Incidental Mutation 'R6035:Krt26'
ID479163
Institutional Source Beutler Lab
Gene Symbol Krt26
Ensembl Gene ENSMUSG00000075570
Gene Namekeratin 26
Synonyms
MMRRC Submission 044207-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.042) question?
Stock #R6035 (G1)
Quality Score225.009
Status Not validated
Chromosome11
Chromosomal Location99328550-99337966 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 99333589 bp
ZygosityHeterozygous
Amino Acid Change Glutamic Acid to Lysine at position 368 (E368K)
Ref Sequence ENSEMBL: ENSMUSP00000098051 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100482]
Predicted Effect probably benign
Transcript: ENSMUST00000100482
AA Change: E368K

PolyPhen 2 Score 0.430 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000098051
Gene: ENSMUSG00000075570
AA Change: E368K

DomainStartEndE-ValueType
low complexity region 40 65 N/A INTRINSIC
Filament 79 394 1.1e-132 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000148770
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 98.9%
  • 10x: 91.8%
  • 20x: 70.9%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the keratin superfamily. This keratin protein is a type I keratin that is specific for the inner root sheath of the hair follicle. This gene exists in a cluster with other keratin genes on chromosome 17q21. [provided by RefSeq, Jul 2009]
Allele List at MGI
Other mutations in this stock
Total: 80 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2m G T 6: 121,638,394 G76W probably damaging Het
Abca17 A T 17: 24,281,245 F1324Y possibly damaging Het
Abca8b A T 11: 109,971,860 probably null Het
Abcc12 A G 8: 86,517,404 M1040T probably damaging Het
Abtb1 A G 6: 88,841,806 F7L probably damaging Het
Adcy9 T C 16: 4,304,513 T558A probably benign Het
Adgrb1 A T 15: 74,540,443 T424S possibly damaging Het
Afg3l2 G T 18: 67,421,259 L458M probably damaging Het
Ankrd31 C A 13: 96,832,213 P786Q probably benign Het
Arhgap39 G T 15: 76,737,224 Y392* probably null Het
Ash1l T C 3: 88,985,019 Y1402H probably damaging Het
Carmil2 G T 8: 105,692,563 W749L probably benign Het
Ccar1 A G 10: 62,751,785 Y867H unknown Het
Cdh13 A G 8: 118,505,698 D47G probably benign Het
Chst9 T A 18: 15,452,853 T218S probably benign Het
Clec2i G A 6: 128,893,624 V67I probably benign Het
Cox7a2 T A 9: 79,759,746 probably benign Het
Cpz A G 5: 35,517,585 C107R probably damaging Het
Dapk1 T A 13: 60,761,199 C1209S possibly damaging Het
Ddx41 T C 13: 55,533,968 M307V probably benign Het
Defa24 A G 8: 21,734,549 I5V probably benign Het
Dgcr8 A T 16: 18,258,314 N2K probably damaging Het
Ebf2 A G 14: 67,238,974 D131G probably damaging Het
Fam149b C T 14: 20,377,917 R424C probably damaging Het
Fbln2 G A 6: 91,263,353 V714M probably damaging Het
Fgf5 T C 5: 98,275,526 Y257H probably damaging Het
Fmo3 A C 1: 162,964,036 V224G probably damaging Het
Gigyf2 T C 1: 87,410,728 I394T possibly damaging Het
Glmn T A 5: 107,593,880 probably null Het
Greb1l T C 18: 10,501,025 I385T possibly damaging Het
Grhl1 C A 12: 24,608,450 Q365K probably benign Het
Gsdme G A 6: 50,229,326 T179M probably damaging Het
Gtf2a1l A G 17: 88,711,534 T349A probably benign Het
Hax1 GTCATCATCATCATCATC GTCATCATCATCATCATCATC 3: 89,997,940 probably benign Het
Il5ra G A 6: 106,741,265 T76I probably damaging Het
Itga8 T C 2: 12,191,714 T631A probably benign Het
Kcnh6 G A 11: 106,019,152 probably null Het
Lhx9 T C 1: 138,838,543 D169G possibly damaging Het
Lman1l A G 9: 57,611,747 probably null Het
Lmod3 A G 6: 97,247,273 L529P probably damaging Het
Mroh2a G A 1: 88,230,668 V146M probably damaging Het
