Incidental Mutation 'R6980:Zfp318'
ID |
543805 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp318
|
Ensembl Gene |
ENSMUSG00000015597 |
Gene Name |
zinc finger protein 318 |
Synonyms |
2610034E08Rik, TZF, D530032D06Rik |
MMRRC Submission |
045088-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R6980 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
17 |
Chromosomal Location |
46694657-46731846 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 46708138 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Asparagine
at position 399
(Y399N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000116544
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000113481]
[ENSMUST00000138127]
[ENSMUST00000152472]
|
AlphaFold |
Q99PP2 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000113481
AA Change: Y399N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000109109 Gene: ENSMUSG00000015597 AA Change: Y399N
Domain | Start | End | E-Value | Type |
low complexity region
|
3 |
15 |
N/A |
INTRINSIC |
low complexity region
|
30 |
127 |
N/A |
INTRINSIC |
low complexity region
|
150 |
169 |
N/A |
INTRINSIC |
low complexity region
|
208 |
221 |
N/A |
INTRINSIC |
low complexity region
|
291 |
304 |
N/A |
INTRINSIC |
coiled coil region
|
348 |
376 |
N/A |
INTRINSIC |
SCOP:d1eq1a_
|
916 |
995 |
2e-4 |
SMART |
low complexity region
|
1018 |
1055 |
N/A |
INTRINSIC |
ZnF_U1
|
1085 |
1119 |
5.99e-7 |
SMART |
ZnF_C2H2
|
1088 |
1112 |
4.5e1 |
SMART |
ZnF_U1
|
1155 |
1189 |
2.1e-11 |
SMART |
ZnF_C2H2
|
1158 |
1180 |
4.62e1 |
SMART |
low complexity region
|
1225 |
1238 |
N/A |
INTRINSIC |
low complexity region
|
1358 |
1371 |
N/A |
INTRINSIC |
low complexity region
|
1640 |
1651 |
N/A |
INTRINSIC |
Blast:HNHc
|
1660 |
1710 |
3e-17 |
BLAST |
low complexity region
|
2001 |
2013 |
N/A |
INTRINSIC |
low complexity region
|
2110 |
2121 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000138127
AA Change: Y399N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000116544 Gene: ENSMUSG00000015597 AA Change: Y399N
Domain | Start | End | E-Value | Type |
low complexity region
|
3 |
15 |
N/A |
INTRINSIC |
low complexity region
|
30 |
127 |
N/A |
INTRINSIC |
low complexity region
|
150 |
169 |
N/A |
INTRINSIC |
low complexity region
|
208 |
221 |
N/A |
INTRINSIC |
low complexity region
|
291 |
304 |
N/A |
INTRINSIC |
coiled coil region
|
348 |
376 |
N/A |
INTRINSIC |
Blast:HOLI
|
854 |
1114 |
8e-19 |
BLAST |
SCOP:d1eq1a_
|
916 |
995 |
6e-5 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000152472
|
SMART Domains |
Protein: ENSMUSP00000116132 Gene: ENSMUSG00000015597
Domain | Start | End | E-Value | Type |
coiled coil region
|
3 |
30 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.2%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Mice homozygous for an ENU-induced allele exhibit reduced male fertility and altered IgM and IgD levels. Null mutants displayed normal level of circulating B cells with decreased IgD and increased IgM levels. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
C |
A |
2: 25,330,878 (GRCm39) |
R1189S |
possibly damaging |
Het |
Abcf2 |
T |
C |
5: 24,770,970 (GRCm39) |
