTSW 12 84,876,128 (GRCm39) missense probably damaging 0.99
X0017:Ltbp2 UTSW 12 84,875,302 (GRCm39) missense probably damaging 1.00
X0026:Ltbp2 UTSW 12 84,876,973 (GRCm39) missense probably damaging 1.00
Z1176:Ltbp2 UTSW 12 84,922,627 (GRCm39) missense probably benign 0.01
Z1177:Ltbp2 UTSW 12 84,876,090 (GRCm39) missense possibly damaging 0.87
Posted On 2014-05-07