Incidental Mutation 'R1982:Aatk'
ID |
219995 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Aatk
|
Ensembl Gene |
ENSMUSG00000025375 |
Gene Name |
apoptosis-associated tyrosine kinase |
Synonyms |
AATYK1 |
MMRRC Submission |
039994-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.135)
|
Stock # |
R1982 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
11 |
Chromosomal Location |
119898139-119937993 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 119904340 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Glutamine
at position 252
(P252Q)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000099309
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000064307]
[ENSMUST00000103019]
[ENSMUST00000103020]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000064307
AA Change: P309Q
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000067181 Gene: ENSMUSG00000025375 AA Change: P309Q
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
low complexity region
|
30 |
49 |
N/A |
INTRINSIC |
Pfam:Pkinase_Tyr
|
135 |
405 |
3.9e-63 |
PFAM |
Pfam:Pkinase
|
136 |
404 |
2.6e-33 |
PFAM |
low complexity region
|
425 |
457 |
N/A |
INTRINSIC |
low complexity region
|
502 |
514 |
N/A |
INTRINSIC |
low complexity region
|
615 |
624 |
N/A |
INTRINSIC |
low complexity region
|
647 |
666 |
N/A |
INTRINSIC |
low complexity region
|
684 |
695 |
N/A |
INTRINSIC |
low complexity region
|
808 |
819 |
N/A |
INTRINSIC |
low complexity region
|
913 |
927 |
N/A |
INTRINSIC |
low complexity region
|
934 |
943 |
N/A |
INTRINSIC |
low complexity region
|
985 |
1004 |
N/A |
INTRINSIC |
low complexity region
|
1063 |
1082 |
N/A |
INTRINSIC |
low complexity region
|
1085 |
1096 |
N/A |
INTRINSIC |
low complexity region
|
1160 |
1174 |
N/A |
INTRINSIC |
low complexity region
|
1179 |
1204 |
N/A |
INTRINSIC |
low complexity region
|
1319 |
1333 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000083666
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000103019
AA Change: P252Q
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000099308 Gene: ENSMUSG00000025375 AA Change: P252Q
Domain | Start | End | E-Value | Type |
Pfam:Pkinase
|
78 |
347 |
3e-36 |
PFAM |
Pfam:Pkinase_Tyr
|
78 |
348 |
1.9e-62 |
PFAM |
low complexity region
|
368 |
400 |
N/A |
INTRINSIC |
low complexity region
|
445 |
457 |
N/A |
INTRINSIC |
low complexity region
|
558 |
567 |
N/A |
INTRINSIC |
low complexity region
|
590 |
609 |
N/A |
INTRINSIC |
low complexity region
|
627 |
638 |
N/A |
INTRINSIC |
low complexity region
|
751 |
762 |
N/A |
INTRINSIC |
low complexity region
|
856 |
870 |
N/A |
INTRINSIC |
low complexity region
|
877 |
886 |
N/A |
INTRINSIC |
low complexity region
|
928 |
947 |
N/A |
INTRINSIC |
low complexity region
|
1006 |
1025 |
N/A |
INTRINSIC |
low complexity region
|
1028 |
1039 |
N/A |
INTRINSIC |
low complexity region
|
1103 |
1117 |
N/A |
INTRINSIC |
low complexity region
|
1122 |
1147 |
N/A |
INTRINSIC |
low complexity region
|
1262 |
1276 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000103020
AA Change: P252Q
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000099309 Gene: ENSMUSG00000025375 AA Change: P252Q
Domain | Start | End | E-Value | Type |
Pfam:Pkinase
|
78 |
347 |
3e-36 |
PFAM |
Pfam:Pkinase_Tyr
|
78 |
348 |
1.9e-62 |
PFAM |
low complexity region
|
368 |
400 |
N/A |
INTRINSIC |
low complexity region
|
445 |
457 |
N/A |
INTRINSIC |
low complexity region
|
558 |
567 |
N/A |
INTRINSIC |
low complexity region
|
590 |
609 |
N/A |
INTRINSIC |
low complexity region
|
627 |
638 |
N/A |
INTRINSIC |
