Incidental Mutation 'R9113:Krtap6-2'
ID 692378
Institutional Source Beutler Lab
Gene Symbol Krtap6-2
Ensembl Gene ENSMUSG00000062433
Gene Name keratin associated protein 6-2
Synonyms
MMRRC Submission 068920-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.065) question?
Stock # R9113 (G1)
Quality Score 139.459
Status Not validated
Chromosome 16
Chromosomal Location 89216214-89216999 bp(-) (GRCm39)
Type of Mutation small deletion (8 aa in frame mutation)
DNA Base Change (assembly) GAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCGTATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCAGAGCCACAGCCATAGCCAGAACCATAGCCACAGCCATAGCCAGAGCCATAGCCACAGCCATAGCCAGAGCCAGAGCCACAGCCATAGCCAGAGCCATAGCCACAGCCATAGCCA to GAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCGTATCCACAGCCATAGCCAGAGCCATATCCACAGCCATAGCCAGAGCCAGAGCCACAGCCATAGCCAGAACCATAGCCACAGCCATAGCCAGAGCCATAGCCACAGCCATAGCCAGAGCCAGAGCCACAGCCATAGCCAGAGCCATAGCCACAGCCATAGCCA at 89216613 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000139661 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000082065]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000082065
SMART Domains Protein: ENSMUSP00000139661
Gene: ENSMUSG00000062433

DomainStartEndE-ValueType
low complexity region 2 152 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.9%
  • 20x: 99.6%
Validation Efficiency 100% (50/50)
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc9 T A 6: 142,591,656 (GRCm39) I791F probably damaging Het
Adamts15 A G 9: 30,822,498 (GRCm39) M389T probably damaging Het
Adgrb2 G A 4: 129,910,877 (GRCm39) V1065M probably damaging Het
Agbl1 C A 7: 76,239,225 (GRCm39) A827E unknown Het
Alox5ap T C 5: 149,216,015 (GRCm39) F67S probably damaging Het
Ankrd11 T C 8: 123,614,072 (GRCm39) N2566S possibly damaging Het
Arhgap10 T C 8: 77,985,701 (GRCm39) D722G probably damaging Het
Atp5mf A G 5: 145,128,315 (GRCm39) L4P probably benign Het
Bean1 T C 8: 104,940,557 (GRCm39) V130A probably benign Het
Ccdc88b T C 19: 6,833,213 (GRCm39) E278G probably damaging Het
Cdhr2 A G 13: 54,882,700 (GRCm39) D1222G probably benign Het
Chrm4 T A 2: 91,758,075 (GRCm39) V161E probably benign Het
Ckap5 T C 2: 91,426,144 (GRCm39) S1335P probably damaging Het
Col11a1 T A 3: 113,888,192 (GRCm39) Y267* probably null Het
Col14a1 T C 15: 55,201,825 (GRCm39) Y38H unknown Het
Coro2a C T 4: 46,563,047 (GRCm39) G36S Het
Ctsc A T 7: 87,959,104 (GRCm39) K461N possibly damaging Het
Dcaf1 A G 9: 106,712,831 (GRCm39) probably benign Het
Dnah9 A G 11: 65,880,713 (GRCm39) I2628T probably damaging Het
Dnajb5 T C 4: 42,953,233 (GRCm39) I20T probably damaging Het
Dus2 C T 8: 106,775,333 (GRCm39) Q287* probably null Het
Fbxl17 A G 17: 63,532,085 (GRCm39) V586A probably benign Het
Glg1 A T 8: 111,887,452 (GRCm39) probably benign Het
Gm4924 G A 10: 82,214,113 (GRCm39) C637Y unknown Het
