Incidental Mutation 'R4426:Lama2'
ID 328181
Institutional Source Beutler Lab
Gene Symbol Lama2
Ensembl Gene ENSMUSG00000019899
Gene Name laminin, alpha 2
Synonyms mer, merosin
MMRRC Submission 041697-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.320) question?
Stock # R4426 (G1)
Quality Score 225
Status Not validated
Chromosome 10
Chromosomal Location 26857281-27493021 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 27298554 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Cysteine at position 181 (R181C)
Ref Sequence ENSEMBL: ENSMUSP00000140716 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092639] [ENSMUST00000189575]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000092639
AA Change: R181C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000090304
Gene: ENSMUSG00000019899
AA Change: R181C

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
LamNT 29 281 5.35e-129 SMART
EGF_Lam 283 337 2.11e-4 SMART
EGF_Lam 340 407 1.59e-8 SMART
EGF_Lam 410 462 5.44e-7 SMART
EGF_Lam 465 511 9.05e-4 SMART
LamB 574 706 2.26e-44 SMART
Pfam:Laminin_EGF 715 745 2.8e-4 PFAM
EGF_Lam 753 800 4.03e-10 SMART
EGF_Lam 803 858 3.01e-9 SMART
EGF_Lam 861 911 1.35e-11 SMART
EGF_Lam 914 960 7.23e-12 SMART
EGF_Lam 963 1007 5.87e-12 SMART
EGF_Lam 1010 1053 1.28e-12 SMART
EGF_Lam 1056 1099 2.37e-7 SMART
EGF_Lam 1102 1159 3.22e-9 SMART
LamB 1225 1360 1.95e-57 SMART
EGF_like 1364 1413 8.13e-1 SMART
EGF_Lam 1416 1462 5.48e-12 SMART
EGF_Lam 1465 1520 1.27e-7 SMART
EGF_Lam 1523 1567 2.4e-8 SMART
Pfam:Laminin_I 1584 1849 2e-92 PFAM
Blast:MA 1881 2113 1e-112 BLAST
LamG 2162 2307 1.28e-25 SMART
LamG 2356 2500 2.2e-33 SMART
LamG 2542 2688 3.31e-28 SMART
low complexity region 2725 2741 N/A INTRINSIC
LamG 2781 2914 2.25e-39 SMART
LamG 2956 3092 1.53e-32 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185839
Predicted Effect noncoding transcript
Transcript: ENSMUST00000186965
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188963
Predicted Effect probably damaging
Transcript: ENSMUST00000189575
AA Change: R181C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000140716
Gene: ENSMUSG00000019899
AA Change: R181C

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
LamNT 29 281 2.5e-131 SMART
EGF_Lam 283 337 1e-6 SMART
EGF_Lam 340 407 7.7e-11 SMART
EGF_Lam 410 462 2.6e-9 SMART
EGF_Lam 465 511 4.5e-6 SMART
LamB 574 706 1.4e-46 SMART
Pfam:Laminin_EGF 715 745 1.7e-2 PFAM
EGF_Lam 753 800 1.9e-12 SMART
EGF_Lam 803 858 1.4e-11 SMART
EGF_Lam 861 911 6.7e-14 SMART
EGF_Lam 914 960 3.6e-14 SMART
EGF_Lam 963 1007 2.9e-14 SMART
EGF_Lam 1010 1053 6.1e-15 SMART
EGF_Lam 1056 1099 1.1e-9 SMART
EGF_Lam 1102 1159 1.5e-11 SMART
LamB 1225 1349 1.4e-45 SMART
