Incidental Mutation 'R6980:Mdn1'
ID 543749
Institutional Source Beutler Lab
Gene Symbol Mdn1
Ensembl Gene ENSMUSG00000058006
Gene Name midasin AAA ATPase 1
Synonyms 4833432B22Rik, D4Abb1e, LOC213784
MMRRC Submission 045088-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R6980 (G1)
Quality Score 225.009
Status Not validated
Chromosome 4
Chromosomal Location 32657119-32775217 bp(+) (GRCm39)
Type of Mutation critical splice donor site (1 bp from exon)
DNA Base Change (assembly) G to A at 32726942 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000136222 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071642] [ENSMUST00000178134]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000071642
SMART Domains Protein: ENSMUSP00000071569
Gene: ENSMUSG00000058006

DomainStartEndE-ValueType
low complexity region 48 75 N/A INTRINSIC
low complexity region 258 270 N/A INTRINSIC
Pfam:AAA_5 324 459 7.4e-19 PFAM
AAA 666 908 1.06e-6 SMART
AAA 1072 1217 2.09e-1 SMART
AAA 1378 1544 8.27e-9 SMART
AAA 1740 1893 6.78e-2 SMART
AAA 2053 2309 1.62e0 SMART
low complexity region 3181 3193 N/A INTRINSIC
low complexity region 3541 3552 N/A INTRINSIC
low complexity region 3557 3565 N/A INTRINSIC
low complexity region 4189 4203 N/A INTRINSIC
low complexity region 4339 4353 N/A INTRINSIC
low complexity region 4672 4681 N/A INTRINSIC
low complexity region 4735 4756 N/A INTRINSIC
low complexity region 4769 4790 N/A INTRINSIC
low complexity region 4886 4905 N/A INTRINSIC
low complexity region 4924 4937 N/A INTRINSIC
coiled coil region 4957 4983 N/A INTRINSIC
low complexity region 5000 5017 N/A INTRINSIC
low complexity region 5176 5192 N/A INTRINSIC
low complexity region 5315 5329 N/A INTRINSIC
VWA 5375 5556 2.73e-6 SMART
Predicted Effect probably null
Transcript: ENSMUST00000178134
SMART Domains Protein: ENSMUSP00000136222
Gene: ENSMUSG00000058006

DomainStartEndE-ValueType
low complexity region 48 75 N/A INTRINSIC
low complexity region 258 270 N/A INTRINSIC
Pfam:AAA_5 324 459 4.4e-19 PFAM
AAA 666 908 1.06e-6 SMART
AAA 1072 1217 2.09e-1 SMART
AAA 1378 1544 8.27e-9 SMART
AAA 1740 1893 6.78e-2 SMART
AAA 2053 2309 1.62e0 SMART
low complexity region 3181 3193 N/A INTRINSIC
low complexity region 3541 3552 N/A INTRINSIC
low complexity region 3557 3565 N/A INTRINSIC
low complexity region 4189 4203 N/A INTRINSIC
low complexity region 4339 4353 N/A INTRINSIC
low complexity region 4667 4676 N/A INTRINSIC
low complexity region 4730 4751 N/A INTRINSIC
low complexity region 4764 4785 N/A INTRINSIC
low complexity region 4881 4900 N/A INTRINSIC
low complexity region 4919 4932 N/A INTRINSIC
coiled coil region 4952 4978 N/A INTRINSIC
low complexity region 4992 5010 N/A INTRINSIC
low complexity region 5169 5185 N/A INTRINSIC
low complexity region 5308 5322 N/A INTRINSIC
VWA 5368 5549 2.73e-6 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.2%
Validation Efficiency
Allele List at MGI

All alleles(29) : Targeted, other(2) Gene trapped(27)

Other mutations in this stock
Total: 88 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca2 C A 2: 25,330,878 (GRCm39) R1189S possibly damaging Het
