Incidental Mutation 'R7229:Lama1'
ID 562390
Institutional Source Beutler Lab
Gene Symbol Lama1
Ensembl Gene ENSMUSG00000032796
Gene Name laminin, alpha 1
Synonyms Lama
MMRRC Submission 045301-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R7229 (G1)
Quality Score 225.009
Status Validated
Chromosome 17
Chromosomal Location 67697265-67822645 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 67752446 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Valine at position 608 (D608V)
Ref Sequence ENSEMBL: ENSMUSP00000043957 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035471]
AlphaFold no structure available at present
Predicted Effect
SMART Domains Protein: ENSMUSP00000043957
Gene: ENSMUSG00000032796
AA Change: D608V

DomainStartEndE-ValueType
low complexity region 3 22 N/A INTRINSIC
LamNT 23 275 1.2e-131 SMART
EGF_Lam 277 331 1e-5 SMART
EGF_Lam 334 401 6.6e-6 SMART
EGF_Lam 404 458 9.11e-9 SMART
EGF_Lam 461 507 8.12e-6 SMART
LamB 570 702 2.09e-57 SMART
EGF_like 715 746 3.36e0 SMART
EGF_Lam 749 795 7.01e-10 SMART
EGF_Lam 798 853 3.59e-7 SMART
EGF_Lam 856 906 1.53e-10 SMART
EGF_Lam 909 955 1.13e-13 SMART
EGF_Lam 958 1002 1.36e-7 SMART
EGF_Lam 1005 1048 7.29e-8 SMART
EGF_like 1034 1082 4.83e1 SMART
EGF_Lam 1051 1094 1.67e-7 SMART
EGF_Lam 1097 1154 1.32e-5 SMART
LamB 1220 1352 8.7e-46 SMART
Pfam:Laminin_EGF 1367 1397 1.7e-6 PFAM
EGF_Lam 1410 1456 7.12e-11 SMART
EGF_Lam 1459 1513 3.25e-5 SMART
EGF_like 1497 1547 6.41e1 SMART
EGF_Lam 1516 1560 1.71e-13 SMART
Pfam:Laminin_I 1574 1838 1.7e-91 PFAM
low complexity region 2012 2031 N/A INTRINSIC
low complexity region 2087 2098 N/A INTRINSIC
LamG 2145 2287 3.66e-30 SMART
LamG 2332 2473 5.98e-35 SMART
LamG 2513 2661 1.11e-29 SMART
low complexity region 2695 2708 N/A INTRINSIC
LamG 2743 2877 9.72e-35 SMART
LamG 2920 3056 4.63e-41 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.8%
Validation Efficiency 100% (73/73)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes one of the alpha 1 subunits of laminin. The laminins are a family of extracellular matrix glycoproteins that have a heterotrimeric structure consisting of an alpha, beta and gamma chain. These proteins make up a major component of the basement membrane and have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Mutations in this gene may be associated with Poretti-Boltshauser syndrome. [provided by RefSeq, Sep 2014]
PHENOTYPE: Homozygous null mice display embryonic lethality before somite formation with impaired formation of Reichert's membrane. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 73 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931414P19Rik T C 14: 54,595,352 (GRCm38) E122G probably benign Het
Adamts2 T C 11: 50,791,820 (GRCm38) Y880H probably damaging Het
Atp13a4 A G 16: 29,420,905 (GRCm38) S830P probably benign Het
