Incidental Mutation 'R7488:Ahnak2'
| ID |
580363 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ahnak2
|
| Ensembl Gene |
ENSMUSG00000072812 |
| Gene Name |
AHNAK nucleoprotein 2 |
| Synonyms |
LOC382643 |
| MMRRC Submission |
045562-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.075)
|
| Stock # |
R7488 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
12 |
| Chromosomal Location |
112738631-112766278 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 112748641 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 402
(I402T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000114522
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000124526]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
|
| SMART Domains |
Protein: ENSMUSP00000114522
Gene: ENSMUSG00000072812
AA Change: I402T
| 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: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.6%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 80 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2700049A03Rik |
T |
A |
12: 71,197,179 (GRCm39) |
F251I |
possibly damaging |
Het |
| Abcb11 |
C |
T |
2: 69,108,146 (GRCm39) |
G717D |
probably benign |
Het |
| Abcc1 |
G |
A |
16: 14,207,763 (GRCm39) |
W47* |
probably null |
Het |
| Ankfy1 |
G |
A |
11: 72,650,769 (GRCm39) |
R984Q |
probably benign |
Het |
| Apaf1 |
A |
G |
10: 90,890,242 (GRCm39) |
I598T |
probably benign |
Het |
| Apobec1 |
G |
T |
6: 122,558,521 (GRCm39) |
P78Q |
possibly damaging |
Het |
| Asap1 |
A |
T |
15: 63,991,974 (GRCm39) |
I737N |
probably benign |
Het |
| Aste1 |
T |
A |
9: 105,279,904 (GRCm39) |
|
probably null |
Het |
| Bcr |
A |
C |
10: 74,996,162 (GRCm39) |
D902A |
possibly damaging |
Het |
| Bicra |
T |
C |
7: 15,723,367 (GRCm39) |
|
probably null |
Het |
| Ccdc27 |
T |
C |
4: 154,117,424 (GRCm39) |
T508A |
probably benign |
Het |
| Ccz1 |
T |
A |
5: 143,928,401 (GRCm39) |
N383I |
probably damaging |
Het |
| Cdh24 |
T |
C |
14: 54,869,637 (GRCm39) |
D760G |
possibly damaging |
Het |
| Cdhr2 |
T |
C |
13: 54,865,728 (GRCm39) |
I242T |
probably benign |
Het |
| Cdk4 |
T |
A |
10: 126,900,106 (GRCm39) |
M1K |
probably null |
Het |
| Cfap96 |
A |
G |
8: 46,415,331 (GRCm39) |
V225A |
probably benign |
Het |
| Cntn5 |
A |
T |
9: 9,970,570 (GRCm39) |
S302T |
probably damaging |
Het |
| Col25a1 |
G |
T |
3: 130,378,350 (GRCm39) |
G601V |
probably damaging |
Het |
| Cpb1 |
A |
G |
3: 20,324,488 (GRCm39) |
L62P |
possibly damaging |
Het |
| Cpne1 |
T |
C |
2: 155,919,857 (GRCm39) |
T264A |
probably benign |
Het |
| Cpvl |
T |
A |
6: 53,924,727 (GRCm39) |
N198Y |
probably damaging |
Het |
| Cyp2u1 |
A |
C |
3: 131,091,596 (GRCm39) |
L308R |
probably damaging |
Het |
| Ddx54 |
G |
T |
5: 120,762,789 (GRCm39) |
V637L |
probably benign |
Het |
| Dglucy |
C |
A |
12: 100,823,310 (GRCm39) |
P472T |
possibly damaging |
Het |
| Dync2h1 |
A |
G |
9: 7,124,855 (GRCm39) |
Y2006H |
probably benign |
Het |
| Eif5b |
T |
C |
1: 38,089,387 (GRCm39) |
M1121T |
possibly damaging |
Het |
| Emsy |
A |
G |
7: 98,264,762 (GRCm39) |
V545A |
possibly damaging |
Het |
| Ezh1 |
G |
A |
11: 101,091,726 (GRCm39) |
L480F |
possibly damaging |
Het |
| Fbln2 |
T |
A |
6: 91,242,845 (GRCm39) |
|
probably null |
Het |
| Gja10 |
T |
A |
4: 32,602,058 (GRCm39) |
K109* |
probably null |
Het |
| Gm28042 |
A |
G |
2: 119,870,438 (GRCm39) |
N762S |
probably benign |
Het |
| Gnb1l |
C |
A |
16: 18,359,220 (GRCm39) |
P7Q |
possibly damaging |
Het |
| Grem2 |
A |
T |
1: 174,664,685 (GRCm39) |
S55T |
probably damaging |
Het |
| Gsn |
A |
T |
2: 35,186,433 (GRCm39) |
N393I |
possibly damaging |
Het |
| H6pd |
T |
A |
4: 150,067,093 (GRCm39) |
Q439L |
probably benign |
Het |
| Hmcn2 |
G |
A |
2: 31,310,842 (GRCm39) |
