Incidental Mutation 'IGL01391:Zfp142'
ID |
79218 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Zfp142
|
Ensembl Gene |
ENSMUSG00000026135 |
Gene Name |
zinc finger protein 142 |
Synonyms |
9330177B18Rik |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
IGL01391
|
Quality Score |
|
Status
|
|
Chromosome |
1 |
Chromosomal Location |
74605490-74627308 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 74618699 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Alanine
at position 120
(V120A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000109366
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027315]
[ENSMUST00000066986]
[ENSMUST00000113737]
[ENSMUST00000127921]
[ENSMUST00000156613]
|
AlphaFold |
G5E869 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000027315
AA Change: V223A
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000027315 Gene: ENSMUSG00000026135 AA Change: V223A
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 damaging
Transcript: ENSMUST00000113737
AA Change: V120A
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000109366 Gene: ENSMUSG00000026135 AA Change: V120A
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
|
Coding Region Coverage |
|
Validation Efficiency |
|
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: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ap3m2 |
T |
A |
8: 23,289,663 (GRCm39) |
I147F |
probably benign |
Het |
Areg |
T |
A |
5: 91,288,954 (GRCm39) |
S87T |
probably damaging |
Het |
Arid1b |
T |
A |
17: 5,369,133 (GRCm39) |
|
probably benign |
Het |
Arl6ip6 |
A |
G |
2: 53,082,156 (GRCm39) |
R8G |
probably benign |
Het |
Brms1 |
A |
G |
19: 5,096,723 (GRCm39) |
E135G |
possibly damaging |
Het |
Ccser1 |
A |
G |
6: 61,615,505 (GRCm39) |
|
probably benign |
Het |
Dock3 |
A |
T |
9: 106,784,433 (GRCm39) |
M258K |
possibly damaging |
Het |
Epb41l4a |
T |
G |
18: 33,934,678 (GRCm39) |
D562A |
possibly damaging |
Het |
Etaa1 |
G |
A |
11: 17,896,005 (GRCm39) |
T704I |
probably damaging |
Het |
Fer1l4 |
T |
A |
2: 155,878,376 (GRCm39) |
H972L |
probably damaging |
Het |
Foxn1 |
A |
G |
11: 78,252,320 (GRCm39) |
M356T |
probably damaging |
Het |
Gfral |
C |
A |
9: 76,072,107 (GRCm39) |
G388* |
probably null |
Het |
Gm12258 |
A |
G |
11: 58,739,520 (GRCm39) |
T3A |
probably benign |
Het |
Hoxa5 |
T |
C |
6: 52,181,311 (GRCm39) |
N7S |
probably damaging |
Het |
Itgb4 |
T |
C |
11: 115,881,746 (GRCm39) |
L765P |
probably damaging |
Het |
Jchain |
C |
T |
5: 88,669,383 (GRCm39) |
C90Y |
probably damaging |
Het |
Klhl40 |
A |
G |
9: 121,607,983 (GRCm39) |
Y381C |
probably damaging |
Het |
Lhx6 |
A |
T |
2: 35,993,477 (GRCm39) |
C74S |
probably benign |
Het |
Magel2 |
A |
G |
7: 62,030,632 (GRCm39) |
S1179G |
unknown |
Het |
Mapre3 |
T |
C |
5: 31,022,241 (GRCm39) |
I236T |
probably damaging |
Het |
Mcf2l |
A |
T |
8: 13,064,010 (GRCm39) |
|
probably null |
Het |
Med13 |
A |
T |
11: 86,219,323 (GRCm39) |
H374Q |
probably benign |
Het |
Meioc |
A |
G |
11: 102,565,113 (GRCm39) |
Y187C |
probably benign |
Het |
Myh1 |
G |
A |
11: 67,108,689 (GRCm39) |
M1368I |
probably benign |
Het |
Or14a258 |
A |
T |
7: 86,035,208 (GRCm39) |
I220N |
possibly damaging |
Het |
Or8b54 |
A |
G |
9: 38,686,826 (GRCm39) |
I92V |
probably damaging |
Het |
Phrf1 |
T |
C |
7: 140,842,394 (GRCm39) |
Y1501H |
probably damaging |
Het |
Pigb |
T |
C |
9: 72,929,573 (GRCm39) |
T337A |
probably damaging |
Het |
Pls1 |
T |
C |
9: 95,655,751 (GRCm39) |
K334E |
probably benign |
Het |
Pramel51 |
C |
T |
12: 88,145,225 (GRCm39) |
V34I |
possibly damaging |
Het |
Rab3b |
T |
C |
4: 108,797,999 (GRCm39) |
C226R |
probably damaging |
Het |
Ryr2 |
A |
T |
13: 11,571,571 (GRCm39) |
I4889N |
possibly damaging |
Het |
Serpinb1a |
G |
A |
13: 33,029,398 (GRCm39) |
S210L |
probably benign |
Het |
Slc52a3 |
A |
G |
2: 151,849,522 (GRCm39) |
I390V |
probably benign |
Het |
Slc6a7 |
C |
A |
18: 61,136,382 (GRCm39) |
A340S |
probably damaging |
Het |
Tcaf3 |
T |
C |
6: 42,570,615 (GRCm39) |
Y379C |
probably damaging |
Het |
Tex261 |
A |
G |
6: 83,748,222 (GRCm39) |
V180A |
probably benign |
Het |
Tnnt1 |
C |
T |
7: 4,517,211 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,798,847 (GRCm39) |
T476A |
possibly damaging |
Het |
Vcan |
A |
G |
13: 89,852,288 (GRCm39) |
S891P |
probably benign |
Het |
Vmn2r16 |
T |
A |
5: 109,511,627 (GRCm39) |
D611E |
possibly damaging |
Het |
Vmn2r68 |
T |
C |
7: 84,886,819 (GRCm39) |
T32A |
probably benign |
Het |
Vwde |
T |
G |
6: 13,190,526 (GRCm39) |
S522R |
probably benign |
Het |
Wdr3 |
G |
A |
3: 100,054,105 (GRCm39) |
|
probably benign |
Het |
Wfs1 |
G |
T |
5: 37,128,907 (GRCm39) |
Q288K |
probably benign |
Het |
Zfp672 |
A |
G |
11: 58,208,192 (GRCm39) |
F43S |
probably damaging |
Het |
Znhit3 |
A |
T |
11: 84,802,283 (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 |
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 |
|
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 |
|
Posted On |
2013-11-05 |