Incidental Mutation 'R7363:Zfp236'
ID |
571506 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp236
|
Ensembl Gene |
ENSMUSG00000041258 |
Gene Name |
zinc finger protein 236 |
Synonyms |
LOC240456 |
MMRRC Submission |
045448-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R7363 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
18 |
Chromosomal Location |
82611718-82711008 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 82639456 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Glycine
at position 1264
(R1264G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000138557
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000171071]
[ENSMUST00000182122]
[ENSMUST00000183048]
|
AlphaFold |
S4R299 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000171071
AA Change: R1216G
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000130004 Gene: ENSMUSG00000041258 AA Change: R1216G
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
39 |
61 |
2.24e-3 |
SMART |
ZnF_C2H2
|
68 |
90 |
2.29e0 |
SMART |
ZnF_C2H2
|
95 |
117 |
1.26e-2 |
SMART |
ZnF_C2H2
|
123 |
145 |
6.67e-2 |
SMART |
ZnF_C2H2
|
155 |
177 |
6.42e-4 |
SMART |
ZnF_C2H2
|
199 |
221 |
1.75e-5 |
SMART |
ZnF_C2H2
|
227 |
249 |
1.52e-5 |
SMART |
ZnF_C2H2
|
255 |
278 |
8.94e-3 |
SMART |
low complexity region
|
290 |
309 |
N/A |
INTRINSIC |
low complexity region
|
403 |
426 |
N/A |
INTRINSIC |
ZnF_C2H2
|
436 |
458 |
1.98e-4 |
SMART |
ZnF_C2H2
|
464 |
486 |
9.58e-3 |
SMART |
ZnF_C2H2
|
492 |
514 |
6.42e-4 |
SMART |
ZnF_C2H2
|
520 |
542 |
1.18e-2 |
SMART |
low complexity region
|
592 |
605 |
N/A |
INTRINSIC |
ZnF_C2H2
|
611 |
633 |
1.62e0 |
SMART |
ZnF_C2H2
|
639 |
661 |
5.21e-4 |
SMART |
ZnF_C2H2
|
667 |
689 |
6.78e-3 |
SMART |
ZnF_C2H2
|
695 |
717 |
7.37e-4 |
SMART |
low complexity region
|
720 |
733 |
N/A |
INTRINSIC |
ZnF_C2H2
|
922 |
944 |
5.21e-4 |
SMART |
ZnF_C2H2
|
950 |
972 |
1.04e-3 |
SMART |
ZnF_C2H2
|
978 |
1000 |
8.6e-5 |
SMART |
ZnF_C2H2
|
1006 |
1028 |
2.75e-3 |
SMART |
low complexity region
|
1030 |
1039 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1122 |
1144 |
7.78e-3 |
SMART |
ZnF_C2H2
|
1150 |
1172 |
3.63e-3 |
SMART |
ZnF_C2H2
|
1178 |
1200 |
6.88e-4 |
SMART |
ZnF_C2H2
|
1206 |
1228 |
5.42e-2 |
SMART |
low complexity region
|
1243 |
1258 |
N/A |
INTRINSIC |
low complexity region
|
1462 |
1477 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1612 |
1635 |
7.15e-2 |
SMART |
ZnF_C2H2
|
1641 |
1663 |
2.91e-2 |
SMART |
ZnF_C2H2
|
1677 |
1699 |
7.26e-3 |
SMART |
ZnF_C2H2
|
1705 |
1727 |
1.84e-4 |
SMART |
ZnF_C2H2
|
1733 |
1756 |
2.95e-3 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000182122
AA Change: R1264G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000138557 Gene: ENSMUSG00000041258 AA Change: R1264G
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
39 |
61 |
2.24e-3 |
SMART |
ZnF_C2H2
|
68 |
90 |
2.29e0 |
SMART |
ZnF_C2H2
|
95 |
117 |
1.26e-2 |
SMART |
ZnF_C2H2
|
123 |
145 |
6.67e-2 |
SMART |
ZnF_C2H2
|
155 |
177 |
6.42e-4 |
SMART |
ZnF_C2H2
|
199 |
221 |
