Incidental Mutation 'R4605:Krtap9-1'
Institutional Source Beutler Lab
Gene Symbol Krtap9-1
Ensembl Gene ENSMUSG00000070335
Gene Namekeratin associated protein 9-1
Accession Numbers
Is this an essential gene? Not available question?
Stock #R4605 (G1)
Quality Score225
Status Not validated
Chromosomal Location99873389-99874432 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to C at 99873753 bp
Amino Acid Change Glutamic Acid to Alanine at position 105 (E105A)
Ref Sequence ENSEMBL: ENSMUSP00000091468 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000093936]
Predicted Effect unknown
Transcript: ENSMUST00000093936
AA Change: E105A
SMART Domains Protein: ENSMUSP00000091468
Gene: ENSMUSG00000070335
AA Change: E105A

Pfam:Keratin_B2_2 1 37 6.8e-6 PFAM
Pfam:Keratin_B2_2 86 135 3.6e-9 PFAM
Pfam:Keratin_B2_2 122 164 9.8e-11 PFAM
low complexity region 170 186 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 95.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931408C20Rik T C 1: 26,683,186 K971R probably benign Het
Ankra2 A G 13: 98,266,234 probably benign Het
Atp9b T A 18: 80,753,149 probably null Het
Birc6 G A 17: 74,639,934 D2885N probably damaging Het
Chaf1b A T 16: 93,888,089 N142I possibly damaging Het
Ckap5 G A 2: 91,576,214 G787S probably damaging Het
Ctc1 G T 11: 69,029,726 C372F possibly damaging Het
Dip2b A G 15: 100,209,636 T1176A probably benign Het
Epha10 A G 4: 124,885,757 E132G probably damaging Het
Extl1 A G 4: 134,359,834 V471A probably benign Het
Fgd6 T C 10: 94,044,355 L357P probably benign Het
Gapvd1 A T 2: 34,728,537 C275S probably damaging Het
Kcnj2 G A 11: 111,072,850 C356Y probably damaging Het
Kcnk10 T C 12: 98,489,960 D204G probably damaging Het
Loxhd1 G A 18: 77,405,946 V668I probably benign Het
Ly86 T C 13: 37,375,011 I62T possibly damaging Het
Maip1 A G 1: 57,411,732 I178V probably benign Het
Mical3 G A 6: 121,034,080 Q386* probably null Het
Olfr1057 G A 2: 86,374,797 T205I probably benign Het
Olfr1461 T A 19: 13,165,248 V78D probably damaging Het
Olfr235 T C 19: 12,269,168 *313Q probably null Het
Olfr472 A C 7: 107,903,238 I174L probably benign Het
Pcdha12 T C 18: 37,021,523 S432P probably damaging Het
Prex1 A T 2: 166,713,544 Y59N probably benign Het
Sbf1 A G 15: 89,303,481 F654L probably damaging Het
Sh2d5 T A 4: 138,257,255 Y187* probably null Het
Slc9a4 T C 1: 40,601,035 probably null Het
Smyd2 A G 1: 189,897,426 S136P probably damaging Het
Srsf11 A T 3: 158,022,923 L115* probably null Het
Tbx19 C T 1: 165,153,584 V114I possibly damaging Het
Unc5b A G 10: 60,774,403 V545A probably benign Het
Ush2a A G 1: 188,910,801 Y4120C probably damaging Het
Vps13a T C 19: 16,640,039 T3002A probably damaging Het
Zkscan2 A T 7: 123,498,724 W150R probably damaging Het
Other mutations in Krtap9-1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00158:Krtap9-1 APN 11 99873854 missense unknown
R7882:Krtap9-1 UTSW 11 99873530 missense unknown
R7965:Krtap9-1 UTSW 11 99873530 missense unknown
Predicted Primers PCR Primer

Sequencing Primer
Posted On2015-09-25