Incidental Mutation 'R1723:Myo18a'
ID 191623
Institutional Source Beutler Lab
Gene Symbol Myo18a
Ensembl Gene ENSMUSG00000000631
Gene Name myosin XVIIIA
Synonyms MyoPDZ
MMRRC Submission 039755-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R1723 (G1)
Quality Score 168
Status Validated
Chromosome 11
Chromosomal Location 77654072-77756806 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 77744140 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Lysine at position 1834 (R1834K)
Ref Sequence ENSEMBL: ENSMUSP00000104013 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000000645] [ENSMUST00000092884] [ENSMUST00000092887] [ENSMUST00000100794] [ENSMUST00000102488] [ENSMUST00000108375] [ENSMUST00000168348] [ENSMUST00000167856] [ENSMUST00000169105] [ENSMUST00000130627] [ENSMUST00000130305] [ENSMUST00000172303] [ENSMUST00000164334] [ENSMUST00000108376]
AlphaFold Q9JMH9
Predicted Effect probably benign
Transcript: ENSMUST00000000645
AA Change: R1872K

PolyPhen 2 Score 0.364 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000000645
Gene: ENSMUSG00000000631
AA Change: R1872K

DomainStartEndE-ValueType
low complexity region 6 27 N/A INTRINSIC
low complexity region 202 227 N/A INTRINSIC
PDZ 229 311 5.72e-10 SMART
MYSc 399 1183 1.53e-45 SMART
IQ 1184 1206 1.11e-3 SMART
Pfam:Myosin_tail_1 1219 1867 1.7e-34 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000092884
AA Change: R1540K

PolyPhen 2 Score 0.113 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000090560
Gene: ENSMUSG00000000631
AA Change: R1540K

DomainStartEndE-ValueType
MYSc 68 851 4.16e-47 SMART
IQ 852 874 1.11e-3 SMART
Pfam:Myosin_tail_1 888 1534 2e-34 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000092887
AA Change: R1871K

PolyPhen 2 Score 0.239 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000090563
Gene: ENSMUSG00000000631
AA Change: R1871K

DomainStartEndE-ValueType
low complexity region 6 27 N/A INTRINSIC
low complexity region 202 227 N/A INTRINSIC
PDZ 229 311 5.72e-10 SMART
MYSc 399 1182 4.16e-47 SMART
IQ 1183 1205 1.11e-3 SMART
Pfam:Myosin_tail_1 1218 1866 3e-34 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000100794
AA Change: R1536K

PolyPhen 2 Score 0.925 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000098358
Gene: ENSMUSG00000000631
AA Change: R1536K

DomainStartEndE-ValueType
MYSc 68 847 1.45e-46 SMART
IQ 848 870 1.11e-3 SMART
Pfam:Myosin_tail_1 884 1530 4.9e-35 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000102488
AA Change: R1871K

PolyPhen 2 Score 0.239 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000099546
Gene: ENSMUSG00000000631
AA Change: R1871K

DomainStartEndE-ValueType
low complexity region 6 27 N/A INTRINSIC
low complexity region 202 227 N/A INTRINSIC
PDZ 229 311 5.72e-10 SMART
MYSc 399 1182 4.16e-47 SMART
IQ 1183 1205 1.11e-3 SMART
Pfam:Myosin_tail_1 1218 1866 3e-34 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000108375
AA Change: R1871K

PolyPhen 2 Score 0.239 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000104012
Gene: ENSMUSG00000000631
AA Change: R1871K

DomainStartEndE-ValueType
low complexity region 6 27 N/A INTRINSIC
low complexity region 202 227 N/A INTRINSIC
PDZ 229 311 5.72e-10 SMART
MYSc 399 1182 4.16e-47 SMART
IQ 1183 1205 1.11e-3 SMART
Pfam:Myosin_tail_1 1218 1838 6.8e-36 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000168348
AA Change: R1919K

PolyPhen 2 Score 0.247 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000130696
Gene: ENSMUSG00000000631
AA Change: R1919K

