Incidental Mutation 'R0325:Lama3'
ID 25808
Institutional Source Beutler Lab
Gene Symbol Lama3
Ensembl Gene ENSMUSG00000024421
Gene Name laminin, alpha 3
Synonyms [a]3B, nicein, 150kDa
MMRRC Submission 038535-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R0325 (G1)
Quality Score 225
Status Not validated
Chromosome 18
Chromosomal Location 12466876-12716070 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 12615183 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Alanine at position 1369 (D1369A)
Ref Sequence ENSEMBL: ENSMUSP00000089703 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092070]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000092070
AA Change: D1369A

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000089703
Gene: ENSMUSG00000024421
AA Change: D1369A

DomainStartEndE-ValueType
signal peptide 1 31 N/A INTRINSIC
LamNT 38 294 1.46e-153 SMART
EGF_Lam 296 350 1.39e-4 SMART
EGF_Lam 353 420 2.66e-10 SMART
EGF_Lam 423 464 3.51e-10 SMART
EGF_Lam 488 530 1.73e-9 SMART
EGF_Lam 533 576 3.81e-11 SMART
EGF_like 579 625 1.82e-1 SMART
EGF_Lam 628 678 5.15e-8 SMART
EGF_Lam 681 725 3.54e-6 SMART
low complexity region 768 781 N/A INTRINSIC
EGF_Lam 1263 1306 3.15e-12 SMART
EGF_Lam 1309 1350 6.3e-3 SMART
EGF_Lam 1353 1399 1.49e-13 SMART
EGF_Lam 1402 1450 8.18e-11 SMART
LamB 1509 1638 4.34e-55 SMART
Pfam:Laminin_EGF 1647 1681 7.9e-5 PFAM
EGF_Lam 1684 1728 2.66e-10 SMART
EGF_Lam 1731 1781 7.81e-8 SMART
Pfam:Laminin_I 1836 2102 2.7e-93 PFAM
low complexity region 2185 2200 N/A INTRINSIC
coiled coil region 2211 2238 N/A INTRINSIC
LamG 2406 2566 1.67e-2 SMART
LamG 2614 2742 1.72e-17 SMART
LamG 2785 2900 3.96e-17 SMART
LamG 3005 3133 1.12e-34 SMART
LamG 3175 3308 3.41e-30 SMART
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 95.9%
  • 20x: 92.0%
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 belongs to the laminin family of secreted molecules. Laminins are heterotrimeric molecules that consist of alpha, beta, and gamma subunits that assemble through a coiled-coil domain. Laminins are essential for formation and function of the basement membrane and have additional functions in regulating cell migration and mechanical signal transduction. This gene encodes an alpha subunit and is responsive to several epithelial-mesenchymal regulators including keratinocyte growth factor, epidermal growth factor and insulin-like growth factor. Mutations in this gene have been identified as the cause of Herlitz type junctional epidermolysis bullosa and laryngoonychocutaneous syndrome. Alternative splicing and alternative promoter usage result in multiple transcript variants. [provided by RefSeq, Dec 2014]
PHENOTYPE: Mice homozygous for a targeted null mutation develop a lethal blistering phenotype similar to human junctional epidermolysis bullosa, and die 2-3 days after birth from a failure to thrive. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 103 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4fm2 T C 4: 144,282,081 (GRCm39) Y237C probably damaging Het