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.8%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Laminin, an extracellular protein, is a major component of the basement membrane. It is thought to mediate the attachment, migration, and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. It is composed of three subunits, alpha, beta, and gamma, which are bound to each other by disulfide bonds into a cross-shaped molecule. This gene encodes the alpha 2 chain, which constitutes one of the subunits of laminin 2 (merosin) and laminin 4 (s-merosin). Mutations in this gene have been identified as the cause of congenital merosin-deficient muscular dystrophy. Two transcript variants encoding different proteins have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for targeted and spontaneous mutations exhibit progressive growth retardation, ataxia, muscle atrophy and degeneration, infertility, and premature lethality. Muscle fiber degeneration is evident as early as the first week of life. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Albfm1 G T 5: 90,720,642 (GRCm39) C271F probably damaging Het
Arhgef39 C T 4: 43,497,112 (GRCm39) G293E possibly damaging Het
Atp8a1 A C 5: 67,932,171 (GRCm39) I206S probably benign Het
Cacnb2 A T 2: 14,980,026 (GRCm39) R290* probably null Het
Ccdc137 T C 11: 120,351,074 (GRCm39) S159P probably damaging Het
Chil5 A G 3: 105,926,943 (GRCm39) S231P probably damaging Het
Cic C T 7: 24,993,433 (GRCm39) probably benign Het
Csmd3 A G 15: 47,532,581 (GRCm39) V2434A possibly damaging Het
Csnk1a1 A G 18: 61,718,381 (GRCm39) probably benign Het
Eif4e1b T C 13: 54,932,296 (GRCm39) S49P probably benign Het
Far1 C A 7: 113,149,208 (GRCm39) P194Q probably benign Het
Fut4 T C 9: 14,662,677 (GRCm39) T206A possibly damaging Het
Galnt7 G T 8: 58,005,606 (GRCm39) S209* probably null Het
Gas2l1 A G 11: 5,013,908 (GRCm39) V184A probably benign Het
Herc1 T C 9: 66,403,287 (GRCm39) L4402P probably damaging Het
Hoxa13 C A 6: 52,237,714 (GRCm39) probably benign Het
Ighv1-9 T A 12: 114,547,416 (GRCm39) K42* probably null Het
Kif20a C T 18: 34,764,994 (GRCm39) R743W probably damaging Het
Lrp2 G T 2: 69,336,692 (GRCm39) T1360K probably benign Het
Map4k1 G A 7: 28,688,020 (GRCm39) V177I probably damaging Het
Nbea G A 3: 55,989,800 (GRCm39) T352I probably damaging Het
Nde1 A G 16: 14,006,200 (GRCm39) T82A possibly damaging Het
Nes A G 3: 87,883,349 (GRCm39) E536G probably damaging Het
Nms C T 1: 38,978,377 (GRCm39) P4L probably benign Het
Nrip1 T C 16: 76,088,293 (GRCm39) Q1088R possibly damaging Het
Nwd1 A G 8: 73,393,423 (GRCm39) K229E probably damaging Het
Or51f1d T C 7: 102,701,018 (GRCm39) L171P probably damaging Het
Or52ad1 A G 7: 102,995,290 (GRCm39) Y282H probably damaging Het
Pcdhac2 T A 18: 37,277,796 (GRCm39) S259T probably benign Het
Pdcd5 T C 7: 35,345,605 (GRCm39) D102G possibly damaging Het
Pgm1 T C 4: 99,819,337 (GRCm39) V169A probably benign Het
Pitpnm2 C T 5: 124,280,186 (GRCm39) E121K probably benign Het
Plin3 T C 17: 56,593,555 (GRCm39) Y53C probably damaging Het
Poc1b T C 10: 98,991,001 (GRCm39) probably null Het
Polr2c A T 8: 95,590,090 (GRCm39) N232Y probably damaging Het