low complexity region
|
751 |
762 |
N/A |
INTRINSIC |
low complexity region
|
856 |
870 |
N/A |
INTRINSIC |
low complexity region
|
877 |
886 |
N/A |
INTRINSIC |
low complexity region
|
928 |
947 |
N/A |
INTRINSIC |
low complexity region
|
1006 |
1025 |
N/A |
INTRINSIC |
low complexity region
|
1028 |
1039 |
N/A |
INTRINSIC |
low complexity region
|
1103 |
1117 |
N/A |
INTRINSIC |
low complexity region
|
1122 |
1147 |
N/A |
INTRINSIC |
low complexity region
|
1262 |
1276 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128836
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000132575
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000150730
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000198674
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142959
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134319
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000136386
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.5%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains a tyrosine kinase domain at the N-terminus and a proline-rich domain at the C-terminus. This gene is induced during apoptosis, and expression of this gene may be a necessary pre-requisite for the induction of growth arrest and/or apoptosis of myeloid precursor cells. This gene has been shown to produce neuronal differentiation in a neuroblastoma cell line. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2011] PHENOTYPE: Mice homozygous for a knock-out allele exhibit decreased brain size, longer axons and fewer neurites. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts4 |
T |
C |
1: 171,086,503 (GRCm39) |
V765A |
probably benign |
Het |
Agfg2 |
A |
T |
5: 137,662,515 (GRCm39) |
V184E |
possibly damaging |
Het |
Alas1 |
A |
T |
9: 106,115,384 (GRCm39) |
I48N |
probably damaging |
Het |
Anks1 |
T |
C |
17: 28,204,095 (GRCm39) |
V181A |
probably damaging |
Het |
Anxa8 |
A |
T |
14: 33,818,527 (GRCm39) |
R261S |
probably damaging |
Het |
Aqp4 |
T |
C |
18: 15,526,608 (GRCm39) |
D291G |
probably damaging |
Het |
Atrn |
A |
G |
2: 130,812,142 (GRCm39) |
R696G |
probably benign |
Het |
Barx2 |
A |
C |
9: 31,824,308 (GRCm39) |
I27S |
probably damaging |
Het |
Btnl1 |
A |
T |
17: 34,598,725 (GRCm39) |
I114L |
possibly damaging |
Het |
Casq1 |
C |
T |
1: 172,043,097 (GRCm39) |
A200T |
probably damaging |
Het |
Ccdc33 |
T |
A |
9: 58,024,451 (GRCm39) |
E225D |
probably benign |
Het |
Cd84 |
C |
A |
1: 171,712,152 (GRCm39) |
|
probably null |
Het |
Ceacam9 |
T |
G |
7: 16,459,232 (GRCm39) |
L177R |
probably benign |
Het |
Cenpi |
T |
A |
X: 133,218,782 (GRCm39) |
F161L |
possibly damaging |
Het |
Cep63 |
T |
C |
9: 102,480,079 (GRCm39) |
K251E |
probably damaging |
Het |
Cetn3 |
A |
G |
13: 81,932,816 (GRCm39) |
E25G |
probably damaging |
Het |
Crybg3 |
T |
C |
16: 59,364,488 (GRCm39) |
D2378G |
possibly damaging |
Het |
Ddx19b |
T |
C |
8: 111,735,975 (GRCm39) |
T357A |
possibly damaging |
Het |
Dpep2 |
A |
C |
8: 106,716,087 (GRCm39) |
Y266* |
probably null |
Het |
Dqx1 |
G |
A |
6: 83,035,558 (GRCm39) |
D24N |
probably damaging |
Het |
Dsg4 |
A |
T |
18: 20,604,269 (GRCm39) |
Y912F |
probably damaging |
Het |
Fezf2 |
G |
T |
14: 12,344,405 (GRCm38) |
P261T |
probably benign |
Het |
Fmo1 |
T |
C |
1: 162,667,325 (GRCm39) |
I163M |
possibly damaging |
Het |
Garin1a |
A |
G |
6: 29,285,921 (GRCm39) |
T69A |
probably benign |
Het |
Gatad2a |
G |
A |
8: 70,365,782 (GRCm39) |
R428* |
probably null |
Het |
Gfpt1 |
T |
A |
6: 87,031,612 (GRCm39) |
F85I |
possibly damaging |
Het |
Gimap7 |
A |
T |
6: 48,701,175 (GRCm39) |
