Incidental Mutation 'R4732:Akap9'
| ID |
359052 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Akap9
|
| Ensembl Gene |
ENSMUSG00000040407 |
| Gene Name |
A kinase (PRKA) anchor protein (yotiao) 9 |
| Synonyms |
AKAP450, G1-448-15, 5730481H23Rik, mei2-5, repro12 |
| MMRRC Submission |
042022-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.327)
|
| Stock # |
R4732 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
5 |
| Chromosomal Location |
3928054-4081310 bp(+) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 4013901 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 1750
(D1750G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000046129
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044492]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000044492
AA Change: D1750G
PolyPhen 2
Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000046129
Gene: ENSMUSG00000040407
AA Change: D1750G
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
9 |
18 |
N/A |
INTRINSIC |
|
low complexity region
|
33 |
44 |
N/A |
INTRINSIC |
|
low complexity region
|
98 |
115 |
N/A |
INTRINSIC |
|
Blast:HPT
|
126 |
197 |
6e-21 |
BLAST |
|
low complexity region
|
237 |
249 |
N/A |
INTRINSIC |
|
low complexity region
|
297 |
315 |
N/A |
INTRINSIC |
|
coiled coil region
|
404 |
593 |
N/A |
INTRINSIC |
|
coiled coil region
|
622 |
756 |
N/A |
INTRINSIC |
|
coiled coil region
|
777 |
843 |
N/A |
INTRINSIC |
|
coiled coil region
|
888 |
958 |
N/A |
INTRINSIC |
|
low complexity region
|
982 |
997 |
N/A |
INTRINSIC |
|
coiled coil region
|
1037 |
1065 |
N/A |
INTRINSIC |
|
low complexity region
|
1233 |
1246 |
N/A |
INTRINSIC |
|
internal_repeat_2
|
1247 |
1312 |
7.75e-5 |
PROSPERO |
|
internal_repeat_1
|
1377 |
1485 |
2.63e-5 |
PROSPERO |
|
coiled coil region
|
1522 |
1589 |
N/A |
INTRINSIC |
|
coiled coil region
|
1789 |
2107 |
N/A |
INTRINSIC |
|
coiled coil region
|
2132 |
2318 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
2322 |
2445 |
2.63e-5 |
PROSPERO |
|
coiled coil region
|
2455 |
2494 |
N/A |
INTRINSIC |
|
low complexity region
|
2587 |
2598 |
N/A |
INTRINSIC |
|
low complexity region
|
2627 |
2640 |
N/A |
INTRINSIC |
|
internal_repeat_2
|
2934 |
2997 |
7.75e-5 |
PROSPERO |
|
low complexity region
|
3000 |
3016 |
N/A |
INTRINSIC |
|
coiled coil region
|
3109 |
3307 |
N/A |
INTRINSIC |
|
coiled coil region
|
3455 |
3493 |
N/A |
INTRINSIC |
|
coiled coil region
|
3521 |
3556 |
N/A |
INTRINSIC |
|
Pfam:PACT_coil_coil
|
3576 |
3657 |
1.2e-27 |
PFAM |
|
| Meta Mutation Damage Score |
0.3211 |
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.2%
- 20x: 95.1%
|
| Validation Efficiency |
99% (110/111) |
| MGI Phenotype |
PHENOTYPE: Mice homozygous for a chemically induced allele exhibit male infertily with abnormal spermatogenesis and Sertoli maturation. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 192 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700128F08Rik |
T |
A |
9: 8,222,173 (GRCm38) |
|
noncoding transcript |
Het |
| 3110035E14Rik |
T |
C |
1: 9,606,976 (GRCm38) |
S24P |
probably benign |
Het |
| 4933409G03Rik |
A |
G |
2: 68,614,721 (GRCm38) |
|
probably benign |
Het |
| Acan |
T |
C |
7: 79,098,609 (GRCm38) |
S1043P |
probably damaging |
Het |
| Ackr2 |
A |
G |
9: 121,909,183 (GRCm38) |
Y208C |
probably damaging |
Het |
| Actg1 |
C |
T |
11: 120,347,479 (GRCm38) |
|
probably benign |
Het |
| Adam1a |
T |
A |
5: 121,519,434 (GRCm38) |
T599S |
probably benign |
Het |
| Adamts12 |
A |
T |
15: 11,270,662 (GRCm38) |
S668C |
probably damaging |
Het |
| Adcy8 |
A |
G |
15: 64,754,862 (GRCm38) |
V709A |
possibly damaging |
Het |
| Adgrf2 |
A |
C |
17: 42,710,754 (GRCm38) |
I393S |
probably damaging |
Het |
| Ahnak |
G |
T |
19: 9,007,301 (GRCm38) |
G1983V |
probably damaging |
Het |
| AI413582 |
A |
G |
17: 27,565,270 (GRCm38) |
|
probably benign |
Het |
| Aim2 |
T |
A |
1: 173,463,876 (GRCm38) |
D282E |
possibly damaging |
Het |
| Ak8 |
A |
G |
2: 28,760,071 (GRCm38) |
Y370C |
probably damaging |
Het |
| Als2cl |
T |
A |
9: 110,889,136 (GRCm38) |
V315E |
probably damaging |
Het |
| Ankrd28 |
A |
C |
14: 31,755,741 (GRCm38) |
C115G |
probably benign |
Het |
| Ap3b2 |
C |
T |
7: 81,471,932 (GRCm38) |
A519T |
probably damaging |
Het |
| Apool |
C |
T |
X: 112,372,200 (GRCm38) |
T166I |
probably damaging |
Het |
| Arhgef2 |
A |
