Incidental Mutation 'R6192:Zfp142'
ID |
502609 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp142
|
Ensembl Gene |
ENSMUSG00000026135 |
Gene Name |
zinc finger protein 142 |
Synonyms |
9330177B18Rik |
MMRRC Submission |
044332-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R6192 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
74605490-74627308 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 74609667 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamic Acid to Glycine
at position 1376
(E1376G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000027315
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027315]
[ENSMUST00000027362]
[ENSMUST00000066986]
[ENSMUST00000067916]
[ENSMUST00000113737]
[ENSMUST00000113747]
[ENSMUST00000113749]
[ENSMUST00000141412]
[ENSMUST00000152707]
[ENSMUST00000156613]
[ENSMUST00000127921]
[ENSMUST00000113750]
|
AlphaFold |
G5E869 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000027315
AA Change: E1376G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000027315 Gene: ENSMUSG00000026135 AA Change: E1376G
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
103 |
127 |
1.16e1 |
SMART |
ZnF_C2H2
|
164 |
186 |
1.26e-2 |
SMART |
ZnF_C2H2
|
193 |
218 |
7.78e-3 |
SMART |
ZnF_C2H2
|
223 |
247 |
2.29e0 |
SMART |
ZnF_C2H2
|
250 |
272 |
9.96e-1 |
SMART |
low complexity region
|
317 |
329 |
N/A |
INTRINSIC |
ZnF_C2H2
|
363 |
385 |
9.96e-1 |
SMART |
ZnF_C2H2
|
391 |
411 |
1.26e1 |
SMART |
ZnF_C2H2
|
419 |
442 |
1.47e-3 |
SMART |
ZnF_C2H2
|
453 |
475 |
2.75e-3 |
SMART |
ZnF_C2H2
|
486 |
511 |
3.34e-2 |
SMART |
ZnF_C2H2
|
516 |
540 |
4.81e0 |
SMART |
ZnF_C2H2
|
543 |
566 |
7.05e-1 |
SMART |
ZnF_C2H2
|
572 |
595 |
2.17e-1 |
SMART |
ZnF_C2H2
|
601 |
623 |
1.56e-2 |
SMART |
ZnF_C2H2
|
629 |
651 |
8.94e-3 |
SMART |
ZnF_C2H2
|
657 |
679 |
1.38e-3 |
SMART |
ZnF_C2H2
|
685 |
707 |
9.44e-2 |
SMART |
ZnF_C2H2
|
712 |
735 |
1.26e-2 |
SMART |
ZnF_C2H2
|
744 |
767 |
1.31e0 |
SMART |
ZnF_C2H2
|
773 |
796 |
2.63e0 |
SMART |
low complexity region
|
903 |
919 |
N/A |
INTRINSIC |
low complexity region
|
953 |
969 |
N/A |
INTRINSIC |
low complexity region
|
996 |
1007 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1039 |
1059 |
2.01e1 |
SMART |
ZnF_C2H2
|
1069 |
1089 |
1.91e1 |
SMART |
low complexity region
|
1147 |
1160 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1187 |
1207 |
2.7e2 |
SMART |
low complexity region
|
1209 |
1222 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1265 |
1285 |
3.56e1 |
SMART |
ZnF_C2H2
|
1295 |
1318 |
4.98e-1 |
SMART |
ZnF_C2H2
|
1331 |
1354 |
2.49e-1 |
SMART |
ZnF_C2H2
|
1360 |
1382 |
1.03e-2 |
SMART |
ZnF_C2H2
|
1388 |
1411 |
5.72e-1 |
SMART |
ZnF_C2H2
|
1417 |
1440 |
6.75e0 |
SMART |
ZnF_C2H2
|
1446 |
1469 |
9.58e-3 |
SMART |
ZnF_C2H2
|
1488 |