Abcf2 T C 5: 24,770,970 (GRCm39) Q594R probably benign Het
Abhd18 G A 3: 40,888,215 (GRCm39) S353N probably benign Het
Adrb1 G T 19: 56,712,046 (GRCm39) A415S probably benign Het
Art2b T C 7: 101,229,680 (GRCm39) N73S probably benign Het
BC028528 CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT 3: 95,795,448 (GRCm39) probably benign Het
BC028528 CACTGGTTCTGTGGT CACTGGTTCTGTGGTTACTGGTTCTGTGGT 3: 95,795,480 (GRCm39) probably benign Het
BC028528 ACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTC ACTGGTTCTGTGGTCTCTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTC 3: 95,795,451 (GRCm39) probably benign Het
Cacna1a A G 8: 85,338,914 (GRCm39) M1753V possibly damaging Het
Cbx8 A T 11: 118,930,287 (GRCm39) I102N possibly damaging Het
Ccdc178 T A 18: 22,238,620 (GRCm39) E332D probably benign Het
Cdhr17 T A 5: 17,031,944 (GRCm39) V533D possibly damaging Het
Cfap74 G A 4: 155,550,809 (GRCm39) probably benign Het
Chat A T 14: 32,146,111 (GRCm39) M354K probably benign Het
Cmas A G 6: 142,702,526 (GRCm39) T10A probably damaging Het
Cyb561d1 A T 3: 108,107,475 (GRCm39) L51H probably benign Het
D030056L22Rik A T 19: 18,694,629 (GRCm39) N128I probably damaging Het
D130043K22Rik G T 13: 25,048,764 (GRCm39) A423S probably damaging Het
Dnah14 T C 1: 181,475,795 (GRCm39) I1349T probably benign Het
Dnajb3 T G 1: 88,132,736 (GRCm39) D222A probably damaging Het
Dtx1 T C 5: 120,819,422 (GRCm39) E592G probably damaging Het
Dzank1 C T 2: 144,332,056 (GRCm39) G427R possibly damaging Het
E130308A19Rik A C 4: 59,719,991 (GRCm39) K508Q probably damaging Het
Eif4e1b T A 13: 54,931,916 (GRCm39) probably null Het
Ell2 A G 13: 75,904,495 (GRCm39) M159V probably null Het
Eml4 G A 17: 83,758,446 (GRCm39) V377I probably benign Het
Fryl A T 5: 73,207,773 (GRCm39) S2466T probably benign Het
Gfpt1 C A 6: 87,054,071 (GRCm39) T426K probably damaging Het
Gm49355 T C 14: 12,307,173 (GRCm38) probably benign Het
Gm5114 T C 7: 39,058,624 (GRCm39) I332V probably benign Het
Gpr15 T A 16: 58,539,105 (GRCm39) probably benign Het
Gpr179 T C 11: 97,225,684 (GRCm39) E2157G probably benign Het
Gramd4 A G 15: 86,016,170 (GRCm39) N482S probably benign Het
Hfm1 A T 5: 107,028,343 (GRCm39) I829K probably benign Het
Hydin A T 8: 111,139,916 (GRCm39) E728D possibly damaging Het
Ifngr2 T A 16: 91,356,895 (GRCm39) V143E probably damaging Het
Ift172 T C 5: 31,414,730 (GRCm39) D1390G probably benign Het
Kdf1 A T 4: 133,256,138 (GRCm39) D285V probably damaging Het
Mast4 C T 13: 102,941,155 (GRCm39) V301I probably damaging Het
Megf11 A G 9: 64,613,132 (GRCm39) E1016G probably damaging Het
Mixl1 G A 1: 180,524,453 (GRCm39) A42V possibly damaging Het
Mpp2 A G 11: 101,950,154 (GRCm39) W567R probably damaging Het
Mrgpra6 A G 7: 46,838,697 (GRCm39) L136P probably damaging Het
Mroh7 T A 4: 106,557,434 (GRCm39) I759L probably benign Het
Nrxn2 A G 19: 6,500,609 (GRCm39) D277G probably benign Het
Nup210l A T 3: 90,027,234 (GRCm39) K205N probably benign Het
Or4g17 A G 2: 111,209,620 (GRCm39) I92V possibly damaging Het