T |
3: 88,631,940 (GRCm38) |
K65* |
probably null |
Het |
| Arhgef38 |
G |
T |
3: 133,132,269 (GRCm38) |
Y633* |
probably null |
Het |
| Asah2 |
T |
C |
19: 31,995,358 (GRCm38) |
N659S |
probably benign |
Het |
| Atf7ip2 |
A |
G |
16: 10,241,886 (GRCm38) |
D430G |
possibly damaging |
Het |
| Atp8a1 |
G |
A |
5: 67,813,120 (GRCm38) |
S92L |
probably benign |
Het |
| Bag4 |
C |
T |
8: 25,769,488 (GRCm38) |
A228T |
probably benign |
Het |
| BC024978 |
T |
A |
7: 27,201,043 (GRCm38) |
M149K |
probably damaging |
Het |
| C130073F10Rik |
C |
A |
4: 101,890,710 (GRCm38) |
S89I |
probably benign |
Het |
| Cacna1g |
T |
C |
11: 94,443,215 (GRCm38) |
T867A |
probably damaging |
Het |
| Ccdc88a |
T |
G |
11: 29,485,906 (GRCm38) |
N1276K |
probably benign |
Het |
| Cdc42bpg |
T |
A |
19: 6,311,191 (GRCm38) |
V282E |
probably damaging |
Het |
| Cdipt |
T |
A |
7: 126,978,358 (GRCm38) |
L92H |
probably damaging |
Het |
| Celsr2 |
T |
A |
3: 108,398,952 (GRCm38) |
D2012V |
probably damaging |
Het |
| Cenpt |
A |
G |
8: 105,847,136 (GRCm38) |
V254A |
probably benign |
Het |
| Cep104 |
T |
A |
4: 153,988,426 (GRCm38) |
D380E |
probably damaging |
Het |
| Cers5 |
C |
T |
15: 99,741,637 (GRCm38) |
R123Q |
probably benign |
Het |
| Ces2h |
A |
G |
8: 105,014,604 (GRCm38) |
E76G |
probably damaging |
Het |
| Cfap77 |
T |
A |
2: 28,984,388 (GRCm38) |
E143D |
probably benign |
Het |
| Chmp7 |
C |
A |
14: 69,732,296 (GRCm38) |
R65L |
probably damaging |
Het |
| Cldnd2 |
T |
A |
7: 43,442,189 (GRCm38) |
C65S |
possibly damaging |
Het |
| Clec2g |
C |
A |
6: 128,981,879 (GRCm38) |
Y142* |
probably null |
Het |
| Coch |
A |
T |
12: 51,605,019 (GRCm38) |
E549V |
probably benign |
Het |
| Cog7 |
T |
C |
7: 121,964,244 (GRCm38) |
D215G |
probably benign |
Het |
| Col4a2 |
T |
C |
8: 11,414,779 (GRCm38) |
V348A |
probably benign |
Het |
| Col4a2 |
A |
G |
8: 11,446,197 (GRCm38) |
H1606R |
probably benign |
Het |
| Cpd |
T |
C |
11: 76,811,794 (GRCm38) |
N583D |
probably damaging |
Het |
| Cyp2d11 |
T |
A |
15: 82,389,227 (GRCm38) |
Y481F |
probably benign |
Het |
| D130043K22Rik |
T |
C |
13: 24,899,665 (GRCm38) |
S1038P |
probably damaging |
Het |
| Deptor |
C |
A |
15: 55,181,010 (GRCm38) |
H191N |
probably benign |
Het |
| Dgkz |
A |
T |
2: 91,938,339 (GRCm38) |
I699N |
probably damaging |
Het |
| Dnah12 |
C |
T |
14: 26,781,784 (GRCm38) |
T1653I |
probably damaging |
Het |
| Dnah7c |
T |
A |
1: 46,770,173 (GRCm38) |
N3550K |
probably damaging |
Het |
| Dnah8 |
A |
G |
17: 30,775,061 (GRCm38) |
K3384R |
probably null |
Het |
| Dnajc11 |
A |
G |
4: 151,970,967 (GRCm38) |
|
probably benign |
Het |
| Dnajc13 |
CT |
C |
9: 104,186,805 (GRCm38) |
|
probably benign |
Het |
| Dnhd1 |
C |
A |
7: 105,673,849 (GRCm38) |
N521K |
probably benign |
Het |
| Drg2 |
T |
C |
11: 60,461,396 (GRCm38) |
|
probably null |
Het |
| Dync1h1 |
C |
T |
12: 110,649,507 (GRCm38) |
Q3030* |
probably null |
Het |
| Efhb |
G |
A |
17: 53,426,244 (GRCm38) |
T533I |
probably damaging |
Het |
| Eif2d |
T |
C |
1: 131,164,727 (GRCm38) |
V374A |
probably damaging |
Het |
| Etfb |
T |
C |
7: 43,444,200 (GRCm38) |
V17A |
probably damaging |
Het |
| F5 |
C |
T |
1: 164,181,657 (GRCm38) |
T332M |
probably damaging |
Het |
| Fcho1 |
T |
C |
8: 71,716,795 (GRCm38) |
T156A |
probably benign |
Het |
| Fn1 |
A |
T |
1: 71,602,512 (GRCm38) |
|
probably null |
Het |
| Fnip2 |
A |
T |
3: 79,481,652 (GRCm38) |
S561T |
probably damaging |
Het |
| Frs2 |
T |
A |
10: 117,074,093 (GRCm38) |
T455S |
probably benign |
Het |
| Fry |
G |
A |
5: 150,386,007 (GRCm38) |
E639K |
|
Het |
| Fto |
T |
A |
8: 91,409,714 (GRCm38) |
D205E |
probably damaging |
Het |
| Galntl6 |
G |
A |
8: 58,427,813 (GRCm38) |
P147L |
probably damaging |
Het |
| Gigyf1 |
T |
A |
5: 137,524,770 (GRCm38) |
D844E |
probably benign |
Het |
| Gle1 |
T |
C |
2: 29,940,232 (GRCm38) |
S267P |
probably damaging |
Het |
| Glg1 |
G |
A |
8: 111,187,755 (GRCm38) |
R466W |
probably damaging |
Het |
| Gm10277 |
T |
C |
11: 77,786,097 (GRCm38) |
|
probably benign |
Het |
| Gm20388 |
A |
G |
8: 122,270,274 (GRCm38) |
|
probably benign |
Het |
| Gm5724 |
A |
T |
6: 141,723,179 (GRCm38) |
M509K |
probably benign |
Het |
| Gm6871 |
T |
C |
7: 41,546,749 (GRCm38) |
I39V |
probably benign |
Het |
| Gm9970 |
A |
G |
5: 31,241,066 (GRCm38) |
|
probably benign |
Het |
| Gpr35 |
T |
G |
