Incidental Mutation 'R5807:Krtap9-5'
ID 448603
Institutional Source Beutler Lab
Gene Symbol Krtap9-5
Ensembl Gene ENSMUSG00000078255
Gene Name keratin associated protein 9-5
Synonyms OTTMUSG00000002205
MMRRC Submission 043393-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.102) question?
Stock # R5807 (G1)
Quality Score 225
Status Validated
Chromosome 11
Chromosomal Location 99948475-99949551 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to A at 99949069 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Cysteine to Serine at position 199 (C199S)
Ref Sequence ENSEMBL: ENSMUSP00000100673 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000105052]
AlphaFold A2A5X3
Predicted Effect unknown
Transcript: ENSMUST00000105052
AA Change: C199S
SMART Domains Protein: ENSMUSP00000100673
Gene: ENSMUSG00000078255
AA Change: C199S

DomainStartEndE-ValueType
internal_repeat_3 4 21 5.14e-6 PROSPERO
internal_repeat_2 5 26 9e-8 PROSPERO
low complexity region 37 48 N/A INTRINSIC
Pfam:Keratin_B2_2 52 94 2.7e-9 PFAM
Pfam:Keratin_B2_2 75 128 2e-5 PFAM
Pfam:Keratin_B2_2 125 169 1.7e-9 PFAM
Pfam:Keratin_B2_2 198 245 6.7e-9 PFAM
Pfam:Keratin_B2_2 241 288 1.1e-8 PFAM
Pfam:Keratin_B2_2 284 317 5.6e-7 PFAM
Pfam:Keratin_B2_2 313 357 1.5e-5 PFAM
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.7%
Validation Efficiency 98% (65/66)
Allele List at MGI
Other mutations in this stock
Total: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca12 A G 1: 71,303,492 L943P probably damaging Het
Abcg5 C A 17: 84,672,291 V214F probably damaging Het
Ang T A 14: 51,101,429 probably benign Het
Arfgef3 A G 10: 18,647,798 probably null Het
Arhgef4 A G 1: 34,807,615 probably benign Het
Atp11b T C 3: 35,812,279 I409T probably damaging Het
Atp5b G A 10: 128,088,562 probably benign Het
Atp9a G A 2: 168,653,534 A660V probably damaging Het
Avpr1a A G 10: 122,449,471 T223A probably benign Het
Bmp2k T C 5: 97,063,494 M507T unknown Het
Cep295 A G 9: 15,332,532 S287P probably damaging Het
Chrna7 T A 7: 63,148,601 D111V probably damaging Het
Cnr2 A G 4: 135,917,436 D275G probably benign Het
Col28a1 T A 6: 8,158,144 M305L probably benign Het
Cpb1 T A 3: 20,263,742 D206V probably damaging Het
Cyp2c50 T C 19: 40,113,500 L453S probably damaging Het
Ddx52 T G 11: 83,949,682 S284A probably benign Het
Efcab1 A T 16: 14,916,972 I69F probably benign Het
Eif2ak4 G T 2: 118,388,851 R48L probably benign Het
Esrrb A G 12: 86,514,401 E303G possibly damaging Het
Fbxo21 A G 5: 117,976,868 E23G probably benign Het
Fcamr T C 1: 130,811,526 S188P probably damaging Het
Fer1l6 C A 15: 58,590,550 S818* probably null Het
Fn1 T C 1: 71,648,059 D213G probably damaging Het
Gcg A G 2: 62,475,725 I176T possibly damaging Het
Glis1 T A 4: 107,568,082 S109T probably benign Het
Gm266 T C 12: 111,485,739 D11G probably benign Het
Gm5070 C A 3: 95,410,654 noncoding transcript Het
Gm8444 T C 15: 81,843,453 probably benign Het
Gm8989 T A 7: 106,330,223 noncoding transcript Het
Golga4 A G 9: 118,527,130 T117A probably damaging Het
Gpr132 G A 12: 112,852,796 R137C probably damaging Het
Herc2 T A 7: 56,230,919 F4766L probably damaging Het
Inhbc C A 10: 127,357,542 E202* probably null Het
Kcnu1 C T 8: 25,849,714 T20I possibly damaging Het
Klhdc3 T C 17: 46,677,465 D161G probably damaging Het
Krt84 T A 15: 101,530,212 K280M probably damaging Het
Mrgprb3 A G 7: 48,643,362 V147A probably benign Het
Ndufs6 A T 13: 73,327,434 F48L probably damaging Het
Obscn T C 11: 59,079,650 S2586G probably damaging Het
Olfr148 A G 9: 39,614,463 R299G probably benign Het
Olfr156 C A 4: 43,820,912 V150L probably benign Het
Olfr559 C T 7: 102,724,202 R96H possibly damaging Het
Osbpl6 A G 2: 76,584,513 D416G probably damaging Het
Pdilt A G 7: 119,500,543 probably benign Het
Phf12 C A 11: 78,022,426 D401E probably benign Het
Pla2r1 C T 2: 60,428,721 V1108M possibly damaging Het
Prim2 A G 1: 33,480,406 probably benign Het
Ptpn6 T C 6: 124,724,984 H406R probably benign Het
Qpctl G T 7: 19,143,207 H329N probably damaging Het
Ripk3 T A 14: 55,785,298 N390Y probably damaging Het
Rnase1 A G 14: 51,145,450 V149A probably benign Het
Rtn3 T A 19: 7,456,827 D581V probably damaging Het
Slamf1 A G 1: 171,775,062 Y119C probably damaging Het
Slc25a34 A G 4: 141,623,662 M12T probably benign Het
Tmem38a A G 8: 72,580,100 Y141C probably damaging Het
Tnr C T 1: 159,886,930 T793I possibly damaging Het
Tns3 T C 11: 8,493,211 D384G probably damaging Het
Vmn2r116 T A 17: 23,387,307 Y398N probably damaging Het
Wee1 TCCCC TCCC 7: 110,124,569 probably null Het
Other mutations in Krtap9-5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00969:Krtap9-5 APN 11 99948465 unclassified probably benign
IGL01105:Krtap9-5 APN 11 99948633 missense unknown
IGL01673:Krtap9-5 APN 11 99949551 makesense probably null
IGL02931:Krtap9-5 APN 11 99949105 missense unknown
IGL03340:Krtap9-5 APN 11 99948601 missense possibly damaging 0.86
R0038:Krtap9-5 UTSW 11 99948602 missense possibly damaging 0.86
R1067:Krtap9-5 UTSW 11 99948763 missense unknown
R2051:Krtap9-5 UTSW 11 99949204 missense unknown
R2102:Krtap9-5 UTSW 11 99949444 missense unknown
R4689:Krtap9-5 UTSW 11 99949460 missense unknown
R5076:Krtap9-5 UTSW 11 99949468 missense unknown
R7468:Krtap9-5 UTSW 11 99949306 missense unknown
R7485:Krtap9-5 UTSW 11 99948974 missense unknown
R8876:Krtap9-5 UTSW 11 99949514 missense unknown
R9727:Krtap9-5 UTSW 11 99948514 missense possibly damaging 0.71
X0050:Krtap9-5 UTSW 11 99948941 missense unknown
Predicted Primers PCR Primer
(F):5'- AGCTGTGAAACCACCTGCTAC -3'
(R):5'- TGATCACACAGGTTGGTTTACAG -3'

Sequencing Primer
(F):5'- GTAAGCCAACCTGTGTGA -3'
(R):5'- TTTACAGCAGGTGGTCCTACAGC -3'
Posted On 2016-12-15