Incidental Mutation 'R1770:Zfp142'
ID |
196460 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp142
|
Ensembl Gene |
ENSMUSG00000026135 |
Gene Name |
zinc finger protein 142 |
Synonyms |
9330177B18Rik |
MMRRC Submission |
039801-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1770 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
74605490-74627308 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 74618790 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Isoleucine
at position 193
(F193I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000027315
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027315]
[ENSMUST00000066986]
[ENSMUST00000113737]
[ENSMUST00000127921]
[ENSMUST00000156613]
|
AlphaFold |
G5E869 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000027315
AA Change: F193I
PolyPhen 2
Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000027315 Gene: ENSMUSG00000026135 AA Change: F193I
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: ENSMUST00000066986
|
SMART Domains |
Protein: ENSMUSP00000065149 Gene: ENSMUSG00000026135
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: ENSMUST00000113737
|
SMART Domains |
Protein: ENSMUSP00000109366 Gene: ENSMUSG00000026135
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: ENSMUST00000127921
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000130112
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000136865
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000156613
|
Meta Mutation Damage Score |
0.6467 |
Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 95.1%
- 20x: 91.8%
|
Validation Efficiency |
92% (69/75) |
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: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd4 |
T |
C |
12: 84,661,874 (GRCm39) |
T84A |
probably benign |
Het |
Adgra1 |
T |
A |
7: 139,453,947 (GRCm39) |
Y161* |
probably null |
Het |
Aldoart1 |
G |
T |
4: 72,770,173 (GRCm39) |
H212N |
probably benign |
Het |
Aldob |
A |
G |
4: 49,536,861 (GRCm39) |
Y343H |
probably damaging |
Het |
Ankrd17 |
A |
T |
5: 90,391,235 (GRCm39) |
V2036E |
possibly damaging |
Het |
Ass1 |
A |
G |
2: 31,376,528 (GRCm39) |
T131A |
probably benign |
Het |
Baz1a |
C |
T |
12: 54,945,293 (GRCm39) |
R1354H |
probably damaging |
Het |
C2cd2l |
A |
G |
9: 44,228,108 (GRCm39) |
V71A |
probably benign |
Het |
C4b |
T |
A |
17: 34,955,901 (GRCm39) |
N678I |
possibly damaging |
Het |
Carmil1 |
A |
G |
13: 24,357,657 (GRCm39) |
L64P |
probably damaging |
Het |
Cdh18 |
T |
C |
15: 23,474,487 (GRCm39) |
S786P |
probably benign |
Het |
Cep135 |
A |
G |
5: 76,751,042 (GRCm39) |
E296G |
possibly damaging |
Het |
Chml |
G |
A |
1: 175,515,444 (GRCm39) |
T159I |
probably benign |
Het |
Cntn3 |
C |
T |
6: 102,246,166 (GRCm39) |
E328K |
possibly damaging |
Het |
Cstf1 |
A |
G |
2: 172,214,983 (GRCm39) |
I35V |
possibly damaging |
Het |
Cyp2c65 |
A |
G |
19: 39,070,642 (GRCm39) |
K275R |
probably benign |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dbx2 |
T |
C |
15: 95,522,615 (GRCm39) |
E364G |
probably benign |
Het |
Dcaf13 |
A |
T |
15: 38,993,633 (GRCm39) |
N242I |
probably damaging |
Het |
Dcc |
A |
G |
18: 71,579,470 (GRCm39) |
V701A |
probably benign |
Het |
Elapor2 |
A |
T |
5: 9,468,021 (GRCm39) |
T230S |
probably benign |
Het |
Fastkd5 |
A |
T |
2: 130,456,200 (GRCm39) |
Y797N |
probably damaging |
Het |
Fat4 |
T |
A |
3: 39,064,417 (GRCm39) |
I4791K |
probably damaging |
Het |
Gm3852 |
T |
C |
1: 46,051,048 (GRCm39) |
I45V |
possibly damaging |
Het |
Gng4 |
A |
G |
13: 13,999,851 (GRCm39) |
D40G |
probably damaging |
Het |
Gns |
A |
G |