I254F |
possibly damaging |
Het |
Glcci1 |
T |
C |
6: 8,592,980 (GRCm39) |
S261P |
probably damaging |
Het |
Glis3 |
A |
T |
19: 28,508,674 (GRCm39) |
F437I |
probably damaging |
Het |
Glp1r |
C |
A |
17: 31,144,601 (GRCm39) |
S258* |
probably null |
Het |
Gpt2 |
C |
T |
8: 86,242,832 (GRCm39) |
A288V |
possibly damaging |
Het |
Grin2c |
G |
T |
11: 115,151,731 (GRCm39) |
S76R |
possibly damaging |
Het |
Guf1 |
T |
A |
5: 69,724,569 (GRCm39) |
Y447* |
probably null |
Het |
H2-T9 |
T |
A |
17: 36,439,614 (GRCm39) |
D122V |
probably damaging |
Het |
Hectd1 |
A |
C |
12: 51,832,624 (GRCm39) |
L916V |
probably damaging |
Het |
Hnf4g |
A |
G |
3: 3,703,268 (GRCm39) |
K96E |
probably damaging |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Ifi207 |
T |
G |
1: 173,562,805 (GRCm39) |
M114L |
probably benign |
Het |
Ifi35 |
A |
T |
11: 101,349,112 (GRCm39) |
E252V |
probably damaging |
Het |
Igsf9b |
G |
A |
9: 27,233,535 (GRCm39) |
R345H |
possibly damaging |
Het |
Itih3 |
T |
C |
14: 30,645,540 (GRCm39) |
|
probably benign |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
Kidins220 |
A |
T |
12: 25,101,193 (GRCm39) |
M1252L |
probably benign |
Het |
Kifap3 |
T |
A |
1: 163,689,591 (GRCm39) |
L525* |
probably null |
Het |
Limk2 |
A |
T |
11: 3,305,461 (GRCm39) |
D35E |
probably benign |
Het |
Lrrc37a |
G |
A |
11: 103,389,792 (GRCm39) |
P1878S |
probably benign |
Het |
Mansc4 |
T |
A |
6: 146,977,173 (GRCm39) |
I148F |
probably benign |
Het |
Mei1 |
A |
G |
15: 81,987,513 (GRCm39) |
N859S |
probably benign |
Het |
Mib1 |
A |
G |
18: 10,812,064 (GRCm39) |
D987G |
probably damaging |
Het |
Mroh8 |
A |
G |
2: 157,113,895 (GRCm39) |
V132A |
possibly damaging |
Het |
Npnt |
T |
C |
3: 132,653,893 (GRCm39) |
I29M |
probably benign |
Het |
Nrap |
T |
C |
19: 56,372,537 (GRCm39) |
D138G |
probably damaging |
Het |
Or10a3m |
A |
G |
7: 108,312,902 (GRCm39) |
Y102C |
probably damaging |
Het |
Or1e16 |
A |
T |
11: 73,285,918 (GRCm39) |
I310N |
probably benign |
Het |
Or2h1 |
T |
A |
17: 37,404,700 (GRCm39) |
E22V |
probably damaging |
Het |
Or6z7 |
T |
C |
7: 6,483,931 (GRCm39) |
M75V |
probably benign |
Het |
Osbpl5 |
A |
C |
7: 143,295,408 (GRCm39) |
|
probably null |
Het |
Pcna-ps2 |
T |
C |
19: 9,261,047 (GRCm39) |
V102A |
possibly damaging |
Het |
Pik3c2g |
T |
C |
6: 139,599,546 (GRCm39) |
S221P |
probably damaging |
Het |
Plppr3 |
A |
G |
10: 79,702,259 (GRCm39) |
I271T |
probably damaging |
Het |
Ppp4r3c1 |
A |
T |
X: 88,975,051 (GRCm39) |
V382E |
probably damaging |
Het |
Pramel25 |
C |
A |
4: 143,521,720 (GRCm39) |
H445Q |
probably benign |
Het |
Prkar1b |
C |
T |
5: 139,113,398 (GRCm39) |
A41T |
probably benign |
Het |
Prkcsh |
A |
G |
9: 21,924,164 (GRCm39) |
D458G |
probably damaging |
Het |
Prr14 |
G |
T |
7: 127,074,662 (GRCm39) |
R398L |
possibly damaging |
Het |
Ptafr |
A |
G |
4: 132,307,296 (GRCm39) |
R229G |
probably damaging |
Het |
Rbp3 |
T |
C |
14: 33,676,502 (GRCm39) |
F150S |
probably damaging |
Het |
Rel |
C |
T |
11: 23,692,761 (GRCm39) |
G424D |
probably benign |
Het |
Rlf |
T |
C |
4: 121,007,309 (GRCm39) |
Y557C |
probably damaging |
Het |
Samt3 |
A |
C |
X: 85,090,740 (GRCm39) |
M211L |
probably benign |
Het |
Selenop |
A |
T |
15: 3,305,176 (GRCm39) |
I111F |
probably damaging |
Het |
Slc2a2 |
G |
A |
3: 28,771,590 (GRCm39) |
M173I |
probably benign |
Het |
Slc43a1 |
G |
T |
2: 84,687,233 (GRCm39) |
G361V |
possibly damaging |
Het |
Slit2 |
G |
A |
5: 48,407,178 (GRCm39) |
V870M |
probably damaging |
Het |
Ssxb10 |
A |
G |
X: 8,197,258 (GRCm39) |
D77G |
probably benign |
Het |