1511 |
1.64e-1 |
SMART |
ZnF_C2H2
|
1514 |
1536 |
1.1e-2 |
SMART |
ZnF_C2H2
|
1540 |
1563 |
4.05e-1 |
SMART |
ZnF_C2H2
|
1580 |
1602 |
4.45e0 |
SMART |
ZnF_C2H2
|
1608 |
1630 |
8.81e-2 |
SMART |
ZnF_C2H2
|
1636 |
1658 |
1.18e-2 |
SMART |
ZnF_C2H2
|
1664 |
1686 |
1.2e-3 |
SMART |
ZnF_C2H2
|
1692 |
1715 |
3.89e-3 |
SMART |
ZnF_C2H2
|
1721 |
1743 |
4.54e-4 |
SMART |
ZnF_C2H2
|
1749 |
1771 |
1.18e-2 |
SMART |
ZnF_C2H2
|
1777 |
1799 |
3.52e-1 |
SMART |
low complexity region
|
1829 |
1838 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000027362
|
SMART Domains |
Protein: ENSMUSP00000027362 Gene: ENSMUSG00000026173
Domain | Start | End | E-Value | Type |
PH
|
17 |
126 |
2.6e-12 |
SMART |
EFh
|
138 |
166 |
9.97e-1 |
SMART |
EFh
|
174 |
202 |
1.83e1 |
SMART |
EFh
|
207 |
234 |
4.45e1 |
SMART |
PLCXc
|
290 |
435 |
2.03e-79 |
SMART |
low complexity region
|
441 |
459 |
N/A |
INTRINSIC |
PLCYc
|
538 |
654 |
1.26e-75 |
SMART |
C2
|
673 |
779 |
5.68e-20 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000066986
AA Change: E1175G
PolyPhen 2
Score 0.025 (Sensitivity: 0.95; Specificity: 0.81)
|
SMART Domains |
Protein: ENSMUSP00000065149 Gene: ENSMUSG00000026135 AA Change: E1175G
Domain | Start | End | E-Value | Type |
low complexity region
|
116 |
128 |
N/A |
INTRINSIC |
ZnF_C2H2
|
162 |
184 |
9.96e-1 |
SMART |
ZnF_C2H2
|
190 |
210 |
1.26e1 |
SMART |
ZnF_C2H2
|
218 |
241 |
1.47e-3 |
SMART |
ZnF_C2H2
|
252 |
274 |
2.75e-3 |
SMART |
ZnF_C2H2
|
285 |
310 |
3.34e-2 |
SMART |
ZnF_C2H2
|
315 |
339 |
4.81e0 |
SMART |
ZnF_C2H2
|
342 |
365 |
7.05e-1 |
SMART |
ZnF_C2H2
|
371 |
394 |
2.17e-1 |
SMART |
ZnF_C2H2
|
400 |
422 |
1.56e-2 |
SMART |
ZnF_C2H2
|
428 |
450 |
8.94e-3 |
SMART |
ZnF_C2H2
|
456 |
478 |
1.38e-3 |
SMART |
ZnF_C2H2
|
484 |
506 |
9.44e-2 |
SMART |
ZnF_C2H2
|
511 |
534 |
1.26e-2 |
SMART |
ZnF_C2H2
|
543 |
566 |
1.31e0 |
SMART |
ZnF_C2H2
|
572 |
595 |
2.63e0 |
SMART |
low complexity region
|
702 |
718 |
N/A |
INTRINSIC |
low complexity region
|
752 |
768 |
N/A |
INTRINSIC |
low complexity region
|
795 |
806 |
N/A |
INTRINSIC |
ZnF_C2H2
|
838 |
858 |
2.01e1 |
SMART |
ZnF_C2H2
|
868 |
888 |
1.91e1 |
SMART |
low complexity region
|
946 |
959 |
N/A |
INTRINSIC |
ZnF_C2H2
|
986 |
1006 |
2.7e2 |
SMART |
low complexity region
|
1008 |
1021 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1064 |
1084 |
3.56e1 |
SMART |
ZnF_C2H2
|
1094 |
1117 |
4.98e-1 |
SMART |
ZnF_C2H2
|
1130 |
1153 |
2.49e-1 |
SMART |
ZnF_C2H2
|
1159 |
1181 |
1.03e-2 |
SMART |
ZnF_C2H2
|
1187 |
1210 |
5.72e-1 |
SMART |
ZnF_C2H2
|
1216 |
1239 |
6.75e0 |
SMART |
ZnF_C2H2
|
1245 |
1268 |
9.58e-3 |
SMART |
ZnF_C2H2
|
1287 |
1310 |
1.64e-1 |
SMART |
ZnF_C2H2
|
1313 |
1335 |
1.1e-2 |
SMART |
ZnF_C2H2
|
1339 |
1362 |
4.05e-1 |
SMART |
ZnF_C2H2
|
1379 |
1401 |
4.45e0 |
SMART |
