Incidental Mutation 'R8177:Muc5ac'
ID 634421
Institutional Source Beutler Lab
Gene Symbol Muc5ac
Ensembl Gene ENSMUSG00000037974
Gene Name mucin 5, subtypes A and C, tracheobronchial/gastric
Synonyms MGM, 2210005L13Rik
MMRRC Submission 067602-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R8177 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 141788972-141819231 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) G to C at 141807331 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Glycine to Arginine at position 1460 (G1460R)
Ref Sequence ENSEMBL: ENSMUSP00000122353 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000041924] [ENSMUST00000155534] [ENSMUST00000163321]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000041924
AA Change: G1459R

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000039699
Gene: ENSMUSG00000037974
AA Change: G1459R

DomainStartEndE-ValueType
signal peptide 1 27 N/A INTRINSIC
VWD 69 226 4.19e-30 SMART
C8 258 334 1.34e-11 SMART
Pfam:TIL 337 393 1.6e-14 PFAM
VWC 395 462 8.6e-18 SMART
VWD 421 585 1.55e-33 SMART
C8 622 696 8.42e-36 SMART
Pfam:TIL 702 759 6.1e-9 PFAM
VWC 761 825 6.75e-1 SMART
VWC 863 905 4.06e-1 SMART
VWD 890 1050 1.51e-45 SMART
C8 1086 1160 2.78e-36 SMART
low complexity region 1315 1330 N/A INTRINSIC
low complexity region 1333 1366 N/A INTRINSIC
low complexity region 1371 1387 N/A INTRINSIC
Pfam:Mucin2_WxxW 1394 1482 2.3e-25 PFAM
low complexity region 1521 1532 N/A INTRINSIC
low complexity region 1536 1563 N/A INTRINSIC
low complexity region 1578 1595 N/A INTRINSIC
Pfam:Mucin2_WxxW 1604 1692 2.2e-27 PFAM
Pfam:Mucin2_WxxW 1765 1857 8.6e-27 PFAM
low complexity region 1875 1895 N/A INTRINSIC
low complexity region 1949 1968 N/A INTRINSIC
VWD 2030 2199 4.17e-48 SMART
C8 2242 2311 3.95e-9 SMART
VWC 2376 2439 1.04e-11 SMART
VWC 2479 2543 9.31e-5 SMART
CT 2625 2711 3.43e-32 SMART
low complexity region 2720 2733 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000155534
AA Change: G1460R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000122353
Gene: ENSMUSG00000037974
AA Change: G1460R

DomainStartEndE-ValueType
signal peptide 1 27 N/A INTRINSIC
VWD 69 226 4.19e-30 SMART
C8 258 334 1.34e-11 SMART
Pfam:TIL 337 393 9.6e-15 PFAM
VWC 395 437 3.54e-1 SMART
VWD 422 586 2.35e-33 SMART
C8 623 697 8.42e-36 SMART
Pfam:TIL 703 760 3.6e-9 PFAM
VWC 762 826 6.75e-1 SMART
VWC 864 906 4.06e-1 SMART
VWD 891 1051 1.51e-45 SMART
C8 1087 1161 2.78e-36 SMART
low complexity region 1316 1331 N/A INTRINSIC
low complexity region 1334 1367 N/A INTRINSIC
low complexity region 1372 1388 N/A INTRINSIC
Pfam:Mucin2_WxxW 1395 1483 1.3e-25 PFAM
low complexity region 1522 1533 N/A INTRINSIC
low complexity region 1537 1564 N/A INTRINSIC
low complexity region 1579 1596 N/A INTRINSIC
