Incidental Mutation 'IGL01913:Zfp429'
ID |
179851 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Zfp429
|
Ensembl Gene |
ENSMUSG00000078994 |
Gene Name |
zinc finger protein 429 |
Synonyms |
2810487A22Rik |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.069)
|
Stock # |
IGL01913
|
Quality Score |
|
Status
|
|
Chromosome |
13 |
Chromosomal Location |
67536024-67547938 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 67544793 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Cysteine
at position 27
(Y27C)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000153005
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000109732]
[ENSMUST00000181071]
[ENSMUST00000224684]
[ENSMUST00000224825]
|
AlphaFold |
Q7M6Y0 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000109732
AA Change: Y40C
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000105354 Gene: ENSMUSG00000078994 AA Change: Y40C
Domain | Start | End | E-Value | Type |
KRAB
|
15 |
75 |
7.16e-34 |
SMART |
ZnF_C2H2
|
119 |
141 |
5.12e1 |
SMART |
ZnF_C2H2
|
147 |
169 |
2.27e-4 |
SMART |
ZnF_C2H2
|
175 |
197 |
1.28e-3 |
SMART |
ZnF_C2H2
|
203 |
225 |
1.56e-2 |
SMART |
ZnF_C2H2
|
259 |
281 |
4.62e1 |
SMART |
ZnF_C2H2
|
287 |
309 |
5.14e-3 |
SMART |
ZnF_C2H2
|
315 |
337 |
6.78e-3 |
SMART |
ZnF_C2H2
|
343 |
365 |
3.11e-2 |
SMART |
ZnF_C2H2
|
371 |
393 |
1.25e-1 |
SMART |
ZnF_C2H2
|
399 |
421 |
6.32e-3 |
SMART |
ZnF_C2H2
|
427 |
449 |
1.47e-3 |
SMART |
ZnF_C2H2
|
455 |
477 |
5.42e-2 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000181071
AA Change: Y40C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000137755 Gene: ENSMUSG00000078994 AA Change: Y40C
Domain | Start | End | E-Value | Type |
KRAB
|
15 |
75 |
7.16e-34 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000224684
AA Change: Y40C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000224825
AA Change: Y27C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000225810
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr2a |
A |
G |
2: 48,789,625 (GRCm39) |
E456G |
probably damaging |
Het |
Ahnak |
A |
T |
19: 8,983,428 (GRCm39) |
K1571* |
probably null |
Het |
Arhgef2 |
G |
A |
3: 88,539,226 (GRCm39) |
V58M |
probably damaging |
Het |
Ash2l |
A |
G |
8: 26,309,652 (GRCm39) |
|
probably null |
Het |
C3 |
T |
C |
17: 57,520,767 (GRCm39) |
N1163S |
probably null |
Het |
Cbfa2t2 |
A |
G |
2: 154,359,693 (GRCm39) |
T253A |
probably damaging |
Het |
Dnah5 |
T |
C |
15: 28,313,899 (GRCm39) |
V1905A |
possibly damaging |
Het |
Dsg1a |
C |
T |
18: 20,455,293 (GRCm39) |
R86C |
probably damaging |
Het |
Fastkd1 |
A |
T |
2: 69,538,845 (GRCm39) |
|
probably benign |
Het |
Fat3 |
T |
C |
9: 15,910,086 (GRCm39) |
D1972G |
probably damaging |
Het |
Fxyd5 |
T |
C |
7: 30,734,637 (GRCm39) |
T163A |
probably damaging |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
H6pd |
A |
T |
4: 150,078,920 (GRCm39) |
|
probably benign |
Het |
Klhdc2 |
T |
G |
12: 69,349,132 (GRCm39) |
S90A |
probably benign |
Het |
Lcn2 |
A |
G |
2: 32,277,157 (GRCm39) |
V139A |
possibly damaging |
Het |
Nup205 |
A |
G |
6: 35,204,365 (GRCm39) |
E1417G |
probably benign |
Het |
Or4a77 |
T |
G |
2: 89,487,684 (GRCm39) |
I34L |
probably benign |
Het |
Or5ac25 |
A |
T |
16: 59,182,294 (GRCm39) |
C96S |