10: 121,213,952 (GRCm39) |
D209G |
probably benign |
Het |
Kif6 |
C |
A |
17: 50,210,677 (GRCm39) |
Q791K |
possibly damaging |
Het |
Klhl35 |
G |
A |
7: 99,123,082 (GRCm39) |
V569M |
possibly damaging |
Het |
Krt1c |
A |
G |
15: 101,719,589 (GRCm39) |
S694P |
unknown |
Het |
Lrrc8c |
A |
G |
5: 105,754,603 (GRCm39) |
Y126C |
probably damaging |
Het |
Mad2l1bp |
A |
G |
17: 46,463,838 (GRCm39) |
V62A |
probably benign |
Het |
Map1b |
T |
C |
13: 99,567,001 (GRCm39) |
R1907G |
unknown |
Het |
Mertk |
A |
G |
2: 128,592,094 (GRCm39) |
I273V |
probably benign |
Het |
Mfsd4b1 |
A |
G |
10: 39,879,223 (GRCm39) |
Y225H |
probably damaging |
Het |
Mrc2 |
T |
C |
11: 105,229,619 (GRCm39) |
V684A |
probably damaging |
Het |
Msh6 |
G |
A |
17: 88,287,651 (GRCm39) |
W97* |
probably null |
Het |
Mtmr10 |
A |
G |
7: 63,986,469 (GRCm39) |
I516V |
possibly damaging |
Het |
Myo7a |
A |
T |
7: 97,761,813 (GRCm39) |
|
probably benign |
Het |
Ndufs5 |
T |
C |
4: 123,606,661 (GRCm39) |
Y92C |
probably benign |
Het |
Nlrp1b |
C |
T |
11: 71,050,979 (GRCm39) |
V1035I |
probably benign |
Het |
Ntrk2 |
A |
G |
13: 59,009,132 (GRCm39) |
R308G |
possibly damaging |
Het |
Or12e13 |
A |
G |
2: 87,663,643 (GRCm39) |
I87V |
probably benign |
Het |
Pcdhb16 |
G |
T |
18: 37,612,233 (GRCm39) |
G398W |
probably damaging |
Het |
Plpbp |
T |
A |
8: 27,543,326 (GRCm39) |
S237T |
probably damaging |
Het |
Pnpla6 |
T |
A |
8: 3,584,634 (GRCm39) |
F769I |
possibly damaging |
Het |
Polk |
A |
G |
13: 96,631,950 (GRCm39) |
V261A |
probably damaging |
Het |
Prss52 |
C |
T |
14: 64,351,082 (GRCm39) |
A289V |
probably damaging |
Het |
Puf60 |
T |
C |
15: 75,942,723 (GRCm39) |
K407E |
probably benign |
Het |
Pzp |
T |
C |
6: 128,462,580 (GRCm39) |
D1455G |
probably damaging |
Het |
Ranbp17 |
T |
C |
11: 33,167,301 (GRCm39) |
N1054S |
probably benign |
Het |
Sdk2 |
A |
G |
11: 113,684,567 (GRCm39) |
S1965P |
probably benign |
Het |
Spryd7 |
T |
C |
14: 61,777,654 (GRCm39) |
Y142C |
probably damaging |
Het |
Srrt |
A |
T |
5: 137,298,122 (GRCm39) |
|
probably benign |
Het |
Stk10 |
A |
G |
11: 32,572,464 (GRCm39) |
E935G |
possibly damaging |
Het |
Tas2r115 |
G |
A |
6: 132,714,934 (GRCm39) |
R6C |
probably damaging |
Het |
Tdrd7 |
T |
A |
4: 45,987,681 (GRCm39) |
|
probably benign |
Het |
Trim29 |
A |
T |
9: 43,243,673 (GRCm39) |
Q564L |
probably damaging |
Het |
Trim5 |
T |
C |
7: 103,925,868 (GRCm39) |
D231G |
probably damaging |
Het |
Trpv2 |
A |
G |
11: 62,487,787 (GRCm39) |
K676E |
probably benign |
Het |
Ttn |
T |
C |
2: 76,583,859 (GRCm39) |
R22383G |
probably damaging |
Het |
Ugt1a2 |
A |
G |
1: 88,129,160 (GRCm39) |
I268V |
probably benign |
Het |
Ugt8a |
T |
C |
3: 125,667,852 (GRCm39) |
N330D |
probably benign |
Het |
Utrn |
G |
A |
10: 12,351,040 (GRCm39) |
H2822Y |
probably damaging |
Het |
Vmn1r176 |
G |
A |
7: 23,534,946 (GRCm39) |
A69V |
probably benign |
Het |
Vmn2r106 |
T |
C |
17: 20,488,560 (GRCm39) |
Y613C |
probably damaging |
Het |
Wdfy1 |
A |
T |
1: 79,686,857 (GRCm39) |
W296R |
probably damaging |
Het |
Zfp11 |
G |
A |
5: 129,734,822 (GRCm39) |
T213I |
possibly damaging |
Het |
Zfp764 |
G |
A |
7: 127,004,739 (GRCm39) |
Q131* |
probably null |
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 |
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 |
|
R6192:Zfp142
|
UTSW |
1 |
74,609,667 (GRCm39) |
missense |
probably damaging |
1.00 |
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'- TGAACAGCAGCAGAAAGTTCTCCC -3'
(R):5'- CACTGAGACCCATATTCAGGCTGTG -3'
Sequencing Primer
(F):5'- TTGGAGCCCATGAAGCTG -3'
(R):5'- TGTGCAGGACCTCTCTAGTC -3'
|
Posted On |
2014-05-23 |