Pfam:Mucin2_WxxW 1605 1693 1.3e-27 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000163321
AA Change: G1459R

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000131681
Gene: ENSMUSG00000037974
AA Change: G1459R

DomainStartEndE-ValueType
signal peptide 1 27 N/A INTRINSIC
VWD 69 226 4.19e-30 SMART
C8 258 334 1.34e-11 SMART
Pfam:TIL 337 393 7.9e-15 PFAM
VWC 395 462 8.6e-18 SMART
VWD 421 585 1.55e-33 SMART
C8 622 696 8.42e-36 SMART
Pfam:TIL 702 759 1.9e-9 PFAM
VWC 761 825 6.75e-1 SMART
VWC 863 905 4.06e-1 SMART
VWD 890 1050 1.51e-45 SMART
C8 1086 1160 2.78e-36 SMART
low complexity region 1315 1330 N/A INTRINSIC
low complexity region 1333 1366 N/A INTRINSIC
low complexity region 1371 1387 N/A INTRINSIC
Pfam:Mucin2_WxxW 1394 1481 1.1e-23 PFAM
low complexity region 1521 1532 N/A INTRINSIC
low complexity region 1536 1563 N/A INTRINSIC
low complexity region 1578 1595 N/A INTRINSIC
Pfam:Mucin2_WxxW 1604 1691 1.1e-25 PFAM
Pfam:Mucin2_WxxW 1765 1856 6.3e-24 PFAM
low complexity region 1875 1895 N/A INTRINSIC
low complexity region 1949 1968 N/A INTRINSIC
VWD 2030 2199 4.17e-48 SMART
C8 2242 2311 3.95e-9 SMART
VWC 2376 2439 1.04e-11 SMART
VWC 2479 2543 9.31e-5 SMART
CT 2625 2711 3.43e-32 SMART
low complexity region 2720 2733 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.9%
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased susceptibility to T. muris infection with persistent worm burden, goblet cell hyperplasia, and increased serum IFN-gamma despite a normal TH2-type immune response. A portion of mice show corneal opacity and poor tear quality. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9830107B12Rik A T 17: 48,128,564 (GRCm38) Y127* probably null Het
Abcb5 C T 12: 118,872,790 (GRCm38) V1129I possibly damaging Het
Abcc2 A G 19: 43,807,080 (GRCm38) D425G probably damaging Het
Adamts15 T A 9: 30,922,026 (GRCm38) D71V probably damaging Het
Add1 A G 5: 34,616,705 (GRCm38) H435R possibly damaging Het
AI464131 G T 4: 41,497,568 (GRCm38) Y687* probably null Het
Akr1c19 A G 13: 4,242,592 (GRCm38) N204S probably benign Het
Ankub1 C A 3: 57,690,416 (GRCm38) R44S possibly damaging Het
Ano3 T A 2: 110,666,456 (GRCm38) N783Y probably damaging Het
Bbs9 A G 9: 22,514,063 (GRCm38) M138V probably benign Het
Ccdc18 G A 5: 108,197,795 (GRCm38) E936K possibly damaging Het
Cit T G 5: 115,988,159 (GRCm38) L1604V probably benign Het
Col2a1 T A 15: 97,976,773 (GRCm38) S1396C unknown Het
Col3a1 G C 1: 45,335,764 (GRCm38) G653R unknown Het
Col6a1 T C 10: 76,725,029 (GRCm38) E45G probably damaging Het
Col9a3 T A 2: 180,607,657 (GRCm38) F271I probably damaging Het
Cyp2g1 C A 7: 26,819,153 (GRCm38) D364E probably damaging Het
Dmbt1 T A 7: 131,106,432 (GRCm38) V1457D possibly damaging Het
Dnah17 A T 11: 118,128,927 (GRCm38) I98N possibly damaging Het