Q594R |
probably benign |
Het |
Abhd18 |
G |
A |
3: 40,888,215 (GRCm39) |
S353N |
probably benign |
Het |
Adrb1 |
G |
T |
19: 56,712,046 (GRCm39) |
A415S |
probably benign |
Het |
Art2b |
T |
C |
7: 101,229,680 (GRCm39) |
N73S |
probably benign |
Het |
BC028528 |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
3: 95,795,448 (GRCm39) |
|
probably benign |
Het |
BC028528 |
CACTGGTTCTGTGGT |
CACTGGTTCTGTGGTTACTGGTTCTGTGGT |
3: 95,795,480 (GRCm39) |
|
probably benign |
Het |
BC028528 |
ACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTC |
ACTGGTTCTGTGGTCTCTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTC |
3: 95,795,451 (GRCm39) |
|
probably benign |
Het |
Cacna1a |
A |
G |
8: 85,338,914 (GRCm39) |
M1753V |
possibly damaging |
Het |
Cbx8 |
A |
T |
11: 118,930,287 (GRCm39) |
I102N |
possibly damaging |
Het |
Ccdc178 |
T |
A |
18: 22,238,620 (GRCm39) |
E332D |
probably benign |
Het |
Cdhr17 |
T |
A |
5: 17,031,944 (GRCm39) |
V533D |
possibly damaging |
Het |
Cfap74 |
G |
A |
4: 155,550,809 (GRCm39) |
|
probably benign |
Het |
Chat |
A |
T |
14: 32,146,111 (GRCm39) |
M354K |
probably benign |
Het |
Cmas |
A |
G |
6: 142,702,526 (GRCm39) |
T10A |
probably damaging |
Het |
Cyb561d1 |
A |
T |
3: 108,107,475 (GRCm39) |
L51H |
probably benign |
Het |
D030056L22Rik |
A |
T |
19: 18,694,629 (GRCm39) |
N128I |
probably damaging |
Het |
D130043K22Rik |
G |
T |
13: 25,048,764 (GRCm39) |
A423S |
probably damaging |
Het |
Dnah14 |
T |
C |
1: 181,475,795 (GRCm39) |
I1349T |
probably benign |
Het |
Dnajb3 |
T |
G |
1: 88,132,736 (GRCm39) |
D222A |
probably damaging |
Het |
Dtx1 |
T |
C |
5: 120,819,422 (GRCm39) |
E592G |
probably damaging |
Het |
Dzank1 |
C |
T |
2: 144,332,056 (GRCm39) |
G427R |
possibly damaging |
Het |
E130308A19Rik |
A |
C |
4: 59,719,991 (GRCm39) |
K508Q |
probably damaging |
Het |
Eif4e1b |
T |
A |
13: 54,931,916 (GRCm39) |
|
probably null |
Het |
Ell2 |
A |
G |
13: 75,904,495 (GRCm39) |
M159V |
probably null |
Het |
Eml4 |
G |
A |
17: 83,758,446 (GRCm39) |
V377I |
probably benign |
Het |
Fryl |
A |
T |
5: 73,207,773 (GRCm39) |
S2466T |
probably benign |
Het |
Gfpt1 |
C |
A |
6: 87,054,071 (GRCm39) |
T426K |
probably damaging |
Het |
Gm49355 |
T |
C |
14: 12,307,173 (GRCm38) |
|
probably benign |
Het |
Gm5114 |
T |
C |
7: 39,058,624 (GRCm39) |
I332V |
probably benign |
Het |
Gpr15 |
T |
A |
16: 58,539,105 (GRCm39) |
|
probably benign |
Het |
Gpr179 |
T |
C |
11: 97,225,684 (GRCm39) |
E2157G |
probably benign |
Het |
Gramd4 |
A |
G |
15: 86,016,170 (GRCm39) |
N482S |
probably benign |
Het |
Hfm1 |
A |
T |
5: 107,028,343 (GRCm39) |
I829K |
probably benign |
Het |
Hydin |
A |
T |
8: 111,139,916 (GRCm39) |
E728D |
possibly damaging |
Het |
Ifngr2 |
T |
A |
16: 91,356,895 (GRCm39) |
V143E |
probably damaging |
Het |
Ift172 |
T |
C |
5: 31,414,730 (GRCm39) |
D1390G |
probably benign |
Het |
Kdf1 |
A |
T |
4: 133,256,138 (GRCm39) |
D285V |
probably damaging |
Het |
Mast4 |
C |
T |
13: 102,941,155 (GRCm39) |
V301I |
probably damaging |
Het |
Mdn1 |
G |
A |
4: 32,726,942 (GRCm39) |
|
probably null |
Het |
Megf11 |
A |
G |
9: 64,613,132 (GRCm39) |
E1016G |
probably damaging |
