Incidental Mutation 'R2132:Ifi207'
ID |
233340 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ifi207
|
Ensembl Gene |
ENSMUSG00000073490 |
Gene Name |
interferon activated gene 207 |
Synonyms |
AI607873, Pyhin-A |
MMRRC Submission |
040135-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.093)
|
Stock # |
R2132 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
173550993-173569313 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 173557337 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Serine
at position 467
(F467S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000119350
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000042610]
[ENSMUST00000127730]
|
AlphaFold |
E9Q3L4 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000042610
AA Change: F474S
PolyPhen 2
Score 0.838 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000048129 Gene: ENSMUSG00000073490 AA Change: F474S
Domain | Start | End | E-Value | Type |
PYRIN
|
6 |
84 |
3.2e-15 |
SMART |
low complexity region
|
121 |
133 |
N/A |
INTRINSIC |
low complexity region
|
136 |
162 |
N/A |
INTRINSIC |
low complexity region
|
207 |
215 |
N/A |
INTRINSIC |
internal_repeat_1
|
286 |
472 |
4.17e-7 |
PROSPERO |
low complexity region
|
476 |
496 |
N/A |
INTRINSIC |
internal_repeat_1
|
565 |
782 |
4.17e-7 |
PROSPERO |
Pfam:HIN
|
788 |
954 |
4.9e-76 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000127730
AA Change: F467S
PolyPhen 2
Score 0.838 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000119350 Gene: ENSMUSG00000073490 AA Change: F467S
Domain | Start | End | E-Value | Type |
PYRIN
|
6 |
84 |
3.2e-15 |
SMART |
low complexity region
|
121 |
133 |
N/A |
INTRINSIC |
low complexity region
|
136 |
155 |
N/A |
INTRINSIC |
low complexity region
|
200 |
208 |
N/A |
INTRINSIC |
internal_repeat_1
|
279 |
465 |
6.41e-7 |
PROSPERO |
low complexity region
|
469 |
489 |
N/A |
INTRINSIC |
internal_repeat_1
|
558 |
775 |
6.41e-7 |
PROSPERO |
Pfam:HIN
|
781 |
948 |
1.8e-78 |
PFAM |
|
Meta Mutation Damage Score |
0.1795 |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.4%
- 20x: 95.3%
|
Validation Efficiency |
94% (117/124) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 122 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
A |
G |
5: 88,112,335 (GRCm39) |
|
probably benign |
Het |
4930562C15Rik |
A |
C |
16: 4,653,835 (GRCm39) |
Q128P |
unknown |
Het |
Abcc3 |
T |
A |
11: 94,258,426 (GRCm39) |
K473M |
probably benign |
Het |
Acacb |
TGGGG |
TGGG |
5: 114,347,828 (GRCm39) |
|
probably null |
Het |
Adgrg7 |
C |
A |
16: 56,588,281 (GRCm39) |
A199S |
probably damaging |
Het |
Akap13 |
G |
T |
7: 75,261,182 (GRCm39) |
A1269S |
probably benign |
Het |
Aox3 |
A |
G |
1: 58,209,002 (GRCm39) |
H845R |
probably damaging |
Het |
Ap2b1 |
T |
A |
11: 83,215,587 (GRCm39) |
|
probably benign |
Het |
Atat1 |
A |
G |
17: 36,220,331 (GRCm39) |
S54P |
probably damaging |
Het |
Atp13a2 |
T |
A |
4: 140,732,327 (GRCm39) |
M864K |
probably damaging |
Het |
B3gnt3 |
G |
A |
8: 72,145,971 (GRCm39) |
T186M |
probably damaging |
Het |
Cars1 |
C |
A |
7: 143,146,211 (GRCm39) |
R71M |
probably damaging |
Het |
Castor2 |
G |
A |
5: 134,164,992 (GRCm39) |
C187Y |
probably damaging |
Het |
Ccdc157 |
A |
T |
11: 4,100,004 (GRCm39) |
V116E |
probably damaging |
Het |
Ccdc85a |
G |
A |
11: 28,384,151 (GRCm39) |
T408I |
probably benign |
Het |
Celf1 |
G |
T |
2: 90,840,791 (GRCm39) |
G353W |
probably damaging |
Het |
Celsr1 |
T |
A |
15: 85,916,168 (GRCm39) |
