Incidental Mutation 'R1719:Fam186a'
| ID |
191325 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Fam186a
|
| Ensembl Gene |
ENSMUSG00000045350 |
| Gene Name |
family with sequence similarity 186, member A |
| Synonyms |
LOC380973, 1700030F18Rik |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.059)
|
| Stock # |
R1719 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
15 |
| Chromosomal Location |
99816229-99864942 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 99840227 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Serine
at position 2006
(T2006S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000097783
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000100209]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000100209
AA Change: T2006S
PolyPhen 2
Score 0.544 (Sensitivity: 0.88; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000097783
Gene: ENSMUSG00000045350
AA Change: T2006S
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
10 |
21 |
N/A |
INTRINSIC |
|
Blast:FBG
|
44 |
222 |
4e-48 |
BLAST |
|
coiled coil region
|
292 |
340 |
N/A |
INTRINSIC |
|
low complexity region
|
423 |
443 |
N/A |
INTRINSIC |
|
low complexity region
|
446 |
458 |
N/A |
INTRINSIC |
|
low complexity region
|
632 |
644 |
N/A |
INTRINSIC |
|
low complexity region
|
702 |
713 |
N/A |
INTRINSIC |
|
internal_repeat_2
|
743 |
1156 |
1.05e-58 |
PROSPERO |
|
internal_repeat_1
|
833 |
1270 |
7.71e-59 |
PROSPERO |
|
low complexity region
|
1271 |
1285 |
N/A |
INTRINSIC |
|
low complexity region
|
1289 |
1300 |
N/A |
INTRINSIC |
|
low complexity region
|
1309 |
1323 |
N/A |
INTRINSIC |
|
low complexity region
|
1327 |
1338 |
N/A |
INTRINSIC |
|
low complexity region
|
1347 |
1361 |
N/A |
INTRINSIC |
|
low complexity region
|
1365 |
1376 |
N/A |
INTRINSIC |
|
low complexity region
|
1384 |
1395 |
N/A |
INTRINSIC |
|
low complexity region
|
1403 |
1414 |
N/A |
INTRINSIC |
|
low complexity region
|
1423 |
1437 |
N/A |
INTRINSIC |
|
low complexity region
|
1441 |
1452 |
N/A |
INTRINSIC |
|
low complexity region
|
1460 |
1471 |
N/A |
INTRINSIC |
|
low complexity region
|
1479 |
1490 |
N/A |
INTRINSIC |
|
low complexity region
|
1498 |
1509 |
N/A |
INTRINSIC |
|
low complexity region
|
1518 |
1532 |
N/A |
INTRINSIC |
|
low complexity region
|
1536 |
1547 |
N/A |
INTRINSIC |
|
low complexity region
|
1555 |
1566 |
N/A |
INTRINSIC |
|
low complexity region
|
1574 |
1585 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
1586 |
1981 |
7.71e-59 |
PROSPERO |
|
internal_repeat_2
|
1737 |
2197 |
1.05e-58 |
PROSPERO |
|
low complexity region
|
2367 |
2378 |
N/A |
INTRINSIC |
|
low complexity region
|
2549 |
2564 |
N/A |
INTRINSIC |
|
low complexity region
|
2644 |
2655 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000104255
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000177831
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000180309
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.2%
- 20x: 92.3%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 84 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A1cf |
A |
T |
19: 31,904,526 (GRCm39) |
K263M |
probably damaging |
Het |
| Adam26a |
