Incidental Mutation 'IGL01736:Zmym6'
ID 105690
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zmym6
Ensembl Gene ENSMUSG00000042408
Gene Name zinc finger, MYM-type 6
Synonyms 9330177P20Rik, Zfp258, D4Wsu24e
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01736
Quality Score
Status
Chromosome 4
Chromosomal Location 126971176-127018165 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 127002437 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Arginine at position 556 (I556R)
Ref Sequence ENSEMBL: ENSMUSP00000045366 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000046751] [ENSMUST00000094713]
AlphaFold Q8BS54
Predicted Effect probably damaging
Transcript: ENSMUST00000046751
AA Change: I556R

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000045366
Gene: ENSMUSG00000042408
AA Change: I556R

DomainStartEndE-ValueType
Blast:TRASH 77 113 1e-12 BLAST
TRASH 123 163 1.18e-1 SMART
TRASH 197 231 5.47e3 SMART
TRASH 241 277 4.01e1 SMART
TRASH 349 385 2.46e1 SMART
TRASH 391 426 3.32e2 SMART
TRASH 434 472 2.91e-1 SMART
TRASH 478 513 9.99e0 SMART
low complexity region 602 612 N/A INTRINSIC
low complexity region 642 656 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000094713
AA Change: I464R

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000092303
Gene: ENSMUSG00000042408
AA Change: I464R

