Incidental Mutation 'R0125:Ahnak2'
| ID |
21318 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ahnak2
|
| Ensembl Gene |
ENSMUSG00000072812 |
| Gene Name |
AHNAK nucleoprotein 2 |
| Synonyms |
LOC382643 |
| MMRRC Submission |
038410-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.074)
|
| Stock # |
R0125 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
(trace)
|
| Chromosome |
12 |
| Chromosomal Location |
112738631-112766278 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 112748776 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Isoleucine
at position 357
(T357I)
|
| 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: T357I
PolyPhen 2
Score 0.415 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000114522
Gene: ENSMUSG00000072812
AA Change: T357I
| 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 |
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 98.9%
- 3x: 97.9%
- 10x: 94.7%
- 20x: 87.1%
|
| Validation Efficiency |
98% (96/98) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 89 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 9930012K11Rik |
T |
C |
14: 70,394,096 (GRCm39) |
|
probably benign |
Het |
| Adam23 |
T |
C |
1: 63,573,515 (GRCm39) |
L261P |
probably benign |
Het |
| Adgra3 |
G |
A |
5: 50,159,194 (GRCm39) |
|
probably benign |
Het |
| Agtr1b |
A |
G |
3: 20,369,704 (GRCm39) |
F301L |
probably benign |
Het |
| Aldh1a7 |
T |
C |
19: 20,704,430 (GRCm39) |
|
probably benign |
Het |
| Apoh |
A |
T |
11: 108,302,899 (GRCm39) |
N288I |
probably damaging |
Het |
| Arfgap3 |
A |
G |
15: 83,227,340 (GRCm39) |
V24A |
probably benign |
Het |
| Atp6v0a1 |
A |
G |
11: 100,929,677 (GRCm39) |
|
probably null |
Het |
| Axl |
A |
T |
7: 25,486,368 (GRCm39) |
M112K |
probably benign |
Het |
| Bnc2 |
A |
C |
4: 84,211,169 (GRCm39) |
I425S |
probably damaging |
Het |
| Ccn4 |
T |
C |
15: 66,789,194 (GRCm39) |
S227P |
possibly damaging |
Het |
| Cdc42bpa |
C |
T |
1: 179,788,763 (GRCm39) |
T30M |
probably damaging |
Het |
| Cebpz |
C |
A |
17: 79,227,317 (GRCm39) |
R1051M |
possibly damaging |
Het |
| Ces1d |
A |
C |
8: 93,901,810 (GRCm39) |
|
probably benign |
Het |
| Chd1l |
T |
C |
3: 97,494,465 (GRCm39) |
N405S |
probably benign |
Het |
| Chodl |
G |
T |
16: 78,738,311 (GRCm39) |
G93V |
probably damaging |
Het |
| Cpeb2 |
C |
T |
5: 43,395,743 (GRCm39) |
|
probably benign |
Het |
| Crebbp |
A |
G |
16: 3,935,105 (GRCm39) |
|
probably benign |
Het |
| Crybb3 |
T |
C |
5: 113,227,675 (GRCm39) |
T49A |
possibly damaging |
Het |
| Ctps1 |
A |
G |
4: 120,418,722 (GRCm39) |
|
probably benign |
Het |
| Cyp26b1 |
A |
G |
6: 84,551,497 (GRCm39) |
Y240H |
probably damaging |
Het |
| Cyp2d11 |
A |
C |
15: 82,273,422 (GRCm39) |
V483G |
probably benign |
Het |