Ppp1r9b A T 11: 94,892,150 (GRCm39) R188S possibly damaging Het
Rab36 G A 10: 74,880,328 (GRCm39) V63I probably damaging Het
Rab3gap2 G A 1: 184,967,539 (GRCm39) S141N probably damaging Het
Radx T C X: 138,381,645 (GRCm39) V134A possibly damaging Het
Rap1gap2 C A 11: 74,298,148 (GRCm39) A491S possibly damaging Het
Rnf166 A G 8: 123,196,979 (GRCm39) L91P probably damaging Het
Robo2 T A 16: 73,745,154 (GRCm39) M200L probably damaging Het
Rp1 A T 1: 4,418,147 (GRCm39) H988Q probably benign Het
Sbno2 T C 10: 79,908,192 (GRCm39) K69R probably null Het
Sgce G A 6: 4,691,459 (GRCm39) A295V probably damaging Het
Shc3 C G 13: 51,634,130 (GRCm39) probably null Het
Slc44a1 T C 4: 53,563,286 (GRCm39) V671A probably benign Het
Sptbn4 A C 7: 27,123,223 (GRCm39) L233R probably damaging Het
Stx5a A G 19: 8,727,104 (GRCm39) T252A probably benign Het
Timd6 T A 11: 46,475,247 (GRCm39) F147L probably benign Het
Tmem87b C T 2: 128,688,670 (GRCm39) A485V probably benign Het
Tns1 A G 1: 74,024,908 (GRCm39) I403T probably damaging Het
Ttll10 G C 4: 156,133,018 (GRCm39) T22R possibly damaging Het
Uevld A T 7: 46,589,890 (GRCm39) S293T probably benign Het
Utp18 T C 11: 93,757,264 (GRCm39) N467D probably damaging Het
Vmn1r39 A T 6: 66,782,345 (GRCm39) probably null Het
Vmn2r106 A G 17: 20,505,641 (GRCm39) S18P probably benign Het
Vmn2r61 A T 7: 41,950,157 (GRCm39) H859L probably benign Het
Vmn2r61 T C 7: 41,950,159 (GRCm39) S860P probably benign Het
Vmn2r72 G A 7: 85,387,036 (GRCm39) R843* probably null Het
Vwc2 A G 11: 11,104,235 (GRCm39) T256A probably damaging Het
Zfp715 T C 7: 42,960,516 (GRCm39) D25G probably damaging Het
Other mutations in Lama2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00392:Lama2 APN 10 27,064,261 (GRCm39) missense probably benign 0.01
IGL00467:Lama2 APN 10 27,343,193 (GRCm39) splice site probably benign
IGL00470:Lama2 APN 10 27,119,738 (GRCm39) missense probably benign 0.22
IGL00517:Lama2 APN 10 27,073,326 (GRCm39) missense probably benign 0.01
IGL00541:Lama2 APN 10 27,064,302 (GRCm39) missense probably benign 0.14
IGL00931:Lama2 APN 10 26,882,772 (GRCm39) missense possibly damaging 0.92
IGL00951:Lama2 APN 10 26,906,281 (GRCm39) missense probably benign 0.03
IGL00988:Lama2 APN 10 27,245,011 (GRCm39) nonsense probably null
IGL01098:Lama2 APN 10 26,907,108 (GRCm39) missense possibly damaging 0.66
IGL01152:Lama2 APN 10 27,084,425 (GRCm39) missense probably benign 0.00
IGL01293:Lama2 APN 10 27,107,632 (GRCm39) missense probably benign 0.38
IGL01338:Lama2 APN 10 27,064,268 (GRCm39) missense probably benign 0.13
IGL01609:Lama2 APN 10 27,220,417 (GRCm39) missense probably benign 0.03
IGL01643:Lama2 APN 10 26,946,368 (GRCm39) splice site probably benign
IGL01675:Lama2 APN 10 27,064,050 (GRCm39) missense possibly damaging 0.77
IGL01681:Lama2 APN 10 27,141,041 (GRCm39) missense probably benign 0.33
IGL01694:Lama2 APN 10 26,882,738 (GRCm39) missense possibly damaging 0.75