Dyrk1b T A 7: 28,183,176 (GRCm38) M222K possibly damaging Het
Epha8 T C 4: 136,945,663 (GRCm38) D270G probably benign Het
Fbxw17 T C 13: 50,425,624 (GRCm38) L159P probably damaging Het
Fgl2 G A 5: 21,373,309 (GRCm38) probably null Het
Fmnl1 A T 11: 103,189,959 (GRCm38) M309L probably damaging Het
Fn1 T C 1: 71,609,587 (GRCm38) I1479V probably benign Het
Gm11939 A T 11: 99,559,298 (GRCm38) S57T possibly damaging Het
Gm5415 T C 1: 32,546,376 (GRCm38) E151G probably benign Het
Gm9195 C T 14: 72,460,537 (GRCm38) A1268T possibly damaging Het
Gnpda1 A G 18: 38,333,295 (GRCm38) W90R possibly damaging Het
Igkv5-43 T A 6: 69,823,461 (GRCm38) R81W probably damaging Het
Mapk3 T A 7: 126,763,765 (GRCm38) W230R probably null Het
Mplkip A G 13: 17,695,620 (GRCm38) S46G probably benign Het
Mrs2 T C 13: 25,004,978 (GRCm38) T118A probably benign Het
Mst1r T A 9: 107,907,585 (GRCm38) H147Q probably damaging Het
Naip1 T C 13: 100,427,403 (GRCm38) H418R probably benign Het
Ncapg A G 5: 45,693,753 (GRCm38) T763A probably benign Het
Nr6a1 T C 2: 38,729,498 (GRCm38) I462V probably benign Het
Nudcd3 T C 11: 6,193,460 (GRCm38) D70G possibly damaging Het
Nup210 A G 6: 91,014,488 (GRCm38) S1858P probably benign Het
Olfr1080 T A 2: 86,553,279 (GRCm38) I282F noncoding transcript Het
Olfr1110 C A 2: 87,135,950 (GRCm38) V124L possibly damaging Het
Olfr1148 T A 2: 87,833,168 (GRCm38) I43N probably benign Het
Olfr2 G C 7: 107,001,456 (GRCm38) L135V probably damaging Het
Olfr775 A G 10: 129,250,921 (GRCm38) H129R probably benign Het
Pde4dip T C 3: 97,767,532 (GRCm38) T23A probably damaging Het
Pex6 A G 17: 46,714,062 (GRCm38) Q347R probably benign Het
Rbm27 A G 18: 42,324,110 (GRCm38) K694R probably damaging Het
Rnf40 T G 7: 127,596,150 (GRCm38) D549E probably benign Het
Rpl22 A G 4: 152,327,511 (GRCm38) K15E probably damaging Het
Rsph6a T A 7: 19,074,239 (GRCm38) D697E unknown Het
Sec23b C T 2: 144,585,623 (GRCm38) P590L probably benign Het
Slc17a7 T A 7: 45,174,932 (GRCm38) M524K probably benign Het
Slc28a1 G A 7: 81,164,416 (GRCm38) D454N probably benign Het
Slc6a13 C T 6: 121,325,028 (GRCm38) R190* probably null Het
Slc7a9 G A 7: 35,456,133 (GRCm38) V257I probably benign Het
Slco1a6 T A 6: 142,101,734 (GRCm38) M377L probably damaging Het
Slit3 A G 11: 35,579,092 (GRCm38) E307G probably damaging Het
Smchd1 A G 17: 71,390,453 (GRCm38) M1164T probably benign Het
Stk4 T C 2: 164,088,857 (GRCm38) I126T probably damaging Het
Syndig1 A T 2: 149,899,868 (GRCm38) S125C probably damaging Het
Synm T C 7: 67,734,065 (GRCm38) D1283G probably benign Het
Tmprss6 T C 15: 78,465,127 (GRCm38) M73V probably benign Het
Tmprss9 A G 10: 80,895,048 (GRCm38) I803V probably benign Het
Tmx4 A T 2: 134,643,902 (GRCm38) V35E probably damaging Het
Topbp1 T G 9: 103,320,541 (GRCm38) S440A probably benign Het
