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)
|
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
Domain | Start | End | E-Value | Type |
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
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
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 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH 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 |