Incidental Mutation 'R4923:Lama5'
ID 378751
Institutional Source Beutler Lab
Gene Symbol Lama5
Ensembl Gene ENSMUSG00000015647
Gene Name laminin, alpha 5
Synonyms
MMRRC Submission 042525-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R4923 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 179818166-179867652 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 179825942 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Leucine at position 2372 (I2372L)
Ref Sequence ENSEMBL: ENSMUSP00000015791 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000015791]
AlphaFold no structure available at present
PDB Structure LAMININ ALPHA5 CHAIN N-TERMINAL FRAGMENT [X-RAY DIFFRACTION]
Predicted Effect probably benign
Transcript: ENSMUST00000015791
AA Change: I2372L

PolyPhen 2 Score 0.176 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000015791
Gene: ENSMUSG00000015647
AA Change: I2372L

DomainStartEndE-ValueType
signal peptide 1 40 N/A INTRINSIC
LamNT 44 303 1.06e-132 SMART
EGF_Lam 305 361 4.35e-6 SMART
EGF_Lam 364 431 5.78e-11 SMART
EGF_Lam 434 476 1.32e-5 SMART
EGF_Lam 500 544 8.63e-10 SMART
EGF_Lam 547 590 1.16e-10 SMART
EGF_Lam 593 635 4.63e-10 SMART
EGF_Lam 638 680 6.25e-7 SMART
EGF_Lam 683 726 3.1e-11 SMART
EGF_Lam 730 779 2.99e-4 SMART
EGF_Lam 782 831 4.66e-6 SMART
EGF_Lam 834 878 3.48e-5 SMART
low complexity region 1261 1273 N/A INTRINSIC
EGF_Lam 1443 1486 7.01e-10 SMART
EGF_like 1489 1530 3.64e-1 SMART
EGF_Lam 1533 1579 8.56e-14 SMART
EGF_Lam 1582 1630 1.86e-14 SMART
LamB 1689 1819 5.86e-61 SMART
EGF_like 1818 1862 2.74e0 SMART
EGF_Lam 1865 1912 3.32e-11 SMART
EGF_Lam 1915 1968 1.61e-9 SMART
EGF_Lam 1971 2022 6.39e-13 SMART
EGF_Lam 2025 2069 1.94e-12 SMART
EGF_Lam 2072 2116 1.35e-11 SMART
EGF_like 2103 2145 3.1e1 SMART
EGF_Lam 2119 2166 1.18e-2 SMART
Pfam:Laminin_I 2189 2453 1.7e-65 PFAM
low complexity region 2532 2548 N/A INTRINSIC
low complexity region 2557 2569 N/A INTRINSIC
low complexity region 2632 2641 N/A INTRINSIC
low complexity region 2663 2676 N/A INTRINSIC
LamG 2760 2912 3.97e-8 SMART
LamG 2966 3103 1.78e-10 SMART
LamG 3149 3274 1.11e-20 SMART
LamG 3359 3497 4.05e-23 SMART
LamG 3539 3670 3e-26 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000130796
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185089
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.2%
  • 10x: 96.0%
  • 20x: 91.3%
Validation Efficiency 98% (107/109)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes one of the vertebrate laminin alpha chains. Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Laminins are composed of 3 non identical chains: laminin alpha, beta and gamma (formerly A, B1, and B2, respectively) and they form a cruciform structure consisting of 3 short arms, each formed by a different chain, and a long arm composed of all 3 chains. Each laminin chain is a multidomain protein encoded by a distinct gene. The protein encoded by this gene is the alpha-5 subunit of of laminin-10 (laminin-511), laminin-11 (laminin-521) and laminin-15 (laminin-523). [provided by RefSeq, Jun 2013]