Twf1 T C 15: 94,584,395 (GRCm38) I157V possibly damaging Het
Vmn1r205 T C 13: 22,592,245 (GRCm38) N229S probably benign Het
Vmn1r27 T A 6: 58,215,774 (GRCm38) I82L probably benign Het
Vmn2r112 A G 17: 22,603,613 (GRCm38) N424S possibly damaging Het
Vmn2r68 A T 7: 85,222,214 (GRCm38) Y620* probably null Het
Zfp51 A G 17: 21,463,867 (GRCm38) D248G probably benign Het
Other mutations in Muc5ac
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00899:Muc5ac APN 7 141,812,703 (GRCm38) missense possibly damaging 0.93
IGL01064:Muc5ac APN 7 141,807,473 (GRCm38) missense probably benign 0.12
IGL01155:Muc5ac APN 7 141,806,943 (GRCm38) splice site probably benign
IGL01452:Muc5ac APN 7 141,817,555 (GRCm38) missense probably benign 0.00
IGL01590:Muc5ac APN 7 141,798,893 (GRCm38) missense probably benign 0.02
IGL02104:Muc5ac APN 7 141,811,078 (GRCm38) missense probably damaging 0.98
IGL02152:Muc5ac APN 7 141,800,177 (GRCm38) missense possibly damaging 0.86
IGL02153:Muc5ac APN 7 141,818,800 (GRCm38) nonsense probably null
IGL02178:Muc5ac APN 7 141,805,447 (GRCm38) splice site probably benign
IGL02403:Muc5ac APN 7 141,803,450 (GRCm38) missense possibly damaging 0.71
IGL02576:Muc5ac APN 7 141,817,044 (GRCm38) missense probably benign 0.01
IGL02665:Muc5ac APN 7 141,791,086 (GRCm38) missense possibly damaging 0.71
IGL02704:Muc5ac APN 7 141,795,263 (GRCm38) missense possibly damaging 0.71
IGL02808:Muc5ac APN 7 141,805,775 (GRCm38) missense possibly damaging 0.72
IGL03283:Muc5ac APN 7 141,813,781 (GRCm38) missense probably benign 0.34
IGL03384:Muc5ac APN 7 141,812,403 (GRCm38) missense possibly damaging 0.71
IGL03046:Muc5ac UTSW 7 141,795,213 (GRCm38) missense probably benign 0.27
PIT4515001:Muc5ac UTSW 7 141,807,416 (GRCm38) missense probably damaging 0.99
R0092:Muc5ac UTSW 7 141,818,630 (GRCm38) missense possibly damaging 0.72
R0145:Muc5ac UTSW 7 141,795,275 (GRCm38) missense possibly damaging 0.71
R0147:Muc5ac UTSW 7 141,811,039 (GRCm38) missense probably benign 0.08
R0363:Muc5ac UTSW 7 141,800,960 (GRCm38) missense probably benign 0.01
R0384:Muc5ac UTSW 7 141,812,251 (GRCm38) missense possibly damaging 0.71
R0440:Muc5ac UTSW 7 141,792,034 (GRCm38) nonsense probably null
R0583:Muc5ac UTSW 7 141,807,608 (GRCm38) missense probably damaging 0.99
R0616:Muc5ac UTSW 7 141,796,244 (GRCm38) missense probably benign 0.02
R0682:Muc5ac UTSW 7 141,805,669 (GRCm38) missense possibly damaging 0.53
R0685:Muc5ac UTSW 7 141,807,709 (GRCm38) missense probably benign 0.03
R0883:Muc5ac UTSW 7 141,796,265 (GRCm38) missense possibly damaging 0.71
R0924:Muc5ac UTSW 7 141,807,515 (GRCm38) missense possibly damaging 0.68
R1300:Muc5ac UTSW 7 141,816,929 (GRCm38) missense possibly damaging 0.73
R1315:Muc5ac UTSW 7 141,807,323 (GRCm38) missense probably damaging 0.99