1: 92,983,385 (GRCm38) |
I57S |
probably damaging |
Het |
| Gprin1 |
C |
T |
13: 54,739,957 (GRCm38) |
G168E |
possibly damaging |
Het |
| Gtdc1 |
A |
G |
2: 44,789,055 (GRCm38) |
|
probably benign |
Het |
| Gtf3c2 |
G |
T |
5: 31,160,057 (GRCm38) |
P586T |
probably damaging |
Het |
| Gucy1a2 |
A |
T |
9: 3,759,424 (GRCm38) |
H410L |
probably benign |
Het |
| Gucy2c |
A |
G |
6: 136,767,152 (GRCm38) |
S150P |
probably damaging |
Het |
| Ifi214 |
T |
C |
1: 173,526,591 (GRCm38) |
Q171R |
probably benign |
Het |
| Ifit1bl1 |
T |
C |
19: 34,594,321 (GRCm38) |
I245M |
probably benign |
Het |
| Igkv4-50 |
T |
C |
6: 69,701,000 (GRCm38) |
K40R |
probably benign |
Het |
| Igkv8-18 |
T |
A |
6: 70,356,296 (GRCm38) |
I74N |
probably damaging |
Het |
| Il2ra |
T |
A |
2: 11,676,920 (GRCm38) |
M112K |
probably benign |
Het |
| Itpr2 |
A |
G |
6: 146,373,173 (GRCm38) |
F837S |
probably damaging |
Het |
| Kbtbd7 |
T |
C |
14: 79,428,800 (GRCm38) |
*691Q |
probably null |
Het |
| Kcnn2 |
T |
A |
18: 45,560,349 (GRCm38) |
S331T |
possibly damaging |
Het |
| Khnyn |
T |
A |
14: 55,886,489 (GRCm38) |
|
probably null |
Het |
| Kif26a |
G |
A |
12: 112,175,573 (GRCm38) |
A754T |
probably benign |
Het |
| Klra3 |
T |
A |
6: 130,327,132 (GRCm38) |
Y199F |
possibly damaging |
Het |
| Lhx2 |
A |
G |
2: 38,359,991 (GRCm38) |
K274R |
probably damaging |
Het |
| Lrp2 |
T |
C |
2: 69,533,555 (GRCm38) |
I313V |
probably benign |
Het |
| Lrrfip1 |
A |
T |
1: 91,115,647 (GRCm38) |
E591D |
probably benign |
Het |
| Lrrk2 |
G |
A |
15: 91,765,747 (GRCm38) |
E1696K |
probably damaging |
Het |
| Lrrk2 |
A |
C |
15: 91,688,849 (GRCm38) |
E200A |
probably damaging |
Het |
| Mast4 |
A |
T |
13: 102,772,572 (GRCm38) |
M465K |
probably damaging |
Het |
| Moxd2 |
T |
G |
6: 40,878,859 (GRCm38) |
I599L |
probably benign |
Het |
| Mug2 |
T |
C |
6: 122,071,872 (GRCm38) |
S866P |
probably damaging |
Het |
| Ncam2 |
A |
G |
16: 81,434,884 (GRCm38) |
T79A |
possibly damaging |
Het |
| Ncoa6 |
C |
A |
2: 155,421,301 (GRCm38) |
Q404H |
probably damaging |
Het |
| Neb |
A |
G |
2: 52,279,079 (GRCm38) |
Y1815H |
probably damaging |
Het |
| Nell1 |
A |
G |
7: 50,856,217 (GRCm38) |
D724G |
probably damaging |
Het |
| Nkx3-2 |
A |
G |
5: 41,762,144 (GRCm38) |
V167A |
probably benign |
Het |
| Nsun3 |
C |
A |
16: 62,735,119 (GRCm38) |
C348F |
possibly damaging |
Het |
| Obox6 |
A |
T |
7: 15,834,772 (GRCm38) |
S60T |
possibly damaging |
Het |
| Olfr1 |
T |
C |
11: 73,395,695 (GRCm38) |
D109G |
probably benign |
Het |
| Olfr1378 |
G |
A |
11: 50,969,266 (GRCm38) |
V83M |
possibly damaging |
Het |
| Olfr138 |
T |
A |
17: 38,275,547 (GRCm38) |
Y259N |
probably damaging |
Het |
| Olfr466 |
T |
C |
13: 65,152,653 (GRCm38) |
V143A |
possibly damaging |
Het |
| Olfr744 |
T |
A |
14: 50,618,569 (GRCm38) |
C116S |
probably benign |
Het |
| Olfr94 |
T |
C |
17: 37,197,024 (GRCm38) |
T315A |
probably damaging |
Het |
| Olfr980 |
A |
T |
9: 40,006,268 (GRCm38) |
I227N |
probably damaging |
Het |
| Oog2 |
T |
A |
4: 144,193,941 (GRCm38) |
|
probably benign |
Het |
| Pabpc1 |
A |
T |
15: 36,599,284 (GRCm38) |
V389E |
probably benign |
Het |
| Pank4 |
A |
T |
4: 154,971,390 (GRCm38) |
M291L |
probably benign |
Het |
| Pcf11 |
T |
C |
7: 92,658,833 (GRCm38) |
D709G |
probably benign |
Het |
| Pcgf1 |
T |
A |
6: 83,079,957 (GRCm38) |
|
probably benign |
Het |
| Pcnx |
A |
G |
12: 81,995,751 (GRCm38) |
I2256V |
probably benign |
Het |
| Pex6 |
A |
G |
17: 46,722,288 (GRCm38) |
D579G |
probably benign |
Het |
| Pex6 |
A |
G |
17: 46,724,707 (GRCm38) |
|
probably null |
Het |
| Piezo2 |
C |
T |
18: 63,030,401 (GRCm38) |
A2149T |
probably damaging |
Het |
| Pik3c2g |
A |
G |
6: 139,935,985 (GRCm38) |
E781G |
probably benign |
Het |
| Pik3r4 |
G |
A |
9: 105,678,176 (GRCm38) |
V1111I |
possibly damaging |
Het |
| Pkd1l2 |
T |
A |
8: 116,995,842 (GRCm38) |
|
probably null |
Het |
| Plekhg1 |
T |
A |
10: 3,957,506 (GRCm38) |
S808T |
probably benign |
Het |
| Pnkp |
T |
A |
7: 44,860,454 (GRCm38) |
|
probably benign |
Het |
| Polr3c |
A |
T |
3: 96,723,661 (GRCm38) |
F148I |
probably damaging |
Het |
| Ppard |
A |
T |
17: 28,286,443 (GRCm38) |
T35S |
probably benign |
Het |
| Ptov1 |
T |
C |
7: 44,867,109 (GRCm38) |
D134G |
probably benign |
Het |
| Ptprz1 |
T |
A |
6: 23,002,610 (GRCm38) |
S1566R |
probably benign |
Het |
| Pum1 |
T |
C |
