Incidental Mutation 'R0345:Zyg11b'
ID 38377
Institutional Source Beutler Lab
Gene Symbol Zyg11b
Ensembl Gene ENSMUSG00000034636
Gene Name zyg-ll family member B, cell cycle regulator
Synonyms 1110046I03Rik, 2810482G21Rik, D4Mgi23, LOC242610
MMRRC Submission 038552-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.710) question?
Stock # R0345 (G1)
Quality Score 225
Status Validated
Chromosome 4
Chromosomal Location 108086921-108158293 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 108123604 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 121 (I121T)
Ref Sequence ENSEMBL: ENSMUSP00000043844 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000043616]
AlphaFold Q3UFS0
Predicted Effect probably damaging
Transcript: ENSMUST00000043616
AA Change: I121T

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000043844
Gene: ENSMUSG00000034636
AA Change: I121T

DomainStartEndE-ValueType
SCOP:d1jdha_ 370 722 3e-16 SMART
Blast:ARM 480 526 1e-17 BLAST
Blast:ARM 528 570 3e-19 BLAST
Blast:ARM 638 679 3e-10 BLAST
Meta Mutation Damage Score 0.3307 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.7%
  • 20x: 94.1%
Validation Efficiency 100% (58/58)
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700129C05Rik T C 14: 59,377,079 (GRCm39) N105D possibly damaging Het
A2m T C 6: 121,615,231 (GRCm39) probably benign Het
Adgrb1 A G 15: 74,415,198 (GRCm39) N641S probably damaging Het
Aff4 T A 11: 53,263,708 (GRCm39) S243T probably benign Het
Agap2 A G 10: 126,923,764 (GRCm39) H713R unknown Het
Ap2a2 T A 7: 141,211,206 (GRCm39) M914K probably damaging Het
Bcl7c A T 7: 127,307,635 (GRCm39) M22K possibly damaging Het
Cacna1i A T 15: 80,256,663 (GRCm39) D1019V probably damaging Het
Cd7 T C 11: 120,929,012 (GRCm39) T80A probably benign Het
Chia1 T C 3: 106,029,755 (GRCm39) Y130H probably damaging Het
Chmp6 T C 11: 119,808,872 (GRCm39) probably benign Het
Chrnb4 A G 9: 54,942,878 (GRCm39) V132A probably benign Het
Ctnna3 A G 10: 63,402,619 (GRCm39) D110G probably benign Het
Cyp2d37-ps A T 15: 82,573,975 (GRCm39) noncoding transcript Het
Dnah6 T C 6: 72,998,240 (GRCm39) M4061V probably benign Het
Dydc2 C A 14: 40,783,903 (GRCm39) M73I probably benign Het
Egflam G T 15: 7,319,475 (GRCm39) probably null Het
Fam228b C T 12: 4,798,351 (GRCm39) V151I possibly damaging Het
Fanca C T 8: 124,031,552 (GRCm39) V380I probably damaging Het
Gbp2b T C 3: 142,313,944 (GRCm39) L408S probably damaging Het
Kcnh4 T C 11: 100,648,507 (GRCm39) S66G probably benign Het
Kcnq3 A T 15: 65,892,154 (GRCm39) V407D possibly damaging Het
Kif24 A T 4: 41,428,413 (GRCm39) D182E probably benign Het
Llgl2 A G 11: 115,740,818 (GRCm39) probably benign Het
Lmo7 T A 14: 102,114,313 (GRCm39) N140K probably damaging Het
Myo5c A G 9: 75,204,701 (GRCm39) E1518G probably damaging Het
Myof A T 19: 38,012,793 (GRCm39) N47K probably damaging Het
Nckap1 G T 2: 80,375,321 (GRCm39) probably benign Het
Nlrp1a C A 11: 71,014,501 (GRCm39) G250W probably damaging Het
Nol4l T A 2: 153,253,672 (GRCm39) S390C probably benign Het
Or2ag2b T C 7: 106,417,908 (GRCm39) F206S probably benign Het
Or52e18 T A 7: 104,609,388 (GRCm39) M184L probably damaging Het
Or5ak22 T C 2: 85,230,685 (GRCm39) Q64R possibly damaging Het
Or5h26 G A 16: 58,988,269 (GRCm39) P79L possibly damaging Het
Plec G T 15: 76,061,367 (GRCm39) P2886T probably damaging Het
Prdm16 T C 4: 154,425,568 (GRCm39) Y738C probably benign Het
Ptprz1 A G 6: 23,016,164 (GRCm39) Y820C probably damaging Het
Rif1 GCCACCA GCCA 2: 52,000,336 (GRCm39) probably benign Het