IGL01705:Lama2 APN 10 27,065,270 (GRCm39) splice site probably benign
IGL01885:Lama2 APN 10 26,981,135 (GRCm39) nonsense probably null
IGL01935:Lama2 APN 10 27,298,600 (GRCm39) missense probably damaging 0.98
IGL01994:Lama2 APN 10 27,343,199 (GRCm39) critical splice donor site probably null
IGL02041:Lama2 APN 10 26,860,322 (GRCm39) missense probably damaging 1.00
IGL02067:Lama2 APN 10 27,052,792 (GRCm39) missense probably benign 0.02
IGL02097:Lama2 APN 10 27,014,956 (GRCm39) missense probably benign 0.09
IGL02179:Lama2 APN 10 26,946,360 (GRCm39) missense probably benign 0.01
IGL02268:Lama2 APN 10 26,877,112 (GRCm39) splice site probably benign
IGL02302:Lama2 APN 10 27,088,039 (GRCm39) missense probably benign 0.06
IGL02363:Lama2 APN 10 27,242,062 (GRCm39) missense probably damaging 1.00
IGL02378:Lama2 APN 10 26,919,652 (GRCm39) missense probably damaging 0.99
IGL02642:Lama2 APN 10 27,343,269 (GRCm39) missense probably damaging 1.00
IGL02676:Lama2 APN 10 26,994,489 (GRCm39) missense probably benign 0.00
IGL02695:Lama2 APN 10 26,876,771 (GRCm39) missense probably benign
IGL02735:Lama2 APN 10 26,980,124 (GRCm39) missense probably damaging 1.00
IGL02794:Lama2 APN 10 26,917,227 (GRCm39) missense possibly damaging 0.73
IGL02823:Lama2 APN 10 26,877,141 (GRCm39) missense probably damaging 1.00
IGL02869:Lama2 APN 10 26,891,534 (GRCm39) missense probably damaging 0.99
IGL02942:Lama2 APN 10 26,917,216 (GRCm39) missense probably damaging 1.00
IGL03201:Lama2 APN 10 27,220,566 (GRCm39) nonsense probably null
IGL03268:Lama2 APN 10 27,298,649 (GRCm39) missense probably damaging 1.00
IGL03288:Lama2 APN 10 27,245,047 (GRCm39) missense probably damaging 1.00
IGL03380:Lama2 APN 10 26,926,261 (GRCm39) missense probably damaging 1.00
IGL03407:Lama2 APN 10 27,223,017 (GRCm39) missense probably damaging 1.00
cowboy UTSW 10 26,919,639 (GRCm39) frame shift probably null
petri UTSW 10 26,869,394 (GRCm39) splice site probably null
PIT4362001:Lama2 UTSW 10 27,245,132 (GRCm39) missense probably damaging 1.00
PIT4382001:Lama2 UTSW 10 27,080,901 (GRCm39) missense probably damaging 1.00
PIT4431001:Lama2 UTSW 10 26,977,426 (GRCm39) missense probably damaging 1.00
R0038:Lama2 UTSW 10 26,862,793 (GRCm39) missense probably benign 0.02
R0038:Lama2 UTSW 10 26,862,793 (GRCm39) missense probably benign 0.02
R0114:Lama2 UTSW 10 26,869,064 (GRCm39) nonsense probably null
R0142:Lama2 UTSW 10 27,063,841 (GRCm39) missense probably benign
R0313:Lama2 UTSW 10 26,869,394 (GRCm39) splice site probably null
R0376:Lama2 UTSW 10 26,891,542 (GRCm39) missense possibly damaging 0.68
R0412:Lama2 UTSW 10 27,066,621 (GRCm39) missense possibly damaging 0.58
R0472:Lama2 UTSW 10 26,866,863 (GRCm39) missense probably damaging 1.00
R0607:Lama2 UTSW 10 27,065,127 (GRCm39) missense probably benign 0.34
R0648:Lama2 UTSW 10 26,865,372 (GRCm39) missense probably benign 0.00
R0667:Lama2 UTSW 10 27,220,406 (GRCm39) splice site probably null