Het |
Mixl1 |
G |
A |
1: 180,524,453 (GRCm39) |
A42V |
possibly damaging |
Het |
Mpp2 |
A |
G |
11: 101,950,154 (GRCm39) |
W567R |
probably damaging |
Het |
Mrgpra6 |
A |
G |
7: 46,838,697 (GRCm39) |
L136P |
probably damaging |
Het |
Mroh7 |
T |
A |
4: 106,557,434 (GRCm39) |
I759L |
probably benign |
Het |
Nrxn2 |
A |
G |
19: 6,500,609 (GRCm39) |
D277G |
probably benign |
Het |
Nup210l |
A |
T |
3: 90,027,234 (GRCm39) |
K205N |
probably benign |
Het |
Or4g17 |
A |
G |
2: 111,209,620 (GRCm39) |
I92V |
possibly damaging |
Het |
Or4p4b-ps1 |
A |
G |
2: 88,453,939 (GRCm39) |
*97W |
probably null |
Het |
Or52e19b |
T |
C |
7: 103,032,303 (GRCm39) |
E302G |
probably benign |
Het |
Or5al6 |
A |
T |
2: 85,976,681 (GRCm39) |
Y132* |
probably null |
Het |
Oxnad1 |
C |
T |
14: 31,807,576 (GRCm39) |
|
probably benign |
Het |
Pamr1 |
C |
T |
2: 102,472,549 (GRCm39) |
T616I |
probably benign |
Het |
Pcdhgb5 |
C |
T |
18: 37,866,592 (GRCm39) |
H796Y |
possibly damaging |
Het |
Pdlim7 |
G |
T |
13: 55,656,041 (GRCm39) |
D126E |
probably benign |
Het |
Pfdn2 |
C |
T |
1: 171,185,465 (GRCm39) |
|
probably benign |
Het |
Piezo2 |
T |
A |
18: 63,216,032 (GRCm39) |
|
probably null |
Het |
Pms2 |
A |
T |
5: 143,848,842 (GRCm39) |
I43L |
probably benign |
Het |
Prex2 |
T |
A |
1: 11,232,487 (GRCm39) |
S851R |
probably benign |
Het |
Ptpn4 |
T |
A |
1: 119,671,151 (GRCm39) |
E202D |
possibly damaging |
Het |
Rnf40 |
T |
A |
7: 127,193,849 (GRCm39) |
V455E |
probably damaging |
Het |
Rp1l1 |
A |
G |
14: 64,266,169 (GRCm39) |
N585S |
probably benign |
Het |
Rrp12 |
A |
G |
19: 41,878,582 (GRCm39) |
S188P |
probably damaging |
Het |
Rsbn1l |
T |
A |
5: 21,101,482 (GRCm39) |
H686L |
probably benign |
Het |
Runx2 |
C |
T |
17: 45,046,203 (GRCm39) |
V107I |
possibly damaging |
Het |
Rusc2 |
A |
G |
4: 43,422,846 (GRCm39) |
I994M |
probably benign |
Het |
Ryr1 |
T |
A |
7: 28,808,812 (GRCm39) |
D420V |
probably benign |
Het |
Sash1 |
T |
C |
10: 8,605,612 (GRCm39) |
Q926R |
probably benign |
Het |
Scgb3a2 |
T |
A |
18: 43,897,499 (GRCm39) |
I6N |
probably damaging |
Het |
Sdc3 |
T |
A |
4: 130,544,233 (GRCm39) |
|
probably benign |
Het |
Sik2 |
A |
G |
9: 50,808,755 (GRCm39) |
V658A |
probably benign |
Het |
Slc25a39 |
A |
G |
11: 102,296,601 (GRCm39) |
V81A |
probably damaging |
Het |
Snai2 |
T |
A |
16: 14,526,113 (GRCm39) |
S255T |
possibly damaging |
Het |
Sorbs1 |
A |
T |
19: 40,316,060 (GRCm39) |
Y371* |
probably null |
Het |
Spata31d1b |
A |
T |
13: 59,863,236 (GRCm39) |
H128L |
probably benign |
Het |
Spdl1 |
A |
T |
11: 34,721,706 (GRCm39) |
M1K |
probably null |
Het |
Tgm3 |
T |
A |
2: 129,868,697 (GRCm39) |
N211K |
probably benign |
Het |
Tmem116 |
T |
C |
5: 121,606,050 (GRCm39) |
|
probably null |
Het |
Tmem132e |
T |
A |
11: 82,329,212 (GRCm39) |
|
probably null |
Het |
Tmem53 |
T |
C |
4: 117,125,705 (GRCm39) |
C251R |
probably damaging |
Het |
Trcg1 |
A |
C |
9: 57,152,856 (GRCm39) |
D551A |
probably damaging |
Het |
Trp63 |
T |
A |
16: 25,620,843 (GRCm39) |
F12I |
probably benign |
Het |
Ttn |
C |
T |
2: 76,709,401 (GRCm39) |
|
probably null |
Het |
Tubgcp4 |
T |
C |
2: 121,025,946 (GRCm39) |