Gorasp1 A G 9: 119,757,442 (GRCm39) F310S probably damaging Het
Gsta5 A T 9: 78,212,667 (GRCm39) I213F probably benign Het
Igfn1 G A 1: 135,883,328 (GRCm39) T2726I probably damaging Het
Inppl1 G T 7: 101,475,231 (GRCm39) P940Q probably benign Het
Klk1b22 G A 7: 43,765,692 (GRCm39) V183M possibly damaging Het
Krt12 A G 11: 99,309,378 (GRCm39) M294T probably damaging Het
Lep T C 6: 29,071,093 (GRCm39) L139P probably damaging Het
Ltn1 T C 16: 87,224,532 (GRCm39) D64G probably damaging Het
Lyzl1 C T 18: 4,168,604 (GRCm39) A28V probably null Het
Mcam T C 9: 44,051,693 (GRCm39) V483A probably benign Het
Mia2 C T 12: 59,217,053 (GRCm39) probably benign Het
Mzf1 T A 7: 12,778,279 (GRCm39) H454L probably damaging Het
Pde10a A G 17: 9,197,782 (GRCm39) T742A probably benign Het
Rapgef4 A G 2: 71,861,493 (GRCm39) Y61C probably benign Het
Ryr2 A T 13: 11,618,741 (GRCm39) probably benign Het
Setbp1 G T 18: 78,900,948 (GRCm39) H906Q probably damaging Het
Slc12a4 A G 8: 106,670,984 (GRCm39) V1032A probably benign Het
Slc6a15 T C 10: 103,236,140 (GRCm39) M285T probably damaging Het
Spata31h1 G A 10: 82,131,352 (GRCm39) Q553* probably null Het
Steap2 A G 5: 5,727,475 (GRCm39) Y287H probably damaging Het
Tas2r135 T G 6: 42,383,315 (GRCm39) F285V probably benign Het
Tmco1 C T 1: 167,136,132 (GRCm39) probably benign Het
Ttn T C 2: 76,618,538 (GRCm39) T16249A probably benign Het
Usp8 A G 2: 126,579,343 (GRCm39) T299A probably benign Het
Vmn2r101 A G 17: 19,811,288 (GRCm39) I457M possibly damaging Het
Vps41 A G 13: 19,023,883 (GRCm39) E437G probably benign Het
Zfp638 A T 6: 83,953,894 (GRCm39) E1333V probably damaging Het
Other mutations in Krtap6-2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03375:Krtap6-2 APN 16 89,216,644 (GRCm39) missense unknown
R1566:Krtap6-2 UTSW 16 89,216,626 (GRCm39) missense unknown
R4896:Krtap6-2 UTSW 16 89,216,806 (GRCm39) missense unknown
R5857:Krtap6-2 UTSW 16 89,216,530 (GRCm39) missense unknown
R6390:Krtap6-2 UTSW 16 89,216,834 (GRCm39) nonsense probably null
R6958:Krtap6-2 UTSW 16 89,216,698 (GRCm39) missense unknown
R7432:Krtap6-2 UTSW 16 89,216,761 (GRCm39) missense unknown
R7454:Krtap6-2 UTSW 16 89,216,800 (GRCm39) missense unknown
R7780:Krtap6-2 UTSW 16 89,216,510 (GRCm39) nonsense probably null
R7981:Krtap6-2 UTSW 16 89,216,562 (GRCm39) missense unknown
R8949:Krtap6-2 UTSW 16 89,216,703 (GRCm39) missense unknown
R9562:Krtap6-2 UTSW 16 89,216,722 (GRCm39) missense unknown
R9565:Krtap6-2 UTSW 16 89,216,722 (GRCm39) missense unknown
R9747:Krtap6-2 UTSW 16 89,216,776 (GRCm39) missense unknown
R9757:Krtap6-2 UTSW 16 89,216,958 (GRCm39) missense unknown
R9762:Krtap6-2 UTSW 16 89,216,763 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- AGCTGGAGGTCAAAGACTTTG -3'
(R):5'- TGGATACGGCTCTGGCTATG -3'

Sequencing Primer
(F):5'- ATATAGAGCTCTTGGCCATGGATC -3'
(R):5'- CTATGGCTGTGGATATGGCTC -3'
Posted On 2021-12-30