Incidental Mutation 'IGL01963:Krtap26-1'
ID 182472
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Krtap26-1
Ensembl Gene ENSMUSG00000071471
Gene Name keratin associated protein 26-1
Synonyms 2310002B14Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.051) question?
Stock # IGL01963
Quality Score
Status
Chromosome 16
Chromosomal Location 88443712-88444684 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 88444556 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Arginine at position 22 (C22R)
Ref Sequence ENSEMBL: ENSMUSP00000093626 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095934]
AlphaFold Q9D7N2
Predicted Effect probably damaging
Transcript: ENSMUST00000095934
AA Change: C22R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000093626
Gene: ENSMUSG00000071471
AA Change: C22R

DomainStartEndE-ValueType
Pfam:PMG 4 213 2.9e-65 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2610042L04Rik G A 14: 4,350,856 (GRCm38) G130D probably damaging Het
Abca8b T A 11: 109,862,589 (GRCm39) D392V probably damaging Het
Cep43 A T 17: 8,411,109 (GRCm39) D354V probably damaging Het
Clptm1l T A 13: 73,765,688 (GRCm39) probably benign Het
Creb3l1 G A 2: 91,823,678 (GRCm39) T178I probably benign Het
Ctsd A G 7: 141,930,336 (GRCm39) probably null Het
Dcstamp A T 15: 39,623,755 (GRCm39) I401F possibly damaging Het
Dnah5 A G 15: 28,370,682 (GRCm39) D2874G probably benign Het
Fcsk A G 8: 111,620,034 (GRCm39) F281S probably damaging Het
Fli1 T A 9: 32,335,503 (GRCm39) K310* probably null Het
Fndc4 C T 5: 31,452,556 (GRCm39) probably null Het
Gc G A 5: 89,569,981 (GRCm39) probably benign Het
Obscn C T 11: 58,911,367 (GRCm39) G6422S probably benign Het
Or10d5 C A 9: 39,861,536 (GRCm39) C177F probably damaging Het
Or10j2 T A 1: 173,097,919 (GRCm39) M59K probably damaging Het
Or5b21 T A 19: 12,839,746 (GRCm39) F202L probably benign Het
Pgr C T 9: 8,922,669 (GRCm39) P613L probably damaging Het
Pnpla8 C A 12: 44,342,816 (GRCm39) A524E possibly damaging Het
Psma2 A T 13: 14,793,948 (GRCm39) I105F probably damaging Het
Ptprg A G 14: 12,220,661 (GRCm38) R458G probably damaging Het
Rbm44 A G 1: 91,090,830 (GRCm39) I755V probably benign Het
Rev3l A G 10: 39,698,733 (GRCm39) K1077E possibly damaging Het
Rps20 A C 4: 3,834,494 (GRCm39) probably benign Het
Sel1l3 A C 5: 53,357,680 (GRCm39) V104G probably damaging Het
Sirpb1c T C 3: 15,892,937 (GRCm39) N89S probably benign Het
Slc25a16 G A 10: 62,766,220 (GRCm39) probably null Het
Sulf1 C T 1: 12,888,731 (GRCm39) R339C probably damaging Het
Tedc2 C T 17: 24,436,926 (GRCm39) A270T probably benign Het
Trem3 T C 17: 48,554,880 (GRCm39) S2P possibly damaging Het
Vps37a G T 8: 40,993,771 (GRCm39) Q255H probably damaging Het
Zfp352 C T 4: 90,112,391 (GRCm39) A177V possibly damaging Het
Other mutations in Krtap26-1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00886:Krtap26-1 APN 16 88,444,267 (GRCm39) missense possibly damaging 0.62
IGL01721:Krtap26-1 APN 16 88,444,060 (GRCm39) missense probably damaging 1.00
IGL02524:Krtap26-1 APN 16 88,444,367 (GRCm39) missense possibly damaging 0.70
R0383:Krtap26-1 UTSW 16 88,444,131 (GRCm39) nonsense probably null
R2367:Krtap26-1 UTSW 16 88,444,213 (GRCm39) missense probably benign 0.28
R4694:Krtap26-1 UTSW 16 88,444,108 (GRCm39) missense possibly damaging 0.70
R6699:Krtap26-1 UTSW 16 88,444,603 (GRCm39) missense unknown
R6884:Krtap26-1 UTSW 16 88,444,467 (GRCm39) missense probably damaging 1.00
R7299:Krtap26-1 UTSW 16 88,444,132 (GRCm39) missense possibly damaging 0.49
R7808:Krtap26-1 UTSW 16 88,444,198 (GRCm39) missense not run
R8824:Krtap26-1 UTSW 16 88,444,324 (GRCm39) missense probably damaging 0.99
R8824:Krtap26-1 UTSW 16 88,444,303 (GRCm39) missense probably damaging 1.00
R9034:Krtap26-1 UTSW 16 88,444,161 (GRCm39) missense probably benign 0.14
R9186:Krtap26-1 UTSW 16 88,444,609 (GRCm39) missense unknown
R9279:Krtap26-1 UTSW 16 88,444,342 (GRCm39) missense probably benign 0.00
Posted On 2014-05-07