G |
A |
8: 44,023,073 (GRCm39) |
T139M |
possibly damaging |
Het |
| Agrp |
G |
T |
8: 106,293,467 (GRCm39) |
T106K |
probably damaging |
Het |
| Akap9 |
C |
T |
5: 4,007,645 (GRCm39) |
Q238* |
probably null |
Het |
| Ankrd6 |
A |
T |
4: 32,828,774 (GRCm39) |
V85E |
probably damaging |
Het |
| Ap2b1 |
C |
A |
11: 83,215,430 (GRCm39) |
P125T |
probably damaging |
Het |
| Arhgef7 |
C |
A |
8: 11,858,713 (GRCm39) |
|
probably null |
Het |
| Cblc |
A |
T |
7: 19,524,399 (GRCm39) |
D280E |
probably benign |
Het |
| Cdk11b |
T |
C |
4: 155,732,854 (GRCm39) |
|
probably benign |
Het |
| Cela2a |
G |
T |
4: 141,545,257 (GRCm39) |
F239L |
probably damaging |
Het |
| Cfap57 |
A |
T |
4: 118,463,828 (GRCm39) |
C342S |
probably benign |
Het |
| Clca4a |
C |
A |
3: 144,669,516 (GRCm39) |
W345L |
probably damaging |
Het |
| Col6a5 |
T |
C |
9: 105,808,492 (GRCm39) |
D852G |
unknown |
Het |
| Cyp4a32 |
T |
C |
4: 115,468,505 (GRCm39) |
V329A |
possibly damaging |
Het |
| Dcaf8 |
C |
T |
1: 172,003,062 (GRCm39) |
P287S |
probably damaging |
Het |
| Dmxl1 |
T |
A |
18: 50,067,704 (GRCm39) |
D2654E |
probably damaging |
Het |
| Dpep1 |
A |
T |
8: 123,927,486 (GRCm39) |
I347F |
possibly damaging |
Het |
| Dtnb |
T |
A |
12: 3,693,936 (GRCm39) |
Y56* |
probably null |
Het |
| Duox1 |
T |
C |
2: 122,169,125 (GRCm39) |
Y1182H |
possibly damaging |
Het |
| Dusp10 |
T |
A |
1: 183,769,422 (GRCm39) |
S129R |
probably benign |
Het |
| Dync2i1 |
T |
C |
12: 116,219,532 (GRCm39) |
I137V |
probably benign |
Het |
| Epcam |
G |
A |
17: 87,949,556 (GRCm39) |
R173Q |
probably damaging |
Het |
| Ephb3 |
A |
G |
16: 21,039,400 (GRCm39) |
E384G |
probably damaging |
Het |
| Exosc10 |
A |
T |
4: 148,652,960 (GRCm39) |
D525V |
probably damaging |
Het |
| Fbxw21 |
T |
A |
9: 108,977,242 (GRCm39) |
T156S |
possibly damaging |
Het |
| Fcrl5 |
A |
G |
3: 87,364,704 (GRCm39) |
E568G |
probably damaging |
Het |
| Fmn2 |
C |
T |
1: 174,436,024 (GRCm39) |
|
probably benign |
Het |
| Fut9 |
A |
G |
4: 25,619,744 (GRCm39) |
F357L |
possibly damaging |
Het |
| Garre1 |
A |
T |
7: 33,947,631 (GRCm39) |
M459K |
probably damaging |
Het |
| Gas2l1 |
G |
A |
11: 5,014,266 (GRCm39) |
H65Y |
probably damaging |
Het |
| Gjd2 |
A |
T |
2: 113,843,614 (GRCm39) |
M1K |
probably null |
Het |
| Hdgfl3 |
T |
C |
7: 81,549,432 (GRCm39) |
Y149C |
probably damaging |
Het |
| Hmcn2 |
T |
C |
2: 31,244,733 (GRCm39) |
V730A |
probably damaging |
Het |
| Inpp4a |
A |
T |
1: 37,437,880 (GRCm39) |
S223C |
probably damaging |
Het |
| Ip6k1 |
G |
A |
9: 107,918,195 (GRCm39) |
E77K |
possibly damaging |
Het |
| Knl1 |
T |
A |
2: 118,902,219 (GRCm39) |
W1307R |
probably benign |
Het |
| Kpna3 |
A |
G |
14: 61,624,926 (GRCm39) |
L139P |
probably damaging |
Het |
| Lama3 |
T |
C |
18: 12,612,929 (GRCm39) |
|
probably null |
Het |
| Lin54 |
G |
A |
5: 100,633,108 (GRCm39) |
P192L |
possibly damaging |
Het |
| Lpo |
T |
A |
11: 87,700,018 (GRCm39) |
|
probably null |
Het |
| Lrrc37 |
T |
A |
11: 103,507,897 (GRCm39) |
|
probably benign |
Het |
| Lrrd1 |
T |
G |
5: 3,900,483 (GRCm39) |
|
probably null |
Het |
| Nbas |
T |
A |
12: 13,610,978 (GRCm39) |
|
probably null |
Het |
| Nemp1 |
G |
A |