V596A |
probably benign |
Het |
Ugt2a3 |
A |
C |
5: 87,473,491 (GRCm39) |
H475Q |
probably damaging |
Het |
Unc79 |
G |
A |
12: 103,025,759 (GRCm39) |
R382K |
probably damaging |
Het |
Vmn2r58 |
T |
C |
7: 41,513,662 (GRCm39) |
H327R |
possibly damaging |
Het |
Vmn2r7 |
G |
A |
3: 64,623,987 (GRCm39) |
T111I |
possibly damaging |
Het |
|
Other mutations in Zfp318 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00705:Zfp318
|
APN |
17 |
46,723,398 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00978:Zfp318
|
APN |
17 |
46,724,652 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01016:Zfp318
|
APN |
17 |
46,711,003 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01310:Zfp318
|
APN |
17 |
46,724,153 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01453:Zfp318
|
APN |
17 |
46,719,942 (GRCm39) |
splice site |
probably null |
|
IGL01887:Zfp318
|
APN |
17 |
46,710,094 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02025:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02026:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02070:Zfp318
|
APN |
17 |
46,707,644 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02182:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02187:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02188:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02189:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02190:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02191:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02192:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02203:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02224:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02230:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02231:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02232:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02233:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02234:Zfp318
|
APN |
17 |
46,707,736 (GRCm39) |
nonsense |
probably null |
|
IGL02412:Zfp318
|
APN |
17 |
46,720,043 (GRCm39) |
nonsense |
probably null |
|
IGL02792:Zfp318
|
APN |
17 |
46,720,104 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02826:Zfp318
|
APN |
17 |
46,709,680 (GRCm39) |
missense |
probably damaging |
1.00 |
Wonton
|
UTSW |
17 |
46,720,618 (GRCm39) |
missense |
possibly damaging |
0.89 |
I0000:Zfp318
|
UTSW |
17 |
46,710,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R0206:Zfp318
|
UTSW |
17 |
46,709,945 (GRCm39) |
missense |
probably benign |
0.07 |
R0240:Zfp318
|
UTSW |
17 |
46,707,739 (GRCm39) |
missense |
probably benign |
0.00 |
R0240:Zfp318
|
UTSW |
17 |
46,707,739 (GRCm39) |
missense |
probably benign |
0.00 |
R0281:Zfp318
|
UTSW |
17 |
46,723,540 (GRCm39) |
missense |
probably benign |
0.05 |
R0350:Zfp318
|
UTSW |
17 |
46,724,124 (GRCm39) |
missense |
probably benign |
0.00 |
R0383:Zfp318
|
UTSW |
17 |
46,724,222 (GRCm39) |
missense |
probably damaging |
0.99 |
R0453:Zfp318
|
UTSW |
17 |
46,707,634 (GRCm39) |
missense |
probably damaging |
0.96 |
R1014:Zfp318
|
UTSW |
17 |
46,723,462 (GRCm39) |
nonsense |
probably null |
|
R1166:Zfp318
|
UTSW |
17 |
