Incidental Mutation 'R5696:Krt9'
ID 450688
Institutional Source Beutler Lab
Gene Symbol Krt9
Ensembl Gene ENSMUSG00000051617
Gene Name keratin 9
Synonyms K9, Krt1-9
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R5696 (G1)
Quality Score 109
Status Not validated
Chromosome 11
Chromosomal Location 100077607-100084072 bp(-) (GRCm39)
Type of Mutation small deletion (8 aa in frame mutation)
DNA Base Change (assembly) TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC to TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC at 100079903 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000055255 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059707]
AlphaFold Q6RHW0
Predicted Effect probably benign
Transcript: ENSMUST00000059707
SMART Domains Protein: ENSMUSP00000055255
Gene: ENSMUSG00000051617

DomainStartEndE-ValueType
low complexity region 6 125 N/A INTRINSIC
Filament 130 442 2.96e-124 SMART
low complexity region 462 716 N/A INTRINSIC
low complexity region 721 737 N/A INTRINSIC
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.6%
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit hyperpigmented calluses on the footpad with acanthosis, hyperkeratosis, thick epidermis and increased keratinocyte proliferation. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 73 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam8 G A 7: 139,569,159 (GRCm39) R186W probably benign Het
Afg3l2 A G 18: 67,540,529 (GRCm39) I660T probably damaging Het
Amtn T A 5: 88,532,944 (GRCm39) Y186* probably null Het
Atosa A G 9: 74,917,399 (GRCm39) E666G probably benign Het
Atrip A G 9: 108,894,569 (GRCm39) S453P possibly damaging Het
Bahcc1 T C 11: 120,164,813 (GRCm39) L840P probably damaging Het
Capn2 T C 1: 182,306,165 (GRCm39) E527G possibly damaging Het
Caprin2 A T 6: 148,779,316 (GRCm39) Y164N possibly damaging Het
Ccnh T A 13: 85,344,446 (GRCm39) probably null Het
Cdon G T 9: 35,403,162 (GRCm39) V1091F possibly damaging Het
Ceacam14 A G 7: 17,548,267 (GRCm39) Y119C probably damaging Het
Ces2h A G 8: 105,745,611 (GRCm39) K445E possibly damaging Het
Cfap46 A G 7: 139,191,947 (GRCm39) S2357P probably damaging Het
Commd4 A T 9: 57,063,499 (GRCm39) S86R possibly damaging Het
Cpsf6 A T 10: 117,196,934 (GRCm39) probably benign Het
Dag1 A T 9: 108,086,646 (GRCm39) V165E probably benign Het
Dmxl1 A T 18: 50,065,008 (GRCm39) K2618* probably null Het
Dnah17 A G 11: 117,991,882 (GRCm39) Y1229H probably benign Het
Endov T A 11: 119,382,625 (GRCm39) L24Q probably damaging Het
Fap C T 2: 62,332,803 (GRCm39) V717M probably damaging Het
Fbxl2 A G 9: 113,815,546 (GRCm39) L239P probably damaging Het
Fbxl5 A T 5: 43,916,182 (GRCm39) V367D possibly damaging Het
Fkbp10 G T 11: 100,314,352 (GRCm39) W384L probably damaging Het
Gbp8 C T 5: 105,166,682 (GRCm39) V216I possibly damaging Het
Gclm G A 3: 122,059,936 (GRCm39) A239T probably benign Het
Gm11569 C T 11: 99,689,556 (GRCm39) probably benign Het
Gnas C A 2: 174,141,468 (GRCm39) probably benign Het
Grb10 T A 11: 11,883,566 (GRCm39) N508I probably benign Het
Gykl1 T G 18: 52,827,267 (GRCm39) I158M probably benign Het
Ide G A 19: 37,295,420 (GRCm39) T214M unknown Het
Il12rb2 T A 6: 67,272,262 (GRCm39) Q341H possibly damaging Het
