Incidental Mutation 'R1885:D430041D05Rik'
ID |
209411 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
D430041D05Rik
|
Ensembl Gene |
ENSMUSG00000068373 |
Gene Name |
RIKEN cDNA D430041D05 gene |
Synonyms |
G2 |
MMRRC Submission |
039906-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.236)
|
Stock # |
R1885 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
2 |
Chromosomal Location |
103973418-104241358 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 104060800 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Methionine to Valine
at position 1365
(M1365V)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000155485
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000089726]
[ENSMUST00000136156]
[ENSMUST00000141159]
[ENSMUST00000230671]
|
AlphaFold |
A0A2R8VKG2 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000089726
AA Change: M681V
PolyPhen 2
Score 0.119 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000106756 Gene: ENSMUSG00000068373 AA Change: M681V
Domain | Start | End | E-Value | Type |
low complexity region
|
55 |
70 |
N/A |
INTRINSIC |
low complexity region
|
206 |
215 |
N/A |
INTRINSIC |
low complexity region
|
218 |
230 |
N/A |
INTRINSIC |
low complexity region
|
234 |
253 |
N/A |
INTRINSIC |
Pfam:DUF3827
|
498 |
1134 |
2.4e-282 |
PFAM |
low complexity region
|
1196 |
1217 |
N/A |
INTRINSIC |
low complexity region
|
1331 |
1351 |
N/A |
INTRINSIC |
low complexity region
|
1360 |
1372 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000136156
AA Change: M681V
PolyPhen 2
Score 0.097 (Sensitivity: 0.93; Specificity: 0.85)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000141159
AA Change: M566V
PolyPhen 2
Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)
|
SMART Domains |
Protein: ENSMUSP00000117041 Gene: ENSMUSG00000068373 AA Change: M566V
Domain | Start | End | E-Value | Type |
low complexity region
|
55 |
70 |
N/A |
INTRINSIC |
low complexity region
|
91 |
100 |
N/A |
INTRINSIC |
low complexity region
|
103 |
115 |
N/A |
INTRINSIC |
low complexity region
|
119 |
138 |
N/A |
INTRINSIC |
Pfam:DUF3827
|
383 |
1020 |
8.2e-280 |
PFAM |
low complexity region
|
1082 |
1103 |
N/A |
INTRINSIC |
low complexity region
|
1217 |
1237 |
N/A |
INTRINSIC |
low complexity region
|
1246 |
1258 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000149165
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000156278
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000158981
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000230671
AA Change: M1365V
PolyPhen 2
Score 0.387 (Sensitivity: 0.90; Specificity: 0.89)
|
Coding Region Coverage |
- 1x: 97.0%
- 3x: 96.1%
- 10x: 92.7%
- 20x: 85.1%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700102P08Rik |
T |
A |
9: 108,270,809 (GRCm39) |
D124E |
possibly damaging |
Het |
Aarsd1 |
T |
C |
11: 101,302,227 (GRCm39) |
T278A |
probably benign |
Het |
Acox2 |
C |
T |
14: 8,248,102 (GRCm38) |
M393I |
probably benign |
Het |
Adcy10 |
A |
G |
1: 165,398,377 (GRCm39) |
I1491M |
probably benign |
Het |
Adcy3 |
T |
A |
12: 4,184,951 (GRCm39) |
V209E |
probably damaging |
Het |
Adora3 |
A |
C |
3: 105,812,152 (GRCm39) |
N13H |
possibly damaging |
Het |
Ap2b1 |
T |
A |
11: 83,281,561 (GRCm39) |
N822K |
probably damaging |
