Incidental Mutation 'IGL02898:Krtap6-1'
ID363473
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Krtap6-1
Ensembl Gene ENSMUSG00000058172
Gene Namekeratin associated protein 6-1
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.087) question?
Stock #IGL02898
Quality Score
Status
Chromosome16
Chromosomal Location89031699-89032292 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 89031755 bp
ZygosityHeterozygous
Amino Acid Change Glycine to Aspartic acid at position 13 (G13D)
Ref Sequence ENSEMBL: ENSMUSP00000076172 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076906]
Predicted Effect unknown
Transcript: ENSMUST00000076906
AA Change: G13D
SMART Domains Protein: ENSMUSP00000076172
Gene: ENSMUSG00000058172
AA Change: G13D

DomainStartEndE-ValueType
Pfam:KRTAP 1 62 2.4e-8 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamtsl5 A G 10: 80,342,231 probably benign Het
Brd3 A G 2: 27,459,741 S267P possibly damaging Het
Btaf1 A G 19: 36,969,068 T425A probably benign Het
Caskin1 A T 17: 24,502,409 E544D probably benign Het
Col20a1 C T 2: 180,989,112 Q58* probably null Het
Eif2ak1 G A 5: 143,889,452 V428I probably damaging Het
Fez2 A G 17: 78,384,755 I345T probably benign Het
Focad A T 4: 88,391,997 M1388L probably benign Het
Gfer T C 17: 24,695,947 R41G probably benign Het
Gm6614 T A 6: 141,994,297 Y140F probably benign Het
Gm9956 C T 10: 56,745,254 S4L unknown Het
Megf8 A G 7: 25,346,508 E1492G possibly damaging Het
Myh7 T C 14: 54,983,740 I909V probably damaging Het
Olfr380 T A 11: 73,453,735 H159L probably damaging Het
Olfr741 T A 14: 50,486,186 S243T probably damaging Het
Otog A G 7: 46,310,138 E717G probably damaging Het
Pik3r4 A G 9: 105,650,406 I319M probably benign Het
Piwil4 A T 9: 14,706,287 probably benign Het
Plekho1 T A 3: 95,992,181 H100L probably damaging Het
Prr30 T G 14: 101,198,481 D215A probably benign Het
Prss52 C T 14: 64,113,666 A300V possibly damaging Het
Ralgps2 C A 1: 156,817,744 K514N probably benign Het
Robo4 T C 9: 37,408,176 I463T probably damaging Het
Sars A T 3: 108,429,263 F268Y probably damaging Het
Sidt1 C T 16: 44,282,495 R289Q possibly damaging Het
Slco2a1 T C 9: 103,079,606 V539A probably damaging Het
Snrnp200 A G 2: 127,216,756 probably benign Het
Spag17 A G 3: 100,101,386 D1944G probably benign Het
Spata1 C T 3: 146,475,339 R288Q possibly damaging Het
Tatdn3 T C 1: 191,046,310 *233W probably null Het
Ttc3 T A 16: 94,419,426 V536E probably damaging Het
V1rd19 A C 7: 24,003,429 T107P probably damaging Het
Other mutations in Krtap6-1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4169:Krtap6-1 UTSW 16 89031696 unclassified probably null
R7051:Krtap6-1 UTSW 16 89031718 start codon destroyed unknown
Posted On2015-12-18