Incidental Mutation 'IGL01953:Iqcd'
ID 181345
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Iqcd
Ensembl Gene ENSMUSG00000029601
Gene Name IQ motif containing D
Synonyms 4933433C09Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # IGL01953
Quality Score
Status
Chromosome 5
Chromosomal Location 120727081-120745183 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 120738554 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Isoleucine at position 124 (N124I)
Ref Sequence ENSEMBL: ENSMUSP00000091955 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000069259] [ENSMUST00000094391] [ENSMUST00000111884] [ENSMUST00000156356]
AlphaFold Q9D3V1
Predicted Effect probably benign
Transcript: ENSMUST00000069259
AA Change: N124I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000069167
Gene: ENSMUSG00000029601
AA Change: N124I

DomainStartEndE-ValueType
coiled coil region 97 137 N/A INTRINSIC
coiled coil region 209 257 N/A INTRINSIC
coiled coil region 298 348 N/A INTRINSIC
IQ 363 385 5.53e-4 SMART
low complexity region 387 425 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000094391
AA Change: N124I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000091955
Gene: ENSMUSG00000029601
AA Change: N124I

DomainStartEndE-ValueType
coiled coil region 97 137 N/A INTRINSIC
coiled coil region 209 257 N/A INTRINSIC
coiled coil region 331 381 N/A INTRINSIC
IQ 396 418 5.53e-4 SMART
low complexity region 420 458 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000111884
Predicted Effect noncoding transcript
Transcript: ENSMUST00000147596
Predicted Effect probably benign
Transcript: ENSMUST00000156356
SMART Domains Protein: ENSMUSP00000122910
Gene: ENSMUSG00000029600