4: 130,718,193 (GRCm38) |
S158P |
probably benign |
Het |
| Qk |
T |
C |
17: 10,216,288 (GRCm38) |
H269R |
probably damaging |
Het |
| Qrsl1 |
T |
C |
10: 43,876,663 (GRCm38) |
Y388C |
probably damaging |
Het |
| Rapgef1 |
T |
G |
2: 29,689,160 (GRCm38) |
I182S |
probably damaging |
Het |
| Ret |
T |
C |
6: 118,163,193 (GRCm38) |
S1013G |
possibly damaging |
Het |
| Rimbp3 |
A |
G |
16: 17,210,601 (GRCm38) |
R630G |
possibly damaging |
Het |
| Rnmt |
A |
T |
18: 68,317,960 (GRCm38) |
|
probably benign |
Het |
| Ryr2 |
A |
T |
13: 11,577,909 (GRCm38) |
M4653K |
possibly damaging |
Het |
| Sacm1l |
G |
A |
9: 123,590,830 (GRCm38) |
V553I |
probably benign |
Het |
| Sec31b |
A |
T |
19: 44,532,677 (GRCm38) |
S110T |
probably damaging |
Het |
| Serpina3k |
G |
A |
12: 104,340,860 (GRCm38) |
G117D |
probably damaging |
Het |
| Sesn2 |
T |
C |
4: 132,494,591 (GRCm38) |
Y410C |
probably damaging |
Het |
| Slc24a1 |
G |
A |
9: 64,949,554 (GRCm38) |
R24C |
probably benign |
Het |
| Slc35g2 |
A |
C |
9: 100,552,502 (GRCm38) |
V372G |
probably benign |
Het |
| Slc7a7 |
T |
C |
14: 54,408,733 (GRCm38) |
Y91C |
probably damaging |
Het |
| Slc7a9 |
T |
A |
7: 35,453,563 (GRCm38) |
Y135* |
probably null |
Het |
| Slco4a1 |
A |
G |
2: 180,473,615 (GRCm38) |
N662D |
probably damaging |
Het |
| Slfn4 |
T |
A |
11: 83,189,282 (GRCm38) |
|
probably benign |
Het |
| Slmap |
T |
C |
14: 26,468,535 (GRCm38) |
N156S |
probably damaging |
Het |
| Snx18 |
A |
G |
13: 113,617,774 (GRCm38) |
S208P |
probably benign |
Het |
| Sorbs1 |
T |
A |
19: 40,314,689 (GRCm38) |
R485S |
probably benign |
Het |
| Spib |
A |
G |
7: 44,528,885 (GRCm38) |
S154P |
probably damaging |
Het |
| Spty2d1 |
T |
C |
7: 46,996,110 (GRCm38) |
D595G |
probably damaging |
Het |
| St7 |
T |
A |
6: 17,906,516 (GRCm38) |
|
probably null |
Het |
| Susd1 |
T |
C |
4: 59,428,029 (GRCm38) |
T52A |
possibly damaging |
Het |
| Svs2 |
T |
A |
2: 164,237,123 (GRCm38) |
D288V |
possibly damaging |
Het |
| Syt7 |
T |
A |
19: 10,442,924 (GRCm38) |
I355N |
probably damaging |
Het |
| Tarm1 |
G |
A |
7: 3,496,900 (GRCm38) |
Q145* |
probably null |
Het |
| Teddm2 |
T |
A |
1: 153,850,741 (GRCm38) |
E76V |
probably damaging |
Het |
| Thsd7b |
T |
C |
1: 129,613,186 (GRCm38) |
S343P |
probably damaging |
Het |
| Tigd2 |
T |
A |
6: 59,211,415 (GRCm38) |
H422Q |
probably benign |
Het |
| Tle1 |
T |
C |
4: 72,125,019 (GRCm38) |
N538D |
possibly damaging |
Het |
| Tmc2 |
A |
G |
2: 130,261,397 (GRCm38) |
|
probably null |
Het |
| Tmtc1 |
A |
C |
6: 148,284,980 (GRCm38) |
|
probably null |
Het |
| Tns3 |
C |
T |
11: 8,450,986 (GRCm38) |
R1104H |
probably benign |
Het |
| Trim6 |
T |
C |
7: 104,232,648 (GRCm38) |
Y369H |
probably damaging |
Het |
| Triobp |
G |
A |
15: 78,967,113 (GRCm38) |
R489K |
probably damaging |
Het |
| Trpv4 |
T |
C |
5: 114,622,753 (GRCm38) |
D732G |
possibly damaging |
Het |
| Trrap |
G |
A |
5: 144,816,570 (GRCm38) |
V1883I |
probably damaging |
Het |
| Tsc2 |
C |
A |
17: 24,603,275 (GRCm38) |
V1141F |
possibly damaging |
Het |
| Ttn |
A |
G |
2: 76,899,827 (GRCm38) |
|
probably benign |
Het |
| Ttn |
A |
T |
2: 76,943,011 (GRCm38) |
M2395K |
unknown |
Het |
| Tyrp1 |
A |
T |
4: 80,844,935 (GRCm38) |
D353V |
possibly damaging |
Het |
| Ubd |
A |
C |
17: 37,195,702 (GRCm38) |
T160P |
probably benign |
Het |
| Ugt2b36 |
G |
T |
5: 87,081,538 (GRCm38) |
Y156* |
probably null |
Het |
| Ulk4 |
G |
A |
9: 121,263,638 (GRCm38) |
R178* |
probably null |
Het |
| Unc13d |
A |
G |
11: 116,073,582 (GRCm38) |
V312A |
possibly damaging |
Het |
| Urb2 |
G |
T |
8: 124,028,897 (GRCm38) |
A448S |
probably damaging |
Het |
| Urod |
G |
A |
4: 116,991,673 (GRCm38) |
A92V |
possibly damaging |
Het |
| Vmn1r33 |
T |
A |
6: 66,611,819 (GRCm38) |
R250S |
probably benign |
Het |
| Vmn1r87 |
A |
T |
7: 13,132,327 (GRCm38) |
M11K |
possibly damaging |
Het |
| Vmn2r77 |
C |
T |
7: 86,800,987 (GRCm38) |
T147I |
probably benign |
Het |
| Vstm4 |
A |
G |
14: 32,917,902 (GRCm38) |
K96E |
possibly damaging |
Het |
| Washc4 |
A |
T |
10: 83,574,479 (GRCm38) |
M644L |
probably benign |
Het |
| Wwp1 |
T |
C |
4: 19,661,990 (GRCm38) |
D172G |
probably benign |
Het |
| Zbtb38 |
A |
T |
9: 96,687,684 (GRCm38) |
V449E |
probably damaging |
Het |
| Zfhx4 |
T |
C |
3: 5,214,807 (GRCm38) |
|
probably benign |
Het |
| Zfp229 |
C |
T |
17: 21,745,286 (GRCm38) |
