Incidental Mutation 'R1456:Krt42'
ID 161811
Institutional Source Beutler Lab
Gene Symbol Krt42
Ensembl Gene ENSMUSG00000053654
Gene Name keratin 42
Synonyms 2410039E07Rik, K17n, Ka22, ecat6
MMRRC Submission 039511-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.067) question?
Stock # R1456 (G1)
Quality Score 225
Status Validated
Chromosome 11
Chromosomal Location 100153708-100160697 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 100160436 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Threonine at position 88 (A88T)
Ref Sequence ENSEMBL: ENSMUSP00000017270 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000017270]
AlphaFold Q6IFX2
Predicted Effect probably benign
Transcript: ENSMUST00000017270
AA Change: A88T

PolyPhen 2 Score 0.041 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000017270
Gene: ENSMUSG00000053654
AA Change: A88T

DomainStartEndE-ValueType
low complexity region 62 84 N/A INTRINSIC
Filament 93 404 5.58e-184 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000107406
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 97.9%
  • 10x: 95.1%
  • 20x: 88.9%
Validation Efficiency 98% (90/92)
Allele List at MGI
Other mutations in this stock
Total: 87 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921504E06Rik C T 2: 19,485,731 (GRCm39) probably null Het
4932414N04Rik A T 2: 68,546,558 (GRCm39) E80V possibly damaging Het
Alkbh3 A G 2: 93,831,764 (GRCm39) probably null Het
Ankar A T 1: 72,704,277 (GRCm39) Y664N probably benign Het
Arhgap18 T C 10: 26,792,436 (GRCm39) I629T probably benign Het
Arhgef28 C T 13: 98,211,510 (GRCm39) E158K probably benign Het
Asxl2 C T 12: 3,551,872 (GRCm39) H1205Y possibly damaging Het
Birc6 A G 17: 74,916,285 (GRCm39) I427V probably benign Het
Camk4 A G 18: 33,262,896 (GRCm39) probably benign Het
Ccdc178 A T 18: 22,283,481 (GRCm39) D16E possibly damaging Het
Cct6b G T 11: 82,644,446 (GRCm39) probably benign Het
Ccz1 A G 5: 143,947,836 (GRCm39) probably benign Het
Cdh23 T C 10: 60,322,899 (GRCm39) N335S possibly damaging Het
Cemip T A 7: 83,647,718 (GRCm39) S121C possibly damaging Het
Cers1 A G 8: 70,783,838 (GRCm39) E262G probably damaging Het
Clec11a G T 7: 43,955,874 (GRCm39) P58T possibly damaging Het
Clec16a T C 16: 10,509,419 (GRCm39) I797T probably damaging Het
Col4a1 A C 8: 11,292,829 (GRCm39) probably benign Het
Colgalt2 G A 1: 152,360,655 (GRCm39) V231I probably damaging Het
D430041D05Rik G T 2: 104,038,428 (GRCm39) N1580K probably damaging Het
Dcdc5 A G 2: 106,181,910 (GRCm39) noncoding transcript Het
Ddx17 T C 15: 79,414,577 (GRCm39) D530G probably benign Het
Dhx9 A T 1: 153,341,441 (GRCm39) D601E probably benign Het
Dnah3 A G 7: 119,646,853 (GRCm39) Y1059H probably damaging Het
Dtx1 C A 5: 120,848,569 (GRCm39) probably benign Het
Egfr A G 11: 16,813,065 (GRCm39) S182G probably benign Het
Fads1 A G 19: 10,163,116 (GRCm39) N131S probably benign Het
Fam243 T A 16: 92,117,553 (GRCm39) Y245F probably damaging Het
Fancm C T 12: 65,165,125 (GRCm39) A1490V possibly damaging Het
Fsd2 C A 7: 81,209,339 (GRCm39) E168* probably null Het
Galnt2l T C 8: 123,568,687 (GRCm39) probably benign Het
Gm9772 A T 17: 22,226,099 (GRCm39) C62S probably damaging Het
H60c C T 10: 3,210,307 (GRCm39) A81T possibly damaging Het
Hira T G 16: 18,744,413 (GRCm39) S377A probably benign Het
Iffo1 T C 6: 125,122,877 (GRCm39) S220P possibly damaging Het
Itih4 A G 14: 30,614,610 (GRCm39) M491V probably benign Het
Khdrbs2 T C 1: 32,559,777 (GRCm39) R102G possibly damaging Het
Klhdc7a T G 4: 139,692,835 (GRCm39) Y704S possibly damaging Het
Klk1b21 G A 7: 43,754,923 (GRCm39) V73I probably benign Het
Limk1 G T 5: 134,686,364 (GRCm39) D580E probably benign Het
Lipk C T 19: 34,024,185 (GRCm39) P323S probably damaging Het
Lipo5 T A 19: 33,443,273 (GRCm39) probably benign Het
Llgl2 A G 11: 115,736,325 (GRCm39) D166G probably benign Het
Mapk8ip3 A T 17: 25,125,923 (GRCm39) N439K probably damaging Het
Mapkbp1 C T 2: 119,803,626 (GRCm39) R32W probably damaging Het
Med23 T A 10: 24,779,550 (GRCm39) probably benign Het
Mrgprb1 A T 7: 48,097,777 (GRCm39) M45K probably damaging Het
Mroh7 G A 4: 106,552,338 (GRCm39) probably benign Het