Atp1a3 T A 7: 24,987,985 (GRCm38) Q696L probably benign Het
Brox G A 1: 183,291,959 (GRCm38) R85* probably null Het
C130073F10Rik T C 4: 101,890,242 (GRCm38) I197V probably benign Het
Cand2 G A 6: 115,791,192 (GRCm38) V433M probably damaging Het
Cep83 A G 10: 94,719,665 (GRCm38) K74E probably damaging Het
Chrng A T 1: 87,209,444 (GRCm38) T275S probably benign Het
Clca2 T C 3: 145,084,108 (GRCm38) D489G probably damaging Het
Cmtr1 A G 17: 29,695,424 (GRCm38) probably null Het
Cnga1 T C 5: 72,618,249 (GRCm38) N43S probably benign Het
Cog8 A T 8: 107,056,352 (GRCm38) C102S probably damaging Het
Cpsf3 G A 12: 21,296,737 (GRCm38) probably null Het
Cyp26b1 G A 6: 84,577,150 (GRCm38) Q162* probably null Het
Elmod3 A G 6: 72,594,753 (GRCm38) F14S probably benign Het
Eps8 A G 6: 137,539,356 (GRCm38) S9P probably benign Het
Fam105a G A 15: 27,658,187 (GRCm38) T199M probably benign Het
Fam184b T C 5: 45,584,175 (GRCm38) Q238R probably damaging Het
Fbxw7 T C 3: 84,977,369 (GRCm38) L654S unknown Het
Foxp1 A T 6: 98,935,412 (GRCm38) L580Q unknown Het
Galr1 A G 18: 82,405,664 (GRCm38) S163P probably damaging Het
Ganc T C 2: 120,427,775 (GRCm38) F201L possibly damaging Het
Gin1 T C 1: 97,785,151 (GRCm38) F310L probably benign Het
Grik2 A T 10: 49,101,416 (GRCm38) probably null Het
Haus1 A T 18: 77,764,134 (GRCm38) F94I probably benign Het
Hcn4 A G 9: 58,853,399 (GRCm38) Y409C unknown Het
Hspa1l A G 17: 34,977,255 (GRCm38) K90R probably benign Het
Icam5 T C 9: 21,037,001 (GRCm38) S702P possibly damaging Het
Ifnar1 A G 16: 91,499,556 (GRCm38) H315R probably benign Het
Klra9 T C 6: 130,191,261 (GRCm38) H14R probably damaging Het
Krt78 A G 15: 101,947,394 (GRCm38) Y661H probably benign Het
Krtap11-1 T C 16: 89,570,925 (GRCm38) T69A possibly damaging Het
L3mbtl3 C A 10: 26,292,662 (GRCm38) S598I unknown Het
Lrrc55 G A 2: 85,196,440 (GRCm38) T80I probably damaging Het
Lyst A T 13: 13,643,509 (GRCm38) T1255S probably benign Het
Magi2 T C 5: 20,465,588 (GRCm38) V310A probably damaging Het
Med23 C A 10: 24,902,004 (GRCm38) A750D probably benign Het
Mmp2 G A 8: 92,831,786 (GRCm38) R161Q probably damaging Het
Myo15 A T 11: 60,496,495 (GRCm38) I733F probably benign Het
Ncan A T 8: 70,100,311 (GRCm38) F1090L possibly damaging Het
Olfr701 T G 7: 106,818,995 (GRCm38) V304G probably damaging Het
Pafah1b1 A G 11: 74,682,278 (GRCm38) I320T probably damaging Het
Pcdhb1 T A 18: 37,266,687 (GRCm38) Y564N probably damaging Het
Pear1 A G 3: 87,750,289 (GRCm38) S988P probably benign Het
Pgam2 A C 11: 5,803,013 (GRCm38) V194G probably damaging Het
Plvap A T 8: 71,511,577 (GRCm38) I47N probably damaging Het
Prdx6 A T 1: 161,247,297 (GRCm38) L71H probably damaging Het
Psmb11 G A 14: 54,625,951 (GRCm38) V209M probably damaging Het
Ptprn2 G A 12: 117,227,225 (GRCm38) probably null Het
Rcn2 T A 9: 56,057,479 (GRCm38) N240K probably benign Het
