Incidental Mutation 'R6173:Foxp1'
ID |
489137 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Foxp1
|
Ensembl Gene |
ENSMUSG00000030067 |
Gene Name |
forkhead box P1 |
Synonyms |
3110052D19Rik, 4932443N09Rik |
MMRRC Submission |
044316-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R6173 (G1)
|
Quality Score |
223.009 |
Status
|
Validated
|
Chromosome |
6 |
Chromosomal Location |
98902299-99499682 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
G to A
at 98992471 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamine to Stop codon
at position 41
(Q41*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000134869
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000074346]
[ENSMUST00000113322]
[ENSMUST00000113324]
[ENSMUST00000113326]
[ENSMUST00000113328]
[ENSMUST00000113329]
[ENSMUST00000123992]
[ENSMUST00000124058]
[ENSMUST00000154163]
[ENSMUST00000175886]
[ENSMUST00000176565]
[ENSMUST00000176632]
[ENSMUST00000176850]
[ENSMUST00000177229]
[ENSMUST00000177230]
[ENSMUST00000177307]
[ENSMUST00000177437]
[ENSMUST00000177507]
[ENSMUST00000175670]
|
AlphaFold |
P58462 |
Predicted Effect |
probably null
Transcript: ENSMUST00000074346
AA Change: Q171*
|
SMART Domains |
Protein: ENSMUSP00000073953 Gene: ENSMUSG00000030067 AA Change: Q171*
Domain | Start | End | E-Value | Type |
coiled coil region
|
62 |
113 |
N/A |
INTRINSIC |
low complexity region
|
140 |
191 |
N/A |
INTRINSIC |
low complexity region
|
200 |
233 |
N/A |
INTRINSIC |
low complexity region
|
236 |
250 |
N/A |
INTRINSIC |
low complexity region
|
264 |
275 |
N/A |
INTRINSIC |
low complexity region
|
317 |
330 |
N/A |
INTRINSIC |
ZnF_C2H2
|
334 |
359 |
8.67e-1 |
SMART |
low complexity region
|
371 |
383 |
N/A |
INTRINSIC |
low complexity region
|
432 |
446 |
N/A |
INTRINSIC |
FH
|
491 |
572 |
2.07e-39 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000113321
|
SMART Domains |
Protein: ENSMUSP00000108947 Gene: ENSMUSG00000030067
Domain | Start | End | E-Value | Type |
low complexity region
|
10 |
62 |
N/A |
INTRINSIC |
low complexity region
|
71 |
104 |
N/A |
INTRINSIC |
low complexity region
|
107 |
124 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000113322
AA Change: Q171*
|
SMART Domains |
Protein: ENSMUSP00000108948 Gene: ENSMUSG00000030067 AA Change: Q171*
Domain | Start | End | E-Value | Type |
coiled coil region
|
62 |
113 |
N/A |
INTRINSIC |
low complexity region
|
140 |
191 |
N/A |
INTRINSIC |
low complexity region
|
200 |
233 |
N/A |
INTRINSIC |
low complexity region
|
236 |
250 |
N/A |
INTRINSIC |
low complexity region
|
264 |
275 |
N/A |
INTRINSIC |
low complexity region
|
317 |
330 |
N/A |
INTRINSIC |
ZnF_C2H2
|
334 |
359 |
8.67e-1 |
SMART |
low complexity region
|
371 |
383 |
N/A |
INTRINSIC |
low complexity region
|
432 |
446 |
N/A |
INTRINSIC |
FH
|
491 |
572 |
2.07e-39 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000113324
AA Change: Q172*
|
SMART Domains |
Protein: ENSMUSP00000108950 Gene: ENSMUSG00000030067 AA Change: Q172*
