Incidental Mutation 'R6198:Zfp236'
ID |
503076 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp236
|
Ensembl Gene |
ENSMUSG00000041258 |
Gene Name |
zinc finger protein 236 |
Synonyms |
LOC240456 |
MMRRC Submission |
044338-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R6198 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
18 |
Chromosomal Location |
82611718-82711008 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 82675278 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Proline
at position 405
(S405P)
|
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: S357P
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000130004 Gene: ENSMUSG00000041258 AA Change: S357P
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: S405P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000138557 Gene: ENSMUSG00000041258 AA Change: S405P
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 damaging
Transcript: ENSMUST00000183048
AA Change: S405P
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000138179 Gene: ENSMUSG00000041258 AA Change: S405P
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 |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
99% (68/69) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
A |
T |
3: 124,210,499 (GRCm39) |
|
probably null |
Het |
2610318N02Rik |
A |
G |
16: 16,936,233 (GRCm39) |
S164P |
probably damaging |
Het |
Acsbg3 |
A |
G |
17: 57,189,679 (GRCm39) |
S265G |
probably damaging |
Het |
Acyp2 |
C |
T |
11: 30,456,354 (GRCm39) |
E98K |
possibly damaging |
Het |
Adam19 |
A |
C |
11: 46,012,329 (GRCm39) |
N275T |
probably damaging |
Het |
Adgrg7 |
T |
A |
16: 56,597,556 (GRCm39) |
T84S |
possibly damaging |
Het |
Asl |
C |
T |
5: 130,047,757 (GRCm39) |
V70I |
probably benign |
Het |
Atp2c1 |
A |
G |
9: 105,398,271 (GRCm39) |
S26P |
probably benign |
Het |
Bcas3 |
A |
T |
11: 85,400,261 (GRCm39) |
D410V |
probably damaging |
Het |
Cc2d1b |
C |
T |
4: 108,490,422 (GRCm39) |
R825W |
probably damaging |
Het |
Ccdc15 |
A |
C |
9: 37,225,581 (GRCm39) |
|
probably null |
Het |
Cfh |
A |
G |
1: 140,033,178 (GRCm39) |
S789P |
probably damaging |
Het |
Cltc |
T |
C |
11: 86,611,188 (GRCm39) |
N561S |
probably benign |
Het |
Cnst |
A |
G |
1: 179,420,430 (GRCm39) |
Q187R |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 48,177,273 (GRCm39) |
T422A |
probably benign |
Het |
Cyp2c55 |
A |
T |
19: 38,995,565 (GRCm39) |
R26* |
probably null |
Het |
Dgkb |
A |
T |
12: 38,223,822 (GRCm39) |
M414L |
probably benign |
Het |
Dgkd |
A |
G |
1: 87,851,930 (GRCm39) |
D444G |
probably damaging |
Het |
Dipk1b |
A |
G |
2: 26,525,710 (GRCm39) |
K215E |
probably damaging |
Het |
Dnmt3c |
T |
C |
2: 153,561,929 (GRCm39) |
V544A |
noncoding transcript |
Het |
Dus3l |
A |
T |
17: 57,074,858 (GRCm39) |
T327S |
possibly damaging |
Het |
Elf2 |
A |
T |
3: 51,184,670 (GRCm39) |
L5Q |
probably damaging |
Het |
Fxyd6 |
A |
G |
9: 45,301,968 (GRCm39) |
Y30C |
probably damaging |
Het |
Gcc2 |
A |
T |
10: 58,128,412 (GRCm39) |
T1375S |
probably benign |
Het |
Git2 |
A |
T |
5: 114,883,556 (GRCm39) |
Y393* |
probably null |
Het |
Gm14403 |
AAACCCTA |
AA |
2: 177,201,448 (GRCm39) |
|
probably benign |
Het |
Golgb1 |
T |
C |
16: 36,713,757 (GRCm39) |
L246P |
probably damaging |
Het |
Grp |
G |
T |
18: 66,013,057 (GRCm39) |
Q74H |
possibly damaging |
Het |
Ifi203 |
A |
T |