Or4p4b-ps1 A G 2: 88,453,939 (GRCm39) *97W probably null Het
Or52e19b T C 7: 103,032,303 (GRCm39) E302G probably benign Het
Or5al6 A T 2: 85,976,681 (GRCm39) Y132* probably null Het
Oxnad1 C T 14: 31,807,576 (GRCm39) probably benign Het
Pamr1 C T 2: 102,472,549 (GRCm39) T616I probably benign Het
Pcdhgb5 C T 18: 37,866,592 (GRCm39) H796Y possibly damaging Het
Pdlim7 G T 13: 55,656,041 (GRCm39) D126E probably benign Het
Pfdn2 C T 1: 171,185,465 (GRCm39) probably benign Het
Piezo2 T A 18: 63,216,032 (GRCm39) probably null Het
Pms2 A T 5: 143,848,842 (GRCm39) I43L probably benign Het
Prex2 T A 1: 11,232,487 (GRCm39) S851R probably benign Het
Ptpn4 T A 1: 119,671,151 (GRCm39) E202D possibly damaging Het
Rnf40 T A 7: 127,193,849 (GRCm39) V455E probably damaging Het
Rp1l1 A G 14: 64,266,169 (GRCm39) N585S probably benign Het
Rrp12 A G 19: 41,878,582 (GRCm39) S188P probably damaging Het
Rsbn1l T A 5: 21,101,482 (GRCm39) H686L probably benign Het
Runx2 C T 17: 45,046,203 (GRCm39) V107I possibly damaging Het
Rusc2 A G 4: 43,422,846 (GRCm39) I994M probably benign Het
Ryr1 T A 7: 28,808,812 (GRCm39) D420V probably benign Het
Sash1 T C 10: 8,605,612 (GRCm39) Q926R probably benign Het
Scgb3a2 T A 18: 43,897,499 (GRCm39) I6N probably damaging Het
Sdc3 T A 4: 130,544,233 (GRCm39) probably benign Het
Sik2 A G 9: 50,808,755 (GRCm39) V658A probably benign Het
Slc25a39 A G 11: 102,296,601 (GRCm39) V81A probably damaging Het
Snai2 T A 16: 14,526,113 (GRCm39) S255T possibly damaging Het
Sorbs1 A T 19: 40,316,060 (GRCm39) Y371* probably null Het
Spata31d1b A T 13: 59,863,236 (GRCm39) H128L probably benign Het
Spdl1 A T 11: 34,721,706 (GRCm39) M1K probably null Het
Tgm3 T A 2: 129,868,697 (GRCm39) N211K probably benign Het
Tmem116 T C 5: 121,606,050 (GRCm39) probably null Het
Tmem132e T A 11: 82,329,212 (GRCm39) probably null Het
Tmem53 T C 4: 117,125,705 (GRCm39) C251R probably damaging Het
Trcg1 A C 9: 57,152,856 (GRCm39) D551A probably damaging Het
Trp63 T A 16: 25,620,843 (GRCm39) F12I probably benign Het
Ttn C T 2: 76,709,401 (GRCm39) probably null Het
Tubgcp4 T C 2: 121,025,946 (GRCm39) V596A probably benign Het
Ugt2a3 A C 5: 87,473,491 (GRCm39) H475Q probably damaging Het
Unc79 G A 12: 103,025,759 (GRCm39) R382K probably damaging Het
Vmn2r58 T C 7: 41,513,662 (GRCm39) H327R possibly damaging Het
Vmn2r7 G A 3: 64,623,987 (GRCm39) T111I possibly damaging Het
Zfp318 T A 17: 46,708,138 (GRCm39) Y399N probably damaging Het
Other mutations in Mdn1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00088:Mdn1 APN 4 32,723,651 (GRCm39) missense probably damaging 1.00
IGL00426:Mdn1 APN 4 32,719,214 (GRCm39) missense possibly damaging 0.91
IGL00570:Mdn1 APN 4 32,735,719 (GRCm39) missense probably benign
IGL00573:Mdn1 APN 4 32,666,619 (GRCm39) critical splice donor site probably null
IGL00983:Mdn1 APN 4 32,735,525 (GRCm39) missense probably damaging 1.00
IGL01288:Mdn1 APN 4 32,730,864 (GRCm39) missense probably benign 0.00
IGL01359:Mdn1 APN 4 32,743,686 (GRCm39) missense probably benign 0.10
IGL01457:Mdn1 APN 4 32,715,922 (GRCm39) missense possibly damaging 0.82