R1354:Muc5ac UTSW 7 141,807,377 (GRCm38) missense probably damaging 0.99
R1484:Muc5ac UTSW 7 141,813,892 (GRCm38) splice site probably null
R1599:Muc5ac UTSW 7 141,798,903 (GRCm38) missense possibly damaging 0.52
R1758:Muc5ac UTSW 7 141,801,531 (GRCm38) missense possibly damaging 0.86
R1837:Muc5ac UTSW 7 141,807,086 (GRCm38) missense probably benign 0.00
R1911:Muc5ac UTSW 7 141,796,304 (GRCm38) missense probably benign 0.18
R1922:Muc5ac UTSW 7 141,793,689 (GRCm38) missense probably benign 0.03
R1966:Muc5ac UTSW 7 141,803,376 (GRCm38) missense possibly damaging 0.92
R1994:Muc5ac UTSW 7 141,813,152 (GRCm38) missense possibly damaging 0.93
R2056:Muc5ac UTSW 7 141,792,035 (GRCm38) missense probably benign 0.01
R2126:Muc5ac UTSW 7 141,810,742 (GRCm38) missense possibly damaging 0.84
R2170:Muc5ac UTSW 7 141,812,347 (GRCm38) missense possibly damaging 0.93
R2258:Muc5ac UTSW 7 141,791,008 (GRCm38) missense probably benign 0.41
R2259:Muc5ac UTSW 7 141,791,008 (GRCm38) missense probably benign 0.41
R2293:Muc5ac UTSW 7 141,807,199 (GRCm38) missense probably damaging 0.99
R2435:Muc5ac UTSW 7 141,818,104 (GRCm38) missense possibly damaging 0.53
R2895:Muc5ac UTSW 7 141,791,140 (GRCm38) missense possibly damaging 0.92
R2910:Muc5ac UTSW 7 141,807,641 (GRCm38) missense probably damaging 0.99
R3154:Muc5ac UTSW 7 141,792,736 (GRCm38) splice site probably null
R3762:Muc5ac UTSW 7 141,807,475 (GRCm38) missense possibly damaging 0.53
R3791:Muc5ac UTSW 7 141,798,501 (GRCm38) missense probably benign 0.32
R3806:Muc5ac UTSW 7 141,813,734 (GRCm38) missense possibly damaging 0.91
R3825:Muc5ac UTSW 7 141,814,723 (GRCm38) missense possibly damaging 0.92
R3888:Muc5ac UTSW 7 141,791,224 (GRCm38) missense possibly damaging 0.51
R3929:Muc5ac UTSW 7 141,802,892 (GRCm38) missense probably benign
R3981:Muc5ac UTSW 7 141,813,775 (GRCm38) missense possibly damaging 0.86
R4034:Muc5ac UTSW 7 141,799,844 (GRCm38) critical splice donor site probably null
R4043:Muc5ac UTSW 7 141,807,478 (GRCm38) missense possibly damaging 0.53
R4061:Muc5ac UTSW 7 141,811,130 (GRCm38) missense possibly damaging 0.85
R4106:Muc5ac UTSW 7 141,802,835 (GRCm38) missense possibly damaging 0.86
R4206:Muc5ac UTSW 7 141,817,110 (GRCm38) missense possibly damaging 0.73
R4613:Muc5ac UTSW 7 141,791,103 (GRCm38) missense possibly damaging 0.93
R4719:Muc5ac UTSW 7 141,789,763 (GRCm38) missense possibly damaging 0.83
R4751:Muc5ac UTSW 7 141,817,601 (GRCm38) missense probably benign 0.00
R4789:Muc5ac UTSW 7 141,798,882 (GRCm38) missense possibly damaging 0.86
R4928:Muc5ac UTSW 7 141,817,902 (GRCm38) nonsense probably null
R4971:Muc5ac UTSW 7 141,816,278 (GRCm38) missense possibly damaging 0.68
R4982:Muc5ac UTSW 7 141,809,456 (GRCm38) intron probably benign
R5088:Muc5ac UTSW 7 141,796,319 (GRCm38) missense possibly damaging 0.53