Rsad2 A T 12: 26,454,123 (GRCm38) Y136N probably damaging Het
Slc12a4 T G 8: 105,946,737 (GRCm38) Q734P probably benign Het
Smarcc2 T A 10: 128,488,048 (GRCm38) M1085K unknown Het
Smg1 A T 7: 118,176,955 (GRCm38) C1371S probably benign Het
Spg11 A T 2: 122,108,104 (GRCm38) F456L probably damaging Het
Srsf10 C T 4: 135,856,217 (GRCm38) probably benign Het
Stxbp5 T C 10: 9,798,187 (GRCm38) Y4C probably damaging Het
Tdrd12 T A 7: 35,480,280 (GRCm38) D881V unknown Het
Tmem171 T C 13: 98,692,625 (GRCm38) T6A probably benign Het
Tmem220 T C 11: 67,026,163 (GRCm38) L55P unknown Het
Ttn G T 2: 76,846,781 (GRCm38) P11037Q unknown Het
Tulp4 C T 17: 6,231,780 (GRCm38) H695Y probably damaging Het
Usp47 T C 7: 112,092,877 (GRCm38) S849P probably benign Het
Vcan G A 13: 89,705,270 (GRCm38) P524S possibly damaging Het
Vmn1r18 A G 6: 57,390,098 (GRCm38) M157T probably benign Het
Vmn2r109 A T 17: 20,540,963 (GRCm38) C711S possibly damaging Het
Wasf3 C T 5: 146,455,653 (GRCm38) R178C probably damaging Het
Wdr76 G A 2: 121,528,920 (GRCm38) V231I probably damaging Het
Xirp2 A T 2: 67,525,551 (GRCm38) N3552I probably damaging Het
Zfp804a A G 2: 82,258,625 (GRCm38) T933A probably benign Het
Zmynd8 A G 2: 165,858,053 (GRCm38) probably null Het
Zranb3 A T 1: 128,040,893 (GRCm38) I95K probably benign Het
Other mutations in Lama1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00157:Lama1 APN 17 67,815,928 (GRCm38) missense probably benign
IGL00336:Lama1 APN 17 67,813,948 (GRCm38) missense probably benign 0.07
IGL01066:Lama1 APN 17 67,743,326 (GRCm38) missense probably damaging 1.00
IGL01140:Lama1 APN 17 67,802,933 (GRCm38) missense probably benign 0.14
IGL01291:Lama1 APN 17 67,738,870 (GRCm38) missense probably damaging 1.00
IGL01296:Lama1 APN 17 67,745,051 (GRCm38) missense probably benign 0.27
IGL01317:Lama1 APN 17 67,818,701 (GRCm38) missense probably damaging 1.00
IGL01490:Lama1 APN 17 67,750,584 (GRCm38) missense possibly damaging 0.54
IGL01506:Lama1 APN 17 67,785,070 (GRCm38) missense probably benign 0.01
IGL01508:Lama1 APN 17 67,809,361 (GRCm38) splice site probably benign
IGL01522:Lama1 APN 17 67,752,774 (GRCm38) splice site probably benign
IGL01530:Lama1 APN 17 67,796,790 (GRCm38) missense probably benign 0.02
IGL01541:Lama1 APN 17 67,785,070 (GRCm38) missense probably benign 0.01
IGL01677:Lama1 APN 17 67,779,148 (GRCm38) missense probably benign 0.15
IGL01886:Lama1 APN 17 67,807,797 (GRCm38) missense probably benign 0.36
IGL01994:Lama1 APN 17 67,752,439 (GRCm38) missense probably benign 0.05
IGL02017:Lama1 APN 17 67,764,725 (GRCm38) missense probably benign 0.00
IGL02021:Lama1 APN 17 67,821,626 (GRCm38) missense probably damaging 1.00
IGL02026:Lama1 APN 17 67,809,292 (GRCm38) missense possibly damaging 0.82
IGL02044:Lama1 APN 17 67,811,490 (GRCm38) missense probably benign 0.01