Domain | Start | End | E-Value | Type |
coiled coil region
|
62 |
113 |
N/A |
INTRINSIC |
low complexity region
|
140 |
192 |
N/A |
INTRINSIC |
low complexity region
|
201 |
234 |
N/A |
INTRINSIC |
low complexity region
|
237 |
251 |
N/A |
INTRINSIC |
low complexity region
|
265 |
276 |
N/A |
INTRINSIC |
low complexity region
|
318 |
331 |
N/A |
INTRINSIC |
ZnF_C2H2
|
335 |
360 |
8.67e-1 |
SMART |
low complexity region
|
372 |
384 |
N/A |
INTRINSIC |
low complexity region
|
433 |
447 |
N/A |
INTRINSIC |
FH
|
492 |
573 |
2.07e-39 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000113326
AA Change: Q139*
|
SMART Domains |
Protein: ENSMUSP00000108952 Gene: ENSMUSG00000030067 AA Change: Q139*
Domain | Start | End | E-Value | Type |
low complexity region
|
108 |
159 |
N/A |
INTRINSIC |
low complexity region
|
168 |
201 |
N/A |
INTRINSIC |
low complexity region
|
204 |
218 |
N/A |
INTRINSIC |
low complexity region
|
232 |
243 |
N/A |
INTRINSIC |
low complexity region
|
285 |
298 |
N/A |
INTRINSIC |
ZnF_C2H2
|
302 |
327 |
8.67e-1 |
SMART |
low complexity region
|
339 |
351 |
N/A |
INTRINSIC |
low complexity region
|
400 |
414 |
N/A |
INTRINSIC |
FH
|
459 |
540 |
2.07e-39 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000113328
AA Change: Q171*
|
SMART Domains |
Protein: ENSMUSP00000108954 Gene: ENSMUSG00000030067 AA Change: Q171*
Domain | Start | End | E-Value | Type |
coiled coil region
|
62 |
113 |
N/A |
INTRINSIC |
low complexity region
|
140 |
191 |
N/A |
INTRINSIC |
low complexity region
|
200 |
234 |
N/A |
INTRINSIC |
low complexity region
|
237 |
251 |
N/A |
INTRINSIC |
low complexity region
|
265 |
276 |
N/A |
INTRINSIC |
low complexity region
|
318 |
331 |
N/A |
INTRINSIC |
ZnF_C2H2
|
335 |
360 |
8.67e-1 |
SMART |
low complexity region
|
372 |
384 |
N/A |
INTRINSIC |
low complexity region
|
433 |
447 |
N/A |
INTRINSIC |
FH
|
492 |
573 |
2.07e-39 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000113329
AA Change: Q171*
|
SMART Domains |
Protein: ENSMUSP00000108955 Gene: ENSMUSG00000030067 AA Change: Q171*
Domain | Start | End | E-Value | Type |
coiled coil region
|
62 |
113 |
N/A |
INTRINSIC |
low complexity region
|
140 |
191 |
N/A |
INTRINSIC |
low complexity region
|
200 |
233 |
N/A |
INTRINSIC |
low complexity region
|
236 |
250 |
N/A |
INTRINSIC |
low complexity region
|
264 |
275 |
N/A |
INTRINSIC |
low complexity region
|
317 |
330 |
N/A |
INTRINSIC |
ZnF_C2H2
|
334 |
359 |
8.67e-1 |
SMART |
low complexity region
|
371 |
383 |
N/A |
INTRINSIC |
low complexity region
|
432 |
446 |
N/A |
INTRINSIC |
FH
|
491 |
579 |
1.76e-10 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000123992
AA Change: Q42*
|
SMART Domains |
Protein: ENSMUSP00000117550 Gene: ENSMUSG00000030067 AA Change: Q42*
Domain | Start | End | E-Value | Type |
low complexity region
|
10 |
62 |
N/A |
INTRINSIC |
low complexity region
|
71 |
104 |
N/A |
INTRINSIC |
low complexity region
|
107 |