R5141:Muc5ac UTSW 7 141,814,742 (GRCm38) missense possibly damaging 0.72
R5224:Muc5ac UTSW 7 141,793,971 (GRCm38) missense probably benign 0.32
R5366:Muc5ac UTSW 7 141,807,550 (GRCm38) missense probably benign 0.01
R5497:Muc5ac UTSW 7 141,807,643 (GRCm38) missense probably damaging 0.99
R5507:Muc5ac UTSW 7 141,807,832 (GRCm38) missense possibly damaging 0.72
R5643:Muc5ac UTSW 7 141,793,715 (GRCm38) critical splice donor site probably null
R5811:Muc5ac UTSW 7 141,798,984 (GRCm38) missense possibly damaging 0.51
R5946:Muc5ac UTSW 7 141,817,907 (GRCm38) missense possibly damaging 0.73
R5970:Muc5ac UTSW 7 141,790,669 (GRCm38) nonsense probably null
R5977:Muc5ac UTSW 7 141,796,367 (GRCm38) missense possibly damaging 0.73
R6051:Muc5ac UTSW 7 141,811,857 (GRCm38) missense possibly damaging 0.53
R6126:Muc5ac UTSW 7 141,801,232 (GRCm38) missense possibly damaging 0.71
R6159:Muc5ac UTSW 7 141,815,586 (GRCm38) missense possibly damaging 0.53
R6256:Muc5ac UTSW 7 141,789,795 (GRCm38) missense possibly damaging 0.53
R6283:Muc5ac UTSW 7 141,816,864 (GRCm38) nonsense probably null
R6341:Muc5ac UTSW 7 141,801,492 (GRCm38) missense probably damaging 0.99
R6356:Muc5ac UTSW 7 141,812,679 (GRCm38) missense probably benign 0.05
R6481:Muc5ac UTSW 7 141,809,071 (GRCm38) intron probably benign
R6483:Muc5ac UTSW 7 141,802,854 (GRCm38) missense probably benign 0.18
R6627:Muc5ac UTSW 7 141,808,690 (GRCm38) intron probably benign
R6636:Muc5ac UTSW 7 141,818,605 (GRCm38) missense possibly damaging 0.86
R6637:Muc5ac UTSW 7 141,818,605 (GRCm38) missense possibly damaging 0.86
R6656:Muc5ac UTSW 7 141,803,328 (GRCm38) missense probably damaging 0.98
R6721:Muc5ac UTSW 7 141,798,992 (GRCm38) missense possibly damaging 0.71
R6794:Muc5ac UTSW 7 141,809,552 (GRCm38) intron probably benign
R6844:Muc5ac UTSW 7 141,809,744 (GRCm38) intron probably benign
R6847:Muc5ac UTSW 7 141,809,744 (GRCm38) intron probably benign
R6852:Muc5ac UTSW 7 141,816,907 (GRCm38) missense probably benign 0.03
R6862:Muc5ac UTSW 7 141,809,744 (GRCm38) intron probably benign
R6863:Muc5ac UTSW 7 141,809,744 (GRCm38) intron probably benign
R6864:Muc5ac UTSW 7 141,809,744 (GRCm38) intron probably benign
R6865:Muc5ac UTSW 7 141,809,744 (GRCm38) intron probably benign
R6874:Muc5ac UTSW 7 141,809,744 (GRCm38) intron probably benign
R6875:Muc5ac UTSW 7 141,809,744 (GRCm38) intron probably benign
R6876:Muc5ac UTSW 7 141,809,744 (GRCm38) intron probably benign
R6877:Muc5ac UTSW 7 141,809,744 (GRCm38) intron probably benign
R6889:Muc5ac UTSW 7 141,809,744 (GRCm38) intron probably benign
R6920:Muc5ac UTSW 7 141,793,298 (GRCm38) missense possibly damaging 0.86
R6998:Muc5ac UTSW 7 141,818,714 (GRCm38) missense possibly damaging 0.92
R7017:Muc5ac UTSW 7 141,809,687 (GRCm38) intron probably benign