ZnF_C2H2
|
1407 |
1429 |
8.81e-2 |
SMART |
ZnF_C2H2
|
1435 |
1457 |
1.18e-2 |
SMART |
ZnF_C2H2
|
1463 |
1485 |
1.2e-3 |
SMART |
ZnF_C2H2
|
1491 |
1514 |
3.89e-3 |
SMART |
ZnF_C2H2
|
1520 |
1542 |
4.54e-4 |
SMART |
ZnF_C2H2
|
1548 |
1570 |
1.18e-2 |
SMART |
ZnF_C2H2
|
1576 |
1598 |
3.52e-1 |
SMART |
low complexity region
|
1628 |
1637 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000067916
|
SMART Domains |
Protein: ENSMUSP00000064413 Gene: ENSMUSG00000026173
Domain | Start | End | E-Value | Type |
PH
|
17 |
126 |
2.6e-12 |
SMART |
EFh
|
138 |
166 |
9.97e-1 |
SMART |
EFh
|
174 |
202 |
1.83e1 |
SMART |
EFh
|
207 |
234 |
4.45e1 |
SMART |
PLCXc
|
290 |
435 |
2.03e-79 |
SMART |
low complexity region
|
441 |
459 |
N/A |
INTRINSIC |
PLCYc
|
506 |
622 |
1.26e-75 |
SMART |
C2
|
641 |
747 |
5.68e-20 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113737
AA Change: E1273G
PolyPhen 2
Score 0.044 (Sensitivity: 0.94; Specificity: 0.83)
|
SMART Domains |
Protein: ENSMUSP00000109366 Gene: ENSMUSG00000026135 AA Change: E1273G
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
93 |
115 |
9.81e1 |
SMART |
ZnF_C2H2
|
120 |
144 |
2.29e0 |
SMART |
ZnF_C2H2
|
147 |
169 |
9.96e-1 |
SMART |
low complexity region
|
214 |
226 |
N/A |
INTRINSIC |
ZnF_C2H2
|
260 |
282 |
9.96e-1 |
SMART |
ZnF_C2H2
|
288 |
308 |
1.26e1 |
SMART |
ZnF_C2H2
|
316 |
339 |
1.47e-3 |
SMART |
ZnF_C2H2
|
350 |
372 |
2.75e-3 |
SMART |
ZnF_C2H2
|
383 |
408 |
3.34e-2 |
SMART |
ZnF_C2H2
|
413 |
437 |
4.81e0 |
SMART |
ZnF_C2H2
|
440 |
463 |
7.05e-1 |
SMART |
ZnF_C2H2
|
469 |
492 |
2.17e-1 |
SMART |
ZnF_C2H2
|
498 |
520 |
1.56e-2 |
SMART |
ZnF_C2H2
|
526 |
548 |
8.94e-3 |
SMART |
ZnF_C2H2
|
554 |
576 |
1.38e-3 |
SMART |
ZnF_C2H2
|
582 |
604 |
9.44e-2 |
SMART |
ZnF_C2H2
|
609 |
632 |
1.26e-2 |
SMART |
ZnF_C2H2
|
641 |
664 |
1.31e0 |
SMART |
ZnF_C2H2
|
670 |
693 |
2.63e0 |
SMART |
low complexity region
|
800 |
816 |
N/A |
INTRINSIC |
low complexity region
|
850 |
866 |
N/A |
INTRINSIC |
low complexity region
|
893 |
904 |
N/A |
INTRINSIC |
ZnF_C2H2
|
936 |
956 |
2.01e1 |
SMART |
ZnF_C2H2
|
966 |
986 |
1.91e1 |
SMART |
low complexity region
|
1044 |
1057 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1084 |
1104 |
2.7e2 |
SMART |
low complexity region
|
1106 |
1119 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1162 |
1182 |
3.56e1 |
SMART |
ZnF_C2H2
|
1192 |
1215 |
4.98e-1 |
SMART |
ZnF_C2H2
|
1228 |
1251 |
2.49e-1 |
SMART |
ZnF_C2H2
|
1257 |
1279 |
1.03e-2 |
SMART |
ZnF_C2H2
|
1285 |
1308 |
5.72e-1 |
SMART |
ZnF_C2H2
|
1314 |
1337 |
6.75e0 |
SMART |
ZnF_C2H2
|
1343 |
1366 |
9.58e-3 |
SMART |
ZnF_C2H2
|
1385 |
1408 |
1.64e-1 |
SMART |
ZnF_C2H2
|
1411 |
1433 |
1.1e-2 |
SMART |
ZnF_C2H2
|
1437 |
1460 |
4.05e-1 |
SMART |
ZnF_C2H2
|
1477 |
1499 |
4.45e0 |
SMART |
ZnF_C2H2
