Incidental Mutation 'R1913:Zfp318'
| ID |
214630 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp318
|
| Ensembl Gene |
ENSMUSG00000015597 |
| Gene Name |
zinc finger protein 318 |
| Synonyms |
2610034E08Rik, TZF, D530032D06Rik |
| MMRRC Submission |
039931-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R1913 (G1)
|
| Quality Score |
189 |
|
Status
|
Not validated
|
| Chromosome |
17 |
| Chromosomal Location |
46694657-46731846 bp(+) (GRCm39) |
| Type of Mutation |
unclassified |
| DNA Base Change (assembly) |
GAAGAA to GAAGAACAAGAA
at 46723450 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000116132
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000113481]
[ENSMUST00000138127]
[ENSMUST00000152472]
|
| AlphaFold |
Q99PP2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000113481
|
| SMART Domains |
Protein: ENSMUSP00000109109
Gene: ENSMUSG00000015597
| 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 |
noncoding transcript
Transcript: ENSMUST00000123733
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000136017
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000138127
|
| SMART Domains |
Protein: ENSMUSP00000116544
Gene: ENSMUSG00000015597
| 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: 97.5%
- 3x: 97.0%
- 10x: 95.6%
- 20x: 93.4%
|
| 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: 104 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca16 |
A |
T |
7: 120,140,463 (GRCm39) |
I1588F |
probably benign |
Het |
| Abcc2 |
A |
T |
19: 43,795,683 (GRCm39) |
T480S |
probably benign |
Het |
| Acnat1 |
A |
G |
4: 49,447,498 (GRCm39) |
I361T |
probably damaging |
Het |
| Adamts10 |
A |
T |
17: 33,768,529 (GRCm39) |
H869L |
probably benign |
Het |
| Agpat5 |
T |
C |
8: 18,929,629 (GRCm39) |
C253R |
probably benign |
Het |
| Agtrap |
T |
A |
4: 148,168,434 (GRCm39) |
H15L |
probably damaging |
Het |
| Ahnak |
T |
A |
19: 8,985,286 (GRCm39) |
V2190E |
probably damaging |
Het |
| Alx4 |
A |
G |
2: 93,505,732 (GRCm39) |
E278G |
probably damaging |
Het |
| Amz2 |
T |
C |
11: 109,319,697 (GRCm39) |
S28P |
probably damaging |
Het |
| Atr |
T |
A |
9: 95,748,786 (GRCm39) |
Y444N |
probably benign |
Het |
| Brdt |
T |
C |
5: 107,496,479 (GRCm39) |
I197T |
probably benign |
Het |
| Ccser1 |
G |
T |
6: 62,356,878 (GRCm39) |
S772I |
probably damaging |
Het |
| Cdh16 |
T |
C |
8: 105,343,100 (GRCm39) |
H657R |
probably benign |
Het |
| Ceacam5 |
A |
T |
7: 17,493,502 (GRCm39) |
K842* |
probably null |
Het |
| Cep120 |
G |
A |
18: 53,856,358 (GRCm39) |
T353I |
probably benign |
Het |
| Chrnb1 |
T |
C |
11: 69,684,410 (GRCm39) |
N164S |
possibly damaging |
Het |
| Cse1l |
T |
C |
2: 166,764,111 (GRCm39) |
F123L |
probably damaging |
Het |
| Cul7 |
T |
A |
17: 46,974,116 (GRCm39) |
L1467H |
probably damaging |
Het |
| Dcx |
G |
C |
X: 142,706,099 (GRCm39) |
L231V |
probably damaging |
Het |
| Dnah12 |
T |
C |
14: 26,514,221 (GRCm39) |
|
probably null |
Het |
| Dnah2 |
A |
T |
11: 69,355,756 (GRCm39) |
M2227K |
probably damaging |
Het |
| Dnajc30 |
G |
A |
5: 135,093,186 (GRCm39) |
A28T |
probably benign |
Het |
| Dnm1l |
T |
C |
16: 16,147,830 (GRCm39) |
T306A |
probably benign |
Het |
| Elapor2 |
T |
G |
5: 9,316,275 (GRCm39) |
L2R |
probably damaging |
Het |
| Enpp3 |
C |
A |
10: 24,652,669 (GRCm39) |