IGL01530:Mdn1 APN 4 32,711,938 (GRCm39) splice site probably benign
IGL01684:Mdn1 APN 4 32,726,857 (GRCm39) missense probably benign
IGL01753:Mdn1 APN 4 32,708,483 (GRCm39) missense probably benign
IGL01901:Mdn1 APN 4 32,669,591 (GRCm39) missense probably damaging 1.00
IGL01952:Mdn1 APN 4 32,723,657 (GRCm39) missense possibly damaging 0.82
IGL01960:Mdn1 APN 4 32,758,393 (GRCm39) missense probably benign 0.14
IGL02019:Mdn1 APN 4 32,749,948 (GRCm39) missense possibly damaging 0.93
IGL02100:Mdn1 APN 4 32,715,708 (GRCm39) missense possibly damaging 0.90
IGL02117:Mdn1 APN 4 32,709,364 (GRCm39) missense probably benign 0.00
IGL02154:Mdn1 APN 4 32,740,395 (GRCm39) missense probably benign 0.35
IGL02216:Mdn1 APN 4 32,739,092 (GRCm39) missense probably benign 0.03
IGL02371:Mdn1 APN 4 32,676,860 (GRCm39) splice site probably benign
IGL02396:Mdn1 APN 4 32,700,120 (GRCm39) missense probably damaging 0.99
IGL02454:Mdn1 APN 4 32,694,674 (GRCm39) critical splice donor site probably null
IGL02502:Mdn1 APN 4 32,670,579 (GRCm39) missense possibly damaging 0.69
IGL02883:Mdn1 APN 4 32,763,199 (GRCm39) missense probably benign 0.05
IGL02946:Mdn1 APN 4 32,734,366 (GRCm39) missense probably damaging 0.98
IGL02950:Mdn1 APN 4 32,713,360 (GRCm39) splice site probably benign
IGL03076:Mdn1 APN 4 32,735,564 (GRCm39) missense probably damaging 0.97
IGL03129:Mdn1 APN 4 32,729,994 (GRCm39) missense possibly damaging 0.47
IGL03234:Mdn1 APN 4 32,732,842 (GRCm39) missense probably benign 0.06
3-1:Mdn1 UTSW 4 32,725,967 (GRCm39) critical splice donor site probably null
IGL03046:Mdn1 UTSW 4 32,694,495 (GRCm39) missense possibly damaging 0.73
P0035:Mdn1 UTSW 4 32,749,934 (GRCm39) missense probably benign 0.05
PIT4508001:Mdn1 UTSW 4 32,719,223 (GRCm39) missense probably damaging 0.97
PIT4618001:Mdn1 UTSW 4 32,746,527 (GRCm39) missense probably benign 0.20
R0008:Mdn1 UTSW 4 32,718,317 (GRCm39) missense possibly damaging 0.47
R0110:Mdn1 UTSW 4 32,738,619 (GRCm39) missense probably benign 0.20
R0125:Mdn1 UTSW 4 32,729,956 (GRCm39) missense probably damaging 0.98
R0257:Mdn1 UTSW 4 32,693,534 (GRCm39) missense probably damaging 0.99
R0266:Mdn1 UTSW 4 32,741,835 (GRCm39) missense probably damaging 0.99
R0349:Mdn1 UTSW 4 32,750,318 (GRCm39) missense probably damaging 1.00
R0362:Mdn1 UTSW 4 32,746,439 (GRCm39) critical splice acceptor site probably null
R0421:Mdn1 UTSW 4 32,684,707 (GRCm39) missense probably benign 0.39
R0450:Mdn1 UTSW 4 32,738,619 (GRCm39) missense probably benign 0.20
R0465:Mdn1 UTSW 4 32,699,204 (GRCm39) splice site probably benign
R0469:Mdn1 UTSW 4 32,738,619 (GRCm39) missense probably benign 0.20
R0477:Mdn1 UTSW 4 32,750,928 (GRCm39) missense probably benign 0.02
R0481:Mdn1 UTSW 4 32,767,182 (GRCm39) splice site probably benign
R0504:Mdn1 UTSW 4 32,698,916 (GRCm39) splice site probably benign
R0522:Mdn1 UTSW 4 32,672,837 (GRCm39) missense probably benign 0.09
R0550:Mdn1 UTSW 4 32,730,479 (GRCm39) missense probably benign 0.13
R0607:Mdn1 UTSW 4 32,732,829 (GRCm39) missense probably benign 0.36
