Incidental Mutation 'R7487:1110002E22Rik'
| ID |
580231 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
1110002E22Rik
|
| Ensembl Gene |
ENSMUSG00000090066 |
| Gene Name |
RIKEN cDNA 1110002E22 gene |
| Synonyms |
|
| MMRRC Submission |
045561-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.431)
|
| Stock # |
R7487 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
3 |
| Chromosomal Location |
137770813-137787267 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 137772629 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Valine
at position 606
(D606V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000123851
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053318]
[ENSMUST00000163080]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000053318
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000163080
AA Change: D606V
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000123851
Gene: ENSMUSG00000090066
AA Change: D606V
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
44 |
55 |
N/A |
INTRINSIC |
|
low complexity region
|
87 |
102 |
N/A |
INTRINSIC |
|
low complexity region
|
229 |
247 |
N/A |
INTRINSIC |
|
low complexity region
|
422 |
438 |
N/A |
INTRINSIC |
|
low complexity region
|
459 |
505 |
N/A |
INTRINSIC |
|
low complexity region
|
667 |
680 |
N/A |
INTRINSIC |
|
low complexity region
|
937 |
948 |
N/A |
INTRINSIC |
|
low complexity region
|
995 |
1007 |
N/A |
INTRINSIC |
|
low complexity region
|
1105 |
1115 |
N/A |
INTRINSIC |
|
low complexity region
|
1224 |
1242 |
N/A |
INTRINSIC |
|
low complexity region
|
1376 |
1385 |
N/A |
INTRINSIC |
|
Pfam:DUF4585
|
1598 |
1667 |
6.9e-32 |
PFAM |
|
low complexity region
|
1723 |
1738 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.1560 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.3%
|
| Validation Efficiency |
100% (89/89) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 87 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700009N14Rik |
T |
A |
4: 39,450,929 (GRCm39) |
V45E |
probably damaging |
Het |
| 2510009E07Rik |
C |
T |
16: 21,472,479 (GRCm39) |
V74M |
probably damaging |
Het |
| Abca2 |
C |
T |
2: 25,327,915 (GRCm39) |
T739M |
probably benign |
Het |
| Abra |
T |
C |
15: 41,732,949 (GRCm39) |
E39G |
probably damaging |
Het |
| Adam34 |
A |
T |
8: 44,104,191 (GRCm39) |
C485S |
probably damaging |
Het |
| Add2 |
G |
T |
6: 86,070,432 (GRCm39) |
V175F |
possibly damaging |
Het |
| Alk |
T |
A |
17: 72,256,893 (GRCm39) |
K655N |
probably benign |
Het |
| Ap3m1 |
A |
G |
14: 21,088,107 (GRCm39) |
V317A |
probably benign |
Het |
| Astn1 |
A |
G |
1: 158,438,352 (GRCm39) |
|
probably null |
Het |
| Atm |
A |
T |
9: 53,435,654 (GRCm39) |
Y219N |
probably benign |
Het |
| Cep128 |
C |
T |
12: 90,966,404 (GRCm39) |
A1068T |
probably benign |
Het |
| Cep20 |
T |
C |
16: 14,128,968 (GRCm39) |
D85G |
probably benign |
Het |
| Cnksr3 |
T |
C |
10: 7,085,097 (GRCm39) |
Q250R |
probably benign |
Het |
| Cst7 |
A |
G |
2: 150,419,624 (GRCm39) |
T97A |
probably benign |
Het |
| Ctps1 |
G |
A |
4: 120,415,997 (GRCm39) |
L209F |
probably damaging |
Het |
| Cyp2d10 |
A |
T |
15: 82,288,793 (GRCm39) |
F230I |
probably benign |
Het |
| Daam2 |
T |
C |
17: 49,793,510 (GRCm39) |
N336D |
probably benign |
Het |
| Dchs2 |
T |
C |
3: 83,263,613 (GRCm39) |
S3294P |
probably damaging |
Het |
| Dhx36 |
G |
T |
3: 62,391,623 (GRCm39) |
N574K |
possibly damaging |
Het |
| Dock10 |
G |
T |
1: 80,562,765 (GRCm39) |
Q533K |
probably benign |
Het |
| Dync2h1 |
A |
G |
9: 7,132,041 (GRCm39) |