46,720,618 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1208:Zfp318
|
UTSW |
17 |
46,723,446 (GRCm39) |
unclassified |
probably benign |
|
R1208:Zfp318
|
UTSW |
17 |
46,723,446 (GRCm39) |
unclassified |
probably benign |
|
R1327:Zfp318
|
UTSW |
17 |
46,724,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R1330:Zfp318
|
UTSW |
17 |
46,724,684 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1737:Zfp318
|
UTSW |
17 |
46,710,403 (GRCm39) |
missense |
probably benign |
0.35 |
R1800:Zfp318
|
UTSW |
17 |
46,722,980 (GRCm39) |
missense |
probably benign |
0.00 |
R1846:Zfp318
|
UTSW |
17 |
46,724,592 (GRCm39) |
missense |
probably benign |
0.00 |
R1848:Zfp318
|
UTSW |
17 |
46,716,981 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1861:Zfp318
|
UTSW |
17 |
46,722,366 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1913:Zfp318
|
UTSW |
17 |
46,723,450 (GRCm39) |
unclassified |
probably benign |
|
R1913:Zfp318
|
UTSW |
17 |
46,723,440 (GRCm39) |
unclassified |
probably benign |
|
R2059:Zfp318
|
UTSW |
17 |
46,707,950 (GRCm39) |
missense |
probably damaging |
0.99 |
R2085:Zfp318
|
UTSW |
17 |
46,720,590 (GRCm39) |
splice site |
probably null |
|
R2122:Zfp318
|
UTSW |
17 |
46,724,297 (GRCm39) |
missense |
probably benign |
0.01 |
R2339:Zfp318
|
UTSW |
17 |
46,710,389 (GRCm39) |
missense |
probably benign |
0.01 |
R4526:Zfp318
|
UTSW |
17 |
46,723,284 (GRCm39) |
missense |
probably benign |
0.00 |
R4564:Zfp318
|
UTSW |
17 |
46,723,741 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4689:Zfp318
|
UTSW |
17 |
46,710,560 (GRCm39) |
missense |
probably damaging |
0.99 |
R4795:Zfp318
|
UTSW |
17 |
46,722,988 (GRCm39) |
missense |
probably benign |
0.07 |
R5256:Zfp318
|
UTSW |
17 |
46,722,995 (GRCm39) |
missense |
probably benign |
0.19 |
R5317:Zfp318
|
UTSW |
17 |
46,723,463 (GRCm39) |
unclassified |
probably benign |
|
R5323:Zfp318
|
UTSW |
17 |
46,697,662 (GRCm39) |
missense |
probably damaging |
0.99 |
R5436:Zfp318
|
UTSW |
17 |
46,723,975 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5485:Zfp318
|
UTSW |
17 |
46,723,180 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5627:Zfp318
|
UTSW |
17 |
46,724,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R5643:Zfp318
|
UTSW |
17 |
46,720,170 (GRCm39) |
intron |
probably benign |
|
R5782:Zfp318
|
UTSW |
17 |
46,723,440 (GRCm39) |
unclassified |
probably benign |
|
R5783:Zfp318
|
UTSW |
17 |
46,723,440 (GRCm39) |
unclassified |
probably benign |
|
R5820:Zfp318
|
UTSW |
17 |
46,723,699 (GRCm39) |
missense |
probably benign |
|
R5895:Zfp318
|
UTSW |
17 |
46,709,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R6189:Zfp318
|
UTSW |
17 |
46,723,440 (GRCm39) |
unclassified |
probably benign |
|
R6385:Zfp318
|
UTSW |
17 |
46,721,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R6428:Zfp318
|
UTSW |
17 |
46,710,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R6471:Zfp318
|
UTSW |
17 |
46,710,431 (GRCm39) |
missense |
probably benign |
0.05 |
R6666:Zfp318
|
UTSW |
17 |
46,720,140 (GRCm39) |
missense |
probably benign |
0.01 |
R6812:Zfp318
|
UTSW |
17 |
46,723,468 (GRCm39) |
unclassified |
probably benign |
|
R6852:Zfp318
