Incidental Mutation 'R2056:Ahnak2'
| ID |
228210 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ahnak2
|
| Ensembl Gene |
ENSMUSG00000072812 |
| Gene Name |
AHNAK nucleoprotein 2 |
| Synonyms |
LOC382643 |
| MMRRC Submission |
040061-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.074)
|
| Stock # |
R2056 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
12 |
| Chromosomal Location |
112738631-112766278 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 112748626 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Valine
at position 407
(D407V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000114522
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000124526]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000124526
AA Change: D407V
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000114522
Gene: ENSMUSG00000072812
AA Change: D407V
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
73 |
94 |
N/A |
INTRINSIC |
|
PDZ
|
118 |
190 |
6e-4 |
SMART |
|
low complexity region
|
268 |
281 |
N/A |
INTRINSIC |
|
low complexity region
|
300 |
319 |
N/A |
INTRINSIC |
|
low complexity region
|
405 |
429 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
465 |
898 |
2.74e-235 |
PROSPERO |
|
low complexity region
|
905 |
923 |
N/A |
INTRINSIC |
|
low complexity region
|
990 |
1013 |
N/A |
INTRINSIC |
|
low complexity region
|
1076 |
1092 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
1145 |
1588 |
2.74e-235 |
PROSPERO |
|
low complexity region
|
1590 |
1632 |
N/A |
INTRINSIC |
|
low complexity region
|
1639 |
1700 |
N/A |
INTRINSIC |
|
low complexity region
|
1709 |
1736 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000137195
|
| SMART Domains |
Protein: ENSMUSP00000116582
Gene: ENSMUSG00000072812
| Domain | Start | End | E-Value | Type |
|---|
|
internal_repeat_1
|
2 |
521 |
3.81e-221 |
PROSPERO |
|
low complexity region
|
557 |
569 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
606 |
1126 |
3.81e-221 |
PROSPERO |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.4%
- 20x: 95.4%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 78 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcg2 |
T |
C |
6: 58,667,525 (GRCm39) |
V129A |
probably benign |
Het |
| Adh1 |
A |
G |
3: 137,992,676 (GRCm39) |
D264G |
probably damaging |
Het |
| Alas1 |
T |
C |
9: 106,118,489 (GRCm39) |
E211G |
probably damaging |
Het |
| Alkbh1 |
C |
T |
12: 87,490,520 (GRCm39) |
|
probably benign |
Het |
| Ankmy1 |
T |
C |
1: 92,809,553 (GRCm39) |
I662V |
possibly damaging |
Het |
| Ano1 |
A |
G |
7: 144,201,789 (GRCm39) |
V334A |
probably damaging |
Het |
| Apc |
A |
G |
18: 34,449,481 (GRCm39) |
R2092G |
probably damaging |
Het |
| Arhgap18 |
C |
T |
10: 26,730,904 (GRCm39) |
T122I |
probably benign |
Het |
| Atp2b4 |
G |
T |
1: 133,654,275 (GRCm39) |
Q777K |
probably benign |
Het |
| Brap |
G |
A |
5: 121,801,529 (GRCm39) |
G95S |
probably damaging |
Het |
| Cbfa2t2 |
G |
A |
2: 154,377,077 (GRCm39) |
A587T |
probably damaging |
Het |
| Ccdc180 |
A |
G |
4: 45,932,477 (GRCm39) |
I1308V |
probably benign |
Het |
| Ccser1 |
T |
A |
6: 61,399,936 (GRCm39) |
|
probably null |
Het |
| Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
| Cmtm4 |
A |
C |
8: 105,081,920 (GRCm39) |
F156V |
probably damaging |
Het |
| Cntln |
G |
A |