DomainStartEndE-ValueType
low complexity region 6 27 N/A INTRINSIC
low complexity region 202 227 N/A INTRINSIC
PDZ 229 311 5.72e-10 SMART
MYSc 447 1230 4.16e-47 SMART
IQ 1231 1253 1.11e-3 SMART
Blast:MYSc 1306 1435 1e-14 BLAST
low complexity region 1444 1455 N/A INTRINSIC
low complexity region 1828 1847 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000167856
AA Change: R1478K

PolyPhen 2 Score 0.871 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000128487
Gene: ENSMUSG00000000631
AA Change: R1478K

DomainStartEndE-ValueType
MYSc 16 789 1.3e-32 SMART
IQ 790 812 1.11e-3 SMART
Blast:MYSc 865 994 1e-14 BLAST
low complexity region 1003 1014 N/A INTRINSIC
low complexity region 1387 1406 N/A INTRINSIC
internal_repeat_1 1569 1627 2.13e-5 PROSPERO
Predicted Effect probably benign
Transcript: ENSMUST00000169105
AA Change: R1883K

PolyPhen 2 Score 0.239 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000132149
Gene: ENSMUSG00000000631
AA Change: R1883K

DomainStartEndE-ValueType
low complexity region 6 27 N/A INTRINSIC
low complexity region 202 227 N/A INTRINSIC
PDZ 229 311 5.72e-10 SMART
MYSc 411 1194 4.16e-47 SMART
IQ 1195 1217 1.11e-3 SMART
Pfam:Myosin_tail_1 1230 1878 7.3e-35 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000130627
AA Change: R1883K

PolyPhen 2 Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000119839
Gene: ENSMUSG00000000631
AA Change: R1883K

DomainStartEndE-ValueType
low complexity region 6 27 N/A INTRINSIC
low complexity region 202 227 N/A INTRINSIC
PDZ 229 311 5.72e-10 SMART
MYSc 411 1194 4.16e-47 SMART
IQ 1195 1217 1.11e-3 SMART
Pfam:Myosin_tail_1 1230 1850 6.9e-36 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000130305
AA Change: R1552K

PolyPhen 2 Score 0.357 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000119574
Gene: ENSMUSG00000000631
AA Change: R1552K

DomainStartEndE-ValueType
MYSc 80 863 4.16e-47 SMART
IQ 864 886 1.11e-3 SMART
Pfam:Myosin_tail_1 902 1547 2.6e-34 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000172303
AA Change: R1558K

PolyPhen 2 Score 0.149 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000129098
Gene: ENSMUSG00000000631
AA Change: R1558K

DomainStartEndE-ValueType
MYSc 80 863 4.16e-47 SMART
IQ 864 886 1.11e-3 SMART
Pfam:Myosin_tail_1 902 1547 2.6e-34 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000164334
AA Change: R1540K

PolyPhen 2 Score 0.233 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000131771
Gene: ENSMUSG00000000631
AA Change: R1540K

DomainStartEndE-ValueType
MYSc 68 851 4.16e-47 SMART
IQ 852 874 1.11e-3 SMART
Pfam:Myosin_tail_1 888 1505 4e-36 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000108376
AA Change: R1834K

PolyPhen 2 Score 0.974 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000104013
Gene: ENSMUSG00000000631
AA Change: R1834K

DomainStartEndE-ValueType
low complexity region 6 27 N/A INTRINSIC
low complexity region 202 227 N/A INTRINSIC
PDZ 229 311 5.72e-10 SMART
MYSc 399 1182 4.16e-47 SMART
IQ 1183 1205 1.11e-3 SMART
Blast:MYSc 1258 1387 1e-14 BLAST
low complexity region 1396 1407 N/A INTRINSIC
low complexity region 1743 1762 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135045
Predicted Effect noncoding transcript
Transcript: ENSMUST00000130956
Predicted Effect noncoding transcript
Transcript: ENSMUST00000142571
Predicted Effect probably benign
Transcript: ENSMUST00000135375
SMART Domains Protein: ENSMUSP00000117044
Gene: ENSMUSG00000000631