1: 173,751,648 (GRCm39) |
M391K |
probably damaging |
Het |
Itih2 |
A |
G |
2: 10,103,352 (GRCm39) |
Y712H |
probably benign |
Het |
Kdm5a |
T |
A |
6: 120,415,958 (GRCm39) |
V1626E |
probably benign |
Het |
Klhl40 |
A |
G |
9: 121,607,833 (GRCm39) |
Y331C |
probably damaging |
Het |
Kprp |
T |
A |
3: 92,731,994 (GRCm39) |
Y352F |
probably damaging |
Het |
Lama2 |
G |
T |
10: 27,064,018 (GRCm39) |
H1286Q |
probably damaging |
Het |
Lgi4 |
T |
A |
7: 30,768,547 (GRCm39) |
|
probably null |
Het |
Lrrc47 |
A |
T |
4: 154,100,129 (GRCm39) |
N235I |
probably damaging |
Het |
Lrrc74b |
T |
A |
16: 17,366,650 (GRCm39) |
I308F |
probably damaging |
Het |
Map7d1 |
T |
A |
4: 126,135,636 (GRCm39) |
K135M |
probably damaging |
Het |
Marchf5 |
A |
G |
19: 37,188,140 (GRCm39) |
R36G |
probably damaging |
Het |
Mtx3 |
C |
A |
13: 92,989,359 (GRCm39) |
P299Q |
probably benign |
Het |
Muc21 |
T |
A |
17: 35,931,808 (GRCm39) |
|
probably benign |
Het |
Ncapd2 |
C |
A |
6: 125,156,286 (GRCm39) |
E500* |
probably null |
Het |
Nckap5l |
T |
C |
15: 99,323,869 (GRCm39) |
K878R |
probably damaging |
Het |
Nphs1 |
T |
C |
7: 30,167,340 (GRCm39) |
I756T |
probably damaging |
Het |
Olfm4 |
T |
G |
14: 80,237,813 (GRCm39) |
S17A |
probably benign |
Het |
Or1j15 |
A |
G |
2: 36,458,963 (GRCm39) |
M118V |
probably damaging |
Het |
Or4b1 |
A |
T |
2: 89,979,782 (GRCm39) |
D189E |
probably damaging |
Het |
Pak1ip1 |
G |
T |
13: 41,154,886 (GRCm39) |
Q27H |
probably benign |
Het |
Piezo2 |
A |
T |
18: 63,290,281 (GRCm39) |
C159* |
probably null |
Het |
Pkn2 |
G |
T |
3: 142,516,165 (GRCm39) |
T538K |
probably benign |
Het |
Ppp3cc |
A |
T |
14: 70,485,060 (GRCm39) |
M198K |
probably benign |
Het |
Rrm1 |
T |
G |
7: 102,095,936 (GRCm39) |
|
probably null |
Het |
Setd3 |
T |
C |
12: 108,131,427 (GRCm39) |
K7E |
possibly damaging |
Het |
Shc1 |
A |
G |
3: 89,329,414 (GRCm39) |
K86R |
probably benign |
Het |
Slc16a7 |
T |
C |
10: 125,064,084 (GRCm39) |
T418A |
probably benign |
Het |
Spocd1 |
C |
T |
4: 129,849,208 (GRCm39) |
P676S |
probably damaging |
Het |
Spp1 |
A |
G |
5: 104,587,374 (GRCm39) |
|
probably null |
Het |
Syne1 |
A |
G |
10: 5,252,269 (GRCm39) |
Y2462H |
probably damaging |
Het |
Tiam2 |
T |
C |
17: 3,464,396 (GRCm39) |
S42P |
probably benign |
Het |
Tmem63b |
C |
T |
17: 45,972,442 (GRCm39) |
V722I |
probably benign |
Het |
Ubqln1 |
A |
G |
13: 58,344,404 (GRCm39) |
S130P |
probably benign |
Het |
Usp34 |
G |
T |
11: 23,434,127 (GRCm39) |
L3215F |
probably damaging |
Het |
Uvssa |
A |
G |
5: 33,566,854 (GRCm39) |
Y517C |
probably damaging |
Het |
Vps13d |
A |
T |
4: 144,875,560 (GRCm39) |
F1649Y |
probably benign |
Het |
Zfp9 |
T |
C |
6: 118,454,282 (GRCm39) |
M1V |
probably null |
Het |
Zfp946 |
A |
T |
17: 22,673,896 (GRCm39) |
S217C |
probably damaging |
Het |
Zfp970 |
T |
A |
2: 177,167,253 (GRCm39) |
C276S |
probably damaging |
Het |
Zswim5 |
T |
A |
4: 116,735,204 (GRCm39) |
F183Y |
probably benign |
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 |
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 |
R7363:Zfp236
|
UTSW |
18 |
82,639,456 (GRCm39) |
missense |
probably damaging |
1.00 |
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'- CAGGTAGGAACGGGGATTTC -3'
(R):5'- AGGGTTATTGCAACGTCTTAGAG -3'
Sequencing Primer
(F):5'- AGGAACGGGGATTTCTTCTTCAG -3'
(R):5'- TGCAACGTCTTAGAGTGTGAAC -3'
|
Posted On |
2018-02-27 |