Nup155 A G 15: 8,144,093 T891A probably benign Het
Olfr20 T C 11: 73,353,756 M1T probably null Het
Olfr341 T A 2: 36,479,984 I49F probably damaging Het
Olfr409-ps1 T C 11: 74,317,459 *145R probably null Het
Olfr739 A G 14: 50,424,527 T3A probably benign Het
Olfr883 ATTGCTGTTT ATTGCTGTTTGCTGTTT 9: 38,026,540 probably null Het
Papln G C 12: 83,774,680 G262A probably damaging Het
Pdcd1lg2 G A 19: 29,446,035 V160I probably benign Het
Pde8b A G 13: 95,027,597 probably benign Het
Ppme1 G A 7: 100,354,795 R68* probably null Het
Ptprn2 A T 12: 117,255,595 N949Y probably damaging Het
Qser1 C A 2: 104,787,123 D1115Y probably damaging Het
Rad54l G T 4: 116,097,469 D674E probably damaging Het
Ripk4 T A 16: 97,744,187 D420V probably damaging Het
Ros1 G T 10: 52,077,971 S1857R probably benign Het
Rsf1 A G 7: 97,662,109 E682G probably benign Het
Rsf1 ATGGCG ATGGCGACGGTGGCG 7: 97,579,904 probably benign Het
Samd4 G A 14: 47,087,872 R515H probably damaging Het
Selp T A 1: 164,141,510 W560R probably benign Het
Shc3 A T 13: 51,461,432 L163Q probably damaging Het
Shh G A 5: 28,461,399 A163V probably damaging Het
Slc17a8 T C 10: 89,592,075 R113G possibly damaging Het
Slc5a6 C A 5: 31,048,824 probably benign Het
Smarcd2 A G 11: 106,266,889 probably null Het
Sytl3 A G 17: 6,728,265 D148G probably damaging Het
Tnks G T 8: 34,918,461 H297Q possibly damaging Het
Trbv21 A T 6: 41,202,634 probably benign Het
Ube3c T C 5: 29,601,163 F268L probably benign Het
Ugt2b5 T C 5: 87,139,682 I209V probably benign Het
Usp1 A G 4: 98,929,845 N140S probably damaging Het
Vcam1 T C 3: 116,125,957 Y226C probably damaging Het
Vmn1r129 T A 7: 21,360,609 Q228L probably damaging Het
Vmn1r209 T A 13: 22,806,032 N163Y probably benign Het
Vmn1r85 A G 7: 13,084,927 S97P probably damaging Het
Vmn2r30 C T 7: 7,334,351 M95I probably benign Het
Vmn2r74 G A 7: 85,951,890 R847C probably damaging Het
Wdr70 G A 15: 7,887,349 T529I possibly damaging Het
Zfp532 T G 18: 65,623,934 S313A possibly damaging Het
Zhx3 A T 2: 160,779,543 N901K probably benign Het
Other mutations in Krt26
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00970:Krt26 APN 11 99331281 missense probably benign 0.00
IGL02019:Krt26 APN 11 99333645 missense probably benign 0.30
IGL02138:Krt26 APN 11 99333645 missense probably benign 0.30
IGL02188:Krt26 APN 11 99333645 missense probably benign 0.30
IGL02189:Krt26 APN 11 99333645 missense probably benign 0.30
IGL02192:Krt26 APN 11 99333645 missense probably benign 0.30
IGL02647:Krt26 APN 11 99333645 missense probably benign 0.30
IGL02651:Krt26 APN 11 99333645 missense probably benign 0.30
R0122:Krt26 UTSW 11 99333719 nonsense probably null
R1842:Krt26 UTSW 11 99333526 small deletion probably benign
R1843:Krt26 UTSW 11 99333526 small deletion probably benign
R1923:Krt26 UTSW 11 99333526 small deletion probably benign
R1924:Krt26 UTSW 11 99333526 small deletion probably benign
R3872:Krt26 UTSW 11 99334744 missense probably damaging 1.00
R3873:Krt26 UTSW 11 99334744 missense probably damaging 1.00
R3874:Krt26 UTSW 11 99334744 missense probably damaging 1.00
R3875:Krt26 UTSW 11 99334744 missense probably damaging 1.00
R4014:Krt26 UTSW 11 99335302 missense probably damaging 0.99
R4939:Krt26 UTSW 11 99334696 missense probably benign 0.03
R5620:Krt26 UTSW 11 99337771 missense possibly damaging 0.86
R6035:Krt26 UTSW 11 99333589 missense probably benign 0.43
R6151:Krt26 UTSW 11 99337489 missense probably benign 0.35
R6578:Krt26 UTSW 11 99334802 missense probably damaging 1.00
R6626:Krt26 UTSW 11 99329702 missense probably benign 0.28
Predicted Primers
Posted On2017-06-26