1.75e-5 |
SMART |
ZnF_C2H2
|
227 |
249 |
1.52e-5 |
SMART |
ZnF_C2H2
|
255 |
278 |
8.94e-3 |
SMART |
ZnF_C2H2
|
287 |
310 |
9.58e-3 |
SMART |
low complexity region
|
338 |
357 |
N/A |
INTRINSIC |
low complexity region
|
451 |
474 |
N/A |
INTRINSIC |
ZnF_C2H2
|
484 |
506 |
1.98e-4 |
SMART |
ZnF_C2H2
|
512 |
534 |
9.58e-3 |
SMART |
ZnF_C2H2
|
540 |
562 |
6.42e-4 |
SMART |
ZnF_C2H2
|
568 |
590 |
1.18e-2 |
SMART |
low complexity region
|
640 |
653 |
N/A |
INTRINSIC |
ZnF_C2H2
|
659 |
681 |
1.62e0 |
SMART |
ZnF_C2H2
|
687 |
709 |
5.21e-4 |
SMART |
ZnF_C2H2
|
715 |
737 |
6.78e-3 |
SMART |
ZnF_C2H2
|
743 |
765 |
7.37e-4 |
SMART |
low complexity region
|
768 |
781 |
N/A |
INTRINSIC |
ZnF_C2H2
|
970 |
992 |
5.21e-4 |
SMART |
ZnF_C2H2
|
998 |
1020 |
1.04e-3 |
SMART |
ZnF_C2H2
|
1026 |
1048 |
8.6e-5 |
SMART |
ZnF_C2H2
|
1054 |
1076 |
2.75e-3 |
SMART |
low complexity region
|
1078 |
1087 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1170 |
1192 |
7.78e-3 |
SMART |
ZnF_C2H2
|
1198 |
1220 |
3.63e-3 |
SMART |
ZnF_C2H2
|
1226 |
1248 |
6.88e-4 |
SMART |
ZnF_C2H2
|
1254 |
1276 |
5.42e-2 |
SMART |
low complexity region
|
1291 |
1306 |
N/A |
INTRINSIC |
low complexity region
|
1510 |
1525 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1660 |
1683 |
7.15e-2 |
SMART |
ZnF_C2H2
|
1689 |
1711 |
2.91e-2 |
SMART |
ZnF_C2H2
|
1725 |
1747 |
7.26e-3 |
SMART |
ZnF_C2H2
|
1753 |
1775 |
1.84e-4 |
SMART |
ZnF_C2H2
|
1781 |
1804 |
2.95e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000183048
|
SMART Domains |
Protein: ENSMUSP00000138179 Gene: ENSMUSG00000041258
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
39 |
61 |
2.24e-3 |
SMART |
ZnF_C2H2
|
68 |
90 |
2.29e0 |
SMART |
ZnF_C2H2
|
95 |
117 |
1.26e-2 |
SMART |
ZnF_C2H2
|
123 |
145 |
6.67e-2 |
SMART |
ZnF_C2H2
|
155 |
177 |
6.42e-4 |
SMART |
ZnF_C2H2
|
199 |
221 |
1.75e-5 |
SMART |
ZnF_C2H2
|
227 |
249 |
1.52e-5 |
SMART |
ZnF_C2H2
|
255 |
278 |
8.94e-3 |
SMART |
ZnF_C2H2
|
287 |
310 |
9.58e-3 |
SMART |
low complexity region
|
338 |
357 |
N/A |
INTRINSIC |
low complexity region
|
454 |
467 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000183324
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
100% (72/72) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930568D16Rik |
T |
A |
2: 35,244,782 (GRCm39) |
N190I |
probably damaging |
Het |
Ablim1 |
G |
T |
19: 57,204,173 (GRCm39) |
L73I |
probably benign |
Het |
Adamts4 |
A |
T |
1: 171,086,608 (GRCm39) |
Q800L |
probably benign |
Het |
Atm |
A |
T |
9: 53,376,598 (GRCm39) |
I2014N |
probably damaging |
Het |
Atp2a1 |
A |
G |
7: 126,062,061 (GRCm39) |
C12R |
possibly damaging |
Het |
B3galnt1 |
A |
T |
3: 69,483,157 (GRCm39) |
Y35N |
probably damaging |
Het |
Bnc2 |
A |
T |
4: 84,210,308 (GRCm39) |
M687K |
probably benign |
Het |
Cacna2d4 |
A |
G |
6: 119,320,939 (GRCm39) |
Y917C |
probably damaging |
Het |
Cemip2 |
T |
C |
19: 21,833,575 (GRCm39) |
F1338L |
probably benign |
Het |
Ces2e |
A |
G |
8: 105,659,632 (GRCm39) |
|
probably null |
Het |
Cldn23 |
A |
G |
