Incidental Mutation 'R6283:Krtap4-16'
ID 508068
Institutional Source Beutler Lab
Gene Symbol Krtap4-16
Ensembl Gene ENSMUSG00000046474
Gene Name keratin associated protein 4-16
Synonyms OTTMUSG00000002196
MMRRC Submission 044453-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.064) question?
Stock # R6283 (G1)
Quality Score 225.009
Status Validated
Chromosome 11
Chromosomal Location 99741481-99742431 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 99741861 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 180 (S180P)
Ref Sequence ENSEMBL: ENSMUSP00000103060 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000107437]
AlphaFold Q91W93
Predicted Effect unknown
Transcript: ENSMUST00000107437
AA Change: S180P
SMART Domains Protein: ENSMUSP00000103060
Gene: ENSMUSG00000046474
AA Change: S180P

DomainStartEndE-ValueType
Pfam:Keratin_B2_2 1 41 8e-7 PFAM
Pfam:Keratin_B2_2 19 63 6.6e-13 PFAM
Pfam:Keratin_B2_2 29 78 3e-8 PFAM
Pfam:Keratin_B2_2 62 98 4.1e-9 PFAM
Pfam:Keratin_B2_2 78 118 6.5e-10 PFAM
Pfam:Keratin_B2_2 96 136 2.4e-10 PFAM
Pfam:Keratin_B2_2 115 157 1.5e-9 PFAM
Pfam:Keratin_B2_2 134 174 7.3e-10 PFAM
Pfam:Keratin_B2_2 168 202 1.6e-7 PFAM
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.0%
  • 20x: 94.1%
Validation Efficiency 100% (59/59)
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsf3 C A 8: 123,512,694 (GRCm39) R372S probably damaging Het
Adamts20 A G 15: 94,249,602 (GRCm39) S472P probably benign Het
Bhlhe40 T C 6: 108,641,992 (GRCm39) L312P probably damaging Het
Ccdc180 A G 4: 45,902,486 (GRCm39) E305G possibly damaging Het
Ccdc83 T A 7: 89,885,615 (GRCm39) R257* probably null Het
Cd209e G A 8: 3,899,212 (GRCm39) Q167* probably null Het
Cd300e G A 11: 114,945,380 (GRCm39) T138I probably benign Het
Ces2c A T 8: 105,576,331 (GRCm39) M115L probably benign Het
Cfap61 T A 2: 145,971,022 (GRCm39) probably null Het
Chd1l G A 3: 97,494,483 (GRCm39) A399V probably damaging Het
Cic C T 7: 24,985,459 (GRCm39) S301L probably damaging Het
Cks2 A G 13: 51,799,495 (GRCm39) H16R probably benign Het
Copa A T 1: 171,946,415 (GRCm39) H953L possibly damaging Het
Ctdsp2 T C 10: 126,831,749 (GRCm39) V145A possibly damaging Het
Cyp2j13 A G 4: 95,945,074 (GRCm39) V377A possibly damaging Het
Dhx57 A G 17: 80,582,234 (GRCm39) V404A probably benign Het
Dock2 T C 11: 34,598,152 (GRCm39) S340G probably damaging Het
Ggps1 A G 13: 14,232,379 (GRCm39) probably null Het
Gm10549 C A 18: 33,597,358 (GRCm39) probably benign Het
Gm11444 T C 11: 85,737,617 (GRCm39) probably null Het
Grina A G 15: 76,132,751 (GRCm39) T173A possibly damaging Het
Hcrtr1 G A 4: 130,029,133 (GRCm39) T223I probably benign Het
Igsf10 T A 3: 59,226,870 (GRCm39) T2268S probably damaging Het
Inhca G A 9: 103,159,834 (GRCm39) R14* probably null Het
Ino80d C T 1: 63,101,285 (GRCm39) R447Q probably damaging Het
Inpp4b C T 8: 82,497,462 (GRCm39) T94M probably damaging Het