|
1505 |
1527 |
8.81e-2 |
SMART |
ZnF_C2H2
|
1533 |
1555 |
1.18e-2 |
SMART |
ZnF_C2H2
|
1561 |
1583 |
1.2e-3 |
SMART |
ZnF_C2H2
|
1589 |
1612 |
3.89e-3 |
SMART |
ZnF_C2H2
|
1618 |
1640 |
4.54e-4 |
SMART |
ZnF_C2H2
|
1646 |
1668 |
1.18e-2 |
SMART |
ZnF_C2H2
|
1674 |
1696 |
3.52e-1 |
SMART |
low complexity region
|
1726 |
1735 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113747
|
SMART Domains |
Protein: ENSMUSP00000109376 Gene: ENSMUSG00000026173
Domain | Start | End | E-Value | Type |
PH
|
17 |
126 |
2.6e-12 |
SMART |
EFh
|
138 |
166 |
9.97e-1 |
SMART |
EFh
|
174 |
202 |
1.83e1 |
SMART |
EFh
|
207 |
234 |
4.45e1 |
SMART |
PLCXc
|
290 |
435 |
2.03e-79 |
SMART |
low complexity region
|
441 |
459 |
N/A |
INTRINSIC |
PLCYc
|
506 |
622 |
1.26e-75 |
SMART |
C2
|
641 |
747 |
5.68e-20 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113749
|
SMART Domains |
Protein: ENSMUSP00000109378 Gene: ENSMUSG00000026173
Domain | Start | End | E-Value | Type |
PH
|
17 |
126 |
2.6e-12 |
SMART |
EFh
|
138 |
166 |
9.97e-1 |
SMART |
EFh
|
174 |
202 |
1.83e1 |
SMART |
EFh
|
207 |
234 |
4.45e1 |
SMART |
PLCXc
|
290 |
435 |
2.03e-79 |
SMART |
low complexity region
|
441 |
459 |
N/A |
INTRINSIC |
PLCYc
|
538 |
654 |
1.26e-75 |
SMART |
C2
|
673 |
779 |
5.68e-20 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000141412
|
SMART Domains |
Protein: ENSMUSP00000115322 Gene: ENSMUSG00000026173
Domain | Start | End | E-Value | Type |
PH
|
17 |
126 |
2.6e-12 |
SMART |
EFh
|
138 |
166 |
9.97e-1 |
SMART |
EFh
|
174 |
202 |
1.83e1 |
SMART |
EFh
|
207 |
234 |
4.45e1 |
SMART |
PLCXc
|
290 |
435 |
2.03e-79 |
SMART |
low complexity region
|
441 |
459 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000152707
|
SMART Domains |
Protein: ENSMUSP00000121732 Gene: ENSMUSG00000026173
Domain | Start | End | E-Value | Type |
PH
|
17 |
126 |
2.6e-12 |
SMART |
EFh
|
138 |
166 |
9.97e-1 |
SMART |
EFh
|
174 |
202 |
1.83e1 |
SMART |
EFh
|
207 |
234 |
4.45e1 |
SMART |
PLCXc
|
290 |
435 |
2.03e-79 |
SMART |
low complexity region
|
441 |
459 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000156613
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000127921
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000135111
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113750
|
SMART Domains |
Protein: ENSMUSP00000109379 Gene: ENSMUSG00000026173
Domain | Start | End | E-Value | Type |
PH
|
17 |
126 |
2.6e-12 |
SMART |
EFh
|
138 |
166 |
9.97e-1 |
SMART |
EFh
|
174 |
202 |
1.83e1 |
SMART |
EFh
|
207 |
234 |
4.45e1 |
SMART |
PLCXc
|
290 |
435 |
2.03e-79 |
SMART |
low complexity region
|
441 |
459 |
N/A |
INTRINSIC |
PLCYc
|
506 |
622 |
1.26e-75 |
SMART |
C2
|
641 |
747 |
7.16e-17 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
Validation Efficiency |