Adcyap1 A G 17: 93,510,260 (GRCm39) D96G probably benign Het
Adgrv1 C T 13: 81,688,134 (GRCm39) V1749M probably damaging Het
Adnp2 A T 18: 80,173,868 (GRCm39) N180K probably benign Het
Ahdc1 G T 4: 132,790,030 (GRCm39) A424S unknown Het
Alpk3 G A 7: 80,717,701 (GRCm39) R86H possibly damaging Het
Atf7ip A C 6: 136,537,987 (GRCm39) T49P possibly damaging Het
Atp7b G A 8: 22,518,467 (GRCm39) L124F probably benign Het
Bub1 A T 2: 127,643,314 (GRCm39) L1010* probably null Het
Cd300c C A 11: 114,850,411 (GRCm39) E131* probably null Het
Cep135 A G 5: 76,763,590 (GRCm39) K527E probably damaging Het
Cfd G T 10: 79,727,592 (GRCm39) E89* probably null Het
Crb1 A C 1: 139,168,904 (GRCm39) C871W probably damaging Het
D6Ertd527e A T 6: 87,088,277 (GRCm39) S147C unknown Het
Ddx60 A T 8: 62,436,889 (GRCm39) E946D probably benign Het
Dmrt1 G A 19: 25,523,371 (GRCm39) E241K probably benign Het
Dnah11 C G 12: 117,976,074 (GRCm39) V2782L probably benign Het
Dzip1 T C 14: 119,146,969 (GRCm39) I313M probably damaging Het
Egln3 T C 12: 54,250,298 (GRCm39) E17G probably benign Het
Eif3d A G 15: 77,852,420 (GRCm39) V42A probably damaging Het
Elapor1 A G 3: 108,368,567 (GRCm39) L808P probably damaging Het
Eogt C A 6: 97,090,916 (GRCm39) G408W probably damaging Het
Fip1l1 T A 5: 74,756,503 (GRCm39) N498K probably damaging Het
Fmn2 T A 1: 174,437,520 (GRCm39) probably null Het
Fndc3b T C 3: 27,521,579 (GRCm39) E532G probably damaging Het
Gabrb3 T C 7: 57,415,278 (GRCm39) L116P probably damaging Het
Galnt6 A T 15: 100,591,352 (GRCm39) probably null Het
Glmp G A 3: 88,232,391 (GRCm39) M1I probably null Het
Gm5478 T C 15: 101,552,761 (GRCm39) D79G probably damaging Het
Gnb1 T G 4: 155,636,140 (GRCm39) D153E probably benign Het
Grik2 T C 10: 49,116,821 (GRCm39) I86V probably damaging Het
Hdac3 C T 18: 38,074,005 (GRCm39) probably null Het
Hdgfl2 G A 17: 56,406,181 (GRCm39) R523H possibly damaging Het
Ifngr1 T A 10: 19,473,180 (GRCm39) N43K probably damaging Het
Iqgap1 A G 7: 80,401,678 (GRCm39) W476R probably benign Het
Jag1 A G 2: 136,937,365 (GRCm39) probably null Het
Kars1 T C 8: 112,734,848 (GRCm39) D46G probably benign Het
Kcnd2 A G 6: 21,216,682 (GRCm39) I129V probably damaging Het
Lars1 A T 18: 42,383,967 (GRCm39) V76E possibly damaging Het
Lgals9 T C 11: 78,854,274 (GRCm39) I337V probably damaging Het
Lrp1b T C 2: 40,741,723 (GRCm39) D3068G probably damaging Het
Med12l A G 3: 58,984,480 (GRCm39) T462A possibly damaging Het
Megf9 T A 4: 70,374,178 (GRCm39) D286V probably damaging Het
Meox1 T A 11: 101,770,227 (GRCm39) S167C probably damaging Het
Mier2 C T 10: 79,378,430 (GRCm39) probably null Het
Mrps2 C A 2: 28,359,791 (GRCm39) T216K probably damaging Het
Mto1 A T 9: 78,360,286 (GRCm39) D258V probably damaging Het
Mug1 A T 6: 121,826,801 (GRCm39) H208L probably benign Het
Myo15b T A 11: 115,775,091 (GRCm39) I751N probably damaging Het
Napg C T 18: 63,120,034 (GRCm39) R149C probably damaging Het
Ndrg4 T A 8: 96,437,563 (GRCm39) M17K probably damaging Het
Nfrkb T G 9: 31,325,476 (GRCm39) M973R probably benign Het
Nxph4 C T 10: 127,362,780 (GRCm39) R37H probably damaging Het