Ints1 T C 5: 139,740,744 (GRCm39) E1946G probably benign Het
Kdelr3 T C 15: 79,410,100 (GRCm39) probably null Het
Kif1b A C 4: 149,358,306 (GRCm39) probably null Het
Kri1 A G 9: 21,191,533 (GRCm39) I320T probably damaging Het
Lin9 T C 1: 180,486,646 (GRCm39) S111P probably benign Het
Lpcat2b C A 5: 107,580,773 (GRCm39) P34Q probably damaging Het
Ltk T A 2: 119,590,080 (GRCm39) T49S probably benign Het
Map3k9 A T 12: 81,780,896 (GRCm39) H421Q probably benign Het
Mapkbp1 T A 2: 119,852,201 (GRCm39) probably null Het
Mcm4 A G 16: 15,443,434 (GRCm39) S830P probably damaging Het
Nek10 T A 14: 14,860,736 (GRCm38) probably null Het
Nlrp9b A T 7: 19,758,417 (GRCm39) R551S probably benign Het
Nol4l T C 2: 153,260,026 (GRCm39) T143A probably damaging Het
Or1r1 T C 11: 73,875,362 (GRCm39) H24R possibly damaging Het
Or51g1 T A 7: 102,633,748 (GRCm39) T208S probably benign Het
Or6z5 T C 7: 6,477,742 (GRCm39) probably null Het
Or7a39 A T 10: 78,715,919 (GRCm39) R304S probably benign Het
Pde4dip G T 3: 97,616,806 (GRCm39) A1812D probably damaging Het
Plekhb1 C A 7: 100,305,960 (GRCm39) G26C probably damaging Het
Polr1a T A 6: 71,906,410 (GRCm39) F409I probably benign Het
Ptpn13 T A 5: 103,702,625 (GRCm39) M1197K probably benign Het
Qrich2 T C 11: 116,335,828 (GRCm39) I2114V probably damaging Het
Rbm27 T C 18: 42,450,731 (GRCm39) Y449H probably damaging Het
Rp1l1 A G 14: 64,267,195 (GRCm39) D927G probably damaging Het
Secisbp2 C A 13: 51,833,857 (GRCm39) Q666K probably damaging Het
Slc45a2 T C 15: 11,001,219 (GRCm39) I106T probably damaging Het
Slx4 G T 16: 3,797,831 (GRCm39) Q1518K probably damaging Het
Smim10l1 T C 6: 133,082,489 (GRCm39) F12S probably damaging Het
Son T C 16: 91,468,301 (GRCm39) V306A possibly damaging Het
Stab1 A G 14: 30,882,178 (GRCm39) S506P probably benign Het
Syne2 A C 12: 76,040,919 (GRCm39) D3859A probably benign Het
Tab1 T A 15: 80,032,930 (GRCm39) Y71* probably null Het
Tarbp1 A C 8: 127,174,079 (GRCm39) M909R probably damaging Het
Tex15 T G 8: 34,063,220 (GRCm39) S1157R probably benign Het
Tnni3 G A 7: 4,523,453 (GRCm39) T120I probably benign Het
Ttn T C 2: 76,747,888 (GRCm39) E4387G probably benign Het
Ugt3a1 G A 15: 9,361,534 (GRCm39) silent Het
Unc5d T C 8: 29,156,870 (GRCm39) I783V probably benign Het
Usp40 T C 1: 87,923,474 (GRCm39) T266A probably benign Het
Vmn2r59 C T 7: 41,695,468 (GRCm39) V315I probably benign Het
Zbtb48 G T 4: 152,105,067 (GRCm39) H532N probably damaging Het
Zfp1005 C T 2: 150,111,394 (GRCm39) H695Y possibly damaging Het
Other mutations in Krt9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00725:Krt9 APN 11 100,080,832 (GRCm39) missense probably damaging 1.00
IGL01695:Krt9 APN 11 100,082,263 (GRCm39) critical splice donor site probably null
IGL02383:Krt9 APN 11 100,082,041 (GRCm39) missense probably damaging 1.00
IGL02529:Krt9 APN 11 100,080,792 (GRCm39) missense probably damaging 0.99
IGL02819:Krt9 APN 11 100,082,346 (GRCm39) missense probably damaging 1.00
droplet UTSW 11 100,081,614 (GRCm39) missense probably damaging 1.00
R5944_Krt9_487 UTSW 11 100,079,265 (GRCm39) missense unknown
G1citation:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R1356:Krt9 UTSW 11 100,079,640 (GRCm39) small insertion probably benign