DomainStartEndE-ValueType
low complexity region 81 91 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Anks3 G A 16: 4,778,408 (GRCm39) A8V probably damaging Het
Atp6v0a4 A G 6: 38,031,552 (GRCm39) S650P probably damaging Het
B3glct C A 5: 149,669,000 (GRCm39) D311E probably benign Het
Cc2d1a G A 8: 84,870,607 (GRCm39) P119S probably benign Het
Cdcp3 T C 7: 130,826,709 (GRCm39) M261T probably benign Het
Chdh T C 14: 29,757,304 (GRCm39) V409A probably benign Het
Cipc T A 12: 86,999,538 (GRCm39) V4E possibly damaging Het
Dock2 G T 11: 34,623,183 (GRCm39) T70K probably benign Het
Dpf1 T C 7: 29,013,732 (GRCm39) V269A probably damaging Het
Drc7 A T 8: 95,785,753 (GRCm39) Y203F probably damaging Het
Dsg3 C T 18: 20,658,361 (GRCm39) T324I probably damaging Het
Gm10718 A T 9: 3,025,118 (GRCm39) Y194F probably benign Het
Kdm7a T C 6: 39,123,836 (GRCm39) N776S probably benign Het
Lama5 C T 2: 179,832,497 (GRCm39) R1684H probably damaging Het
Lrp12 A T 15: 39,741,497 (GRCm39) V406D probably damaging Het
Lrrc74a T A 12: 86,788,494 (GRCm39) L158Q probably damaging Het
Mef2d C T 3: 88,063,813 (GRCm39) T80I probably damaging Het
Megf11 T C 9: 64,597,370 (GRCm39) C681R probably damaging Het
Mex3c A G 18: 73,723,104 (GRCm39) D399G probably damaging Het
Muc20 T C 16: 32,614,073 (GRCm39) T435A probably benign Het
Myo5b T C 18: 74,702,838 (GRCm39) Y10H possibly damaging Het
Or12d13 T C 17: 37,647,766 (GRCm39) D119G probably damaging Het
Or4k40 A G 2: 111,250,657 (GRCm39) L213P probably benign Het
Otoa T A 7: 120,759,548 (GRCm39) probably null Het
P4ha2 T C 11: 54,004,996 (GRCm39) F124S probably benign Het
Phkg2 C T 7: 127,181,512 (GRCm39) P232S probably damaging Het
Piezo1 T A 8: 123,217,923 (GRCm39) Q800L probably damaging Het
Pign C A 1: 105,516,764 (GRCm39) probably benign Het
Pik3r5 A G 11: 68,384,997 (GRCm39) D634G probably benign Het
Ptpn9 A G 9: 56,964,072 (GRCm39) T402A possibly damaging Het
Relb A C 7: 19,349,482 (GRCm39) probably null Het
Scgb1b30 A G 7: 33,799,302 (GRCm39) Q78R probably damaging Het
Sema6a C T 18: 47,423,187 (GRCm39) W273* probably null Het
Sestd1 A G 2: 77,042,813 (GRCm39) V247A possibly damaging Het
Specc1 T A 11: 62,009,122 (GRCm39) S293T probably benign Het
Sptbn2 A G 19: 4,799,721 (GRCm39) D2145G probably benign Het
Trim43b T A 9: 88,967,496 (GRCm39) D380V possibly damaging Het
Vmn1r236 A G 17: 21,507,473 (GRCm39) Y197C possibly damaging Het
Vmn1r79 A G 7: 11,910,382 (GRCm39) Y88C probably damaging Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Vmn2r61 G A 7: 41,949,613 (GRCm39) V678M probably damaging Het
Wdfy3 A T 5: 102,042,894 (GRCm39) Y1937* probably null Het
Other mutations in Iqcd
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1420:Iqcd UTSW 5 120,738,860 (GRCm39) missense probably damaging 1.00
R1574:Iqcd UTSW 5 120,738,300 (GRCm39) missense probably damaging 0.98
R1574:Iqcd UTSW 5 120,738,300 (GRCm39) missense probably damaging 0.98
R4038:Iqcd UTSW 5 120,740,587 (GRCm39) missense probably damaging 0.97
R4178:Iqcd UTSW 5 120,740,476 (GRCm39) missense probably damaging 1.00
R4405:Iqcd UTSW 5 120,740,485 (GRCm39) missense probably damaging 1.00
R5326:Iqcd UTSW 5 120,740,440 (GRCm39) missense probably damaging 1.00
R5364:Iqcd UTSW 5 120,738,332 (GRCm39) missense probably damaging 1.00
R5656:Iqcd UTSW 5 120,743,191 (GRCm39) splice site probably null
R5691:Iqcd UTSW 5 120,740,571 (GRCm39) nonsense probably null
R5711:Iqcd UTSW 5 120,740,571 (GRCm39) nonsense probably null
R6387:Iqcd UTSW 5 120,744,920 (GRCm39) missense probably benign 0.28
R6556:Iqcd UTSW 5 120,740,443 (GRCm39) missense probably damaging 0.99
R6634:Iqcd UTSW 5 120,738,556 (GRCm39) missense probably benign 0.14
R7067:Iqcd UTSW 5 120,743,212 (GRCm39) missense probably damaging 1.00
R7672:Iqcd UTSW 5 120,744,881 (GRCm39) missense probably damaging 1.00
R8207:Iqcd UTSW 5 120,740,514 (GRCm39) missense probably damaging 1.00
R8828:Iqcd UTSW 5 120,738,232 (GRCm39) missense possibly damaging 0.90
R9217:Iqcd UTSW 5 120,738,707 (GRCm39) missense possibly damaging 0.56
R9218:Iqcd UTSW 5 120,738,707 (GRCm39) missense possibly damaging 0.56
R9404:Iqcd UTSW 5 120,738,601 (GRCm39) missense
R9525:Iqcd UTSW 5 120,738,217 (GRCm39) missense probably benign 0.13
R9667:Iqcd UTSW 5 120,744,737 (GRCm39) missense probably damaging 1.00
Posted On 2014-05-07