R7091:Muc5ac UTSW 7 141,809,687 (GRCm38) intron probably benign
R7092:Muc5ac UTSW 7 141,809,687 (GRCm38) intron probably benign
R7092:Muc5ac UTSW 7 141,809,648 (GRCm38) intron probably benign
R7110:Muc5ac UTSW 7 141,799,822 (GRCm38) missense possibly damaging 0.95
R7117:Muc5ac UTSW 7 141,813,822 (GRCm38) nonsense probably null
R7238:Muc5ac UTSW 7 141,809,687 (GRCm38) intron probably benign
R7238:Muc5ac UTSW 7 141,809,517 (GRCm38) missense unknown
R7396:Muc5ac UTSW 7 141,808,415 (GRCm38) missense unknown
R7456:Muc5ac UTSW 7 141,793,167 (GRCm38) missense probably benign 0.32
R7477:Muc5ac UTSW 7 141,816,282 (GRCm38) missense possibly damaging 0.72
R7530:Muc5ac UTSW 7 141,813,799 (GRCm38) missense possibly damaging 0.51
R7545:Muc5ac UTSW 7 141,808,668 (GRCm38) missense unknown
R7604:Muc5ac UTSW 7 141,809,709 (GRCm38) missense unknown
R7635:Muc5ac UTSW 7 141,805,676 (GRCm38) missense probably damaging 0.98
R7635:Muc5ac UTSW 7 141,805,753 (GRCm38) missense possibly damaging 0.53
R7650:Muc5ac UTSW 7 141,809,422 (GRCm38) missense unknown
R7651:Muc5ac UTSW 7 141,796,254 (GRCm38) missense possibly damaging 0.92
R7685:Muc5ac UTSW 7 141,809,383 (GRCm38) missense unknown
R7720:Muc5ac UTSW 7 141,809,303 (GRCm38) missense unknown
R7749:Muc5ac UTSW 7 141,809,303 (GRCm38) missense unknown
R7750:Muc5ac UTSW 7 141,809,303 (GRCm38) missense unknown
R7751:Muc5ac UTSW 7 141,809,303 (GRCm38) missense unknown
R7754:Muc5ac UTSW 7 141,809,303 (GRCm38) missense unknown
R7798:Muc5ac UTSW 7 141,794,041 (GRCm38) critical splice donor site probably null
R7835:Muc5ac UTSW 7 141,809,303 (GRCm38) missense unknown
R7837:Muc5ac UTSW 7 141,815,963 (GRCm38) missense possibly damaging 0.53
R7858:Muc5ac UTSW 7 141,803,429 (GRCm38) missense possibly damaging 0.51
R7866:Muc5ac UTSW 7 141,795,852 (GRCm38) missense probably benign 0.00
R7874:Muc5ac UTSW 7 141,809,303 (GRCm38) missense unknown
R7876:Muc5ac UTSW 7 141,809,303 (GRCm38) missense unknown
R7877:Muc5ac UTSW 7 141,809,303 (GRCm38) missense unknown
R7881:Muc5ac UTSW 7 141,809,303 (GRCm38) missense unknown
R7884:Muc5ac UTSW 7 141,809,303 (GRCm38) missense unknown
R7921:Muc5ac UTSW 7 141,809,687 (GRCm38) intron probably benign
R7976:Muc5ac UTSW 7 141,809,791 (GRCm38) missense unknown
R8104:Muc5ac UTSW 7 141,804,783 (GRCm38) missense possibly damaging 0.96
R8214:Muc5ac UTSW 7 141,802,948 (GRCm38) missense possibly damaging 0.53
R8292:Muc5ac UTSW 7 141,809,263 (GRCm38) missense unknown
R8386:Muc5ac UTSW 7 141,807,634 (GRCm38) missense possibly damaging 0.93
R8400:Muc5ac UTSW 7 141,810,476 (GRCm38) missense probably damaging 0.99
R8504:Muc5ac UTSW 7 141,807,155 (GRCm38) missense probably damaging 1.00
R8709:Muc5ac UTSW 7 141,816,926 (GRCm38) missense possibly damaging 0.96
R8725:Muc5ac UTSW 7 141,809,744 (GRCm38) intron probably benign