121 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000124058
AA Change: Q42*
|
SMART Domains |
Protein: ENSMUSP00000120244 Gene: ENSMUSG00000030067 AA Change: Q42*
Domain | Start | End | E-Value | Type |
low complexity region
|
10 |
62 |
N/A |
INTRINSIC |
low complexity region
|
71 |
104 |
N/A |
INTRINSIC |
low complexity region
|
107 |
121 |
N/A |
INTRINSIC |
low complexity region
|
135 |
146 |
N/A |
INTRINSIC |
low complexity region
|
188 |
201 |
N/A |
INTRINSIC |
ZnF_C2H2
|
205 |
230 |
8.67e-1 |
SMART |
low complexity region
|
242 |
254 |
N/A |
INTRINSIC |
low complexity region
|
303 |
317 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000154163
AA Change: Q42*
|
SMART Domains |
Protein: ENSMUSP00000121404 Gene: ENSMUSG00000030067 AA Change: Q42*
Domain | Start | End | E-Value | Type |
low complexity region
|
10 |
62 |
N/A |
INTRINSIC |
low complexity region
|
71 |
104 |
N/A |
INTRINSIC |
low complexity region
|
107 |
121 |
N/A |
INTRINSIC |
low complexity region
|
135 |
146 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000175886
AA Change: Q42*
|
SMART Domains |
Protein: ENSMUSP00000135517 Gene: ENSMUSG00000030067 AA Change: Q42*
Domain | Start | End | E-Value | Type |
low complexity region
|
10 |
62 |
N/A |
INTRINSIC |
low complexity region
|
71 |
105 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000176565
AA Change: Q171*
|
SMART Domains |
Protein: ENSMUSP00000135181 Gene: ENSMUSG00000030067 AA Change: Q171*
Domain | Start | End | E-Value | Type |
coiled coil region
|
62 |
113 |
N/A |
INTRINSIC |
low complexity region
|
140 |
191 |
N/A |
INTRINSIC |
low complexity region
|
200 |
234 |
N/A |
INTRINSIC |
low complexity region
|
237 |
251 |
N/A |
INTRINSIC |
low complexity region
|
265 |
276 |
N/A |
INTRINSIC |
low complexity region
|
318 |
331 |
N/A |
INTRINSIC |
ZnF_C2H2
|
335 |
360 |
8.67e-1 |
SMART |
low complexity region
|
372 |
384 |
N/A |
INTRINSIC |
low complexity region
|
433 |
447 |
N/A |
INTRINSIC |
FH
|
491 |
572 |
2.07e-39 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000176632
AA Change: Q139*
|
SMART Domains |
Protein: ENSMUSP00000135635 Gene: ENSMUSG00000030067 AA Change: Q139*
Domain | Start | End | E-Value | Type |
low complexity region
|
108 |
159 |
N/A |
INTRINSIC |
low complexity region
|
168 |
202 |
N/A |
INTRINSIC |
low complexity region
|
205 |
219 |
N/A |
INTRINSIC |
low complexity region
|
233 |
244 |
N/A |
INTRINSIC |
low complexity region
|
286 |
299 |
N/A |
INTRINSIC |
ZnF_C2H2
|
303 |
328 |
8.67e-1 |
SMART |
low complexity region
|
340 |
352 |
N/A |
INTRINSIC |
low complexity region
|
401 |
415 |
N/A |
INTRINSIC |
FH
|
460 |
541 |
2.07e-39 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000176850
AA Change: Q140*
|
SMART Domains |
Protein: ENSMUSP00000135041 Gene: ENSMUSG00000030067 AA Change: Q140*
Domain | Start | End | E-Value | Type |
low complexity region
|
108 |
160 |
N/A |
INTRINSIC |
low complexity region
|
169 |
203 |
N/A |
INTRINSIC |
low complexity region
|