Oas1e A G 5: 120,933,460 (GRCm39) I35T probably damaging Het
Oc90 C T 15: 65,769,514 (GRCm39) probably null Het
Or4b12 A T 2: 90,095,880 (GRCm39) M298K probably null Het
Or52d3 A T 7: 104,229,567 (GRCm39) D238V probably damaging Het
Or8j3 G A 2: 86,029,055 (GRCm39) L14F possibly damaging Het
Or8k30 A T 2: 86,339,549 (GRCm39) T249S probably benign Het
Or9a7 A T 6: 40,521,057 (GRCm39) N285K possibly damaging Het
Papola T A 12: 105,773,452 (GRCm39) I157N probably damaging Het
Pcyox1l G C 18: 61,830,964 (GRCm39) P303A possibly damaging Het
Pkdrej T C 15: 85,703,752 (GRCm39) N728S probably benign Het
Pkp4 A G 2: 59,148,873 (GRCm39) D542G probably damaging Het
Pla2g5 C T 4: 138,527,967 (GRCm39) D100N probably benign Het
Poln C T 5: 34,307,108 (GRCm39) R31H probably benign Het
Ppp3ca G A 3: 136,640,900 (GRCm39) A484T probably benign Het
Prag1 A G 8: 36,570,958 (GRCm39) T514A probably benign Het
Pramel28 A T 4: 143,693,310 (GRCm39) V56E probably damaging Het
Prex2 G A 1: 11,270,281 (GRCm39) probably null Het
Prrc2b G T 2: 32,089,103 (GRCm39) W403L probably damaging Het
Pter A T 2: 13,005,748 (GRCm39) K307M probably damaging Het
Ptpn5 G A 7: 46,740,506 (GRCm39) S99L probably benign Het
Ptpn5 A C 7: 46,740,507 (GRCm39) S99A probably benign Het
Rpap1 A C 2: 119,602,321 (GRCm39) H674Q probably benign Het
Rph3a A T 5: 121,081,127 (GRCm39) D623E probably benign Het
Sdr9c7 G T 10: 127,734,588 (GRCm39) E25D probably benign Het
Septin9 T G 11: 117,247,458 (GRCm39) V479G probably damaging Het
Sgo2a A G 1: 58,055,856 (GRCm39) D680G probably benign Het
Sgo2b A T 8: 64,381,410 (GRCm39) I474N probably benign Het
Sgsm1 A T 5: 113,436,701 (GRCm39) I43N probably damaging Het
Shprh G A 10: 11,045,853 (GRCm39) M891I probably benign Het
Skic2 A T 17: 35,063,791 (GRCm39) Y551N possibly damaging Het
Slc12a9 A G 5: 137,321,108 (GRCm39) M469T probably damaging Het
Slc4a2 A T 5: 24,640,941 (GRCm39) I747F probably damaging Het
Slc7a6 T A 8: 106,921,149 (GRCm39) N373K probably damaging Het
Slc7a6os T C 8: 106,927,688 (GRCm39) D296G probably benign Het
Sncaip A G 18: 53,038,881 (GRCm39) T120A probably damaging Het
Sorcs1 G C 19: 50,301,480 (GRCm39) probably null Het
Spata16 A G 3: 26,721,605 (GRCm39) E42G probably damaging Het
Spata31e2 G T 1: 26,724,347 (GRCm39) Q278K possibly damaging Het
Syne2 A T 12: 76,009,415 (GRCm39) M2440L probably benign Het
Taf7l2 T C 10: 115,949,474 (GRCm39) I17M probably damaging Het
Tead2 A G 7: 44,875,179 (GRCm39) E232G probably damaging Het
Tmf1 T G 6: 97,153,465 (GRCm39) T203P possibly damaging Het
Trrap C A 5: 144,753,205 (GRCm39) H1843Q probably benign Het
Unc79 C A 12: 103,137,903 (GRCm39) Q2314K probably damaging Het
Unc80 G T 1: 66,550,040 (GRCm39) G766V probably damaging Het
Vmn1r217 A G 13: 23,298,764 (GRCm39) L46P probably damaging Het
Vmn2r80 A T 10: 78,984,773 (GRCm39) I42F possibly damaging Het
Vwa5a T C 9: 38,639,961 (GRCm39) V403A probably damaging Het
Zfp42 T C 8: 43,748,988 (GRCm39) E171G probably damaging Het
Zfp64 A T 2: 168,767,960 (GRCm39) S551T probably benign Het