DomainStartEndE-ValueType
low complexity region 198 231 N/A INTRINSIC
low complexity region 289 303 N/A INTRINSIC
low complexity region 361 459 N/A INTRINSIC
low complexity region 474 486 N/A INTRINSIC
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 93.1%
Validation Efficiency 100% (62/62)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene can bind GOLPH3, linking the Golgi to the cytoskeleton and influencing Golgi membrane trafficking. The encoded protein is also part of a complex that assembles lamellar actomyosin bundles and may be required for cell migration. [provided by RefSeq, Oct 2016]
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Alms1 G T 6: 85,605,735 (GRCm39) G2462C probably damaging Het
Anapc5 T C 5: 122,937,406 (GRCm39) E464G probably damaging Het
Aoc3 T A 11: 101,227,261 (GRCm39) V378E possibly damaging Het
Atp13a5 T A 16: 29,051,551 (GRCm39) K1152I possibly damaging Het
Auh G A 13: 52,989,532 (GRCm39) P308L probably benign Het
Calcoco1 C A 15: 102,627,988 (GRCm39) G49C probably damaging Het
Cd70 T C 17: 57,453,401 (GRCm39) T88A possibly damaging Het
Cpeb1 C T 7: 81,085,974 (GRCm39) R56Q probably benign Het
Dglucy A G 12: 100,808,938 (GRCm39) Y212C probably damaging Het
Dnhd1 C A 7: 105,364,127 (GRCm39) P4160T possibly damaging Het
Ecel1 T C 1: 87,082,143 (GRCm39) D190G probably benign Het
Exoc6b A G 6: 85,046,326 (GRCm39) L21P probably damaging Het
Fam110c A G 12: 31,124,394 (GRCm39) R119G unknown Het
Gask1b T A 3: 79,843,970 (GRCm39) N32K probably benign Het
Gm42791 C A 5: 148,896,311 (GRCm39) probably benign Het
Hpcal4 A G 4: 123,084,532 (GRCm39) I154V probably benign Het
Itgb1 A G 8: 129,452,519 (GRCm39) D728G probably damaging Het
Kdm5d A T Y: 927,753 (GRCm39) D701V probably damaging Het
Kif18a A G 2: 109,133,227 (GRCm39) K448E probably damaging Het
Kif26a T C 12: 112,140,292 (GRCm39) F507S possibly damaging Het
Kmt2c C T 5: 25,520,003 (GRCm39) G2036R probably damaging Het
Lrrc43 T A 5: 123,630,276 (GRCm39) probably benign Het
Map3k20 T C 2: 72,219,836 (GRCm39) I256T probably damaging Het
Med29 T A 7: 28,092,130 (GRCm39) probably benign Het
Mob3b A G 4: 34,954,026 (GRCm39) C215R probably damaging Het
Mtf2 T C 5: 108,235,936 (GRCm39) Y87H probably damaging Het
Nlrc4 T A 17: 74,748,903 (GRCm39) D779V probably damaging Het
Or51q1c T C 7: 103,652,518 (GRCm39) F18S probably damaging Het
Otud3 T C 4: 138,625,329 (GRCm39) T242A probably damaging Het
Pcare A T 17: 72,057,373 (GRCm39) F768Y probably damaging Het
Pnliprp1 T A 19: 58,720,574 (GRCm39) M150K possibly damaging Het
Polm T A 11: 5,784,776 (GRCm39) Q227L probably benign Het
Poln A G 5: 34,280,016 (GRCm39) V282A probably benign Het
Ppfia2 T A 10: 106,751,533 (GRCm39) probably null Het
Rad51 T G 2: 118,954,295 (GRCm39) M168R probably benign Het
Senp2 A G 16: 21,846,792 (GRCm39) T266A probably benign Het
Sfswap A G 5: 129,616,758 (GRCm39) T401A probably benign Het
Slc35a4 C A 18: 36,815,788 (GRCm39) T206K possibly damaging Het
