Incidental Mutation 'R4902:Zfp236'
ID |
377913 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp236
|
Ensembl Gene |
ENSMUSG00000041258 |
Gene Name |
zinc finger protein 236 |
Synonyms |
LOC240456 |
MMRRC Submission |
042505-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R4902 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
18 |
Chromosomal Location |
82611718-82711008 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 82627543 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Asparagine
at position 1552
(I1552N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000138557
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000171071]
[ENSMUST00000182122]
[ENSMUST00000183048]
|
AlphaFold |
S4R299 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000171071
AA Change: I1504N
PolyPhen 2
Score 0.868 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000130004 Gene: ENSMUSG00000041258 AA Change: I1504N
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 |
possibly damaging
Transcript: ENSMUST00000182122
AA Change: I1552N
PolyPhen 2
Score 0.893 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000138557 Gene: ENSMUSG00000041258 AA Change: I1552N
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
|
Meta Mutation Damage Score |
0.0989 |
Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.2%
- 10x: 95.9%
- 20x: 91.0%
|
Validation Efficiency |
100% (84/84) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930488N24Rik |
T |
C |
17: 14,326,408 (GRCm39) |
|
noncoding transcript |
Het |
Adamdec1 |
T |
C |
14: 68,809,215 (GRCm39) |
N249S |
probably damaging |
Het |
Asxl1 |
T |
A |
2: 153,241,751 (GRCm39) |
V767E |
probably benign |
Het |
Atp6v1f |
T |
C |
6: 29,470,271 (GRCm39) |
|
probably benign |
Het |
Brix1 |
T |
C |
15: 10,483,378 (GRCm39) |
|
probably null |
Het |
Cap2 |
T |
C |
13: 46,684,501 (GRCm39) |
V2A |
probably damaging |
Het |
Chrnb2 |
A |
G |
3: 89,668,248 (GRCm39) |
C356R |
probably damaging |
Het |
Chtf8 |
C |
T |
8: 107,612,424 (GRCm39) |
G172R |
probably damaging |
Het |
Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
Dact2 |
T |
A |
17: 14,416,991 (GRCm39) |
K403M |
possibly damaging |
Het |
Dhx40 |
A |
C |
11: 86,662,036 (GRCm39) |
L674V |
possibly damaging |
Het |
Dlc1 |
A |
G |
8: 37,044,285 (GRCm39) |
V1230A |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,329,935 (GRCm39) |
S3260T |
probably benign |
Het |
Eef1a2 |
T |
A |
2: 180,789,881 (GRCm39) |
D428V |
probably benign |
Het |
Ehd1 |
T |
C |
19: 6,344,273 (GRCm39) |
F178L |
possibly damaging |
Het |
Eif4a3l1 |
T |
G |
6: 136,306,262 (GRCm39) |
V241G |
probably benign |
Het |
F2 |
A |
T |
2: 91,465,316 (GRCm39) |
|
probably benign |
Het |
Fam186a |
T |
C |
15: 99,844,723 (GRCm39) |
D507G |
unknown |
Het |
Fbxo11 |
G |
A |
17: 88,372,702 (GRCm39) |
|
probably benign |
Het |
Fry |
A |
T |
5: 150,419,168 (GRCm39) |
M2871L |
probably benign |
Het |
Gabrr2 |
A |
G |
4: 33,095,512 (GRCm39) |
D442G |
probably damaging |
Het |
Gemin5 |
A |
G |
11: 58,055,103 (GRCm39) |
I214T |
probably benign |
Het |
Gfra2 |
A |
G |
14: 71,204,455 (GRCm39) |
N175S |
probably damaging |
Het |
Gprc5c |
G |
T |
11: 114,755,093 (GRCm39) |
V257L |
possibly damaging |
Het |
Jhy |
C |
T |
9: 40,808,821 (GRCm39) |
|
probably benign |
Het |
Krtap5-5 |
A |
T |
7: 141,783,156 (GRCm39) |
C165S |
unknown |