| Dennd2b |
T |
C |
7: 109,155,545 (GRCm39) |
K402E |
probably benign |
Het |
| Dnah14 |
A |
T |
1: 181,579,628 (GRCm39) |
N3054Y |
probably damaging |
Het |
| Dspp |
A |
C |
5: 104,325,905 (GRCm39) |
D756A |
unknown |
Het |
| Dst |
T |
C |
1: 34,309,984 (GRCm39) |
S1553P |
probably damaging |
Het |
| Elp4 |
A |
G |
2: 105,622,559 (GRCm39) |
|
probably null |
Het |
| Eml6 |
G |
T |
11: 29,832,088 (GRCm39) |
T194K |
probably benign |
Het |
| Evi5 |
A |
G |
5: 107,943,638 (GRCm39) |
I569T |
probably benign |
Het |
| Fancm |
C |
T |
12: 65,168,730 (GRCm39) |
P1698S |
possibly damaging |
Het |
| Fhdc1 |
T |
C |
3: 84,352,852 (GRCm39) |
D791G |
probably benign |
Het |
| Frem1 |
A |
G |
4: 82,930,188 (GRCm39) |
Y253H |
probably damaging |
Het |
| Gpn3 |
A |
G |
5: 122,519,481 (GRCm39) |
Y196C |
probably benign |
Het |
| Hcls1 |
A |
G |
16: 36,782,525 (GRCm39) |
D398G |
probably benign |
Het |
| Hydin |
T |
C |
8: 111,189,163 (GRCm39) |
V1189A |
probably benign |
Het |
| Itgb3 |
G |
A |
11: 104,534,789 (GRCm39) |
D549N |
probably damaging |
Het |
| Itpr2 |
A |
G |
6: 146,141,951 (GRCm39) |
F1697S |
probably benign |
Het |
| Klk1b11 |
A |
G |
7: 43,648,475 (GRCm39) |
T161A |
probably benign |
Het |
| Kntc1 |
G |
A |
5: 123,903,120 (GRCm39) |
|
probably benign |
Het |
| Map3k19 |
A |
T |
1: 127,750,837 (GRCm39) |
F838Y |
probably benign |
Het |
| Map6 |
T |
A |
7: 98,985,187 (GRCm39) |
|
probably null |
Het |
| Mcrs1 |
A |
G |
15: 99,142,608 (GRCm39) |
|
probably benign |
Het |
| Mdn1 |
A |
T |
4: 32,729,956 (GRCm39) |
Y2766F |
probably damaging |
Het |
| Med23 |
C |
T |
10: 24,776,686 (GRCm39) |
H739Y |
probably damaging |
Het |
| Mmp17 |
T |
A |
5: 129,671,646 (GRCm39) |
D65E |
possibly damaging |
Het |
| Mmp9 |
T |
A |
2: 164,793,177 (GRCm39) |
L442Q |
probably damaging |
Het |
| Myo19 |
T |
C |
11: 84,779,001 (GRCm39) |
|
probably benign |
Het |
| Nedd1 |
A |
C |
10: 92,527,791 (GRCm39) |
S468A |
possibly damaging |
Het |
| Niban2 |
T |
A |
2: 32,813,833 (GRCm39) |
V682D |
probably benign |
Het |
| Nlrp4d |
A |
C |
7: 10,116,316 (GRCm39) |
V152G |
probably damaging |
Het |
| Nxf1 |
T |
A |
19: 8,740,170 (GRCm39) |
D112E |
probably benign |
Het |
| Oas1h |
A |
T |
5: 121,000,626 (GRCm39) |
K79* |
probably null |
Het |
| Omg |
T |
A |
11: 79,393,679 (GRCm39) |
I60F |
possibly damaging |
Het |
| Or5p69 |
A |
G |
7: 107,967,576 (GRCm39) |
Y293C |
probably damaging |
Het |
| Or8b101 |
A |
G |
9: 38,020,815 (GRCm39) |
T278A |
probably benign |
Het |
| Or8b1b |
T |
A |
9: 38,375,757 (GRCm39) |
L140* |
probably null |
Het |
| Pck1 |
G |
A |
2: 172,997,874 (GRCm39) |
W314* |
probably null |
Het |
| Pla2g15 |
T |
C |
8: 106,889,756 (GRCm39) |
Y343H |
probably benign |
Het |
| Plcb3 |
T |
C |
19: 6,936,276 (GRCm39) |
