Incidental Mutation 'IGL01868:Micall1'
ID 178604
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Micall1
Ensembl Gene ENSMUSG00000033039
Gene Name microtubule associated monooxygenase, calponin and LIM domain containing -like 1
Synonyms Mus EST 820961, D15Mit260, D15N2e
Accession Numbers
Essential gene? Probably non essential (E-score: 0.082) question?
Stock # IGL01868
Quality Score
Status
Chromosome 15
Chromosomal Location 78993098-79021100 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 78999260 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Valine at position 76 (I76V)
Ref Sequence ENSEMBL: ENSMUSP00000154886 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040320] [ENSMUST00000229031]
AlphaFold Q8BGT6
Predicted Effect unknown
Transcript: ENSMUST00000040320
AA Change: I76V
SMART Domains Protein: ENSMUSP00000042053
Gene: ENSMUSG00000033039
AA Change: I76V

DomainStartEndE-ValueType
CH 4 103 5.64e-19 SMART
low complexity region 113 135 N/A INTRINSIC
LIM 164 219 1.15e-5 SMART
low complexity region 241 250 N/A INTRINSIC
low complexity region 375 394 N/A INTRINSIC
low complexity region 414 467 N/A INTRINSIC
low complexity region 477 497 N/A INTRINSIC
low complexity region 515 530 N/A INTRINSIC
low complexity region 571 586 N/A INTRINSIC
DUF3585 685 825 5.07e-68 SMART
Predicted Effect unknown
Transcript: ENSMUST00000229004
AA Change: I60V
Predicted Effect probably benign
Transcript: ENSMUST00000229031
AA Change: I76V

PolyPhen 2 Score 0.410 (Sensitivity: 0.89; Specificity: 0.90)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000229048
Predicted Effect noncoding transcript
Transcript: ENSMUST00000229113
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Afg3l2 G A 18: 67,547,218 (GRCm39) T569M possibly damaging Het
Aldh1l1 A T 6: 90,560,212 (GRCm39) K620* probably null Het
Amdhd2 G T 17: 24,376,504 (GRCm39) T346K probably damaging Het
Arhgap44 T C 11: 64,902,904 (GRCm39) D521G probably damaging Het
Ccdc146 C A 5: 21,538,052 (GRCm39) A91S probably damaging Het
Ccdc187 C A 2: 26,170,960 (GRCm39) R506L probably benign Het
Cd37 T C 7: 44,885,603 (GRCm39) Q128R probably benign Het
Cdh22 T A 2: 164,999,278 (GRCm39) M185L probably damaging Het
Cib2 A T 9: 54,455,759 (GRCm39) N68K probably damaging Het
Ddx46 C T 13: 55,787,683 (GRCm39) R96* probably null Het
Dnajc13 A T 9: 104,039,944 (GRCm39) H2050Q possibly damaging Het
Drgx C A 14: 32,330,334 (GRCm39) F150L probably damaging Het
Duox1 A G 2: 122,168,888 (GRCm39) H1172R probably benign Het
Eftud2 C T 11: 102,759,953 (GRCm39) V132I probably benign Het
Fcrl5 G A 3: 87,351,014 (GRCm39) D87N possibly damaging Het
Gm10718 A T 9: 3,025,118 (GRCm39) Y194F probably benign Het
Gm5862 A C 5: 26,227,769 (GRCm39) W41G probably benign Het
Kat6a T C 8: 23,416,471 (GRCm39) F660L probably damaging Het
Lipo2 T C 19: 33,708,238 (GRCm39) M259V probably benign Het
Lrrcc1 T A 3: 14,619,417 (GRCm39) L90* probably null Het
Lsm1 G A 8: 26,283,821 (GRCm39) probably null Het
Luzp1 T C 4: 136,270,048 (GRCm39) I757T probably damaging Het
Mmp21 A T 7: 133,277,643 (GRCm39) D394E probably damaging Het
Mtfr1l T C 4: 134,258,018 (GRCm39) D68G probably null Het
Necab2 A G 8: 120,189,315 (GRCm39) S162G probably benign Het
Or11a4 A T 17: 37,536,043 (GRCm39) Q9L probably benign Het
Or4c100 T C 2: 88,356,059 (GRCm39) V44A possibly damaging Het
Or51b17 G A 7: 103,542,583 (GRCm39) R120* probably null Het
Or6n1 C T 1: 173,916,936 (GRCm39) T110I possibly damaging Het
Pde7b A T 10: 20,282,911 (GRCm39) C376* probably null Het
Pira12 G A 7: 3,900,174 (GRCm39) Q143* probably null Het
