Incidental Mutation 'R8390:Ifi206'
| ID |
647306 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ifi206
|
| Ensembl Gene |
ENSMUSG00000037849 |
| Gene Name |
interferon activated gene 206 |
| Synonyms |
Pyblhin-C, Gm4955 |
| MMRRC Submission |
067755-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.175)
|
| Stock # |
R8390 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
1 |
| Chromosomal Location |
173296051-173318607 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 173308511 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Asparagine
at position 495
(T495N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000134646
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000160565]
|
| AlphaFold |
G3UZV2 |
| Predicted Effect |
|
| SMART Domains |
Protein: ENSMUSP00000134646
Gene: ENSMUSG00000037849
AA Change: T495N
| Domain | Start | End | E-Value | Type |
|---|
|
PYRIN
|
6 |
84 |
5.7e-21 |
SMART |
|
low complexity region
|
97 |
108 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
154 |
349 |
6.25e-15 |
PROSPERO |
|
internal_repeat_1
|
342 |
575 |
6.25e-15 |
PROSPERO |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.5%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 48 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700069L16Rik |
A |
T |
5: 113,830,841 (GRCm39) |
F50I |
unknown |
Het |
| Abca9 |
A |
T |
11: 110,036,456 (GRCm39) |
M551K |
probably benign |
Het |
| Adgrl3 |
T |
C |
5: 81,914,057 (GRCm39) |
S1145P |
probably damaging |
Het |
| Brix1 |
C |
T |
15: 10,485,954 (GRCm39) |
R9H |
probably benign |
Het |
| C1d |
T |
C |
11: 17,213,993 (GRCm39) |
V83A |
probably damaging |
Het |
| Ciz1 |
G |
T |
2: 32,257,335 (GRCm39) |
V127L |
probably benign |
Het |
| Csnk1g3 |
A |
T |
18: 54,081,150 (GRCm39) |
T374S |
probably benign |
Het |
| Elavl1 |
T |
A |
8: 4,339,623 (GRCm39) |
K320* |
probably null |
Het |
| Foxn3 |
T |
A |
12: 99,355,000 (GRCm39) |
M55L |
probably benign |
Het |
| Gm14399 |
A |
T |
2: 174,972,605 (GRCm39) |
Y383* |
probably null |
Het |
| H2-M10.5 |
T |
A |
17: 37,085,487 (GRCm39) |
H215Q |
probably benign |
Het |
| Hsd17b13 |
C |
A |
5: 104,120,512 (GRCm39) |
C80F |
probably damaging |
Het |
| Ifi207 |
GTT |
GT |
1: 173,557,016 (GRCm39) |
|
probably null |
Het |
| Ipo13 |
A |
T |
4: 117,769,534 (GRCm39) |
I86N |
probably damaging |
Het |
| Iqcf3 |
T |
G |
9: 106,438,175 (GRCm39) |
E16A |
unknown |
Het |
| Kcnh5 |
T |
A |
12: 75,134,532 (GRCm39) |
D339V |
probably damaging |
Het |
| Lmbr1 |
C |
T |
5: 29,440,040 (GRCm39) |
M441I |
probably benign |
Het |
| Me3 |
G |
T |
7: 89,498,803 (GRCm39) |
G461V |
probably damaging |
Het |
| Mepce |
A |
G |
5: 137,783,441 (GRCm39) |
L295P |
possibly damaging |
Het |
| Mtpap |
T |
A |
18: 4,396,141 (GRCm39) |
Y478N |
probably damaging |
Het |
| Myl12a |
T |
C |
17: 71,303,231 (GRCm39) |
M74V |
probably benign |
Het |
| Neil3 |
A |
T |
8: 54,062,559 (GRCm39) |
M99K |
probably damaging |
Het |
| Nlrp3 |
A |
G |
11: 59,442,616 (GRCm39) |
T723A |
possibly damaging |
Het |
| Obscn |
A |
T |
11: 58,892,870 (GRCm39) |
I6792N |
probably benign |
Het |