Het |
Apobec3 |
A |
T |
15: 79,781,906 (GRCm39) |
H82L |
probably damaging |
Het |
Atg9b |
A |
T |
5: 24,593,252 (GRCm39) |
W384R |
probably damaging |
Het |
Atp8a1 |
A |
G |
5: 67,904,661 (GRCm39) |
V506A |
possibly damaging |
Het |
Atxn1 |
G |
T |
13: 45,721,280 (GRCm39) |
A205D |
probably benign |
Het |
B4galnt3 |
T |
C |
6: 120,200,601 (GRCm39) |
E223G |
probably damaging |
Het |
Brip1 |
C |
A |
11: 86,029,641 (GRCm39) |
G631V |
probably damaging |
Het |
Cacna1i |
A |
G |
15: 80,243,145 (GRCm39) |
E434G |
probably damaging |
Het |
Caprin2 |
A |
T |
6: 148,779,383 (GRCm39) |
|
probably null |
Het |
Cblif |
G |
A |
19: 11,729,688 (GRCm39) |
A216T |
probably benign |
Het |
Ccdc80 |
A |
C |
16: 44,917,083 (GRCm39) |
D613A |
probably benign |
Het |
Ccdc81 |
T |
C |
7: 89,515,819 (GRCm39) |
E620G |
possibly damaging |
Het |
Cdhr18 |
A |
C |
14: 13,828,607 (GRCm38) |
Y718D |
probably damaging |
Het |
Cebpz |
A |
T |
17: 79,239,545 (GRCm39) |
D625E |
probably benign |
Het |
Coq6 |
C |
A |
12: 84,419,238 (GRCm39) |
N388K |
probably damaging |
Het |
Cracd |
A |
G |
5: 77,004,589 (GRCm39) |
T317A |
unknown |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dap3 |
A |
G |
3: 88,838,281 (GRCm39) |
L86P |
probably damaging |
Het |
Dpysl4 |
T |
G |
7: 138,676,723 (GRCm39) |
V391G |
probably damaging |
Het |
Dyrk4 |
G |
T |
6: 126,854,144 (GRCm39) |
Q550K |
probably benign |
Het |
Epas1 |
A |
G |
17: 87,112,723 (GRCm39) |
D107G |
probably damaging |
Het |
Esrp2 |
A |
G |
8: 106,858,453 (GRCm39) |
V636A |
possibly damaging |
Het |
Etl4 |
T |
A |
2: 20,748,795 (GRCm39) |
Y176N |
probably damaging |
Het |
Etnppl |
T |
C |
3: 130,423,111 (GRCm39) |
V264A |
probably benign |
Het |
Ezhip |
GTCATCATCATCATC |
GTCATCATCATCATCATC |
X: 5,994,645 (GRCm39) |
|
probably benign |
Het |
Fer |
T |
A |
17: 64,445,909 (GRCm39) |
V790D |
probably damaging |
Het |
Gdpd5 |
G |
A |
7: 99,109,204 (GRCm39) |
V575I |
probably benign |
Het |
Gfus |
G |
T |
15: 75,798,838 (GRCm39) |
T123N |
possibly damaging |
Het |
Gipc3 |
T |
C |
10: 81,177,181 (GRCm39) |
I130V |
probably benign |
Het |
Iqsec3 |
G |
A |
6: 121,405,326 (GRCm39) |
|
probably benign |
Het |
Kdm5d |
G |
T |
Y: 940,781 (GRCm39) |
|
probably null |
Het |
Kl |
A |
G |
5: 150,876,959 (GRCm39) |
R260G |
possibly damaging |
Het |
Kras |
T |
C |
6: 145,177,843 (GRCm39) |
E143G |
probably damaging |
Het |
Ksr1 |
C |
A |
11: 78,911,204 (GRCm39) |
V11F |
probably null |
Het |
Ksr1 |
T |
C |
11: 78,927,347 (GRCm39) |
T329A |
probably damaging |
Het |
Marchf6 |
A |
G |
15: 31,502,952 (GRCm39) |
V83A |
probably benign |
Het |
Mettl2 |
T |
C |
11: 105,022,446 (GRCm39) |
I212T |
possibly damaging |
Het |
Mgat3 |
A |
G |
15: 80,095,820 (GRCm39) |
I216V |
probably benign |
Het |
Mkrn3 |
G |
A |
7: 62,068,486 (GRCm39) |
A435V |
probably benign |
Het |
Mlh1 |
C |
A |
9: 111,087,624 (GRCm39) |
S24I |
probably benign |
Het |
Mmel1 |
G |
A |
4: 154,975,333 (GRCm39) |
R424Q |
possibly damaging |
Het |
Mob3a |
G |
A |
10: 80,527,068 (GRCm39) |
Q86* |
probably null |
Het |
Myh3 |
A |
G |
11: 66,977,453 (GRCm39) |
K368E |
probably benign |
Het |
Myo16 |
T |
A |
8: 10,372,656 (GRCm39) |
N118K |
probably damaging |
Het |
Myo5c |
A |
G |
9: 75,157,043 (GRCm39) |
S160G |
probably damaging |
Het |