8: 36,292,659 (GRCm39) |
|
probably null |
Het |
Cntn5 |
G |
T |
9: 10,172,021 (GRCm39) |
S54R |
probably benign |
Het |
Cyria |
T |
A |
12: 12,390,665 (GRCm39) |
|
probably null |
Het |
Dido1 |
G |
T |
2: 180,304,310 (GRCm39) |
S1198* |
probably null |
Het |
Dnah12 |
A |
G |
14: 26,445,766 (GRCm39) |
M776V |
probably benign |
Het |
Dnah14 |
A |
G |
1: 181,518,089 (GRCm39) |
|
probably null |
Het |
Dnttip1 |
GGGCCGGC |
GGGC |
2: 164,599,605 (GRCm39) |
|
probably null |
Het |
Dusp28 |
A |
T |
1: 92,834,861 (GRCm39) |
T29S |
probably benign |
Het |
Erich1 |
A |
T |
8: 14,083,688 (GRCm39) |
S127R |
probably benign |
Het |
Fam151a |
T |
A |
4: 106,602,681 (GRCm39) |
L200H |
probably damaging |
Het |
Fbxw8 |
A |
T |
5: 118,263,057 (GRCm39) |
H207Q |
probably damaging |
Het |
Fgf22 |
A |
G |
10: 79,592,676 (GRCm39) |
E116G |
probably benign |
Het |
Gapvd1 |
C |
A |
2: 34,602,207 (GRCm39) |
V647F |
probably benign |
Het |
Garin4 |
A |
T |
1: 190,895,910 (GRCm39) |
S244R |
probably damaging |
Het |
Gja4 |
T |
A |
4: 127,206,487 (GRCm39) |
Y92F |
probably damaging |
Het |
Gtf3c2 |
G |
A |
5: 31,327,600 (GRCm39) |
R288W |
probably damaging |
Het |
Hira |
G |
T |
16: 18,716,532 (GRCm39) |
R99L |
possibly damaging |
Het |
Ighv16-1 |
C |
T |
12: 114,032,721 (GRCm39) |
G27D |
probably damaging |
Het |
Igkv1-133 |
C |
T |
6: 67,702,395 (GRCm39) |
P38S |
probably benign |
Het |
Igkv4-59 |
T |
C |
6: 69,415,396 (GRCm39) |
Y53C |
probably damaging |
Het |
Il23a |
T |
C |
10: 128,133,020 (GRCm39) |
E113G |
probably damaging |
Het |
Kcnip1 |
A |
G |
11: 33,584,589 (GRCm39) |
V188A |
probably benign |
Het |
L3mbtl3 |
T |
C |
10: 26,216,850 (GRCm39) |
K155E |
unknown |
Het |
Lancl2 |
T |
G |
6: 57,699,664 (GRCm39) |
C169G |
probably benign |
Het |
Lrrc26 |
A |
G |
2: 25,180,581 (GRCm39) |
D194G |
probably benign |
Het |
Lrrfip1 |
C |
T |
1: 91,050,842 (GRCm39) |
A545V |
probably benign |
Het |
Lrtm1 |
T |
C |
14: 28,743,850 (GRCm39) |
F106S |
probably damaging |
Het |
Lypd2 |
A |
T |
15: 74,604,848 (GRCm39) |
M49K |
probably damaging |
Het |
Mbd1 |
A |
C |
18: 74,406,357 (GRCm39) |
D63A |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,691,729 (GRCm39) |
F990L |
probably damaging |
Het |
Mtfr1l |
T |
C |
4: 134,256,577 (GRCm39) |
E196G |
probably benign |
Het |
Myh10 |
A |
G |
11: 68,705,874 (GRCm39) |
T2007A |
probably benign |
Het |
Nckap1 |
G |
A |
2: 80,370,512 (GRCm39) |
R393C |
probably damaging |
Het |
Nup205 |
C |
T |
6: 35,209,508 (GRCm39) |
T1605M |
probably benign |
Het |
Or1e33 |
T |
C |
11: 73,738,741 (GRCm39) |
D70G |
probably damaging |
Het |
Or5j3 |
GTACTTTTT |
GT |
2: 86,128,338 (GRCm39) |
|
probably null |
Het |
Pgap2 |
T |
A |
7: 101,875,467 (GRCm39) |
|
probably null |
Het |
Pitrm1 |
A |
G |
13: 6,619,387 (GRCm39) |
S741G |
probably benign |
Het |
Plcd4 |
A |
T |
1: 74,590,231 (GRCm39) |
S155C |
probably null |
Het |
Poc5 |
A |
T |
13: 96,540,925 (GRCm39) |
T365S |
possibly damaging |
Het |
Ppp2r5c |
G |
A |
12: 110,489,041 (GRCm39) |
A71T |
probably benign |
Het |
Prdm6 |
T |
A |