S1589P |
probably benign |
Het |
| Enpp3 |
T |
A |
10: 24,681,821 (GRCm39) |
Y295F |
probably benign |
Het |
| Esrrg |
T |
A |
1: 187,878,620 (GRCm39) |
Y234N |
probably benign |
Het |
| Fadd |
A |
C |
7: 144,134,462 (GRCm39) |
V141G |
probably damaging |
Het |
| Fam114a2 |
C |
T |
11: 57,404,515 (GRCm39) |
G83D |
probably damaging |
Het |
| Fam170b |
T |
A |
14: 32,557,776 (GRCm39) |
C204S |
probably damaging |
Het |
| Fam186a |
T |
A |
15: 99,840,017 (GRCm39) |
I2076F |
possibly damaging |
Het |
| Fdxacb1 |
G |
A |
9: 50,681,519 (GRCm39) |
V147I |
possibly damaging |
Het |
| Frem2 |
C |
A |
3: 53,561,970 (GRCm39) |
V846F |
probably benign |
Het |
| Fry |
G |
A |
5: 150,338,039 (GRCm39) |
S1449N |
possibly damaging |
Het |
| Gucy1b2 |
A |
G |
14: 62,685,672 (GRCm39) |
F98L |
probably damaging |
Het |
| Hps1 |
T |
C |
19: 42,744,700 (GRCm39) |
Y658C |
probably damaging |
Het |
| Igkv3-9 |
T |
A |
6: 70,565,506 (GRCm39) |
L35Q |
probably damaging |
Het |
| Irx2 |
A |
G |
13: 72,778,739 (GRCm39) |
Y101C |
probably damaging |
Het |
| Kcnj11 |
G |
T |
7: 45,748,265 (GRCm39) |
R353S |
probably benign |
Het |
| Kyat3 |
C |
T |
3: 142,431,955 (GRCm39) |
Q228* |
probably null |
Het |
| Lama3 |
T |
A |
18: 12,552,294 (GRCm39) |
D415E |
probably benign |
Het |
| Lcn3 |
G |
A |
2: 25,656,174 (GRCm39) |
|
probably null |
Het |
| Lin7b |
T |
C |
7: 45,019,364 (GRCm39) |
E68G |
possibly damaging |
Het |
| Lmbr1 |
T |
A |
5: 29,459,262 (GRCm39) |
K379M |
probably benign |
Het |
| Lrig1 |
A |
G |
6: 94,583,099 (GRCm39) |
S1006P |
probably benign |
Het |
| Lrrc37a |
T |
G |
11: 103,389,045 (GRCm39) |
T2127P |
unknown |
Het |
| Map4 |
A |
G |
9: 109,856,783 (GRCm39) |
D151G |
probably damaging |
Het |
| Marchf1 |
A |
T |
8: 66,908,726 (GRCm39) |
T149S |
probably benign |
Het |
| Msh4 |
A |
T |
3: 153,569,147 (GRCm39) |
F809I |
probably damaging |
Het |
| Muc16 |
G |
A |
9: 18,496,095 (GRCm39) |
P6699S |
possibly damaging |
Het |
| Mxi1 |
A |
T |
19: 53,360,088 (GRCm39) |
D270V |
probably damaging |
Het |
| Myh6 |
A |
T |
14: 55,190,953 (GRCm39) |
C907* |
probably null |
Het |
| Myo18b |
T |
C |
5: 112,982,299 (GRCm39) |
R1145G |
possibly damaging |
Het |
| Nkx2-6 |
A |
C |
14: 69,409,389 (GRCm39) |
N47H |
probably benign |
Het |
| Nol7 |
G |
A |
13: 43,552,076 (GRCm39) |
A66T |
probably damaging |
Het |
| Ntrk3 |
T |
C |
7: 77,900,461 (GRCm39) |
N626S |
probably damaging |
Het |
| Nwd1 |
A |
G |
8: 73,393,266 (GRCm39) |
Y77C |
unknown |
Het |
| Or12d17 |
G |
T |
17: 37,777,457 (GRCm39) |
R120L |
probably damaging |
Het |
| Or12k5 |
A |
C |
2: 36,894,786 (GRCm39) |
V280G |
probably damaging |
Het |
| Or8c14-ps1 |
A |
G |
9: 38,101,356 (GRCm39) |
S112G |
probably damaging |
Het |
| Or8j3b |
A |
T |
2: 86,205,475 (GRCm39) |
Y94N |
probably damaging |
Het |
| Or9s23 |
G |
A |
1: 92,501,517 (GRCm39) |
G208D |
possibly damaging |
Het |
| Otop3 |
A |
G |
11: 115,235,826 (GRCm39) |
D486G |
probably benign |
Het |
| Pak1ip1 |
A |
G |
13: 41,162,731 (GRCm39) |
K178R |
probably benign |
Het |
| Pcsk1 |
G |
A |
13: 75,259,002 (GRCm39) |
G259S |
probably benign |
Het |
| Pde6a |
A |
G |
18: 61,383,031 (GRCm39) |
D338G |
probably damaging |
Het |
| Pias4 |
A |
T |
10: 80,999,806 (GRCm39) |
D82E |
probably benign |
Het |
| Plekha5 |
C |
A |
6: 140,516,059 (GRCm39) |
Q771K |
probably benign |
Het |
| Plekhh3 |
C |
A |
11: 101,056,405 (GRCm39) |
A397S |
possibly damaging |
Het |
| Prg4 |
G |
T |
1: 150,331,656 (GRCm39) |
T339N |
unknown |
Het |
| Prss22 |
A |
T |
17: 24,216,971 (GRCm39) |
