Incidental Mutation 'R1448:Ltbp4'
ID 159038
Institutional Source Beutler Lab
Gene Symbol Ltbp4
Ensembl Gene ENSMUSG00000040488
Gene Name latent transforming growth factor beta binding protein 4
Synonyms 2310046A13Rik
MMRRC Submission 039503-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R1448 (G1)
Quality Score 135
Status Not validated
Chromosome 7
Chromosomal Location 27004561-27037117 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 27006002 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Cysteine at position 1559 (R1559C)
Ref Sequence ENSEMBL: ENSMUSP00000104006 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000038618] [ENSMUST00000108369] [ENSMUST00000118583] [ENSMUST00000121175] [ENSMUST00000125455]
AlphaFold Q8K4G1
Predicted Effect possibly damaging
Transcript: ENSMUST00000038618
AA Change: R1560C

PolyPhen 2 Score 0.774 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000037536
Gene: ENSMUSG00000040488
AA Change: R1560C

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
low complexity region 87 100 N/A INTRINSIC
low complexity region 112 125 N/A INTRINSIC
EGF 151 180 2.74e-3 SMART
low complexity region 244 265 N/A INTRINSIC
EGF_CA 356 396 3.51e-10 SMART
Pfam:TB 416 457 4.8e-15 PFAM
low complexity region 490 501 N/A INTRINSIC
low complexity region 507 568 N/A INTRINSIC
low complexity region 579 590 N/A INTRINSIC
EGF 591 629 6.06e-5 SMART
EGF_CA 630 671 8.3e-12 SMART
EGF_CA 672 713 7.34e-13 SMART
EGF_CA 714 751 8.43e-13 SMART
EGF_CA 753 794 1.66e-11 SMART
EGF_CA 795 836 3.61e-12 SMART
EGF_CA 837 876 5.61e-9 SMART
EGF_CA 877 919 1.73e-9 SMART
EGF_CA 920 961 7.12e-11 SMART
EGF_CA 962 1002 3.56e-11 SMART
EGF_CA 1003 1046 1.61e-9 SMART
EGF_CA 1047 1090 2.13e-9 SMART
EGF_CA 1091 1132 1.02e-11 SMART
EGF 1136 1175 1.69e1 SMART
low complexity region 1185 1223 N/A INTRINSIC
Pfam:TB 1234 1276 1.7e-13 PFAM
EGF_CA 1295 1337 2.72e-7 SMART
EGF_CA 1338 1379 1.36e-7 SMART
Pfam:TB 1402 1443 4.3e-14 PFAM
low complexity region 1449 1461 N/A INTRINSIC
low complexity region 1478 1500 N/A INTRINSIC
EGF 1578 1615 6.06e-5 SMART
EGF_CA 1616 1660 9.54e-12 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000108369
AA Change: R1559C

PolyPhen 2 Score 0.859 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000104006
Gene: ENSMUSG00000040488
AA Change: R1559C

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
low complexity region 116 145 N/A INTRINSIC
EGF 150 179 2.74e-3 SMART
low complexity region 243 264 N/A INTRINSIC
EGF_CA 355 395 3.51e-10 SMART
Pfam:TB 414 456 2.5e-14 PFAM
low complexity region 489 500 N/A INTRINSIC
low complexity region 506 567 N/A INTRINSIC
low complexity region 578 589 N/A INTRINSIC
EGF 590 628 6.06e-5 SMART
EGF_CA 629 670 8.3e-12 SMART
EGF_CA 671 712 7.34e-13 SMART
EGF_CA 713 750 8.43e-13 SMART
EGF_CA 752 793 1.66e-11 SMART
EGF_CA 794 835 3.61e-12 SMART
EGF_CA 836 875 5.61e-9 SMART
EGF_CA 876 918 1.73e-9 SMART