R0607:Mdn1 UTSW 4 32,712,014 (GRCm39) missense probably damaging 1.00
R0664:Mdn1 UTSW 4 32,768,011 (GRCm39) nonsense probably null
R0701:Mdn1 UTSW 4 32,699,263 (GRCm39) missense probably benign 0.00
R0801:Mdn1 UTSW 4 32,668,895 (GRCm39) missense probably benign 0.04
R0841:Mdn1 UTSW 4 32,752,032 (GRCm39) missense probably benign 0.23
R0849:Mdn1 UTSW 4 32,741,835 (GRCm39) missense probably damaging 0.99
R0893:Mdn1 UTSW 4 32,701,713 (GRCm39) missense probably benign 0.01
R1114:Mdn1 UTSW 4 32,746,568 (GRCm39) critical splice donor site probably null
R1137:Mdn1 UTSW 4 32,694,511 (GRCm39) missense probably damaging 1.00
R1185:Mdn1 UTSW 4 32,735,576 (GRCm39) missense possibly damaging 0.94
R1185:Mdn1 UTSW 4 32,735,576 (GRCm39) missense possibly damaging 0.94
R1185:Mdn1 UTSW 4 32,735,576 (GRCm39) missense possibly damaging 0.94
R1257:Mdn1 UTSW 4 32,667,089 (GRCm39) critical splice acceptor site probably null
R1356:Mdn1 UTSW 4 32,700,334 (GRCm39) splice site probably benign
R1466:Mdn1 UTSW 4 32,730,788 (GRCm39) missense probably benign 0.28
R1466:Mdn1 UTSW 4 32,730,788 (GRCm39) missense probably benign 0.28
R1518:Mdn1 UTSW 4 32,739,977 (GRCm39) missense probably damaging 1.00
R1569:Mdn1 UTSW 4 32,723,501 (GRCm39) missense probably null 0.10
R1574:Mdn1 UTSW 4 32,722,315 (GRCm39) missense probably benign
R1574:Mdn1 UTSW 4 32,722,315 (GRCm39) missense probably benign
R1591:Mdn1 UTSW 4 32,700,092 (GRCm39) missense possibly damaging 0.65
R1678:Mdn1 UTSW 4 32,663,050 (GRCm39) missense probably damaging 0.99
R1696:Mdn1 UTSW 4 32,700,417 (GRCm39) missense possibly damaging 0.91
R1707:Mdn1 UTSW 4 32,693,504 (GRCm39) missense probably damaging 1.00
R1749:Mdn1 UTSW 4 32,773,952 (GRCm39) missense probably damaging 1.00
R1780:Mdn1 UTSW 4 32,700,103 (GRCm39) missense probably damaging 1.00
R1833:Mdn1 UTSW 4 32,720,761 (GRCm39) missense probably damaging 0.97
R1858:Mdn1 UTSW 4 32,730,881 (GRCm39) missense probably benign 0.17
R1870:Mdn1 UTSW 4 32,763,339 (GRCm39) missense probably damaging 1.00
R1887:Mdn1 UTSW 4 32,742,540 (GRCm39) missense probably damaging 1.00
R1909:Mdn1 UTSW 4 32,760,839 (GRCm39) small deletion probably benign
R2075:Mdn1 UTSW 4 32,716,058 (GRCm39) missense probably benign 0.03
R2103:Mdn1 UTSW 4 32,738,712 (GRCm39) missense possibly damaging 0.75
R2104:Mdn1 UTSW 4 32,743,843 (GRCm39) splice site probably null
R2110:Mdn1 UTSW 4 32,700,409 (GRCm39) missense probably damaging 1.00
R2111:Mdn1 UTSW 4 32,700,409 (GRCm39) missense probably damaging 1.00
R2206:Mdn1 UTSW 4 32,716,271 (GRCm39) missense possibly damaging 0.71
R2221:Mdn1 UTSW 4 32,763,306 (GRCm39) missense probably benign 0.37
R2240:Mdn1 UTSW 4 32,765,701 (GRCm39) missense possibly damaging 0.90
R2351:Mdn1 UTSW 4 32,750,010 (GRCm39) missense probably benign 0.21
R2421:Mdn1 UTSW 4 32,723,621 (GRCm39) missense probably damaging 0.96
R3036:Mdn1 UTSW 4 32,750,013 (GRCm39) missense probably damaging 0.99
R3434:Mdn1 UTSW 4 32,733,726 (GRCm39) critical splice donor site probably null
R3435:Mdn1 UTSW 4 32,733,726 (GRCm39) critical splice donor site probably null
R3783:Mdn1 UTSW 4 32,720,818 (GRCm39) missense probably benign 0.01
