Incidental Mutation 'R4864:Ahnak2'
ID |
374773 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ahnak2
|
Ensembl Gene |
ENSMUSG00000072812 |
Gene Name |
AHNAK nucleoprotein 2 |
Synonyms |
LOC382643 |
MMRRC Submission |
042474-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.075)
|
Stock # |
R4864 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
12 |
Chromosomal Location |
112738631-112766278 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 112740040 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Leucine
at position 538
(S538L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000098572
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000063888]
[ENSMUST00000101010]
[ENSMUST00000128258]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000063888
|
SMART Domains |
Protein: ENSMUSP00000067002 Gene: ENSMUSG00000052160
Domain | Start | End | E-Value | Type |
transmembrane domain
|
35 |
57 |
N/A |
INTRINSIC |
low complexity region
|
113 |
124 |
N/A |
INTRINSIC |
PLDc
|
207 |
234 |
1.64e-10 |
SMART |
Pfam:PLDc_3
|
237 |
414 |
5.5e-41 |
PFAM |
PLDc
|
421 |
447 |
4.66e-6 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000101010
AA Change: S538L
PolyPhen 2
Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000098572 Gene: ENSMUSG00000072812 AA Change: S538L
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
14 |
N/A |
INTRINSIC |
low complexity region
|
364 |
375 |
N/A |
INTRINSIC |
low complexity region
|
545 |
564 |
N/A |
INTRINSIC |
low complexity region
|
717 |
733 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000128258
AA Change: S1344L
PolyPhen 2
Score 0.953 (Sensitivity: 0.79; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000122404 Gene: ENSMUSG00000072812 AA Change: S1344L
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
66 |
N/A |
INTRINSIC |
internal_repeat_1
|
67 |
251 |
2.35e-83 |
PROSPERO |
low complexity region
|
285 |
308 |
N/A |
INTRINSIC |
low complexity region
|
371 |
389 |
N/A |
INTRINSIC |
internal_repeat_1
|
413 |
597 |
2.35e-83 |
PROSPERO |
low complexity region
|
734 |
756 |
N/A |
INTRINSIC |
low complexity region
|
811 |
820 |
N/A |
INTRINSIC |
low complexity region
|
1170 |
1181 |
N/A |
INTRINSIC |
low complexity region
|
1351 |
1370 |
N/A |
INTRINSIC |
low complexity region
|
1523 |
1539 |
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 |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000221115
|
Meta Mutation Damage Score |
0.6467 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 93.8%
|
Validation Efficiency |
99% (93/94) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930578I06Rik |
C |
T |
14: 64,210,658 (GRCm39) |
R190H |
probably benign |
Het |
Acp6 |
T |
C |
3: 97,066,683 (GRCm39) |
|
probably null |
Het |
Adora3 |
T |
A |
3: 105,815,131 (GRCm39) |
Y148N |
probably damaging |
Het |
Aox3 |
T |
G |
1: 58,215,646 (GRCm39) |
V1026G |
probably damaging |
Het |
Ap3d1 |
TTCTCTCTCTCTCTCTCT |
TTCTCTCTCTCTCTCT |
10: 80,548,612 (GRCm39) |
|
probably null |
Het |
Arhgef37 |
G |
A |
18: 61,627,996 (GRCm39) |