Other mutations in Lama3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00091:Lama3 APN 18 12,713,349 (GRCm39) missense probably benign
IGL00272:Lama3 APN 18 12,624,605 (GRCm39) missense probably damaging 1.00
IGL00335:Lama3 APN 18 12,582,645 (GRCm39) splice site probably benign
IGL00836:Lama3 APN 18 12,605,285 (GRCm39) missense probably benign 0.01
IGL01017:Lama3 APN 18 12,574,200 (GRCm39) critical splice donor site probably null
IGL01025:Lama3 APN 18 12,614,094 (GRCm39) missense probably benign 0.09
IGL01394:Lama3 APN 18 12,664,983 (GRCm39) missense probably null 0.39
IGL01545:Lama3 APN 18 12,574,188 (GRCm39) missense probably benign 0.01
IGL01685:Lama3 APN 18 12,586,937 (GRCm39) splice site probably benign
IGL01863:Lama3 APN 18 12,552,993 (GRCm39) splice site probably benign
IGL01869:Lama3 APN 18 12,657,820 (GRCm39) missense possibly damaging 0.94
IGL01894:Lama3 APN 18 12,705,121 (GRCm39) missense probably benign 0.09
IGL02027:Lama3 APN 18 12,649,570 (GRCm39) missense probably damaging 1.00
IGL02106:Lama3 APN 18 12,601,371 (GRCm39) missense probably damaging 0.98
IGL02307:Lama3 APN 18 12,714,840 (GRCm39) missense probably benign 0.09
IGL02342:Lama3 APN 18 12,624,533 (GRCm39) missense probably damaging 1.00
IGL02377:Lama3 APN 18 12,689,807 (GRCm39) missense possibly damaging 0.49
IGL02401:Lama3 APN 18 12,690,784 (GRCm39) missense probably benign 0.02
IGL02517:Lama3 APN 18 12,670,915 (GRCm39) critical splice donor site probably null
IGL02644:Lama3 APN 18 12,658,910 (GRCm39) missense probably benign 0.12
IGL02733:Lama3 APN 18 12,711,184 (GRCm39) missense probably damaging 0.99
IGL02932:Lama3 APN 18 12,661,858 (GRCm39) missense probably damaging 1.00
IGL03006:Lama3 APN 18 12,601,425 (GRCm39) splice site probably benign
IGL03038:Lama3 APN 18 12,552,307 (GRCm39) missense probably damaging 0.99
IGL03064:Lama3 APN 18 12,572,406 (GRCm39) missense possibly damaging 0.72
IGL03146:Lama3 APN 18 12,660,681 (GRCm39) missense possibly damaging 0.66
IGL03233:Lama3 APN 18 12,614,095 (GRCm39) missense probably damaging 1.00
IGL03255:Lama3 APN 18 12,672,760 (GRCm39) missense probably damaging 1.00
IGL03369:Lama3 APN 18 12,686,340 (GRCm39) missense probably benign 0.05
IGL03412:Lama3 APN 18 12,552,239 (GRCm39) missense probably damaging 0.99
IGL02980:Lama3 UTSW 18 12,686,288 (GRCm39) missense probably benign 0.01
IGL03014:Lama3 UTSW 18 12,673,024 (GRCm39) missense possibly damaging 0.95
R0007:Lama3 UTSW 18 12,630,938 (GRCm39) splice site probably benign
R0007:Lama3 UTSW 18 12,630,938 (GRCm39) splice site probably benign
R0050:Lama3 UTSW 18 12,537,160 (GRCm39) missense probably damaging 1.00
R0050:Lama3 UTSW 18 12,537,160 (GRCm39) missense probably damaging 1.00
R0063:Lama3 UTSW 18 12,661,762 (GRCm39) splice site probably benign
R0063:Lama3 UTSW 18 12,661,762 (GRCm39) splice site probably benign
R0106:Lama3 UTSW 18 12,537,039 (GRCm39) missense probably damaging 0.96
R0148:Lama3 UTSW 18 12,581,329 (GRCm39) missense probably damaging 1.00
R0165:Lama3 UTSW 18 12,657,867 (GRCm39) missense probably damaging 0.99