Slc40a1 A G 1: 45,963,921 (GRCm39) S23P probably damaging Het
Spef2 T C 15: 9,614,295 (GRCm39) K1217R probably damaging Het
St18 A C 1: 6,880,909 (GRCm39) probably benign Het
Tdrd6 T C 17: 43,939,218 (GRCm39) D610G possibly damaging Het
Tmem163 C A 1: 127,479,108 (GRCm39) R137L probably damaging Het
Tmem94 T A 11: 115,685,574 (GRCm39) D942E probably damaging Het
Ttn T A 2: 76,580,754 (GRCm39) I23380F possibly damaging Het
Uckl1 T A 2: 181,212,393 (GRCm39) probably null Het
Vav2 T C 2: 27,208,976 (GRCm39) D99G possibly damaging Het
Vmn2r30 T A 7: 7,337,259 (GRCm39) I126F probably benign Het
Zbtb41 A T 1: 139,351,301 (GRCm39) Q138L probably benign Het
Zfp599 T C 9: 22,169,361 (GRCm39) Y37C probably damaging Het
Zfp784 T A 7: 5,038,782 (GRCm39) T259S possibly damaging Het
Zfp954 T C 7: 7,118,837 (GRCm39) S236G probably benign Het
Zng1 A G 19: 24,925,458 (GRCm39) V166A possibly damaging Het
Other mutations in Myo18a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00089:Myo18a APN 11 77,738,764 (GRCm39) missense probably damaging 1.00
IGL00753:Myo18a APN 11 77,715,977 (GRCm39) missense probably damaging 1.00
IGL01137:Myo18a APN 11 77,718,655 (GRCm39) missense probably damaging 1.00
IGL01536:Myo18a APN 11 77,711,677 (GRCm39) missense probably damaging 1.00
IGL01642:Myo18a APN 11 77,755,558 (GRCm39) missense probably benign 0.07
IGL01728:Myo18a APN 11 77,668,682 (GRCm39) missense probably damaging 0.99
IGL01780:Myo18a APN 11 77,741,073 (GRCm39) missense probably benign 0.02
IGL02286:Myo18a APN 11 77,668,811 (GRCm39) nonsense probably null
IGL02350:Myo18a APN 11 77,741,073 (GRCm39) missense probably benign 0.02
IGL02357:Myo18a APN 11 77,741,073 (GRCm39) missense probably benign 0.02
IGL02420:Myo18a APN 11 77,709,519 (GRCm39) missense possibly damaging 0.81
IGL02643:Myo18a APN 11 77,668,998 (GRCm39) missense possibly damaging 0.67
IGL02667:Myo18a APN 11 77,748,678 (GRCm39) splice site probably benign
IGL02869:Myo18a APN 11 77,720,699 (GRCm39) splice site probably benign
IGL02869:Myo18a APN 11 77,755,612 (GRCm39) missense probably damaging 1.00
IGL02962:Myo18a APN 11 77,669,061 (GRCm39) missense probably damaging 1.00
IGL02963:Myo18a APN 11 77,732,844 (GRCm39) splice site probably benign
IGL03410:Myo18a APN 11 77,738,830 (GRCm39) missense probably damaging 0.99
IGL03050:Myo18a UTSW 11 77,709,596 (GRCm39) missense probably benign 0.00
R0022:Myo18a UTSW 11 77,734,059 (GRCm39) critical splice donor site probably null
R0064:Myo18a UTSW 11 77,738,170 (GRCm39) missense probably damaging 1.00
R0064:Myo18a UTSW 11 77,738,170 (GRCm39) missense probably damaging 1.00
R0098:Myo18a UTSW 11 77,736,591 (GRCm39) missense probably damaging 1.00
R0322:Myo18a UTSW 11 77,720,626 (GRCm39) missense probably damaging 1.00
R0373:Myo18a UTSW 11 77,711,868 (GRCm39) missense probably benign 0.01
R0379:Myo18a UTSW 11 77,741,632 (GRCm39) missense possibly damaging 0.84