10: 127,532,117 (GRCm39) |
G341D |
probably damaging |
Het |
| Nrp1 |
T |
C |
8: 129,152,366 (GRCm39) |
F192L |
probably damaging |
Het |
| Nufip2 |
T |
A |
11: 77,583,916 (GRCm39) |
V610E |
probably damaging |
Het |
| Nup160 |
T |
G |
2: 90,530,780 (GRCm39) |
Y479* |
probably null |
Het |
| Oas1d |
A |
T |
5: 121,058,025 (GRCm39) |
D323V |
possibly damaging |
Het |
| Or10ak14 |
A |
G |
4: 118,610,797 (GRCm39) |
W315R |
possibly damaging |
Het |
| Or14j1 |
A |
G |
17: 38,146,244 (GRCm39) |
D118G |
possibly damaging |
Het |
| Or4c3d |
T |
C |
2: 89,882,128 (GRCm39) |
Y180C |
probably damaging |
Het |
| Or52e4 |
C |
A |
7: 104,706,001 (GRCm39) |
H183N |
probably damaging |
Het |
| Or5ac22 |
T |
A |
16: 59,135,069 (GRCm39) |
R234* |
probably null |
Het |
| Or8b3 |
G |
A |
9: 38,314,550 (GRCm39) |
V127M |
possibly damaging |
Het |
| Or8c9 |
A |
T |
9: 38,241,803 (GRCm39) |
T307S |
probably benign |
Het |
| Pcm1 |
T |
A |
8: 41,766,396 (GRCm39) |
M1567K |
possibly damaging |
Het |
| Pdxk |
A |
G |
10: 78,279,730 (GRCm39) |
V215A |
probably benign |
Het |
| Phf12 |
T |
A |
11: 77,914,427 (GRCm39) |
L74Q |
probably damaging |
Het |
| Plcg1 |
A |
G |
2: 160,595,663 (GRCm39) |
E537G |
probably null |
Het |
| Plxna2 |
C |
T |
1: 194,326,678 (GRCm39) |
P204L |
possibly damaging |
Het |
| Ppp3cb |
T |
G |
14: 20,574,131 (GRCm39) |
M236L |
probably benign |
Het |
| Qrsl1 |
A |
T |
10: 43,772,026 (GRCm39) |
S55T |
probably damaging |
Het |
| Rbm5 |
T |
C |
9: 107,621,112 (GRCm39) |
|
probably null |
Het |
| Sipa1l2 |
A |
G |
8: 126,171,274 (GRCm39) |
S1403P |
probably damaging |
Het |
| Sis |
C |
T |
3: 72,872,937 (GRCm39) |
C67Y |
probably damaging |
Het |
| Specc1 |
A |
G |
11: 62,019,218 (GRCm39) |
I686V |
possibly damaging |
Het |
| Speg |
G |
A |
1: 75,394,507 (GRCm39) |
E1739K |
probably benign |
Het |
| Sprtn |
C |
A |
8: 125,628,372 (GRCm39) |
H154Q |
probably damaging |
Het |
| St7l |
A |
G |
3: 104,778,303 (GRCm39) |
T147A |
probably benign |
Het |
| Stab1 |
G |
A |
14: 30,867,985 (GRCm39) |
Q1630* |
probably null |
Het |
| Stpg2 |
A |
G |
3: 138,937,960 (GRCm39) |
D173G |
probably benign |
Het |
| Tcf20 |
G |
A |
15: 82,736,978 (GRCm39) |
T1491I |
probably benign |
Het |
| Themis2 |
A |
T |
4: 132,516,960 (GRCm39) |
I180N |
possibly damaging |
Het |
| Timd5 |
T |
C |
11: 46,417,121 (GRCm39) |
L13P |
probably damaging |
Het |
| Tktl2 |
G |
A |
8: 66,964,999 (GRCm39) |
V186M |
probably damaging |
Het |
| Ttn |
A |
G |
2: 76,638,340 (GRCm39) |
V13980A |
probably damaging |
Het |
| Ttn |
C |
T |
2: 76,575,978 (GRCm39) |
V24972M |
probably damaging |
Het |
| Usp5 |
A |
T |
6: 124,800,423 (GRCm39) |
M286K |
possibly damaging |
Het |
| Vmn2r22 |
G |
A |
6: 123,614,802 (GRCm39) |
R263C |
possibly damaging |
Het |
| Vmn2r71 |
T |
G |
7: 85,270,435 (GRCm39) |
C534G |
probably damaging |
Het |
| Wnk2 |
C |
T |
13: 49,214,202 (GRCm39) |
S1460N |
possibly damaging |
Het |
| Zfp445 |
G |
A |
9: 122,681,707 (GRCm39) |
P745S |
probably damaging |
Het |
| Zfp957 |
C |
T |
14: 79,451,436 (GRCm39) |
G121D |
probably damaging |
Het |
| Zscan4f |
A |
G |
7: 11,135,254 (GRCm39) |
E220G |
possibly damaging |
Het |
|