E763* |
probably null |
Het |
| Esyt3 |
T |
C |
9: 99,202,364 (GRCm39) |
S516G |
probably benign |
Het |
| Exoc3 |
T |
C |
13: 74,330,435 (GRCm39) |
Q498R |
probably damaging |
Het |
| Fbn2 |
T |
A |
18: 58,194,814 (GRCm39) |
N1449I |
probably damaging |
Het |
| Fgb |
T |
C |
3: 82,952,287 (GRCm39) |
D194G |
probably benign |
Het |
| Fgd3 |
T |
C |
13: 49,417,324 (GRCm39) |
D713G |
possibly damaging |
Het |
| Foxb1 |
T |
A |
9: 69,667,383 (GRCm39) |
Y49F |
possibly damaging |
Het |
| Fpr3 |
A |
G |
17: 18,191,670 (GRCm39) |
I314V |
probably damaging |
Het |
| Gfod1 |
A |
T |
13: 43,456,921 (GRCm39) |
I18N |
probably damaging |
Het |
| Gm5407 |
T |
C |
16: 49,117,283 (GRCm39) |
|
noncoding transcript |
Het |
| Gpr89 |
A |
G |
3: 96,782,949 (GRCm39) |
F334L |
possibly damaging |
Het |
| Gucy2d |
G |
T |
7: 98,093,054 (GRCm39) |
V144F |
probably benign |
Het |
| H2-M10.5 |
C |
A |
17: 37,085,660 (GRCm39) |
P273H |
probably damaging |
Het |
| H2-T13 |
T |
A |
17: 36,391,908 (GRCm39) |
K237M |
probably damaging |
Het |
| Hcn2 |
A |
G |
10: 79,566,777 (GRCm39) |
M485V |
probably benign |
Het |
| Helz2 |
G |
T |
2: 180,875,543 (GRCm39) |
S1650R |
probably damaging |
Het |
| Ifnar2 |
T |
C |
16: 91,201,058 (GRCm39) |
V433A |
probably benign |
Het |
| Igsf21 |
T |
A |
4: 139,834,623 (GRCm39) |
Y83F |
probably benign |
Het |
| Kcnk18 |
A |
G |
19: 59,223,490 (GRCm39) |
I212V |
possibly damaging |
Het |
| Kcns2 |
T |
C |
15: 34,839,855 (GRCm39) |
I406T |
probably damaging |
Het |
| Krt42 |
C |
T |
11: 100,158,075 (GRCm39) |
V166M |
possibly damaging |
Het |
| Lama3 |
T |
C |
18: 12,628,336 (GRCm39) |
M1476T |
probably benign |
Het |
| Lcor |
A |
G |
19: 41,546,913 (GRCm39) |
R166G |
probably benign |
Het |
| Mapt |
C |
T |
11: 104,218,901 (GRCm39) |
P354L |
probably damaging |
Het |
| Mep1b |
A |
T |
18: 21,226,286 (GRCm39) |
I383F |
probably benign |
Het |
| Mpzl1 |
C |
A |
1: 165,429,374 (GRCm39) |
C222F |
probably benign |
Het |
| Mug2 |
T |
C |
6: 122,047,829 (GRCm39) |
L780P |
probably damaging |
Het |
| Naip2 |
C |
T |
13: 100,288,665 (GRCm39) |
|
probably null |
Het |
| Ndufab1 |
T |
C |
7: 121,695,914 (GRCm39) |
D41G |
probably benign |
Het |
| Ntn1 |
A |
G |
11: 68,104,011 (GRCm39) |
C546R |
probably damaging |
Het |
| Or2a5 |
T |
A |
6: 42,873,687 (GRCm39) |
F101I |
probably damaging |
Het |
| Pakap |
A |
G |
4: 57,892,963 (GRCm39) |
E880G |
probably damaging |
Het |
| Pde6b |
A |
G |
5: 108,575,056 (GRCm39) |
E639G |
probably benign |
Het |
| Phf10 |
T |
C |
17: 15,177,071 (GRCm39) |
T83A |
probably benign |
Het |
| Phkb |
T |
A |
8: 86,628,549 (GRCm39) |
I186N |
possibly damaging |
Het |
| Pkhd1 |
A |
G |
1: 20,636,980 (GRCm39) |
|
probably null |
Het |
| Plxnd1 |
C |
A |
6: 115,954,978 (GRCm39) |
A595S |
possibly damaging |
Het |
| Ppara |
T |
A |
15: 85,685,300 (GRCm39) |
H416Q |
probably damaging |
Het |
| Prodh |
T |
A |
16: 17,898,891 (GRCm39) |
D188V |
probably damaging |
Het |
| Psmd14 |
A |
T |
2: 61,615,800 (GRCm39) |
K223M |
possibly damaging |
Het |
| Ptpn5 |
A |
G |
7: 46,728,616 (GRCm39) |
M528T |
possibly damaging |
Het |
| Rassf9 |
G |
A |
10: 102,380,800 (GRCm39) |
E59K |
probably benign |
Het |
| Rnf2 |
A |
T |
1: 151,351,936 (GRCm39) |
L140H |
probably damaging |
Het |
| Scai |
A |
G |
2: 38,970,093 (GRCm39) |