R0240:Lama3 UTSW 18 12,672,880 (GRCm39) splice site probably null
R0240:Lama3 UTSW 18 12,672,880 (GRCm39) splice site probably null
R0316:Lama3 UTSW 18 12,652,934 (GRCm39) missense probably benign 0.09
R0365:Lama3 UTSW 18 12,640,064 (GRCm39) missense probably damaging 0.96
R0390:Lama3 UTSW 18 12,540,620 (GRCm39) missense probably benign 0.10
R0408:Lama3 UTSW 18 12,589,894 (GRCm39) missense probably benign
R0449:Lama3 UTSW 18 12,633,569 (GRCm39) splice site probably null
R0453:Lama3 UTSW 18 12,598,535 (GRCm39) missense possibly damaging 0.63
R0480:Lama3 UTSW 18 12,583,481 (GRCm39) missense possibly damaging 0.81
R0536:Lama3 UTSW 18 12,658,951 (GRCm39) missense probably damaging 1.00
R0545:Lama3 UTSW 18 12,694,758 (GRCm39) missense possibly damaging 0.90
R0567:Lama3 UTSW 18 12,682,309 (GRCm39) missense probably benign
R0605:Lama3 UTSW 18 12,640,006 (GRCm39) missense probably benign 0.02
R0617:Lama3 UTSW 18 12,552,315 (GRCm39) critical splice donor site probably null
R0629:Lama3 UTSW 18 12,552,302 (GRCm39) missense possibly damaging 0.79
R0671:Lama3 UTSW 18 12,610,647 (GRCm39) missense possibly damaging 0.80
R0730:Lama3 UTSW 18 12,589,907 (GRCm39) splice site probably benign
R1216:Lama3 UTSW 18 12,554,191 (GRCm39) splice site probably benign
R1356:Lama3 UTSW 18 12,633,634 (GRCm39) unclassified probably benign
R1386:Lama3 UTSW 18 12,610,427 (GRCm39) missense probably benign 0.04
R1424:Lama3 UTSW 18 12,653,048 (GRCm39) missense probably benign 0.13
R1426:Lama3 UTSW 18 12,614,155 (GRCm39) critical splice donor site probably null
R1437:Lama3 UTSW 18 12,682,284 (GRCm39) missense possibly damaging 0.46
R1468:Lama3 UTSW 18 12,574,164 (GRCm39) missense probably benign 0.00
R1468:Lama3 UTSW 18 12,574,164 (GRCm39) missense probably benign 0.00
R1472:Lama3 UTSW 18 12,615,102 (GRCm39) missense probably benign 0.23
R1557:Lama3 UTSW 18 12,646,788 (GRCm39) splice site probably benign
R1571:Lama3 UTSW 18 12,672,774 (GRCm39) missense probably damaging 0.98
R1599:Lama3 UTSW 18 12,583,457 (GRCm39) nonsense probably null
R1631:Lama3 UTSW 18 12,540,551 (GRCm39) missense probably damaging 1.00
R1647:Lama3 UTSW 18 12,665,256 (GRCm39) missense possibly damaging 0.90
R1648:Lama3 UTSW 18 12,665,256 (GRCm39) missense possibly damaging 0.90
R1719:Lama3 UTSW 18 12,612,929 (GRCm39) critical splice donor site probably null
R1757:Lama3 UTSW 18 12,598,556 (GRCm39) missense probably benign 0.10
R1766:Lama3 UTSW 18 12,535,119 (GRCm39) missense probably damaging 1.00
R1853:Lama3 UTSW 18 12,646,762 (GRCm39) missense possibly damaging 0.75
R1856:Lama3 UTSW 18 12,670,838 (GRCm39) nonsense probably null
R1909:Lama3 UTSW 18 12,714,855 (GRCm39) missense probably benign 0.19
R1913:Lama3 UTSW 18 12,628,336 (GRCm39) missense probably benign 0.15
R1975:Lama3 UTSW 18 12,586,920 (GRCm39) missense probably damaging 1.00
R2014:Lama3 UTSW 18 12,657,778 (GRCm39) splice site probably benign
R2059:Lama3 UTSW 18 12,661,390 (GRCm39) missense probably damaging 0.98
R2060:Lama3 UTSW 18 12,661,783 (GRCm39) missense probably benign 0.30
R2086:Lama3 UTSW 18 12,657,887 (GRCm39) missense probably benign 0.39