| Or13a19 |
G |
T |
7: 139,903,027 (GRCm39) |
W138C |
possibly damaging |
Het |
| Or2d2 |
A |
G |
7: 106,728,522 (GRCm39) |
L26P |
probably benign |
Het |
| Or5al7 |
A |
G |
2: 85,993,266 (GRCm39) |
V9A |
possibly damaging |
Het |
| Or8b49 |
T |
A |
9: 38,505,887 (GRCm39) |
Y123* |
probably null |
Het |
| Or8h10 |
G |
A |
2: 86,808,501 (GRCm39) |
T213I |
probably benign |
Het |
| Peg10 |
T |
TCCC |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
| Pitx2 |
C |
A |
3: 129,012,507 (GRCm39) |
N312K |
probably damaging |
Het |
| Pot1b |
C |
A |
17: 55,999,739 (GRCm39) |
V229L |
probably benign |
Het |
| Psmd1 |
A |
G |
1: 86,006,329 (GRCm39) |
I232V |
possibly damaging |
Het |
| Rif1 |
A |
G |
2: 52,000,935 (GRCm39) |
E1463G |
probably damaging |
Het |
| Scn5a |
T |
A |
9: 119,368,604 (GRCm39) |
Y307F |
possibly damaging |
Het |
| Shprh |
G |
A |
10: 11,063,727 (GRCm39) |
E1267K |
possibly damaging |
Het |
| Smtnl1 |
A |
T |
2: 84,645,694 (GRCm39) |
Y392* |
probably null |
Het |
| Sry |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
Y: 2,662,638 (GRCm39) |
|
probably benign |
Het |
| Sspo |
G |
A |
6: 48,444,896 (GRCm39) |
G2268R |
probably benign |
Het |
| Tex47 |
G |
A |
5: 7,355,301 (GRCm39) |
E161K |
probably benign |
Het |
| Timd6 |
G |
T |
11: 46,468,082 (GRCm39) |
R52L |
probably damaging |
Het |
| Tmem236 |
T |
C |
2: 14,224,168 (GRCm39) |
L319P |
probably damaging |
Het |
| Tnk1 |
T |
C |
11: 69,742,695 (GRCm39) |
T606A |
possibly damaging |
Het |
| Tnrc6a |
A |
G |
7: 122,761,794 (GRCm39) |
T81A |
probably damaging |
Het |
| Trav6d-4 |
A |
T |
14: 52,991,092 (GRCm39) |
T46S |
probably benign |
Het |
| Wdr19 |
T |
A |
5: 65,381,210 (GRCm39) |
Y411* |
probably null |
Het |
| Zfp553 |
A |
G |
7: 126,835,476 (GRCm39) |
T344A |
probably damaging |
Het |
| Zfp62 |
G |
A |
11: 49,106,019 (GRCm39) |
G37S |
probably benign |
Het |
|
| Other mutations in Ifi206 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01509:Ifi206
|
APN |
1 |
173,313,142 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02044:Ifi206
|
APN |
1 |
173,308,557 (GRCm39) |
missense |
probably benign |
0.41 |
|
IGL02118:Ifi206
|
APN |
1 |
173,309,334 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL02476:Ifi206
|
APN |
1 |
173,309,132 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02824:Ifi206
|
APN |
1 |
173,309,438 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL03375:Ifi206
|
APN |
1 |
173,308,344 (GRCm39) |
missense |
probably benign |
0.06 |
|
PIT4142001:Ifi206
|
UTSW |
1 |
173,308,730 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0069:Ifi206
|
UTSW |
1 |
173,314,413 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0741:Ifi206
|
UTSW |
1 |
173,301,315 (GRCm39) |
missense |
probably benign |
0.41 |
|
R1572:Ifi206
|
UTSW |
1 |
173,314,419 (GRCm39) |
missense |
probably benign |
0.10 |
|
R1742:Ifi206
|
UTSW |
1 |
173,309,537 (GRCm39) |
missense |
probably benign |
0.06 |
|
R4109:Ifi206
|
UTSW |
1 |
173,308,554 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4707:Ifi206
|
UTSW |
1 |
173,308,432 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4783:Ifi206
