Incidental Mutation 'IGL01011:Foxp2'
| ID |
53610 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Foxp2
|
| Ensembl Gene |
ENSMUSG00000029563 |
| Gene Name |
forkhead box P2 |
| Synonyms |
D0Kist7, 2810043D05Rik |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL01011
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
6 |
| Chromosomal Location |
14901348-15441976 bp(+) (GRCm39) |
| Type of Mutation |
makesense |
| DNA Base Change (assembly) |
T to A
at 15438018 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Stop codon to Arginine
at position 715
(*715R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000111137
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000031545]
[ENSMUST00000115472]
[ENSMUST00000115474]
[ENSMUST00000115475]
[ENSMUST00000115477]
|
| AlphaFold |
P58463 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000031545
AA Change: *715R
|
| SMART Domains |
Protein: ENSMUSP00000031545
Gene: ENSMUSG00000029563
AA Change: *715R
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
30 |
42 |
N/A |
INTRINSIC |
|
low complexity region
|
49 |
69 |
N/A |
INTRINSIC |
|
coiled coil region
|
140 |
215 |
N/A |
INTRINSIC |
|
low complexity region
|
291 |
304 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
345 |
370 |
3.02e0 |
SMART |
|
low complexity region
|
437 |
458 |
N/A |
INTRINSIC |
|
FH
|
501 |
582 |
7.5e-37 |
SMART |
|
low complexity region
|
605 |
624 |
N/A |
INTRINSIC |
|
low complexity region
|
697 |
714 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000115472
AA Change: *694R
|
| SMART Domains |
Protein: ENSMUSP00000111132
Gene: ENSMUSG00000029563
AA Change: *694R
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
30 |
42 |
N/A |
INTRINSIC |
|
low complexity region
|
49 |
69 |
N/A |
INTRINSIC |
|
coiled coil region
|
116 |
194 |
N/A |
INTRINSIC |
|
low complexity region
|
270 |
283 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
324 |
349 |
3.02e0 |
SMART |
|
low complexity region
|
416 |
437 |
N/A |
INTRINSIC |
|
FH
|
480 |
561 |
7.5e-37 |
SMART |
|
low complexity region
|
584 |
603 |
N/A |
INTRINSIC |
|
low complexity region
|
676 |
693 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000115474
AA Change: *740R
|
| SMART Domains |
Protein: ENSMUSP00000111134
Gene: ENSMUSG00000029563
AA Change: *740R
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
30 |
42 |
N/A |
INTRINSIC |
|
low complexity region
|
49 |
69 |
N/A |
INTRINSIC |
|
coiled coil region
|
165 |
240 |
N/A |
INTRINSIC |
|
low complexity region
|
316 |
329 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
370 |
395 |
3.02e0 |
SMART |
|
low complexity region
|
462 |
483 |
N/A |
INTRINSIC |
|
FH
|
526 |
607 |
7.5e-37 |
SMART |
|
low complexity region
|
630 |
649 |
N/A |
INTRINSIC |
|
low complexity region
|
722 |
739 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000115475
|
| SMART Domains |
Protein: ENSMUSP00000111135
Gene: ENSMUSG00000029563
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
8 |
46 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000115477
AA Change: *715R
|
| SMART Domains |
Protein: ENSMUSP00000111137
Gene: ENSMUSG00000029563
AA Change: *715R
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
30 |
42 |
N/A |
INTRINSIC |
|
low complexity region
|
49 |
69 |
N/A |
INTRINSIC |
|
coiled coil region
|
140 |
215 |
N/A |
INTRINSIC |
|
low complexity region
|
291 |
304 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
345 |
370 |
3.02e0 |
SMART |
|
low complexity region
|
437 |
458 |
N/A |
INTRINSIC |
|
FH
|
501 |
582 |
7.5e-37 |
SMART |
|
low complexity region
|
605 |
624 |
N/A |
INTRINSIC |
|
low complexity region
|
697 |
714 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Homozygous null mice display postnatal lethality, growth retardation, reduced vocalization, prolonged external granule cell layer presence, abnormal Purkinje and radial glial cells, delayed eye opening and ear emergence, negative geotaxis, impaired righting response, and hypoactivity. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 58 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700017B05Rik |