IGL02120:Lama1 APN 17 67,716,789 (GRCm38) missense probably damaging 1.00
IGL02425:Lama1 APN 17 67,811,485 (GRCm38) missense probably benign 0.45
IGL02549:Lama1 APN 17 67,790,835 (GRCm38) missense possibly damaging 0.93
IGL02642:Lama1 APN 17 67,812,366 (GRCm38) missense probably benign 0.00
IGL02795:Lama1 APN 17 67,738,894 (GRCm38) splice site probably null
IGL02798:Lama1 APN 17 67,795,191 (GRCm38) splice site probably benign
IGL02863:Lama1 APN 17 67,804,536 (GRCm38) missense probably damaging 0.99
IGL02870:Lama1 APN 17 67,804,536 (GRCm38) missense probably damaging 0.99
IGL02876:Lama1 APN 17 67,750,692 (GRCm38) critical splice donor site probably null
IGL02885:Lama1 APN 17 67,804,536 (GRCm38) missense probably damaging 0.99
IGL02891:Lama1 APN 17 67,804,536 (GRCm38) missense probably damaging 0.99
IGL02978:Lama1 APN 17 67,786,081 (GRCm38) nonsense probably null
IGL03064:Lama1 APN 17 67,779,104 (GRCm38) missense probably benign 0.01
IGL03076:Lama1 APN 17 67,716,799 (GRCm38) missense possibly damaging 0.95
IGL03110:Lama1 APN 17 67,798,986 (GRCm38) missense probably benign 0.04
IGL03143:Lama1 APN 17 67,804,536 (GRCm38) missense probably damaging 0.99
IGL03159:Lama1 APN 17 67,804,536 (GRCm38) missense probably damaging 0.99
IGL03268:Lama1 APN 17 67,804,536 (GRCm38) missense probably damaging 0.99
ANU05:Lama1 UTSW 17 67,738,870 (GRCm38) missense probably damaging 1.00
PIT4472001:Lama1 UTSW 17 67,764,704 (GRCm38) missense
R0047:Lama1 UTSW 17 67,795,186 (GRCm38) splice site probably benign
R0047:Lama1 UTSW 17 67,795,186 (GRCm38) splice site probably benign
R0050:Lama1 UTSW 17 67,782,056 (GRCm38) missense possibly damaging 0.66
R0096:Lama1 UTSW 17 67,805,413 (GRCm38) missense probably benign 0.12
R0096:Lama1 UTSW 17 67,805,413 (GRCm38) missense probably benign 0.12
R0111:Lama1 UTSW 17 67,737,498 (GRCm38) missense probably damaging 0.98
R0116:Lama1 UTSW 17 67,776,923 (GRCm38) missense probably benign 0.10
R0121:Lama1 UTSW 17 67,798,513 (GRCm38) splice site probably benign
R0278:Lama1 UTSW 17 67,810,183 (GRCm38) missense probably null 0.98
R0281:Lama1 UTSW 17 67,817,569 (GRCm38) missense probably damaging 1.00
R0312:Lama1 UTSW 17 67,775,851 (GRCm38) missense possibly damaging 0.45
R0419:Lama1 UTSW 17 67,791,610 (GRCm38) critical splice donor site probably null
R0512:Lama1 UTSW 17 67,779,134 (GRCm38) missense possibly damaging 0.67
R0514:Lama1 UTSW 17 67,764,698 (GRCm38) missense probably benign 0.40
R0562:Lama1 UTSW 17 67,815,959 (GRCm38) missense probably damaging 1.00
R0632:Lama1 UTSW 17 67,752,368 (GRCm38) splice site probably benign
R0645:Lama1 UTSW 17 67,773,712 (GRCm38) missense probably benign 0.01
R0712:Lama1 UTSW 17 67,779,042 (GRCm38) splice site probably null
R0763:Lama1 UTSW 17 67,772,818 (GRCm38) missense probably damaging 0.97
R0941:Lama1 UTSW 17 67,775,865 (GRCm38) missense probably benign 0.10