I602F |
possibly damaging |
Het |
Cenpb |
C |
T |
2: 131,021,226 (GRCm39) |
V191M |
probably damaging |
Het |
Cenpn |
G |
A |
8: 117,661,536 (GRCm39) |
|
probably null |
Het |
Cfap65 |
A |
C |
1: 74,946,850 (GRCm39) |
C1287G |
probably damaging |
Het |
Cmya5 |
G |
A |
13: 93,205,891 (GRCm39) |
T3326I |
probably damaging |
Het |
Cnn3 |
A |
T |
3: 121,245,584 (GRCm39) |
E100V |
probably damaging |
Het |
Col4a4 |
G |
A |
1: 82,475,581 (GRCm39) |
R583C |
unknown |
Het |
Commd7 |
A |
C |
2: 153,463,586 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
T |
C |
15: 48,320,899 (GRCm39) |
T304A |
probably benign |
Het |
Cyp4a14 |
A |
T |
4: 115,348,588 (GRCm39) |
S325R |
probably damaging |
Het |
Dclk2 |
T |
C |
3: 86,827,353 (GRCm39) |
N42S |
probably benign |
Het |
Dmrta1 |
A |
T |
4: 89,576,946 (GRCm39) |
Q134L |
probably damaging |
Het |
Dnaaf3 |
T |
A |
7: 4,526,800 (GRCm39) |
I426L |
probably benign |
Het |
Dnah17 |
G |
A |
11: 117,924,573 (GRCm39) |
L3999F |
probably damaging |
Het |
Dock6 |
A |
G |
9: 21,757,814 (GRCm39) |
S97P |
probably benign |
Het |
Dsg1a |
T |
A |
18: 20,473,854 (GRCm39) |
S976T |
probably damaging |
Het |
Dstyk |
T |
A |
1: 132,377,222 (GRCm39) |
M29K |
probably null |
Het |
Eif3i |
A |
T |
4: 129,490,719 (GRCm39) |
H18Q |
probably benign |
Het |
Epm2a |
A |
G |
10: 11,219,426 (GRCm39) |
E71G |
probably benign |
Het |
Eps15l1 |
A |
T |
8: 73,140,712 (GRCm39) |
V260D |
probably benign |
Het |
Faf1 |
A |
G |
4: 109,568,042 (GRCm39) |
N34S |
probably damaging |
Het |
Fat3 |
A |
G |
9: 16,158,015 (GRCm39) |
|
probably null |
Het |
Fbxw10 |
T |
A |
11: 62,750,683 (GRCm39) |
I422N |
probably damaging |
Het |
Fcgbpl1 |
C |
T |
7: 27,854,899 (GRCm39) |
P1842S |
probably damaging |
Het |
Fkbp15 |
C |
A |
4: 62,246,136 (GRCm39) |
G431W |
probably damaging |
Het |
Flnb |
A |
C |
14: 7,873,376 (GRCm38) |
D224A |
probably benign |
Het |
Flnc |
G |
A |
6: 29,443,675 (GRCm39) |
V566M |
probably damaging |
Het |
Gli3 |
T |
A |
13: 15,900,134 (GRCm39) |
S1174T |
possibly damaging |
Het |
Glmn |
A |
T |
5: 107,726,321 (GRCm39) |
V93E |
probably damaging |
Het |
Glrx2 |
T |
C |
1: 143,620,842 (GRCm39) |
S74P |
possibly damaging |
Het |
Gm5422 |
G |
A |
10: 31,124,929 (GRCm39) |
|
noncoding transcript |
Het |
Gpi1 |
T |
C |
7: 33,905,339 (GRCm39) |
K362E |
probably damaging |
Het |
Gtpbp2 |
T |
C |
17: 46,472,128 (GRCm39) |
M21T |
probably benign |
Het |
Gxylt1 |
A |
G |
15: 93,142,851 (GRCm39) |
*405R |
probably null |
Het |
Heyl |
T |
C |
4: 123,139,876 (GRCm39) |
V145A |
probably damaging |
Het |
Hhipl1 |
A |
C |
12: 108,277,949 (GRCm39) |
E92D |
probably damaging |
Het |
Ift70b |
G |
T |
2: 75,767,129 (GRCm39) |
H541Q |
probably damaging |
Het |
Igf2r |
A |
T |
17: 12,941,095 (GRCm39) |
I462N |
probably benign |
Het |
Inpp5b |
A |
T |
4: 124,678,961 (GRCm39) |
|
probably benign |
Het |
Kansl2 |
A |
G |
15: 98,427,278 (GRCm39) |
I201T |
probably damaging |
Het |
Kcnh8 |
T |
C |
17: 53,200,961 (GRCm39) |
V465A |
probably damaging |
Het |
Kcnu1 |
T |
A |
8: 26,341,928 (GRCm39) |
I91N |
probably damaging |
Het |
Kif5c |
T |
A |
2: 49,648,817 (GRCm39) |
|
probably benign |
Het |
Klrc3 |
T |
A |
6: 129,618,501 (GRCm39) |
Y94F |
probably benign |
Het |
Lgals3bp |
T |
A |
11: 118,284,113 (GRCm39) |
T489S |
probably benign |
Het |
Lmo2 |
T |
C |
2: 103,811,407 (GRCm39) |
Y147H |
probably damaging |
Het |
Lmtk2 |
C |
T |
5: 144,111,806 (GRCm39) |
T842I |
possibly damaging |
Het |
Magel2 |
A |
T |