I3N |
probably damaging |
Het |
| Rasgrp1 |
T |
C |
2: 117,118,424 (GRCm39) |
I522V |
probably damaging |
Het |
| Rspo2 |
T |
C |
15: 42,941,510 (GRCm39) |
T138A |
probably benign |
Het |
| Rtcb |
C |
T |
10: 85,789,333 (GRCm39) |
G70S |
probably benign |
Het |
| Selenov |
A |
T |
7: 27,989,803 (GRCm39) |
S234T |
probably damaging |
Het |
| Shtn1 |
T |
C |
19: 58,992,292 (GRCm39) |
T429A |
probably damaging |
Het |
| Slc4a3 |
G |
T |
1: 75,530,021 (GRCm39) |
R622L |
probably benign |
Het |
| Smc2 |
T |
C |
4: 52,478,448 (GRCm39) |
I1015T |
probably damaging |
Het |
| Spata9 |
G |
T |
13: 76,115,959 (GRCm39) |
V3F |
possibly damaging |
Het |
| Tlr4 |
T |
C |
4: 66,842,659 (GRCm39) |
I105T |
probably benign |
Het |
| Trav6d-4 |
A |
T |
14: 52,991,096 (GRCm39) |
Y47F |
possibly damaging |
Het |
| Ttn |
A |
T |
2: 76,657,377 (GRCm39) |
I12450N |
unknown |
Het |
| Umad1 |
G |
T |
6: 8,270,560 (GRCm39) |
A21S |
probably damaging |
Het |
| Unc5a |
G |
A |
13: 55,144,362 (GRCm39) |
R229H |
probably benign |
Het |
| Vmn1r216 |
A |
T |
13: 23,284,030 (GRCm39) |
M238L |
probably damaging |
Het |
| Vps16 |
T |
A |
2: 130,280,977 (GRCm39) |
C255* |
probably null |
Het |
| Wdr89 |
A |
G |
12: 75,679,388 (GRCm39) |
F289L |
probably benign |
Het |
| Zfp180 |
A |
T |
7: 23,805,525 (GRCm39) |
H648L |
probably damaging |
Het |
| Zfp735 |
A |
G |
11: 73,581,154 (GRCm39) |
K64E |
possibly damaging |
Het |
| Zfp990 |
G |
A |
4: 145,264,157 (GRCm39) |
C385Y |
probably damaging |
Het |
| Zswim3 |
G |
T |
2: 164,662,135 (GRCm39) |
S205I |
probably damaging |
Het |
|
| Other mutations in 1110002E22Rik |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
R0026:1110002E22Rik
|
UTSW |
3 |
137,772,566 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0047:1110002E22Rik
|
UTSW |
3 |
137,772,025 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0047:1110002E22Rik
|
UTSW |
3 |
137,772,025 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0102:1110002E22Rik
|
UTSW |
3 |
137,773,874 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0102:1110002E22Rik
|
UTSW |
3 |
137,773,874 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0197:1110002E22Rik
|
UTSW |
3 |
137,775,632 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0239:1110002E22Rik
|
UTSW |
3 |
137,771,595 (GRCm39) |
small deletion |
probably benign |
|
|
R0394:1110002E22Rik
|
UTSW |
3 |
137,773,065 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0401:1110002E22Rik
|
UTSW |
3 |
137,776,067 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R0496:1110002E22Rik
|
UTSW |
3 |
137,774,005 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0591:1110002E22Rik
|
UTSW |
3 |
137,774,704 (GRCm39) |
nonsense |
probably null |
|
|
R0711:1110002E22Rik
|
UTSW |
3 |
137,773,986 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0883:1110002E22Rik
|
UTSW |
3 |
137,775,632 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0908:1110002E22Rik
|
UTSW |
3 |
137,775,838 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0968:1110002E22Rik
|
UTSW |
3 |
137,772,967 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1023:1110002E22Rik
|
UTSW |
3 |
137,772,632 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1168:1110002E22Rik
|
UTSW |
3 |
137,773,661 (GRCm39) |
missense |
probably benign |
0.20 |
|
R1472:1110002E22Rik
|
UTSW |
3 |
137,773,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1538:1110002E22Rik
|
UTSW |
3 |
137,771,162 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1648:1110002E22Rik
|
UTSW |
3 |
137,775,181 (GRCm39) |
