Incidental Mutation 'R6403:Iqcm'
ID 516219
Institutional Source Beutler Lab
Gene Symbol Iqcm
Ensembl Gene ENSMUSG00000031620
Gene Name IQ motif containing M
Synonyms 1700007B14Rik
MMRRC Submission 044382-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.065) question?
Stock # R6403 (G1)
Quality Score 225.009
Status Not validated
Chromosome 8
Chromosomal Location 76175322-76711131 bp(+) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) T to C at 76304624 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000148495 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034033] [ENSMUST00000121983] [ENSMUST00000212704]
AlphaFold Q149I8
Predicted Effect probably null
Transcript: ENSMUST00000034033
SMART Domains Protein: ENSMUSP00000034033
Gene: ENSMUSG00000031620

DomainStartEndE-ValueType
IQ 281 303 2.54e-3 SMART
Predicted Effect probably null
Transcript: ENSMUST00000121983
SMART Domains Protein: ENSMUSP00000112901
Gene: ENSMUSG00000031620

DomainStartEndE-ValueType
IQ 281 303 2.54e-3 SMART
Predicted Effect probably null
Transcript: ENSMUST00000212704
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.5%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aars1 A G 8: 111,768,881 (GRCm39) D227G possibly damaging Het
Aox1 A G 1: 58,107,594 (GRCm39) I623V probably damaging Het
Camsap2 G A 1: 136,208,538 (GRCm39) R317* probably null Het
Carmil1 G A 13: 24,265,950 (GRCm39) R271C probably damaging Het
Ces2b T A 8: 105,562,901 (GRCm39) L323* probably null Het
Copb1 T A 7: 113,837,686 (GRCm39) I286F probably damaging Het
Dnajb11 T A 16: 22,689,691 (GRCm39) V285D probably damaging Het
Dok5 G T 2: 170,671,820 (GRCm39) A79S probably damaging Het
Enpp2 T C 15: 54,727,160 (GRCm39) N557S probably damaging Het
Hexa G A 9: 59,464,644 (GRCm39) R178H probably damaging Het
Iars1 T C 13: 49,840,971 (GRCm39) S35P probably damaging Het
Il3ra G T 14: 14,347,137 (GRCm38) A3S probably damaging Het
Krt9 G T 11: 100,080,485 (GRCm39) S420R probably damaging Het
Lca5l T C 16: 95,975,045 (GRCm39) N293S probably benign Het
Mb21d2 A G 16: 28,647,269 (GRCm39) I235T possibly damaging Het
Ncbp3 A G 11: 72,969,802 (GRCm39) T550A probably benign Het
Nckipsd G T 9: 108,688,882 (GRCm39) R139L possibly damaging Het
Nxn A G 11: 76,289,846 (GRCm39) V14A probably benign Het
Or8d2b T C 9: 38,788,538 (GRCm39) L22P probably damaging Het
Pramel22 G A 4: 143,382,343 (GRCm39) Q118* probably null Het
Rprd2 C A 3: 95,673,399 (GRCm39) C668F possibly damaging Het
Tmem87a A T 2: 120,211,252 (GRCm39) M231K possibly damaging Het
Trappc8 A G 18: 20,999,128 (GRCm39) V333A probably benign Het
Trit1 C A 4: 122,933,372 (GRCm39) T103K possibly damaging Het
Tspan13 A G 12: 36,065,704 (GRCm39) F203S probably damaging Het
Vmn2r114 C T 17: 23,528,939 (GRCm39) D388N probably damaging Het
Zfp617 C T 8: 72,683,015 (GRCm39) A55V probably benign Het
Other mutations in Iqcm
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01895:Iqcm APN 8 76,615,188 (GRCm39) missense probably damaging 1.00
IGL02835:Iqcm APN 8 76,281,511 (GRCm39) utr 5 prime probably benign
R0056:Iqcm UTSW 8 76,480,014 (GRCm39) missense probably benign
R2146:Iqcm UTSW 8 76,615,241 (GRCm39) missense probably damaging 1.00
R2910:Iqcm UTSW 8 76,441,404 (GRCm39) missense probably benign
R3801:Iqcm UTSW 8 76,396,021 (GRCm39) missense possibly damaging 0.59
R3804:Iqcm UTSW 8 76,396,021 (GRCm39) missense possibly damaging 0.59
R3834:Iqcm UTSW 8 76,304,380 (GRCm39) missense possibly damaging 0.93
R3897:Iqcm UTSW 8 76,480,028 (GRCm39) missense probably damaging 1.00
R4447:Iqcm UTSW 8 76,356,394 (GRCm39) missense probably damaging 0.97
R4448:Iqcm UTSW 8 76,356,394 (GRCm39) missense probably damaging 0.97
R4450:Iqcm UTSW 8 76,356,394 (GRCm39) missense probably damaging 0.97
R4687:Iqcm UTSW 8 76,489,617 (GRCm39) missense probably damaging 1.00
R4810:Iqcm UTSW 8 76,615,281 (GRCm39) missense probably damaging 1.00
R4845:Iqcm UTSW 8 76,472,980 (GRCm39) missense probably damaging 0.99
R4856:Iqcm UTSW 8 76,615,228 (GRCm39) missense possibly damaging 0.95
R4886:Iqcm UTSW 8 76,615,228 (GRCm39) missense possibly damaging 0.95
R5063:Iqcm UTSW 8 76,472,914 (GRCm39) missense probably damaging 1.00
R5460:Iqcm UTSW 8 76,441,417 (GRCm39) missense probably benign
R6667:Iqcm UTSW 8 76,479,980 (GRCm39) missense probably damaging 1.00
R7187:Iqcm UTSW 8 76,480,044 (GRCm39) missense probably benign 0.22
R7263:Iqcm UTSW 8 76,489,701 (GRCm39) missense probably benign
R7701:Iqcm UTSW 8 76,281,539 (GRCm39) missense probably benign 0.02
R7916:Iqcm UTSW 8 76,304,578 (GRCm39) missense probably benign
R7938:Iqcm UTSW 8 76,304,596 (GRCm39) missense probably benign
R7974:Iqcm UTSW 8 76,281,520 (GRCm39) start codon destroyed probably null 0.66
R8039:Iqcm UTSW 8 76,489,733 (GRCm39) missense probably damaging 1.00
R8311:Iqcm UTSW 8 76,480,118 (GRCm39) splice site probably benign
R8703:Iqcm UTSW 8 76,615,271 (GRCm39) missense probably damaging 1.00
R9175:Iqcm UTSW 8 76,710,867 (GRCm39) missense possibly damaging 0.84
R9475:Iqcm UTSW 8 76,480,083 (GRCm39) missense probably damaging 1.00
RF002:Iqcm UTSW 8 76,304,527 (GRCm39) missense probably benign 0.01
X0018:Iqcm UTSW 8 76,710,840 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- ACTGTCAAGTTCATACCTTTTGAGG -3'
(R):5'- ACACAACAGCCAGTTCTGG -3'

Sequencing Primer
(F):5'- TCAAGTTCATACCTTTTGAGGTTAAG -3'
(R):5'- AGAATGCTCTCATCACAGTTTCTGG -3'
Posted On 2018-05-04