206 |
220 |
N/A |
INTRINSIC |
low complexity region
|
234 |
245 |
N/A |
INTRINSIC |
low complexity region
|
287 |
300 |
N/A |
INTRINSIC |
ZnF_C2H2
|
304 |
329 |
8.67e-1 |
SMART |
low complexity region
|
341 |
353 |
N/A |
INTRINSIC |
low complexity region
|
402 |
416 |
N/A |
INTRINSIC |
FH
|
461 |
542 |
2.07e-39 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000177229
AA Change: Q42*
|
SMART Domains |
Protein: ENSMUSP00000134817 Gene: ENSMUSG00000030067 AA Change: Q42*
Domain | Start | End | E-Value | Type |
low complexity region
|
10 |
62 |
N/A |
INTRINSIC |
low complexity region
|
71 |
105 |
N/A |
INTRINSIC |
low complexity region
|
108 |
122 |
N/A |
INTRINSIC |
low complexity region
|
136 |
147 |
N/A |
INTRINSIC |
low complexity region
|
189 |
202 |
N/A |
INTRINSIC |
ZnF_C2H2
|
206 |
231 |
8.67e-1 |
SMART |
low complexity region
|
243 |
255 |
N/A |
INTRINSIC |
low complexity region
|
304 |
318 |
N/A |
INTRINSIC |
FH
|
363 |
444 |
2.07e-39 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000177230
AA Change: Q140*
|
SMART Domains |
Protein: ENSMUSP00000135098 Gene: ENSMUSG00000030067 AA Change: Q140*
Domain | Start | End | E-Value | Type |
low complexity region
|
108 |
160 |
N/A |
INTRINSIC |
low complexity region
|
169 |
203 |
N/A |
INTRINSIC |
low complexity region
|
206 |
220 |
N/A |
INTRINSIC |
low complexity region
|
234 |
245 |
N/A |
INTRINSIC |
low complexity region
|
287 |
300 |
N/A |
INTRINSIC |
ZnF_C2H2
|
304 |
329 |
8.67e-1 |
SMART |
low complexity region
|
341 |
353 |
N/A |
INTRINSIC |
low complexity region
|
402 |
416 |
N/A |
INTRINSIC |
FH
|
461 |
542 |
2.07e-39 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000177307
AA Change: Q172*
|
SMART Domains |
Protein: ENSMUSP00000135764 Gene: ENSMUSG00000030067 AA Change: Q172*
Domain | Start | End | E-Value | Type |
coiled coil region
|
62 |
113 |
N/A |
INTRINSIC |
low complexity region
|
140 |
192 |
N/A |
INTRINSIC |
low complexity region
|
201 |
235 |
N/A |
INTRINSIC |
low complexity region
|
238 |
252 |
N/A |
INTRINSIC |
low complexity region
|
266 |
277 |
N/A |
INTRINSIC |
low complexity region
|
319 |
332 |
N/A |
INTRINSIC |
ZnF_C2H2
|
336 |
361 |
8.67e-1 |
SMART |
low complexity region
|
373 |
385 |
N/A |
INTRINSIC |
low complexity region
|
434 |
448 |
N/A |
INTRINSIC |
FH
|
492 |
573 |
2.07e-39 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000177437
AA Change: Q41*
|
SMART Domains |
Protein: ENSMUSP00000135809 Gene: ENSMUSG00000030067 AA Change: Q41*
Domain | Start | End | E-Value | Type |
low complexity region
|
10 |
61 |
N/A |
INTRINSIC |
low complexity region
|
70 |
104 |
N/A |
INTRINSIC |
low complexity region
|
107 |
121 |
N/A |
INTRINSIC |
low complexity region
|
135 |
146 |
N/A |
INTRINSIC |
low complexity region
|
188 |
201 |
N/A |
INTRINSIC |
ZnF_C2H2
|
205 |
230 |
8.67e-1 |
SMART |
low complexity region
|
242 |
254 |
N/A |
INTRINSIC |
low complexity region
|
303 |
317 |
N/A |
INTRINSIC |
FH
|
362 |
443 |