probably damaging |
Het |
Or5t17 |
A |
T |
2: 86,833,164 (GRCm39) |
M284L |
possibly damaging |
Het |
Pcdh18 |
C |
A |
3: 49,709,698 (GRCm39) |
S539I |
possibly damaging |
Het |
Stat1 |
T |
C |
1: 52,165,716 (GRCm39) |
I104T |
probably benign |
Het |
Tmem151a |
G |
A |
19: 5,131,920 (GRCm39) |
R429C |
probably benign |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Wdpcp |
A |
G |
11: 21,698,931 (GRCm39) |
D570G |
probably damaging |
Het |
Zbtb47 |
T |
C |
9: 121,593,035 (GRCm39) |
C452R |
probably damaging |
Het |
Zfp462 |
T |
C |
4: 55,012,138 (GRCm39) |
V1368A |
probably benign |
Het |
|
Other mutations in Zfp429 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01160:Zfp429
|
APN |
13 |
67,539,132 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02343:Zfp429
|
APN |
13 |
67,538,844 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02679:Zfp429
|
APN |
13 |
67,547,855 (GRCm39) |
intron |
probably benign |
|
IGL03396:Zfp429
|
APN |
13 |
67,544,159 (GRCm39) |
splice site |
probably benign |
|
FR4342:Zfp429
|
UTSW |
13 |
67,544,769 (GRCm39) |
missense |
probably benign |
0.02 |
R0012:Zfp429
|
UTSW |
13 |
67,538,796 (GRCm39) |
missense |
probably benign |
0.01 |
R1232:Zfp429
|
UTSW |
13 |
67,538,751 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1330:Zfp429
|
UTSW |
13 |
67,544,262 (GRCm39) |
splice site |
probably null |
|
R1653:Zfp429
|
UTSW |
13 |
67,538,043 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1761:Zfp429
|
UTSW |
13 |
67,544,195 (GRCm39) |
missense |
probably benign |
0.28 |
R1813:Zfp429
|
UTSW |
13 |
67,538,505 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2356:Zfp429
|
UTSW |
13 |
67,538,746 (GRCm39) |
missense |
probably benign |
|
R4280:Zfp429
|
UTSW |
13 |
67,538,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R4283:Zfp429
|
UTSW |
13 |
67,538,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R4464:Zfp429
|
UTSW |
13 |
67,538,617 (GRCm39) |
missense |
probably benign |
0.13 |
R4789:Zfp429
|
UTSW |
13 |
67,538,523 (GRCm39) |
missense |
probably benign |
0.06 |
R5187:Zfp429
|
UTSW |
13 |
67,538,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R5250:Zfp429
|
UTSW |
13 |
67,538,638 (GRCm39) |
missense |
probably benign |
0.00 |
R6688:Zfp429
|
UTSW |
13 |
67,544,249 (GRCm39) |
missense |
probably damaging |
0.98 |
R6772:Zfp429
|
UTSW |
13 |
67,538,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R6989:Zfp429
|
UTSW |
13 |
67,538,080 (GRCm39) |
missense |
probably benign |
0.00 |
R7041:Zfp429
|
UTSW |
13 |
67,538,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R7101:Zfp429
|
UTSW |
13 |
67,538,931 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7593:Zfp429
|
UTSW |
13 |
67,538,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R7792:Zfp429
|
UTSW |
13 |
67,538,558 (GRCm39) |
nonsense |
probably null |
|
R8500:Zfp429
|
UTSW |
13 |
67,538,828 (GRCm39) |
nonsense |
probably null |
|
R8721:Zfp429
|
UTSW |
13 |
67,538,331 (GRCm39) |
missense |
probably damaging |
0.98 |
R8891:Zfp429
|
UTSW |
13 |
67,538,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R9364:Zfp429
|
UTSW |
13 |
67,538,531 (GRCm39) |
missense |
probably benign |
0.12 |
R9554:Zfp429
|
UTSW |
13 |
67,538,531 (GRCm39) |
missense |
probably benign |
0.12 |
|
Posted On |
2014-05-07 |