|
UTSW |
1 |
173,308,432 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4785:Ifi206
|
UTSW |
1 |
173,308,432 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4805:Ifi206
|
UTSW |
1 |
173,308,952 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R4918:Ifi206
|
UTSW |
1 |
173,309,610 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R5043:Ifi206
|
UTSW |
1 |
173,314,284 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5080:Ifi206
|
UTSW |
1 |
173,301,414 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R5419:Ifi206
|
UTSW |
1 |
173,308,797 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5420:Ifi206
|
UTSW |
1 |
173,308,599 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R5777:Ifi206
|
UTSW |
1 |
173,308,928 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R5988:Ifi206
|
UTSW |
1 |
173,308,906 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R6772:Ifi206
|
UTSW |
1 |
173,308,773 (GRCm39) |
missense |
unknown |
|
|
R6782:Ifi206
|
UTSW |
1 |
173,308,923 (GRCm39) |
missense |
unknown |
|
|
R6806:Ifi206
|
UTSW |
1 |
173,309,137 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7042:Ifi206
|
UTSW |
1 |
173,308,808 (GRCm39) |
missense |
|
|
|
R7091:Ifi206
|
UTSW |
1 |
173,301,441 (GRCm39) |
missense |
unknown |
|
|
R7292:Ifi206
|
UTSW |
1 |
173,301,428 (GRCm39) |
missense |
unknown |
|
|
R7429:Ifi206
|
UTSW |
1 |
173,308,157 (GRCm39) |
missense |
|
|
|
R7499:Ifi206
|
UTSW |
1 |
173,309,607 (GRCm39) |
missense |
|
|
|
R7772:Ifi206
|
UTSW |
1 |
173,308,640 (GRCm39) |
missense |
|
|
|
R7853:Ifi206
|
UTSW |
1 |
173,299,100 (GRCm39) |
nonsense |
probably null |
|
|
R7971:Ifi206
|
UTSW |
1 |
173,298,976 (GRCm39) |
missense |
unknown |
|
|
R8079:Ifi206
|
UTSW |
1 |
173,308,724 (GRCm39) |
missense |
|
|
|
R8205:Ifi206
|
UTSW |
1 |
173,309,450 (GRCm39) |
missense |
|
|
|
R8289:Ifi206
|
UTSW |
1 |
173,308,032 (GRCm39) |
missense |
|
|
|
R8500:Ifi206
|
UTSW |
1 |
173,314,311 (GRCm39) |
missense |
|
|
|
R8712:Ifi206
|
UTSW |
1 |
173,308,074 (GRCm39) |
missense |
|
|
|
R8753:Ifi206
|
UTSW |
1 |
173,301,223 (GRCm39) |
missense |
unknown |
|
|
R8875:Ifi206
|
UTSW |
1 |
173,301,353 (GRCm39) |
missense |
unknown |
|
|
R9128:Ifi206
|
UTSW |
1 |
173,299,022 (GRCm39) |
missense |
unknown |
|
|
R9369:Ifi206
|
UTSW |
1 |
173,301,489 (GRCm39) |
missense |
unknown |
|
|
R9569:Ifi206
|
UTSW |
1 |
173,314,209 (GRCm39) |
missense |
|
|
|
R9676:Ifi206
|
UTSW |
1 |
173,308,718 (GRCm39) |
missense |
|
|
|
R9695:Ifi206
|
UTSW |
1 |
173,301,249 (GRCm39) |
missense |
unknown |
|
|
R9776:Ifi206
|
UTSW |
1 |
173,308,075 (GRCm39) |
missense |
|
|
|
X0052:Ifi206
|
UTSW |
1 |
173,309,535 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
Z1088:Ifi206
|
UTSW |
1 |
173,301,577 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Ifi206
|
UTSW |
1 |
173,309,614 (GRCm39) |
missense |
|
|
|
| Predicted Primers |
PCR Primer
(F):5'- ACTGTTGCTGGAGTTACCTGAG -3'
(R):5'- TTCCTCAAGTAGCAGTGCC -3'
Sequencing Primer
(F):5'- CTGGATATTGTTGCTGCAGACATC -3'
(R):5'- CCAGCAGTGCCTTTCAAATG -3'
|
| Posted On |
2020-09-02 |
Incidental Mutation