R1025:Lama1 UTSW 17 67,752,898 (GRCm38) missense probably benign 0.00
R1084:Lama1 UTSW 17 67,804,469 (GRCm38) missense probably benign 0.12
R1103:Lama1 UTSW 17 67,790,947 (GRCm38) missense probably damaging 0.98
R1420:Lama1 UTSW 17 67,790,947 (GRCm38) missense probably damaging 0.98
R1430:Lama1 UTSW 17 67,782,155 (GRCm38) missense possibly damaging 0.95
R1569:Lama1 UTSW 17 67,780,618 (GRCm38) splice site probably null
R1575:Lama1 UTSW 17 67,810,409 (GRCm38) missense possibly damaging 0.96
R1613:Lama1 UTSW 17 67,807,923 (GRCm38) missense probably benign 0.42
R1620:Lama1 UTSW 17 67,767,033 (GRCm38) missense probably benign 0.01
R1629:Lama1 UTSW 17 67,805,428 (GRCm38) missense probably benign 0.00
R1645:Lama1 UTSW 17 67,737,682 (GRCm38) missense probably benign 0.14
R1652:Lama1 UTSW 17 67,807,846 (GRCm38) missense probably damaging 0.97
R1674:Lama1 UTSW 17 67,791,244 (GRCm38) missense probably benign
R1678:Lama1 UTSW 17 67,810,155 (GRCm38) missense possibly damaging 0.56
R1710:Lama1 UTSW 17 67,753,791 (GRCm38) missense probably benign 0.00
R1712:Lama1 UTSW 17 67,717,186 (GRCm38) missense possibly damaging 0.95
R1737:Lama1 UTSW 17 67,802,921 (GRCm38) missense probably benign 0.36
R1757:Lama1 UTSW 17 67,697,383 (GRCm38) missense unknown
R1757:Lama1 UTSW 17 67,763,836 (GRCm38) missense probably benign 0.40
R1813:Lama1 UTSW 17 67,791,223 (GRCm38) missense probably benign
R1896:Lama1 UTSW 17 67,791,223 (GRCm38) missense probably benign
R1945:Lama1 UTSW 17 67,745,853 (GRCm38) missense probably benign 0.14
R2086:Lama1 UTSW 17 67,817,623 (GRCm38) missense probably damaging 1.00
R2149:Lama1 UTSW 17 67,773,865 (GRCm38) missense possibly damaging 0.95
R2178:Lama1 UTSW 17 67,769,515 (GRCm38) missense probably benign 0.07
R2183:Lama1 UTSW 17 67,791,009 (GRCm38) missense probably damaging 0.98
R2197:Lama1 UTSW 17 67,752,941 (GRCm38) missense probably benign 0.02
R2213:Lama1 UTSW 17 67,777,034 (GRCm38) nonsense probably null
R2260:Lama1 UTSW 17 67,737,507 (GRCm38) missense probably damaging 0.96
R2356:Lama1 UTSW 17 67,810,114 (GRCm38) missense probably damaging 1.00
R2420:Lama1 UTSW 17 67,750,553 (GRCm38) missense probably benign 0.00
R2421:Lama1 UTSW 17 67,750,553 (GRCm38) missense probably benign 0.00
R2422:Lama1 UTSW 17 67,750,553 (GRCm38) missense probably benign 0.00
R2424:Lama1 UTSW 17 67,798,665 (GRCm38) missense probably benign 0.09
R2442:Lama1 UTSW 17 67,768,317 (GRCm38) missense probably benign 0.04
R3147:Lama1 UTSW 17 67,737,658 (GRCm38) missense probably damaging 0.98
R3414:Lama1 UTSW 17 67,737,603 (GRCm38) missense probably damaging 1.00
R3683:Lama1 UTSW 17 67,768,333 (GRCm38) missense probably benign 0.40
R3820:Lama1 UTSW 17 67,779,046 (GRCm38) splice site probably null
R3821:Lama1 UTSW 17 67,779,046 (GRCm38) splice site probably null
R3822:Lama1 UTSW 17 67,779,046 (GRCm38) splice site probably null
