Incidental Mutation 'RF008:Krtap28-10'
ID 602957
Institutional Source Beutler Lab
Gene Symbol Krtap28-10
Ensembl Gene ENSMUSG00000100190
Gene Name keratin associated protein 28-10
Synonyms 4733401N17Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.144) question?
Stock # RF008 (G1)
Quality Score 214.467
Status Not validated
Chromosome 1
Chromosomal Location 83019245-83020201 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) CAGCCA to CAGCCATAGCCA at 83019849 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000152431 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000045560] [ENSMUST00000164473] [ENSMUST00000188323] [ENSMUST00000222567]
AlphaFold A0A1Y7VP58
Predicted Effect probably benign
Transcript: ENSMUST00000045560
SMART Domains Protein: ENSMUSP00000041683
Gene: ENSMUSG00000038496

DomainStartEndE-ValueType
Pfam:Folate_carrier 11 435 1.4e-178 PFAM
Pfam:MFS_1 16 416 1.6e-17 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000164473
SMART Domains Protein: ENSMUSP00000126646
Gene: ENSMUSG00000038496

DomainStartEndE-ValueType
Pfam:Folate_carrier 11 435 1.3e-178 PFAM
Pfam:MFS_1 16 416 1.9e-17 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000188323
Predicted Effect probably benign
Transcript: ENSMUST00000222567
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.7%
  • 10x: 99.4%
  • 20x: 98.7%
Validation Efficiency 100% (45/45)
Allele List at MGI
Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abi3bp CCACGACC CCACGACCACGACC 16: 56,447,952 (GRCm39) probably benign Het
Acan T G 7: 78,742,148 (GRCm39) V515G possibly damaging Het
Acap3 TGG TGGACTGCTGCATCCAGG 4: 155,989,555 (GRCm39) probably benign Het
AI837181 G GGCT 19: 5,475,266 (GRCm39) probably benign Het
Ankhd1 GGCGGC GGCGGCAGCGGC 18: 36,693,977 (GRCm39) probably benign Het
Anks1b G A 10: 89,869,087 (GRCm39) G49D probably damaging Het
Arid1b GCG GCGACG 17: 5,045,869 (GRCm39) probably benign Het
Arid1b CGG CGGAGG 17: 5,045,870 (GRCm39) probably benign Het
Begain G GCCGCCC 12: 108,999,363 (GRCm39) probably null Het
Cacna1e A G 1: 154,317,882 (GRCm39) M1500T probably damaging Het
Casp16 C A 17: 23,774,201 (GRCm39) probably benign Het
Ccdc174 T C 6: 91,876,347 (GRCm39) S395P possibly damaging Het
Ccdc7a T G 8: 129,691,434 (GRCm39) Q396H probably damaging Het
Ccdc85c CC CCGGC 12: 108,240,887 (GRCm39) probably benign Het
Cemip T C 7: 83,610,843 (GRCm39) T704A probably damaging Het
Cfap68 C T 9: 50,677,067 (GRCm39) R8H probably benign Het
Col7a1 C T 9: 108,793,547 (GRCm39) P1370S unknown Het
Cts8 T C 13: 61,397,102 (GRCm39) I273V probably benign Het
Cyp2c50 T A 19: 40,078,268 (GRCm39) I42N probably damaging Het
Dbt T G 3: 116,341,717 (GRCm39) Y439* probably null Het
Dennd1b T A 1: 138,981,135 (GRCm39) D116E probably damaging Het
Dkk2 T A 3: 131,883,863 (GRCm39) H254Q probably damaging Het
Dpy30 C A 17: 74,622,902 (GRCm39) V27F possibly damaging Het
Efhd2 GCCGCC GCCGCCCCCGCC 4: 141,602,069 (GRCm39) probably benign Het
Eif4g3 A T 4: 137,903,235 (GRCm39) E1020V probably damaging Het
Elmo1 T A 13: 20,458,706 (GRCm39) S156T probably benign Het
Fancd2os T C 6: 113,574,881 (GRCm39) T42A probably damaging Het
Fbrsl1 TGTGC TGTGCGGGTGTGGGTGC 5: 110,525,984 (GRCm39) probably benign Het
Fsip2 T C 2: 82,808,184 (GRCm39) V1501A probably benign Het