PHENOTYPE: Homozygotes for a targeted null mutation exhibit disrupted basal laminae leading to exencephaly, syndactyly, placentopathy, kidney defects, abnormal lobar septation with absence of a visceral pleural membrane, and lethality in late gestation. [provided by MGI curators]
Allele List at MGI

All alleles(49) : Targeted(5) Gene trapped(44)

Other mutations in this stock
Total: 95 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aim2 A G 1: 173,287,372 (GRCm39) D124G probably benign Het
Akr1c6 T C 13: 4,504,494 (GRCm39) M293T probably damaging Het
Albfm1 A G 5: 90,709,158 (GRCm39) T23A probably benign Het
Ankhd1 A G 18: 36,722,505 (GRCm39) T343A probably damaging Het
Ano2 T C 6: 125,880,018 (GRCm39) probably benign Het
Arfgap2 G A 2: 91,104,004 (GRCm39) G353R probably damaging Het
Armc3 A G 2: 19,297,791 (GRCm39) probably null Het
Atp11b T C 3: 35,889,528 (GRCm39) probably null Het
Brd4 A G 17: 32,418,214 (GRCm39) M13T probably benign Het
Btd T A 14: 31,384,044 (GRCm39) M10K possibly damaging Het
C1s2 T C 6: 124,602,649 (GRCm39) K515E probably benign Het
Cars1 A T 7: 143,123,587 (GRCm39) Y455N probably damaging Het
Ccdc110 A G 8: 46,396,460 (GRCm39) S784G probably benign Het
Chic2 A G 5: 75,171,872 (GRCm39) probably benign Het
Chka A T 19: 3,942,105 (GRCm39) probably null Het
Chrne A G 11: 70,506,101 (GRCm39) I420T possibly damaging Het
Clstn1 T C 4: 149,729,486 (GRCm39) V747A probably benign Het
Cobll1 A G 2: 64,929,602 (GRCm39) S575P possibly damaging Het
Col6a6 A T 9: 105,666,147 (GRCm39) L3Q probably damaging Het
Comtd1 A T 14: 21,898,813 (GRCm39) probably benign Het
Cpsf2 T C 12: 101,948,243 (GRCm39) V13A probably benign Het
Creb3l4 T A 3: 90,149,521 (GRCm39) I115L probably benign Het
Cyp2j12 C T 4: 95,990,346 (GRCm39) A407T possibly damaging Het
Ddr2 A G 1: 169,825,498 (GRCm39) probably null Het
Dennd4c T C 4: 86,725,775 (GRCm39) L743P probably damaging Het
Egfl8 T C 17: 34,833,171 (GRCm39) T192A probably benign Het
Elapor1 C T 3: 108,379,284 (GRCm39) probably null Het
Elf3 A G 1: 135,184,473 (GRCm39) probably benign Het
Entrep2 A G 7: 64,417,439 (GRCm39) S322P probably benign Het
Etv3 T G 3: 87,443,223 (GRCm39) L269R possibly damaging Het
Fah C A 7: 84,251,260 (GRCm39) probably benign Het
Fbll1 C A 11: 35,688,407 (GRCm39) L285F probably benign Het
Fcrla A T 1: 170,748,682 (GRCm39) F154I probably damaging Het
Fnip2 T A 3: 79,396,701 (GRCm39) probably null Het
Focad T C 4: 88,115,083 (GRCm39) probably benign Het
Gabrr1 T A 4: 33,162,820 (GRCm39) I462N possibly damaging Het
Gm57859 C A 11: 113,579,805 (GRCm39) T400K probably benign Het
Gnptab A G 10: 88,265,485 (GRCm39) T366A probably benign Het
Hnrnpu G A 1: 178,159,017 (GRCm39) probably benign Het
Il17ra T A 6: 120,454,406 (GRCm39) V299E possibly damaging Het
Impg1 G A 9: 80,252,360 (GRCm39) Q607* probably null Het
Impg1 T A 9: 80,252,827 (GRCm39) E374V probably damaging Het
Itgax C T 7: 127,747,700 (GRCm39) L1039F probably benign Het
