Incidental Mutation 'R9239:Muc5ac'
ID 700635
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
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R9239 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 141788972-141819231 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 141800217 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Valine at position 851 (D851V)
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: D850V

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000039699
Gene: ENSMUSG00000037974
AA Change: D850V

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: D851V

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000122353
Gene: ENSMUSG00000037974
AA Change: D851V

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: D850V

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000131681
Gene: ENSMUSG00000037974
AA Change: D850V

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: 98.5%
Validation Efficiency 100% (44/44)
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: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acot8 A G 2: 164,804,688 (GRCm38) probably null Het
Aldh1l2 A G 10: 83,506,632 (GRCm38) F438S probably damaging Het
Alk T A 17: 71,949,869 (GRCm38) N665I probably benign Het
Anxa4 T A 6: 86,757,830 (GRCm38) T59S probably benign Het
B3gnt8 ACCCC ACCC 7: 25,628,251 (GRCm38) probably null Het
Cabs1 G A 5: 87,979,526 (GRCm38) R12Q probably benign Het
Cep152 A G 2: 125,583,910 (GRCm38) V845A probably benign Het
Dsg1a T A 18: 20,340,693 (GRCm38) V941E probably damaging Het
Fam69a T C 5: 107,911,706 (GRCm38) E127G possibly damaging Het
Fam84a A G 12: 14,150,184 (GRCm38) W181R probably damaging Het
Fbxo11 G T 17: 88,009,094 (GRCm38) H284N Het
Fubp1 A G 3: 152,217,849 (GRCm38) E98G probably damaging Het
Fyco1 A G 9: 123,797,572 (GRCm38) I1358T probably damaging Het
Ginm1 T C 10: 7,774,061 (GRCm38) N156S possibly damaging Het
Gm3739 T C 14: 7,299,352 (GRCm38) Y101C probably damaging Het
Gm4778 T A 3: 94,266,564 (GRCm38) V289E probably benign Het
Ide T C 19: 37,330,499 (GRCm38) N38S Het
Itgb4 T C 11: 116,007,304 (GRCm38) V1644A probably damaging Het
Itpka A G 2: 119,749,542 (GRCm38) D254G probably damaging Het
Kat7 T A 11: 95,306,194 (GRCm38) R6S probably benign Het
Klhl40 A T 9: 121,778,571 (GRCm38) T266S probably benign Het
Mmaa T C 8: 79,269,227 (GRCm38) D289G probably damaging Het
Olfr1414 T C 1: 92,511,732 (GRCm38) T99A probably benign Het
Olfr389 A G 11: 73,776,520 (GRCm38) V269A probably benign Het
Olfr658 G T 7: 104,644,539 (GRCm38) H278N probably damaging Het
Pcdh17 T G 14: 84,533,209 (GRCm38) I1042M probably benign Het
Pipox A G 11: 77,883,939 (GRCm38) I106T probably benign Het
Ppcs C T 4: 119,419,038 (GRCm38) V290M possibly damaging Het
Rnasel T A 1: 153,754,351 (GRCm38) N204K probably damaging Het
Runx1 A G 16: 92,606,047 (GRCm38) Y336H probably damaging Het
Sell A G 1: 164,065,607 (GRCm38) I131V possibly damaging Het
Serpina3f A G 12: 104,218,451 (GRCm38) R285G possibly damaging Het
Slc25a2 A T 18: 37,638,116 (GRCm38) M120K possibly damaging Het
Slc47a1 A T 11: 61,359,518 (GRCm38) probably null Het
Slc4a11 C T 2: 130,691,744 (GRCm38) A100T probably damaging Het
Spats2l A G 1: 57,832,098 (GRCm38) probably benign Het
Taf1b T A 12: 24,556,016 (GRCm38) L431H probably damaging Het
Tectb CT C 19: 55,192,662 (GRCm38) probably null Het
Thsd7b G A 1: 130,159,716 (GRCm38) probably null Het
Tmtc4 A G 14: 122,927,666 (GRCm38) Y594H possibly damaging Het
Trim33 T C 3: 103,330,137 (GRCm38) F599L probably benign Het
Vcl A G 14: 21,022,024 (GRCm38) D819G probably damaging Het
Vmn1r43 G A 6: 89,869,895 (GRCm38) T203M probably damaging Het
Vmn2r1 G T 3: 64,104,538 (GRCm38) V607L probably damaging 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
R8177:Muc5ac UTSW 7 141,807,331 (GRCm38) missense probably damaging 1.00
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
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'- AGGGCCTTCAGACTATTGTGG -3'
(R):5'- AACTTAGTCCATTCCTAACCAGG -3'

Sequencing Primer
(F):5'- GTGGCTACACTGTATTCTCAGAACAC -3'
(R):5'- AACCAGGACCTCTGTACTTGGTG -3'
Posted On 2022-02-07