Incidental Mutation 'R6493:Lama3'
ID 522894
Institutional Source Beutler Lab
Gene Symbol Lama3
Ensembl Gene ENSMUSG00000024421
Gene Name laminin, alpha 3
Synonyms [a]3B, nicein, 150kDa
MMRRC Submission 044625-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R6493 (G1)
Quality Score 193.009
Status Not validated
Chromosome 18
Chromosomal Location 12466876-12716070 bp(+) (GRCm39)
Type of Mutation critical splice donor site (1 bp from exon)
DNA Base Change (assembly) G to A at 12615205 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000089703 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092070]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000092070
SMART Domains Protein: ENSMUSP00000089703
Gene: ENSMUSG00000024421

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: 99.8%
  • 3x: 99.4%
  • 10x: 97.3%
  • 20x: 91.3%
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: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca5 T A 11: 110,184,704 (GRCm39) H934L probably benign Het
Abcb1b G A 5: 8,874,698 (GRCm39) D453N probably damaging Het
Ampd3 A G 7: 110,395,018 (GRCm39) probably null Het
Axdnd1 A T 1: 156,208,383 (GRCm39) I485N probably damaging Het
Bscl2 A G 19: 8,817,138 (GRCm39) D22G probably damaging Het
Ccdc96 A G 5: 36,643,596 (GRCm39) E534G probably damaging Het
Cdc42bpg G T 19: 6,368,485 (GRCm39) G1061V probably damaging Het
Cers3 T C 7: 66,393,468 (GRCm39) Y26H probably benign Het
Chd1l G A 3: 97,494,483 (GRCm39) A399V probably damaging Het
Clca4a T A 3: 144,663,059 (GRCm39) T597S probably benign Het
Daxx T A 17: 34,131,345 (GRCm39) probably null Het
Egf T C 3: 129,512,737 (GRCm39) probably benign Het
Eps15 A G 4: 109,226,145 (GRCm39) D629G probably damaging Het
Fancm G A 12: 65,144,262 (GRCm39) A575T probably benign Het
Fat4 G A 3: 38,945,036 (GRCm39) D1310N probably damaging Het
Gm11595 G A 11: 99,663,381 (GRCm39) R100C unknown Het
Grxcr2 G A 18: 42,131,766 (GRCm39) P101L possibly damaging Het
Hsd17b12 A T 2: 93,874,228 (GRCm39) I225N probably damaging Het
Kcnj8 T C 6: 142,511,773 (GRCm39) Y278C probably damaging Het
Lax1 C T 1: 133,607,530 (GRCm39) D404N probably benign Het
Lipg T C 18: 75,081,095 (GRCm39) K329E probably damaging Het
Lysmd2 T G 9: 75,542,984 (GRCm39) L197R probably damaging Het
Maneal A T 4: 124,750,964 (GRCm39) I264N probably damaging Het
Myh4 A G 11: 67,149,455 (GRCm39) N1729S probably benign Het
Myl2 A G 5: 122,244,791 (GRCm39) N154D possibly damaging Het
Nlrp9c T A 7: 26,081,812 (GRCm39) D638V probably damaging Het
Notch1 T C 2: 26,362,110 (GRCm39) H74R unknown Het
Olfml3 A T 3: 103,643,523 (GRCm39) V286D possibly damaging Het
Or14c46 T G 7: 85,918,090 (GRCm39) K302N probably benign Het
Or4b12 G A 2: 90,096,052 (GRCm39) H241Y probably damaging Het
Or51a25 G T 7: 102,373,287 (GRCm39) R137S possibly damaging Het
Or51f23c-ps1 A G 7: 102,431,603 (GRCm39) K307E probably benign Het
Or8k41 T C 2: 86,313,565 (GRCm39) I174V possibly damaging Het
Parn A C 16: 13,474,789 (GRCm39) F127V probably damaging Het
Pcdhac2 T C 18: 37,277,758 (GRCm39) V246A probably damaging Het
Plin2 G A 4: 86,580,224 (GRCm39) T90I possibly damaging Het
Podxl C T 6: 31,501,981 (GRCm39) C326Y probably damaging Het
Pramel46 A G 5: 95,418,684 (GRCm39) L104P probably damaging Het
Prl8a8 T A 13: 27,691,335 (GRCm39) K223* probably null Het
Ptprh T G 7: 4,583,989 (GRCm39) E201A possibly damaging Het
Rtn1 A C 12: 72,355,103 (GRCm39) V281G probably damaging Het
Scaf8 T C 17: 3,221,394 (GRCm39) S294P unknown Het
Shroom3 C A 5: 93,089,420 (GRCm39) N723K probably benign Het
Spata22 T C 11: 73,244,572 (GRCm39) *312R probably null Het
Stx7 T C 10: 24,060,969 (GRCm39) probably null Het
Taar6 T C 10: 23,861,021 (GRCm39) D175G probably benign Het
Tbccd1 A C 16: 22,641,216 (GRCm39) L387R probably damaging Het
Tecpr1 T C 5: 144,146,792 (GRCm39) M525V probably benign Het
Tex10 A T 4: 48,436,450 (GRCm39) I756N probably damaging Het
Tfap2d G C 1: 19,174,702 (GRCm39) G52R probably benign Het
Ttn T C 2: 76,572,341 (GRCm39) E24438G probably damaging Het
Tut4 A G 4: 108,384,002 (GRCm39) K1053R probably damaging Het
Wdpcp C T 11: 21,661,631 (GRCm39) T301I possibly damaging Het
Zbtb1 C T 12: 76,433,247 (GRCm39) T411I probably benign Het
Zzef1 G A 11: 72,804,129 (GRCm39) G2624R 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
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
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
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'- CCTTTGTGAAGAGGTGACAGGG -3'
(R):5'- CTGGCATACATGAGCAAGGC -3'

Sequencing Primer
(F):5'- GAAGTGTCTCTGCCCACC -3'
(R):5'- CCTGGCTGCCCTGAGTC -3'
Posted On 2018-06-06