R0760:Lama2 UTSW 10 26,920,429 (GRCm39) critical splice donor site probably null
R1240:Lama2 UTSW 10 26,917,120 (GRCm39) missense probably damaging 1.00
R1385:Lama2 UTSW 10 27,100,039 (GRCm39) missense probably benign 0.11
R1433:Lama2 UTSW 10 27,063,750 (GRCm39) missense probably damaging 1.00
R1434:Lama2 UTSW 10 27,084,366 (GRCm39) missense probably damaging 1.00
R1574:Lama2 UTSW 10 27,200,750 (GRCm39) missense possibly damaging 0.65
R1574:Lama2 UTSW 10 27,200,750 (GRCm39) missense possibly damaging 0.65
R1645:Lama2 UTSW 10 27,244,981 (GRCm39) missense probably damaging 1.00
R1702:Lama2 UTSW 10 27,066,525 (GRCm39) missense probably benign
R1703:Lama2 UTSW 10 27,142,667 (GRCm39) missense probably damaging 1.00
R1769:Lama2 UTSW 10 27,084,403 (GRCm39) missense probably benign
R1769:Lama2 UTSW 10 27,084,402 (GRCm39) missense probably damaging 1.00
R1846:Lama2 UTSW 10 27,088,092 (GRCm39) missense probably damaging 1.00
R1859:Lama2 UTSW 10 26,907,078 (GRCm39) missense possibly damaging 0.51
R1871:Lama2 UTSW 10 26,860,490 (GRCm39) missense probably damaging 1.00
R1903:Lama2 UTSW 10 27,064,395 (GRCm39) missense probably damaging 1.00
R1906:Lama2 UTSW 10 26,932,523 (GRCm39) critical splice donor site probably null
R1958:Lama2 UTSW 10 26,857,594 (GRCm39) missense probably damaging 0.97
R1959:Lama2 UTSW 10 27,298,614 (GRCm39) missense probably damaging 1.00
R1977:Lama2 UTSW 10 26,866,796 (GRCm39) splice site probably null
R2063:Lama2 UTSW 10 27,040,922 (GRCm39) missense probably damaging 1.00
R2079:Lama2 UTSW 10 27,245,049 (GRCm39) missense probably damaging 0.99
R2085:Lama2 UTSW 10 27,080,837 (GRCm39) nonsense probably null
R2125:Lama2 UTSW 10 26,920,449 (GRCm39) nonsense probably null
R2140:Lama2 UTSW 10 26,930,690 (GRCm39) splice site probably null
R2219:Lama2 UTSW 10 26,919,565 (GRCm39) missense probably damaging 0.99
R2259:Lama2 UTSW 10 26,907,123 (GRCm39) missense probably benign 0.00
R2265:Lama2 UTSW 10 26,868,932 (GRCm39) missense probably damaging 1.00
R2266:Lama2 UTSW 10 26,862,793 (GRCm39) missense probably benign 0.02
R2267:Lama2 UTSW 10 26,868,932 (GRCm39) missense probably damaging 1.00
R2268:Lama2 UTSW 10 26,868,932 (GRCm39) missense probably damaging 1.00
R2269:Lama2 UTSW 10 26,868,932 (GRCm39) missense probably damaging 1.00
R2862:Lama2 UTSW 10 27,298,608 (GRCm39) nonsense probably null
R2912:Lama2 UTSW 10 26,876,799 (GRCm39) missense probably benign
R2999:Lama2 UTSW 10 26,865,417 (GRCm39) missense probably benign 0.18
R3034:Lama2 UTSW 10 26,877,231 (GRCm39) missense probably benign 0.11
R3081:Lama2 UTSW 10 26,877,231 (GRCm39) missense probably benign 0.11
R3107:Lama2 UTSW 10 26,877,231 (GRCm39) missense probably benign 0.11
R3109:Lama2 UTSW 10 26,877,231 (GRCm39) missense probably benign 0.11
R3436:Lama2 UTSW 10 26,877,231 (GRCm39) missense probably benign 0.11
R3437:Lama2 UTSW 10 26,877,231 (GRCm39) missense probably benign 0.11
R3706:Lama2 UTSW 10 27,014,992 (GRCm39) missense probably damaging 1.00