EGF_CA 919 960 7.12e-11 SMART
EGF_CA 961 1001 3.56e-11 SMART
EGF_CA 1002 1045 1.61e-9 SMART
EGF_CA 1046 1089 2.13e-9 SMART
EGF_CA 1090 1131 1.02e-11 SMART
EGF 1135 1174 1.69e1 SMART
low complexity region 1184 1222 N/A INTRINSIC
Pfam:TB 1232 1275 2.4e-13 PFAM
EGF_CA 1294 1336 2.72e-7 SMART
EGF_CA 1337 1378 1.36e-7 SMART
Pfam:TB 1400 1442 7.6e-15 PFAM
low complexity region 1448 1460 N/A INTRINSIC
low complexity region 1477 1499 N/A INTRINSIC
EGF 1577 1614 6.06e-5 SMART
EGF_CA 1615 1659 9.54e-12 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000118583
AA Change: R1494C

PolyPhen 2 Score 0.600 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000113523
Gene: ENSMUSG00000040488
AA Change: R1494C

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
low complexity region 69 80 N/A INTRINSIC
EGF 85 114 2.74e-3 SMART
low complexity region 178 199 N/A INTRINSIC
EGF_CA 290 330 3.51e-10 SMART
Pfam:TB 349 391 2.3e-14 PFAM
low complexity region 424 435 N/A INTRINSIC
low complexity region 441 502 N/A INTRINSIC
low complexity region 513 524 N/A INTRINSIC
EGF 525 563 6.06e-5 SMART
EGF_CA 564 605 8.3e-12 SMART
EGF_CA 606 647 7.34e-13 SMART
EGF_CA 648 685 8.43e-13 SMART
EGF_CA 687 728 1.66e-11 SMART
EGF_CA 729 770 3.61e-12 SMART
EGF_CA 771 810 5.61e-9 SMART
EGF_CA 811 853 1.73e-9 SMART
EGF_CA 854 895 7.12e-11 SMART
EGF_CA 896 936 3.56e-11 SMART
EGF_CA 937 980 1.61e-9 SMART
EGF_CA 981 1024 2.13e-9 SMART
EGF_CA 1025 1066 1.02e-11 SMART
EGF 1070 1109 1.69e1 SMART
low complexity region 1119 1157 N/A INTRINSIC
Pfam:TB 1167 1210 2.2e-13 PFAM
EGF_CA 1229 1271 2.72e-7 SMART
EGF_CA 1272 1313 1.36e-7 SMART
Pfam:TB 1335 1377 7.1e-15 PFAM
low complexity region 1383 1395 N/A INTRINSIC
low complexity region 1412 1434 N/A INTRINSIC
EGF 1512 1549 6.06e-5 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000121175
AA Change: R1494C

PolyPhen 2 Score 0.855 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000113674
Gene: ENSMUSG00000040488
AA Change: R1494C

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
low complexity region 69 80 N/A INTRINSIC
EGF 85 114 2.74e-3 SMART
low complexity region 178 199 N/A INTRINSIC
EGF_CA 290 330 3.51e-10 SMART
Pfam:TB 349 391 3.4e-14 PFAM
low complexity region 424 435 N/A INTRINSIC
low complexity region 441 502 N/A INTRINSIC
low complexity region 513 524 N/A INTRINSIC
EGF 525 563 6.06e-5 SMART
EGF_CA 564 605 8.3e-12 SMART
EGF_CA 606 647 7.34e-13 SMART
EGF_CA 648 685 8.43e-13 SMART
EGF_CA 687 728 1.66e-11 SMART
EGF_CA 729 770 3.61e-12 SMART
EGF_CA 771 810 5.61e-9 SMART
EGF_CA 811 853 1.73e-9 SMART
EGF_CA 854 895 7.12e-11 SMART
EGF_CA 896 936 3.56e-11 SMART
EGF_CA 937 980 1.61e-9 SMART
EGF_CA 981 1024 2.13e-9 SMART
EGF_CA 1025 1066 1.02e-11 SMART
EGF 1070 1109 1.69e1 SMART
low complexity region 1119 1157 N/A INTRINSIC
Pfam:TB 1167 1210 3.3e-13 PFAM
EGF_CA 1229 1271 2.72e-7 SMART
EGF_CA 1272 1313 1.36e-7 SMART
Pfam:TB 1335 1377 1e-14 PFAM