R4012:Lama1 UTSW 17 67,812,373 (GRCm38) nonsense probably null
R4113:Lama1 UTSW 17 67,764,703 (GRCm38) missense probably benign 0.01
R4133:Lama1 UTSW 17 67,812,486 (GRCm38) missense probably damaging 1.00
R4133:Lama1 UTSW 17 67,750,655 (GRCm38) missense probably damaging 0.98
R4259:Lama1 UTSW 17 67,752,418 (GRCm38) missense possibly damaging 0.95
R4278:Lama1 UTSW 17 67,791,517 (GRCm38) missense probably null 0.00
R4321:Lama1 UTSW 17 67,771,083 (GRCm38) missense probably benign 0.03
R4374:Lama1 UTSW 17 67,804,518 (GRCm38) missense probably benign 0.00
R4386:Lama1 UTSW 17 67,773,712 (GRCm38) missense probably benign 0.01
R4463:Lama1 UTSW 17 67,761,700 (GRCm38) missense probably damaging 1.00
R4629:Lama1 UTSW 17 67,805,360 (GRCm38) critical splice acceptor site probably null
R4630:Lama1 UTSW 17 67,794,300 (GRCm38) missense probably benign 0.00
R4633:Lama1 UTSW 17 67,798,584 (GRCm38) missense probably damaging 0.96
R4668:Lama1 UTSW 17 67,752,434 (GRCm38) missense probably benign 0.27
R4684:Lama1 UTSW 17 67,773,778 (GRCm38) missense possibly damaging 0.88
R4745:Lama1 UTSW 17 67,738,780 (GRCm38) missense probably damaging 1.00
R4786:Lama1 UTSW 17 67,773,859 (GRCm38) missense possibly damaging 0.77
R4797:Lama1 UTSW 17 67,716,775 (GRCm38) missense probably benign 0.04
R4803:Lama1 UTSW 17 67,809,271 (GRCm38) missense probably damaging 1.00
R4925:Lama1 UTSW 17 67,794,314 (GRCm38) missense probably benign 0.02
R4939:Lama1 UTSW 17 67,737,475 (GRCm38) missense possibly damaging 0.91
R4952:Lama1 UTSW 17 67,767,566 (GRCm38) critical splice donor site probably null
R4975:Lama1 UTSW 17 67,738,834 (GRCm38) missense possibly damaging 0.95
R4977:Lama1 UTSW 17 67,737,682 (GRCm38) missense probably damaging 1.00
R5039:Lama1 UTSW 17 67,745,893 (GRCm38) missense possibly damaging 0.66
R5047:Lama1 UTSW 17 67,743,281 (GRCm38) nonsense probably null
R5195:Lama1 UTSW 17 67,764,800 (GRCm38) missense probably benign 0.13
R5230:Lama1 UTSW 17 67,745,083 (GRCm38) nonsense probably null
R5236:Lama1 UTSW 17 67,804,492 (GRCm38) missense probably benign 0.24
R5254:Lama1 UTSW 17 67,756,716 (GRCm38) missense probably benign 0.01
R5345:Lama1 UTSW 17 67,817,563 (GRCm38) missense probably benign
R5438:Lama1 UTSW 17 67,800,774 (GRCm38) missense possibly damaging 0.92
R5521:Lama1 UTSW 17 67,780,894 (GRCm38) nonsense probably null
R5568:Lama1 UTSW 17 67,768,298 (GRCm38) critical splice acceptor site probably null
R5645:Lama1 UTSW 17 67,802,948 (GRCm38) missense probably damaging 1.00
R5665:Lama1 UTSW 17 67,770,987 (GRCm38) missense probably damaging 1.00
R5727:Lama1 UTSW 17 67,815,224 (GRCm38) missense possibly damaging 0.81
R5757:Lama1 UTSW 17 67,738,787 (GRCm38) missense possibly damaging 0.59
R5795:Lama1 UTSW 17 67,796,727 (GRCm38) missense probably benign 0.02
R5857:Lama1 UTSW 17 67,807,843 (GRCm38) missense probably damaging 0.99