A649V |
probably benign |
Het |
Atp5f1a |
G |
A |
18: 77,869,015 (GRCm39) |
R413H |
possibly damaging |
Het |
Bace1 |
A |
T |
9: 45,766,109 (GRCm39) |
I179F |
probably damaging |
Het |
Brinp1 |
A |
G |
4: 68,717,123 (GRCm39) |
F242L |
probably damaging |
Het |
Brk1 |
T |
C |
6: 113,592,805 (GRCm39) |
Y63H |
possibly damaging |
Het |
Ccdc74a |
A |
G |
16: 17,466,736 (GRCm39) |
T148A |
probably benign |
Het |
Cenpc1 |
T |
A |
5: 86,193,180 (GRCm39) |
L236F |
probably damaging |
Het |
Col13a1 |
C |
T |
10: 61,698,439 (GRCm39) |
E541K |
unknown |
Het |
Copg1 |
T |
A |
6: 87,866,678 (GRCm39) |
C44S |
probably damaging |
Het |
D130043K22Rik |
A |
G |
13: 25,047,595 (GRCm39) |
E380G |
probably damaging |
Het |
Dchs1 |
T |
C |
7: 105,404,460 (GRCm39) |
D2694G |
probably damaging |
Het |
Dgkd |
A |
T |
1: 87,844,560 (GRCm39) |
N242I |
possibly damaging |
Het |
Dnah2 |
C |
T |
11: 69,313,416 (GRCm39) |
V4248I |
probably damaging |
Het |
Dpy19l3 |
T |
A |
7: 35,411,607 (GRCm39) |
K376* |
probably null |
Het |
Eef1d |
A |
G |
15: 75,775,255 (GRCm39) |
S135P |
possibly damaging |
Het |
Epc2 |
T |
A |
2: 49,427,177 (GRCm39) |
S574T |
probably benign |
Het |
Eps15 |
G |
A |
4: 109,223,727 (GRCm39) |
|
probably benign |
Het |
Eps8 |
T |
C |
6: 137,455,967 (GRCm39) |
|
probably benign |
Het |
Exoc5 |
A |
T |
14: 49,289,839 (GRCm39) |
V13E |
probably benign |
Het |
Fbn1 |
A |
T |
2: 125,214,317 (GRCm39) |
C765S |
possibly damaging |
Het |
Fbxo5 |
A |
T |
10: 5,752,392 (GRCm39) |
C74S |
probably benign |
Het |
Fbxw9 |
T |
C |
8: 85,792,530 (GRCm39) |
S322P |
probably damaging |
Het |
Fmo5 |
T |
A |
3: 97,553,195 (GRCm39) |
I381N |
probably damaging |
Het |
Fmo6 |
T |
C |
1: 162,751,964 (GRCm39) |
D175G |
probably benign |
Het |
Gm7361 |
A |
G |
5: 26,467,008 (GRCm39) |
|
probably null |
Het |
Gm9961 |
G |
A |
16: 11,720,899 (GRCm39) |
|
probably benign |
Het |
Golga7b |
T |
A |
19: 42,255,405 (GRCm39) |
|
probably null |
Het |
Gorab |
T |
C |
1: 163,213,967 (GRCm39) |
E321G |
probably benign |
Het |
Gpx1 |
T |
A |
9: 108,216,594 (GRCm39) |
V28E |
probably benign |
Het |
H2-T15 |
T |
A |
17: 36,369,253 (GRCm39) |
|
probably benign |
Het |
H3c14 |
T |
C |
3: 96,154,575 (GRCm39) |
I125T |
probably damaging |
Het |
Hk1 |
T |
C |
10: 62,178,318 (GRCm39) |
S8G |
probably benign |
Het |
Iqsec1 |
C |
T |
6: 90,641,038 (GRCm39) |
R1026H |
probably damaging |
Het |
Kdm4b |
A |
T |
17: 56,660,091 (GRCm39) |
Y86F |
probably benign |
Het |
Kprp |
C |
T |
3: 92,731,829 (GRCm39) |
R407Q |
unknown |
Het |
Lamb1 |
C |
T |
12: 31,371,005 (GRCm39) |
T1400M |
probably benign |
Het |
Lcor |
G |
T |
19: 41,573,803 (GRCm39) |
A853S |
probably benign |
Het |
Lrriq3 |
T |
A |
3: 154,893,447 (GRCm39) |
Y383N |
possibly damaging |
Het |
Map3k21 |
T |
C |
8: 126,654,294 (GRCm39) |
I371T |
probably benign |
Het |
Mllt1 |
A |
T |
17: 57,212,819 (GRCm39) |
F105I |
probably damaging |
Het |
Nfatc2 |
A |
G |
2: 168,378,312 (GRCm39) |
M451T |
probably damaging |
Het |
Nfkbiz |
A |
C |
16: 55,638,787 (GRCm39) |
N224K |
probably damaging |
Het |
Nlrp4d |