Stk32b |
T |
A |
5: 37,806,458 (GRCm39) |
I29F |
probably damaging |
Het |
Stra6l |
T |
A |
4: 45,867,237 (GRCm39) |
C161* |
probably null |
Het |
Tecpr2 |
T |
A |
12: 110,921,219 (GRCm39) |
M1264K |
probably benign |
Het |
Tfap2c |
A |
T |
2: 172,399,156 (GRCm39) |
I468F |
probably damaging |
Het |
Ticam1 |
C |
T |
17: 56,578,555 (GRCm39) |
R180H |
probably damaging |
Het |
Tlr4 |
T |
A |
4: 66,759,272 (GRCm39) |
N688K |
probably benign |
Het |
Tmem35b |
A |
T |
4: 127,019,846 (GRCm39) |
|
probably benign |
Het |
Ugt2b34 |
T |
C |
5: 87,054,172 (GRCm39) |
E203G |
probably damaging |
Het |
Vegfa |
A |
C |
17: 46,329,786 (GRCm39) |
*393G |
probably null |
Het |
Vmn2r16 |
T |
C |
5: 109,511,890 (GRCm39) |
V699A |
probably benign |
Het |
Zfp324 |
T |
C |
7: 12,705,145 (GRCm39) |
S445P |
probably damaging |
Het |
Zfp982 |
T |
A |
4: 147,597,049 (GRCm39) |
C135* |
probably null |
Het |
Zfp990 |
A |
C |
4: 145,263,439 (GRCm39) |
N146H |
probably damaging |
Het |
Zfyve26 |
A |
G |
12: 79,302,017 (GRCm39) |
Y431H |
possibly damaging |
Het |
|
Other mutations in Aatk |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00497:Aatk
|
APN |
11 |
119,901,012 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00953:Aatk
|
APN |
11 |
119,902,047 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01019:Aatk
|
APN |
11 |
119,903,101 (GRCm39) |
missense |
probably benign |
|
IGL01758:Aatk
|
APN |
11 |
119,901,645 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02377:Aatk
|
APN |
11 |
119,937,689 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02902:Aatk
|
APN |
11 |
119,902,603 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03067:Aatk
|
APN |
11 |
119,900,909 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03116:Aatk
|
APN |
11 |
119,907,577 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03279:Aatk
|
APN |
11 |
119,904,504 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03405:Aatk
|
APN |
11 |
119,907,229 (GRCm39) |
missense |
probably benign |
0.02 |
PIT4366001:Aatk
|
UTSW |
11 |
119,901,786 (GRCm39) |
missense |
possibly damaging |
0.55 |
PIT4802001:Aatk
|
UTSW |
11 |
119,902,172 (GRCm39) |
missense |
probably benign |
|
R0101:Aatk
|
UTSW |
11 |
119,901,739 (GRCm39) |
missense |
probably benign |
0.19 |
R0497:Aatk
|
UTSW |
11 |
119,909,606 (GRCm39) |
missense |
probably damaging |
0.99 |
R0535:Aatk
|
UTSW |
11 |
119,901,019 (GRCm39) |
missense |
probably benign |
0.00 |
R0638:Aatk
|
UTSW |
11 |
119,900,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0939:Aatk
|
UTSW |
11 |
119,902,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R1475:Aatk
|
UTSW |
11 |
119,901,714 (GRCm39) |
missense |
probably damaging |
0.96 |
R1840:Aatk
|
UTSW |
11 |
119,904,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R1865:Aatk
|
UTSW |
11 |
119,901,048 (GRCm39) |
missense |
probably benign |
0.00 |
R2027:Aatk
|
UTSW |
11 |
119,900,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R2115:Aatk
|
UTSW |
11 |
119,900,562 (GRCm39) |
missense |
probably benign |
|
R2220:Aatk
|
UTSW |
11 |
119,903,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R2264:Aatk
|
UTSW |
11 |
119,901,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Aatk
|
UTSW |
11 |
119,909,681 (GRCm39) |
missense |
probably benign |
0.00 |
R3872:Aatk
|
UTSW |
11 |
119,901,045 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4551:Aatk
|
UTSW |
11 |
119,902,395 (GRCm39) |
missense |
probably benign |
0.03 |
R4657:Aatk
|
UTSW |
11 |
119,904,304 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4744:Aatk
|
UTSW |
11 |