R2115:Lama3 UTSW 18 12,535,906 (GRCm39) missense possibly damaging 0.94
R2291:Lama3 UTSW 18 12,658,136 (GRCm39) missense probably damaging 0.98
R2860:Lama3 UTSW 18 12,586,807 (GRCm39) missense probably damaging 1.00
R2861:Lama3 UTSW 18 12,586,807 (GRCm39) missense probably damaging 1.00
R2862:Lama3 UTSW 18 12,586,807 (GRCm39) missense probably damaging 1.00
R3410:Lama3 UTSW 18 12,546,915 (GRCm39) critical splice donor site probably null
R3614:Lama3 UTSW 18 12,581,345 (GRCm39) missense probably benign 0.03
R3696:Lama3 UTSW 18 12,572,532 (GRCm39) splice site probably benign
R3752:Lama3 UTSW 18 12,640,086 (GRCm39) missense probably damaging 1.00
R3967:Lama3 UTSW 18 12,713,398 (GRCm39) missense probably damaging 1.00
R3968:Lama3 UTSW 18 12,713,398 (GRCm39) missense probably damaging 1.00
R3969:Lama3 UTSW 18 12,713,398 (GRCm39) missense probably damaging 1.00
R3970:Lama3 UTSW 18 12,713,398 (GRCm39) missense probably damaging 1.00
R4088:Lama3 UTSW 18 12,637,365 (GRCm39) nonsense probably null
R4118:Lama3 UTSW 18 12,583,488 (GRCm39) missense probably benign 0.01
R4222:Lama3 UTSW 18 12,583,460 (GRCm39) missense probably damaging 1.00
R4223:Lama3 UTSW 18 12,583,460 (GRCm39) missense probably damaging 1.00
R4224:Lama3 UTSW 18 12,583,460 (GRCm39) missense probably damaging 1.00
R4225:Lama3 UTSW 18 12,583,460 (GRCm39) missense probably damaging 1.00
R4367:Lama3 UTSW 18 12,646,747 (GRCm39) missense probably damaging 1.00
R4404:Lama3 UTSW 18 12,715,588 (GRCm39) missense probably benign 0.01
R4424:Lama3 UTSW 18 12,652,929 (GRCm39) nonsense probably null
R4483:Lama3 UTSW 18 12,682,310 (GRCm39) missense probably benign 0.32
R4484:Lama3 UTSW 18 12,614,145 (GRCm39) missense probably benign
R4516:Lama3 UTSW 18 12,628,415 (GRCm39) missense probably damaging 1.00
R4556:Lama3 UTSW 18 12,612,816 (GRCm39) missense possibly damaging 0.63
R4616:Lama3 UTSW 18 12,637,454 (GRCm39) critical splice donor site probably null
R4702:Lama3 UTSW 18 12,711,086 (GRCm39) nonsense probably null
R4704:Lama3 UTSW 18 12,686,280 (GRCm39) missense probably benign 0.08
R4750:Lama3 UTSW 18 12,637,416 (GRCm39) missense probably benign 0.25
R4753:Lama3 UTSW 18 12,615,141 (GRCm39) missense probably damaging 1.00
R4767:Lama3 UTSW 18 12,633,620 (GRCm39) missense probably benign 0.32
R4777:Lama3 UTSW 18 12,546,828 (GRCm39) missense probably damaging 1.00
R4782:Lama3 UTSW 18 12,544,627 (GRCm39) nonsense probably null
R4784:Lama3 UTSW 18 12,582,601 (GRCm39) missense probably benign 0.20
R4816:Lama3 UTSW 18 12,610,661 (GRCm39) missense possibly damaging 0.93
R4833:Lama3 UTSW 18 12,574,188 (GRCm39) missense probably benign 0.01
R4854:Lama3 UTSW 18 12,544,599 (GRCm39) missense probably benign 0.00
R4863:Lama3 UTSW 18 12,631,735 (GRCm39) intron probably benign
R4863:Lama3 UTSW 18 12,672,850 (GRCm39) missense probably damaging 0.99
R4953:Lama3 UTSW 18 12,581,362 (GRCm39) missense probably damaging 1.00
R4974:Lama3 UTSW 18 12,685,883 (GRCm39) missense probably damaging 0.98
R4996:Lama3 UTSW 18 12,651,800 (GRCm39) missense probably benign 0.24
