Incidental Mutation 'R6191:Lama5'
ID 502541
Institutional Source Beutler Lab
Gene Symbol Lama5
Ensembl Gene ENSMUSG00000015647
Gene Name laminin, alpha 5
Synonyms
MMRRC Submission 044331-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R6191 (G1)
Quality Score 225.009
Status Validated
Chromosome 2
Chromosomal Location 179818166-179867652 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 179822404 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Serine at position 2890 (T2890S)
Ref Sequence ENSEMBL: ENSMUSP00000015791 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000015791] [ENSMUST00000061437]
AlphaFold no structure available at present
PDB Structure LAMININ ALPHA5 CHAIN N-TERMINAL FRAGMENT [X-RAY DIFFRACTION]
Predicted Effect probably damaging
Transcript: ENSMUST00000015791
AA Change: T2890S

PolyPhen 2 Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000015791
Gene: ENSMUSG00000015647
AA Change: T2890S

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 probably benign
Transcript: ENSMUST00000061437
SMART Domains Protein: ENSMUSP00000050076
Gene: ENSMUSG00000039041

DomainStartEndE-ValueType
Pfam:Proteasom_Rpn13 29 111 3.5e-35 PFAM
low complexity region 135 161 N/A INTRINSIC
low complexity region 173 254 N/A INTRINSIC
Pfam:RPN13_C 268 381 7.3e-38 PFAM
low complexity region 390 403 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000123906
Predicted Effect noncoding transcript
Transcript: ENSMUST00000128029
Predicted Effect noncoding transcript
Transcript: ENSMUST00000130796
Predicted Effect noncoding transcript
Transcript: ENSMUST00000145230
Predicted Effect noncoding transcript
Transcript: ENSMUST00000152850
Predicted Effect noncoding transcript
Transcript: ENSMUST00000149812
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185089
Predicted Effect noncoding transcript
Transcript: ENSMUST00000152540
Predicted Effect noncoding transcript
Transcript: ENSMUST00000147383
Meta Mutation Damage Score 0.0650 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.8%
Validation Efficiency 99% (84/85)
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: 83 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930563M21Rik A C 9: 55,909,807 (GRCm39) D144E possibly damaging Het
Amigo2 T A 15: 97,143,419 (GRCm39) K334N probably benign Het
Ano6 T C 15: 95,846,380 (GRCm39) probably null Het
Ap1m2 C A 9: 21,210,601 (GRCm39) V343F probably benign Het
Apol6 T C 15: 76,940,098 (GRCm39) V307A probably benign Het
Arsi C A 18: 61,045,544 (GRCm39) A78E probably damaging Het
B2m A T 2: 121,981,396 (GRCm39) N37I possibly damaging Het
Bltp3b G T 10: 89,641,180 (GRCm39) G784C possibly damaging Het
C8a T C 4: 104,703,100 (GRCm39) K363R probably benign Het
Ccdc117 C A 11: 5,484,242 (GRCm39) probably null Het
Ccdc154 C A 17: 25,386,945 (GRCm39) Q325K probably damaging Het
Cd300e A T 11: 114,945,359 (GRCm39) V145E possibly damaging Het
Col19a1 G T 1: 24,356,474 (GRCm39) P673Q probably damaging Het
Csn2 A G 5: 87,843,885 (GRCm39) probably null Het
Ctnna1 T C 18: 35,307,408 (GRCm39) V135A probably damaging Het
Dnah11 T A 12: 118,154,632 (GRCm39) D216V probably benign Het
Dnah12 A G 14: 26,431,412 (GRCm39) H410R probably benign Het
Dock2 C T 11: 34,181,652 (GRCm39) R1637H possibly damaging Het
Dspp A G 5: 104,325,214 (GRCm39) N526D unknown Het
Frem2 T C 3: 53,562,701 (GRCm39) H602R probably benign Het
Galc A T 12: 98,218,293 (GRCm39) H186Q probably damaging Het
Grina T C 15: 76,133,218 (GRCm39) V262A probably damaging Het
Gse1 G A 8: 121,280,542 (GRCm39) probably null Het
H2-Oa C A 17: 34,312,842 (GRCm39) Q40K probably damaging Het
Hfm1 C A 5: 107,034,419 (GRCm39) D763Y possibly damaging Het
Hmcn2 T A 2: 31,348,758 (GRCm39) Y4925N probably damaging Het
Hs3st3b1 C A 11: 63,780,029 (GRCm39) R366L probably benign Het