Gabrb2 A G 11: 42,517,705 (GRCm39) Y509C probably damaging Het
Gm8369 GTGT GTGTTTGT 19: 11,489,118 (GRCm39) probably null Het
Gpr139 T C 7: 118,744,090 (GRCm39) D165G probably benign Het
Grik2 T C 10: 49,120,480 (GRCm39) E603G probably damaging Het
H13 G A 2: 152,511,589 (GRCm39) E30K probably damaging Het
Ifitm10 T A 7: 141,882,330 (GRCm39) M147L unknown Het
Itpkb C T 1: 180,160,887 (GRCm39) R338W probably damaging Het
Kif1b T A 4: 149,336,195 (GRCm39) probably null Het
Las1l AGTGG AGTGGTGG X: 94,984,422 (GRCm39) probably benign Het
Mical2 T C 7: 111,922,833 (GRCm39) Y613H probably damaging Het
Mlf2 C A 6: 124,911,259 (GRCm39) H91Q probably benign Het
Nat9 A T 11: 115,074,212 (GRCm39) I152N probably damaging Het
Or10d4c T C 9: 39,558,559 (GRCm39) M179T probably benign Het
Or4a75 A T 2: 89,447,711 (GRCm39) I275N possibly damaging Het
Pdik1l CACCAC CACCACAACCAC 4: 134,006,822 (GRCm39) probably benign Het
Phldb2 T C 16: 45,583,337 (GRCm39) S1054G probably damaging Het
Pkhd1l1 TTTT TTTTTTTTTTGTTT 15: 44,421,901 (GRCm39) probably benign Het
Plcg2 T A 8: 118,300,263 (GRCm39) probably null Het
Polr1has CACCACCACCACCACCAC CACCACCACCACCACCACCACAACCACCACCACCACCAC 17: 37,275,946 (GRCm39) probably benign Het
Prdm16 T A 4: 154,426,452 (GRCm39) R444S probably damaging Het
Rgs6 T C 12: 83,110,223 (GRCm39) F163L probably damaging Het
Rnaseh2a A T 8: 85,686,687 (GRCm39) L154* probably null Het
Rpp38 A G 2: 3,330,072 (GRCm39) S277P unknown Het
Setd1a GGTAGTGGT GGTAGTGGTTGTAGTGGT 7: 127,384,486 (GRCm39) probably benign Het
Shisa6 CGACAGCAGCAGAG CG 11: 66,416,749 (GRCm39) probably benign Het
Slc27a2 T A 2: 126,395,175 (GRCm39) L34Q possibly damaging Het
Slc7a6 G A 8: 106,922,030 (GRCm39) V386I probably benign Het
Spry1 C T 3: 37,697,264 (GRCm39) T169I possibly damaging Het
Sry TGCTGCTGCTG TGCTGCTGCTGCTG Y: 2,662,826 (GRCm39) probably benign Het
Stk24 A T 14: 121,532,172 (GRCm39) I275N probably benign Het
Strn TC TCCGTGCTCCCTTACCCCAGTCCGTGCTCCCTTACCCCAGGC 17: 78,984,716 (GRCm39) probably null Het
Tcp11l2 C A 10: 84,449,388 (GRCm39) P451Q probably damaging Het
Tfeb AGC AGCTGC 17: 48,097,027 (GRCm39) probably benign Het
Trappc9 TGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT TGCTGCTGCTGCTGCGGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT 15: 72,673,138 (GRCm39) probably benign Het
V1ra8 A G 6: 90,180,591 (GRCm39) T265A probably benign Het
Zfp106 CTCCTGGCAGT CT 2: 120,355,026 (GRCm39) probably benign Het
Zfp612 C A 8: 110,816,193 (GRCm39) H467N probably damaging Het
Zfp777 A T 6: 48,018,982 (GRCm39) Y317* probably null Het
Other mutations in Krtap28-10
AlleleSourceChrCoordTypePredicted EffectPPH Score
FR4737:Krtap28-10 UTSW 1 83,019,844 (GRCm39) unclassified probably benign
R8865:Krtap28-10 UTSW 1 83,019,808 (GRCm39) missense unknown
R8984:Krtap28-10 UTSW 1 83,019,894 (GRCm39) missense unknown
RF001:Krtap28-10 UTSW 1 83,020,003 (GRCm39) unclassified probably benign
RF001:Krtap28-10 UTSW 1 83,019,976 (GRCm39) unclassified probably benign
RF001:Krtap28-10 UTSW 1 83,020,001 (GRCm39) unclassified probably benign
RF008:Krtap28-10 UTSW 1 83,020,000 (GRCm39) unclassified probably benign
RF008:Krtap28-10 UTSW 1 83,019,856 (GRCm39) unclassified probably benign
RF008:Krtap28-10 UTSW 1 83,019,974 (GRCm39) unclassified probably benign