R5049:Lama3 UTSW 18 12,715,668 (GRCm39) missense probably benign 0.19
R5057:Lama3 UTSW 18 12,665,005 (GRCm39) missense probably null 0.82
R5090:Lama3 UTSW 18 12,675,459 (GRCm39) missense possibly damaging 0.94
R5122:Lama3 UTSW 18 12,672,823 (GRCm39) missense possibly damaging 0.53
R5215:Lama3 UTSW 18 12,710,957 (GRCm39) missense probably damaging 1.00
R5245:Lama3 UTSW 18 12,552,950 (GRCm39) missense probably damaging 1.00
R5259:Lama3 UTSW 18 12,598,565 (GRCm39) missense probably damaging 1.00
R5320:Lama3 UTSW 18 12,685,912 (GRCm39) missense probably damaging 0.99
R5377:Lama3 UTSW 18 12,586,803 (GRCm39) missense probably damaging 0.99
R5432:Lama3 UTSW 18 12,705,123 (GRCm39) missense probably damaging 1.00
R5500:Lama3 UTSW 18 12,589,821 (GRCm39) missense possibly damaging 0.93
R5534:Lama3 UTSW 18 12,686,267 (GRCm39) missense probably benign 0.00
R5589:Lama3 UTSW 18 12,605,277 (GRCm39) missense possibly damaging 0.46
R5604:Lama3 UTSW 18 12,572,405 (GRCm39) missense probably benign
R5617:Lama3 UTSW 18 12,631,993 (GRCm39) intron probably benign
R5709:Lama3 UTSW 18 12,672,856 (GRCm39) missense probably damaging 1.00
R5965:Lama3 UTSW 18 12,562,944 (GRCm39) missense possibly damaging 0.67
R6042:Lama3 UTSW 18 12,707,311 (GRCm39) missense probably damaging 1.00
R6065:Lama3 UTSW 18 12,602,985 (GRCm39) missense possibly damaging 0.53
R6085:Lama3 UTSW 18 12,615,156 (GRCm39) missense probably benign 0.01
R6212:Lama3 UTSW 18 12,646,702 (GRCm39) missense probably damaging 1.00
R6268:Lama3 UTSW 18 12,657,794 (GRCm39) missense probably damaging 0.98
R6276:Lama3 UTSW 18 12,640,006 (GRCm39) missense probably benign 0.02
R6366:Lama3 UTSW 18 12,615,194 (GRCm39) missense probably damaging 1.00
R6393:Lama3 UTSW 18 12,612,813 (GRCm39) missense probably benign 0.44
R6493:Lama3 UTSW 18 12,615,205 (GRCm39) critical splice donor site probably null
R6505:Lama3 UTSW 18 12,628,405 (GRCm39) missense probably benign 0.02
R6563:Lama3 UTSW 18 12,670,823 (GRCm39) missense probably damaging 1.00
R6582:Lama3 UTSW 18 12,710,897 (GRCm39) missense probably damaging 1.00
R6585:Lama3 UTSW 18 12,552,314 (GRCm39) critical splice donor site probably null
R6609:Lama3 UTSW 18 12,646,735 (GRCm39) missense probably damaging 0.99
R6656:Lama3 UTSW 18 12,682,283 (GRCm39) missense possibly damaging 0.66
R6833:Lama3 UTSW 18 12,624,605 (GRCm39) missense probably damaging 1.00
R6834:Lama3 UTSW 18 12,624,605 (GRCm39) missense probably damaging 1.00
R7019:Lama3 UTSW 18 12,661,475 (GRCm39) missense probably damaging 0.97
R7026:Lama3 UTSW 18 12,649,605 (GRCm39) missense probably damaging 0.98
R7088:Lama3 UTSW 18 12,715,602 (GRCm39) missense possibly damaging 0.90
R7100:Lama3 UTSW 18 12,715,701 (GRCm39) missense possibly damaging 0.80
R7102:Lama3 UTSW 18 12,685,870 (GRCm39) missense possibly damaging 0.66
R7103:Lama3 UTSW 18 12,664,936 (GRCm39) missense probably benign 0.00
R7121:Lama3 UTSW 18 12,595,839 (GRCm39) missense probably benign 0.06
R7133:Lama3 UTSW 18 12,672,843 (GRCm39) missense probably benign 0.05
R7150:Lama3 UTSW 18 12,601,346 (GRCm39) missense probably damaging 1.00