Het |
Lce1k |
T |
A |
3: 92,714,134 (GRCm39) |
T17S |
unknown |
Het |
Map3k1 |
C |
T |
13: 111,909,146 (GRCm39) |
R268Q |
probably damaging |
Het |
Med13l |
T |
A |
5: 118,883,195 (GRCm39) |
H1351Q |
probably damaging |
Het |
Met |
T |
C |
6: 17,546,995 (GRCm39) |
V876A |
probably damaging |
Het |
Mical2 |
T |
C |
7: 111,936,107 (GRCm39) |
S903P |
probably benign |
Het |
Mkks |
A |
G |
2: 136,718,094 (GRCm39) |
V396A |
probably benign |
Het |
Mvk |
T |
C |
5: 114,594,060 (GRCm39) |
V305A |
probably benign |
Het |
Myo5a |
A |
G |
9: 75,081,360 (GRCm39) |
T982A |
probably benign |
Het |
N4bp1 |
A |
G |
8: 87,588,311 (GRCm39) |
V209A |
probably benign |
Het |
Nfkbib |
G |
T |
7: 28,461,173 (GRCm39) |
S158* |
probably null |
Het |
Nkx3-1 |
G |
A |
14: 69,428,367 (GRCm39) |
G72S |
probably benign |
Het |
Ogfr |
A |
G |
2: 180,235,518 (GRCm39) |
|
probably benign |
Het |
Or10a3 |
G |
A |
7: 108,480,624 (GRCm39) |
T63I |
probably benign |
Het |
Or2t43 |
G |
A |
11: 58,457,451 (GRCm39) |
S240F |
possibly damaging |
Het |
Or8s8 |
T |
C |
15: 98,354,796 (GRCm39) |
S202P |
probably damaging |
Het |
Pcdhga8 |
T |
A |
18: 37,948,978 (GRCm39) |
D131E |
probably damaging |
Het |
Plch1 |
A |
G |
3: 63,648,264 (GRCm39) |
|
probably benign |
Het |
Polrmt |
A |
G |
10: 79,582,385 (GRCm39) |
M1T |
probably null |
Het |
Ppp1r12a |
T |
C |
10: 108,066,451 (GRCm39) |
V214A |
probably damaging |
Het |
Prr5l |
A |
G |
2: 101,628,027 (GRCm39) |
|
probably benign |
Het |
Prss35 |
A |
G |
9: 86,638,175 (GRCm39) |
Q315R |
probably damaging |
Het |
Psg29 |
G |
T |
7: 16,945,837 (GRCm39) |
*469L |
probably null |
Het |
Psmd4 |
A |
G |
3: 94,943,170 (GRCm39) |
V78A |
probably damaging |
Het |
Rad9a |
C |
A |
19: 4,251,552 (GRCm39) |
|
probably benign |
Het |
Rfx7 |
G |
T |
9: 72,524,573 (GRCm39) |
V588F |
probably benign |
Het |
Rnase13 |
A |
C |
14: 52,160,052 (GRCm39) |
I29S |
probably benign |
Het |
Steap2 |
T |
C |
5: 5,725,866 (GRCm39) |
N386S |
possibly damaging |
Het |
Ston1 |
A |
G |
17: 88,952,680 (GRCm39) |
E719G |
probably damaging |
Het |
Stx4a |
A |
G |
7: 127,441,934 (GRCm39) |
|
probably null |
Het |
Tekt2 |
A |
G |
4: 126,217,263 (GRCm39) |
S212P |
possibly damaging |
Het |
Tex19.2 |
A |
T |
11: 121,007,782 (GRCm39) |
L222Q |
probably damaging |
Het |
Tmem50a |
A |
G |
4: 134,637,017 (GRCm39) |
I38T |
probably damaging |
Het |
Ubr2 |
A |
G |
17: 47,296,922 (GRCm39) |
V286A |
possibly damaging |
Het |
Ugt2b35 |
T |
C |
5: 87,151,159 (GRCm39) |
M255T |
possibly damaging |
Het |
Vmn2r17 |
T |
A |
5: 109,601,220 (GRCm39) |
F839L |
probably benign |
Het |
Wdr36 |
T |
C |
18: 32,992,314 (GRCm39) |
V617A |
possibly damaging |
Het |
Wtip |
A |
T |
7: 33,818,437 (GRCm39) |
|
probably null |
Het |
Yeats2 |
G |
A |
16: 20,026,418 (GRCm39) |
G765S |
probably benign |
Het |
Zbtb3 |
T |
C |
19: 8,781,331 (GRCm39) |
S315P |
probably benign |
Het |
Zdhhc8 |
T |
C |
16: 18,045,030 (GRCm39) |
M259V |
probably benign |
Het |
Zfp120 |
A |
G |
2: 149,961,440 (GRCm39) |
|
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 |
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 |
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'- AGTTTGACCCAGTTCATAATTTCTC -3'
(R):5'- AGAAAGCCTCTCTTCATTTGCATCG -3'
Sequencing Primer
(F):5'- GACCCAGTTCATAATTTCTCCTTTG -3'
(R):5'- ATTTCCTTATTGTGGTGCCAGG -3'
|
Posted On |
2016-04-15 |