| Other mutations in Fam186a |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00588:Fam186a
|
APN |
15 |
99,825,572 (GRCm39) |
splice site |
probably benign |
|
|
IGL03047:Fam186a
|
UTSW |
15 |
99,843,589 (GRCm39) |
missense |
unknown |
|
|
R0172:Fam186a
|
UTSW |
15 |
99,852,768 (GRCm39) |
missense |
unknown |
|
|
R0194:Fam186a
|
UTSW |
15 |
99,839,644 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R0381:Fam186a
|
UTSW |
15 |
99,840,055 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0799:Fam186a
|
UTSW |
15 |
99,839,893 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1295:Fam186a
|
UTSW |
15 |
99,837,670 (GRCm39) |
splice site |
probably benign |
|
|
R1366:Fam186a
|
UTSW |
15 |
99,841,270 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R1519:Fam186a
|
UTSW |
15 |
99,845,536 (GRCm39) |
missense |
unknown |
|
|
R1592:Fam186a
|
UTSW |
15 |
99,838,199 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1636:Fam186a
|
UTSW |
15 |
99,839,539 (GRCm39) |
missense |
unknown |
|
|
R1759:Fam186a
|
UTSW |
15 |
99,864,762 (GRCm39) |
nonsense |
probably null |
|
|
R1856:Fam186a
|
UTSW |
15 |
99,838,183 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R2131:Fam186a
|
UTSW |
15 |
99,831,557 (GRCm39) |
unclassified |
probably benign |
|
|
R2192:Fam186a
|
UTSW |
15 |
99,838,192 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R2239:Fam186a
|
UTSW |
15 |
99,852,745 (GRCm39) |
missense |
unknown |
|
|
R2251:Fam186a
|
UTSW |
15 |
99,842,978 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2902:Fam186a
|
UTSW |
15 |
99,843,049 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R3037:Fam186a
|
UTSW |
15 |
99,841,675 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3744:Fam186a
|
UTSW |
15 |
99,845,416 (GRCm39) |
missense |
unknown |
|
|
R4021:Fam186a
|
UTSW |
15 |
99,839,680 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R4183:Fam186a
|
UTSW |
15 |
99,831,566 (GRCm39) |
unclassified |
probably benign |
|
|
R4238:Fam186a
|
UTSW |
15 |
99,841,523 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4667:Fam186a
|
UTSW |
15 |
99,842,413 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R4817:Fam186a
|
UTSW |
15 |
99,831,419 (GRCm39) |
unclassified |
probably benign |
|
|
R4835:Fam186a
|
UTSW |
15 |
99,843,689 (GRCm39) |
missense |
unknown |
|
|
R4837:Fam186a
|
UTSW |
15 |
99,838,678 (GRCm39) |
missense |
unknown |
|
|
R4897:Fam186a
|
UTSW |
15 |
99,843,158 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R4902:Fam186a
|
UTSW |
15 |
99,844,723 (GRCm39) |
missense |
unknown |
|
|
R4950:Fam186a
|
UTSW |
15 |
99,839,534 (GRCm39) |
missense |
unknown |
|
|
R4995:Fam186a
|
UTSW |
15 |
99,842,980 (GRCm39) |
missense |
probably benign |
0.27 |
|
R5062:Fam186a
|
UTSW |
15 |
99,842,527 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R5124:Fam186a
|
UTSW |
15 |
99,840,977 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5133:Fam186a
|
UTSW |
15 |
99,853,374 (GRCm39) |
missense |
unknown |
|
|
R5424:Fam186a
|
UTSW |
15 |
99,843,644 (GRCm39) |
missense |
unknown |
|
|
R5624:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5628:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5637:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5639:Fam186a