R7158:Lama3 UTSW 18 12,589,869 (GRCm39) missense probably benign 0.20
R7170:Lama3 UTSW 18 12,537,133 (GRCm39) missense probably benign 0.26
R7216:Lama3 UTSW 18 12,563,057 (GRCm39) missense probably damaging 1.00
R7223:Lama3 UTSW 18 12,715,665 (GRCm39) missense possibly damaging 0.53
R7243:Lama3 UTSW 18 12,552,902 (GRCm39) missense probably damaging 1.00
R7282:Lama3 UTSW 18 12,572,449 (GRCm39) missense probably damaging 0.99
R7337:Lama3 UTSW 18 12,640,097 (GRCm39) splice site probably null
R7442:Lama3 UTSW 18 12,605,238 (GRCm39) critical splice acceptor site probably null
R7487:Lama3 UTSW 18 12,552,294 (GRCm39) missense probably benign
R7604:Lama3 UTSW 18 12,633,550 (GRCm39) missense possibly damaging 0.93
R7609:Lama3 UTSW 18 12,664,891 (GRCm39) critical splice acceptor site probably null
R7650:Lama3 UTSW 18 12,670,895 (GRCm39) missense probably benign 0.01
R7894:Lama3 UTSW 18 12,595,864 (GRCm39) missense probably benign 0.07
R7975:Lama3 UTSW 18 12,670,796 (GRCm39) missense probably damaging 1.00
R8099:Lama3 UTSW 18 12,667,120 (GRCm39) missense probably damaging 0.97
R8168:Lama3 UTSW 18 12,639,999 (GRCm39) missense probably null
R8219:Lama3 UTSW 18 12,572,417 (GRCm39) missense probably benign 0.07
R8227:Lama3 UTSW 18 12,540,608 (GRCm39) missense probably benign
R8229:Lama3 UTSW 18 12,540,608 (GRCm39) missense probably benign
R8298:Lama3 UTSW 18 12,658,910 (GRCm39) missense probably benign 0.12
R8351:Lama3 UTSW 18 12,673,670 (GRCm39) missense probably damaging 1.00
R8364:Lama3 UTSW 18 12,661,404 (GRCm39) missense probably damaging 0.99
R8463:Lama3 UTSW 18 12,582,896 (GRCm39) missense probably damaging 0.96
R8515:Lama3 UTSW 18 12,544,688 (GRCm39) missense probably null 0.01
R8784:Lama3 UTSW 18 12,554,212 (GRCm39) missense probably benign
R8799:Lama3 UTSW 18 12,624,000 (GRCm39) missense probably damaging 0.96
R8874:Lama3 UTSW 18 12,582,643 (GRCm39) critical splice donor site probably null
R8938:Lama3 UTSW 18 12,689,762 (GRCm39) missense probably damaging 1.00
R8967:Lama3 UTSW 18 12,665,096 (GRCm39) missense possibly damaging 0.46
R9039:Lama3 UTSW 18 12,614,120 (GRCm39) nonsense probably null
R9126:Lama3 UTSW 18 12,583,527 (GRCm39) missense probably damaging 1.00
R9200:Lama3 UTSW 18 12,605,297 (GRCm39) missense probably benign 0.00
R9203:Lama3 UTSW 18 12,595,869 (GRCm39) missense probably benign 0.04
R9246:Lama3 UTSW 18 12,710,959 (GRCm39) missense probably damaging 0.99
R9284:Lama3 UTSW 18 12,583,541 (GRCm39) nonsense probably null
R9553:Lama3 UTSW 18 12,563,019 (GRCm39) missense probably damaging 1.00
R9716:Lama3 UTSW 18 12,583,460 (GRCm39) missense probably damaging 1.00
R9734:Lama3 UTSW 18 12,682,320 (GRCm39) missense possibly damaging 0.94
X0019:Lama3 UTSW 18 12,715,631 (GRCm39) missense possibly damaging 0.94
Z1177:Lama3 UTSW 18 12,562,936 (GRCm39) critical splice acceptor site probably null
Predicted Primers PCR Primer
(F):5'- GGGGCTGCTTCAGAATGTCTTGAAC -3'
(R):5'- ACCTGCCCAGCAAAATCTCTTCTTG -3'

Sequencing Primer
(F):5'- TGCTATGAGCAGTTCAGATCACC -3'
(R):5'- CAAAATCTCTTCTTGCTGGGAAGC -3'
Posted On 2013-04-16