R5894:Lama1 UTSW 17 67,779,047 (GRCm38) critical splice acceptor site probably null
R5974:Lama1 UTSW 17 67,773,727 (GRCm38) missense probably benign 0.31
R6032:Lama1 UTSW 17 67,750,643 (GRCm38) missense probably benign 0.01
R6032:Lama1 UTSW 17 67,750,643 (GRCm38) missense probably benign 0.01
R6120:Lama1 UTSW 17 67,780,617 (GRCm38) critical splice donor site probably null
R6219:Lama1 UTSW 17 67,790,856 (GRCm38) missense probably benign 0.08
R6224:Lama1 UTSW 17 67,802,987 (GRCm38) missense possibly damaging 0.56
R6249:Lama1 UTSW 17 67,798,604 (GRCm38) missense probably benign
R6265:Lama1 UTSW 17 67,750,655 (GRCm38) missense probably damaging 0.98
R6276:Lama1 UTSW 17 67,784,088 (GRCm38) splice site probably null
R6284:Lama1 UTSW 17 67,810,096 (GRCm38) missense probably damaging 0.99
R6337:Lama1 UTSW 17 67,786,019 (GRCm38) missense probably benign 0.27
R6414:Lama1 UTSW 17 67,746,910 (GRCm38) critical splice donor site probably null
R6631:Lama1 UTSW 17 67,774,482 (GRCm38) missense probably benign 0.21
R6659:Lama1 UTSW 17 67,818,635 (GRCm38) missense probably damaging 1.00
R6660:Lama1 UTSW 17 67,804,500 (GRCm38) missense probably benign 0.05
R6677:Lama1 UTSW 17 67,795,233 (GRCm38) missense probably benign 0.14
R6763:Lama1 UTSW 17 67,746,873 (GRCm38) missense unknown
R6787:Lama1 UTSW 17 67,784,025 (GRCm38) missense unknown
R6831:Lama1 UTSW 17 67,756,754 (GRCm38) missense possibly damaging 0.89
R6855:Lama1 UTSW 17 67,782,155 (GRCm38) missense possibly damaging 0.95
R6910:Lama1 UTSW 17 67,791,464 (GRCm38) missense possibly damaging 0.60
R6934:Lama1 UTSW 17 67,774,543 (GRCm38) missense probably benign 0.04
R6945:Lama1 UTSW 17 67,813,866 (GRCm38) missense
R6984:Lama1 UTSW 17 67,779,112 (GRCm38) missense
R6989:Lama1 UTSW 17 67,753,758 (GRCm38) missense
R6994:Lama1 UTSW 17 67,753,825 (GRCm38) missense
R6995:Lama1 UTSW 17 67,753,825 (GRCm38) missense
R7035:Lama1 UTSW 17 67,781,049 (GRCm38) missense
R7133:Lama1 UTSW 17 67,782,146 (GRCm38) missense
R7172:Lama1 UTSW 17 67,804,545 (GRCm38) missense
R7197:Lama1 UTSW 17 67,737,705 (GRCm38) nonsense probably null
R7217:Lama1 UTSW 17 67,764,673 (GRCm38) missense
R7264:Lama1 UTSW 17 67,743,297 (GRCm38) missense
R7311:Lama1 UTSW 17 67,767,385 (GRCm38) missense
R7394:Lama1 UTSW 17 67,717,261 (GRCm38) missense
R7419:Lama1 UTSW 17 67,717,174 (GRCm38) missense
R7460:Lama1 UTSW 17 67,767,018 (GRCm38) missense
R7492:Lama1 UTSW 17 67,817,651 (GRCm38) missense
R7494:Lama1 UTSW 17 67,811,446 (GRCm38) missense
R7552:Lama1 UTSW 17 67,737,667 (GRCm38) missense
R7576:Lama1 UTSW 17 67,782,041 (GRCm38) missense
R7583:Lama1 UTSW 17 67,761,621 (GRCm38) missense
R7649:Lama1 UTSW 17 67,737,554 (GRCm38) missense
R7663:Lama1 UTSW 17 67,780,880 (GRCm38) missense
R7667:Lama1 UTSW 17 67,780,597 (GRCm38) missense
R7688:Lama1 UTSW 17 67,761,628 (GRCm38) missense
R7693:Lama1 UTSW 17 67,817,031 (GRCm38) missense