R0513:Myo18a UTSW 11 77,702,420 (GRCm39) intron probably benign
R0688:Myo18a UTSW 11 77,714,966 (GRCm39) missense probably damaging 1.00
R0734:Myo18a UTSW 11 77,738,230 (GRCm39) missense probably damaging 1.00
R0790:Myo18a UTSW 11 77,731,535 (GRCm39) missense possibly damaging 0.95
R1099:Myo18a UTSW 11 77,709,727 (GRCm39) splice site probably null
R1103:Myo18a UTSW 11 77,714,156 (GRCm39) missense probably damaging 1.00
R1183:Myo18a UTSW 11 77,748,571 (GRCm39) missense probably damaging 1.00
R1216:Myo18a UTSW 11 77,709,473 (GRCm39) missense probably benign 0.35
R1331:Myo18a UTSW 11 77,732,405 (GRCm39) missense probably benign 0.28
R1479:Myo18a UTSW 11 77,733,020 (GRCm39) missense probably benign 0.04
R1742:Myo18a UTSW 11 77,732,293 (GRCm39) missense probably damaging 0.99
R1796:Myo18a UTSW 11 77,720,170 (GRCm39) missense possibly damaging 0.94
R1823:Myo18a UTSW 11 77,715,923 (GRCm39) splice site probably benign
R1827:Myo18a UTSW 11 77,709,597 (GRCm39) missense probably benign 0.00
R2033:Myo18a UTSW 11 77,733,925 (GRCm39) splice site probably null
R2043:Myo18a UTSW 11 77,714,189 (GRCm39) missense probably damaging 0.99
R2105:Myo18a UTSW 11 77,741,060 (GRCm39) missense probably benign
R2191:Myo18a UTSW 11 77,709,441 (GRCm39) missense probably damaging 0.99
R2264:Myo18a UTSW 11 77,710,798 (GRCm39) splice site probably benign
R2370:Myo18a UTSW 11 77,668,596 (GRCm39) missense probably benign 0.03
R3015:Myo18a UTSW 11 77,749,846 (GRCm39) intron probably benign
R3433:Myo18a UTSW 11 77,708,870 (GRCm39) splice site probably null
R3739:Myo18a UTSW 11 77,736,441 (GRCm39) missense probably damaging 1.00
R3825:Myo18a UTSW 11 77,668,292 (GRCm39) missense possibly damaging 0.47
R4056:Myo18a UTSW 11 77,702,839 (GRCm39) missense possibly damaging 0.72
R4163:Myo18a UTSW 11 77,720,534 (GRCm39) missense possibly damaging 0.72
R4184:Myo18a UTSW 11 77,748,613 (GRCm39) missense probably damaging 1.00
R4620:Myo18a UTSW 11 77,708,773 (GRCm39) missense possibly damaging 0.93
R4628:Myo18a UTSW 11 77,714,962 (GRCm39) missense probably damaging 1.00
R4647:Myo18a UTSW 11 77,708,776 (GRCm39) missense probably damaging 1.00
R4701:Myo18a UTSW 11 77,708,491 (GRCm39) missense probably damaging 1.00
R4729:Myo18a UTSW 11 77,668,511 (GRCm39) splice site probably null
R4731:Myo18a UTSW 11 77,720,585 (GRCm39) missense probably benign 0.00
R4739:Myo18a UTSW 11 77,714,149 (GRCm39) missense probably damaging 1.00
R4814:Myo18a UTSW 11 77,750,062 (GRCm39) intron probably benign
R4889:Myo18a UTSW 11 77,723,238 (GRCm39) missense probably damaging 1.00
R4988:Myo18a UTSW 11 77,736,347 (GRCm39) critical splice donor site probably null
R5172:Myo18a UTSW 11 77,714,924 (GRCm39) missense probably damaging 1.00
R5177:Myo18a UTSW 11 77,755,668 (GRCm39) utr 3 prime probably benign
R5394:Myo18a UTSW 11 77,744,176 (GRCm39) missense probably benign 0.14
R5643:Myo18a UTSW 11 77,745,513 (GRCm39) missense probably benign 0.12