2.07e-39 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000177507
AA Change: Q41*
|
SMART Domains |
Protein: ENSMUSP00000134869 Gene: ENSMUSG00000030067 AA Change: Q41*
Domain | Start | End | E-Value | Type |
low complexity region
|
10 |
61 |
N/A |
INTRINSIC |
low complexity region
|
70 |
104 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000175670
|
Meta Mutation Damage Score |
0.9755 |
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.3%
- 20x: 95.2%
|
Validation Efficiency |
96% (52/54) |
MGI Phenotype |
PHENOTYPE: Homozygous null mice display embryonic lethality with abnormal outflow tract septation, ventricular septal defects, abnormal cardiac valve morphology, decreased and irregular heart rate, thin ventricular compact zone, and edema. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ank2 |
T |
C |
3: 126,846,395 (GRCm39) |
D219G |
probably damaging |
Het |
Arap2 |
A |
T |
5: 62,906,965 (GRCm39) |
I18N |
probably damaging |
Het |
Baz1b |
T |
C |
5: 135,271,361 (GRCm39) |
S1315P |
probably benign |
Het |
Bbs7 |
A |
T |
3: 36,646,523 (GRCm39) |
C432* |
probably null |
Het |
Bend3 |
A |
G |
10: 43,385,864 (GRCm39) |
T86A |
probably benign |
Het |
Cadm2 |
C |
T |
16: 66,679,729 (GRCm39) |
V35I |
probably benign |
Het |
Ch25h |
A |
G |
19: 34,451,896 (GRCm39) |
S211P |
probably damaging |
Het |
Chd5 |
A |
T |
4: 152,463,848 (GRCm39) |
H1476L |
probably damaging |
Het |
Chia1 |
T |
C |
3: 106,036,338 (GRCm39) |
|
probably null |
Het |
Clpx |
C |
A |
9: 65,209,161 (GRCm39) |
S92* |
probably null |
Het |
Dazl |
A |
T |
17: 50,594,599 (GRCm39) |
M152K |
probably benign |
Het |
Dnah17 |
A |
G |
11: 117,930,772 (GRCm39) |
S3748P |
probably damaging |
Het |
Dock2 |
T |
C |
11: 34,212,388 (GRCm39) |
K1251R |
probably null |
Het |
Esr1 |
T |
C |
10: 4,696,760 (GRCm39) |
V203A |
probably damaging |
Het |
F830045P16Rik |
A |
G |
2: 129,305,588 (GRCm39) |
I262T |
probably damaging |
Het |
Fshb |
T |
C |
2: 106,887,638 (GRCm39) |
E127G |
possibly damaging |
Het |
Galk2 |
A |
G |
2: 125,701,137 (GRCm39) |
|
probably benign |
Het |
Gid4 |
A |
G |
11: 60,323,241 (GRCm39) |
D111G |
probably damaging |
Het |
Gm14412 |
G |
A |
2: 177,006,330 (GRCm39) |
P522S |
probably damaging |
Het |
Iqank1 |
A |
G |
15: 75,917,237 (GRCm39) |
E290G |
probably damaging |
Het |
Mfap4 |
A |
G |
11: 61,376,245 (GRCm39) |
|
probably null |
Het |
Mfsd2a |
A |
G |
4: 122,845,039 (GRCm39) |
V224A |
probably benign |
Het |
Mocos |
A |
T |
18: 24,809,639 (GRCm39) |
Y414F |
probably benign |
Het |
Mrto4 |
T |
C |
4: 139,077,755 (GRCm39) |
I27V |
probably benign |
Het |
Muc4 |
A |
G |
16: 32,554,958 (GRCm39) |
|
probably benign |
Het |
Mug1 |
T |
A |
6: 121,840,752 (GRCm39) |
I534N |
probably damaging |
Het |
Mup20 |
A |
T |
4: 61,972,267 (GRCm39) |
L7Q |
unknown |
Het |
Nlrp2 |
T |
C |
7: 5,340,808 (GRCm39) |
E2G |
probably damaging |
Het |
Or11g1 |
A |
G |
14: 50,651,654 (GRCm39) |
I218V |
possibly damaging |
Het |
Or12k7 |
A |
G |
2: 36,959,091 (GRCm39) |