H166Y |
possibly damaging |
Het |
| Zfp512b |
A |
G |
2: 181,588,739 (GRCm38) |
S453P |
probably benign |
Het |
| Zp2 |
C |
A |
7: 120,138,120 (GRCm38) |
V282L |
probably damaging |
Het |
|
| Other mutations in Akap9 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00478:Akap9
|
APN |
5 |
4,046,639 (GRCm38) |
missense |
probably damaging |
0.97 |
|
IGL00642:Akap9
|
APN |
5 |
3,960,842 (GRCm38) |
missense |
probably damaging |
0.99 |
|
IGL00786:Akap9
|
APN |
5 |
4,070,522 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL00788:Akap9
|
APN |
5 |
4,060,480 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL00969:Akap9
|
APN |
5 |
4,001,550 (GRCm38) |
missense |
probably benign |
|
|
IGL01014:Akap9
|
APN |
5 |
3,968,683 (GRCm38) |
missense |
probably benign |
0.41 |
|
IGL01302:Akap9
|
APN |
5 |
3,970,711 (GRCm38) |
missense |
probably benign |
0.27 |
|
IGL01610:Akap9
|
APN |
5 |
4,032,839 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
IGL01620:Akap9
|
APN |
5 |
3,960,218 (GRCm38) |
missense |
probably benign |
0.11 |
|
IGL01862:Akap9
|
APN |
5 |
4,065,856 (GRCm38) |
missense |
probably damaging |
0.99 |
|
IGL01862:Akap9
|
APN |
5 |
3,951,705 (GRCm38) |
missense |
probably damaging |
0.99 |
|
IGL02151:Akap9
|
APN |
5 |
4,032,728 (GRCm38) |
nonsense |
probably null |
|
|
IGL02635:Akap9
|
APN |
5 |
4,070,500 (GRCm38) |
missense |
possibly damaging |
0.59 |
|
IGL02858:Akap9
|
APN |
5 |
4,069,130 (GRCm38) |
missense |
possibly damaging |
0.88 |
|
IGL02967:Akap9
|
APN |
5 |
3,976,164 (GRCm38) |
missense |
probably benign |
0.07 |
|
IGL03064:Akap9
|
APN |
5 |
3,968,755 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL03289:Akap9
|
APN |
5 |
4,077,261 (GRCm38) |
missense |
probably damaging |
1.00 |
|
Andy
|
UTSW |
5 |
3,961,764 (GRCm38) |
nonsense |
probably null |
|
|
blimey
|
UTSW |
5 |
4,070,397 (GRCm38) |
nonsense |
probably null |
|
|
hoarder
|
UTSW |
5 |
4,069,089 (GRCm38) |
missense |
probably benign |
0.00 |
|
marinarum
|
UTSW |
5 |
4,013,875 (GRCm38) |
nonsense |
probably null |
|
|
miser
|
UTSW |
5 |
4,046,064 (GRCm38) |
missense |
probably benign |
0.13 |
|
naviculus
|
UTSW |
5 |
3,960,865 (GRCm38) |
missense |
probably damaging |
0.98 |
|
thrifty
|
UTSW |
5 |
3,976,209 (GRCm38) |
missense |
probably damaging |
0.99 |
|
wee_one
|
UTSW |
5 |
4,043,925 (GRCm38) |
missense |
probably damaging |
1.00 |
|
FR4449:Akap9
|
UTSW |
5 |
3,981,214 (GRCm38) |
unclassified |
probably benign |
|
|
PIT1430001:Akap9
|
UTSW |
5 |
4,029,849 (GRCm38) |
missense |
probably damaging |
1.00 |
|
PIT4366001:Akap9
|
UTSW |
5 |
4,046,221 (GRCm38) |
missense |
probably benign |
0.24 |
|
R0088:Akap9
|
UTSW |
5 |
3,961,946 (GRCm38) |
missense |
probably benign |
0.22 |
|
R0309:Akap9
|
UTSW |
5 |
4,069,038 (GRCm38) |
missense |
probably benign |
0.01 |
|
R0387:Akap9
|
UTSW |
5 |
3,951,678 (GRCm38) |
splice site |
probably benign |
|
|
R0440:Akap9
|
UTSW |
5 |
4,064,569 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R0441:Akap9
|
UTSW |
5 |
3,961,714 (GRCm38) |
missense |
probably benign |
0.15 |
|
R0491:Akap9
|
UTSW |
5 |
3,972,851 (GRCm38) |
unclassified |
probably benign |
|
|
R0501:Akap9
|
UTSW |
5 |
3,970,685 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0507:Akap9
|
UTSW |
5 |
4,069,043 (GRCm38) |
missense |
probably benign |
0.41 |
|
R0544:Akap9
|
UTSW |
5 |
4,069,185 (GRCm38) |
missense |
probably benign |
0.22 |
|
R0581:Akap9
|
UTSW |
5 |
4,050,620 (GRCm38) |
missense |
probably benign |
0.03 |
|
R0611:Akap9
|
UTSW |
5 |
3,954,870 (GRCm38) |
missense |
probably benign |
0.00 |
|
R0620:Akap9
|
UTSW |
5 |
4,064,136 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R0639:Akap9
|
UTSW |
5 |
4,060,318 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0932:Akap9
|
UTSW |
5 |
4,046,492 (GRCm38) |
missense |
possibly damaging |
0.77 |
|
R0944:Akap9
|
UTSW |
5 |
4,064,742 (GRCm38) |
splice site |
probably null |
|
|
R1101:Akap9
|
UTSW |
5 |
4,046,205 (GRCm38) |
missense |
probably benign |
0.00 |
|
R1159:Akap9
|
UTSW |
5 |
3,960,865 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R1170:Akap9
|
UTSW |
5 |
4,055,671 (GRCm38) |
missense |
probably benign |
|
|
R1185:Akap9
|
UTSW |
5 |
3,948,783 (GRCm38) |
missense |
probably benign |
0.13 |
|
R1185:Akap9
|
UTSW |
5 |
3,948,783 (GRCm38) |
missense |
probably benign |
0.13 |
|
R1185:Akap9