low complexity region 1383 1395 N/A INTRINSIC
low complexity region 1412 1434 N/A INTRINSIC
EGF 1512 1549 6.06e-5 SMART
EGF_CA 1550 1594 9.54e-12 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000125455
SMART Domains Protein: ENSMUSP00000120326
Gene: ENSMUSG00000040488

DomainStartEndE-ValueType
Pfam:TB 9 52 1.9e-14 PFAM
Pfam:TB 85 127 6e-16 PFAM
low complexity region 133 145 N/A INTRINSIC
low complexity region 162 184 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000129471
Predicted Effect noncoding transcript
Transcript: ENSMUST00000134464
Predicted Effect noncoding transcript
Transcript: ENSMUST00000148594
Predicted Effect noncoding transcript
Transcript: ENSMUST00000206413
Coding Region Coverage
  • 1x: 98.8%
  • 3x: 97.8%
  • 10x: 94.6%
  • 20x: 87.0%
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 binds transforming growth factor beta (TGFB) as it is secreted and targeted to the extracellular matrix. TGFB is biologically latent after secretion and insertion into the extracellular matrix, and sheds TGFB and other proteins upon activation. Defects in this gene may be a cause of cutis laxa and severe pulmonary, gastrointestinal, and urinary abnormalities. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]
PHENOTYPE: Homozygous disruption of this locus results in pulmonary emphysema, cardiomyopathy, and colon cancer. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 85 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5330417H12Rik T A 7: 107,223,952 (GRCm39) probably benign Het
A1cf A T 19: 31,886,196 (GRCm39) N35I possibly damaging Het
Abca2 T C 2: 25,330,542 (GRCm39) I1106T possibly damaging Het
Abca4 G A 3: 121,956,577 (GRCm39) probably null Het
Adgrv1 T C 13: 81,581,632 (GRCm39) D4804G probably benign Het
Adk T A 14: 21,102,708 (GRCm39) M1K probably null Het
Aff3 T C 1: 38,230,364 (GRCm39) N1006D probably damaging Het
Akap12 A G 10: 4,305,475 (GRCm39) T762A probably benign Het
Atosa C G 9: 74,917,456 (GRCm39) S685* probably null Het
Atp12a T A 14: 56,623,296 (GRCm39) M843K probably damaging Het
Bbx T A 16: 50,086,633 (GRCm39) K169* probably null Het
Bicra A T 7: 15,722,284 (GRCm39) V411E possibly damaging Het
Camk1d A T 2: 5,366,836 (GRCm39) Y126* probably null Het
Cel T C 2: 28,446,338 (GRCm39) Y511C probably damaging Het
Celf4 G T 18: 25,636,140 (GRCm39) probably null Het
Clasp1 A G 1: 118,436,646 (GRCm39) N310S probably benign Het
Col6a3 T C 1: 90,709,577 (GRCm39) K1873R unknown Het
Cstf1 A G 2: 172,217,795 (GRCm39) D136G probably damaging Het
Cwc22 T A 2: 77,741,899 (GRCm39) E470D probably damaging Het
Cxcr2 A T 1: 74,197,527 (GRCm39) D7V probably benign Het
Cytip A G 2: 58,035,192 (GRCm39) I168T probably damaging Het
D5Ertd579e A G 5: 36,760,083 (GRCm39) L1359P probably benign Het
Ddx25 A C 9: 35,469,034 (GRCm39) V26G probably benign Het
Dennd4a T A 9: 64,813,327 (GRCm39) S1429T possibly damaging Het
Dmd A G X: 83,892,306 (GRCm39) D2990G probably damaging Het
