Incidental Mutation 'R7029:Iqcn'
ID 546183
Institutional Source Beutler Lab
Gene Symbol Iqcn
Ensembl Gene ENSMUSG00000110622
Gene Name IQ motif containing N
Synonyms Gm16486
MMRRC Submission 045130-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.094) question?
Stock # R7029 (G1)
Quality Score 225.009
Status Not validated
Chromosome 8
Chromosomal Location 71156106-71170299 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 71161511 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Leucine at position 235 (V235L)
Ref Sequence ENSEMBL: ENSMUSP00000148728 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000212436]
AlphaFold A0A1D5RMD1
Predicted Effect possibly damaging
Transcript: ENSMUST00000212436
AA Change: V235L

PolyPhen 2 Score 0.455 (Sensitivity: 0.89; Specificity: 0.90)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700034J05Rik T C 6: 146,853,841 (GRCm39) Q271R probably benign Het
Abhd4 T A 14: 54,500,164 (GRCm39) W63R probably damaging Het
Adcy5 A G 16: 35,120,018 (GRCm39) M1176V probably null Het
Bach1 G A 16: 87,516,179 (GRCm39) R240Q probably benign Het
Brox G A 1: 183,065,750 (GRCm39) P206L possibly damaging Het
Ccn3 A G 15: 54,611,171 (GRCm39) D102G possibly damaging Het
Def6 A G 17: 28,444,943 (GRCm39) K447R probably benign Het
Dna2 T C 10: 62,799,773 (GRCm39) S726P probably damaging Het
Ell G A 8: 71,031,879 (GRCm39) V15I probably damaging Het
Entrep2 T A 7: 64,409,075 (GRCm39) T440S probably benign Het
Epha3 T A 16: 63,593,698 (GRCm39) D130V probably benign Het
Gys1 A G 7: 45,089,008 (GRCm39) T200A possibly damaging Het
Habp4 A T 13: 64,309,939 (GRCm39) H47L probably benign Het
Kcnj10 C A 1: 172,196,563 (GRCm39) R26S probably benign Het
Klhl1 T A 14: 96,755,632 (GRCm39) D41V probably benign Het
Lyn A G 4: 3,782,996 (GRCm39) T410A probably damaging Het
Mga A G 2: 119,754,031 (GRCm39) T847A probably damaging Het
Mrgpra3 G T 7: 47,239,290 (GRCm39) T212N probably benign Het
Myh4 T C 11: 67,137,251 (GRCm39) F491L probably benign Het
Neurl4 T A 11: 69,801,562 (GRCm39) I1206N probably damaging Het
Pcdhb15 T A 18: 37,608,621 (GRCm39) W618R possibly damaging Het
Pomc A G 12: 4,010,146 (GRCm39) H129R probably damaging Het
Ppm1l C A 3: 69,460,399 (GRCm39) H325Q probably benign Het
Psme4 A G 11: 30,722,474 (GRCm39) probably benign Het
Reep2 A G 18: 34,978,342 (GRCm39) I74V probably null Het
Robo2 T G 16: 73,745,225 (GRCm39) E850A probably damaging Het
Scrn2 T A 11: 96,921,262 (GRCm39) probably benign Het
Sfpq G A 4: 126,923,675 (GRCm39) R673K probably benign Het
Sh2d3c T C 2: 32,644,581 (GRCm39) *703R probably null Het
Spp1 A G 5: 104,587,167 (GRCm39) M85V probably benign Het
Srebf1 T C 11: 60,097,810 (GRCm39) E98G probably damaging Het
Srrm4 T A 5: 116,582,851 (GRCm39) probably benign Het
Ticam1 A T 17: 56,578,154 (GRCm39) S314T possibly damaging Het
Tie1 T C 4: 118,341,823 (GRCm39) I209V possibly damaging Het
Vapa G A 17: 65,889,586 (GRCm39) R194* probably null Het
Vcan C T 13: 89,838,360 (GRCm39) D2395N probably damaging Het
Whamm A G 7: 81,241,574 (GRCm39) H295R probably benign Het
Zdhhc14 A G 17: 5,698,186 (GRCm39) Y85C probably damaging Het
Zfp35 T A 18: 24,136,583 (GRCm39) F309Y probably damaging Het
Zfp423 C A 8: 88,414,694 (GRCm39) C1187F probably damaging Het
Zfp874b T C 13: 67,622,392 (GRCm39) Y302C probably damaging Het
Other mutations in Iqcn
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6811:Iqcn UTSW 8 71,169,422 (GRCm39) missense probably benign 0.05
R6850:Iqcn UTSW 8 71,163,425 (GRCm39) missense probably damaging 0.97
R7203:Iqcn UTSW 8 71,169,597 (GRCm39) missense probably benign 0.26
R7260:Iqcn UTSW 8 71,161,397 (GRCm39) missense probably benign 0.00
R7263:Iqcn UTSW 8 71,163,425 (GRCm39) missense possibly damaging 0.66
R7327:Iqcn UTSW 8 71,169,453 (GRCm39) missense possibly damaging 0.65
R7401:Iqcn UTSW 8 71,169,921 (GRCm39) missense probably benign 0.03
R7542:Iqcn UTSW 8 71,161,415 (GRCm39) missense possibly damaging 0.66
R7572:Iqcn UTSW 8 71,162,075 (GRCm39) missense probably benign 0.00
R7733:Iqcn UTSW 8 71,170,100 (GRCm39) missense possibly damaging 0.95
R7873:Iqcn UTSW 8 71,163,989 (GRCm39) missense probably benign 0.29
R8015:Iqcn UTSW 8 71,169,441 (GRCm39) missense probably benign 0.02
R8039:Iqcn UTSW 8 71,163,555 (GRCm39) missense probably benign 0.09
R8061:Iqcn UTSW 8 71,161,224 (GRCm39) missense probably benign
R8094:Iqcn UTSW 8 71,162,067 (GRCm39) missense probably benign
R8498:Iqcn UTSW 8 71,162,625 (GRCm39) missense probably benign 0.19
R8542:Iqcn UTSW 8 71,166,520 (GRCm39) splice site probably null
R8709:Iqcn UTSW 8 71,162,372 (GRCm39) missense possibly damaging 0.83
R9141:Iqcn UTSW 8 71,162,421 (GRCm39) missense probably benign 0.15
R9313:Iqcn UTSW 8 71,161,353 (GRCm39) missense probably damaging 1.00
R9324:Iqcn UTSW 8 71,161,794 (GRCm39) missense possibly damaging 0.92
Z1177:Iqcn UTSW 8 71,169,752 (GRCm39) missense possibly damaging 0.92
Predicted Primers PCR Primer
(F):5'- GTGACTAAAGAGACTCAGTTCCC -3'
(R):5'- CAGCCATTGGACACACCTTG -3'

Sequencing Primer
(F):5'- AAAGAGACTCAGTTCCCGTCCTTTG -3'
(R):5'- ACACCTTGGTGTGGGTCTTG -3'
Posted On 2019-05-13