G3362E |
probably damaging |
Het |
| Ighv11-2 |
T |
C |
12: 114,011,978 (GRCm39) |
Y79C |
probably damaging |
Het |
| Ikzf2 |
T |
A |
1: 69,578,544 (GRCm39) |
N322Y |
probably benign |
Het |
| Il25 |
A |
G |
14: 55,170,459 (GRCm39) |
I11V |
probably benign |
Het |
| Jak2 |
C |
T |
19: 29,275,783 (GRCm39) |
T741I |
probably damaging |
Het |
| Kdm3b |
T |
C |
18: 34,957,934 (GRCm39) |
S1300P |
probably damaging |
Het |
| Ldb3 |
T |
A |
14: 34,289,402 (GRCm39) |
Q268L |
probably damaging |
Het |
| Lrrc23 |
T |
A |
6: 124,756,075 (GRCm39) |
D6V |
unknown |
Het |
| Megf10 |
A |
G |
18: 57,324,187 (GRCm39) |
Y76C |
probably damaging |
Het |
| Neb |
A |
T |
2: 52,110,233 (GRCm39) |
M205K |
probably benign |
Het |
| Or12e8 |
T |
C |
2: 87,188,597 (GRCm39) |
S270P |
probably damaging |
Het |
| Or6c2b |
G |
T |
10: 128,947,605 (GRCm39) |
Q230K |
probably benign |
Het |
| Or8a1 |
A |
G |
9: 37,641,983 (GRCm39) |
S99P |
probably damaging |
Het |
| Pcnx3 |
G |
A |
19: 5,717,487 (GRCm39) |
R1541W |
possibly damaging |
Het |
| Pdgfd |
A |
G |
9: 6,359,739 (GRCm39) |
Y270C |
probably damaging |
Het |
| Pds5b |
A |
T |
5: 150,646,802 (GRCm39) |
D197V |
probably damaging |
Het |
| Pknox2 |
A |
G |
9: 36,866,127 (GRCm39) |
M30T |
probably benign |
Het |
| Plekhg1 |
A |
T |
10: 3,907,491 (GRCm39) |
S858C |
|
Het |
| Por |
A |
T |
5: 135,762,498 (GRCm39) |
E400D |
probably benign |
Het |
| Pou2af2 |
C |
A |
9: 51,201,360 (GRCm39) |
R232L |
probably damaging |
Het |
| Psip1 |
A |
G |
4: 83,391,275 (GRCm39) |
|
probably null |
Het |
| Retreg1 |
G |
T |
15: 25,889,628 (GRCm39) |
V111F |
|
Het |
| Rock1 |
G |
A |
18: 10,122,762 (GRCm39) |
A353V |
probably damaging |
Het |
| Rpl6 |
C |
G |
5: 121,346,591 (GRCm39) |
R231G |
probably benign |
Het |
| Scn7a |
C |
T |
2: 66,587,574 (GRCm39) |
R43H |
probably benign |
Het |
| Scnn1g |
T |
A |
7: 121,362,657 (GRCm39) |
N488K |
probably benign |
Het |
| Slc24a1 |
A |
G |
9: 64,831,764 (GRCm39) |
V1111A |
probably benign |
Het |
| Snapc1 |
C |
T |
12: 74,029,285 (GRCm39) |
S356L |
probably benign |
Het |
| Spata31e2 |
T |
C |
1: 26,723,039 (GRCm39) |
T714A |
possibly damaging |
Het |
| Ssbp2 |
T |
A |
13: 91,823,209 (GRCm39) |
N201K |
probably damaging |
Het |
| Tfdp2 |
A |
G |
9: 96,179,695 (GRCm39) |
N43D |
probably damaging |
Het |
| Tmprss11d |
A |
G |
5: 86,474,309 (GRCm39) |
I216T |
probably damaging |
Het |
| Tmprss4 |
A |
G |
9: 45,086,853 (GRCm39) |
S303P |
probably benign |
Het |
| Tnpo2 |
A |
G |
8: 85,781,663 (GRCm39) |
E815G |
probably benign |
Het |
| Trav6-1 |
A |
C |
14: 52,875,972 (GRCm39) |
M1L |
possibly damaging |
Het |
| Trpm3 |
T |
C |
19: 22,955,937 (GRCm39) |
V1133A |
probably damaging |
Het |
| Trpv1 |
C |
T |
11: 73,129,355 (GRCm39) |
P91S |
probably benign |
Het |
| Trpv2 |
T |
C |
11: 62,480,576 (GRCm39) |
Y338H |
probably damaging |
Het |
| Txnip |
T |
C |
3: 96,467,539 (GRCm39) |
M336T |
probably benign |
Het |
| Vmn1r61 |
A |
T |
7: 5,613,767 (GRCm39) |
H182Q |
possibly damaging |
Het |
| Vmn2r105 |
A |
G |
17: 20,429,045 (GRCm39) |
V677A |
probably damaging |
Het |
| Wwp1 |
G |
T |
4: 19,627,660 (GRCm39) |
T745K |
probably damaging |
Het |
| Xkr5 |
C |
A |
8: 18,983,608 (GRCm39) |
E645* |
probably null |
Het |
| Zfp451 |
C |
T |
1: 33,818,221 (GRCm39) |
R303H |
probably benign |
Het |
| Zyg11b |
T |
C |
4: 108,123,655 (GRCm39) |
H104R |
possibly 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 |
|
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 |
|
|
|
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'- TCTTTCAGAGACAGTCTTGCAATG -3'
(R):5'- GAGCCCAGATACAAGTGAGC -3'
Sequencing Primer
(F):5'- GAGACAGTCTTGCAATGCCAATTTC -3'
(R):5'- GGAGATGCTGGAGCGCTG -3'
|
| Posted On |
2019-10-07 |
Incidental Mutation