|
UTSW |
5 |
3,948,783 (GRCm38) |
missense |
probably benign |
0.13 |
|
R1453:Akap9
|
UTSW |
5 |
3,975,614 (GRCm38) |
splice site |
probably null |
|
|
R1551:Akap9
|
UTSW |
5 |
4,069,174 (GRCm38) |
missense |
probably benign |
0.02 |
|
R1608:Akap9
|
UTSW |
5 |
3,961,783 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1652:Akap9
|
UTSW |
5 |
4,077,210 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1659:Akap9
|
UTSW |
5 |
4,064,633 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1713:Akap9
|
UTSW |
5 |
4,039,345 (GRCm38) |
critical splice donor site |
probably null |
|
|
R1719:Akap9
|
UTSW |
5 |
3,957,645 (GRCm38) |
nonsense |
probably null |
|
|
R1720:Akap9
|
UTSW |
5 |
3,972,791 (GRCm38) |
missense |
possibly damaging |
0.63 |
|
R1757:Akap9
|
UTSW |
5 |
4,001,667 (GRCm38) |
missense |
probably benign |
0.41 |
|
R1872:Akap9
|
UTSW |
5 |
4,001,406 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1876:Akap9
|
UTSW |
5 |
3,961,809 (GRCm38) |
missense |
probably benign |
0.28 |
|
R1881:Akap9
|
UTSW |
5 |
4,050,173 (GRCm38) |
missense |
probably benign |
|
|
R1950:Akap9
|
UTSW |
5 |
3,960,677 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1980:Akap9
|
UTSW |
5 |
3,972,771 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R1993:Akap9
|
UTSW |
5 |
4,038,520 (GRCm38) |
splice site |
probably null |
|
|
R2008:Akap9
|
UTSW |
5 |
3,960,131 (GRCm38) |
missense |
possibly damaging |
0.47 |
|
R2020:Akap9
|
UTSW |
5 |
3,961,967 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2051:Akap9
|
UTSW |
5 |
3,975,685 (GRCm38) |
nonsense |
probably null |
|
|
R2061:Akap9
|
UTSW |
5 |
3,961,010 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2109:Akap9
|
UTSW |
5 |
4,044,847 (GRCm38) |
missense |
possibly damaging |
0.47 |
|
R2135:Akap9
|
UTSW |
5 |
4,064,509 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2225:Akap9
|
UTSW |
5 |
4,077,271 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R2232:Akap9
|
UTSW |
5 |
4,046,603 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2424:Akap9
|
UTSW |
5 |
4,065,279 (GRCm38) |
missense |
probably damaging |
0.97 |
|
R2483:Akap9
|
UTSW |
5 |
3,976,235 (GRCm38) |
missense |
possibly damaging |
0.65 |
|
R2879:Akap9
|
UTSW |
5 |
3,976,353 (GRCm38) |
intron |
probably benign |
|
|
R3622:Akap9
|
UTSW |
5 |
3,976,235 (GRCm38) |
missense |
possibly damaging |
0.65 |
|
R3623:Akap9
|
UTSW |
5 |
3,976,235 (GRCm38) |
missense |
possibly damaging |
0.65 |
|
R3624:Akap9
|
UTSW |
5 |
3,976,235 (GRCm38) |
missense |
possibly damaging |
0.65 |
|
R3722:Akap9
|
UTSW |
5 |
4,070,351 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R3806:Akap9
|
UTSW |
5 |
3,954,410 (GRCm38) |
missense |
probably benign |
0.00 |
|
R3919:Akap9
|
UTSW |
5 |
3,961,764 (GRCm38) |
nonsense |
probably null |
|
|
R4023:Akap9
|
UTSW |
5 |
3,992,077 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R4093:Akap9
|
UTSW |
5 |
4,043,996 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4434:Akap9
|
UTSW |
5 |
4,032,708 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4529:Akap9
|
UTSW |
5 |
4,043,948 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4530:Akap9
|
UTSW |
5 |
4,043,948 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4532:Akap9
|
UTSW |
5 |
4,043,948 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4533:Akap9
|
UTSW |
5 |
4,043,948 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4585:Akap9
|
UTSW |
5 |
3,976,151 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4586:Akap9
|
UTSW |
5 |
3,976,151 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4655:Akap9
|
UTSW |
5 |
4,046,403 (GRCm38) |
missense |
probably benign |
0.14 |
|
R4676:Akap9
|
UTSW |
5 |
4,064,515 (GRCm38) |
nonsense |
probably null |
|
|
R4676:Akap9
|
UTSW |
5 |
4,032,774 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4724:Akap9
|
UTSW |
5 |
4,055,339 (GRCm38) |
missense |
probably benign |
|
|
R4731:Akap9
|
UTSW |
5 |
3,962,266 (GRCm38) |
missense |
possibly damaging |
0.54 |
|
R4733:Akap9
|
UTSW |
5 |
4,013,901 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R4743:Akap9
|
UTSW |
5 |
3,961,013 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4749:Akap9
|
UTSW |
5 |
3,968,737 (GRCm38) |
missense |
probably benign |
0.41 |
|
R4756:Akap9
|
UTSW |
5 |
4,001,418 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4757:Akap9