E749G |
probably damaging |
Het |
| Plgrkt |
A |
G |
19: 29,328,442 (GRCm39) |
|
probably null |
Het |
| Pprc1 |
A |
G |
19: 46,057,951 (GRCm39) |
|
probably benign |
Het |
| Prkdc |
A |
T |
16: 15,516,871 (GRCm39) |
I1082F |
probably damaging |
Het |
| Rapgef6 |
T |
A |
11: 54,516,701 (GRCm39) |
Y172* |
probably null |
Het |
| Ros1 |
G |
T |
10: 52,001,885 (GRCm39) |
A1079D |
probably benign |
Het |
| Sap30 |
T |
C |
8: 57,938,545 (GRCm39) |
E147G |
probably null |
Het |
| Sell |
T |
C |
1: 163,899,674 (GRCm39) |
|
probably benign |
Het |
| Senp1 |
A |
T |
15: 97,946,112 (GRCm39) |
D544E |
probably damaging |
Het |
| Shpk |
G |
A |
11: 73,105,048 (GRCm39) |
|
probably benign |
Het |
| Slc35b1 |
A |
T |
11: 95,277,353 (GRCm39) |
T74S |
probably benign |
Het |
| Slc6a3 |
T |
A |
13: 73,718,098 (GRCm39) |
|
probably benign |
Het |
| Slf1 |
T |
C |
13: 77,191,864 (GRCm39) |
N990S |
probably benign |
Het |
| Smgc |
A |
G |
15: 91,738,746 (GRCm39) |
|
probably benign |
Het |
| Snx19 |
T |
A |
9: 30,351,515 (GRCm39) |
V861D |
probably damaging |
Het |
| Sprr2e |
C |
T |
3: 92,260,285 (GRCm39) |
P39S |
unknown |
Het |
| Sstr2 |
T |
A |
11: 113,515,303 (GRCm39) |
M74K |
probably damaging |
Het |
| Svep1 |
T |
C |
4: 58,099,937 (GRCm39) |
|
probably benign |
Het |
| Tas2r143 |
A |
G |
6: 42,377,889 (GRCm39) |
I240V |
probably benign |
Het |
| Tbrg1 |
T |
C |
9: 37,563,937 (GRCm39) |
I233V |
probably benign |
Het |
| Tecpr1 |
G |
T |
5: 144,134,717 (GRCm39) |
D1055E |
probably damaging |
Het |
| Thap2 |
A |
T |
10: 115,212,277 (GRCm39) |
|
probably null |
Het |
| Tinagl1 |
A |
G |
4: 130,060,101 (GRCm39) |
Y388H |
probably damaging |
Het |
| Ttn |
T |
A |
2: 76,585,896 (GRCm39) |
Y21945F |
probably damaging |
Het |
| Ugt2b1 |
A |
T |
5: 87,073,961 (GRCm39) |
W133R |
probably benign |
Het |
| Usp24 |
C |
T |
4: 106,254,496 (GRCm39) |
P1491L |
possibly damaging |
Het |
| Utp15 |
A |
G |
13: 98,387,390 (GRCm39) |
S395P |
possibly damaging |
Het |
| Vav1 |
T |
A |
17: 57,606,847 (GRCm39) |
L254Q |
probably damaging |
Het |
| Vmn2r104 |
T |
C |
17: 20,250,069 (GRCm39) |
Y734C |
probably damaging |
Het |
| Vps8 |
T |
A |
16: 21,288,904 (GRCm39) |
V421E |
probably benign |
Het |
| Xkr7 |
G |
T |
2: 152,874,346 (GRCm39) |
A138S |
probably benign |
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 |
|
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 |
|
R2056:Ahnak2
|
UTSW |
12 |
112,748,626 (GRCm39) |
missense |
probably benign |
0.00 |
|
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'- TCTTTCAGAGACAGTCTTGCAATGCC -3'
(R):5'- CAGTTCTTCAGAAGCCTCAGAACACAG -3'
Sequencing Primer
(F):5'- GACAGTCTTGCAATGCCAATTTC -3'
(R):5'- GACACAGAAGTCCACAGGACAG -3'
|
| Posted On |
2013-04-11 |
Incidental Mutation