Kcnk2 A T 1: 189,072,133 (GRCm39) V65D probably damaging Het
Kif20b A C 19: 34,918,611 (GRCm39) probably null Het
Krt9 TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC 11: 100,079,903 (GRCm39) probably benign Het
Lilrb4a A G 10: 51,368,139 (GRCm39) T85A possibly damaging Het
Mapk13 C A 17: 28,997,197 (GRCm39) H330N probably benign Het
Mars1 C A 10: 127,132,549 (GRCm39) probably benign Het
Mdga1 C A 17: 30,057,052 (GRCm39) R818L probably damaging Het
Mdn1 T A 4: 32,671,608 (GRCm39) L476Q possibly damaging Het
Mup21 T C 4: 62,066,202 (GRCm39) E178G probably benign Het
Myg1 A G 15: 102,240,288 (GRCm39) N38S probably benign Het
Ncam1 A T 9: 49,416,779 (GRCm39) D837E probably benign Het
Ncam2 C T 16: 81,386,679 (GRCm39) P686L possibly damaging Het
Nck2 T C 1: 43,500,231 (GRCm39) probably benign Het
Nfya T C 17: 48,707,563 (GRCm39) probably benign Het
Npat A G 9: 53,482,330 (GRCm39) K1346R probably damaging Het
Odad2 C G 18: 7,181,787 (GRCm39) D846H probably damaging Het
Or12j3 G T 7: 139,952,920 (GRCm39) T201K probably benign Het
Or4a72 T C 2: 89,406,023 (GRCm39) T16A probably damaging Het
Or6c212 A G 10: 129,558,681 (GRCm39) V244A probably benign Het
Pde7b G T 10: 20,288,873 (GRCm39) Q325K probably damaging Het
Pla2r1 A T 2: 60,253,056 (GRCm39) M1345K probably benign Het
Prkcz T C 4: 155,441,946 (GRCm39) D62G probably damaging Het
Pros1 T A 16: 62,723,935 (GRCm39) C228S possibly damaging Het
Ptprc A G 1: 138,006,236 (GRCm39) M782T possibly damaging Het
Rcn1 T C 2: 105,219,518 (GRCm39) D225G probably benign Het
Recql4 G A 15: 76,594,381 (GRCm39) R46C probably damaging Het
Rnf220 C T 4: 117,346,797 (GRCm39) R205Q possibly damaging Het
Samd13 T C 3: 146,368,502 (GRCm39) D11G probably benign Het
Scp2d1 T A 2: 144,666,030 (GRCm39) I123K probably benign Het
Skap1 A T 11: 96,644,870 (GRCm39) Y311F probably damaging Het
Slc2a10 T C 2: 165,356,676 (GRCm39) I112T possibly damaging Het
Slc34a1 G A 13: 24,003,078 (GRCm39) V243M probably benign Het
Slc39a2 G A 14: 52,132,711 (GRCm39) G218D probably damaging Het
Sos1 T C 17: 80,742,381 (GRCm39) N382S probably benign Het
Spam1 C T 6: 24,796,655 (GRCm39) T202I probably damaging Het
Tas2r138 T A 6: 40,589,820 (GRCm39) Q142L possibly damaging Het
Tec T A 5: 72,939,365 (GRCm39) R217* probably null Het
Tmeff2 T A 1: 50,969,804 (GRCm39) V90D probably benign Het
Tmem119 T C 5: 113,933,405 (GRCm39) Y132C probably damaging Het
Topbp1 A G 9: 103,190,035 (GRCm39) I204V probably benign Het
Trappc14 A T 5: 138,260,641 (GRCm39) probably benign Het
Ttn A T 2: 76,601,232 (GRCm39) I17001N probably damaging Het
Vit T A 17: 78,894,270 (GRCm39) M224K probably benign Het
Vmn1r179 T G 7: 23,628,491 (GRCm39) H227Q possibly damaging Het
Vmn1r84 T C 7: 12,095,743 (GRCm39) N305D probably benign Het
Vmn2r61 A G 7: 41,916,520 (GRCm39) N378D probably damaging Het
Vmn2r87 A G 10: 130,314,435 (GRCm39) Y384H probably damaging Het
Wiz C T 17: 32,580,570 (GRCm39) A294T probably benign Het