18: 53,598,199 (GRCm39) |
I187N |
possibly damaging |
Het |
Pxk |
A |
G |
14: 8,152,118 (GRCm38) |
Q478R |
probably benign |
Het |
Rgl1 |
T |
C |
1: 152,394,914 (GRCm39) |
Y718C |
probably damaging |
Het |
Ring1 |
G |
T |
17: 34,243,336 (GRCm39) |
T2K |
possibly damaging |
Het |
Sdk1 |
A |
G |
5: 142,173,897 (GRCm39) |
S2022G |
probably benign |
Het |
Sec61a1 |
C |
A |
6: 88,492,533 (GRCm39) |
V32F |
probably benign |
Het |
Sv2b |
G |
A |
7: 74,797,402 (GRCm39) |
P331S |
probably damaging |
Het |
Syne1 |
T |
C |
10: 5,090,970 (GRCm39) |
S795G |
possibly damaging |
Het |
Tmod2 |
T |
C |
9: 75,484,023 (GRCm39) |
E309G |
probably damaging |
Het |
Tpp2 |
T |
G |
1: 44,024,582 (GRCm39) |
S987A |
probably benign |
Het |
Trim75 |
G |
C |
8: 65,435,539 (GRCm39) |
H304D |
probably damaging |
Het |
Trp53bp2 |
G |
T |
1: 182,272,231 (GRCm39) |
D447Y |
probably damaging |
Het |
Ube3a |
A |
G |
7: 58,936,751 (GRCm39) |
K697E |
probably benign |
Het |
Vmn2r13 |
T |
A |
5: 109,339,909 (GRCm39) |
H22L |
probably benign |
Het |
Vmn2r4 |
G |
A |
3: 64,314,432 (GRCm39) |
S183F |
probably damaging |
Het |
Vwa8 |
T |
C |
14: 79,256,147 (GRCm39) |
Y721H |
probably benign |
Het |
Wbp1l |
C |
T |
19: 46,642,569 (GRCm39) |
P190L |
possibly damaging |
Het |
Zcchc4 |
A |
T |
5: 52,942,510 (GRCm39) |
Q105L |
possibly damaging |
Het |
Zfpm2 |
T |
A |
15: 40,616,413 (GRCm39) |
N54K |
probably damaging |
Het |
Zkscan3 |
C |
T |
13: 21,571,992 (GRCm39) |
G547S |
probably damaging |
Het |
|
Other mutations in Zfp236 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01016:Zfp236
|
APN |
18 |
82,686,815 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01760:Zfp236
|
APN |
18 |
82,639,547 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01923:Zfp236
|
APN |
18 |
82,700,344 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01934:Zfp236
|
APN |
18 |
82,651,245 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01949:Zfp236
|
APN |
18 |
82,642,521 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02063:Zfp236
|
APN |
18 |
82,676,276 (GRCm39) |
missense |
probably benign |
|
IGL02496:Zfp236
|
APN |
18 |
82,648,117 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02513:Zfp236
|
APN |
18 |
82,648,239 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02626:Zfp236
|
APN |
18 |
82,676,120 (GRCm39) |
splice site |
probably benign |
|
IGL02880:Zfp236
|
APN |
18 |
82,642,584 (GRCm39) |
missense |
probably benign |
0.15 |
IGL03156:Zfp236
|
APN |
18 |
82,698,827 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03261:Zfp236
|
APN |
18 |
82,648,733 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0047:Zfp236
|
UTSW |
18 |
82,698,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R0052:Zfp236
|
UTSW |
18 |
82,657,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R0194:Zfp236
|
UTSW |
18 |
82,675,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R0207:Zfp236
|
UTSW |
18 |
82,658,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R0234:Zfp236
|
UTSW |
18 |