missense |
probably benign |
0.18 |
|
R1800:1110002E22Rik
|
UTSW |
3 |
137,772,479 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1919:1110002E22Rik
|
UTSW |
3 |
137,773,031 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1974:1110002E22Rik
|
UTSW |
3 |
137,773,028 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1990:1110002E22Rik
|
UTSW |
3 |
137,771,419 (GRCm39) |
nonsense |
probably null |
|
|
R1991:1110002E22Rik
|
UTSW |
3 |
137,771,419 (GRCm39) |
nonsense |
probably null |
|
|
R2102:1110002E22Rik
|
UTSW |
3 |
137,770,934 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2761:1110002E22Rik
|
UTSW |
3 |
137,773,541 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2899:1110002E22Rik
|
UTSW |
3 |
137,771,443 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3618:1110002E22Rik
|
UTSW |
3 |
137,774,168 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3904:1110002E22Rik
|
UTSW |
3 |
137,772,400 (GRCm39) |
missense |
probably benign |
0.15 |
|
R3955:1110002E22Rik
|
UTSW |
3 |
137,773,834 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4520:1110002E22Rik
|
UTSW |
3 |
137,776,027 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4619:1110002E22Rik
|
UTSW |
3 |
137,775,520 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4736:1110002E22Rik
|
UTSW |
3 |
137,774,246 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4752:1110002E22Rik
|
UTSW |
3 |
137,775,751 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R4777:1110002E22Rik
|
UTSW |
3 |
137,771,503 (GRCm39) |
missense |
probably benign |
0.09 |
|
R4780:1110002E22Rik
|
UTSW |
3 |
137,771,131 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4824:1110002E22Rik
|
UTSW |
3 |
137,771,437 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4829:1110002E22Rik
|
UTSW |
3 |
137,774,780 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4965:1110002E22Rik
|
UTSW |
3 |
137,775,433 (GRCm39) |
missense |
probably benign |
|
|
R5206:1110002E22Rik
|
UTSW |
3 |
137,772,272 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5212:1110002E22Rik
|
UTSW |
3 |
137,771,611 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R5373:1110002E22Rik
|
UTSW |
3 |
137,773,396 (GRCm39) |
missense |
probably benign |
|
|
R5374:1110002E22Rik
|
UTSW |
3 |
137,773,396 (GRCm39) |
missense |
probably benign |
|
|
R5506:1110002E22Rik
|
UTSW |
3 |
137,773,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5528:1110002E22Rik
|
UTSW |
3 |
137,772,260 (GRCm39) |
missense |
probably benign |
|
|
R5536:1110002E22Rik
|
UTSW |
3 |
137,772,149 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R5587:1110002E22Rik
|
UTSW |
3 |
137,771,170 (GRCm39) |
missense |
probably benign |
|
|
R5759:1110002E22Rik
|
UTSW |
3 |
137,774,419 (GRCm39) |
missense |
probably benign |
|
|
R5933:1110002E22Rik
|
UTSW |
3 |
137,776,109 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5957:1110002E22Rik
|
UTSW |
3 |
137,775,922 (GRCm39) |
missense |
probably benign |
|
|
R6092:1110002E22Rik
|
UTSW |
3 |
137,774,701 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6305:1110002E22Rik
|
UTSW |
3 |
137,773,741 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6457:1110002E22Rik
|
UTSW |
3 |
137,772,383 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6469:1110002E22Rik
|
UTSW |
3 |
137,772,736 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6499:1110002E22Rik
|
UTSW |
3 |
137,774,561 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6527:1110002E22Rik
|
UTSW |
3 |
137,773,288 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6580:1110002E22Rik