Xdh C A 17: 74,231,931 (GRCm39) V260L possibly damaging Het
Xirp2 A G 2: 67,343,237 (GRCm39) K1826R probably benign Het
Zfp445 A C 9: 122,681,358 (GRCm39) I861R probably benign Het
Zfp691 T C 4: 119,027,999 (GRCm39) T78A probably benign Het
Other mutations in Lama5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01067:Lama5 APN 2 179,818,336 (GRCm39) unclassified probably benign
IGL01370:Lama5 APN 2 179,839,193 (GRCm39) missense possibly damaging 0.87
IGL01474:Lama5 APN 2 179,838,363 (GRCm39) missense probably damaging 1.00
IGL01614:Lama5 APN 2 179,822,657 (GRCm39) missense probably damaging 1.00
IGL01941:Lama5 APN 2 179,834,185 (GRCm39) missense possibly damaging 0.71
IGL01953:Lama5 APN 2 179,832,497 (GRCm39) missense probably damaging 0.97
IGL02093:Lama5 APN 2 179,830,380 (GRCm39) missense probably damaging 1.00
IGL02197:Lama5 APN 2 179,849,012 (GRCm39) missense possibly damaging 0.82
IGL02308:Lama5 APN 2 179,832,120 (GRCm39) splice site probably benign
IGL02314:Lama5 APN 2 179,836,275 (GRCm39) splice site probably benign
IGL02317:Lama5 APN 2 179,833,112 (GRCm39) missense probably damaging 1.00
IGL02354:Lama5 APN 2 179,835,677 (GRCm39) nonsense probably null
IGL02361:Lama5 APN 2 179,835,677 (GRCm39) nonsense probably null
IGL02557:Lama5 APN 2 179,832,725 (GRCm39) nonsense probably null
IGL03026:Lama5 APN 2 179,837,760 (GRCm39) missense probably benign 0.34
IGL03160:Lama5 APN 2 179,822,128 (GRCm39) missense probably damaging 1.00
IGL03238:Lama5 APN 2 179,830,367 (GRCm39) missense probably benign
IGL03390:Lama5 APN 2 179,849,011 (GRCm39) missense probably damaging 1.00
blancmange UTSW 2 179,822,404 (GRCm39) missense probably damaging 0.98
cupcake UTSW 2 179,827,752 (GRCm39) missense probably damaging 1.00
layercake UTSW 2 179,822,511 (GRCm39) missense possibly damaging 0.83
poundcake UTSW 2 179,837,401 (GRCm39) missense probably damaging 1.00
Salty UTSW 2 179,823,444 (GRCm39) missense possibly damaging 0.84
PIT4378001:Lama5 UTSW 2 179,831,238 (GRCm39) missense possibly damaging 0.89
R0003:Lama5 UTSW 2 179,819,872 (GRCm39) splice site probably null
R0056:Lama5 UTSW 2 179,828,899 (GRCm39) intron probably benign
R0147:Lama5 UTSW 2 179,832,199 (GRCm39) missense probably benign
R0148:Lama5 UTSW 2 179,832,199 (GRCm39) missense probably benign
R0310:Lama5 UTSW 2 179,823,359 (GRCm39) splice site probably benign
R0326:Lama5 UTSW 2 179,824,219 (GRCm39) missense possibly damaging 0.90
R0368:Lama5 UTSW 2 179,823,023 (GRCm39) nonsense probably null
R0479:Lama5 UTSW 2 179,826,250 (GRCm39) missense probably benign 0.03
R0490:Lama5 UTSW 2 179,821,962 (GRCm39) missense possibly damaging 0.90
R0636:Lama5 UTSW 2 179,831,124 (GRCm39) critical splice donor site probably null
R0704:Lama5 UTSW 2 179,821,277 (GRCm39) missense possibly damaging 0.84
R0733:Lama5 UTSW 2 179,822,511 (GRCm39) missense possibly damaging 0.83
R1017:Lama5 UTSW 2 179,837,213 (GRCm39) missense probably damaging 1.00
R1078:Lama5 UTSW 2 179,821,557 (GRCm39) unclassified probably benign