4: 84,967,911 (GRCm39) |
R710K |
probably benign |
Het |
| Csn1s1 |
A |
T |
5: 87,819,387 (GRCm39) |
T15S |
possibly damaging |
Het |
| Cul9 |
T |
C |
17: 46,854,298 (GRCm39) |
T135A |
probably benign |
Het |
| Cyp2d10 |
T |
A |
15: 82,288,015 (GRCm39) |
I363F |
probably damaging |
Het |
| Dhx38 |
G |
T |
8: 110,289,352 (GRCm39) |
|
probably benign |
Het |
| Dis3 |
A |
T |
14: 99,336,251 (GRCm39) |
I85N |
possibly damaging |
Het |
| Dmbt1 |
G |
A |
7: 130,707,900 (GRCm39) |
A1381T |
possibly damaging |
Het |
| Dscaml1 |
A |
G |
9: 45,661,430 (GRCm39) |
D1776G |
probably damaging |
Het |
| Erbin |
A |
G |
13: 103,966,824 (GRCm39) |
S1209P |
probably benign |
Het |
| Fat4 |
T |
A |
3: 38,945,319 (GRCm39) |
M1404K |
possibly damaging |
Het |
| Fbxo45 |
G |
T |
16: 32,057,346 (GRCm39) |
Q183K |
possibly damaging |
Het |
| Frmd4b |
C |
T |
6: 97,389,448 (GRCm39) |
|
probably null |
Het |
| Fzd7 |
A |
G |
1: 59,523,361 (GRCm39) |
S415G |
probably benign |
Het |
| Gpd2 |
T |
A |
2: 57,229,025 (GRCm39) |
|
probably null |
Het |
| Gsk3b |
T |
A |
16: 38,008,271 (GRCm39) |
D192E |
probably benign |
Het |
| Gstcd |
T |
C |
3: 132,787,814 (GRCm39) |
I295V |
probably benign |
Het |
| Gucy1a1 |
A |
G |
3: 82,016,592 (GRCm39) |
L132P |
possibly damaging |
Het |
| Il12b |
A |
C |
11: 44,298,727 (GRCm39) |
T61P |
probably damaging |
Het |
| Il7 |
A |
T |
3: 7,638,975 (GRCm39) |
N130K |
probably damaging |
Het |
| Itih3 |
A |
C |
14: 30,631,481 (GRCm39) |
|
probably null |
Het |
| Kdm5b |
T |
A |
1: 134,540,952 (GRCm39) |
D681E |
probably benign |
Het |
| Kif11 |
A |
G |
19: 37,390,660 (GRCm39) |
N408D |
probably benign |
Het |
| Kng2 |
TATGACCATGACCATGACCATGACCATGACCATGACCAT |
TATGACCATGACCATGACCATGACCATGACCAT |
16: 22,806,703 (GRCm39) |
|
probably benign |
Het |
| Kremen2 |
T |
C |
17: 23,961,691 (GRCm39) |
E272G |
possibly damaging |
Het |
| Krt9 |
G |
T |
11: 100,082,321 (GRCm39) |
N201K |
probably damaging |
Het |
| Lmbr1 |
G |
A |
5: 29,438,092 (GRCm39) |
P304L |
probably benign |
Het |
| Lrrfip1 |
A |
G |
1: 91,043,539 (GRCm39) |
N648S |
probably benign |
Het |
| Mab21l3 |
C |
A |
3: 101,722,469 (GRCm39) |
V386L |
possibly damaging |
Het |
| Mamdc4 |
T |
C |
2: 25,454,180 (GRCm39) |
Q1149R |
probably benign |
Het |
| Mast1 |
A |
G |
8: 85,646,995 (GRCm39) |
F677L |
possibly damaging |
Het |
| Mcoln3 |
A |
G |
3: 145,833,979 (GRCm39) |
D173G |
probably benign |
Het |
| Mmrn1 |
C |
T |
6: 60,921,789 (GRCm39) |
T82I |
probably benign |
Het |
| Mtcl2 |
C |
T |
2: 156,864,747 (GRCm39) |
G1154S |
probably benign |
Het |
| Muc5ac |
A |
G |
7: 141,345,772 (GRCm39) |
T203A |
probably benign |
Het |
| Myo9b |
T |
C |
8: 71,812,334 (GRCm39) |
I2035T |
possibly damaging |
Het |
| Ndst3 |
T |
C |
3: 123,465,534 (GRCm39) |
N146S |
probably damaging |
Het |
| Neu4 |
A |
G |
1: 93,950,172 (GRCm39) |
T21A |
possibly damaging |
Het |
| Nos1ap |
G |
A |
1: 170,155,215 (GRCm39) |
L267F |
probably damaging |
Het |
| Or14c40 |
A |
T |
7: 86,313,591 (GRCm39) |
K240N |
probably damaging |
Het |
| Or3a4 |
A |
T |
11: 73,944,819 (GRCm39) |
Y255* |
probably null |
Het |
| Or4p8 |
A |
G |
2: 88,727,105 (GRCm39) |
F279L |
probably damaging |
Het |
| Phc1 |
T |
C |
6: 122,310,299 (GRCm39) |
N136S |
probably damaging |
Het |
| Prkdc |
A |
G |
16: 15,545,469 (GRCm39) |
T1862A |
probably benign |