R8727:Muc5ac UTSW 7 141,809,744 (GRCm38) intron probably benign
R8754:Muc5ac UTSW 7 141,800,271 (GRCm38) missense possibly damaging 0.85
R8769:Muc5ac UTSW 7 141,818,872 (GRCm38) missense probably damaging 1.00
R8933:Muc5ac UTSW 7 141,789,756 (GRCm38) missense possibly damaging 0.59
R8939:Muc5ac UTSW 7 141,793,354 (GRCm38) missense probably damaging 0.98
R9049:Muc5ac UTSW 7 141,808,975 (GRCm38) missense unknown
R9124:Muc5ac UTSW 7 141,809,792 (GRCm38) missense unknown
R9131:Muc5ac UTSW 7 141,809,792 (GRCm38) missense unknown
R9132:Muc5ac UTSW 7 141,809,792 (GRCm38) missense unknown
R9135:Muc5ac UTSW 7 141,798,481 (GRCm38) missense probably damaging 0.99
R9156:Muc5ac UTSW 7 141,809,792 (GRCm38) missense unknown
R9157:Muc5ac UTSW 7 141,809,792 (GRCm38) missense unknown
R9159:Muc5ac UTSW 7 141,809,792 (GRCm38) missense unknown
R9160:Muc5ac UTSW 7 141,809,792 (GRCm38) missense unknown
R9161:Muc5ac UTSW 7 141,799,289 (GRCm38) missense possibly damaging 0.53
R9175:Muc5ac UTSW 7 141,812,356 (GRCm38) missense possibly damaging 0.92
R9183:Muc5ac UTSW 7 141,798,900 (GRCm38) missense possibly damaging 0.71
R9218:Muc5ac UTSW 7 141,807,361 (GRCm38) missense probably damaging 0.99
R9219:Muc5ac UTSW 7 141,817,063 (GRCm38) nonsense probably null
R9239:Muc5ac UTSW 7 141,800,217 (GRCm38) missense probably damaging 0.99
R9246:Muc5ac UTSW 7 141,810,478 (GRCm38) missense probably benign 0.11
R9287:Muc5ac UTSW 7 141,807,889 (GRCm38) missense probably damaging 0.99
R9320:Muc5ac UTSW 7 141,815,518 (GRCm38) missense probably benign 0.01
R9327:Muc5ac UTSW 7 141,811,692 (GRCm38) missense possibly damaging 0.86
R9428:Muc5ac UTSW 7 141,808,822 (GRCm38) missense unknown
R9430:Muc5ac UTSW 7 141,808,832 (GRCm38) missense unknown
R9454:Muc5ac UTSW 7 141,808,694 (GRCm38) missense unknown
R9483:Muc5ac UTSW 7 141,811,728 (GRCm38) nonsense probably null
R9581:Muc5ac UTSW 7 141,810,062 (GRCm38) missense unknown
R9610:Muc5ac UTSW 7 141,796,341 (GRCm38) missense possibly damaging 0.86
R9642:Muc5ac UTSW 7 141,795,864 (GRCm38) missense possibly damaging 0.71
R9684:Muc5ac UTSW 7 141,811,061 (GRCm38) missense probably benign 0.41
R9760:Muc5ac UTSW 7 141,807,248 (GRCm38) missense probably benign 0.05
R9778:Muc5ac UTSW 7 141,795,284 (GRCm38) nonsense probably null
X0060:Muc5ac UTSW 7 141,803,333 (GRCm38) missense possibly damaging 0.71
Z1088:Muc5ac UTSW 7 141,811,692 (GRCm38) missense possibly damaging 0.86
Z1088:Muc5ac UTSW 7 141,809,744 (GRCm38) intron probably benign
Z1177:Muc5ac UTSW 7 141,818,040 (GRCm38) missense probably benign 0.33
Z1177:Muc5ac UTSW 7 141,809,224 (GRCm38) missense unknown
Predicted Primers PCR Primer
(F):5'- GCCCTGTTACAGCTCCTATGAC -3'
(R):5'- TGCTCAGTTGAGGTAACAGGG -3'

Sequencing Primer
(F):5'- CTCCCTGGATGGATGTTAGCC -3'
(R):5'- GACTGAGGAGGTTGTGTTATCC -3'
Posted On 2020-07-13