R7748:Lama1 UTSW 17 67,750,590 (GRCm38) missense
R7778:Lama1 UTSW 17 67,804,473 (GRCm38) missense
R7824:Lama1 UTSW 17 67,804,473 (GRCm38) missense
R7861:Lama1 UTSW 17 67,809,221 (GRCm38) missense
R7884:Lama1 UTSW 17 67,769,435 (GRCm38) missense
R8029:Lama1 UTSW 17 67,817,594 (GRCm38) missense
R8078:Lama1 UTSW 17 67,791,294 (GRCm38) missense
R8101:Lama1 UTSW 17 67,745,922 (GRCm38) missense
R8313:Lama1 UTSW 17 67,750,520 (GRCm38) missense
R8356:Lama1 UTSW 17 67,737,496 (GRCm38) missense
R8366:Lama1 UTSW 17 67,818,704 (GRCm38) missense
R8403:Lama1 UTSW 17 67,745,923 (GRCm38) missense
R8456:Lama1 UTSW 17 67,737,496 (GRCm38) missense
R8466:Lama1 UTSW 17 67,813,953 (GRCm38) missense
R8678:Lama1 UTSW 17 67,817,103 (GRCm38) missense
R8728:Lama1 UTSW 17 67,818,668 (GRCm38) missense
R8796:Lama1 UTSW 17 67,810,151 (GRCm38) missense
R8885:Lama1 UTSW 17 67,773,784 (GRCm38) missense
R8893:Lama1 UTSW 17 67,805,372 (GRCm38) missense
R8898:Lama1 UTSW 17 67,821,615 (GRCm38) missense
R8909:Lama1 UTSW 17 67,772,741 (GRCm38) missense
R9025:Lama1 UTSW 17 67,812,496 (GRCm38) missense
R9045:Lama1 UTSW 17 67,753,843 (GRCm38) missense
R9098:Lama1 UTSW 17 67,804,513 (GRCm38) missense
R9114:Lama1 UTSW 17 67,821,674 (GRCm38) missense
R9173:Lama1 UTSW 17 67,769,602 (GRCm38) missense
R9190:Lama1 UTSW 17 67,804,519 (GRCm38) missense
R9381:Lama1 UTSW 17 67,737,484 (GRCm38) missense
R9429:Lama1 UTSW 17 67,811,454 (GRCm38) missense
R9504:Lama1 UTSW 17 67,821,666 (GRCm38) missense
R9558:Lama1 UTSW 17 67,817,009 (GRCm38) missense
R9647:Lama1 UTSW 17 67,717,175 (GRCm38) missense
R9651:Lama1 UTSW 17 67,794,220 (GRCm38) missense
R9654:Lama1 UTSW 17 67,794,271 (GRCm38) missense
R9710:Lama1 UTSW 17 67,822,409 (GRCm38) missense
R9733:Lama1 UTSW 17 67,809,945 (GRCm38) missense
RF001:Lama1 UTSW 17 67,752,902 (GRCm38) missense
RF013:Lama1 UTSW 17 67,781,062 (GRCm38) missense
V8831:Lama1 UTSW 17 67,752,883 (GRCm38) missense probably benign 0.00
X0024:Lama1 UTSW 17 67,738,888 (GRCm38) missense probably damaging 1.00
X0028:Lama1 UTSW 17 67,794,310 (GRCm38) missense probably benign 0.06
X0028:Lama1 UTSW 17 67,767,422 (GRCm38) missense probably benign 0.00
X0066:Lama1 UTSW 17 67,811,566 (GRCm38) missense probably damaging 1.00
Z1088:Lama1 UTSW 17 67,810,171 (GRCm38) missense probably damaging 1.00
Z1088:Lama1 UTSW 17 67,771,082 (GRCm38) missense probably benign 0.25
Z1088:Lama1 UTSW 17 67,752,883 (GRCm38) missense probably benign 0.00
Z1176:Lama1 UTSW 17 67,752,883 (GRCm38) missense probably benign 0.00
Z1177:Lama1 UTSW 17 67,752,883 (GRCm38) missense probably benign 0.00
Z1191:Lama1 UTSW 17 67,798,644 (GRCm38) missense
Predicted Primers PCR Primer
(F):5'- TCTTTCATATGGTCATCAGGATGGC -3'
(R):5'- TGACCCAATCCAGAGTTACCAG -3'

Sequencing Primer
(F):5'- GCTCCTGCCTGTGGATCTCAG -3'
(R):5'- AGGTGGCAGTTGACTGAACTC -3'
Posted On 2019-06-26