Incidental Mutation 'R4605:Krtap9-1'
ID 345972
Institutional Source Beutler Lab
Gene Symbol Krtap9-1
Ensembl Gene ENSMUSG00000070335
Gene Name keratin associated protein 9-1
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # R4605 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 99764215-99764826 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 99764579 bp (GRCm39)
Zygosity Heterozygous
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]
AlphaFold Q64526
Predicted Effect unknown
Transcript: ENSMUST00000093936
AA Change: E105A
SMART Domains Protein: ENSMUSP00000091468
Gene: ENSMUSG00000070335
AA Change: E105A

DomainStartEndE-ValueType
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
Ankra2 A G 13: 98,402,742 (GRCm39) probably benign Het
Atp9b T A 18: 80,796,364 (GRCm39) probably null Het
Birc6 G A 17: 74,946,929 (GRCm39) D2885N probably damaging Het
Chaf1b A T 16: 93,684,977 (GRCm39) N142I possibly damaging Het
Ckap5 G A 2: 91,406,559 (GRCm39) G787S probably damaging Het
Ctc1 G T 11: 68,920,552 (GRCm39) C372F possibly damaging Het
Dip2b A G 15: 100,107,517 (GRCm39) T1176A probably benign Het
Epha10 A G 4: 124,779,550 (GRCm39) E132G probably damaging Het
Extl1 A G 4: 134,087,145 (GRCm39) V471A probably benign Het
Fgd6 T C 10: 93,880,217 (GRCm39) L357P probably benign Het
Gapvd1 A T 2: 34,618,549 (GRCm39) C275S probably damaging Het
Kcnj2 G A 11: 110,963,676 (GRCm39) C356Y probably damaging Het
Kcnk10 T C 12: 98,456,219 (GRCm39) D204G probably damaging Het
Loxhd1 G A 18: 77,493,642 (GRCm39) V668I probably benign Het
Ly86 T C 13: 37,558,987 (GRCm39) I62T possibly damaging Het
Maip1 A G 1: 57,450,891 (GRCm39) I178V probably benign Het
Mical3 G A 6: 121,011,041 (GRCm39) Q386* probably null Het
Or5an11 T C 19: 12,246,532 (GRCm39) *313Q probably null Het
Or5b107 T A 19: 13,142,612 (GRCm39) V78D probably damaging Het
Or5p52 A C 7: 107,502,445 (GRCm39) I174L probably benign Het
Or8j3b G A 2: 86,205,141 (GRCm39) T205I probably benign Het
Pcdha12 T C 18: 37,154,576 (GRCm39) S432P probably damaging Het
Prex1 A T 2: 166,555,464 (GRCm39) Y59N probably benign Het
Sbf1 A G 15: 89,187,684 (GRCm39) F654L probably damaging Het
Sh2d5 T A 4: 137,984,566 (GRCm39) Y187* probably null Het
Slc9a4 T C 1: 40,640,195 (GRCm39) probably null Het
Smyd2 A G 1: 189,629,623 (GRCm39) S136P probably damaging Het
Spata31e2 T C 1: 26,722,267 (GRCm39) K971R probably benign Het
Srsf11 A T 3: 157,728,560 (GRCm39) L115* probably null Het
Tbx19 C T 1: 164,981,153 (GRCm39) V114I possibly damaging Het
Unc5b A G 10: 60,610,182 (GRCm39) V545A probably benign Het
Ush2a A G 1: 188,642,998 (GRCm39) Y4120C probably damaging Het
Vps13a T C 19: 16,617,403 (GRCm39) T3002A probably damaging Het
Zkscan2 A T 7: 123,097,947 (GRCm39) W150R probably damaging Het
Other mutations in Krtap9-1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00158:Krtap9-1 APN 11 99,764,680 (GRCm39) missense unknown
R7882:Krtap9-1 UTSW 11 99,764,356 (GRCm39) missense unknown
R8726:Krtap9-1 UTSW 11 99,764,577 (GRCm39) nonsense probably null
R9393:Krtap9-1 UTSW 11 99,764,664 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- AAGCTGTGTGACCAGCTGTTG -3'
(R):5'- ACACATGTTGGCTGGTAGC -3'

Sequencing Primer
(F):5'- TGTGGCTCCAGCTGCTG -3'
(R):5'- GTAGCAAGTCCTGGTGCAG -3'
Posted On 2015-09-25