Dop1a C A 9: 86,424,785 (GRCm39) probably null Het
Eps8 T C 6: 137,499,852 (GRCm39) Q209R possibly damaging Het
Fabp6 T A 11: 43,486,992 (GRCm39) I112F probably benign Het
Fbxw10 T C 11: 62,738,418 (GRCm39) V104A possibly damaging Het
Gp1ba C T 11: 70,532,253 (GRCm39) P673L probably damaging Het
Grin3a T C 4: 49,702,804 (GRCm39) Y894C probably damaging Het
Hydin C T 8: 111,173,217 (GRCm39) H967Y probably benign Het
Ip6k3 T C 17: 27,364,242 (GRCm39) K269E possibly damaging Het
Jup T C 11: 100,274,026 (GRCm39) K172E probably damaging Het
Katnal1 T C 5: 148,841,486 (GRCm39) D126G probably benign Het
Knl1 A T 2: 118,898,788 (GRCm39) K163M probably damaging Het
Krt17 C T 11: 100,148,365 (GRCm39) E359K possibly damaging Het
Lct T A 1: 128,235,559 (GRCm39) I483F probably damaging Het
Loxl2 G A 14: 69,930,489 (GRCm39) G751D probably damaging Het
Man2c1 T A 9: 57,042,503 (GRCm39) D183E probably benign Het
Med17 T C 9: 15,187,139 (GRCm39) probably null Het
Mrgpra9 A C 7: 46,885,561 (GRCm39) S34R probably benign Het
Mrpl44 T A 1: 79,755,677 (GRCm39) N94K probably damaging Het
Nat8f1 A G 6: 85,887,924 (GRCm39) V12A probably benign Het
Nr2e3 C A 9: 59,850,797 (GRCm39) G354V probably damaging Het
Nrbp1 T A 5: 31,403,157 (GRCm39) I210N probably damaging Het
Nup155 T C 15: 8,141,890 (GRCm39) V94A probably benign Het
Or14a256 A T 7: 86,265,569 (GRCm39) C95S probably damaging Het
Or52h2 C T 7: 103,839,082 (GRCm39) V111I possibly damaging Het
Or5p76 T C 7: 108,122,525 (GRCm39) I211V probably benign Het
Or9q2 A T 19: 13,772,140 (GRCm39) Y278* probably null Het
Pcdhb10 A T 18: 37,545,556 (GRCm39) I211F possibly damaging Het
Phip A C 9: 82,797,476 (GRCm39) I509S possibly damaging Het
Pkhd1 C T 1: 20,655,381 (GRCm39) probably null Het
Psme4 T G 11: 30,802,744 (GRCm39) L1487R probably damaging Het
Ptgdr2 A G 19: 10,917,857 (GRCm39) S125G probably damaging Het
Ptpro A G 6: 137,418,114 (GRCm39) K126E probably damaging Het
Rdh16f2 T A 10: 127,712,794 (GRCm39) V264E probably benign Het
Ric8b C T 10: 84,783,535 (GRCm39) A131V possibly damaging Het
Rock1 A T 18: 10,070,233 (GRCm39) I1280N probably damaging Het
Rprd2 A G 3: 95,725,888 (GRCm39) V59A possibly damaging Het
Ruvbl1 T A 6: 88,444,551 (GRCm39) C49S probably benign Het
Scn2a A G 2: 65,514,189 (GRCm39) N291S probably benign Het
Serbp1 T A 6: 67,254,904 (GRCm39) H325Q probably damaging Het
Shf G A 2: 122,199,163 (GRCm39) P51S probably damaging Het
Shisal2b T C 13: 104,982,470 (GRCm39) I151V probably benign Het
Slitrk3 G A 3: 72,957,674 (GRCm39) T366I probably damaging Het
Spryd3 A T 15: 102,026,827 (GRCm39) H307Q possibly damaging Het
Spx A T 6: 142,364,239 (GRCm39) D100V probably benign Het
Surf4 A G 2: 26,814,476 (GRCm39) F142L probably damaging Het
Syne2 T A 12: 76,067,099 (GRCm39) probably null Het
Syne2 T C 12: 76,098,952 (GRCm39) M5278T possibly damaging Het
Thap12 T C 7: 98,365,230 (GRCm39) V466A probably benign Het