F557S |
probably damaging |
Het |
| Sdk2 |
A |
G |
11: 113,747,552 (GRCm39) |
S653P |
possibly damaging |
Het |
| Sec24c |
A |
G |
14: 20,739,179 (GRCm39) |
D534G |
probably benign |
Het |
| Semp2l2a |
T |
A |
8: 13,887,143 (GRCm39) |
Q316L |
probably benign |
Het |
| Septin4 |
T |
C |
11: 87,457,838 (GRCm39) |
S71P |
probably benign |
Het |
| Serinc1 |
A |
G |
10: 57,395,561 (GRCm39) |
V375A |
probably benign |
Het |
| Serpinb9f |
C |
T |
13: 33,509,829 (GRCm39) |
A7V |
probably damaging |
Het |
| Smco1 |
T |
C |
16: 32,092,700 (GRCm39) |
S124P |
probably damaging |
Het |
| Smim23 |
C |
A |
11: 32,774,441 (GRCm39) |
C26F |
possibly damaging |
Het |
| Sppl2c |
T |
A |
11: 104,078,715 (GRCm39) |
M505K |
probably benign |
Het |
| Sprr1b |
C |
A |
3: 92,344,775 (GRCm39) |
V34F |
possibly damaging |
Het |
| Sun1 |
G |
A |
5: 139,221,487 (GRCm39) |
|
probably null |
Het |
| Supt16 |
A |
G |
14: 52,415,592 (GRCm39) |
L381P |
possibly damaging |
Het |
| Syne2 |
A |
G |
12: 75,946,020 (GRCm39) |
D364G |
possibly damaging |
Het |
| Tax1bp1 |
G |
T |
6: 52,742,937 (GRCm39) |
V775F |
probably damaging |
Het |
| Tial1 |
T |
A |
7: 128,046,383 (GRCm39) |
I231F |
probably damaging |
Het |
| Tiam1 |
C |
A |
16: 89,595,582 (GRCm39) |
V1300L |
probably damaging |
Het |
| Tmem132e |
A |
G |
11: 82,334,243 (GRCm39) |
T585A |
probably damaging |
Het |
| Tnni3k |
C |
T |
3: 154,684,836 (GRCm39) |
A165T |
probably benign |
Het |
| Tomm40 |
A |
T |
7: 19,444,886 (GRCm39) |
I165N |
probably damaging |
Het |
| Tomt |
T |
C |
7: 101,550,454 (GRCm39) |
E104G |
probably damaging |
Het |
| Topaz1 |
T |
C |
9: 122,596,078 (GRCm39) |
S950P |
possibly damaging |
Het |
| Traf3ip2 |
C |
G |
10: 39,501,936 (GRCm39) |
P28R |
probably benign |
Het |
| Trim24 |
C |
T |
6: 37,934,750 (GRCm39) |
P822S |
probably damaging |
Het |
| Upf3a |
T |
G |
8: 13,842,108 (GRCm39) |
Y175D |
probably damaging |
Het |
| Vars2 |
G |
A |
17: 35,977,814 (GRCm39) |
P69S |
probably benign |
Het |
| Veph1 |
T |
C |
3: 66,151,976 (GRCm39) |
Y151C |
probably damaging |
Het |
| Vmn2r11 |
T |
A |
5: 109,202,654 (GRCm39) |
D141V |
probably benign |
Het |
| Vwa5b1 |
G |
A |
4: 138,319,331 (GRCm39) |
Q442* |
probably null |
Het |
| Wdr17 |
T |
A |
8: 55,140,761 (GRCm39) |
D197V |
probably damaging |
Het |
| Wdr70 |
G |
T |
15: 7,913,891 (GRCm39) |
T586N |
possibly damaging |
Het |
| Wfdc18 |
G |
A |
11: 83,600,754 (GRCm39) |
G52R |
probably benign |
Het |
| Zc3h6 |
T |
C |
2: 128,858,540 (GRCm39) |
I857T |
probably damaging |
Het |
| Zfp647 |
C |
T |
15: 76,796,151 (GRCm39) |
V170I |
probably benign |
Het |
| Zfp871 |
T |
C |
17: 32,994,891 (GRCm39) |
N76D |
possibly damaging |
Het |
| Zpld2 |
A |
G |
4: 133,919,986 (GRCm39) |
|
probably null |
Het |
| Zwilch |
A |
G |
9: 64,068,234 (GRCm39) |
Y194H |
probably 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 |
46,723,440 (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 |
|
|
R6980:Zfp318
|
UTSW |
17 |
46,708,138 (GRCm39) |
missense |
probably damaging |
1.00 |
|
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'- TCAGATTTGACCTGGGAGAGC -3'
(R):5'- GAGACGGACTCAATTCAATTACTAC -3'
Sequencing Primer
(F):5'- GGTACAGATTCAACTTCTCATCTATC -3'
(R):5'- ACTTTACTTGTATTCTCATGTCCGG -3'
|
| Posted On |
2014-07-14 |
Incidental Mutation