7: 62,027,486 (GRCm39) |
H130L |
unknown |
Het |
Magi1 |
T |
C |
6: 93,674,255 (GRCm39) |
E951G |
probably damaging |
Het |
Mcm7 |
T |
C |
5: 138,167,364 (GRCm39) |
Q86R |
probably damaging |
Het |
Med12l |
G |
T |
3: 59,172,703 (GRCm39) |
|
probably null |
Het |
Morc2a |
A |
G |
11: 3,629,787 (GRCm39) |
E402G |
possibly damaging |
Het |
Mphosph8 |
T |
C |
14: 56,916,161 (GRCm39) |
C486R |
probably benign |
Het |
Mpo |
A |
G |
11: 87,688,187 (GRCm39) |
D282G |
possibly damaging |
Het |
Mtcl1 |
G |
T |
17: 66,650,618 (GRCm39) |
H1616N |
probably benign |
Het |
Myh10 |
A |
G |
11: 68,698,115 (GRCm39) |
|
probably benign |
Het |
Myh8 |
A |
G |
11: 67,183,702 (GRCm39) |
E777G |
probably damaging |
Het |
Nid1 |
A |
G |
13: 13,684,071 (GRCm39) |
H1186R |
probably benign |
Het |
Nppb |
T |
A |
4: 148,070,454 (GRCm39) |
S8T |
probably benign |
Het |
Nrp1 |
A |
T |
8: 129,224,997 (GRCm39) |
E782D |
probably damaging |
Het |
Ntrk3 |
G |
A |
7: 78,127,683 (GRCm39) |
|
probably benign |
Het |
Or1ak2 |
A |
G |
2: 36,827,704 (GRCm39) |
N191S |
probably benign |
Het |
Or1j13 |
A |
G |
2: 36,370,059 (GRCm39) |
S28P |
possibly damaging |
Het |
Or2f1 |
C |
A |
6: 42,721,069 (GRCm39) |
L33M |
possibly damaging |
Het |
Or5al5 |
A |
G |
2: 85,961,605 (GRCm39) |
V134A |
possibly damaging |
Het |
Or5b99 |
T |
A |
19: 12,976,402 (GRCm39) |
D17E |
probably benign |
Het |
Or6f1 |
C |
T |
7: 85,970,687 (GRCm39) |
V158M |
possibly damaging |
Het |
Osbpl6 |
T |
A |
2: 76,416,558 (GRCm39) |
I546K |
probably damaging |
Het |
Pard6g |
T |
C |
18: 80,160,523 (GRCm39) |
V212A |
probably damaging |
Het |
Pate6 |
T |
G |
9: 35,701,039 (GRCm39) |
|
probably benign |
Het |
Pdlim4 |
A |
G |
11: 53,954,563 (GRCm39) |
L48S |
possibly damaging |
Het |
Phactr3 |
T |
C |
2: 177,925,759 (GRCm39) |
F345L |
probably benign |
Het |
Plcb1 |
T |
A |
2: 135,167,587 (GRCm39) |
Y460* |
probably null |
Het |
Prcp |
T |
A |
7: 92,550,488 (GRCm39) |
V95D |
probably benign |
Het |
Rfwd3 |
A |
T |
8: 112,024,034 (GRCm39) |
V96E |
probably benign |
Het |
Ror1 |
A |
G |
4: 100,267,222 (GRCm39) |
N308D |
probably benign |
Het |
Sdccag8 |
C |
A |
1: 176,783,455 (GRCm39) |
Q655K |
probably damaging |
Het |
Senp1 |
T |
A |
15: 97,973,848 (GRCm39) |
T132S |
probably benign |
Het |
Skap1 |
T |
C |
11: 96,355,559 (GRCm39) |
I10T |
possibly damaging |
Het |
Slc9a4 |
T |
G |
1: 40,646,901 (GRCm39) |
|
probably null |
Het |
Smad2 |
T |
A |
18: 76,421,155 (GRCm39) |
C161* |
probably null |
Het |
Spata31d1a |
G |
T |
13: 59,848,857 (GRCm39) |
D1090E |
probably damaging |
Het |
Stard13 |
T |
C |
5: 150,968,633 (GRCm39) |
Y879C |
probably damaging |
Het |
Tdrd6 |
T |
C |
17: 43,935,724 (GRCm39) |
T1775A |
probably benign |
Het |
Tecpr1 |
T |
A |
5: 144,145,463 (GRCm39) |
T595S |
probably benign |
Het |
Terf1 |
A |
G |
1: 15,875,909 (GRCm39) |
E3G |
probably benign |
Het |
Tjp3 |
T |
A |
10: 81,113,888 (GRCm39) |
M457L |
possibly damaging |
Het |
Tnfrsf26 |
C |
T |
7: 143,171,577 (GRCm39) |
|
probably null |
Het |
Tor1aip1 |
A |
C |
1: 155,883,308 (GRCm39) |
M180R |
probably damaging |
Het |
Trabd2b |
A |
T |
4: 114,467,205 (GRCm39) |
Q478L |
probably benign |
Het |
Trim41 |
C |
A |
11: 48,698,419 (GRCm39) |
G516W |
probably damaging |
Het |
Ttc39a |
A |
G |
4: 109,299,903 (GRCm39) |
Y464C |
probably damaging |
Het |
Unc5a |
A |
G |
13: 55,138,896 (GRCm39) |
S92G |
probably damaging |
Het |
Unc5d |
A |
C |
8: 29,365,557 (GRCm39) |
S143A |
possibly damaging |
Het |
Usp34 |
A |
T |