A |
T |
9: 57,165,529 (GRCm39) |
C282S |
probably damaging |
Het |
| Abca12 |
T |
C |
1: 71,302,791 (GRCm39) |
I2143V |
probably benign |
Het |
| Adgrg6 |
A |
C |
10: 14,285,542 (GRCm39) |
I1148S |
probably damaging |
Het |
| Aox4 |
C |
T |
1: 58,279,934 (GRCm39) |
R517* |
probably null |
Het |
| Arnt2 |
T |
A |
7: 83,935,037 (GRCm39) |
D289V |
probably benign |
Het |
| Atad2b |
A |
G |
12: 5,015,984 (GRCm39) |
N570S |
probably benign |
Het |
| Aven |
G |
A |
2: 112,460,130 (GRCm39) |
D208N |
possibly damaging |
Het |
| Bcl9l |
A |
G |
9: 44,416,476 (GRCm39) |
D183G |
possibly damaging |
Het |
| Cd300lf |
A |
G |
11: 115,015,159 (GRCm39) |
S144P |
probably benign |
Het |
| Chd8 |
C |
A |
14: 52,468,989 (GRCm39) |
G543V |
possibly damaging |
Het |
| Chrm2 |
A |
G |
6: 36,501,373 (GRCm39) |
N410S |
probably benign |
Het |
| Clip4 |
A |
G |
17: 72,156,934 (GRCm39) |
I590V |
probably benign |
Het |
| Cnbp |
C |
T |
6: 87,822,682 (GRCm39) |
R27H |
probably benign |
Het |
| Col4a3 |
T |
C |
1: 82,660,022 (GRCm39) |
V889A |
unknown |
Het |
| Cxcl5 |
T |
C |
5: 90,908,382 (GRCm39) |
|
probably benign |
Het |
| Dennd6a |
G |
T |
14: 26,324,209 (GRCm39) |
V171F |
probably damaging |
Het |
| Dhx38 |
T |
C |
8: 110,289,323 (GRCm39) |
I26V |
probably benign |
Het |
| Dscaml1 |
A |
G |
9: 45,594,970 (GRCm39) |
D691G |
possibly damaging |
Het |
| Etfdh |
A |
T |
3: 79,519,368 (GRCm39) |
|
probably benign |
Het |
| Fbn2 |
G |
A |
18: 58,228,312 (GRCm39) |
|
probably benign |
Het |
| Ftl1 |
A |
T |
7: 45,108,070 (GRCm39) |
D65E |
probably benign |
Het |
| Galm |
A |
G |
17: 80,490,709 (GRCm39) |
T289A |
probably benign |
Het |
| Gm20721 |
A |
G |
2: 174,187,531 (GRCm39) |
D1049G |
probably damaging |
Het |
| Gm28778 |
T |
C |
1: 53,338,277 (GRCm39) |
V47A |
probably benign |
Het |
| Gm5414 |
T |
C |
15: 101,536,569 (GRCm39) |
S19G |
probably benign |
Het |
| H1f6 |
C |
T |
13: 23,880,032 (GRCm39) |
L62F |
probably damaging |
Het |
| Hdac7 |
T |
A |
15: 97,691,816 (GRCm39) |
E835D |
possibly damaging |
Het |
| Hspg2 |
C |
T |
4: 137,286,646 (GRCm39) |
T3663I |
probably damaging |
Het |
| Kdm4d |
A |
T |
9: 14,375,515 (GRCm39) |
D114E |
probably benign |
Het |
| Kif5a |
A |
T |
10: 127,075,065 (GRCm39) |
V516E |
probably benign |
Het |
| Lrrtm1 |
A |
G |
6: 77,221,218 (GRCm39) |
|
probably null |
Het |
| Miga1 |
G |
T |
3: 151,982,327 (GRCm39) |
T519K |
probably benign |
Het |
| Mtfr1l |
G |
A |
4: 134,256,511 (GRCm39) |
P182S |
probably damaging |
Het |
| Myo15a |
A |
G |
11: 60,367,818 (GRCm39) |
I193V |
probably benign |
Het |
| Myo1e |
T |
C |
9: 70,223,871 (GRCm39) |
|
probably benign |
Het |
| Or13a26 |
A |
T |
7: 140,284,350 (GRCm39) |
Y62F |
probably damaging |
Het |
| Or1e1c |
A |
T |
11: 73,265,833 (GRCm39) |
Q86L |
probably benign |
Het |
| Or5h22 |
T |
A |
16: 58,894,793 (GRCm39) |
T217S |
probably benign |
Het |
| Pias1 |
T |
C |
9: 62,820,137 (GRCm39) |
T277A |
probably benign |
Het |
| Skic3 |
G |
A |
13: 76,270,784 (GRCm39) |
C127Y |
probably damaging |
Het |
| Slamf6 |
T |
A |
1: 171,765,666 (GRCm39) |
H263Q |
probably benign |
Het |
| Snrnp48 |
A |
G |
13: 38,404,740 (GRCm39) |
D202G |
probably damaging |
Het |
| Snx13 |
T |
A |
12: 35,148,279 (GRCm39) |
D269E |
probably damaging |
Het |
| Tiam2 |
A |
T |
17: 3,465,303 (GRCm39) |
D344V |
probably benign |
Het |
| Tmem62 |
G |
T |
2: 120,809,700 (GRCm39) |
K127N |
possibly damaging |
Het |
| Trav15-1-dv6-1 |
C |
T |
14: 53,797,492 (GRCm39) |
T46I |
possibly damaging |
Het |
| Trav16d-dv11 |
C |
T |
14: 53,285,041 (GRCm39) |
T39M |
possibly damaging |
Het |
| Trio |
T |
C |
15: 27,736,575 (GRCm39) |
D2794G |
probably damaging |
Het |
| Trpc7 |
C |
T |
13: 56,952,353 (GRCm39) |
G551D |
probably damaging |
Het |
| Ttn |
A |
G |
2: 76,644,634 (GRCm39) |
V11294A |
possibly damaging |
Het |
| Ubap2 |
G |
A |
4: 41,195,328 (GRCm39) |
|
probably benign |
Het |
| Ubap2l |
G |
A |
3: 89,916,563 (GRCm39) |
Q915* |
probably null |
Het |
| Ubfd1 |
A |
G |
7: 121,677,695 (GRCm39) |
E340G |
probably benign |
Het |
| Vil1 |
T |
C |