DomainStartEndE-ValueType
Blast:TRASH 77 113 1e-12 BLAST
TRASH 123 163 1.18e-1 SMART
TRASH 197 231 5.47e3 SMART
TRASH 262 293 6.03e2 SMART
TRASH 299 334 3.32e2 SMART
TRASH 342 380 2.91e-1 SMART
TRASH 386 421 9.99e0 SMART
low complexity region 510 520 N/A INTRINSIC
low complexity region 550 564 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000125160
Predicted Effect noncoding transcript
Transcript: ENSMUST00000151461
Predicted Effect noncoding transcript
Transcript: ENSMUST00000158357
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acacb A G 5: 114,326,503 (GRCm39) T290A possibly damaging Het
Apip G A 2: 102,917,486 (GRCm39) V62M probably damaging Het
Appbp2 T C 11: 85,105,143 (GRCm39) K141R possibly damaging Het
Arhgef18 T A 8: 3,501,624 (GRCm39) probably benign Het
B3galt2 A G 1: 143,522,583 (GRCm39) T240A probably benign Het
Bivm A T 1: 44,180,973 (GRCm39) N385I probably damaging Het
Brd4 A T 17: 32,417,649 (GRCm39) probably benign Het
Cage1 T C 13: 38,206,789 (GRCm39) D352G possibly damaging Het
Ceacam10 A G 7: 24,480,535 (GRCm39) Y102C probably damaging Het
Diaph3 T C 14: 87,156,282 (GRCm39) D677G probably benign Het
Dis3l T C 9: 64,226,536 (GRCm39) probably null Het
Dnah6 C T 6: 73,165,360 (GRCm39) V582M probably benign Het
Fndc3b A G 3: 27,521,552 (GRCm39) L541P probably damaging Het
Folh1 T C 7: 86,391,444 (GRCm39) T384A possibly damaging Het
Gdpd3 T C 7: 126,365,695 (GRCm39) L18P probably damaging Het
Grxcr2 T A 18: 42,132,047 (GRCm39) K7N probably damaging Het
Gulo A G 14: 66,234,325 (GRCm39) F246L probably benign Het
Inpp4b A T 8: 82,723,968 (GRCm39) D500V probably benign Het
Ints4 C T 7: 97,175,849 (GRCm39) L647F probably benign Het
Kif17 T A 4: 138,013,876 (GRCm39) L264Q possibly damaging Het
Kif21a T C 15: 90,843,948 (GRCm39) N1104S possibly damaging Het
Ly6e T G 15: 74,830,546 (GRCm39) L132R probably benign Het
Mis18bp1 T A 12: 65,185,452 (GRCm39) H905L probably damaging Het
Nr2f2 A G 7: 70,004,446 (GRCm39) S269P probably damaging Het
Or2b2b C A 13: 21,858,787 (GRCm39) C109F probably benign Het
Or2o1 G A 11: 49,051,354 (GRCm39) C171Y probably damaging Het
Or5d46 T A 2: 88,170,771 (GRCm39) N287K probably damaging Het
Pde8b T C 13: 95,166,910 (GRCm39) I757V probably damaging Het
Psg23 A T 7: 18,346,122 (GRCm39) I191N possibly damaging Het
Slc12a4 A T 8: 106,672,475 (GRCm39) probably null Het
Snph A T 2: 151,436,093 (GRCm39) Y209* probably null Het
Tnfaip3 T C 10: 18,882,649 (GRCm39) H256R probably damaging Het
Tnip3 T A 6: 65,573,107 (GRCm39) probably benign Het
Ttc3 T A 16: 94,243,386 (GRCm39) F1130Y probably damaging Het
Twnk T G 19: 44,998,627 (GRCm39) V515G probably damaging Het
Usp24 T A 4: 106,280,658 (GRCm39) I2324K probably benign Het
Vwa7 T C 17: 35,238,827 (GRCm39) F305S probably damaging Het
Ythdc2 A T 18: 44,983,735 (GRCm39) Q567L probably damaging Het
Zbtb11 T A 16: 55,818,523 (GRCm39) I649K probably damaging Het
Zbtb49 T C 5: 38,358,204 (GRCm39) Y683C probably damaging Het
Zfhx4 A T 3: 5,309,152 (GRCm39) M793L possibly damaging Het
Zswim8 C T 14: 20,764,780 (GRCm39) P717S probably benign Het
Other mutations in Zmym6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00430:Zmym6 APN 4 126,995,742 (GRCm39) nonsense probably null
IGL00486:Zmym6 APN 4 127,017,978 (GRCm39) utr 5 prime probably benign
IGL01017:Zmym6 APN 4 126,982,152 (GRCm39) missense probably benign 0.00
IGL01385:Zmym6 APN 4 127,017,899 (GRCm39) missense probably benign 0.02
IGL01577:Zmym6 APN 4 126,999,223 (GRCm39) missense probably damaging 1.00
IGL01654:Zmym6 APN 4 127,017,519 (GRCm39) missense probably damaging 1.00
IGL01824:Zmym6 APN 4 127,002,499 (GRCm39) missense probably damaging 0.99
IGL01916:Zmym6 APN 4 127,017,549 (GRCm39) missense probably damaging 0.98
IGL01985:Zmym6 APN 4 126,994,541 (GRCm39) missense probably damaging 1.00
IGL02056:Zmym6 APN 4 126,997,207 (GRCm39) missense probably damaging 1.00
IGL02477:Zmym6 APN 4 126,972,295 (GRCm39) nonsense probably null
IGL02754:Zmym6 APN 4 127,003,764 (GRCm39) splice site probably benign
IGL03344:Zmym6 APN 4 127,014,314 (GRCm39) missense probably damaging 1.00
IGL03412:Zmym6 APN 4 126,986,731 (GRCm39) missense probably damaging 1.00
R0335:Zmym6 UTSW 4 127,016,601 (GRCm39) missense probably damaging 1.00
R0448:Zmym6 UTSW 4 127,002,487 (GRCm39) missense probably benign 0.01
R0463:Zmym6 UTSW 4 127,016,565 (GRCm39) missense probably damaging 0.98
R0538:Zmym6 UTSW 4 127,017,162 (GRCm39) missense probably benign 0.21
R0789:Zmym6 UTSW 4 127,016,615 (GRCm39) missense possibly damaging 0.52
R0798:Zmym6 UTSW 4 126,997,316 (GRCm39) missense probably benign 0.00
R1311:Zmym6 UTSW 4 127,017,151 (GRCm39) missense probably damaging 1.00
R1351:Zmym6 UTSW 4 127,016,798 (GRCm39) missense probably benign 0.00
R1429:Zmym6 UTSW 4 127,017,672 (GRCm39) missense probably damaging 1.00
R1636:Zmym6 UTSW 4 127,017,560 (GRCm39) missense probably damaging 0.99
R1666:Zmym6 UTSW 4 127,016,652 (GRCm39) missense probably damaging 0.98
R1919:Zmym6 UTSW 4 126,997,207 (GRCm39) missense probably damaging 1.00
R2058:Zmym6 UTSW 4 126,982,208 (GRCm39) nonsense probably null
R3957:Zmym6 UTSW 4 127,017,089 (GRCm39) missense possibly damaging 0.68
R3978:Zmym6 UTSW 4 127,017,348 (GRCm39) missense possibly damaging 0.71
R4417:Zmym6 UTSW 4 126,986,781 (GRCm39) missense probably damaging 1.00
R4801:Zmym6 UTSW 4 127,017,009 (GRCm39) missense probably benign 0.19
R4802:Zmym6 UTSW 4 127,017,009 (GRCm39) missense probably benign 0.19
R5052:Zmym6 UTSW 4 127,017,767 (GRCm39) missense possibly damaging 0.92
R5105:Zmym6 UTSW 4 127,017,551 (GRCm39) missense probably benign 0.33
R5217:Zmym6 UTSW 4 126,999,167 (GRCm39) missense possibly damaging 0.76
R5682:Zmym6 UTSW 4 126,998,200 (GRCm39) missense probably damaging 1.00
R5841:Zmym6 UTSW 4 126,994,463 (GRCm39) missense possibly damaging 0.71
R5991:Zmym6 UTSW 4 127,002,266 (GRCm39) splice site probably null
R6478:Zmym6 UTSW 4 127,017,176 (GRCm39) missense possibly damaging 0.86
R7014:Zmym6 UTSW 4 127,017,337 (GRCm39) nonsense probably null
R7287:Zmym6 UTSW 4 127,016,775 (GRCm39) missense possibly damaging 0.50
R7290:Zmym6 UTSW 4 127,017,294 (GRCm39) missense possibly damaging 0.73
R7371:Zmym6 UTSW 4 126,998,106 (GRCm39) missense probably damaging 1.00
R7967:Zmym6 UTSW 4 127,016,453 (GRCm39) missense probably benign 0.03
R8237:Zmym6 UTSW 4 127,016,544 (GRCm39) missense probably damaging 0.99
R8306:Zmym6 UTSW 4 127,016,355 (GRCm39) missense probably damaging 1.00
R8312:Zmym6 UTSW 4 127,017,627 (GRCm39) missense probably damaging 1.00
R9090:Zmym6 UTSW 4 127,017,854 (GRCm39) missense probably damaging 0.99
R9216:Zmym6 UTSW 4 127,002,500 (GRCm39) missense probably benign 0.00
R9271:Zmym6 UTSW 4 127,017,854 (GRCm39) missense probably damaging 0.99
R9695:Zmym6 UTSW 4 127,016,340 (GRCm39) missense probably benign
X0025:Zmym6 UTSW 4 127,016,143 (GRCm39) missense possibly damaging 0.60
X0067:Zmym6 UTSW 4 126,998,107 (GRCm39) missense probably damaging 1.00
Z1177:Zmym6 UTSW 4 127,017,590 (GRCm39) missense not run
Posted On 2014-01-21