100% (75/75) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the Kruppel family of C2H2-type zinc finger proteins. It contains 31 C2H2-type zinc fingers and may be involved in transcriptional regulation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts9 |
T |
C |
6: 92,774,002 (GRCm39) |
E1137G |
probably damaging |
Het |
Adcy9 |
T |
C |
16: 4,105,818 (GRCm39) |
I1099V |
probably benign |
Het |
Angptl4 |
A |
T |
17: 33,996,015 (GRCm39) |
N320K |
probably benign |
Het |
Atp6v0a2 |
G |
A |
5: 124,767,268 (GRCm39) |
M10I |
probably benign |
Het |
Bltp1 |
C |
T |
3: 37,042,318 (GRCm39) |
T2768I |
probably benign |
Het |
Cbfa2t3 |
A |
G |
8: 123,361,135 (GRCm39) |
S395P |
probably benign |
Het |
Cenpe |
C |
T |
3: 134,954,291 (GRCm39) |
T1716I |
possibly damaging |
Het |
Chsy1 |
T |
C |
7: 65,820,625 (GRCm39) |
Y287H |
probably benign |
Het |
Col4a4 |
G |
T |
1: 82,462,151 (GRCm39) |
P1075T |
probably damaging |
Het |
Cryab |
T |
A |
9: 50,665,813 (GRCm39) |
M68K |
probably damaging |
Het |
Cybrd1 |
T |
A |
2: 70,967,858 (GRCm39) |
L143Q |
probably null |
Het |
Dcaf7 |
T |
C |
11: 105,942,584 (GRCm39) |
V177A |
probably damaging |
Het |
Dclk2 |
T |
C |
3: 86,722,457 (GRCm39) |
Y392C |
probably damaging |
Het |
Ddx20 |
T |
C |
3: 105,586,036 (GRCm39) |
T770A |
probably benign |
Het |
Dennd1b |
T |
A |
1: 139,095,456 (GRCm39) |
D501E |
probably benign |
Het |
Dgkh |
A |
T |
14: 78,865,504 (GRCm39) |
Y26* |
probably null |
Het |
Dnajc2 |
A |
G |
5: 21,973,646 (GRCm39) |
V196A |
probably damaging |
Het |
Etl4 |
A |
G |
2: 20,806,362 (GRCm39) |
K827E |
probably damaging |
Het |
Fam8a1 |
C |
T |
13: 46,823,099 (GRCm39) |
P13L |
probably damaging |
Het |
Gfra3 |
T |
C |
18: 34,837,582 (GRCm39) |
S139G |
possibly damaging |
Het |
Ggnbp1 |
G |
A |
17: 27,248,847 (GRCm39) |
V139I |
possibly damaging |
Het |
Gja1 |
T |
A |
10: 56,264,330 (GRCm39) |
Y230N |
probably damaging |
Het |
Gldc |
A |
G |
19: 30,111,172 (GRCm39) |
S535P |
probably damaging |
Het |
Gm45871 |
A |
G |
18: 90,610,357 (GRCm39) |
T532A |
probably benign |
Het |
Gm5431 |
T |
A |
11: 48,785,220 (GRCm39) |
D107V |
probably benign |
Het |
Herc2 |
C |
T |
7: 55,857,510 (GRCm39) |
T4031M |
probably damaging |
Het |
Iffo2 |
G |
A |
4: 139,333,769 (GRCm39) |
A282T |
probably damaging |
Het |
Ifi44 |
T |
G |
3: 151,451,276 (GRCm39) |
|
probably null |
Het |
Igkv4-53 |
C |
T |
6: 69,625,915 (GRCm39) |
R62H |
possibly damaging |
Het |
Lrp11 |
A |
C |
10: 7,474,454 (GRCm39) |
|
probably null |
Het |
Lrp4 |
A |
G |
2: 91,338,833 (GRCm39) |
T1755A |
probably benign |
Het |
Mcm3ap |
A |
T |
10: 76,336,934 (GRCm39) |
K1316M |
probably damaging |
Het |
Mctp1 |
T |
G |
13: 76,971,082 (GRCm39) |
|
probably null |
Het |
Mroh5 |
A |
T |
15: 73,662,630 (GRCm39) |
I396N |
probably damaging |
Het |