R3780:Lama2 UTSW 10 27,335,335 (GRCm39) missense probably damaging 1.00
R3807:Lama2 UTSW 10 27,066,661 (GRCm39) frame shift probably null
R3919:Lama2 UTSW 10 26,994,501 (GRCm39) missense probably damaging 1.00
R4014:Lama2 UTSW 10 26,860,372 (GRCm39) missense probably damaging 1.00
R4131:Lama2 UTSW 10 26,917,170 (GRCm39) missense probably benign 0.00
R4190:Lama2 UTSW 10 27,142,660 (GRCm39) missense probably damaging 0.96
R4273:Lama2 UTSW 10 27,223,050 (GRCm39) missense probably damaging 1.00
R4358:Lama2 UTSW 10 26,860,489 (GRCm39) missense probably damaging 1.00
R4407:Lama2 UTSW 10 27,088,124 (GRCm39) small deletion probably benign
R4415:Lama2 UTSW 10 26,865,340 (GRCm39) nonsense probably null
R4590:Lama2 UTSW 10 26,865,410 (GRCm39) missense probably benign 0.00
R4615:Lama2 UTSW 10 26,857,520 (GRCm39) missense probably damaging 0.99
R4736:Lama2 UTSW 10 27,080,925 (GRCm39) missense probably damaging 1.00
R4754:Lama2 UTSW 10 26,994,527 (GRCm39) missense possibly damaging 0.58
R4791:Lama2 UTSW 10 27,343,267 (GRCm39) missense probably damaging 1.00
R4834:Lama2 UTSW 10 26,882,745 (GRCm39) missense probably benign 0.30
R4856:Lama2 UTSW 10 26,919,639 (GRCm39) frame shift probably null
R4858:Lama2 UTSW 10 26,919,639 (GRCm39) frame shift probably null
R4859:Lama2 UTSW 10 26,919,639 (GRCm39) frame shift probably null
R4897:Lama2 UTSW 10 26,919,639 (GRCm39) frame shift probably null
R4898:Lama2 UTSW 10 26,919,639 (GRCm39) frame shift probably null
R4899:Lama2 UTSW 10 26,919,639 (GRCm39) frame shift probably null
R4907:Lama2 UTSW 10 27,040,942 (GRCm39) missense probably benign 0.11
R4911:Lama2 UTSW 10 27,014,923 (GRCm39) missense probably damaging 1.00
R4924:Lama2 UTSW 10 27,245,137 (GRCm39) missense probably damaging 0.98
R5023:Lama2 UTSW 10 27,066,500 (GRCm39) missense probably damaging 0.97
R5057:Lama2 UTSW 10 27,040,982 (GRCm39) missense probably damaging 1.00
R5070:Lama2 UTSW 10 27,226,247 (GRCm39) critical splice donor site probably null
R5116:Lama2 UTSW 10 26,994,556 (GRCm39) missense probably benign 0.08
R5177:Lama2 UTSW 10 27,066,699 (GRCm39) missense possibly damaging 0.94
R5198:Lama2 UTSW 10 27,222,999 (GRCm39) missense probably damaging 0.96
R5289:Lama2 UTSW 10 27,088,069 (GRCm39) nonsense probably null
R5327:Lama2 UTSW 10 27,014,942 (GRCm39) missense probably benign
R5424:Lama2 UTSW 10 26,860,392 (GRCm39) missense probably damaging 1.00
R5469:Lama2 UTSW 10 26,917,185 (GRCm39) missense possibly damaging 0.92
R5620:Lama2 UTSW 10 26,866,876 (GRCm39) missense probably damaging 0.99
R5667:Lama2 UTSW 10 27,066,540 (GRCm39) missense probably damaging 1.00
R5671:Lama2 UTSW 10 27,066,540 (GRCm39) missense probably damaging 1.00
R5815:Lama2 UTSW 10 26,862,847 (GRCm39) missense probably damaging 1.00
R5917:Lama2 UTSW 10 27,066,693 (GRCm39) missense probably damaging 1.00
R5935:Lama2 UTSW 10 26,891,494 (GRCm39) missense probably benign