Nat1 |
A |
T |
8: 67,943,653 (GRCm39) |
I13F |
probably damaging |
Het |
Ncoa7 |
T |
C |
10: 30,524,448 (GRCm39) |
N823S |
possibly damaging |
Het |
Nwd1 |
T |
C |
8: 73,431,622 (GRCm39) |
S1207P |
probably benign |
Het |
Or2y17 |
T |
C |
11: 49,231,662 (GRCm39) |
L101P |
probably damaging |
Het |
Or4k49 |
G |
T |
2: 111,495,099 (GRCm39) |
S176I |
probably damaging |
Het |
Or5p57 |
T |
C |
7: 107,665,985 (GRCm39) |
N7D |
probably benign |
Het |
Or5w22 |
T |
C |
2: 87,363,168 (GRCm39) |
S264P |
probably damaging |
Het |
Paqr8 |
A |
T |
1: 21,005,704 (GRCm39) |
H286L |
probably damaging |
Het |
Pdzd4 |
G |
A |
X: 72,839,052 (GRCm39) |
R419C |
probably damaging |
Het |
Pes1 |
A |
G |
11: 3,919,482 (GRCm39) |
K52E |
probably damaging |
Het |
Ppp1r13l |
T |
C |
7: 19,111,496 (GRCm39) |
S774P |
probably damaging |
Het |
Robo2 |
T |
C |
16: 73,713,033 (GRCm39) |
D1283G |
probably benign |
Het |
Rp1l1 |
T |
C |
14: 64,265,839 (GRCm39) |
V475A |
probably benign |
Het |
Scml4 |
A |
G |
10: 42,788,223 (GRCm39) |
Y51C |
probably damaging |
Het |
Skic3 |
A |
T |
13: 76,261,166 (GRCm39) |
R112S |
probably benign |
Het |
Skic3 |
A |
G |
13: 76,278,354 (GRCm39) |
Q556R |
probably benign |
Het |
Slc2a4 |
C |
T |
11: 69,835,833 (GRCm39) |
V339I |
probably benign |
Het |
Slc39a6 |
G |
A |
18: 24,734,539 (GRCm39) |
|
probably null |
Het |
Slco1b2 |
A |
T |
6: 141,628,951 (GRCm39) |
Y551F |
probably damaging |
Het |
Snx33 |
T |
C |
9: 56,833,121 (GRCm39) |
H316R |
probably benign |
Het |
Spata31d1a |
T |
G |
13: 59,849,821 (GRCm39) |
D769A |
probably damaging |
Het |
Stmn2 |
A |
T |
3: 8,606,964 (GRCm39) |
E28V |
probably damaging |
Het |
Syt9 |
A |
G |
7: 107,035,736 (GRCm39) |
D251G |
probably damaging |
Het |
Tjap1 |
T |
C |
17: 46,573,347 (GRCm39) |
T37A |
probably damaging |
Het |
Tmc7 |
A |
T |
7: 118,160,310 (GRCm39) |
F176I |
possibly damaging |
Het |
Tprg1 |
A |
G |
16: 25,231,641 (GRCm39) |
T206A |
probably benign |
Het |
Ubqlnl |
A |
T |
7: 103,799,272 (GRCm39) |
M75K |
possibly damaging |
Het |
Vmn2r115 |
ATCTTCT |
ATCT |
17: 23,578,962 (GRCm39) |
|
probably benign |
Het |
Vmn2r12 |
C |
T |
5: 109,239,942 (GRCm39) |
G207E |
probably damaging |
Het |
Xrn2 |
T |
G |
2: 146,891,281 (GRCm39) |
L697* |
probably null |
Het |
Zfp764 |
A |
G |
7: 127,004,211 (GRCm39) |
F307L |
probably benign |
Het |
Zfp804b |
T |
C |
5: 6,820,376 (GRCm39) |
R860G |
probably damaging |
Het |
Zranb2 |
A |
T |
3: 157,248,793 (GRCm39) |
|
probably null |
Het |
|
Other mutations in D430041D05Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00838:D430041D05Rik
|
APN |
2 |
104,031,648 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01114:D430041D05Rik
|
APN |
2 |
104,088,511 (GRCm39) |
nonsense |
probably null |
|
IGL01669:D430041D05Rik
|
APN |
2 |
104,085,306 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02015:D430041D05Rik
|
APN |
2 |
104,060,749 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02037:D430041D05Rik
|
APN |
2 |
104,038,559 (GRCm39) |
splice site |
probably benign |
|
IGL02268:D430041D05Rik
|
APN |
2 |
104,071,500 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02294:D430041D05Rik
|
APN |
2 |
104,085,351 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02457:D430041D05Rik
|
APN |
2 |