A |
G |
7: 10,115,088 (GRCm39) |
V531A |
noncoding transcript |
Het |
Noc3l |
A |
G |
19: 38,778,081 (GRCm39) |
Y778H |
probably benign |
Het |
Nup98 |
C |
A |
7: 101,802,403 (GRCm39) |
A734S |
possibly damaging |
Het |
Or2ag18 |
T |
C |
7: 106,405,171 (GRCm39) |
Y166C |
probably damaging |
Het |
Or4k2 |
T |
A |
14: 50,424,039 (GRCm39) |
I212F |
probably damaging |
Het |
Or9g20 |
A |
G |
2: 85,630,033 (GRCm39) |
Y194H |
probably damaging |
Het |
Or9r7 |
T |
A |
10: 129,962,756 (GRCm39) |
R57* |
probably null |
Het |
Pate4 |
A |
T |
9: 35,519,535 (GRCm39) |
C52S |
probably damaging |
Het |
Pecr |
C |
A |
1: 72,316,490 (GRCm39) |
A72S |
probably benign |
Het |
Pomt1 |
A |
G |
2: 32,142,004 (GRCm39) |
N578S |
probably benign |
Het |
Ppm1a |
T |
C |
12: 72,830,738 (GRCm39) |
S88P |
probably benign |
Het |
Ppm1l |
T |
A |
3: 69,449,844 (GRCm39) |
|
probably benign |
Het |
Prdm13 |
A |
G |
4: 21,685,543 (GRCm39) |
S86P |
unknown |
Het |
Prph2 |
T |
C |
17: 47,221,848 (GRCm39) |
S76P |
probably benign |
Het |
Sarnp |
G |
A |
10: 128,669,212 (GRCm39) |
R23H |
probably damaging |
Het |
Septin1 |
T |
C |
7: 126,816,064 (GRCm39) |
|
probably benign |
Het |
Serpini1 |
T |
C |
3: 75,520,481 (GRCm39) |
I26T |
probably benign |
Het |
Setdb2 |
A |
G |
14: 59,646,715 (GRCm39) |
I616T |
probably benign |
Het |
Slc2a10 |
T |
C |
2: 165,356,541 (GRCm39) |
F67S |
probably benign |
Het |
Slc38a6 |
T |
A |
12: 73,390,424 (GRCm39) |
|
probably null |
Het |
Smg6 |
T |
C |
11: 74,820,988 (GRCm39) |
S420P |
possibly damaging |
Het |
Srp72 |
T |
A |
5: 77,132,009 (GRCm39) |
H229Q |
probably benign |
Het |
Ston2 |
A |
G |
12: 91,615,448 (GRCm39) |
V320A |
possibly damaging |
Het |
Stx3 |
A |
T |
19: 11,754,515 (GRCm39) |
I269N |
possibly damaging |
Het |
Tdg-ps |
A |
G |
15: 82,400,843 (GRCm39) |
|
noncoding transcript |
Het |
Tecpr1 |
T |
A |
5: 144,150,935 (GRCm39) |
N291I |
probably benign |
Het |
Tmem177 |
A |
G |
1: 119,838,553 (GRCm39) |
V42A |
probably benign |
Het |
Trim26 |
T |
A |
17: 37,168,886 (GRCm39) |
|
probably benign |
Het |
Ttc17 |
A |
G |
2: 94,196,980 (GRCm39) |
S456P |
probably benign |
Het |
Tubgcp6 |
T |
C |
15: 88,988,021 (GRCm39) |
Y984C |
probably benign |
Het |
Unc5cl |
A |
G |
17: 48,766,872 (GRCm39) |
E82G |
possibly damaging |
Het |
Uncx |
T |
C |
5: 139,529,875 (GRCm39) |
S43P |
probably damaging |
Het |
Vmn1r1 |
A |
G |
1: 181,985,332 (GRCm39) |
V111A |
probably benign |
Het |
Vmn1r168 |
A |
G |
7: 23,240,907 (GRCm39) |
I255V |
probably damaging |
Het |
Vwce |
A |
G |
19: 10,628,000 (GRCm39) |
T487A |
probably benign |
Het |
Xaf1 |
A |
G |
11: 72,197,682 (GRCm39) |
|
probably benign |
Het |
Zfp27 |
G |
T |
7: 29,594,261 (GRCm39) |
P568Q |
probably damaging |
Het |
Zfp382 |
A |
T |
7: 29,832,885 (GRCm39) |
I179F |
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 |
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'- TCAAGAATCTCTGCGGGCTC -3'
(R):5'- TTCAGGGGTCTCGAGGTGAAAG -3'
Sequencing Primer
(F):5'- TGCGGGCTCCTCATCAGAG -3'
(R):5'- AAGTCGCTCTTCCTAGCAGG -3'
|
Posted On |
2016-03-17 |