Mrps5 |
T |
A |
2: 127,443,305 (GRCm39) |
H294Q |
probably damaging |
Het |
Muc16 |
A |
T |
9: 18,569,985 (GRCm39) |
S845T |
unknown |
Het |
Mycbpap |
A |
T |
11: 94,398,557 (GRCm39) |
V474E |
probably damaging |
Het |
Mzt2 |
G |
C |
16: 15,666,551 (GRCm39) |
S122W |
probably benign |
Het |
Neb |
T |
C |
2: 52,146,802 (GRCm39) |
I2821V |
probably benign |
Het |
Ngef |
A |
T |
1: 87,415,622 (GRCm39) |
D347E |
probably damaging |
Het |
Nlrp14 |
T |
C |
7: 106,781,646 (GRCm39) |
V281A |
probably benign |
Het |
Obscn |
A |
T |
11: 58,888,864 (GRCm39) |
Y7597N |
unknown |
Het |
Or4k47 |
T |
C |
2: 111,451,520 (GRCm39) |
R300G |
possibly damaging |
Het |
Patj |
G |
T |
4: 98,344,394 (GRCm39) |
G569W |
probably damaging |
Het |
Pdzrn4 |
A |
T |
15: 92,655,562 (GRCm39) |
E485V |
probably damaging |
Het |
Phf2 |
T |
A |
13: 48,973,583 (GRCm39) |
T361S |
unknown |
Het |
Pik3r6 |
A |
G |
11: 68,434,455 (GRCm39) |
E552G |
probably damaging |
Het |
Pitx2 |
A |
G |
3: 129,009,521 (GRCm39) |
T147A |
probably benign |
Het |
Pkmyt1 |
G |
A |
17: 23,953,167 (GRCm39) |
G241D |
probably damaging |
Het |
Pola2 |
A |
T |
19: 6,003,802 (GRCm39) |
V191D |
possibly damaging |
Het |
Ralgapb |
T |
A |
2: 158,291,367 (GRCm39) |
|
probably null |
Het |
Rapgef4 |
T |
C |
2: 71,811,661 (GRCm39) |
S11P |
probably benign |
Het |
Rnf10 |
G |
A |
5: 115,395,136 (GRCm39) |
R151C |
probably damaging |
Het |
Rpl34 |
G |
A |
3: 130,522,716 (GRCm39) |
P50L |
probably benign |
Het |
Rptn |
C |
G |
3: 93,305,437 (GRCm39) |
H923Q |
possibly damaging |
Het |
Sbno2 |
A |
T |
10: 79,895,850 (GRCm39) |
L977Q |
probably damaging |
Het |
Sec14l3 |
G |
A |
11: 4,025,566 (GRCm39) |
|
probably null |
Het |
Serping1 |
A |
T |
2: 84,600,612 (GRCm39) |
N243K |
possibly damaging |
Het |
Slco2b1 |
T |
A |
7: 99,334,779 (GRCm39) |
I231F |
probably damaging |
Het |
Spag8 |
A |
G |
4: 43,652,458 (GRCm39) |
F294S |
probably damaging |
Het |
Speer4f1 |
G |
A |
5: 17,684,493 (GRCm39) |
A174T |
probably damaging |
Het |
Spred3 |
T |
C |
7: 28,862,402 (GRCm39) |
D147G |
probably benign |
Het |
Stard9 |
A |
G |
2: 120,527,241 (GRCm39) |
D1166G |
probably damaging |
Het |
Svep1 |
G |
T |
4: 58,104,536 (GRCm39) |
T1229K |
possibly damaging |
Het |
Tanc1 |
T |
A |
2: 59,669,305 (GRCm39) |
|
probably null |
Het |
Tmem232 |
T |
C |
17: 65,737,800 (GRCm39) |
Y420C |
probably damaging |
Het |
Tubd1 |
A |
T |
11: 86,448,619 (GRCm39) |
M311L |
probably benign |
Het |
Tulp3 |
G |
A |
6: 128,332,703 (GRCm39) |
|
probably null |
Het |
Usp42 |
T |
C |
5: 143,702,942 (GRCm39) |
T560A |
possibly damaging |
Het |
Vmn1r170 |
A |
T |
7: 23,305,934 (GRCm39) |
Y112F |
probably damaging |
Het |
Vmn2r4 |
A |
T |
3: 64,322,699 (GRCm39) |
C7S |
probably benign |
Het |
Wrn |
A |
G |
8: 33,774,682 (GRCm39) |
M652T |