104,079,690 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02601:D430041D05Rik
|
APN |
2 |
104,060,631 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02647:D430041D05Rik
|
APN |
2 |
104,078,611 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02679:D430041D05Rik
|
APN |
2 |
104,060,650 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02926:D430041D05Rik
|
APN |
2 |
104,044,604 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03171:D430041D05Rik
|
APN |
2 |
104,071,508 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03178:D430041D05Rik
|
APN |
2 |
104,051,556 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03371:D430041D05Rik
|
APN |
2 |
104,078,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:D430041D05Rik
|
UTSW |
2 |
104,085,389 (GRCm39) |
missense |
probably benign |
|
R0064:D430041D05Rik
|
UTSW |
2 |
104,079,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R0135:D430041D05Rik
|
UTSW |
2 |
104,085,379 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0227:D430041D05Rik
|
UTSW |
2 |
104,035,545 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0265:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0268:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0282:D430041D05Rik
|
UTSW |
2 |
104,031,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R0366:D430041D05Rik
|
UTSW |
2 |
104,085,685 (GRCm39) |
missense |
probably damaging |
0.99 |
R0402:D430041D05Rik
|
UTSW |
2 |
103,998,509 (GRCm39) |
missense |
probably damaging |
0.99 |
R0436:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0441:D430041D05Rik
|
UTSW |
2 |
103,998,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R0540:D430041D05Rik
|
UTSW |
2 |
104,063,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:D430041D05Rik
|
UTSW |
2 |
104,063,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R0613:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0747:D430041D05Rik
|
UTSW |
2 |
104,060,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R0864:D430041D05Rik
|
UTSW |
2 |
104,060,773 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0980:D430041D05Rik
|
UTSW |
2 |
104,079,690 (GRCm39) |
missense |
probably damaging |
0.99 |
R1014:D430041D05Rik
|
UTSW |
2 |
104,088,674 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1254:D430041D05Rik
|
UTSW |
2 |
104,031,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R1364:D430041D05Rik
|
UTSW |
2 |
103,985,363 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1456:D430041D05Rik
|
UTSW |
2 |
104,038,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:D430041D05Rik
|
UTSW |
2 |
104,051,553 (GRCm39) |
small deletion |
probably benign |
|
R1604:D430041D05Rik
|
UTSW |
2 |
104,035,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:D430041D05Rik
|
UTSW |
2 |
104,085,915 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1623:D430041D05Rik
|
UTSW |
2 |
103,983,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R1634:D430041D05Rik
|
UTSW |
2 |
104,051,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R1834:D430041D05Rik
|
UTSW |
2 |
103,998,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R2080:D430041D05Rik
|
UTSW |
2 |
103,987,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R2101:D430041D05Rik
|
UTSW |
2 |