Het |
| Psd2 |
A |
G |
18: 36,139,744 (GRCm39) |
D596G |
possibly damaging |
Het |
| Psmc3 |
T |
C |
2: 90,888,433 (GRCm39) |
F315L |
probably benign |
Het |
| Rerg |
G |
A |
6: 137,034,878 (GRCm39) |
T42I |
probably benign |
Het |
| Rif1 |
T |
A |
2: 51,983,588 (GRCm39) |
M577K |
probably damaging |
Het |
| Sap30 |
T |
C |
8: 57,940,282 (GRCm39) |
|
probably null |
Het |
| Scn2b |
T |
C |
9: 45,036,815 (GRCm39) |
Y108H |
probably damaging |
Het |
| Senp2 |
C |
T |
16: 21,832,949 (GRCm39) |
T79I |
probably damaging |
Het |
| Serpinb2 |
T |
C |
1: 107,451,543 (GRCm39) |
V232A |
probably damaging |
Het |
| Sgpp2 |
T |
A |
1: 78,393,588 (GRCm39) |
L197Q |
probably damaging |
Het |
| Slc27a4 |
T |
C |
2: 29,700,953 (GRCm39) |
W320R |
probably damaging |
Het |
| Spmip4 |
T |
C |
6: 50,550,725 (GRCm39) |
R575G |
possibly damaging |
Het |
| Tgm4 |
T |
C |
9: 122,890,835 (GRCm39) |
I54T |
probably damaging |
Het |
| Thbs4 |
T |
A |
13: 92,927,387 (GRCm39) |
D34V |
probably benign |
Het |
| Tlcd4 |
T |
G |
3: 121,001,070 (GRCm39) |
I188L |
probably benign |
Het |
| Tmem176b |
G |
A |
6: 48,813,267 (GRCm39) |
T64I |
probably damaging |
Het |
| Tmod2 |
T |
C |
9: 75,484,524 (GRCm39) |
E248G |
probably benign |
Het |
| Ttc6 |
T |
A |
12: 57,784,479 (GRCm39) |
D1849E |
probably benign |
Het |
| Ttn |
T |
C |
2: 76,615,882 (GRCm39) |
D8360G |
possibly damaging |
Het |
| Unc80 |
A |
G |
1: 66,679,711 (GRCm39) |
E2094G |
possibly damaging |
Het |
| Vmn2r18 |
A |
T |
5: 151,508,160 (GRCm39) |
D321E |
probably damaging |
Het |
|
| Other mutations in Ahnak2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02257:Ahnak2
|
APN |
12 |
112,748,905 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
IGL02994:Ahnak2
|
APN |
12 |
112,749,827 (GRCm39) |
missense |
probably damaging |
0.99 |
|
PIT4480001:Ahnak2
|
UTSW |
12 |
112,740,358 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
PIT4810001:Ahnak2
|
UTSW |
12 |
112,749,214 (GRCm39) |
missense |
|
|
|
R0025:Ahnak2
|
UTSW |
12 |
112,749,154 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0025:Ahnak2
|
UTSW |
12 |
112,749,154 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0038:Ahnak2
|
UTSW |
12 |
112,740,896 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0125:Ahnak2
|
UTSW |
12 |
112,748,776 (GRCm39) |
missense |
probably benign |
0.41 |
|
R1173:Ahnak2
|
UTSW |
12 |
112,749,409 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1494:Ahnak2
|
UTSW |
12 |
112,751,570 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1712:Ahnak2
|
UTSW |
12 |
112,748,998 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1888:Ahnak2
|
UTSW |
12 |
112,740,325 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R1888:Ahnak2
|
UTSW |
12 |
112,740,325 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R2042:Ahnak2
|
UTSW |
12 |
112,749,439 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2417:Ahnak2
|
UTSW |
12 |
112,741,805 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2762:Ahnak2
|
UTSW |
12 |
112,748,984 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R3618:Ahnak2
|
UTSW |
12 |
112,749,842 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3706:Ahnak2
|
UTSW |
12 |
112,740,085 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R3739:Ahnak2
|
UTSW |
12 |
112,740,992 (GRCm39) |
missense |