R3811:Mdn1 UTSW 4 32,693,506 (GRCm39) nonsense probably null
R3973:Mdn1 UTSW 4 32,722,363 (GRCm39) missense probably benign 0.00
R4154:Mdn1 UTSW 4 32,707,475 (GRCm39) missense probably damaging 0.96
R4372:Mdn1 UTSW 4 32,743,809 (GRCm39) missense probably benign 0.03
R4393:Mdn1 UTSW 4 32,754,482 (GRCm39) missense possibly damaging 0.48
R4438:Mdn1 UTSW 4 32,704,635 (GRCm39) missense probably damaging 1.00
R4471:Mdn1 UTSW 4 32,668,860 (GRCm39) missense probably benign 0.00
R4509:Mdn1 UTSW 4 32,715,883 (GRCm39) missense probably damaging 1.00
R4538:Mdn1 UTSW 4 32,722,334 (GRCm39) missense probably damaging 1.00
R4557:Mdn1 UTSW 4 32,754,437 (GRCm39) missense probably damaging 1.00
R4570:Mdn1 UTSW 4 32,741,812 (GRCm39) missense probably damaging 1.00
R4591:Mdn1 UTSW 4 32,707,636 (GRCm39) missense probably damaging 1.00
R4658:Mdn1 UTSW 4 32,730,749 (GRCm39) splice site probably null
R4667:Mdn1 UTSW 4 32,679,572 (GRCm39) missense probably damaging 1.00
R4684:Mdn1 UTSW 4 32,666,430 (GRCm39) missense probably damaging 1.00
R4778:Mdn1 UTSW 4 32,683,583 (GRCm39) nonsense probably null
R4807:Mdn1 UTSW 4 32,685,651 (GRCm39) splice site probably null
R4923:Mdn1 UTSW 4 32,671,608 (GRCm39) missense possibly damaging 0.89
R4951:Mdn1 UTSW 4 32,707,459 (GRCm39) missense probably damaging 1.00
R4963:Mdn1 UTSW 4 32,756,512 (GRCm39) missense probably benign 0.00
R4971:Mdn1 UTSW 4 32,739,827 (GRCm39) missense probably damaging 1.00
R4973:Mdn1 UTSW 4 32,734,418 (GRCm39) missense probably benign 0.01
R5122:Mdn1 UTSW 4 32,670,593 (GRCm39) missense probably damaging 1.00
R5159:Mdn1 UTSW 4 32,774,008 (GRCm39) missense possibly damaging 0.93
R5164:Mdn1 UTSW 4 32,759,011 (GRCm39) splice site probably null
R5215:Mdn1 UTSW 4 32,741,418 (GRCm39) missense possibly damaging 0.78
R5217:Mdn1 UTSW 4 32,723,690 (GRCm39) missense probably damaging 0.98
R5219:Mdn1 UTSW 4 32,723,690 (GRCm39) missense probably damaging 0.98
R5365:Mdn1 UTSW 4 32,723,690 (GRCm39) missense probably damaging 0.98
R5366:Mdn1 UTSW 4 32,723,690 (GRCm39) missense probably damaging 0.98
R5368:Mdn1 UTSW 4 32,723,690 (GRCm39) missense probably damaging 0.98
R5445:Mdn1 UTSW 4 32,723,690 (GRCm39) missense probably damaging 0.98
R5462:Mdn1 UTSW 4 32,720,897 (GRCm39) missense probably benign
R5522:Mdn1 UTSW 4 32,685,783 (GRCm39) missense probably damaging 1.00
R5525:Mdn1 UTSW 4 32,767,961 (GRCm39) missense possibly damaging 0.73
R5578:Mdn1 UTSW 4 32,728,167 (GRCm39) missense probably benign 0.04
R5605:Mdn1 UTSW 4 32,765,664 (GRCm39) missense probably benign
R5621:Mdn1 UTSW 4 32,716,371 (GRCm39) missense possibly damaging 0.46
R5636:Mdn1 UTSW 4 32,695,480 (GRCm39) missense probably damaging 1.00
R5650:Mdn1 UTSW 4 32,667,467 (GRCm39) splice site probably null
R5780:Mdn1 UTSW 4 32,722,950 (GRCm39) missense probably benign 0.02
R5838:Mdn1 UTSW 4 32,754,547 (GRCm39) missense probably damaging 0.99
R5857:Mdn1 UTSW 4 32,670,646 (GRCm39) missense probably benign 0.09
R5895:Mdn1 UTSW 4 32,695,400 (GRCm39) missense probably damaging 1.00
