Incidental Mutation 'R9722:Krtap4-13'
ID 730870
Institutional Source Beutler Lab
Gene Symbol Krtap4-13
Ensembl Gene ENSMUSG00000048294
Gene Name keratin associated protein 4-13
Synonyms 2300006N05Rik
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.049) question?
Stock # R9722 (G1)
Quality Score 225.009
Status Not validated
Chromosome 11
Chromosomal Location 99699904-99700718 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 99700180 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 160 (S160P)
Ref Sequence ENSEMBL: ENSMUSP00000053810 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050106] [ENSMUST00000105056]
AlphaFold Q9D7P3
Predicted Effect unknown
Transcript: ENSMUST00000050106
AA Change: S160P
SMART Domains Protein: ENSMUSP00000053810
Gene: ENSMUSG00000048294
AA Change: S160P

DomainStartEndE-ValueType
Pfam:Keratin_B2_2 1 43 1.3e-9 PFAM
Pfam:Keratin_B2 1 80 7.3e-10 PFAM
Pfam:Keratin_B2_2 14 58 6.4e-14 PFAM
Pfam:Keratin_B2_2 24 68 7.8e-15 PFAM
Pfam:Keratin_B2_2 39 83 9.1e-15 PFAM
Pfam:Keratin_B2_2 54 98 1.3e-14 PFAM
Pfam:Keratin_B2_2 64 107 1.1e-14 PFAM
Pfam:Keratin_B2_2 99 143 1.3e-12 PFAM
Pfam:Keratin_B2_2 124 165 5.3e-9 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000105056
SMART Domains Protein: ENSMUSP00000100677
Gene: ENSMUSG00000078259