|
UTSW |
5 |
4,008,382 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4860:Akap9
|
UTSW |
5 |
4,034,916 (GRCm38) |
intron |
probably benign |
|
|
R4937:Akap9
|
UTSW |
5 |
4,050,145 (GRCm38) |
splice site |
probably null |
|
|
R4960:Akap9
|
UTSW |
5 |
3,957,664 (GRCm38) |
missense |
probably benign |
0.15 |
|
R4974:Akap9
|
UTSW |
5 |
3,961,466 (GRCm38) |
missense |
possibly damaging |
0.81 |
|
R5101:Akap9
|
UTSW |
5 |
4,001,748 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R5160:Akap9
|
UTSW |
5 |
4,030,007 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5200:Akap9
|
UTSW |
5 |
3,960,734 (GRCm38) |
missense |
probably benign |
0.00 |
|
R5245:Akap9
|
UTSW |
5 |
3,976,209 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5293:Akap9
|
UTSW |
5 |
3,948,687 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5408:Akap9
|
UTSW |
5 |
4,058,458 (GRCm38) |
missense |
possibly damaging |
0.84 |
|
R5507:Akap9
|
UTSW |
5 |
3,968,683 (GRCm38) |
missense |
probably benign |
0.41 |
|
R5517:Akap9
|
UTSW |
5 |
4,001,665 (GRCm38) |
missense |
possibly damaging |
0.76 |
|
R5579:Akap9
|
UTSW |
5 |
4,064,714 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R5619:Akap9
|
UTSW |
5 |
3,954,760 (GRCm38) |
intron |
probably benign |
|
|
R5645:Akap9
|
UTSW |
5 |
4,050,590 (GRCm38) |
missense |
probably benign |
0.09 |
|
R5669:Akap9
|
UTSW |
5 |
4,050,540 (GRCm38) |
nonsense |
probably null |
|
|
R5686:Akap9
|
UTSW |
5 |
3,971,926 (GRCm38) |
missense |
probably benign |
0.00 |
|
R5697:Akap9
|
UTSW |
5 |
3,960,170 (GRCm38) |
missense |
possibly damaging |
0.92 |
|
R5821:Akap9
|
UTSW |
5 |
4,046,064 (GRCm38) |
missense |
probably benign |
0.13 |
|
R5875:Akap9
|
UTSW |
5 |
4,077,285 (GRCm38) |
missense |
probably benign |
0.01 |
|
R5897:Akap9
|
UTSW |
5 |
4,077,904 (GRCm38) |
missense |
probably benign |
0.23 |
|
R5999:Akap9
|
UTSW |
5 |
4,043,925 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6025:Akap9
|
UTSW |
5 |
4,032,801 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6078:Akap9
|
UTSW |
5 |
4,067,924 (GRCm38) |
critical splice donor site |
probably null |
|
|
R6138:Akap9
|
UTSW |
5 |
4,067,924 (GRCm38) |
critical splice donor site |
probably null |
|
|
R6225:Akap9
|
UTSW |
5 |
3,962,105 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6243:Akap9
|
UTSW |
5 |
4,065,000 (GRCm38) |
splice site |
probably null |
|
|
R6326:Akap9
|
UTSW |
5 |
3,962,061 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6564:Akap9
|
UTSW |
5 |
4,028,491 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R6617:Akap9
|
UTSW |
5 |
3,968,745 (GRCm38) |
missense |
probably benign |
0.04 |
|
R6625:Akap9
|
UTSW |
5 |
3,968,745 (GRCm38) |
missense |
probably benign |
0.04 |
|
R6632:Akap9
|
UTSW |
5 |
4,013,842 (GRCm38) |
splice site |
probably null |
|
|
R6677:Akap9
|
UTSW |
5 |
4,029,869 (GRCm38) |
missense |
probably benign |
0.21 |
|
R6717:Akap9
|
UTSW |
5 |
4,064,086 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6893:Akap9
|
UTSW |
5 |
3,961,709 (GRCm38) |
missense |
probably benign |
0.32 |
|
R6915:Akap9
|
UTSW |
5 |
3,960,551 (GRCm38) |
missense |
probably benign |
0.03 |
|
R6938:Akap9
|
UTSW |
5 |
4,046,628 (GRCm38) |
missense |
possibly damaging |
0.91 |
|
R6972:Akap9
|
UTSW |
5 |
4,046,699 (GRCm38) |
missense |
possibly damaging |
0.62 |
|
R6973:Akap9
|
UTSW |
5 |
4,046,699 (GRCm38) |
missense |
possibly damaging |
0.62 |
|
R6993:Akap9
|
UTSW |
5 |
4,065,866 (GRCm38) |
missense |
possibly damaging |
0.65 |
|
R7032:Akap9
|
UTSW |
5 |
3,954,896 (GRCm38) |
missense |
probably benign |
|
|
R7164:Akap9
|
UTSW |
5 |
4,060,364 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R7170:Akap9
|
UTSW |
5 |
3,968,745 (GRCm38) |
missense |
probably benign |
0.04 |
|
R7192:Akap9
|
UTSW |
5 |
4,005,723 (GRCm38) |
splice site |
probably null |
|
|
R7284:Akap9
|
UTSW |
5 |
3,956,246 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7299:Akap9
|
UTSW |
5 |
4,032,696 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7313:Akap9
|
UTSW |
5 |
4,004,933 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7326:Akap9
|
UTSW |
5 |
4,045,930 (GRCm38) |
missense |
possibly damaging |
0.47 |
|
R7343:Akap9
|
UTSW |
5 |
4,046,364 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7455:Akap9
|
UTSW |
5 |
3,972,792 (GRCm38) |
missense |
probably benign |
0.03 |
|
R7482:Akap9