|
UTSW |
3 |
137,772,386 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6693:1110002E22Rik
|
UTSW |
3 |
137,774,915 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6751:1110002E22Rik
|
UTSW |
3 |
137,771,971 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6852:1110002E22Rik
|
UTSW |
3 |
137,770,930 (GRCm39) |
nonsense |
probably null |
|
|
R6920:1110002E22Rik
|
UTSW |
3 |
137,773,811 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7001:1110002E22Rik
|
UTSW |
3 |
137,771,272 (GRCm39) |
missense |
probably benign |
|
|
R7145:1110002E22Rik
|
UTSW |
3 |
137,775,820 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7238:1110002E22Rik
|
UTSW |
3 |
137,775,712 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7278:1110002E22Rik
|
UTSW |
3 |
137,771,237 (GRCm39) |
missense |
probably benign |
|
|
R7425:1110002E22Rik
|
UTSW |
3 |
137,771,456 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7557:1110002E22Rik
|
UTSW |
3 |
137,774,044 (GRCm39) |
nonsense |
probably null |
|
|
R7663:1110002E22Rik
|
UTSW |
3 |
137,771,887 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7743:1110002E22Rik
|
UTSW |
3 |
137,774,516 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7799:1110002E22Rik
|
UTSW |
3 |
137,775,362 (GRCm39) |
missense |
probably benign |
0.33 |
|
R8181:1110002E22Rik
|
UTSW |
3 |
137,774,156 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8264:1110002E22Rik
|
UTSW |
3 |
137,773,543 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8273:1110002E22Rik
|
UTSW |
3 |
137,772,211 (GRCm39) |
missense |
probably benign |
|
|
R8434:1110002E22Rik
|
UTSW |
3 |
137,773,021 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8530:1110002E22Rik
|
UTSW |
3 |
137,774,586 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8754:1110002E22Rik
|
UTSW |
3 |
137,771,798 (GRCm39) |
missense |
probably benign |
|
|
R8808:1110002E22Rik
|
UTSW |
3 |
137,775,874 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8891:1110002E22Rik
|
UTSW |
3 |
137,772,520 (GRCm39) |
nonsense |
probably null |
|
|
R9026:1110002E22Rik
|
UTSW |
3 |
137,770,909 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R9177:1110002E22Rik
|
UTSW |
3 |
137,775,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9250:1110002E22Rik
|
UTSW |
3 |
137,772,389 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9291:1110002E22Rik
|
UTSW |
3 |
137,772,464 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9293:1110002E22Rik
|
UTSW |
3 |
137,771,839 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R9307:1110002E22Rik
|
UTSW |
3 |
137,771,183 (GRCm39) |
missense |
probably benign |
0.04 |
|
R9439:1110002E22Rik
|
UTSW |
3 |
137,772,048 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9509:1110002E22Rik
|
UTSW |
3 |
137,771,595 (GRCm39) |
small deletion |
probably benign |
|
|
R9582:1110002E22Rik
|
UTSW |
3 |
137,772,766 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9599:1110002E22Rik
|
UTSW |
3 |
137,774,267 (GRCm39) |
missense |
probably benign |
0.16 |
|
R9613:1110002E22Rik
|
UTSW |
3 |
137,771,126 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9670:1110002E22Rik
|
UTSW |
3 |
137,770,894 (GRCm39) |
missense |
probably benign |
|
|
X0003:1110002E22Rik
|
UTSW |
3 |
137,774,857 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CCAAGCATGAAGGCGACATG -3'
(R):5'- TTTGCTGACCACAAACTCCAAG -3'
Sequencing Primer
(F):5'- GAGTCTCTTCAGCTGCTGAACAC -3'
(R):5'- AAGGCCTTGGTCTGCGACTTC -3'
|
| Posted On |
2019-10-07 |
Incidental Mutation