Mrpl27 G A 11: 94,544,659 (GRCm39) probably benign Het
Ms4a10 T A 19: 10,942,097 (GRCm39) T175S possibly damaging Het
Muc17 T C 5: 137,166,799 (GRCm39) H330R probably benign Het
Myo15a A T 11: 60,399,028 (GRCm39) I2787F probably damaging Het
Ndst1 A G 18: 60,846,277 (GRCm39) C11R possibly damaging Het
Obsl1 C A 1: 75,464,300 (GRCm39) G1669* probably null Het
Or5p56 A G 7: 107,589,605 (GRCm39) E11G probably benign Het
Or6c208 A T 10: 129,223,652 (GRCm39) D50V probably damaging Het
Or7e177 T C 9: 20,212,134 (GRCm39) Y214H probably benign Het
Pafah2 T A 4: 134,131,468 (GRCm39) I52N probably damaging Het
Pcsk6 A T 7: 65,693,283 (GRCm39) I693F possibly damaging Het
Pde4c G T 8: 71,199,262 (GRCm39) R228L probably benign Het
Pdzd8 T C 19: 59,288,904 (GRCm39) N832S probably benign Het
Plbd1 T A 6: 136,590,814 (GRCm39) M451L probably benign Het
Pramel14 G T 4: 143,719,851 (GRCm39) D171E probably benign Het
Prom1 T C 5: 44,194,965 (GRCm39) D260G probably damaging Het
Ranbp17 A G 11: 33,216,310 (GRCm39) S813P probably damaging Het
Scn10a T C 9: 119,520,544 (GRCm39) I119V probably benign Het
Sh3pxd2b A G 11: 32,365,967 (GRCm39) T353A probably damaging Het
Shq1 A T 6: 100,646,659 (GRCm39) probably null Het
Slc22a28 T A 19: 8,049,223 (GRCm39) H342L possibly damaging Het
Slco2b1 C T 7: 99,314,114 (GRCm39) E9K probably null Het
Specc1l T C 10: 75,082,118 (GRCm39) F505L probably damaging Het
Sptan1 G T 2: 29,870,215 (GRCm39) probably null Het
St6gal2 A G 17: 55,797,932 (GRCm39) probably benign Het
Taok2 T C 7: 126,479,313 (GRCm39) I73V probably benign Het
Tax1bp1 C T 6: 52,721,229 (GRCm39) T478I probably benign Het
Tbc1d4 A T 14: 101,744,542 (GRCm39) N361K probably damaging Het
Tph1 A T 7: 46,296,907 (GRCm39) Y429* probably null Het
Tprkb A T 6: 85,901,403 (GRCm39) R14W probably damaging Het
Trio A T 15: 27,753,890 (GRCm39) probably benign Het
Ttc23 T C 7: 67,316,902 (GRCm39) probably benign Het
Vmn1r211 T C 13: 23,036,415 (GRCm39) Y84C probably damaging Het
Vmn2r22 C G 6: 123,614,624 (GRCm39) G322A possibly damaging Het
Wdr74 A G 19: 8,717,776 (GRCm39) Q330R probably benign Het
Wdtc1 C A 4: 133,024,739 (GRCm39) S486I possibly damaging Het
Zbtb24 T C 10: 41,340,989 (GRCm39) V673A possibly damaging Het
Zfpm2 A T 15: 40,965,877 (GRCm39) R655S probably damaging Het
Zkscan5 A G 5: 145,157,798 (GRCm39) N694D probably benign Het
Other mutations in Krt42
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01411:Krt42 APN 11 100,154,167 (GRCm39) missense possibly damaging 0.93
PIT4377001:Krt42 UTSW 11 100,153,931 (GRCm39) missense probably damaging 0.97
R0135:Krt42 UTSW 11 100,153,985 (GRCm39) missense possibly damaging 0.95
R0535:Krt42 UTSW 11 100,155,412 (GRCm39) missense probably damaging 1.00
R1169:Krt42 UTSW 11 100,154,171 (GRCm39) critical splice acceptor site probably null
R1456:Krt42 UTSW 11 100,160,435 (GRCm39) missense probably benign 0.00
R1913:Krt42 UTSW 11 100,158,075 (GRCm39) missense possibly damaging 0.78
R4655:Krt42 UTSW 11 100,160,671 (GRCm39) missense probably damaging 0.99
R5527:Krt42 UTSW 11 100,154,121 (GRCm39) unclassified probably benign
R6049:Krt42 UTSW 11 100,157,886 (GRCm39) missense probably damaging 1.00
R6901:Krt42 UTSW 11 100,160,542 (GRCm39) missense probably benign 0.00
R7748:Krt42 UTSW 11 100,157,792 (GRCm39) missense probably damaging 1.00
R7979:Krt42 UTSW 11 100,155,865 (GRCm39) missense possibly damaging 0.67
R8030:Krt42 UTSW 11 100,155,865 (GRCm39) missense possibly damaging 0.67
R8031:Krt42 UTSW 11 100,155,865 (GRCm39) missense possibly damaging 0.67
R8063:Krt42 UTSW 11 100,155,865 (GRCm39) missense possibly damaging 0.67
R8108:Krt42 UTSW 11 100,157,783 (GRCm39) missense probably benign 0.01
R9040:Krt42 UTSW 11 100,157,859 (GRCm39) missense probably damaging 1.00
R9211:Krt42 UTSW 11 100,155,867 (GRCm39) missense possibly damaging 0.52
R9265:Krt42 UTSW 11 100,157,808 (GRCm39) missense probably damaging 1.00
Z1177:Krt42 UTSW 11 100,157,894 (GRCm39) missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- CTTGGAGAGTTCCCAAAGACCACAC -3'
(R):5'- GACCTGAGGATAACATGGCTTCCAC -3'

Sequencing Primer
(F):5'- CCAGAGACACTGGGTTATTCC -3'
(R):5'- AACTTCTGGCTCCGTTAAGG -3'
Posted On 2014-03-14