Incidental Mutation 'IGL02092:Zfp947'
ID |
279444 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Zfp947
|
Ensembl Gene |
ENSMUSG00000063383 |
Gene Name |
zinc finger protein 947 |
Synonyms |
Gm4769 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.106)
|
Stock # |
IGL02092
|
Quality Score |
|
Status
|
|
Chromosome |
17 |
Chromosomal Location |
22363336-22385153 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to G
at 22366477 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Alanine
at position 17
(D17A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000079137
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000080249]
|
AlphaFold |
Q8BIQ6 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000080249
AA Change: D17A
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000079137 Gene: ENSMUSG00000063383 AA Change: D17A
Domain | Start | End | E-Value | Type |
KRAB
|
13 |
73 |
9.26e-19 |
SMART |
ZnF_C2H2
|
183 |
205 |
7.05e-1 |
SMART |
ZnF_C2H2
|
211 |
233 |
1.5e-4 |
SMART |
ZnF_C2H2
|
239 |
261 |
7.67e-2 |
SMART |
ZnF_C2H2
|
267 |
289 |
2.79e-4 |
SMART |
ZnF_C2H2
|
295 |
317 |
5.59e-4 |
SMART |
ZnF_C2H2
|
323 |
345 |
4.24e-4 |
SMART |
ZnF_C2H2
|
351 |
373 |
3.21e-4 |
SMART |
ZnF_C2H2
|
379 |
401 |
5.99e-4 |
SMART |
ZnF_C2H2
|
407 |
429 |
8.02e-5 |
SMART |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010H22Rik |
T |
A |
5: 98,714,627 (GRCm39) |
|
probably benign |
Het |
Birc7 |
A |
T |
2: 180,574,979 (GRCm39) |
R238S |
probably benign |
Het |
Cdc42bpg |
C |
A |
19: 6,366,856 (GRCm39) |
|
probably benign |
Het |
Ces3a |
T |
C |
8: 105,776,962 (GRCm39) |
|
probably benign |
Het |
Cntnap2 |
T |
C |
6: 46,211,137 (GRCm39) |
F517S |
probably damaging |
Het |
Cracr2b |
A |
G |
7: 141,044,869 (GRCm39) |
E201G |
probably damaging |
Het |
Cyth3 |
T |
C |
5: 143,693,140 (GRCm39) |
|
probably benign |
Het |
Exoc2 |
A |
T |
13: 31,059,260 (GRCm39) |
N611K |
probably benign |
Het |
Fign |
A |
T |
2: 63,810,927 (GRCm39) |
N114K |
possibly damaging |
Het |
Gabrb3 |
A |
G |
7: 57,415,334 (GRCm39) |
T135A |
probably damaging |
Het |
Htra3 |
T |
C |
5: 35,828,416 (GRCm39) |
K155E |
probably damaging |
Het |
Inpp5f |
T |
C |
7: 128,286,948 (GRCm39) |
L609S |
probably damaging |
Het |
Kcp |
C |
A |
6: 29,489,031 (GRCm39) |
|
probably null |
Het |
Map4k4 |
A |
G |
1: 40,025,943 (GRCm39) |
K311R |
probably benign |
Het |
Map4k4 |
A |
G |
1: 40,063,508 (GRCm39) |
K1228E |
probably damaging |
Het |
Muc20 |
G |
A |
16: 32,614,642 (GRCm39) |
S245F |
probably damaging |
Het |
Or10ak8 |
A |
G |
4: 118,774,187 (GRCm39) |
L159S |
possibly damaging |
Het |
Or7g33 |
T |
A |
9: 19,449,046 (GRCm39) |
Y60F |
probably damaging |
Het |
Or8b36 |
T |
G |
9: 37,937,917 (GRCm39) |
S272A |
possibly damaging |
Het |
Pi4ka |
A |
G |
16: 17,136,360 (GRCm39) |
M892T |
probably benign |
Het |
Ptpn22 |
A |
G |
3: 103,784,637 (GRCm39) |
T234A |
probably damaging |
Het |
Sema4g |
G |
A |
19: 44,981,078 (GRCm39) |
|
probably null |
Het |
Slc35a3 |
A |
G |
3: 116,474,781 (GRCm39) |
S204P |
probably damaging |
Het |
Speer4f2 |
C |
T |
5: 17,581,627 (GRCm39) |
Q190* |
probably null |
Het |
Szt2 |
A |
G |
4: 118,220,529 (GRCm39) |
|
probably benign |
Het |
Tacr1 |
T |
C |
6: 82,380,900 (GRCm39) |
Y104H |