RF012:Krtap28-10 UTSW 1 83,019,857 (GRCm39) unclassified probably benign
RF013:Krtap28-10 UTSW 1 83,019,995 (GRCm39) unclassified probably benign
RF013:Krtap28-10 UTSW 1 83,019,856 (GRCm39) unclassified probably benign
RF014:Krtap28-10 UTSW 1 83,019,972 (GRCm39) unclassified probably benign
RF016:Krtap28-10 UTSW 1 83,019,844 (GRCm39) unclassified probably benign
RF017:Krtap28-10 UTSW 1 83,019,987 (GRCm39) unclassified probably benign
RF017:Krtap28-10 UTSW 1 83,019,859 (GRCm39) unclassified probably benign
RF018:Krtap28-10 UTSW 1 83,019,974 (GRCm39) unclassified probably benign
RF019:Krtap28-10 UTSW 1 83,019,990 (GRCm39) unclassified probably benign
RF023:Krtap28-10 UTSW 1 83,020,007 (GRCm39) unclassified probably benign
RF023:Krtap28-10 UTSW 1 83,019,867 (GRCm39) nonsense probably null
RF024:Krtap28-10 UTSW 1 83,019,973 (GRCm39) unclassified probably benign
RF024:Krtap28-10 UTSW 1 83,019,844 (GRCm39) unclassified probably benign
RF025:Krtap28-10 UTSW 1 83,019,979 (GRCm39) unclassified probably benign
RF026:Krtap28-10 UTSW 1 83,019,847 (GRCm39) unclassified probably benign
RF027:Krtap28-10 UTSW 1 83,020,006 (GRCm39) unclassified probably benign
RF028:Krtap28-10 UTSW 1 83,019,979 (GRCm39) unclassified probably benign
RF029:Krtap28-10 UTSW 1 83,019,991 (GRCm39) unclassified probably benign
RF032:Krtap28-10 UTSW 1 83,019,979 (GRCm39) unclassified probably benign
RF034:Krtap28-10 UTSW 1 83,020,003 (GRCm39) unclassified probably benign
RF035:Krtap28-10 UTSW 1 83,020,002 (GRCm39) unclassified probably benign
RF035:Krtap28-10 UTSW 1 83,019,867 (GRCm39) unclassified probably benign
RF037:Krtap28-10 UTSW 1 83,019,866 (GRCm39) unclassified probably benign
RF037:Krtap28-10 UTSW 1 83,020,007 (GRCm39) unclassified probably benign
RF038:Krtap28-10 UTSW 1 83,019,978 (GRCm39) unclassified probably benign
RF038:Krtap28-10 UTSW 1 83,019,849 (GRCm39) unclassified probably benign
RF042:Krtap28-10 UTSW 1 83,019,846 (GRCm39) unclassified probably benign
RF044:Krtap28-10 UTSW 1 83,019,852 (GRCm39) unclassified probably benign
RF045:Krtap28-10 UTSW 1 83,019,982 (GRCm39) unclassified probably benign
RF045:Krtap28-10 UTSW 1 83,019,864 (GRCm39) unclassified probably benign
RF049:Krtap28-10 UTSW 1 83,020,006 (GRCm39) unclassified probably benign
RF049:Krtap28-10 UTSW 1 83,019,859 (GRCm39) unclassified probably benign
RF053:Krtap28-10 UTSW 1 83,019,999 (GRCm39) unclassified probably benign
RF055:Krtap28-10 UTSW 1 83,019,991 (GRCm39) unclassified probably benign
RF055:Krtap28-10 UTSW 1 83,019,983 (GRCm39) unclassified probably benign
RF055:Krtap28-10 UTSW 1 83,019,851 (GRCm39) unclassified probably benign
RF058:Krtap28-10 UTSW 1 83,019,983 (GRCm39) unclassified probably benign
RF059:Krtap28-10 UTSW 1 83,020,011 (GRCm39) unclassified probably benign
RF059:Krtap28-10 UTSW 1 83,019,996 (GRCm39) unclassified probably benign
RF061:Krtap28-10 UTSW 1 83,020,002 (GRCm39) unclassified probably benign
RF064:Krtap28-10 UTSW 1 83,019,852 (GRCm39) unclassified probably benign
Z1177:Krtap28-10 UTSW 1 83,019,880 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- AGCATTTCCAGTGGGTAGATG -3'
(R):5'- TCCTCTCTACTGACAACATGGG -3'

Sequencing Primer
(F):5'- CATTTCCAGTGGGTAGATGAAAAG -3'
(R):5'- CTGTGGAGGCTGCGGAG -3'
Posted On 2019-12-04