82,648,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R0234:Zfp236
|
UTSW |
18 |
82,648,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R0302:Zfp236
|
UTSW |
18 |
82,676,213 (GRCm39) |
missense |
probably damaging |
0.99 |
R0730:Zfp236
|
UTSW |
18 |
82,658,369 (GRCm39) |
splice site |
probably benign |
|
R0755:Zfp236
|
UTSW |
18 |
82,638,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R1202:Zfp236
|
UTSW |
18 |
82,646,291 (GRCm39) |
missense |
probably benign |
0.00 |
R1449:Zfp236
|
UTSW |
18 |
82,664,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R1550:Zfp236
|
UTSW |
18 |
82,692,549 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1785:Zfp236
|
UTSW |
18 |
82,639,429 (GRCm39) |
missense |
probably benign |
0.08 |
R1786:Zfp236
|
UTSW |
18 |
82,639,429 (GRCm39) |
missense |
probably benign |
0.08 |
R2042:Zfp236
|
UTSW |
18 |
82,651,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Zfp236
|
UTSW |
18 |
82,639,429 (GRCm39) |
missense |
probably benign |
0.08 |
R2133:Zfp236
|
UTSW |
18 |
82,639,429 (GRCm39) |
missense |
probably benign |
0.08 |
R2247:Zfp236
|
UTSW |
18 |
82,622,423 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2484:Zfp236
|
UTSW |
18 |
82,686,762 (GRCm39) |
missense |
probably benign |
0.05 |
R3715:Zfp236
|
UTSW |
18 |
82,651,095 (GRCm39) |
splice site |
probably benign |
|
R4003:Zfp236
|
UTSW |
18 |
82,698,870 (GRCm39) |
nonsense |
probably null |
|
R4031:Zfp236
|
UTSW |
18 |
82,642,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R4482:Zfp236
|
UTSW |
18 |
82,662,346 (GRCm39) |
missense |
probably benign |
0.04 |
R4492:Zfp236
|
UTSW |
18 |
82,648,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R4502:Zfp236
|
UTSW |
18 |
82,655,079 (GRCm39) |
missense |
probably benign |
0.13 |
R4561:Zfp236
|
UTSW |
18 |
82,638,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R4649:Zfp236
|
UTSW |
18 |
82,615,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R4902:Zfp236
|
UTSW |
18 |
82,627,543 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5064:Zfp236
|
UTSW |
18 |
82,709,701 (GRCm39) |
critical splice donor site |
probably null |
|
R5084:Zfp236
|
UTSW |
18 |
82,627,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R5090:Zfp236
|
UTSW |
18 |
82,637,006 (GRCm39) |
missense |
probably benign |
0.08 |
R5191:Zfp236
|
UTSW |
18 |
82,639,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R5264:Zfp236
|
UTSW |
18 |
82,676,198 (GRCm39) |
missense |
probably damaging |
0.99 |
R5264:Zfp236
|
UTSW |
18 |
82,648,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R5339:Zfp236
|
UTSW |
18 |
82,642,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R5375:Zfp236
|
UTSW |
18 |
82,615,813 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5445:Zfp236
|
UTSW |
18 |
82,700,281 (GRCm39) |
missense |
probably benign |
0.02 |
R5513:Zfp236
|
UTSW |
18 |
82,676,147 (GRCm39) |
missense |
probably damaging |
0.97 |
R5527:Zfp236
|
UTSW |
18 |
82,676,159 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5628:Zfp236
|
UTSW |
18 |