DomainStartEndE-ValueType
Pfam:Keratin_B2_2 1 52 7.4e-9 PFAM
Pfam:Keratin_B2 1 122 3.8e-11 PFAM
Pfam:Keratin_B2_2 34 78 8.9e-14 PFAM
Pfam:Keratin_B2_2 74 117 2.5e-12 PFAM
Pfam:Keratin_B2_2 109 157 2.5e-7 PFAM
Pfam:Keratin_B2_2 149 190 5.8e-10 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9330159F19Rik A T 10: 29,094,269 (GRCm39) I52F probably benign Het
Abcc3 A T 11: 94,250,072 (GRCm39) L1017Q probably damaging Het
Antxr2 T C 5: 98,096,186 (GRCm39) D366G possibly damaging Het
Astn2 C T 4: 65,831,978 (GRCm39) V563I probably benign Het
Atrn C A 2: 130,803,536 (GRCm39) D575E probably damaging Het
Baz1a C T 12: 54,946,882 (GRCm39) D1228N probably benign Het
Canx A G 11: 50,195,301 (GRCm39) S256P probably benign Het
Ccnt2 T A 1: 127,729,925 (GRCm39) D267E probably damaging Het
Cd209c G T 8: 3,995,905 (GRCm39) R2S probably benign Het
Cyfip2 T C 11: 46,087,135 (GRCm39) T1252A probably benign Het
Dchs2 A G 3: 83,261,301 (GRCm39) Y2523C probably benign Het
Dmxl2 G A 9: 54,323,892 (GRCm39) P990L probably benign Het
Dnajc9 T C 14: 20,438,279 (GRCm39) I108V probably benign Het
Eif2d T C 1: 131,092,948 (GRCm39) probably null Het
Ephb2 T C 4: 136,384,768 (GRCm39) D881G probably damaging Het
Esr1 A G 10: 4,951,215 (GRCm39) N531S probably benign Het
Fbxo2 G A 4: 148,248,883 (GRCm39) R125H probably damaging Het
Foxred1 C T 9: 35,117,300 (GRCm39) S277N possibly damaging Het
Gemin5 T C 11: 58,041,418 (GRCm39) E518G probably damaging Het
Gm17655 A G 5: 110,194,226 (GRCm39) Y519H probably benign Het
Igkv4-57-1 A T 6: 69,521,493 (GRCm39) W70R probably damaging Het
Map3k3 A G 11: 106,033,361 (GRCm39) I205V possibly damaging Het
Map3k4 A C 17: 12,490,523 (GRCm39) F303V probably benign Het
Mpdz T C 4: 81,304,504 (GRCm39) Q132R probably damaging Het
Myo10 T A 15: 25,801,227 (GRCm39) V1472E probably damaging Het
Nckap1 G A 2: 80,401,568 (GRCm39) Q39* probably null Het
Nog A G 11: 89,192,396 (GRCm39) S151P probably damaging Het
Obox6 G A 7: 15,568,831 (GRCm39) S15F probably benign Het
Odf2 A G 2: 29,813,594 (GRCm39) H647R possibly damaging Het
Or6c74 A G 10: 129,869,500 (GRCm39) R2G probably benign Het
Pcdhga11 T C 18: 37,890,398 (GRCm39) S469P possibly damaging Het
Pcnx4 T C 12: 72,603,039 (GRCm39) Y434H probably damaging Het
Pfpl G C 19: 12,406,297 (GRCm39) E183Q probably damaging Het
Pglyrp3 A G 3: 91,938,695 (GRCm39) K290R possibly damaging Het
Phactr3 G A 2: 177,898,043 (GRCm39) E86K probably damaging Het
Piezo1 A C 8: 123,225,497 (GRCm39) L530R Het
Pigg A T 5: 108,495,767 (GRCm39) I935F possibly damaging Het
Pofut2 T C 10: 77,102,759 (GRCm39) S282P possibly damaging Het
Ppfia1 A G 7: 144,071,402 (GRCm39) S337P probably benign Het
Sdr16c5 A T 4: 4,005,595 (GRCm39) D246E probably benign Het
Sgsm1 T A 5: 113,428,207 (GRCm39) H327L possibly damaging Het
Slc39a4 A G 15: 76,500,211 (GRCm39) I113T possibly damaging Het
Slc5a7 A G 17: 54,603,985 (GRCm39) probably null Het
Snx11 A G 11: 96,661,925 (GRCm39) S86P probably benign Het
Srm T A 4: 148,676,245 (GRCm39) probably null Het
Tas2r126 T C 6: 42,412,082 (GRCm39) I205T possibly damaging Het
Tek T G 4: 94,692,539 (GRCm39) W216G possibly damaging Het
Tenm3 A T 8: 48,753,849 (GRCm39) S851R probably benign Het
Tnip2 A G 5: 34,654,212 (GRCm39) V288A probably benign Het
Tpx2 T A 2: 152,733,476 (GRCm39) probably null Het
Trim33 C A 3: 103,261,146 (GRCm39) T1115K possibly damaging Het
Tspan13 T A 12: 36,074,017 (GRCm39) I40F probably damaging Het
Ube2v2 T C 16: 15,394,899 (GRCm39) I91V probably benign Het
Vmn1r22 A T 6: 57,877,631 (GRCm39) F115L probably benign Het
Vmn2r7 G A 3: 64,598,407 (GRCm39) P717S probably damaging Het
Zan T C 5: 137,387,324 (GRCm39) T4910A unknown Het
Zfp599 T A 9: 22,160,741 (GRCm39) T475S probably damaging Het
Zfp638 T A 6: 83,923,301 (GRCm39) F700I probably damaging Het
Zfp985 A C 4: 147,667,618 (GRCm39) K162T possibly damaging Het
Other mutations in Krtap4-13
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00401:Krtap4-13 APN 11 99,700,543 (GRCm39) missense unknown
R4632:Krtap4-13 UTSW 11 99,700,354 (GRCm39) missense unknown
R6845:Krtap4-13 UTSW 11 99,700,192 (GRCm39) unclassified probably benign
R7284:Krtap4-13 UTSW 11 99,700,238 (GRCm39) nonsense probably null
R8118:Krtap4-13 UTSW 11 99,700,224 (GRCm39) missense unknown
R9180:Krtap4-13 UTSW 11 99,700,165 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- ACTAAGCAGGCTGGAGTGTG -3'
(R):5'- CCTAGCTGCTGCATTTCCAG -3'

Sequencing Primer
(F):5'- GTGGCAAATAGTTGTTGTCCAAATC -3'
(R):5'- ATTTCCAGCTGCTGCAGG -3'
Posted On 2022-10-06