R1294:Lama5 UTSW 2 179,832,714 (GRCm39) missense probably benign 0.00
R1423:Lama5 UTSW 2 179,837,434 (GRCm39) missense probably damaging 1.00
R1438:Lama5 UTSW 2 179,824,593 (GRCm39) missense probably benign 0.01
R1447:Lama5 UTSW 2 179,827,671 (GRCm39) missense probably damaging 0.99
R1540:Lama5 UTSW 2 179,821,944 (GRCm39) missense probably benign
R1601:Lama5 UTSW 2 179,839,538 (GRCm39) missense probably damaging 1.00
R1624:Lama5 UTSW 2 179,848,551 (GRCm39) missense probably benign 0.02
R1674:Lama5 UTSW 2 179,843,780 (GRCm39) missense probably benign 0.00
R1687:Lama5 UTSW 2 179,835,859 (GRCm39) missense probably benign 0.00
R1696:Lama5 UTSW 2 179,844,279 (GRCm39) missense probably damaging 1.00
R1701:Lama5 UTSW 2 179,863,162 (GRCm39) missense probably damaging 1.00
R1778:Lama5 UTSW 2 179,837,274 (GRCm39) splice site probably benign
R1936:Lama5 UTSW 2 179,832,714 (GRCm39) missense probably benign 0.00
R1939:Lama5 UTSW 2 179,832,714 (GRCm39) missense probably benign 0.00
R1940:Lama5 UTSW 2 179,832,714 (GRCm39) missense probably benign 0.00
R1953:Lama5 UTSW 2 179,832,540 (GRCm39) missense possibly damaging 0.94
R1966:Lama5 UTSW 2 179,830,145 (GRCm39) missense probably damaging 1.00
R2024:Lama5 UTSW 2 179,820,923 (GRCm39) missense probably benign 0.00
R2079:Lama5 UTSW 2 179,867,301 (GRCm39) missense possibly damaging 0.68
R2115:Lama5 UTSW 2 179,828,678 (GRCm39) missense probably damaging 1.00
R2173:Lama5 UTSW 2 179,838,035 (GRCm39) missense probably benign 0.00
R2272:Lama5 UTSW 2 179,820,396 (GRCm39) missense possibly damaging 0.93
R2357:Lama5 UTSW 2 179,821,890 (GRCm39) missense probably benign 0.01
R2860:Lama5 UTSW 2 179,829,040 (GRCm39) missense probably benign 0.00
R2861:Lama5 UTSW 2 179,829,040 (GRCm39) missense probably benign 0.00
R2939:Lama5 UTSW 2 179,840,747 (GRCm39) missense probably damaging 1.00
R3053:Lama5 UTSW 2 179,824,860 (GRCm39) missense probably damaging 0.99
R3430:Lama5 UTSW 2 179,838,110 (GRCm39) missense probably benign 0.00
R3752:Lama5 UTSW 2 179,829,015 (GRCm39) missense probably damaging 1.00
R3782:Lama5 UTSW 2 179,836,356 (GRCm39) missense possibly damaging 0.57
R3901:Lama5 UTSW 2 179,824,144 (GRCm39) splice site probably benign
R4248:Lama5 UTSW 2 179,822,220 (GRCm39) missense possibly damaging 0.84
R4626:Lama5 UTSW 2 179,826,253 (GRCm39) missense probably damaging 0.98
R4638:Lama5 UTSW 2 179,832,206 (GRCm39) missense possibly damaging 0.89
R4669:Lama5 UTSW 2 179,822,430 (GRCm39) missense probably damaging 1.00
R4673:Lama5 UTSW 2 179,841,059 (GRCm39) missense probably damaging 1.00
R4677:Lama5 UTSW 2 179,821,159 (GRCm39) missense possibly damaging 0.69
R4701:Lama5 UTSW 2 179,833,489 (GRCm39) missense probably damaging 1.00
R4774:Lama5 UTSW 2 179,827,734 (GRCm39) missense probably damaging 1.00
R4880:Lama5 UTSW 2 179,818,861 (GRCm39) unclassified probably benign
R4960:Lama5 UTSW 2 179,850,045 (GRCm39) critical splice donor site probably null
R4983:Lama5 UTSW 2 179,835,242 (GRCm39) missense probably benign 0.13