11: 23,414,556 (GRCm39) |
H2833L |
possibly damaging |
Het |
Vps35l |
T |
C |
7: 118,393,798 (GRCm39) |
Y516H |
probably damaging |
Het |
Wdr17 |
T |
G |
8: 55,125,541 (GRCm39) |
K446N |
probably damaging |
Het |
Xirp2 |
A |
T |
2: 67,338,392 (GRCm39) |
Q211L |
possibly damaging |
Het |
Xkr7 |
G |
A |
2: 152,894,816 (GRCm39) |
R256Q |
probably benign |
Het |
Zfp236 |
T |
C |
18: 82,639,429 (GRCm39) |
M1225V |
probably benign |
Het |
Zfp268 |
T |
A |
4: 145,350,803 (GRCm39) |
|
probably benign |
Het |
Zfp280d |
T |
C |
9: 72,215,287 (GRCm39) |
F133L |
probably damaging |
Het |
Zfp747l1 |
T |
C |
7: 126,986,107 (GRCm39) |
D8G |
probably benign |
Het |
Zfp758 |
A |
G |
17: 22,594,951 (GRCm39) |
H479R |
probably damaging |
Het |
Zfp827 |
A |
G |
8: 79,912,350 (GRCm39) |
N284S |
possibly damaging |
Het |
Zfyve26 |
T |
A |
12: 79,315,208 (GRCm39) |
I1423F |
possibly damaging |
Het |
|
Other mutations in Ifi207 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01776:Ifi207
|
APN |
1 |
173,552,610 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01864:Ifi207
|
APN |
1 |
173,564,007 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02293:Ifi207
|
APN |
1 |
173,551,314 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02402:Ifi207
|
APN |
1 |
173,555,159 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03160:Ifi207
|
APN |
1 |
173,562,670 (GRCm39) |
splice site |
probably benign |
|
PIT4458001:Ifi207
|
UTSW |
1 |
173,562,738 (GRCm39) |
missense |
unknown |
|
R0043:Ifi207
|
UTSW |
1 |
173,556,678 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0212:Ifi207
|
UTSW |
1 |
173,563,964 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0395:Ifi207
|
UTSW |
1 |
173,557,431 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0506:Ifi207
|
UTSW |
1 |
173,563,878 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0843:Ifi207
|
UTSW |
1 |
173,555,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R1302:Ifi207
|
UTSW |
1 |
173,562,861 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1373:Ifi207
|
UTSW |
1 |
173,557,913 (GRCm39) |
missense |
unknown |
|
R1462:Ifi207
|
UTSW |
1 |
173,552,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Ifi207
|
UTSW |
1 |
173,552,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Ifi207
|
UTSW |
1 |
173,557,629 (GRCm39) |
missense |
unknown |
|
R1502:Ifi207
|
UTSW |
1 |
173,556,872 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1533:Ifi207
|
UTSW |
1 |
173,555,306 (GRCm39) |
missense |
probably benign |
0.30 |
R1831:Ifi207
|
UTSW |
1 |
173,559,992 (GRCm39) |
missense |
unknown |
|
R1928:Ifi207
|
UTSW |
1 |
173,557,211 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1982:Ifi207
|
UTSW |
1 |
173,562,805 (GRCm39) |
missense |
probably benign |
0.01 |
R2248:Ifi207
|
UTSW |
1 |
173,564,036 (GRCm39) |
splice site |
probably benign |
|
R3703:Ifi207
|
UTSW |
1 |
173,555,029 (GRCm39) |
nonsense |
probably null |
|
R3741:Ifi207
|
UTSW |
1 |
173,555,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R3846:Ifi207
|
UTSW |
1 |
173,562,869 (GRCm39) |
missense |
probably benign |
0.33 |
R4747:Ifi207
|
UTSW |
1 |
173,556,633 (GRCm39) |
missense |
probably benign |
0.00 |
R4772:Ifi207
|
UTSW |
1 |
173,555,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R4776:Ifi207
|
UTSW |
1 |
173,557,622 (GRCm39) |
missense |
unknown |
|
R4855:Ifi207
|
UTSW |
1 |
173,557,381 (GRCm39) |
missense |
probably damaging |
0.96 |
R5170:Ifi207
|
UTSW |
1 |
173,558,064 (GRCm39) |
missense |
