Incidental Mutation 'IGL02238:Krt88'
ID 285993
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Krt88
Ensembl Gene ENSMUSG00000063971
Gene Name keratin 88
Synonyms 1700011A15Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02238
Quality Score
Status
Chromosome 15
Chromosomal Location 101345625-101351788 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 101350486 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000023781 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023781]
AlphaFold Q9CPR6
Predicted Effect probably benign
Transcript: ENSMUST00000023781
SMART Domains Protein: ENSMUSP00000023781
Gene: ENSMUSG00000063971

DomainStartEndE-ValueType
Pfam:Filament 1 109 5e-24 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca15 T A 7: 119,995,829 (GRCm39) I1322N probably benign Het
Adamts1 A T 16: 85,592,713 (GRCm39) M565K probably benign Het
Akr1b7 T A 6: 34,392,333 (GRCm39) Y49N probably damaging Het
Cacna2d2 T A 9: 107,390,757 (GRCm39) V363E probably damaging Het
Cdc45 C T 16: 18,617,479 (GRCm39) M200I probably benign Het
Cdh10 C T 15: 19,013,605 (GRCm39) T735I probably damaging Het
Cds1 T A 5: 101,962,302 (GRCm39) C306S possibly damaging Het
Cfap251 T C 5: 123,440,486 (GRCm39) Y1091H probably damaging Het
Clasp2 T C 9: 113,709,088 (GRCm39) C644R probably damaging Het
Coil T C 11: 88,872,580 (GRCm39) S314P probably benign Het
D630045J12Rik T A 6: 38,173,329 (GRCm39) M280L probably benign Het
Dmxl2 C T 9: 54,352,717 (GRCm39) V795M probably damaging Het
Dock10 A G 1: 80,511,510 (GRCm39) V1533A probably damaging Het
Fbxo40 T C 16: 36,789,536 (GRCm39) N525D possibly damaging Het
Fezf2 T C 14: 12,344,494 (GRCm38) E231G probably damaging Het
Fmn1 T C 2: 113,412,470 (GRCm39) V870A possibly damaging Het
Ifi44 A G 3: 151,438,019 (GRCm39) *423Q probably null Het
Invs T C 4: 48,390,029 (GRCm39) V173A probably damaging Het
Mctp2 A T 7: 71,739,953 (GRCm39) Y812* probably null Het
Neto2 T C 8: 86,396,292 (GRCm39) I118V probably damaging Het
Nutm2 T G 13: 50,625,075 (GRCm39) M264R probably damaging Het
Or2d2 A G 7: 106,728,244 (GRCm39) S119P probably damaging Het
Or8u8 T C 2: 86,011,939 (GRCm39) probably null Het
Pcnx1 G A 12: 81,964,688 (GRCm39) R285Q probably damaging Het
Pi16 G T 17: 29,545,269 (GRCm39) K177N probably damaging Het
Pigg C T 5: 108,466,794 (GRCm39) S225F possibly damaging Het
Prrc2b T A 2: 32,103,429 (GRCm39) V969E probably damaging Het
Rab4b A C 7: 26,872,154 (GRCm39) Y189D probably benign Het
Ran A G 5: 129,099,246 (GRCm39) N143D possibly damaging Het
Rfc4 A T 16: 22,933,219 (GRCm39) F286L probably damaging Het
Sel1l2 T C 2: 140,089,859 (GRCm39) Y418C probably damaging Het
Slc13a1 T C 6: 24,103,482 (GRCm39) I354V probably benign Het
Slc7a2 A T 8: 41,361,193 (GRCm39) T386S probably benign Het
Tm2d2 G T 8: 25,512,787 (GRCm39) V212F probably benign Het
Tmem247 A T 17: 87,225,721 (GRCm39) N54Y probably damaging Het
Txnrd3 T A 6: 89,633,117 (GRCm39) Y206N probably benign Het
Uba5 T C 9: 103,931,259 (GRCm39) probably benign Het
Vmn2r54 A G 7: 12,369,910 (GRCm39) L51P probably damaging Het
Zfp735 A G 11: 73,601,319 (GRCm39) K88E probably benign Het
Other mutations in Krt88
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01069:Krt88 APN 15 101,351,508 (GRCm39) makesense probably null
R3916:Krt88 UTSW 15 101,350,809 (GRCm39) splice site probably null
R3917:Krt88 UTSW 15 101,350,809 (GRCm39) splice site probably null
R5161:Krt88 UTSW 15 101,348,349 (GRCm39) missense probably benign 0.28
R7253:Krt88 UTSW 15 101,348,392 (GRCm39) missense probably damaging 1.00
R7360:Krt88 UTSW 15 101,345,643 (GRCm39) start gained probably benign
R8163:Krt88 UTSW 15 101,351,389 (GRCm39) missense probably damaging 1.00
R8498:Krt88 UTSW 15 101,351,406 (GRCm39) missense probably benign
R8745:Krt88 UTSW 15 101,351,460 (GRCm39) missense possibly damaging 0.95
Posted On 2015-04-16