probably benign |
Het |
Wsb1 |
G |
A |
11: 79,139,336 (GRCm39) |
P120L |
possibly damaging |
Het |
Zfp709 |
TCGACG |
TCG |
8: 72,644,552 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Zfp142 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00581:Zfp142
|
APN |
1 |
74,606,131 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00711:Zfp142
|
APN |
1 |
74,611,593 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01391:Zfp142
|
APN |
1 |
74,618,699 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01808:Zfp142
|
APN |
1 |
74,615,184 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02074:Zfp142
|
APN |
1 |
74,609,022 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02134:Zfp142
|
APN |
1 |
74,609,022 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02567:Zfp142
|
APN |
1 |
74,617,309 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02567:Zfp142
|
APN |
1 |
74,617,306 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02567:Zfp142
|
APN |
1 |
74,617,308 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02669:Zfp142
|
APN |
1 |
74,610,432 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02694:Zfp142
|
APN |
1 |
74,609,307 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02884:Zfp142
|
APN |
1 |
74,611,142 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03000:Zfp142
|
APN |
1 |
74,612,777 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03080:Zfp142
|
APN |
1 |
74,610,368 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03238:Zfp142
|
APN |
1 |
74,615,437 (GRCm39) |
missense |
probably benign |
0.37 |
IGL03277:Zfp142
|
APN |
1 |
74,610,193 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4402001:Zfp142
|
UTSW |
1 |
74,618,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R0124:Zfp142
|
UTSW |
1 |
74,607,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R0256:Zfp142
|
UTSW |
1 |
74,617,317 (GRCm39) |
missense |
probably benign |
|
R0267:Zfp142
|
UTSW |
1 |
74,615,223 (GRCm39) |
missense |
probably benign |
0.05 |
R0306:Zfp142
|
UTSW |
1 |
74,609,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R0321:Zfp142
|
UTSW |
1 |
74,608,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R0466:Zfp142
|
UTSW |
1 |
74,624,570 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0513:Zfp142
|
UTSW |
1 |
74,610,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R1084:Zfp142
|
UTSW |
1 |
74,610,985 (GRCm39) |
missense |
probably benign |
|
R1534:Zfp142
|
UTSW |
1 |
74,611,247 (GRCm39) |
missense |
probably benign |
0.00 |
R1548:Zfp142
|
UTSW |
1 |
74,609,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R1623:Zfp142
|
UTSW |
1 |
74,610,934 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1628:Zfp142
|
UTSW |
1 |
74,611,047 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1710:Zfp142