103,979,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R2240:D430041D05Rik
|
UTSW |
2 |
103,987,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R2923:D430041D05Rik
|
UTSW |
2 |
104,085,660 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3751:D430041D05Rik
|
UTSW |
2 |
104,085,403 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3862:D430041D05Rik
|
UTSW |
2 |
104,044,522 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3863:D430041D05Rik
|
UTSW |
2 |
104,044,522 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3864:D430041D05Rik
|
UTSW |
2 |
104,044,522 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3949:D430041D05Rik
|
UTSW |
2 |
104,087,713 (GRCm39) |
missense |
probably benign |
0.02 |
R4493:D430041D05Rik
|
UTSW |
2 |
104,086,684 (GRCm39) |
missense |
probably benign |
0.02 |
R4526:D430041D05Rik
|
UTSW |
2 |
104,022,778 (GRCm39) |
critical splice donor site |
probably null |
|
R4592:D430041D05Rik
|
UTSW |
2 |
104,063,824 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4598:D430041D05Rik
|
UTSW |
2 |
104,038,528 (GRCm39) |
missense |
probably damaging |
0.99 |
R4599:D430041D05Rik
|
UTSW |
2 |
104,038,528 (GRCm39) |
missense |
probably damaging |
0.99 |
R4647:D430041D05Rik
|
UTSW |
2 |
104,088,788 (GRCm39) |
missense |
probably damaging |
0.99 |
R4765:D430041D05Rik
|
UTSW |
2 |
104,044,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R4808:D430041D05Rik
|
UTSW |
2 |
104,031,455 (GRCm39) |
critical splice donor site |
probably null |
|
R4868:D430041D05Rik
|
UTSW |
2 |
104,085,754 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4982:D430041D05Rik
|
UTSW |
2 |
104,085,732 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5144:D430041D05Rik
|
UTSW |
2 |
104,088,847 (GRCm39) |
missense |
probably damaging |
0.99 |
R5255:D430041D05Rik
|
UTSW |
2 |
104,086,945 (GRCm39) |
missense |
probably benign |
0.26 |
R5356:D430041D05Rik
|
UTSW |
2 |
104,085,754 (GRCm39) |
missense |
probably damaging |
0.99 |
R5368:D430041D05Rik
|
UTSW |
2 |
104,078,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R5963:D430041D05Rik
|
UTSW |
2 |
104,078,630 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5993:D430041D05Rik
|
UTSW |
2 |
103,998,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R6122:D430041D05Rik
|
UTSW |
2 |
104,086,637 (GRCm39) |
missense |
probably benign |
0.01 |
R6410:D430041D05Rik
|
UTSW |
2 |
103,998,548 (GRCm39) |
splice site |
probably null |
|
R6804:D430041D05Rik
|
UTSW |
2 |
103,979,371 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6850:D430041D05Rik
|
UTSW |
2 |
104,031,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R6853:D430041D05Rik
|
UTSW |
2 |
104,071,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R7034:D430041D05Rik
|
UTSW |
2 |
104,022,883 (GRCm39) |
missense |
probably damaging |
0.99 |
R7146:D430041D05Rik
|
UTSW |
2 |
104,088,698 (GRCm39) |
missense |
probably benign |
0.06 |
R7250:D430041D05Rik
|
UTSW |
2 |
104,086,961 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7251:D430041D05Rik
|
UTSW |
2 |
104,051,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:D430041D05Rik
|
UTSW |
2 |
104,085,910 (GRCm39) |
missense |
probably benign |
|
R7359:D430041D05Rik
|
UTSW |
2 |
104,044,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:D430041D05Rik