119,906,948 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4924:Aatk
|
UTSW |
11 |
119,902,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R5063:Aatk
|
UTSW |
11 |
119,901,315 (GRCm39) |
missense |
probably benign |
0.07 |
R5223:Aatk
|
UTSW |
11 |
119,904,278 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5243:Aatk
|
UTSW |
11 |
119,907,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R5376:Aatk
|
UTSW |
11 |
119,902,860 (GRCm39) |
missense |
probably damaging |
0.98 |
R5442:Aatk
|
UTSW |
11 |
119,909,594 (GRCm39) |
missense |
probably benign |
0.02 |
R5550:Aatk
|
UTSW |
11 |
119,900,129 (GRCm39) |
missense |
probably benign |
0.42 |
R5678:Aatk
|
UTSW |
11 |
119,900,980 (GRCm39) |
missense |
probably benign |
0.00 |
R5932:Aatk
|
UTSW |
11 |
119,912,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R6026:Aatk
|
UTSW |
11 |
119,903,190 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6129:Aatk
|
UTSW |
11 |
119,912,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R6409:Aatk
|
UTSW |
11 |
119,902,558 (GRCm39) |
missense |
probably benign |
0.01 |
R6477:Aatk
|
UTSW |
11 |
119,909,696 (GRCm39) |
missense |
probably benign |
0.00 |
R6478:Aatk
|
UTSW |
11 |
119,901,817 (GRCm39) |
missense |
probably benign |
0.00 |
R6749:Aatk
|
UTSW |
11 |
119,901,600 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6753:Aatk
|
UTSW |
11 |
119,900,977 (GRCm39) |
missense |
probably benign |
|
R6787:Aatk
|
UTSW |
11 |
119,901,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R6852:Aatk
|
UTSW |
11 |
119,901,294 (GRCm39) |
missense |
probably benign |
0.10 |
R7114:Aatk
|
UTSW |
11 |
119,900,445 (GRCm39) |
missense |
probably benign |
|
R7557:Aatk
|
UTSW |
11 |
119,900,256 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7818:Aatk
|
UTSW |
11 |
119,912,281 (GRCm39) |
missense |
probably benign |
|
R7954:Aatk
|
UTSW |
11 |
119,903,169 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8176:Aatk
|
UTSW |
11 |
119,907,241 (GRCm39) |
missense |
probably damaging |
0.99 |
R8420:Aatk
|
UTSW |
11 |
119,937,746 (GRCm39) |
missense |
unknown |
|
R8963:Aatk
|
UTSW |
11 |
119,902,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R9090:Aatk
|
UTSW |
11 |
119,901,940 (GRCm39) |
missense |
probably damaging |
0.98 |
R9167:Aatk
|
UTSW |
11 |
119,901,952 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9271:Aatk
|
UTSW |
11 |
119,901,940 (GRCm39) |
missense |
probably damaging |
0.98 |
R9357:Aatk
|
UTSW |
11 |
119,901,696 (GRCm39) |
missense |
probably benign |
0.01 |
R9373:Aatk
|
UTSW |
11 |
119,906,343 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9420:Aatk
|
UTSW |
11 |
119,912,277 (GRCm39) |
missense |
probably benign |
0.01 |
R9423:Aatk
|
UTSW |
11 |
119,901,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R9476:Aatk
|
UTSW |
11 |
119,901,094 (GRCm39) |
missense |
probably benign |
0.01 |
R9510:Aatk
|
UTSW |
11 |
119,901,094 (GRCm39) |
missense |
probably benign |
0.01 |
R9519:Aatk
|
UTSW |
11 |
119,912,309 (GRCm39) |
start gained |
probably benign |
|
R9605:Aatk
|
UTSW |
11 |
119,902,209 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9649:Aatk
|
UTSW |
11 |
119,901,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R9766:Aatk
|
UTSW |
11 |
119,902,565 (GRCm39) |
missense |
probably benign |
0.00 |
X0064:Aatk
|
UTSW |
11 |
119,902,002 (GRCm39) |
splice site |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- AGCCCTAATCCTAGCCAGAG -3'
(R):5'- CTGACCTGACAGTGAAGGTTGG -3'
Sequencing Primer
(F):5'- CTAATCCTAGCCAGAGAAGGAAGTC -3'
(R):5'- GTGATTATGGCCTGTCGCATTGC -3'
|
Posted On |
2014-08-25 |