|
UTSW |
1 |
74,611,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R1722:Zfp142
|
UTSW |
1 |
74,608,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R1770:Zfp142
|
UTSW |
1 |
74,618,790 (GRCm39) |
missense |
probably damaging |
0.99 |
R2042:Zfp142
|
UTSW |
1 |
74,609,778 (GRCm39) |
missense |
probably benign |
0.10 |
R2112:Zfp142
|
UTSW |
1 |
74,612,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R2249:Zfp142
|
UTSW |
1 |
74,606,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R4393:Zfp142
|
UTSW |
1 |
74,611,219 (GRCm39) |
missense |
probably benign |
0.00 |
R4700:Zfp142
|
UTSW |
1 |
74,609,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R4750:Zfp142
|
UTSW |
1 |
74,611,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R4763:Zfp142
|
UTSW |
1 |
74,615,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R5208:Zfp142
|
UTSW |
1 |
74,610,027 (GRCm39) |
missense |
probably benign |
0.18 |
R5233:Zfp142
|
UTSW |
1 |
74,624,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R5585:Zfp142
|
UTSW |
1 |
74,617,404 (GRCm39) |
nonsense |
probably null |
|
R6461:Zfp142
|
UTSW |
1 |
74,606,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R6482:Zfp142
|
UTSW |
1 |
74,609,376 (GRCm39) |
splice site |
probably null |
|
R7320:Zfp142
|
UTSW |
1 |
74,609,167 (GRCm39) |
nonsense |
probably null |
|
R7438:Zfp142
|
UTSW |
1 |
74,624,679 (GRCm39) |
missense |
probably benign |
|
R7528:Zfp142
|
UTSW |
1 |
74,610,061 (GRCm39) |
missense |
probably benign |
0.00 |
R7600:Zfp142
|
UTSW |
1 |
74,612,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R8007:Zfp142
|
UTSW |
1 |
74,610,655 (GRCm39) |
missense |
probably benign |
0.01 |
R8681:Zfp142
|
UTSW |
1 |
74,610,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R8772:Zfp142
|
UTSW |
1 |
74,610,825 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9058:Zfp142
|
UTSW |
1 |
74,608,955 (GRCm39) |
nonsense |
probably null |
|
R9233:Zfp142
|
UTSW |
1 |
74,610,288 (GRCm39) |
missense |
probably benign |
|
R9281:Zfp142
|
UTSW |
1 |
74,607,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R9302:Zfp142
|
UTSW |
1 |
74,606,302 (GRCm39) |
missense |
probably damaging |
0.98 |
R9454:Zfp142
|
UTSW |
1 |
74,609,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R9569:Zfp142
|
UTSW |
1 |
74,615,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R9595:Zfp142
|
UTSW |
1 |
74,611,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R9680:Zfp142
|
UTSW |
1 |
74,610,933 (GRCm39) |
missense |
probably benign |
0.16 |
Z1177:Zfp142
|
UTSW |
1 |
74,609,325 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TGGCGAGTGATGTCATGACG -3'
(R):5'- GAGATCTGCACTGTGGTCTCTG -3'
Sequencing Primer
(F):5'- TGATGTCATGACGAAGATAACCAC -3'
(R):5'- TGAGGCTCCATCAAAAACGG -3'
|
Posted On |
2018-02-27 |