probably benign |
0.05 |
|
R3950:Ahnak2
|
UTSW |
12 |
112,749,409 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4485:Ahnak2
|
UTSW |
12 |
112,745,944 (GRCm39) |
unclassified |
probably benign |
|
|
R4651:Ahnak2
|
UTSW |
12 |
112,741,271 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R4652:Ahnak2
|
UTSW |
12 |
112,741,271 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R4831:Ahnak2
|
UTSW |
12 |
112,742,183 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4836:Ahnak2
|
UTSW |
12 |
112,740,550 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4837:Ahnak2
|
UTSW |
12 |
112,749,359 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4864:Ahnak2
|
UTSW |
12 |
112,740,040 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4908:Ahnak2
|
UTSW |
12 |
112,741,706 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5067:Ahnak2
|
UTSW |
12 |
112,748,936 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5146:Ahnak2
|
UTSW |
12 |
112,742,160 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5228:Ahnak2
|
UTSW |
12 |
112,741,820 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5255:Ahnak2
|
UTSW |
12 |
112,739,812 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R5323:Ahnak2
|
UTSW |
12 |
112,745,989 (GRCm39) |
unclassified |
probably benign |
|
|
R5523:Ahnak2
|
UTSW |
12 |
112,741,642 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5733:Ahnak2
|
UTSW |
12 |
112,742,100 (GRCm39) |
nonsense |
probably null |
|
|
R5799:Ahnak2
|
UTSW |
12 |
112,745,365 (GRCm39) |
unclassified |
probably benign |
|
|
R5817:Ahnak2
|
UTSW |
12 |
112,740,437 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5835:Ahnak2
|
UTSW |
12 |
112,742,230 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R6083:Ahnak2
|
UTSW |
12 |
112,746,589 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6083:Ahnak2
|
UTSW |
12 |
112,746,715 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6167:Ahnak2
|
UTSW |
12 |
112,747,750 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6168:Ahnak2
|
UTSW |
12 |
112,747,750 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6405:Ahnak2
|
UTSW |
12 |
112,739,771 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6460:Ahnak2
|
UTSW |
12 |
112,750,610 (GRCm39) |
missense |
probably null |
0.27 |
|
R6495:Ahnak2
|
UTSW |
12 |
112,740,148 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6544:Ahnak2
|
UTSW |
12 |
112,746,829 (GRCm39) |
unclassified |
probably benign |
|
|
R6656:Ahnak2
|
UTSW |
12 |
112,748,991 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6679:Ahnak2
|
UTSW |
12 |
112,739,410 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6723:Ahnak2
|
UTSW |
12 |
112,745,228 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6774:Ahnak2
|
UTSW |
12 |
112,740,172 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R6884:Ahnak2
|
UTSW |
12 |
112,741,863 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R6906:Ahnak2
|
UTSW |
12 |
112,748,933 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6919:Ahnak2
|
UTSW |
12 |
112,741,118 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R7036:Ahnak2
|
UTSW |
12 |
112,745,216 (GRCm39) |
unclassified |
probably benign |
|
|
R7037:Ahnak2
|
UTSW |
12 |
112,740,712 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7064:Ahnak2
|
UTSW |
12 |