R5943:Mdn1 UTSW 4 32,678,330 (GRCm39) missense probably damaging 1.00
R6008:Mdn1 UTSW 4 32,741,073 (GRCm39) missense probably damaging 1.00
R6013:Mdn1 UTSW 4 32,715,713 (GRCm39) missense probably damaging 1.00
R6075:Mdn1 UTSW 4 32,689,581 (GRCm39) missense possibly damaging 0.48
R6151:Mdn1 UTSW 4 32,684,735 (GRCm39) missense probably damaging 1.00
R6163:Mdn1 UTSW 4 32,716,040 (GRCm39) missense probably damaging 1.00
R6181:Mdn1 UTSW 4 32,715,953 (GRCm39) missense probably damaging 1.00
R6211:Mdn1 UTSW 4 32,696,269 (GRCm39) missense probably benign 0.12
R6249:Mdn1 UTSW 4 32,708,484 (GRCm39) missense possibly damaging 0.85
R6251:Mdn1 UTSW 4 32,748,590 (GRCm39) missense probably benign 0.13
R6253:Mdn1 UTSW 4 32,749,593 (GRCm39) missense probably benign 0.25
R6273:Mdn1 UTSW 4 32,715,979 (GRCm39) missense probably benign 0.01
R6297:Mdn1 UTSW 4 32,730,054 (GRCm39) nonsense probably null
R6384:Mdn1 UTSW 4 32,670,607 (GRCm39) missense probably damaging 1.00
R6463:Mdn1 UTSW 4 32,773,308 (GRCm39) missense probably damaging 1.00
R6528:Mdn1 UTSW 4 32,713,780 (GRCm39) missense probably damaging 1.00
R6688:Mdn1 UTSW 4 32,774,041 (GRCm39) missense possibly damaging 0.74
R6762:Mdn1 UTSW 4 32,676,786 (GRCm39) missense possibly damaging 0.50
R6794:Mdn1 UTSW 4 32,741,893 (GRCm39) missense probably damaging 1.00
R6894:Mdn1 UTSW 4 32,748,614 (GRCm39) missense possibly damaging 0.75
R6935:Mdn1 UTSW 4 32,774,041 (GRCm39) missense possibly damaging 0.74
R6995:Mdn1 UTSW 4 32,733,374 (GRCm39) missense probably benign 0.03
R7048:Mdn1 UTSW 4 32,767,969 (GRCm39) missense probably benign 0.00
R7082:Mdn1 UTSW 4 32,762,341 (GRCm39) missense probably benign
R7158:Mdn1 UTSW 4 32,725,121 (GRCm39) missense probably benign 0.09
R7166:Mdn1 UTSW 4 32,746,446 (GRCm39) missense probably damaging 1.00
R7168:Mdn1 UTSW 4 32,719,184 (GRCm39) missense probably damaging 1.00
R7175:Mdn1 UTSW 4 32,694,634 (GRCm39) missense probably damaging 1.00
R7195:Mdn1 UTSW 4 32,701,823 (GRCm39) missense probably damaging 1.00
R7250:Mdn1 UTSW 4 32,695,427 (GRCm39) missense probably damaging 1.00
R7274:Mdn1 UTSW 4 32,725,944 (GRCm39) missense probably benign 0.12
R7330:Mdn1 UTSW 4 32,723,685 (GRCm39) missense probably benign 0.16
R7363:Mdn1 UTSW 4 32,691,729 (GRCm39) missense probably damaging 0.99
R7369:Mdn1 UTSW 4 32,773,375 (GRCm39) missense probably damaging 0.99
R7452:Mdn1 UTSW 4 32,739,030 (GRCm39) missense possibly damaging 0.87
R7523:Mdn1 UTSW 4 32,667,270 (GRCm39) critical splice acceptor site probably null
R7594:Mdn1 UTSW 4 32,696,359 (GRCm39) missense probably benign 0.27
R7605:Mdn1 UTSW 4 32,694,599 (GRCm39) missense probably damaging 1.00
R7661:Mdn1 UTSW 4 32,691,229 (GRCm39) missense probably benign 0.08
R7689:Mdn1 UTSW 4 32,739,912 (GRCm39) missense probably damaging 1.00
R7699:Mdn1 UTSW 4 32,741,344 (GRCm39) missense probably damaging 1.00
R7700:Mdn1 UTSW 4 32,741,344 (GRCm39) missense probably damaging 1.00
R7714:Mdn1 UTSW 4 32,722,360 (GRCm39) missense possibly damaging 0.75
R7718:Mdn1 UTSW 4 32,718,420 (GRCm39) missense probably damaging 1.00
R7762:Mdn1 UTSW 4 32,734,421 (GRCm39) missense probably benign