82,675,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R5758:Zfp236
|
UTSW |
18 |
82,689,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R5890:Zfp236
|
UTSW |
18 |
82,658,276 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6137:Zfp236
|
UTSW |
18 |
82,689,919 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6193:Zfp236
|
UTSW |
18 |
82,622,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R6198:Zfp236
|
UTSW |
18 |
82,675,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R6239:Zfp236
|
UTSW |
18 |
82,675,229 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6705:Zfp236
|
UTSW |
18 |
82,651,862 (GRCm39) |
missense |
probably damaging |
0.97 |
R6948:Zfp236
|
UTSW |
18 |
82,662,187 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6989:Zfp236
|
UTSW |
18 |
82,646,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R7002:Zfp236
|
UTSW |
18 |
82,709,701 (GRCm39) |
critical splice donor site |
probably null |
|
R7113:Zfp236
|
UTSW |
18 |
82,638,462 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7261:Zfp236
|
UTSW |
18 |
82,627,470 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7447:Zfp236
|
UTSW |
18 |
82,651,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R7564:Zfp236
|
UTSW |
18 |
82,662,366 (GRCm39) |
nonsense |
probably null |
|
R7731:Zfp236
|
UTSW |
18 |
82,698,798 (GRCm39) |
missense |
probably benign |
0.27 |
R7857:Zfp236
|
UTSW |
18 |
82,686,726 (GRCm39) |
nonsense |
probably null |
|
R7860:Zfp236
|
UTSW |
18 |
82,692,481 (GRCm39) |
nonsense |
probably null |
|
R7904:Zfp236
|
UTSW |
18 |
82,627,507 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7948:Zfp236
|
UTSW |
18 |
82,642,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R7995:Zfp236
|
UTSW |
18 |
82,657,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R8153:Zfp236
|
UTSW |
18 |
82,648,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R8435:Zfp236
|
UTSW |
18 |
82,658,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R8560:Zfp236
|
UTSW |
18 |
82,664,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R8878:Zfp236
|
UTSW |
18 |
82,617,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8916:Zfp236
|
UTSW |
18 |
82,664,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R9046:Zfp236
|
UTSW |
18 |
82,637,042 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9076:Zfp236
|
UTSW |
18 |
82,638,469 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9243:Zfp236
|
UTSW |
18 |
82,662,050 (GRCm39) |
intron |
probably benign |
|
R9594:Zfp236
|
UTSW |
18 |
82,664,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R9642:Zfp236
|
UTSW |
18 |
82,622,384 (GRCm39) |
missense |
probably benign |
0.00 |
R9707:Zfp236
|
UTSW |
18 |
82,664,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R9748:Zfp236
|
UTSW |
18 |
82,637,008 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
Predicted Primers |
PCR Primer
(F):5'- TTCTGATCAAACTGCCCTGTTAG -3'
(R):5'- TGCTATCTGAAGCCAGGGTG -3'
Sequencing Primer
(F):5'- GTTAGGACAGAGTTGTTCATGATG -3'
(R):5'- GTCCATACTGGCTGTGAGC -3'
|
Posted On |
2019-09-13 |