Plcb2 A G 2: 118,540,071 (GRCm39) L1074P probably damaging Het
Plcb2 G T 2: 118,541,868 (GRCm39) T914N probably benign Het
Prph C A 15: 98,954,224 (GRCm39) D207E probably damaging Het
Rbp4 C A 19: 38,112,968 (GRCm39) R37L probably damaging Het
Ryr3 T C 2: 112,633,503 (GRCm39) probably benign Het
Sardh T G 2: 27,117,159 (GRCm39) Q496P probably benign Het
Serpina1f T A 12: 103,659,704 (GRCm39) N193Y probably benign Het
Slc10a7 G A 8: 79,423,965 (GRCm39) probably null Het
Spg7 T C 8: 123,816,975 (GRCm39) probably null Het
Sphkap T C 1: 83,258,120 (GRCm39) probably null Het
Tas2r121 T A 6: 132,677,235 (GRCm39) I246L probably benign Het
Tbc1d9b T C 11: 50,052,460 (GRCm39) F889S probably damaging Het
Tcp10a T C 17: 7,597,263 (GRCm39) M140T possibly damaging Het
Tctn2 G A 5: 124,754,591 (GRCm39) noncoding transcript Het
Tfap2b G T 1: 19,284,506 (GRCm39) R138L probably damaging Het
Tnrc18 T C 5: 142,757,567 (GRCm39) T985A unknown Het
Treml1 G A 17: 48,673,035 (GRCm39) V211I probably benign Het
Ubr4 C T 4: 139,139,989 (GRCm39) Q1191* probably null Het
Vim G A 2: 13,583,249 (GRCm39) R217H possibly damaging Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Vmn2r77 A G 7: 86,452,224 (GRCm39) D468G probably benign Het
Vmn2r98 G T 17: 19,286,548 (GRCm39) V349F probably benign Het
Vwa7 A T 17: 35,240,235 (GRCm39) E401V probably null Het
Zfp119b C A 17: 56,246,866 (GRCm39) V75L possibly damaging Het
Zfp287 C T 11: 62,606,083 (GRCm39) E275K probably benign Het
Other mutations in Micall1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00493:Micall1 APN 15 78,999,221 (GRCm39) splice site probably benign
IGL00496:Micall1 APN 15 78,999,221 (GRCm39) splice site probably benign
IGL00508:Micall1 APN 15 79,014,768 (GRCm39) missense probably damaging 0.99
IGL01626:Micall1 APN 15 79,014,712 (GRCm39) missense possibly damaging 0.46
IGL03062:Micall1 APN 15 78,998,881 (GRCm39) missense probably damaging 1.00
R0086:Micall1 UTSW 15 79,009,689 (GRCm39) utr 3 prime probably benign
R0099:Micall1 UTSW 15 79,016,101 (GRCm39) splice site probably benign
R0282:Micall1 UTSW 15 79,016,101 (GRCm39) splice site probably benign
R0727:Micall1 UTSW 15 79,004,978 (GRCm39) missense probably benign 0.00
R1859:Micall1 UTSW 15 79,007,145 (GRCm39) intron probably benign
R2142:Micall1 UTSW 15 79,014,995 (GRCm39) missense probably damaging 0.98
R2228:Micall1 UTSW 15 79,014,036 (GRCm39) missense probably damaging 1.00
R3508:Micall1 UTSW 15 79,006,965 (GRCm39) missense probably damaging 1.00
R4858:Micall1 UTSW 15 79,007,146 (GRCm39) intron probably benign
R4888:Micall1 UTSW 15 79,016,048 (GRCm39) nonsense probably null
R5059:Micall1 UTSW 15 79,007,034 (GRCm39) intron probably benign
R5097:Micall1 UTSW 15 79,014,078 (GRCm39) missense probably benign 0.17
R5451:Micall1 UTSW 15 79,011,104 (GRCm39) splice site probably null
R5710:Micall1 UTSW 15 79,011,290 (GRCm39) missense probably damaging 1.00
R5727:Micall1 UTSW 15 79,014,678 (GRCm39) missense possibly damaging 0.64
R7135:Micall1 UTSW 15 78,993,624 (GRCm39) missense unknown
R7186:Micall1 UTSW 15 79,009,575 (GRCm39) missense unknown
R7297:Micall1 UTSW 15 79,005,097 (GRCm39) missense unknown
R7472:Micall1 UTSW 15 79,006,760 (GRCm39) missense unknown
R8494:Micall1 UTSW 15 79,005,080 (GRCm39) missense probably damaging 1.00
R8714:Micall1 UTSW 15 79,011,510 (GRCm39) missense probably benign 0.03
R8937:Micall1 UTSW 15 79,011,198 (GRCm39) missense probably damaging 1.00
R9440:Micall1 UTSW 15 79,011,159 (GRCm39) missense
R9760:Micall1 UTSW 15 79,005,032 (GRCm39) missense unknown
Posted On 2014-05-07