1: 74,474,046 (GRCm39) |
|
probably null |
Het |
| Vmn1r6 |
T |
G |
6: 56,979,529 (GRCm39) |
L42V |
probably benign |
Het |
| Vps13c |
A |
G |
9: 67,834,237 (GRCm39) |
T1635A |
probably damaging |
Het |
| Zfhx3 |
T |
A |
8: 109,520,226 (GRCm39) |
H449Q |
probably benign |
Het |
| Zfp750 |
A |
T |
11: 121,403,922 (GRCm39) |
S318T |
probably benign |
Het |
|
| Other mutations in Foxp2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00515:Foxp2
|
APN |
6 |
15,403,818 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01412:Foxp2
|
APN |
6 |
15,376,757 (GRCm39) |
intron |
probably benign |
|
|
IGL01769:Foxp2
|
APN |
6 |
15,409,834 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
IGL02578:Foxp2
|
APN |
6 |
15,376,814 (GRCm39) |
intron |
probably benign |
|
|
IGL03368:Foxp2
|
APN |
6 |
15,394,717 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0004:Foxp2
|
UTSW |
6 |
15,197,095 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R0081:Foxp2
|
UTSW |
6 |
15,405,643 (GRCm39) |
critical splice donor site |
probably benign |
|
|
R0095:Foxp2
|
UTSW |
6 |
15,196,976 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0233:Foxp2
|
UTSW |
6 |
15,409,752 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0294:Foxp2
|
UTSW |
6 |
15,376,773 (GRCm39) |
intron |
probably benign |
|
|
R0357:Foxp2
|
UTSW |
6 |
15,409,839 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0432:Foxp2
|
UTSW |
6 |
15,254,278 (GRCm39) |
intron |
probably benign |
|
|
R0659:Foxp2
|
UTSW |
6 |
15,254,278 (GRCm39) |
intron |
probably benign |
|
|
R1381:Foxp2
|
UTSW |
6 |
15,409,765 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R1813:Foxp2
|
UTSW |
6 |
15,379,767 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R1896:Foxp2
|
UTSW |
6 |
15,379,767 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R2007:Foxp2
|
UTSW |
6 |
15,396,818 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2020:Foxp2
|
UTSW |
6 |
15,324,643 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R2167:Foxp2
|
UTSW |
6 |
15,437,901 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2326:Foxp2
|
UTSW |
6 |
15,409,938 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R3829:Foxp2
|
UTSW |
6 |
15,379,830 (GRCm39) |
unclassified |
probably benign |
|
|
R3978:Foxp2
|
UTSW |
6 |
15,197,207 (GRCm39) |
unclassified |
probably benign |
|
|
R4393:Foxp2
|
UTSW |
6 |
15,377,689 (GRCm39) |
intron |
probably benign |
|
|
R4703:Foxp2
|
UTSW |
6 |
15,411,247 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5202:Foxp2
|
UTSW |
6 |
15,394,770 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5303:Foxp2
|
UTSW |
6 |
15,324,636 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5368:Foxp2
|
UTSW |
6 |
15,377,913 (GRCm39) |
intron |
probably benign |
|
|
R5533:Foxp2
|
UTSW |
6 |
15,197,119 (GRCm39) |
nonsense |
probably null |
|
|
R5655:Foxp2
|
UTSW |
6 |
15,197,112 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6220:Foxp2
|
UTSW |
6 |
15,437,947 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6241:Foxp2
|
UTSW |
6 |
15,394,761 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6365:Foxp2
|
UTSW |
6 |
15,286,684 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6384:Foxp2
|
UTSW |
6 |
15,437,947 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7217:Foxp2
|
UTSW |
6 |
15,416,023 (GRCm39) |
missense |
unknown |
|
|
R7553:Foxp2
|
UTSW |
6 |
15,437,881 (GRCm39) |
missense |
unknown |
|
|
R7881:Foxp2
|
UTSW |
6 |
15,409,888 (GRCm39) |
missense |
unknown |
|
|
R8420:Foxp2
|
UTSW |
6 |
15,403,866 (GRCm39) |
missense |
unknown |
|
|
R8865:Foxp2
|
UTSW |
6 |
15,415,093 (GRCm39) |
missense |
unknown |
|
|
R9147:Foxp2
|
UTSW |
6 |
15,286,711 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R9148:Foxp2
|
UTSW |
6 |
15,286,711 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R9290:Foxp2
|
UTSW |
6 |
15,197,120 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R9373:Foxp2
|
UTSW |
6 |
15,377,969 (GRCm39) |
missense |
unknown |
|
|
X0023:Foxp2
|
UTSW |
6 |
15,409,834 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-06-28 |
Incidental Mutation