Incidental Mutation 'IGL01080:Zyg11b'
ID 50864
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zyg11b
Ensembl Gene ENSMUSG00000034636
Gene Name zyg-ll family member B, cell cycle regulator
Synonyms 1110046I03Rik, 2810482G21Rik, D4Mgi23, LOC242610
Accession Numbers
Essential gene? Possibly essential (E-score: 0.710) question?
Stock # IGL01080
Quality Score
Status
Chromosome 4
Chromosomal Location 108086921-108158293 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 108094613 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Glutamine at position 657 (L657Q)
Ref Sequence ENSEMBL: ENSMUSP00000043844 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000043616]
AlphaFold Q3UFS0
Predicted Effect probably damaging
Transcript: ENSMUST00000043616
AA Change: L657Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000043844
Gene: ENSMUSG00000034636
AA Change: L657Q

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
Predicted Effect noncoding transcript
Transcript: ENSMUST00000130508
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb4 A T 5: 8,984,258 (GRCm39) R663W probably damaging Het
Cacng5 A T 11: 107,768,754 (GRCm39) F179L probably damaging Het
Cacng5 C T 11: 107,772,531 (GRCm39) V106I probably benign Het
Cd96 T C 16: 45,870,056 (GRCm39) E471G possibly damaging Het
Cpt1c T C 7: 44,610,333 (GRCm39) D621G probably damaging Het
Csmd3 T C 15: 47,744,799 (GRCm39) I1503V probably benign Het
Dmgdh T C 13: 93,840,286 (GRCm39) probably benign Het
Flg A T 3: 93,186,906 (GRCm39) K119N probably benign Het
Gale T C 4: 135,693,389 (GRCm39) Y104H probably damaging Het
Gm8005 T C 14: 42,258,971 (GRCm39) D119G unknown Het
Gstk1 A T 6: 42,223,560 (GRCm39) D50V possibly damaging Het
Kmt2a T C 9: 44,720,389 (GRCm39) D3866G unknown Het
Mastl A G 2: 23,036,160 (GRCm39) S119P probably damaging Het
Or2aj4 A T 16: 19,384,958 (GRCm39) V225E probably damaging Het
Phf11c G A 14: 59,630,648 (GRCm39) T19I probably benign Het
Ppp1r16b A G 2: 158,599,092 (GRCm39) T355A probably damaging Het
Prmt7 T G 8: 106,963,846 (GRCm39) probably benign Het
Rad50 T C 11: 53,596,895 (GRCm39) T44A probably damaging Het
Rangap1 C T 15: 81,589,953 (GRCm39) probably benign Het
Slc27a3 A T 3: 90,292,767 (GRCm39) V634E probably benign Het
Tbxas1 T A 6: 38,998,115 (GRCm39) L228I probably damaging Het
Tnfaip3 T C 10: 18,887,403 (GRCm39) K41E probably benign Het
Tti1 C T 2: 157,824,379 (GRCm39) V1025I probably damaging Het
Tyrobp T C 7: 30,116,841 (GRCm39) probably null Het
Wfdc16 A T 2: 164,480,406 (GRCm39) W30R probably damaging Het
Other mutations in Zyg11b
AlleleSourceChrCoordTypePredicted EffectPPH Score
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
R0345:Zyg11b UTSW 4 108,123,604 (GRCm39) missense probably damaging 1.00
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
Posted On 2013-06-21