R5061:Lama5 UTSW 2 179,840,579 (GRCm39) nonsense probably null
R5080:Lama5 UTSW 2 179,848,993 (GRCm39) nonsense probably null
R5135:Lama5 UTSW 2 179,844,013 (GRCm39) missense possibly damaging 0.89
R5206:Lama5 UTSW 2 179,833,097 (GRCm39) missense probably damaging 1.00
R5296:Lama5 UTSW 2 179,835,594 (GRCm39) missense probably damaging 1.00
R5319:Lama5 UTSW 2 179,822,911 (GRCm39) missense probably damaging 1.00
R5355:Lama5 UTSW 2 179,823,444 (GRCm39) missense possibly damaging 0.84
R5388:Lama5 UTSW 2 179,832,539 (GRCm39) missense possibly damaging 0.83
R5528:Lama5 UTSW 2 179,836,356 (GRCm39) missense probably benign 0.21
R5536:Lama5 UTSW 2 179,831,142 (GRCm39) missense probably damaging 0.99
R5658:Lama5 UTSW 2 179,850,069 (GRCm39) nonsense probably null
R5823:Lama5 UTSW 2 179,834,285 (GRCm39) missense probably benign 0.04
R5885:Lama5 UTSW 2 179,843,624 (GRCm39) missense probably damaging 1.00
R5889:Lama5 UTSW 2 179,835,467 (GRCm39) intron probably benign
R5912:Lama5 UTSW 2 179,837,268 (GRCm39) missense probably damaging 1.00
R5955:Lama5 UTSW 2 179,839,267 (GRCm39) missense probably damaging 1.00
R6015:Lama5 UTSW 2 179,827,185 (GRCm39) missense probably benign 0.36
R6037:Lama5 UTSW 2 179,848,806 (GRCm39) missense probably damaging 1.00
R6037:Lama5 UTSW 2 179,848,806 (GRCm39) missense probably damaging 1.00
R6191:Lama5 UTSW 2 179,827,752 (GRCm39) missense probably damaging 1.00
R6191:Lama5 UTSW 2 179,822,404 (GRCm39) missense probably damaging 0.98
R6359:Lama5 UTSW 2 179,837,775 (GRCm39) missense probably benign 0.01
R6385:Lama5 UTSW 2 179,838,326 (GRCm39) missense probably damaging 1.00
R6406:Lama5 UTSW 2 179,839,257 (GRCm39) nonsense probably null
R6552:Lama5 UTSW 2 179,822,947 (GRCm39) missense probably damaging 0.98
R6632:Lama5 UTSW 2 179,833,455 (GRCm39) missense probably damaging 1.00
R6633:Lama5 UTSW 2 179,833,455 (GRCm39) missense probably damaging 1.00
R6645:Lama5 UTSW 2 179,821,463 (GRCm39) missense probably damaging 1.00
R6731:Lama5 UTSW 2 179,830,367 (GRCm39) missense probably benign 0.09
R6744:Lama5 UTSW 2 179,833,455 (GRCm39) missense probably damaging 1.00
R6798:Lama5 UTSW 2 179,833,455 (GRCm39) missense probably damaging 1.00
R6799:Lama5 UTSW 2 179,833,455 (GRCm39) missense probably damaging 1.00
R6801:Lama5 UTSW 2 179,833,455 (GRCm39) missense probably damaging 1.00
R6851:Lama5 UTSW 2 179,833,455 (GRCm39) missense probably damaging 1.00
R6869:Lama5 UTSW 2 179,833,455 (GRCm39) missense probably damaging 1.00
R6881:Lama5 UTSW 2 179,833,455 (GRCm39) missense probably damaging 1.00
R6882:Lama5 UTSW 2 179,833,455 (GRCm39) missense probably damaging 1.00
R6884:Lama5 UTSW 2 179,833,455 (GRCm39) missense probably damaging 1.00
R7022:Lama5 UTSW 2 179,822,524 (GRCm39) missense probably damaging 1.00
R7204:Lama5 UTSW 2 179,843,970 (GRCm39) missense probably damaging 1.00
R7207:Lama5 UTSW 2 179,848,877 (GRCm39) missense probably damaging 0.98
R7282:Lama5 UTSW 2 179,843,588 (GRCm39) missense probably damaging 1.00
R7367:Lama5 UTSW 2 179,834,751 (GRCm39) missense probably benign 0.01