Itga2 A G 13: 115,005,786 (GRCm39) Y465H probably damaging Het
Knl1 A G 2: 118,900,767 (GRCm39) T823A probably damaging Het
Ldc1 A G 4: 130,115,534 (GRCm39) S5P probably benign Het
Lpar6 A T 14: 73,476,297 (GRCm39) D86V probably damaging Het
Muc5ac C A 7: 141,370,601 (GRCm39) C2500* probably null Het
Mzf1 T C 7: 12,787,296 (GRCm39) probably benign Het
Or4f58 A C 2: 111,851,605 (GRCm39) M198R possibly damaging Het
Or5d46 T A 2: 88,170,002 (GRCm39) I31N probably benign Het
Or5m3 G T 2: 85,838,443 (GRCm39) V108L possibly damaging Het
Or7a36 T C 10: 78,820,113 (GRCm39) V163A probably benign Het
Otogl T G 10: 107,626,361 (GRCm39) E1501A probably damaging Het
Pcdh10 T A 3: 45,335,989 (GRCm39) S768T possibly damaging Het
Pcnx2 G T 8: 126,604,325 (GRCm39) Q644K probably damaging Het
Pdzd9 T A 7: 120,259,449 (GRCm39) I180F possibly damaging Het
Pinx1 A C 14: 64,115,621 (GRCm39) N152T probably benign Het
Prr14l T C 5: 32,987,608 (GRCm39) E629G probably benign Het
Qpctl T A 7: 18,882,345 (GRCm39) I104F probably benign Het
Rabep1 C T 11: 70,808,505 (GRCm39) A444V probably damaging Het
Rnf150 A G 8: 83,717,183 (GRCm39) Y230C probably damaging Het
Slc25a27 A C 17: 43,968,621 (GRCm39) V152G probably damaging Het
Swt1 A G 1: 151,260,084 (GRCm39) S772P possibly damaging Het
Tenm4 A G 7: 96,523,701 (GRCm39) T1711A probably benign Het
Tfap2d G C 1: 19,174,702 (GRCm39) G52R probably benign Het
Tmem265 T G 7: 127,164,044 (GRCm39) V86G possibly damaging Het
Trpm8 C T 1: 88,276,054 (GRCm39) H551Y probably benign Het
Ttc6 T G 12: 57,749,048 (GRCm39) Y1327D possibly damaging Het
Uevld G T 7: 46,587,729 (GRCm39) Q324K possibly damaging Het
Vmn2r111 T C 17: 22,778,032 (GRCm39) N549S possibly damaging Het
Vmn2r73 C T 7: 85,521,049 (GRCm39) M306I probably benign Het
Vmn2r93 T A 17: 18,524,366 (GRCm39) M120K probably benign Het
Zfp804b T A 5: 6,819,908 (GRCm39) I1016F probably benign Het
Zfp90 T C 8: 107,152,026 (GRCm39) C580R probably damaging Het
Other mutations in Krtap4-16
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00095:Krtap4-16 APN 11 99,742,032 (GRCm39) missense possibly damaging 0.86
IGL02750:Krtap4-16 APN 11 99,742,106 (GRCm39) missense possibly damaging 0.71
IGL02973:Krtap4-16 APN 11 99,742,167 (GRCm39) missense possibly damaging 0.71
IGL03236:Krtap4-16 APN 11 99,741,962 (GRCm39) missense unknown
IGL02837:Krtap4-16 UTSW 11 99,741,863 (GRCm39) missense unknown
R1803:Krtap4-16 UTSW 11 99,741,998 (GRCm39) missense possibly damaging 0.93
R1959:Krtap4-16 UTSW 11 99,742,373 (GRCm39) missense unknown
R1986:Krtap4-16 UTSW 11 99,742,322 (GRCm39) missense unknown
R5818:Krtap4-16 UTSW 11 99,742,349 (GRCm39) missense unknown
R9643:Krtap4-16 UTSW 11 99,742,271 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- AGTTTCTTACTGGTGTCAGGAC -3'
(R):5'- GTGATCAAAGTCCCTGCCAG -3'

Sequencing Primer
(F):5'- CAACAAAGGTAGGAGGCATTTAGTAC -3'
(R):5'- TCAAAGTCCCTGCCAGGAGAG -3'
Posted On 2018-03-15