Incidental Mutation 'R9757:Gm17093'
ID 732809
Institutional Source Beutler Lab
Gene Symbol Gm17093
Ensembl Gene ENSMUSG00000091429
Gene Name predicted gene 17093
Synonyms
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.245) question?
Stock # R9757 (G1)
Quality Score 146.008
Status Not validated
Chromosome 14
Chromosomal Location 44518276-44523444 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to A at 44521533 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Tryptophan to Arginine at position 171 (W171R)
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect
SMART Domains Protein: ENSMUSP00000132075
Gene: ENSMUSG00000091429
AA Change: W171R

DomainStartEndE-ValueType
Pfam:Takusan 57 137 2.6e-27 PFAM
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 99.3%
  • 20x: 98.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrl3 T C 5: 81,465,239 V105A probably benign Het
Agrn C A 4: 156,176,778 V621L probably benign Het
Anapc1 A G 2: 128,675,756 S323P probably damaging Het
Anxa6 T A 11: 54,994,356 K456* probably null Het
C7 G T 15: 5,045,652 T186K probably damaging Het
Cacna1b T C 2: 24,719,101 E396G probably damaging Het
Ccdc191 C T 16: 43,941,807 T20I Het
Ces1b G T 8: 93,079,873 P15Q probably benign Het
Dnah14 G T 1: 181,685,784 A1901S probably benign Het
Dock3 T C 9: 107,023,836 H310R possibly damaging Het
Eif2ak4 T G 2: 118,438,917 S23R probably benign Het
Gli2 A G 1: 118,845,922 C485R probably damaging Het
Gm13078 A G 4: 143,728,422 D430G probably benign Het
Ing2 G A 8: 47,675,040 probably benign Het
Itpkb T C 1: 180,332,807 I166T probably benign Het
Kcnj8 T A 6: 142,570,079 I101F probably benign Het
Krtap6-2 C T 16: 89,420,070 C3Y unknown Het
Lep A G 6: 29,069,084 I45V probably benign Het
Lrrk2 A T 15: 91,811,026 I2355L probably benign Het
Mettl3 C A 14: 52,299,904 A174S probably benign Het
Mmp23 T C 4: 155,651,058 N317S probably damaging Het
Mybpc1 A T 10: 88,536,395 V777E probably damaging Het
Nlrp9b T A 7: 20,048,692 C844S probably damaging Het
Obscn T C 11: 59,001,512 E6823G probably benign Het
Olfr220 A T 1: 174,449,300 I226F probably damaging Het
Pcdhb1 A T 18: 37,267,249 Q751L probably benign Het
Pdgfrl T A 8: 40,926,417 L16Q possibly damaging Het
Pdzph1 A C 17: 58,974,903 L128* probably null Het
Prr36 A T 8: 4,210,998 S940T probably damaging Het
Rad54l2 A T 9: 106,717,921 I279N probably damaging Het
Rasgrp3 A T 17: 75,500,724 T259S probably damaging Het
Rrn3 T A 16: 13,810,569 I538N probably damaging Het
Sdf2l1 A T 16: 17,130,534 D213E probably benign Het
Sorcs3 T C 19: 48,722,924 Y643H probably damaging Het
Sval2 G T 6: 41,861,840 C4F possibly damaging Het
Taldo1 A G 7: 141,400,350 E131G probably benign Het
Tas2r130 T C 6: 131,630,333 I166M probably benign Het
Tmem178 A G 17: 81,000,860 Y228C probably damaging Het
Ttn A T 2: 76,782,079 L17188* probably null Het
Unc45b A G 11: 82,919,732 K273E probably damaging Het
Usp32 A C 11: 85,077,329 Y169* probably null Het
Vmn2r9 A T 5: 108,848,042 Y247N possibly damaging Het
Zkscan2 A T 7: 123,480,087 C882* probably null Het
Other mutations in Gm17093
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01401:Gm17093 APN 14 44521527 missense unknown
IGL01431:Gm17093 APN 14 44521665 splice site probably benign
IGL01911:Gm17093 APN 14 44520820 splice site probably benign
IGL02324:Gm17093 APN 14 44518350 missense unknown
IGL02418:Gm17093 APN 14 44520728 missense unknown
IGL03072:Gm17093 APN 14 44520672 splice site probably benign
R3419:Gm17093 UTSW 14 44521590 missense unknown
R4838:Gm17093 UTSW 14 44518348 missense unknown
R4994:Gm17093 UTSW 14 44519322 missense probably damaging 1.00
R5819:Gm17093 UTSW 14 44521529 missense unknown
R8167:Gm17093 UTSW 14 44520682 missense
R8962:Gm17093 UTSW 14 44520692 missense
Predicted Primers PCR Primer
(F):5'- TCTCCCTCTAAGGCCAATCTGG -3'
(R):5'- TGCAGGATGGTTACATAGGC -3'

Sequencing Primer
(F):5'- AGGCCAATCTGGATACTTGTC -3'
(R):5'- CAGGATGGTTACATAGGCTTGAC -3'
Posted On 2022-11-14