Sgce G A 6: 4,718,019 (GRCm39) P98S probably damaging Het
Siglecf T C 7: 43,001,368 (GRCm39) F112S probably damaging Het
Slc6a16 C T 7: 44,908,672 (GRCm39) A84V possibly damaging Het
Sntb2 T C 8: 107,728,170 (GRCm39) S373P probably damaging Het
Sorcs2 C T 5: 36,185,218 (GRCm39) V953I probably benign Het
Spata31f1a T C 4: 42,851,116 (GRCm39) I347V probably benign Het
St7l T C 3: 104,803,125 (GRCm39) probably benign Het
Stap2 A G 17: 56,307,097 (GRCm39) V217A probably damaging Het
Stxbp5l A T 16: 37,108,670 (GRCm39) D215E probably damaging Het
Synm C T 7: 67,385,569 (GRCm39) V256I probably benign Het
Syt13 A C 2: 92,776,412 (GRCm39) E233A possibly damaging Het
Tecta T A 9: 42,295,514 (GRCm39) E327V probably damaging Het
Tent5b A T 4: 133,213,522 (GRCm39) Q131L probably benign Het
Themis3 A T 17: 66,866,540 (GRCm39) probably null Het
Ttll13 T A 7: 79,897,084 (GRCm39) D14E probably benign Het
Tubb2a A C 13: 34,260,620 (GRCm39) D26E probably benign Het
Ubr1 T C 2: 120,734,584 (GRCm39) probably null Het
Vps13d A T 4: 144,844,195 (GRCm39) V2537E possibly damaging Het
Zscan10 T A 17: 23,829,056 (GRCm39) F456I probably damaging Het
Other mutations in Zyg11b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01080:Zyg11b APN 4 108,094,613 (GRCm39) missense probably damaging 1.00
IGL01143:Zyg11b APN 4 108,102,191 (GRCm39) missense possibly damaging 0.69
IGL01627:Zyg11b APN 4 108,107,985 (GRCm39) missense probably benign 0.19
IGL02517:Zyg11b APN 4 108,123,515 (GRCm39) missense probably damaging 0.96
IGL03166:Zyg11b APN 4 108,123,086 (GRCm39) missense probably benign 0.32
R0326:Zyg11b UTSW 4 108,129,450 (GRCm39) missense possibly damaging 0.77
R0396:Zyg11b UTSW 4 108,112,505 (GRCm39) missense probably damaging 1.00
R0571:Zyg11b UTSW 4 108,117,239 (GRCm39) missense probably damaging 1.00
R0718:Zyg11b UTSW 4 108,099,273 (GRCm39) missense possibly damaging 0.94
R1426:Zyg11b UTSW 4 108,108,009 (GRCm39) missense probably damaging 1.00
R1495:Zyg11b UTSW 4 108,123,410 (GRCm39) missense probably damaging 1.00
R1829:Zyg11b UTSW 4 108,123,290 (GRCm39) missense possibly damaging 0.65
R1907:Zyg11b UTSW 4 108,112,423 (GRCm39) missense probably damaging 1.00
R1916:Zyg11b UTSW 4 108,129,480 (GRCm39) missense probably damaging 0.99
R1980:Zyg11b UTSW 4 108,123,127 (GRCm39) missense probably damaging 0.99
R2070:Zyg11b UTSW 4 108,108,016 (GRCm39) missense possibly damaging 0.73
R2495:Zyg11b UTSW 4 108,101,921 (GRCm39) critical splice donor site probably null
R4717:Zyg11b UTSW 4 108,099,069 (GRCm39) missense probably damaging 0.99
R5889:Zyg11b UTSW 4 108,094,577 (GRCm39) nonsense probably null
R5957:Zyg11b UTSW 4 108,102,210 (GRCm39) missense probably damaging 1.00
R6606:Zyg11b UTSW 4 108,093,286 (GRCm39) missense probably benign 0.00
R7151:Zyg11b UTSW 4 108,102,119 (GRCm39) missense possibly damaging 0.49
R7316:Zyg11b UTSW 4 108,107,699 (GRCm39) missense possibly damaging 0.81
R7488:Zyg11b UTSW 4 108,123,655 (GRCm39) missense possibly damaging 0.65
R8936:Zyg11b UTSW 4 108,109,356 (GRCm39) missense
R9291:Zyg11b UTSW 4 108,108,014 (GRCm39) missense probably benign 0.37
R9642:Zyg11b UTSW 4 108,117,185 (GRCm39) missense probably damaging 1.00
X0022:Zyg11b UTSW 4 108,093,298 (GRCm39) missense probably benign
X0067:Zyg11b UTSW 4 108,112,543 (GRCm39) missense probably benign
Z1177:Zyg11b UTSW 4 108,112,561 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TAGGCAGCGAAGCAACTTCAGC -3'
(R):5'- AGTGAATCTCCGCAATGTCTGTTCC -3'

Sequencing Primer
(F):5'- CAGCCAGATCTTCATTGTAAAAGAGC -3'
(R):5'- GCTCCATAATCTTGGAAAGTTCTC -3'
Posted On 2013-05-23