Idh2 TCCCAGG T 7: 79,748,079 (GRCm39) probably benign Het
Iqank1 T C 15: 75,918,218 (GRCm39) probably null Het
Itpr2 A G 6: 146,229,833 (GRCm39) V1221A probably benign Het
Kdm6b T C 11: 69,297,584 (GRCm39) N285S probably benign Het
Klk1b1 T A 7: 43,620,081 (GRCm39) N181K probably damaging Het
Kmt2a C A 9: 44,738,125 (GRCm39) probably benign Het
Lsm2 T A 17: 35,201,131 (GRCm39) probably benign Het
Map3k5 G T 10: 19,899,415 (GRCm39) C232F probably damaging Het
Mapk9 T G 11: 49,754,383 (GRCm39) D45E probably damaging Het
Mpnd T C 17: 56,319,482 (GRCm39) V315A possibly damaging Het
Msh2 A G 17: 88,030,900 (GRCm39) I926V probably benign Het
Mtcl1 C T 17: 66,650,521 (GRCm39) R1345H probably damaging Het
Nbeal2 A G 9: 110,457,058 (GRCm39) probably null Het
Neo1 T C 9: 58,796,312 (GRCm39) D1205G probably damaging Het
Nhlrc2 A G 19: 56,559,291 (GRCm39) S259G probably benign Het
Nkain4 G A 2: 180,577,796 (GRCm39) P186L probably damaging Het
Nkain4 G A 2: 180,577,797 (GRCm39) P186S probably damaging Het
Nlrp1b T A 11: 71,109,283 (GRCm39) R73* probably null Het
Nr5a2 T C 1: 136,818,536 (GRCm39) D330G probably damaging Het
Nup54 A G 5: 92,572,153 (GRCm39) L299P probably damaging Het
Or2v1 T C 11: 49,025,877 (GRCm39) L286P probably damaging Het
Or5aq7 A G 2: 86,938,296 (GRCm39) V145A probably damaging Het
Pcdhb8 T A 18: 37,489,279 (GRCm39) V319E probably benign Het
Pcsk6 T A 7: 65,578,875 (GRCm39) D129E probably benign Het
Pld5 G A 1: 175,798,100 (GRCm39) T433I probably benign Het
Plin1 A T 7: 79,371,347 (GRCm39) L459H probably benign Het
Psd4 T C 2: 24,284,499 (GRCm39) V121A probably damaging Het
Pxdn A T 12: 30,032,716 (GRCm39) I167F possibly damaging Het
R3hdm2 T C 10: 127,320,384 (GRCm39) S569P probably damaging Het
Rfng T A 11: 120,673,516 (GRCm39) T202S probably damaging Het
Robo1 T C 16: 72,730,696 (GRCm39) S266P probably benign Het
Sema3c G T 5: 17,858,804 (GRCm39) V68L probably damaging Het
Slco6c1 C T 1: 96,993,808 (GRCm39) R645H possibly damaging Het
Slfn8 A G 11: 82,907,626 (GRCm39) Y306H possibly damaging Het
Snap91 T C 9: 86,720,105 (GRCm39) D144G probably damaging Het
St7l T G 3: 104,775,349 (GRCm39) F75C probably damaging Het
Stard10 A G 7: 100,992,468 (GRCm39) I145V probably damaging Het
Tekt3 C T 11: 62,968,999 (GRCm39) A242V probably damaging Het
Tex44 A G 1: 86,354,306 (GRCm39) probably benign Het
Thg1l T C 11: 45,844,988 (GRCm39) Q88R probably benign Het
Trav8n-2 T A 14: 53,583,744 (GRCm39) I67N probably damaging Het
Ttn G A 2: 76,677,770 (GRCm39) probably benign Het
Ube4a A T 9: 44,861,051 (GRCm39) L253* probably null Het
Uggt1 A T 1: 36,201,289 (GRCm39) N1150K probably damaging Het
Ush2a T A 1: 187,995,298 (GRCm39) L23* probably null Het
Usp22 T A 11: 61,065,602 (GRCm39) N37I probably benign Het
Usp53 T A 3: 122,743,390 (GRCm39) K515N probably damaging Het
Vmn2r4 T C 3: 64,322,702 (GRCm39) K6E probably benign Het
Vps13d C T 4: 144,875,918 (GRCm39) V1530M probably damaging Het
Vwa3b A G 1: 37,153,612 (GRCm39) I485V possibly damaging Het
Wnk4 T C 11: 101,155,156 (GRCm39) Y356H probably damaging Het
Zcchc2 A G 1: 105,917,900 (GRCm39) probably benign Het
Zfp345 A C 2: 150,315,010 (GRCm39) Y176D probably benign Het
Zfp598 T C 17: 24,896,850 (GRCm39) F238S possibly damaging Het
Zkscan17 T C 11: 59,393,820 (GRCm39) D10G probably damaging Het
Zmat4 T G 8: 24,392,083 (GRCm39) M13R probably damaging 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
R4923:Lama5 UTSW 2 179,825,942 (GRCm39) missense probably benign 0.18
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
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'- TCTCAATGCAGCCCAGGTAG -3'
(R):5'- AGACTTGTATTTCCAGGTGCTG -3'

Sequencing Primer
(F):5'- CCAGGTAGCCAGGGAATCG -3'
(R):5'- GTGCTGTGTCTGTGTCTCACC -3'
Posted On 2018-02-27