|
UTSW |
5 |
3,968,745 (GRCm38) |
missense |
probably benign |
0.04 |
|
R7489:Akap9
|
UTSW |
5 |
4,004,933 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7525:Akap9
|
UTSW |
5 |
3,968,745 (GRCm38) |
missense |
probably benign |
0.04 |
|
R7528:Akap9
|
UTSW |
5 |
3,968,745 (GRCm38) |
missense |
probably benign |
0.04 |
|
R7576:Akap9
|
UTSW |
5 |
3,968,745 (GRCm38) |
missense |
probably benign |
0.04 |
|
R7577:Akap9
|
UTSW |
5 |
3,968,745 (GRCm38) |
missense |
probably benign |
0.04 |
|
R7578:Akap9
|
UTSW |
5 |
3,968,745 (GRCm38) |
missense |
probably benign |
0.04 |
|
R7610:Akap9
|
UTSW |
5 |
3,957,677 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R7658:Akap9
|
UTSW |
5 |
3,968,745 (GRCm38) |
missense |
probably benign |
0.04 |
|
R7754:Akap9
|
UTSW |
5 |
4,046,736 (GRCm38) |
missense |
probably benign |
0.03 |
|
R7818:Akap9
|
UTSW |
5 |
4,013,875 (GRCm38) |
nonsense |
probably null |
|
|
R7979:Akap9
|
UTSW |
5 |
4,050,381 (GRCm38) |
missense |
probably benign |
|
|
R7991:Akap9
|
UTSW |
5 |
4,064,949 (GRCm38) |
splice site |
probably null |
|
|
R8036:Akap9
|
UTSW |
5 |
4,070,397 (GRCm38) |
nonsense |
probably null |
|
|
R8054:Akap9
|
UTSW |
5 |
4,038,707 (GRCm38) |
critical splice donor site |
probably null |
|
|
R8116:Akap9
|
UTSW |
5 |
4,061,183 (GRCm38) |
missense |
probably benign |
0.04 |
|
R8150:Akap9
|
UTSW |
5 |
3,961,982 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8234:Akap9
|
UTSW |
5 |
4,044,845 (GRCm38) |
missense |
probably benign |
0.18 |
|
R8348:Akap9
|
UTSW |
5 |
3,948,897 (GRCm38) |
critical splice donor site |
probably null |
|
|
R8365:Akap9
|
UTSW |
5 |
3,968,745 (GRCm38) |
missense |
probably benign |
0.04 |
|
R8366:Akap9
|
UTSW |
5 |
3,968,745 (GRCm38) |
missense |
probably benign |
0.04 |
|
R8448:Akap9
|
UTSW |
5 |
3,948,897 (GRCm38) |
critical splice donor site |
probably null |
|
|
R8466:Akap9
|
UTSW |
5 |
4,038,659 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8772:Akap9
|
UTSW |
5 |
4,046,255 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8881:Akap9
|
UTSW |
5 |
3,961,279 (GRCm38) |
missense |
|
|
|
R8937:Akap9
|
UTSW |
5 |
4,044,048 (GRCm38) |
missense |
possibly damaging |
0.78 |
|
R8956:Akap9
|
UTSW |
5 |
3,948,805 (GRCm38) |
missense |
possibly damaging |
0.79 |
|
R9000:Akap9
|
UTSW |
5 |
4,055,650 (GRCm38) |
missense |
probably benign |
|
|
R9049:Akap9
|
UTSW |
5 |
4,064,597 (GRCm38) |
missense |
|
|
|
R9074:Akap9
|
UTSW |
5 |
4,077,959 (GRCm38) |
missense |
probably benign |
0.40 |
|
R9124:Akap9
|
UTSW |
5 |
4,061,284 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R9129:Akap9
|
UTSW |
5 |
4,069,089 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9371:Akap9
|
UTSW |
5 |
3,961,852 (GRCm38) |
missense |
possibly damaging |
0.83 |
|
R9424:Akap9
|
UTSW |
5 |
3,962,224 (GRCm38) |
nonsense |
probably null |
|
|
R9424:Akap9
|
UTSW |
5 |
3,962,223 (GRCm38) |
nonsense |
probably null |
|
|
R9509:Akap9
|
UTSW |
5 |
4,046,349 (GRCm38) |
missense |
probably benign |
|
|
R9515:Akap9
|
UTSW |
5 |
4,055,709 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9567:Akap9
|
UTSW |
5 |
4,077,311 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R9587:Akap9
|
UTSW |
5 |
4,069,149 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9619:Akap9
|
UTSW |
5 |
4,044,833 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9635:Akap9
|
UTSW |
5 |
4,050,545 (GRCm38) |
missense |
probably benign |
0.20 |
|
R9680:Akap9
|
UTSW |
5 |
3,961,587 (GRCm38) |
missense |
probably benign |
0.03 |
|
R9691:Akap9
|
UTSW |
5 |
3,960,491 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9726:Akap9
|
UTSW |
5 |
4,003,757 (GRCm38) |
missense |
probably benign |
0.39 |
|
U15987:Akap9
|
UTSW |
5 |
4,067,924 (GRCm38) |
critical splice donor site |
probably null |
|
|
X0026:Akap9
|
UTSW |
5 |
4,014,039 (GRCm38) |
missense |
probably damaging |
1.00 |
|
X0057:Akap9
|
UTSW |
5 |
3,975,598 (GRCm38) |
critical splice acceptor site |
probably null |
|
|
Z1176:Akap9
|
UTSW |
5 |
3,962,251 (GRCm38) |
missense |
probably damaging |
0.96 |
|
Z1177:Akap9
|
UTSW |
5 |
4,046,189 (GRCm38) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGCTTTGCATGTTCACTCTGTTAAG -3'
(R):5'- GCATTACGCTCTGCAGACAC -3'
Sequencing Primer
(F):5'- GTTGTTATTGAAAGACCTTGGAATTG -3'
(R):5'- ACTCCAAGAAAAGAGGTTACCTG -3'
|
| Posted On |
2015-11-11 |
Incidental Mutation