Incidental Mutation 'IGL02889:Krtap19-4'
ID 363107
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Krtap19-4
Ensembl Gene ENSMUSG00000043982
Gene Name keratin associated protein 19-4
Synonyms Krtap16-4
Accession Numbers
Essential gene? Probably non essential (E-score: 0.165) question?
Stock # IGL02889
Quality Score
Status
Chromosome 16
Chromosomal Location 88681674-88681977 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 88681944 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 4 (Y4C)
Ref Sequence ENSEMBL: ENSMUSP00000056250 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000051103]
AlphaFold Q925H7
Predicted Effect unknown
Transcript: ENSMUST00000051103
AA Change: Y4C
SMART Domains Protein: ENSMUSP00000056250
Gene: ENSMUSG00000043982
AA Change: Y4C

DomainStartEndE-ValueType
Pfam:KRTAP 1 47 1e-15 PFAM
Pfam:KRTAP 45 78 3.2e-8 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adarb1 C T 10: 77,149,375 (GRCm39) V371I probably benign Het
Amdhd2 A G 17: 24,376,761 (GRCm39) L308P probably damaging Het
Antxr2 G T 5: 98,125,509 (GRCm39) H249Q probably benign Het
Arg1 A T 10: 24,791,653 (GRCm39) M276K probably damaging Het
Bloc1s6 T C 2: 122,584,604 (GRCm39) Y60H probably damaging Het
Btnl9 A T 11: 49,069,604 (GRCm39) V225E probably damaging Het
Col1a1 T C 11: 94,842,335 (GRCm39) Y1418H unknown Het
Ct45a C A X: 55,592,551 (GRCm39) K19N probably damaging Het
Dhx57 A T 17: 80,554,581 (GRCm39) I1162K possibly damaging Het
Dmgdh T C 13: 93,852,185 (GRCm39) probably null Het
Ear10 A G 14: 44,160,726 (GRCm39) F34L probably damaging Het
Fli1 A G 9: 32,376,992 (GRCm39) I92T probably damaging Het
Fpgs G A 2: 32,575,891 (GRCm39) probably benign Het
Glp1r T A 17: 31,150,118 (GRCm39) probably benign Het
Hectd4 T A 5: 121,503,116 (GRCm39) Y4362N possibly damaging Het
Ifitm3 C T 7: 140,589,792 (GRCm39) R87Q probably damaging Het
Ints3 G T 3: 90,300,143 (GRCm39) H925N probably damaging Het
Itgb4 T A 11: 115,879,731 (GRCm39) C628S probably damaging Het
Itprid1 A T 6: 55,878,443 (GRCm39) D402V possibly damaging Het
Kcnh3 A T 15: 99,124,991 (GRCm39) E147V probably null Het
Lrp2 A T 2: 69,382,794 (GRCm39) S30R possibly damaging Het
Or11g27 A G 14: 50,770,970 (GRCm39) I34V probably benign Het
Or8g2b A G 9: 39,751,533 (GRCm39) M268V probably benign Het
Prima1 A G 12: 103,163,575 (GRCm39) V132A probably benign Het
Psme1 A G 14: 55,817,383 (GRCm39) probably benign Het
Rab11fip3 C A 17: 26,286,653 (GRCm39) R500L possibly damaging Het
Rnf40 C A 7: 127,190,601 (GRCm39) S255* probably null Het
Sebox T C 11: 78,395,156 (GRCm39) V166A probably benign Het
Spata24 C A 18: 35,789,805 (GRCm39) R194L probably benign Het
Spata31h1 C T 10: 82,119,654 (GRCm39) S482N probably damaging Het
Tbx4 T A 11: 85,790,621 (GRCm39) Y154* probably null Het
Trim24 G A 6: 37,934,696 (GRCm39) E768K probably benign Het
Ttn A G 2: 76,562,304 (GRCm39) V28847A possibly damaging Het
Utp6 T A 11: 79,839,896 (GRCm39) Q264L possibly damaging Het
Vim A G 2: 13,585,491 (GRCm39) R424G probably damaging Het
Vmn1r216 A C 13: 23,283,649 (GRCm39) T111P probably damaging Het
Wnt11 G A 7: 98,499,566 (GRCm39) A244T probably damaging Het
Zbtb26 A C 2: 37,326,261 (GRCm39) N247K probably benign Het
Zfp629 T G 7: 127,209,203 (GRCm39) probably benign Het
Other mutations in Krtap19-4
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1803:Krtap19-4 UTSW 16 88,681,879 (GRCm39) missense unknown
R4678:Krtap19-4 UTSW 16 88,681,734 (GRCm39) missense unknown
R7219:Krtap19-4 UTSW 16 88,681,797 (GRCm39) missense unknown
R7958:Krtap19-4 UTSW 16 88,681,833 (GRCm39) missense unknown
R8720:Krtap19-4 UTSW 16 88,681,846 (GRCm39) missense unknown
R9056:Krtap19-4 UTSW 16 88,681,801 (GRCm39) missense unknown
Posted On 2015-12-18