R5808:Myo18a UTSW 11 77,720,127 (GRCm39) missense probably benign 0.34
R5871:Myo18a UTSW 11 77,723,306 (GRCm39) missense probably damaging 1.00
R5936:Myo18a UTSW 11 77,709,039 (GRCm39) missense probably damaging 1.00
R6017:Myo18a UTSW 11 77,732,349 (GRCm39) missense probably damaging 0.96
R6053:Myo18a UTSW 11 77,709,002 (GRCm39) missense probably damaging 1.00
R6271:Myo18a UTSW 11 77,711,635 (GRCm39) missense probably damaging 1.00
R6486:Myo18a UTSW 11 77,755,648 (GRCm39) missense possibly damaging 0.83
R6558:Myo18a UTSW 11 77,741,678 (GRCm39) missense probably damaging 0.99
R6884:Myo18a UTSW 11 77,709,875 (GRCm39) missense possibly damaging 0.67
R6983:Myo18a UTSW 11 77,736,341 (GRCm39) missense probably benign 0.06
R6993:Myo18a UTSW 11 77,749,900 (GRCm39) intron probably benign
R7071:Myo18a UTSW 11 77,714,653 (GRCm39) missense probably damaging 1.00
R7074:Myo18a UTSW 11 77,733,387 (GRCm39) missense probably benign 0.03
R7238:Myo18a UTSW 11 77,733,059 (GRCm39) missense probably damaging 0.96
R7328:Myo18a UTSW 11 77,698,737 (GRCm39) missense
R7527:Myo18a UTSW 11 77,734,406 (GRCm39) missense probably benign 0.00
R7598:Myo18a UTSW 11 77,738,172 (GRCm39) missense probably damaging 1.00
R7671:Myo18a UTSW 11 77,750,246 (GRCm39) missense
R7958:Myo18a UTSW 11 77,732,383 (GRCm39) missense probably damaging 1.00
R8098:Myo18a UTSW 11 77,736,227 (GRCm39) missense probably damaging 0.97
R8168:Myo18a UTSW 11 77,711,968 (GRCm39) missense probably damaging 0.99
R8318:Myo18a UTSW 11 77,714,215 (GRCm39) missense probably benign 0.02
R8685:Myo18a UTSW 11 77,745,520 (GRCm39) missense probably benign 0.00
R8778:Myo18a UTSW 11 77,714,150 (GRCm39) missense probably damaging 1.00
R9023:Myo18a UTSW 11 77,718,477 (GRCm39) missense probably damaging 1.00
R9059:Myo18a UTSW 11 77,668,899 (GRCm39) missense possibly damaging 0.78
R9186:Myo18a UTSW 11 77,749,847 (GRCm39) missense
R9321:Myo18a UTSW 11 77,733,370 (GRCm39) missense probably damaging 0.97
R9357:Myo18a UTSW 11 77,733,014 (GRCm39) missense probably damaging 1.00
R9407:Myo18a UTSW 11 77,709,596 (GRCm39) missense probably benign 0.00
R9430:Myo18a UTSW 11 77,709,410 (GRCm39) missense possibly damaging 0.64
R9576:Myo18a UTSW 11 77,709,827 (GRCm39) missense probably damaging 1.00
R9585:Myo18a UTSW 11 77,709,495 (GRCm39) missense probably benign 0.06
R9698:Myo18a UTSW 11 77,720,681 (GRCm39) missense probably damaging 0.99
R9743:Myo18a UTSW 11 77,723,304 (GRCm39) missense probably benign 0.10
R9777:Myo18a UTSW 11 77,733,080 (GRCm39) missense possibly damaging 0.94
Y5407:Myo18a UTSW 11 77,668,641 (GRCm39) missense probably benign 0.44
Z1177:Myo18a UTSW 11 77,732,821 (GRCm39) missense probably damaging 1.00
Z1187:Myo18a UTSW 11 77,744,643 (GRCm39) missense possibly damaging 0.95
Predicted Primers PCR Primer
(F):5'- ACCTCTAGCATCCCTTAGCCATAGC -3'
(R):5'- TGTCAGGACTGAACTGTCCCCTAC -3'

Sequencing Primer
(F):5'- CCCTTAGCCATAGCTGAGTTGG -3'
(R):5'- CATATACTTAACAGGACTTGGGGAC -3'
Posted On 2014-05-14