Y258C |
possibly damaging |
Het |
Or2y16 |
T |
C |
11: 49,335,299 (GRCm39) |
V207A |
probably benign |
Het |
Or6z5 |
C |
T |
7: 6,477,835 (GRCm39) |
A242V |
probably damaging |
Het |
Parn |
T |
C |
16: 13,469,675 (GRCm39) |
T209A |
possibly damaging |
Het |
Psip1 |
T |
A |
4: 83,391,286 (GRCm39) |
|
probably null |
Het |
Ptprc |
A |
C |
1: 137,995,628 (GRCm39) |
C1157G |
probably damaging |
Het |
Rad17 |
A |
C |
13: 100,759,389 (GRCm39) |
V546G |
probably benign |
Het |
Rc3h2 |
GCC |
GCCC |
2: 37,304,745 (GRCm39) |
|
probably null |
Het |
Safb |
A |
G |
17: 56,904,798 (GRCm39) |
E124G |
probably damaging |
Het |
Sart3 |
C |
T |
5: 113,881,267 (GRCm39) |
A938T |
probably benign |
Het |
Skint5 |
T |
C |
4: 113,392,907 (GRCm39) |
T1242A |
unknown |
Het |
Slc13a5 |
C |
T |
11: 72,144,023 (GRCm39) |
E352K |
probably benign |
Het |
Sohlh2 |
G |
T |
3: 55,104,419 (GRCm39) |
V263F |
probably benign |
Het |
Strn |
A |
G |
17: 79,008,298 (GRCm39) |
Y107H |
probably damaging |
Het |
Tbx15 |
G |
T |
3: 99,161,203 (GRCm39) |
E3* |
probably null |
Het |
Tespa1 |
A |
G |
10: 130,183,172 (GRCm39) |
D39G |
probably benign |
Het |
Trp73 |
A |
T |
4: 154,188,798 (GRCm39) |
D54E |
probably damaging |
Het |
Ttll5 |
A |
T |
12: 85,980,151 (GRCm39) |
S912C |
probably damaging |
Het |
Utp14b |
A |
T |
1: 78,643,554 (GRCm39) |
D484V |
probably benign |
Het |
Utp14b |
A |
C |
1: 78,643,557 (GRCm39) |
N485T |
probably benign |
Het |
Vmn2r29 |
T |
C |
7: 7,234,369 (GRCm39) |
E839G |
probably benign |
Het |
Vmn2r6 |
G |
C |
3: 64,467,176 (GRCm39) |
P108A |
probably damaging |
Het |
Vps8 |
T |
G |
16: 21,314,682 (GRCm39) |
|
probably null |
Het |
Zfp36l1 |
A |
T |
12: 80,156,320 (GRCm39) |
|
probably null |
Het |
Zfp998 |
T |
A |
13: 66,579,608 (GRCm39) |
T292S |
probably benign |
Het |
Zp3r |
A |
T |
1: 130,519,305 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Foxp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02191:Foxp1
|
APN |
6 |
98,922,561 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02330:Foxp1
|
APN |
6 |
98,922,373 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02869:Foxp1
|
APN |
6 |
98,907,044 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02968:Foxp1
|
APN |
6 |
99,052,822 (GRCm39) |
missense |
probably damaging |
1.00 |
Foxy
|
UTSW |
6 |
98,992,471 (GRCm39) |
nonsense |
probably null |
|
Moxie
|
UTSW |
6 |
98,992,475 (GRCm39) |
critical splice acceptor site |
probably null |
|
Roxie
|
UTSW |
6 |
98,918,595 (GRCm39) |
missense |
unknown |
|
R0037:Foxp1
|
UTSW |
6 |
99,139,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Foxp1
|
UTSW |
6 |
98,921,684 (GRCm39) |
splice site |
probably benign |
|
R0063:Foxp1
|
UTSW |
6 |
98,921,684 (GRCm39) |
splice site |
probably benign |
|
R0427:Foxp1
|
UTSW |
6 |
98,907,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Foxp1
|
UTSW |
6 |
98,907,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R1356:Foxp1
|
UTSW |
6 |
98,993,637 (GRCm39) |
splice site |
probably benign |