|
UTSW |
17 |
46,723,464 (GRCm39) |
unclassified |
probably benign |
|
R6852:Zfp318
|
UTSW |
17 |
46,723,459 (GRCm39) |
unclassified |
probably benign |
|
R6852:Zfp318
|
UTSW |
17 |
46,723,460 (GRCm39) |
unclassified |
probably benign |
|
R6854:Zfp318
|
UTSW |
17 |
46,723,468 (GRCm39) |
unclassified |
probably benign |
|
R6999:Zfp318
|
UTSW |
17 |
46,710,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R7164:Zfp318
|
UTSW |
17 |
46,716,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R7164:Zfp318
|
UTSW |
17 |
46,708,232 (GRCm39) |
critical splice donor site |
probably null |
|
R7175:Zfp318
|
UTSW |
17 |
46,697,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R7233:Zfp318
|
UTSW |
17 |
46,716,978 (GRCm39) |
missense |
probably damaging |
0.99 |
R7339:Zfp318
|
UTSW |
17 |
46,722,173 (GRCm39) |
missense |
probably damaging |
0.99 |
R7426:Zfp318
|
UTSW |
17 |
46,710,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R7600:Zfp318
|
UTSW |
17 |
46,695,210 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7608:Zfp318
|
UTSW |
17 |
46,710,935 (GRCm39) |
missense |
probably damaging |
0.96 |
R7779:Zfp318
|
UTSW |
17 |
46,710,820 (GRCm39) |
missense |
probably benign |
0.16 |
R8057:Zfp318
|
UTSW |
17 |
46,710,692 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8273:Zfp318
|
UTSW |
17 |
46,723,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R8274:Zfp318
|
UTSW |
17 |
46,723,915 (GRCm39) |
missense |
probably benign |
|
R8695:Zfp318
|
UTSW |
17 |
46,723,576 (GRCm39) |
missense |
probably benign |
0.01 |
R8822:Zfp318
|
UTSW |
17 |
46,723,831 (GRCm39) |
missense |
probably benign |
0.00 |
R8851:Zfp318
|
UTSW |
17 |
46,710,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R8913:Zfp318
|
UTSW |
17 |
46,722,699 (GRCm39) |
missense |
probably benign |
0.07 |
R8953:Zfp318
|
UTSW |
17 |
46,731,356 (GRCm39) |
missense |
probably benign |
0.38 |
R9031:Zfp318
|
UTSW |
17 |
46,723,433 (GRCm39) |
missense |
probably benign |
0.15 |
R9327:Zfp318
|
UTSW |
17 |
46,721,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R9329:Zfp318
|
UTSW |
17 |
46,722,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R9352:Zfp318
|
UTSW |
17 |
46,721,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R9633:Zfp318
|
UTSW |
17 |
46,710,421 (GRCm39) |
missense |
probably damaging |
0.99 |
R9662:Zfp318
|
UTSW |
17 |
46,724,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R9728:Zfp318
|
UTSW |
17 |
46,707,713 (GRCm39) |
missense |
probably benign |
0.10 |
R9755:Zfp318
|
UTSW |
17 |
46,722,055 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Zfp318
|
UTSW |
17 |
46,721,564 (GRCm39) |
missense |
possibly damaging |
0.89 |
X0054:Zfp318
|
UTSW |
17 |
46,723,535 (GRCm39) |
missense |
possibly damaging |
0.79 |
X0065:Zfp318
|
UTSW |
17 |
46,721,915 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Zfp318
|
UTSW |
17 |
46,716,904 (GRCm39) |
missense |
probably benign |
0.03 |
|
Predicted Primers |
PCR Primer
(F):5'- AGCCCTAGGTTTCTAGATCCC -3'
(R):5'- AACAGAAGCCCTTGTTGATACG -3'
Sequencing Primer
(F):5'- TCTAGATCCCGAGTTTCGAGAAC -3'
(R):5'- CAGAAGCCCTTGTTGATACGCTATG -3'
|
Posted On |
2019-05-13 |