R1397:Krt9 UTSW 11 100,083,464 (GRCm39) missense probably damaging 1.00
R1498:Krt9 UTSW 11 100,079,195 (GRCm39) nonsense probably null
R1772:Krt9 UTSW 11 100,082,131 (GRCm39) missense probably damaging 0.99
R1871:Krt9 UTSW 11 100,081,614 (GRCm39) missense probably damaging 1.00
R1883:Krt9 UTSW 11 100,079,523 (GRCm39) missense unknown
R1985:Krt9 UTSW 11 100,080,817 (GRCm39) missense probably benign 0.02
R2056:Krt9 UTSW 11 100,082,321 (GRCm39) missense probably damaging 1.00
R2253:Krt9 UTSW 11 100,081,685 (GRCm39) missense possibly damaging 0.83
R2305:Krt9 UTSW 11 100,083,942 (GRCm39) missense unknown
R2875:Krt9 UTSW 11 100,080,031 (GRCm39) nonsense probably null
R3813:Krt9 UTSW 11 100,080,503 (GRCm39) missense probably damaging 1.00
R3874:Krt9 UTSW 11 100,081,675 (GRCm39) missense probably damaging 1.00
R4157:Krt9 UTSW 11 100,079,475 (GRCm39) missense unknown
R4762:Krt9 UTSW 11 100,081,675 (GRCm39) missense probably damaging 1.00
R4873:Krt9 UTSW 11 100,080,863 (GRCm39) missense probably benign 0.06
R4875:Krt9 UTSW 11 100,080,863 (GRCm39) missense probably benign 0.06
R4923:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R4973:Krt9 UTSW 11 100,079,538 (GRCm39) missense unknown
R5153:Krt9 UTSW 11 100,082,068 (GRCm39) missense probably damaging 0.99
R5658:Krt9 UTSW 11 100,081,593 (GRCm39) missense probably damaging 0.98
R5944:Krt9 UTSW 11 100,079,265 (GRCm39) missense unknown
R6147:Krt9 UTSW 11 100,079,665 (GRCm39) missense unknown
R6403:Krt9 UTSW 11 100,080,485 (GRCm39) missense probably damaging 0.99
R6476:Krt9 UTSW 11 100,081,640 (GRCm39) missense probably damaging 1.00
R6822:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R7159:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R7174:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R7203:Krt9 UTSW 11 100,081,617 (GRCm39) missense probably damaging 1.00
R7805:Krt9 UTSW 11 100,083,522 (GRCm39) missense possibly damaging 0.85
R7817:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R7822:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R7834:Krt9 UTSW 11 100,083,492 (GRCm39) missense probably benign 0.06
R7947:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R7977:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R8943:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R9092:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R9099:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R9203:Krt9 UTSW 11 100,079,734 (GRCm39) missense unknown
R9313:Krt9 UTSW 11 100,079,547 (GRCm39) missense unknown
R9361:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R9370:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R9438:Krt9 UTSW 11 100,079,824 (GRCm39) missense unknown
R9448:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R9455:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R9620:Krt9 UTSW 11 100,079,186 (GRCm39) missense unknown
R9676:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
R9719:Krt9 UTSW 11 100,079,903 (GRCm39) small deletion probably benign
Predicted Primers PCR Primer
(F):5'- AGAGCTGCTTCCTCCTCCATAA -3'
(R):5'- GGGATGCCTCAGTTCACACT -3'

Sequencing Primer
(F):5'- TAACCTCCTCCACTTTTTCCACCATG -3'
(R):5'- GGATGCCTCAGTTCACACTTAAGTC -3'
Posted On 2017-01-03