Thap3 T C 4: 152,067,673 (GRCm39) K135R possibly damaging Het
Tmem131 G T 1: 36,866,439 (GRCm39) D448E probably benign Het
Tmem63b C G 17: 45,989,904 (GRCm39) R88P possibly damaging Het
Trim43a G T 9: 88,464,146 (GRCm39) C19F probably damaging Het
Trp63 C T 16: 25,707,870 (GRCm39) P526L possibly damaging Het
Ubqln3 T C 7: 103,791,997 (GRCm39) D31G probably damaging Het
Utp14b C A 1: 78,643,162 (GRCm39) N353K probably damaging Het
Vmn1r40 A G 6: 89,691,558 (GRCm39) K125R probably damaging Het
Vmn2r1 A G 3: 64,008,734 (GRCm39) Y471C probably damaging Het
Vmn2r13 A G 5: 109,322,001 (GRCm39) I232T probably damaging Het
Zfp263 A C 16: 3,564,323 (GRCm39) E204D probably benign Het
Zfp865 A T 7: 5,032,278 (GRCm39) K88* probably null Het
Other mutations in Ltbp4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00434:Ltbp4 APN 7 27,028,230 (GRCm39) missense probably damaging 0.96
IGL00585:Ltbp4 APN 7 27,026,158 (GRCm39) missense probably damaging 0.98
IGL01320:Ltbp4 APN 7 27,027,784 (GRCm39) splice site probably benign
IGL01860:Ltbp4 APN 7 27,019,071 (GRCm39) missense probably damaging 1.00
IGL02026:Ltbp4 APN 7 27,026,842 (GRCm39) nonsense probably null
IGL02226:Ltbp4 APN 7 27,006,359 (GRCm39) missense probably damaging 1.00
IGL02422:Ltbp4 APN 7 27,019,097 (GRCm39) missense probably damaging 1.00
IGL02611:Ltbp4 APN 7 27,010,080 (GRCm39) missense probably damaging 1.00
IGL02892:Ltbp4 APN 7 27,010,074 (GRCm39) missense probably damaging 1.00
IGL02926:Ltbp4 APN 7 27,028,297 (GRCm39) splice site probably null
IGL02950:Ltbp4 APN 7 27,006,143 (GRCm39) missense probably damaging 0.99
IGL03008:Ltbp4 APN 7 27,023,789 (GRCm39) missense probably damaging 0.99
IGL03271:Ltbp4 APN 7 27,029,240 (GRCm39) missense unknown
IGL02837:Ltbp4 UTSW 7 27,013,806 (GRCm39) missense probably damaging 1.00
R0792:Ltbp4 UTSW 7 27,024,485 (GRCm39) missense probably damaging 1.00
R0980:Ltbp4 UTSW 7 27,023,587 (GRCm39) missense probably damaging 1.00
R1017:Ltbp4 UTSW 7 27,005,501 (GRCm39) missense possibly damaging 0.95
R1185:Ltbp4 UTSW 7 27,009,960 (GRCm39) missense probably damaging 1.00
R1185:Ltbp4 UTSW 7 27,009,960 (GRCm39) missense probably damaging 1.00
R1185:Ltbp4 UTSW 7 27,009,960 (GRCm39) missense probably damaging 1.00
R1403:Ltbp4 UTSW 7 27,028,464 (GRCm39) missense unknown
R1403:Ltbp4 UTSW 7 27,028,464 (GRCm39) missense unknown
R1575:Ltbp4 UTSW 7 27,022,245 (GRCm39) missense probably damaging 1.00
R1918:Ltbp4 UTSW 7 27,036,994 (GRCm39) unclassified probably benign
R1932:Ltbp4 UTSW 7 27,007,191 (GRCm39) critical splice donor site probably null
R1959:Ltbp4 UTSW 7 27,028,443 (GRCm39) missense unknown
R1960:Ltbp4 UTSW 7 27,028,443 (GRCm39) missense unknown
R1976:Ltbp4 UTSW 7 27,026,195 (GRCm39) missense probably damaging 1.00
R2060:Ltbp4 UTSW 7 27,008,378 (GRCm39) missense probably damaging 1.00
R2333:Ltbp4 UTSW 7 27,027,203 (GRCm39) missense possibly damaging 0.82