112,746,919 (GRCm39) |
unclassified |
probably benign |
|
|
R7072:Ahnak2
|
UTSW |
12 |
112,751,786 (GRCm39) |
missense |
|
|
|
R7112:Ahnak2
|
UTSW |
12 |
112,747,747 (GRCm39) |
missense |
|
|
|
R7268:Ahnak2
|
UTSW |
12 |
112,780,802 (GRCm38) |
missense |
|
|
|
R7269:Ahnak2
|
UTSW |
12 |
112,780,802 (GRCm38) |
missense |
|
|
|
R7270:Ahnak2
|
UTSW |
12 |
112,780,802 (GRCm38) |
missense |
|
|
|
R7271:Ahnak2
|
UTSW |
12 |
112,780,802 (GRCm38) |
missense |
|
|
|
R7444:Ahnak2
|
UTSW |
12 |
112,745,831 (GRCm39) |
missense |
|
|
|
R7448:Ahnak2
|
UTSW |
12 |
112,746,605 (GRCm39) |
missense |
|
|
|
R7488:Ahnak2
|
UTSW |
12 |
112,748,641 (GRCm39) |
missense |
|
|
|
R7508:Ahnak2
|
UTSW |
12 |
112,740,839 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R7560:Ahnak2
|
UTSW |
12 |
112,745,851 (GRCm39) |
missense |
|
|
|
R7611:Ahnak2
|
UTSW |
12 |
112,751,749 (GRCm39) |
missense |
|
|
|
R7743:Ahnak2
|
UTSW |
12 |
112,748,383 (GRCm39) |
missense |
not run |
|
|
R7762:Ahnak2
|
UTSW |
12 |
112,742,114 (GRCm39) |
missense |
probably benign |
0.27 |
|
R7780:Ahnak2
|
UTSW |
12 |
112,746,716 (GRCm39) |
missense |
|
|
|
R7930:Ahnak2
|
UTSW |
12 |
112,745,560 (GRCm39) |
missense |
|
|
|
R7985:Ahnak2
|
UTSW |
12 |
112,745,398 (GRCm39) |
missense |
|
|
|
R8114:Ahnak2
|
UTSW |
12 |
112,741,163 (GRCm39) |
missense |
probably benign |
0.05 |
|
R8122:Ahnak2
|
UTSW |
12 |
112,742,510 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R8240:Ahnak2
|
UTSW |
12 |
112,741,082 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8289:Ahnak2
|
UTSW |
12 |
112,742,242 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R8315:Ahnak2
|
UTSW |
12 |
112,745,756 (GRCm39) |
missense |
|
|
|
R8430:Ahnak2
|
UTSW |
12 |
112,741,121 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R8476:Ahnak2
|
UTSW |
12 |
112,747,100 (GRCm39) |
unclassified |
probably benign |
|
|
R8712:Ahnak2
|
UTSW |
12 |
112,750,709 (GRCm39) |
missense |
|
|
|
R8712:Ahnak2
|
UTSW |
12 |
112,749,872 (GRCm39) |
missense |
|
|
|
R8778:Ahnak2
|
UTSW |
12 |
112,783,158 (GRCm38) |
missense |
|
|
|
R8830:Ahnak2
|
UTSW |
12 |
112,750,656 (GRCm39) |
missense |
|
|
|
R9014:Ahnak2
|
UTSW |
12 |
112,740,170 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9055:Ahnak2
|
UTSW |
12 |
112,741,019 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R9327:Ahnak2
|
UTSW |
12 |
112,748,446 (GRCm39) |
missense |
|
|
|
R9386:Ahnak2
|
UTSW |
12 |
112,745,428 (GRCm39) |
missense |
|
|
|
R9445:Ahnak2
|
UTSW |
12 |
112,745,978 (GRCm39) |
missense |
|
|
|
R9462:Ahnak2
|
UTSW |
12 |
112,750,655 (GRCm39) |
missense |
|
|
|
R9559:Ahnak2
|
UTSW |
12 |
112,749,782 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9571:Ahnak2
|
UTSW |
12 |
112,742,510 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R9589:Ahnak2
|
UTSW |
12 |
112,746,831 (GRCm39) |
missense |
|
|
|
R9664:Ahnak2
|
UTSW |
12 |
112,741,363 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9711:Ahnak2
|
UTSW |
12 |
112,739,468 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
Z1177:Ahnak2
|
UTSW |
12 |
112,745,822 (GRCm39) |
missense |
|
|
|
| Predicted Primers |
PCR Primer
(F):5'- AACTTGCTGTCTTTGGCCAC -3'
(R):5'- GCCCAGATACAAGTGAGCAG -3'
Sequencing Primer
(F):5'- GGCACTAGGGACCTGTATATTTAC -3'
(R):5'- AGATGCTGGAGCGCTGG -3'
|
| Posted On |
2014-09-17 |
Incidental Mutation