unknown |
|
R5244:Ifi207
|
UTSW |
1 |
173,557,503 (GRCm39) |
missense |
probably benign |
0.04 |
R5280:Ifi207
|
UTSW |
1 |
173,557,870 (GRCm39) |
missense |
unknown |
|
R5301:Ifi207
|
UTSW |
1 |
173,556,977 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5334:Ifi207
|
UTSW |
1 |
173,555,097 (GRCm39) |
missense |
probably benign |
0.21 |
R5445:Ifi207
|
UTSW |
1 |
173,555,363 (GRCm39) |
missense |
probably damaging |
0.99 |
R5691:Ifi207
|
UTSW |
1 |
173,559,992 (GRCm39) |
missense |
unknown |
|
R5838:Ifi207
|
UTSW |
1 |
173,559,953 (GRCm39) |
missense |
unknown |
|
R6060:Ifi207
|
UTSW |
1 |
173,558,093 (GRCm39) |
missense |
unknown |
|
R6220:Ifi207
|
UTSW |
1 |
173,557,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R6264:Ifi207
|
UTSW |
1 |
173,555,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R6307:Ifi207
|
UTSW |
1 |
173,552,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:Ifi207
|
UTSW |
1 |
173,557,532 (GRCm39) |
missense |
probably benign |
0.01 |
R6394:Ifi207
|
UTSW |
1 |
173,556,581 (GRCm39) |
missense |
probably benign |
0.43 |
R6532:Ifi207
|
UTSW |
1 |
173,557,211 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6660:Ifi207
|
UTSW |
1 |
173,556,972 (GRCm39) |
missense |
probably benign |
0.01 |
R6893:Ifi207
|
UTSW |
1 |
173,555,208 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7190:Ifi207
|
UTSW |
1 |
173,557,818 (GRCm39) |
missense |
unknown |
|
R7192:Ifi207
|
UTSW |
1 |
173,556,584 (GRCm39) |
missense |
not run |
|
R7194:Ifi207
|
UTSW |
1 |
173,557,490 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7327:Ifi207
|
UTSW |
1 |
173,556,581 (GRCm39) |
missense |
probably benign |
0.43 |
R7348:Ifi207
|
UTSW |
1 |
173,556,762 (GRCm39) |
small deletion |
probably benign |
|
R7404:Ifi207
|
UTSW |
1 |
173,556,494 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7442:Ifi207
|
UTSW |
1 |
173,554,997 (GRCm39) |
missense |
probably benign |
0.03 |
R7784:Ifi207
|
UTSW |
1 |
173,557,698 (GRCm39) |
missense |
unknown |
|
R8041:Ifi207
|
UTSW |
1 |
173,555,268 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8116:Ifi207
|
UTSW |
1 |
173,557,746 (GRCm39) |
missense |
unknown |
|
R8166:Ifi207
|
UTSW |
1 |
173,557,504 (GRCm39) |
missense |
probably benign |
0.10 |
R8166:Ifi207
|
UTSW |
1 |
173,557,166 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8168:Ifi207
|
UTSW |
1 |
173,557,504 (GRCm39) |
missense |
probably benign |
0.10 |
R8383:Ifi207
|
UTSW |
1 |
173,556,770 (GRCm39) |
small deletion |
probably benign |
|
R8388:Ifi207
|
UTSW |
1 |
173,557,016 (GRCm39) |
frame shift |
probably null |
|
R8389:Ifi207
|
UTSW |
1 |
173,557,016 (GRCm39) |
frame shift |
probably null |
|
R8390:Ifi207
|
UTSW |
1 |
173,557,016 (GRCm39) |
frame shift |
probably null |
|
R8399:Ifi207
|
UTSW |
1 |
173,557,844 (GRCm39) |
missense |
unknown |
|
R8431:Ifi207
|
UTSW |
1 |
173,558,070 (GRCm39) |
missense |
unknown |
|
R8474:Ifi207
|
UTSW |
1 |
173,556,605 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8505:Ifi207
|
UTSW |
1 |
173,557,016 (GRCm39) |
frame shift |
probably null |
|
R9009:Ifi207
|
UTSW |
1 |
173,555,382 (GRCm39) |
missense |
probably damaging |
0.97 |
R9061:Ifi207
|
UTSW |
1 |
173,564,153 (GRCm39) |
intron |
probably benign |
|
R9071:Ifi207
|
UTSW |
1 |
173,557,764 (GRCm39) |
missense |
unknown |
|
R9090:Ifi207
|
UTSW |
1 |
173,556,762 (GRCm39) |
small deletion |
probably benign |
|
R9323:Ifi207
|
UTSW |
1 |
173,555,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R9407:Ifi207
