Incidental Mutation 'IGL00870:Krtap20-2'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Krtap20-2
Ensembl Gene ENSMUSG00000091039
Gene Namekeratin associated protein 20-2
SynonymsGm6371, 1190004K03Rik
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.195) question?
Stock #IGL00870
Quality Score
Chromosomal Location89205861-89206394 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 89205987 bp
Amino Acid Change Glycine to Aspartic acid at position 25 (G25D)
Ref Sequence ENSEMBL: ENSMUSP00000126264 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000169954]
Predicted Effect unknown
Transcript: ENSMUST00000169954
AA Change: G25D
SMART Domains Protein: ENSMUSP00000126264
Gene: ENSMUSG00000091039
AA Change: G25D

Pfam:KRTAP 1 54 3e-14 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ahnak T A 19: 9,013,698 D4115E probably damaging Het
Asb5 T C 8: 54,583,660 probably null Het
Cpeb3 A T 19: 37,054,295 I569N probably damaging Het
Cpsf7 T C 19: 10,539,650 probably null Het
Dlat A G 9: 50,650,869 L285P probably damaging Het
Dytn T C 1: 63,677,113 probably benign Het
Ears2 A T 7: 122,055,676 L123Q probably damaging Het
Gad2 T C 2: 22,629,971 V212A probably benign Het
Gon4l T C 3: 88,857,185 Y358H probably damaging Het
Gys1 T C 7: 45,448,013 probably null Het
Hnrnpm C A 17: 33,649,902 R517L probably damaging Het
Lrif1 T C 3: 106,734,641 probably null Het
Naip2 A G 13: 100,152,060 probably benign Het
Olfr884 A T 9: 38,047,740 I173F probably damaging Het
Oxct1 T A 15: 4,101,818 L396Q probably damaging Het
Pclo A T 5: 14,539,983 R766W unknown Het
Pkhd1 T A 1: 20,571,390 I275F probably damaging Het
Rxfp3 A G 15: 11,036,215 F357S probably damaging Het
Rxfp3 A G 15: 11,036,305 V327A probably damaging Het
Serpinb2 A G 1: 107,523,070 I181V probably damaging Het
Smad5 A G 13: 56,723,667 D25G probably benign Het
Strada A G 11: 106,171,257 L82P probably damaging Het
Tek T A 4: 94,873,081 Y1079* probably null Het
Tenm3 T C 8: 48,417,132 T209A probably benign Het
Tnks1bp1 C T 2: 85,062,236 Q836* probably null Het
Toporsl T C 4: 52,610,172 S22P probably benign Het
Ttc17 T C 2: 94,371,733 probably null Het
Ttc39a A G 4: 109,442,345 probably benign Het
Vangl1 T C 3: 102,189,440 D60G probably damaging Het
Vmn1r13 A T 6: 57,210,113 M86L probably benign Het
Vmn1r220 C T 13: 23,184,477 M16I probably null Het
Other mutations in Krtap20-2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01634:Krtap20-2 APN 16 89206089 missense unknown
R5086:Krtap20-2 UTSW 16 89205918 missense unknown
Posted On2012-12-06