R5976:Lama2 UTSW 10 27,066,672 (GRCm39) missense probably benign 0.00
R5979:Lama2 UTSW 10 27,111,728 (GRCm39) missense probably damaging 0.99
R6004:Lama2 UTSW 10 27,111,781 (GRCm39) missense probably benign 0.01
R6180:Lama2 UTSW 10 26,857,495 (GRCm39) missense probably benign 0.03
R6198:Lama2 UTSW 10 27,064,018 (GRCm39) missense probably damaging 1.00
R6257:Lama2 UTSW 10 26,862,895 (GRCm39) missense possibly damaging 0.85
R6271:Lama2 UTSW 10 26,899,325 (GRCm39) missense possibly damaging 0.67
R6322:Lama2 UTSW 10 27,066,543 (GRCm39) missense probably damaging 0.96
R6354:Lama2 UTSW 10 27,088,064 (GRCm39) missense probably damaging 1.00
R6431:Lama2 UTSW 10 26,929,027 (GRCm39) missense possibly damaging 0.50
R6499:Lama2 UTSW 10 26,907,154 (GRCm39) missense probably damaging 1.00
R6535:Lama2 UTSW 10 26,980,127 (GRCm39) missense probably damaging 1.00
R6545:Lama2 UTSW 10 27,052,793 (GRCm39) missense probably benign
R6636:Lama2 UTSW 10 27,000,564 (GRCm39) missense probably benign 0.13
R6891:Lama2 UTSW 10 27,204,078 (GRCm39) nonsense probably null
R6891:Lama2 UTSW 10 27,204,068 (GRCm39) nonsense probably null
R6902:Lama2 UTSW 10 26,857,625 (GRCm39) missense probably damaging 1.00
R6908:Lama2 UTSW 10 26,907,192 (GRCm39) splice site probably null
R7168:Lama2 UTSW 10 27,242,148 (GRCm39) critical splice acceptor site probably null
R7233:Lama2 UTSW 10 27,107,659 (GRCm39) missense probably damaging 1.00
R7272:Lama2 UTSW 10 27,000,552 (GRCm39) missense probably damaging 1.00
R7274:Lama2 UTSW 10 26,995,976 (GRCm39) missense probably damaging 0.99
R7419:Lama2 UTSW 10 27,142,630 (GRCm39) missense probably benign
R7423:Lama2 UTSW 10 27,088,222 (GRCm39) missense probably benign 0.00
R7554:Lama2 UTSW 10 27,031,492 (GRCm39) missense probably damaging 1.00
R7569:Lama2 UTSW 10 27,141,046 (GRCm39) missense probably damaging 1.00
R7574:Lama2 UTSW 10 26,882,726 (GRCm39) missense probably benign 0.03
R7584:Lama2 UTSW 10 26,980,257 (GRCm39) missense possibly damaging 0.78
R7586:Lama2 UTSW 10 26,977,389 (GRCm39) missense probably benign 0.00
R7603:Lama2 UTSW 10 27,142,676 (GRCm39) missense possibly damaging 0.55
R7691:Lama2 UTSW 10 27,084,389 (GRCm39) missense possibly damaging 0.67
R7750:Lama2 UTSW 10 26,866,920 (GRCm39) missense probably damaging 0.97
R7841:Lama2 UTSW 10 27,031,529 (GRCm39) missense probably benign 0.00
R7864:Lama2 UTSW 10 26,932,611 (GRCm39) missense probably benign 0.08
R7960:Lama2 UTSW 10 26,869,094 (GRCm39) missense probably benign 0.04
R7964:Lama2 UTSW 10 27,099,977 (GRCm39) critical splice donor site probably null
R7980:Lama2 UTSW 10 27,239,609 (GRCm39) missense probably damaging 0.98
R8013:Lama2 UTSW 10 27,220,494 (GRCm39) missense probably benign 0.00
R8028:Lama2 UTSW 10 27,204,145 (GRCm39) missense probably benign 0.13
R8097:Lama2 UTSW 10 27,066,660 (GRCm39) nonsense probably null
R8100:Lama2 UTSW 10 26,917,113 (GRCm39) missense probably benign 0.03
R8110:Lama2 UTSW 10 26,866,866 (GRCm39) missense probably damaging 1.00