R7410:Lama5 UTSW 2 179,844,183 (GRCm39) critical splice donor site probably null
R7699:Lama5 UTSW 2 179,822,654 (GRCm39) missense probably damaging 1.00
R7849:Lama5 UTSW 2 179,843,605 (GRCm39) missense probably damaging 1.00
R7909:Lama5 UTSW 2 179,834,069 (GRCm39) missense possibly damaging 0.95
R7948:Lama5 UTSW 2 179,843,994 (GRCm39) missense probably damaging 1.00
R8153:Lama5 UTSW 2 179,829,724 (GRCm39) missense probably benign 0.37
R8317:Lama5 UTSW 2 179,848,784 (GRCm39) missense probably damaging 1.00
R8351:Lama5 UTSW 2 179,837,401 (GRCm39) missense probably damaging 1.00
R8370:Lama5 UTSW 2 179,843,280 (GRCm39) missense possibly damaging 0.80
R8398:Lama5 UTSW 2 179,838,827 (GRCm39) critical splice donor site probably null
R8401:Lama5 UTSW 2 179,840,580 (GRCm39) missense probably damaging 1.00
R8404:Lama5 UTSW 2 179,837,015 (GRCm39) missense probably damaging 1.00
R8502:Lama5 UTSW 2 179,837,015 (GRCm39) missense probably damaging 1.00
R8694:Lama5 UTSW 2 179,822,677 (GRCm39) missense probably damaging 0.98
R8705:Lama5 UTSW 2 179,820,354 (GRCm39) missense probably damaging 1.00
R8732:Lama5 UTSW 2 179,828,481 (GRCm39) missense probably damaging 1.00
R8755:Lama5 UTSW 2 179,832,714 (GRCm39) missense probably benign 0.00
R8786:Lama5 UTSW 2 179,838,100 (GRCm39) missense probably damaging 1.00
R8926:Lama5 UTSW 2 179,835,783 (GRCm39) missense probably benign 0.08
R8928:Lama5 UTSW 2 179,843,832 (GRCm39) missense probably damaging 1.00
R8953:Lama5 UTSW 2 179,835,313 (GRCm39) missense probably damaging 0.99
R8958:Lama5 UTSW 2 179,835,592 (GRCm39) missense probably benign
R9002:Lama5 UTSW 2 179,838,311 (GRCm39) missense probably damaging 1.00
R9081:Lama5 UTSW 2 179,833,930 (GRCm39) nonsense probably null
R9165:Lama5 UTSW 2 179,821,286 (GRCm39) missense probably damaging 0.99
R9233:Lama5 UTSW 2 179,840,502 (GRCm39) nonsense probably null
R9264:Lama5 UTSW 2 179,838,271 (GRCm39) splice site probably benign
R9311:Lama5 UTSW 2 179,838,275 (GRCm39) critical splice donor site probably null
R9443:Lama5 UTSW 2 179,843,522 (GRCm39) missense probably benign 0.00
R9488:Lama5 UTSW 2 179,823,234 (GRCm39) missense possibly damaging 0.95
R9674:Lama5 UTSW 2 179,840,267 (GRCm39) critical splice donor site probably null
R9684:Lama5 UTSW 2 179,849,038 (GRCm39) missense probably damaging 1.00
R9749:Lama5 UTSW 2 179,825,433 (GRCm39) missense probably benign 0.00
RF020:Lama5 UTSW 2 179,837,971 (GRCm39) missense probably benign
X0065:Lama5 UTSW 2 179,823,524 (GRCm39) missense probably benign 0.26
Z1177:Lama5 UTSW 2 179,832,507 (GRCm39) missense possibly damaging 0.95
Z1177:Lama5 UTSW 2 179,831,212 (GRCm39) missense probably damaging 1.00
Z1177:Lama5 UTSW 2 179,825,423 (GRCm39) missense probably benign 0.03
Z1177:Lama5 UTSW 2 179,840,603 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CCTGGGTCTGAGAGAACATG -3'
(R):5'- TGCTTCTGAGGTGGACTAGAC -3'

Sequencing Primer
(F):5'- TTGACAGAAGACCAGGGCCTG -3'
(R):5'- TGGACTAGACCGGTGCTG -3'
Posted On 2016-04-15