|
UTSW |
2 |
104,085,363 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7436:D430041D05Rik
|
UTSW |
2 |
104,087,447 (GRCm39) |
missense |
probably benign |
0.02 |
R7472:D430041D05Rik
|
UTSW |
2 |
104,240,484 (GRCm39) |
missense |
unknown |
|
R7492:D430041D05Rik
|
UTSW |
2 |
104,031,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R7631:D430041D05Rik
|
UTSW |
2 |
103,979,363 (GRCm39) |
nonsense |
probably null |
|
R7672:D430041D05Rik
|
UTSW |
2 |
104,071,581 (GRCm39) |
missense |
probably benign |
0.01 |
R7721:D430041D05Rik
|
UTSW |
2 |
104,088,874 (GRCm39) |
missense |
probably benign |
0.00 |
R7754:D430041D05Rik
|
UTSW |
2 |
104,087,504 (GRCm39) |
missense |
probably benign |
0.01 |
R7882:D430041D05Rik
|
UTSW |
2 |
104,087,974 (GRCm39) |
nonsense |
probably null |
|
R7896:D430041D05Rik
|
UTSW |
2 |
104,088,385 (GRCm39) |
missense |
probably benign |
0.05 |
R7986:D430041D05Rik
|
UTSW |
2 |
104,087,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R8005:D430041D05Rik
|
UTSW |
2 |
104,088,599 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8016:D430041D05Rik
|
UTSW |
2 |
104,022,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R8054:D430041D05Rik
|
UTSW |
2 |
103,985,390 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8058:D430041D05Rik
|
UTSW |
2 |
103,979,128 (GRCm39) |
makesense |
probably null |
|
R8100:D430041D05Rik
|
UTSW |
2 |
104,087,287 (GRCm39) |
missense |
probably benign |
0.00 |
R8461:D430041D05Rik
|
UTSW |
2 |
103,998,280 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8695:D430041D05Rik
|
UTSW |
2 |
104,085,299 (GRCm39) |
critical splice donor site |
probably null |
|
R8885:D430041D05Rik
|
UTSW |
2 |
104,071,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R9007:D430041D05Rik
|
UTSW |
2 |
104,087,930 (GRCm39) |
missense |
probably benign |
0.08 |
R9009:D430041D05Rik
|
UTSW |
2 |
104,240,521 (GRCm39) |
start gained |
probably benign |
|
R9335:D430041D05Rik
|
UTSW |
2 |
104,078,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R9348:D430041D05Rik
|
UTSW |
2 |
104,088,337 (GRCm39) |
missense |
probably benign |
0.05 |
R9384:D430041D05Rik
|
UTSW |
2 |
104,087,920 (GRCm39) |
missense |
probably benign |
|
R9483:D430041D05Rik
|
UTSW |
2 |
104,087,563 (GRCm39) |
missense |
probably benign |
0.44 |
R9489:D430041D05Rik
|
UTSW |
2 |
104,087,189 (GRCm39) |
missense |
probably benign |
0.20 |
R9605:D430041D05Rik
|
UTSW |
2 |
104,087,189 (GRCm39) |
missense |
probably benign |
0.20 |
R9613:D430041D05Rik
|
UTSW |
2 |
104,060,737 (GRCm39) |
missense |
probably benign |
0.09 |
R9698:D430041D05Rik
|
UTSW |
2 |
103,985,396 (GRCm39) |
missense |
probably damaging |
1.00 |
X0024:D430041D05Rik
|
UTSW |
2 |
104,022,911 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:D430041D05Rik
|
UTSW |
2 |
104,087,201 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:D430041D05Rik
|
UTSW |
2 |
103,985,280 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:D430041D05Rik
|
UTSW |
2 |
104,071,536 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
Predicted Primers |
PCR Primer
(F):5'- TTAGAGGACCGCTGTGATGC -3'
(R):5'- AACTGTGGCTGTAGGGAGGATC -3'
Sequencing Primer
(F):5'- GTGAATACAGAGACTCCTTACGGTC -3'
(R):5'- AGGATCATAGGCCTAGTGTCTAGCC -3'
|
Posted On |
2014-06-30 |