R2431:Ltbp4 UTSW 7 27,019,101 (GRCm39) missense possibly damaging 0.91
R3125:Ltbp4 UTSW 7 27,027,203 (GRCm39) missense possibly damaging 0.82
R4093:Ltbp4 UTSW 7 27,024,641 (GRCm39) missense possibly damaging 0.93
R4095:Ltbp4 UTSW 7 27,024,641 (GRCm39) missense possibly damaging 0.93
R4592:Ltbp4 UTSW 7 27,024,608 (GRCm39) missense probably damaging 0.96
R4610:Ltbp4 UTSW 7 27,006,125 (GRCm39) missense probably damaging 1.00
R4650:Ltbp4 UTSW 7 27,013,734 (GRCm39) missense probably damaging 1.00
R4912:Ltbp4 UTSW 7 27,005,541 (GRCm39) nonsense probably null
R5002:Ltbp4 UTSW 7 27,027,110 (GRCm39) frame shift probably null
R5016:Ltbp4 UTSW 7 27,027,110 (GRCm39) frame shift probably null
R5216:Ltbp4 UTSW 7 27,026,736 (GRCm39) small deletion probably benign
R5218:Ltbp4 UTSW 7 27,026,736 (GRCm39) small deletion probably benign
R5219:Ltbp4 UTSW 7 27,026,746 (GRCm39) missense probably benign 0.01
R5219:Ltbp4 UTSW 7 27,026,736 (GRCm39) small deletion probably benign
R5539:Ltbp4 UTSW 7 27,027,149 (GRCm39) missense probably damaging 0.97
R5991:Ltbp4 UTSW 7 27,008,741 (GRCm39) missense probably damaging 1.00
R6082:Ltbp4 UTSW 7 27,035,105 (GRCm39) unclassified probably benign
R6125:Ltbp4 UTSW 7 27,027,180 (GRCm39) missense probably damaging 1.00
R6146:Ltbp4 UTSW 7 27,019,149 (GRCm39) missense probably damaging 0.99
R6156:Ltbp4 UTSW 7 27,029,587 (GRCm39) missense unknown
R6414:Ltbp4 UTSW 7 27,010,140 (GRCm39) missense probably damaging 1.00
R6563:Ltbp4 UTSW 7 27,008,488 (GRCm39) missense probably damaging 1.00
R6719:Ltbp4 UTSW 7 27,028,188 (GRCm39) missense probably damaging 0.99
R6940:Ltbp4 UTSW 7 27,008,369 (GRCm39) missense probably damaging 1.00
R7054:Ltbp4 UTSW 7 27,007,191 (GRCm39) critical splice donor site probably null
R7116:Ltbp4 UTSW 7 27,004,852 (GRCm39) missense probably damaging 0.99
R7326:Ltbp4 UTSW 7 27,029,180 (GRCm39) missense unknown
R7419:Ltbp4 UTSW 7 27,029,192 (GRCm39) missense unknown
R8068:Ltbp4 UTSW 7 27,023,593 (GRCm39) missense probably damaging 0.99
R8435:Ltbp4 UTSW 7 27,034,870 (GRCm39) missense unknown
R8543:Ltbp4 UTSW 7 27,024,666 (GRCm39) missense possibly damaging 0.84
R8897:Ltbp4 UTSW 7 27,026,119 (GRCm39) missense probably benign 0.09
R9103:Ltbp4 UTSW 7 27,028,186 (GRCm39) missense unknown
R9131:Ltbp4 UTSW 7 27,036,976 (GRCm39) missense unknown
R9206:Ltbp4 UTSW 7 27,022,350 (GRCm39) missense probably damaging 1.00
R9301:Ltbp4 UTSW 7 27,021,578 (GRCm39) missense probably damaging 0.98
R9302:Ltbp4 UTSW 7 27,008,481 (GRCm39) missense possibly damaging 0.80
X0025:Ltbp4 UTSW 7 27,025,227 (GRCm39) missense probably damaging 1.00
X0066:Ltbp4 UTSW 7 27,005,490 (GRCm39) critical splice donor site probably null
Z1088:Ltbp4 UTSW 7 27,007,217 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ATGAGTCACCAACACTCCTGCTTTC -3'
(R):5'- TTTGCAATGTGCTGCGTCCACC -3'

Sequencing Primer
(F):5'- ACTCCTGCTTTCCAGGTGC -3'
(R):5'- GAATTCCCTATGAATATGGCCCAG -3'
Posted On 2014-03-14