Incidental Mutation 'R5589:Lama3'
ID 437388
Institutional Source Beutler Lab
Gene Symbol Lama3
Ensembl Gene ENSMUSG00000024421
Gene Name laminin, alpha 3
Synonyms [a]3B, nicein, 150kDa
MMRRC Submission 043142-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R5589 (G1)
Quality Score 225
Status Not validated
Chromosome 18
Chromosomal Location 12466876-12716070 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 12605277 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 1077 (T1077I)
Ref Sequence ENSEMBL: ENSMUSP00000089703 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092070]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000092070
AA Change: T1077I

PolyPhen 2 Score 0.463 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000089703
Gene: ENSMUSG00000024421
AA Change: T1077I

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: 99.9%
  • 3x: 99.7%
  • 10x: 98.7%
  • 20x: 96.4%
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: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700093K21Rik T A 11: 23,468,066 (GRCm39) M76L probably benign Het
Adrm1b T A 3: 92,336,112 (GRCm39) probably benign Het
Alg1 T A 16: 5,053,086 (GRCm39) W116R probably benign Het
Ano3 A T 2: 110,715,340 (GRCm39) S33T probably damaging Het
Atp2b2 T C 6: 113,751,400 (GRCm39) E556G possibly damaging Het
Brca2 T A 5: 150,480,597 (GRCm39) I2761K possibly damaging Het
Ccdc68 G A 18: 70,079,577 (GRCm39) G141E probably benign Het
Cckbr T C 7: 105,083,732 (GRCm39) V220A probably damaging Het
Ccnd3 G A 17: 47,909,544 (GRCm39) R45Q probably damaging Het
Cdh24 G T 14: 54,874,832 (GRCm39) T391N probably damaging Het
Cldn11 A G 3: 31,204,395 (GRCm39) T33A probably damaging Het
Clec2e T A 6: 129,075,391 (GRCm39) Y50F probably benign Het
Cntnap1 A G 11: 101,075,944 (GRCm39) N943D probably benign Het
Cspg4b A G 13: 113,454,484 (GRCm39) R177G possibly damaging Het
Dmgdh T C 13: 93,813,665 (GRCm39) V70A probably damaging Het
Gm14496 C A 2: 181,637,674 (GRCm39) Y249* probably null Het
Gmnc T A 16: 26,781,714 (GRCm39) H105L probably damaging Het
Gpt2 A G 8: 86,219,740 (GRCm39) Y62C probably damaging Het
Ift80 T C 3: 68,838,233 (GRCm39) R413G probably damaging Het
Kctd16 C A 18: 40,392,061 (GRCm39) D216E probably damaging Het
Kif26b T C 1: 178,743,864 (GRCm39) V873A probably benign Het
Klra4 G T 6: 130,039,117 (GRCm39) Q92K probably benign Het
L1td1 C A 4: 98,626,341 (GRCm39) N845K possibly damaging Het
Loxhd1 T C 18: 77,429,751 (GRCm39) I230T possibly damaging Het
Lsg1 T C 16: 30,399,819 (GRCm39) N160S probably damaging Het
Lyzl4 G A 9: 121,413,469 (GRCm39) R24C probably damaging Het
Mib1 A G 18: 10,794,488 (GRCm39) N658S probably benign Het
Mmp8 T C 9: 7,566,275 (GRCm39) I377T probably damaging Het
Mtmr14 T C 6: 113,238,243 (GRCm39) probably null Het
Myo1c A G 11: 75,548,414 (GRCm39) T58A possibly damaging Het
Myo9a C T 9: 59,802,527 (GRCm39) Q2005* probably null Het
Neu3 G T 7: 99,472,636 (GRCm39) P34T probably benign Het
Nlrp4b G A 7: 10,449,512 (GRCm39) V205I probably benign Het
Or4b1b C T 2: 90,112,313 (GRCm39) G202D probably damaging Het
Or4k38 T C 2: 111,165,850 (GRCm39) N191S possibly damaging Het
Or5h23 A T 16: 58,906,334 (GRCm39) S171T probably benign Het
Or5t15 A G 2: 86,681,118 (GRCm39) I308T unknown Het
Or6c66 T G 10: 129,461,319 (GRCm39) T204P probably damaging Het
Or9m1 T C 2: 87,733,691 (GRCm39) T110A probably benign Het
Pcsk6 T C 7: 65,578,933 (GRCm39) probably null Het
Pik3c2a A G 7: 116,016,893 (GRCm39) V288A probably benign Het
Plcd3 T C 11: 102,968,629 (GRCm39) D354G probably benign Het
Prkdc C A 16: 15,524,655 (GRCm39) N1219K probably benign Het
Prl3d1 T A 13: 27,278,927 (GRCm39) Y41N probably damaging Het
Qrich2 C T 11: 116,332,234 (GRCm39) G2321R probably damaging Het
Rrbp1 T C 2: 143,831,886 (GRCm39) I94V probably benign Het
Serinc1 C A 10: 57,399,262 (GRCm39) V214L probably benign Het
Serpina9 G T 12: 103,967,728 (GRCm39) N222K probably benign Het
Smchd1 A G 17: 71,747,956 (GRCm39) Y429H probably damaging Het
Smyd1 C T 6: 71,239,164 (GRCm39) V9M probably damaging Het
Sostdc1 C T 12: 36,367,246 (GRCm39) Q141* probably null Het
Spam1 C T 6: 24,796,109 (GRCm39) T20I probably benign Het
Tex47 T C 5: 7,354,834 (GRCm39) V5A probably benign Het
Thbs4 T C 13: 92,912,582 (GRCm39) probably null Het
Trim45 C T 3: 100,837,257 (GRCm39) P531L probably damaging Het
Tshb A T 3: 102,685,478 (GRCm39) Y50* probably null Het
Ttn T C 2: 76,599,320 (GRCm39) I19230V probably damaging Het
Ttn A T 2: 76,641,587 (GRCm39) L5176Q possibly damaging Het
Uba6 G A 5: 86,270,288 (GRCm39) T832I probably damaging Het
Unc13d A T 11: 115,960,579 (GRCm39) V497D probably damaging Het
Usp13 T C 3: 32,892,007 (GRCm39) V62A probably damaging Het
Vmn1r215 A C 13: 23,260,189 (GRCm39) L76F probably damaging Het
Vmn1r215 G T 13: 23,260,190 (GRCm39) G77C probably damaging Het
Vmn2r5 T C 3: 64,411,497 (GRCm39) D357G probably damaging Het
Zbtb40 T C 4: 136,722,594 (GRCm39) D828G probably damaging Het
Zfp74 A T 7: 29,633,990 (GRCm39) C573S probably damaging 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
R0325:Lama3 UTSW 18 12,615,183 (GRCm39) missense probably damaging 1.00
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
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'- ACAATCTCTAGGCTCCTCCG -3'
(R):5'- GAGTGCAAGTTCCCAAATTGG -3'

Sequencing Primer
(F):5'- CCTCCGGTTCCTTGGTGG -3'
(R):5'- GATGACTAGTCCCATTCCATAGC -3'
Posted On 2016-10-26