probably damaging |
Het |
Trim23 |
A |
G |
13: 104,324,120 (GRCm39) |
E173G |
probably benign |
Het |
Trpm6 |
T |
C |
19: 18,749,695 (GRCm39) |
I8T |
possibly damaging |
Het |
Trpv1 |
T |
A |
11: 73,136,905 (GRCm39) |
|
probably benign |
Het |
Ufsp2 |
T |
C |
8: 46,448,701 (GRCm39) |
|
probably null |
Het |
Wwc2 |
T |
C |
8: 48,317,570 (GRCm39) |
D669G |
unknown |
Het |
Zfp940 |
T |
C |
7: 29,545,626 (GRCm39) |
T94A |
probably benign |
Het |
|
Other mutations in Zfp947 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02592:Zfp947
|
APN |
17 |
22,365,233 (GRCm39) |
missense |
possibly damaging |
0.95 |
deformity
|
UTSW |
17 |
22,364,594 (GRCm39) |
missense |
probably damaging |
1.00 |
Gnarled
|
UTSW |
17 |
22,365,165 (GRCm39) |
missense |
probably benign |
0.00 |
R0070:Zfp947
|
UTSW |
17 |
22,365,165 (GRCm39) |
missense |
probably benign |
0.00 |
R1519:Zfp947
|
UTSW |
17 |
22,365,273 (GRCm39) |
missense |
probably benign |
0.02 |
R1521:Zfp947
|
UTSW |
17 |
22,364,813 (GRCm39) |
missense |
probably benign |
0.00 |
R1639:Zfp947
|
UTSW |
17 |
22,365,074 (GRCm39) |
missense |
probably benign |
|
R1721:Zfp947
|
UTSW |
17 |
22,365,184 (GRCm39) |
missense |
probably benign |
|
R1801:Zfp947
|
UTSW |
17 |
22,365,443 (GRCm39) |
missense |
probably benign |
|
R2264:Zfp947
|
UTSW |
17 |
22,364,919 (GRCm39) |
missense |
probably benign |
|
R3943:Zfp947
|
UTSW |
17 |
22,364,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R4561:Zfp947
|
UTSW |
17 |
22,365,124 (GRCm39) |
nonsense |
probably null |
|
R4562:Zfp947
|
UTSW |
17 |
22,365,124 (GRCm39) |
nonsense |
probably null |
|
R4943:Zfp947
|
UTSW |
17 |
22,364,813 (GRCm39) |
missense |
probably benign |
|
R5688:Zfp947
|
UTSW |
17 |
22,365,066 (GRCm39) |
missense |
probably benign |
0.00 |
R6037:Zfp947
|
UTSW |
17 |
22,366,415 (GRCm39) |
missense |
probably damaging |
0.99 |
R6037:Zfp947
|
UTSW |
17 |
22,366,415 (GRCm39) |
missense |
probably damaging |
0.99 |
R6414:Zfp947
|
UTSW |
17 |
22,365,395 (GRCm39) |
missense |
probably damaging |
0.98 |
R6786:Zfp947
|
UTSW |
17 |
22,364,750 (GRCm39) |
missense |
probably benign |
0.01 |
R6993:Zfp947
|
UTSW |
17 |
22,364,961 (GRCm39) |
missense |
probably benign |
0.11 |
R7556:Zfp947
|
UTSW |
17 |
22,364,597 (GRCm39) |
missense |
probably benign |
|
R8224:Zfp947
|
UTSW |
17 |
22,364,363 (GRCm39) |
missense |
probably benign |
|
R8398:Zfp947
|
UTSW |
17 |
22,365,102 (GRCm39) |
missense |
probably benign |
0.03 |
R8670:Zfp947
|
UTSW |
17 |
22,364,687 (GRCm39) |
missense |
probably benign |
0.09 |
R8871:Zfp947
|
UTSW |
17 |
22,364,695 (GRCm39) |
missense |
probably benign |
0.13 |
R9000:Zfp947
|
UTSW |
17 |
22,365,161 (GRCm39) |
missense |
probably benign |
0.12 |
R9099:Zfp947
|
UTSW |
17 |
22,364,855 (GRCm39) |
missense |
probably benign |
0.00 |
R9180:Zfp947
|
UTSW |
17 |
22,364,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R9287:Zfp947
|
UTSW |
17 |
22,364,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R9371:Zfp947
|
UTSW |
17 |
22,364,384 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9507:Zfp947
|
UTSW |
17 |
22,364,582 (GRCm39) |
missense |
probably benign |
0.00 |
R9738:Zfp947
|
UTSW |
17 |
22,365,341 (GRCm39) |
missense |
probably benign |
0.01 |
|
Posted On |
2015-04-16 |