R8122:Lama2 UTSW 10 26,930,592 (GRCm39) missense possibly damaging 0.87
R8264:Lama2 UTSW 10 27,343,218 (GRCm39) missense probably benign 0.07
R8315:Lama2 UTSW 10 27,298,655 (GRCm39) missense probably damaging 1.00
R8318:Lama2 UTSW 10 26,860,334 (GRCm39) missense probably damaging 1.00
R8419:Lama2 UTSW 10 27,298,559 (GRCm39) missense probably benign 0.26
R8475:Lama2 UTSW 10 26,977,369 (GRCm39) missense possibly damaging 0.69
R8735:Lama2 UTSW 10 27,066,530 (GRCm39) missense probably damaging 1.00
R8754:Lama2 UTSW 10 26,877,147 (GRCm39) missense possibly damaging 0.83
R8817:Lama2 UTSW 10 27,063,869 (GRCm39) missense probably damaging 1.00
R8851:Lama2 UTSW 10 27,242,119 (GRCm39) missense possibly damaging 0.94
R8859:Lama2 UTSW 10 27,335,384 (GRCm39) missense possibly damaging 0.58
R8886:Lama2 UTSW 10 27,245,157 (GRCm39) splice site probably benign
R8937:Lama2 UTSW 10 26,862,816 (GRCm39) missense probably damaging 1.00
R8993:Lama2 UTSW 10 27,298,710 (GRCm39) missense possibly damaging 0.91
R9025:Lama2 UTSW 10 26,860,367 (GRCm39) missense probably benign 0.00
R9027:Lama2 UTSW 10 27,080,881 (GRCm39) missense probably damaging 1.00
R9047:Lama2 UTSW 10 26,882,697 (GRCm39) missense possibly damaging 0.50
R9075:Lama2 UTSW 10 26,857,588 (GRCm39) missense probably damaging 1.00
R9135:Lama2 UTSW 10 27,298,515 (GRCm39) missense probably damaging 1.00
R9165:Lama2 UTSW 10 26,929,022 (GRCm39) critical splice donor site probably null
R9192:Lama2 UTSW 10 27,204,181 (GRCm39) missense possibly damaging 0.95
R9254:Lama2 UTSW 10 27,298,685 (GRCm39) missense probably damaging 0.96
R9326:Lama2 UTSW 10 26,906,193 (GRCm39) missense probably benign 0.04
R9356:Lama2 UTSW 10 27,088,186 (GRCm39) missense probably damaging 0.99
R9358:Lama2 UTSW 10 27,492,761 (GRCm39) missense unknown
R9358:Lama2 UTSW 10 27,064,378 (GRCm39) missense possibly damaging 0.95
R9376:Lama2 UTSW 10 26,994,620 (GRCm39) missense probably benign 0.11
R9381:Lama2 UTSW 10 27,064,023 (GRCm39) nonsense probably null
R9397:Lama2 UTSW 10 26,981,117 (GRCm39) missense probably benign 0.01
R9460:Lama2 UTSW 10 27,298,475 (GRCm39) missense probably damaging 1.00
R9478:Lama2 UTSW 10 26,891,478 (GRCm39) missense probably damaging 0.98
R9503:Lama2 UTSW 10 26,865,440 (GRCm39) missense possibly damaging 0.57
R9514:Lama2 UTSW 10 27,100,015 (GRCm39) missense probably benign 0.00
R9515:Lama2 UTSW 10 26,877,170 (GRCm39) missense probably benign 0.23
R9516:Lama2 UTSW 10 27,100,015 (GRCm39) missense probably benign 0.00
R9533:Lama2 UTSW 10 26,862,871 (GRCm39) missense probably damaging 1.00
R9619:Lama2 UTSW 10 27,064,282 (GRCm39) missense probably damaging 1.00
R9721:Lama2 UTSW 10 27,343,338 (GRCm39) missense possibly damaging 0.58
Predicted Primers PCR Primer
(F):5'- CTTCTGTTAAAAGTGCACTGACG -3'
(R):5'- TTTGGAATGACTGAGAGAGTGC -3'

Sequencing Primer
(F):5'- GTGCACTGACGTTAGTTACTGACAC -3'
(R):5'- GAACTCAGAGTGATGCTTTTGTCACC -3'
Posted On 2015-07-07