R7787:Mdn1 UTSW 4 32,741,794 (GRCm39) missense probably damaging 1.00
R8111:Mdn1 UTSW 4 32,674,003 (GRCm39) missense possibly damaging 0.81
R8222:Mdn1 UTSW 4 32,707,477 (GRCm39) missense probably benign 0.09
R8246:Mdn1 UTSW 4 32,657,284 (GRCm39) missense probably benign 0.06
R8267:Mdn1 UTSW 4 32,742,485 (GRCm39) missense possibly damaging 0.82
R8286:Mdn1 UTSW 4 32,731,960 (GRCm39) missense possibly damaging 0.91
R8305:Mdn1 UTSW 4 32,725,107 (GRCm39) missense probably benign
R8318:Mdn1 UTSW 4 32,735,897 (GRCm39) critical splice donor site probably null
R8379:Mdn1 UTSW 4 32,756,453 (GRCm39) missense probably null 1.00
R8384:Mdn1 UTSW 4 32,765,680 (GRCm39) missense probably benign 0.05
R8514:Mdn1 UTSW 4 32,739,857 (GRCm39) missense probably damaging 1.00
R8560:Mdn1 UTSW 4 32,743,830 (GRCm39) missense probably benign 0.08
R8672:Mdn1 UTSW 4 32,768,793 (GRCm39) missense probably damaging 1.00
R8708:Mdn1 UTSW 4 32,725,854 (GRCm39) missense probably damaging 1.00
R8769:Mdn1 UTSW 4 32,751,390 (GRCm39) missense probably damaging 0.97
R8896:Mdn1 UTSW 4 32,678,328 (GRCm39) missense probably benign 0.28
R8918:Mdn1 UTSW 4 32,744,579 (GRCm39) nonsense probably null
R8920:Mdn1 UTSW 4 32,719,280 (GRCm39) missense probably damaging 1.00
R8966:Mdn1 UTSW 4 32,672,837 (GRCm39) nonsense probably null
R8997:Mdn1 UTSW 4 32,773,275 (GRCm39) missense probably damaging 1.00
R9120:Mdn1 UTSW 4 32,701,814 (GRCm39) missense probably damaging 1.00
R9129:Mdn1 UTSW 4 32,676,812 (GRCm39) missense probably benign 0.24
R9131:Mdn1 UTSW 4 32,762,275 (GRCm39) missense possibly damaging 0.69
R9200:Mdn1 UTSW 4 32,760,791 (GRCm39) missense probably benign 0.00
R9226:Mdn1 UTSW 4 32,694,612 (GRCm39) missense probably benign 0.25
R9235:Mdn1 UTSW 4 32,739,122 (GRCm39) missense probably benign 0.10
R9293:Mdn1 UTSW 4 32,707,579 (GRCm39) missense probably damaging 1.00
R9315:Mdn1 UTSW 4 32,760,911 (GRCm39) missense probably benign 0.00
R9338:Mdn1 UTSW 4 32,666,536 (GRCm39) missense probably benign 0.00
R9353:Mdn1 UTSW 4 32,693,504 (GRCm39) missense probably damaging 1.00
R9393:Mdn1 UTSW 4 32,713,825 (GRCm39) missense
R9420:Mdn1 UTSW 4 32,678,414 (GRCm39) missense probably damaging 1.00
R9475:Mdn1 UTSW 4 32,739,849 (GRCm39) missense possibly damaging 0.65
R9583:Mdn1 UTSW 4 32,741,372 (GRCm39) missense probably damaging 1.00
R9600:Mdn1 UTSW 4 32,684,723 (GRCm39) nonsense probably null
R9640:Mdn1 UTSW 4 32,754,539 (GRCm39) missense probably damaging 1.00
R9688:Mdn1 UTSW 4 32,745,590 (GRCm39) missense probably damaging 1.00
R9744:Mdn1 UTSW 4 32,715,711 (GRCm39) missense possibly damaging 0.91
X0066:Mdn1 UTSW 4 32,739,030 (GRCm39) missense probably damaging 1.00
Z1176:Mdn1 UTSW 4 32,696,244 (GRCm39) missense probably damaging 1.00
Z1176:Mdn1 UTSW 4 32,668,944 (GRCm39) missense probably damaging 1.00
Z1176:Mdn1 UTSW 4 32,667,102 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- GGCTCCGTGAGAGGATATTTAC -3'
(R):5'- GGGCCATTGTGAGGATACAG -3'

Sequencing Primer
(F):5'- GAGGATATTTACCTAGTGTGCTCAC -3'
(R):5'- CCATTGTGAGGATACAGAAACAGC -3'
Posted On 2019-05-13