|
R1468:Foxp1
|
UTSW |
6 |
98,955,181 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1468:Foxp1
|
UTSW |
6 |
98,955,181 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1548:Foxp1
|
UTSW |
6 |
98,922,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R1696:Foxp1
|
UTSW |
6 |
98,922,663 (GRCm39) |
missense |
probably benign |
0.18 |
R1933:Foxp1
|
UTSW |
6 |
99,052,926 (GRCm39) |
small deletion |
probably benign |
|
R2152:Foxp1
|
UTSW |
6 |
98,993,502 (GRCm39) |
missense |
probably damaging |
0.99 |
R2338:Foxp1
|
UTSW |
6 |
98,980,254 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3896:Foxp1
|
UTSW |
6 |
99,052,897 (GRCm39) |
missense |
probably benign |
0.33 |
R5006:Foxp1
|
UTSW |
6 |
99,139,819 (GRCm39) |
missense |
probably damaging |
0.98 |
R5143:Foxp1
|
UTSW |
6 |
98,922,493 (GRCm39) |
critical splice donor site |
probably null |
|
R5428:Foxp1
|
UTSW |
6 |
98,993,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5765:Foxp1
|
UTSW |
6 |
98,992,423 (GRCm39) |
missense |
probably damaging |
0.99 |
R5816:Foxp1
|
UTSW |
6 |
99,052,926 (GRCm39) |
small deletion |
probably benign |
|
R6172:Foxp1
|
UTSW |
6 |
98,992,475 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6172:Foxp1
|
UTSW |
6 |
98,992,471 (GRCm39) |
nonsense |
probably null |
|
R6173:Foxp1
|
UTSW |
6 |
98,992,475 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6175:Foxp1
|
UTSW |
6 |
98,943,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6776:Foxp1
|
UTSW |
6 |
99,052,926 (GRCm39) |
small deletion |
probably benign |
|
R6782:Foxp1
|
UTSW |
6 |
98,907,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R7229:Foxp1
|
UTSW |
6 |
98,912,373 (GRCm39) |
missense |
unknown |
|
R7559:Foxp1
|
UTSW |
6 |
98,922,521 (GRCm39) |
missense |
unknown |
|
R7715:Foxp1
|
UTSW |
6 |
98,922,621 (GRCm39) |
missense |
unknown |
|
R8007:Foxp1
|
UTSW |
6 |
98,918,595 (GRCm39) |
missense |
unknown |
|
R8099:Foxp1
|
UTSW |
6 |
98,922,510 (GRCm39) |
missense |
unknown |
|
R8317:Foxp1
|
UTSW |
6 |
99,052,866 (GRCm39) |
small deletion |
probably benign |
|
R8408:Foxp1
|
UTSW |
6 |
98,922,543 (GRCm39) |
missense |
unknown |
|
R8704:Foxp1
|
UTSW |
6 |
98,993,507 (GRCm39) |
missense |
unknown |
|
R8705:Foxp1
|
UTSW |
6 |
98,993,507 (GRCm39) |
missense |
unknown |
|
R9014:Foxp1
|
UTSW |
6 |
99,052,866 (GRCm39) |
small deletion |
probably benign |
|
R9147:Foxp1
|
UTSW |
6 |
99,052,866 (GRCm39) |
small deletion |
probably benign |
|
R9399:Foxp1
|
UTSW |
6 |
99,052,866 (GRCm39) |
small deletion |
probably benign |
|
R9604:Foxp1
|
UTSW |
6 |
99,052,926 (GRCm39) |
small deletion |
probably benign |
|
X0066:Foxp1
|
UTSW |
6 |
99,052,976 (GRCm39) |
nonsense |
probably null |
|
Z1177:Foxp1
|
UTSW |
6 |
98,955,122 (GRCm39) |
missense |
unknown |
|
|
Predicted Primers |
PCR Primer
(F):5'- CAATAACTCTCCGTCTGAAAGC -3'
(R):5'- CAAGAATAGTCAGTGTGCGTGG -3'
Sequencing Primer
(F):5'- CCGATAGAGTCAGCTGAGTTG -3'
(R):5'- GGAATTTATTGTCCGGTTTCAAAG -3'
|
Posted On |
2017-10-10 |