|
UTSW |
1 |
173,555,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R9493:Ifi207
|
UTSW |
1 |
173,556,522 (GRCm39) |
missense |
probably benign |
0.00 |
R9629:Ifi207
|
UTSW |
1 |
173,556,561 (GRCm39) |
small deletion |
probably benign |
|
RF009:Ifi207
|
UTSW |
1 |
173,556,558 (GRCm39) |
missense |
probably benign |
0.00 |
RF011:Ifi207
|
UTSW |
1 |
173,556,687 (GRCm39) |
missense |
not run |
|
RF032:Ifi207
|
UTSW |
1 |
173,562,723 (GRCm39) |
small deletion |
probably benign |
|
X0003:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0004:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0005:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0009:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0010:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0011:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0012:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0013:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0014:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0017:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0018:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0019:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0020:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0021:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0022:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0023:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0024:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0025:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0026:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0027:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0028:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0033:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0034:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0035:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0036:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0037:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0038:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0039:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0040:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0050:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0052:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0053:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0054:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0057:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0058:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0060:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0061:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0062:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0063:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0064:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0065:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0066:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
X0067:Ifi207
|
UTSW |
1 |
173,556,548 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Ifi207
|
UTSW |
1 |
173,557,145 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1187:Ifi207
|
UTSW |
1 |
173,558,093 (GRCm39) |
missense |
unknown |
|
Z1192:Ifi207
|
UTSW |
1 |
173,558,093 (GRCm39) |
missense |
unknown |
|
|
Predicted Primers |
PCR Primer
(F):5'- TGTGTCAACTGAGTGGTGCAC -3'
(R):5'- CCCAGCTCCTAAAGATGCCTTC -3'
Sequencing Primer
(F):5'- CAACTGAGTGGTGCACTTATTTC -3'
(R):5'- ACATCATCCAGCAGTGTTCAGG -3'
|
Posted On |
2014-10-01 |