|
UTSW |
15 |
99,844,931 (GRCm39) |
missense |
unknown |
|
|
R5652:Fam186a
|
UTSW |
15 |
99,843,253 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R5673:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5799:Fam186a
|
UTSW |
15 |
99,864,705 (GRCm39) |
nonsense |
probably null |
|
|
R5965:Fam186a
|
UTSW |
15 |
99,842,978 (GRCm39) |
missense |
probably benign |
0.37 |
|
R6044:Fam186a
|
UTSW |
15 |
99,839,878 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6077:Fam186a
|
UTSW |
15 |
99,840,584 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R6120:Fam186a
|
UTSW |
15 |
99,838,244 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6185:Fam186a
|
UTSW |
15 |
99,845,530 (GRCm39) |
missense |
unknown |
|
|
R6186:Fam186a
|
UTSW |
15 |
99,845,206 (GRCm39) |
missense |
unknown |
|
|
R6242:Fam186a
|
UTSW |
15 |
99,837,788 (GRCm39) |
missense |
unknown |
|
|
R6351:Fam186a
|
UTSW |
15 |
99,839,623 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6368:Fam186a
|
UTSW |
15 |
99,841,198 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R6369:Fam186a
|
UTSW |
15 |
99,845,212 (GRCm39) |
missense |
unknown |
|
|
R6559:Fam186a
|
UTSW |
15 |
99,842,356 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R6855:Fam186a
|
UTSW |
15 |
99,852,756 (GRCm39) |
missense |
unknown |
|
|
R6867:Fam186a
|
UTSW |
15 |
99,843,731 (GRCm39) |
missense |
unknown |
|
|
R6957:Fam186a
|
UTSW |
15 |
99,844,357 (GRCm39) |
missense |
unknown |
|
|
R6961:Fam186a
|
UTSW |
15 |
99,838,082 (GRCm39) |
missense |
probably benign |
0.16 |
|
R6994:Fam186a
|
UTSW |
15 |
99,840,347 (GRCm39) |
missense |
probably benign |
0.35 |
|
R6996:Fam186a
|
UTSW |
15 |
99,853,374 (GRCm39) |
missense |
unknown |
|
|
R7062:Fam186a
|
UTSW |
15 |
99,831,521 (GRCm39) |
unclassified |
probably benign |
|
|
R7064:Fam186a
|
UTSW |
15 |
99,839,557 (GRCm39) |
missense |
unknown |
|
|
R7173:Fam186a
|
UTSW |
15 |
99,843,531 (GRCm39) |
missense |
unknown |
|
|
R7244:Fam186a
|
UTSW |
15 |
99,844,273 (GRCm39) |
missense |
unknown |
|
|
R7270:Fam186a
|
UTSW |
15 |
99,842,033 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R7410:Fam186a
|
UTSW |
15 |
99,844,826 (GRCm39) |
nonsense |
probably null |
|
|
R7437:Fam186a
|
UTSW |
15 |
99,840,775 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7475:Fam186a
|
UTSW |
15 |
99,845,395 (GRCm39) |
missense |
unknown |
|
|
R7487:Fam186a
|
UTSW |
15 |
99,840,017 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R7526:Fam186a
|
UTSW |
15 |
99,839,796 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R7650:Fam186a
|
UTSW |
15 |
99,837,788 (GRCm39) |
missense |
unknown |
|
|
R7658:Fam186a
|
UTSW |
15 |
99,837,725 (GRCm39) |
missense |
unknown |
|
|
R7663:Fam186a
|
UTSW |
15 |
99,842,950 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7703:Fam186a
|
UTSW |
15 |
99,852,678 (GRCm39) |
missense |
unknown |
|
|
R7814:Fam186a
|
UTSW |
15 |
99,842,545 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R7958:Fam186a
|
UTSW |
15 |
99,841,189 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7970:Fam186a
|
UTSW |
15 |
99,831,467 (GRCm39) |
missense |
unknown |
|
|
R8076:Fam186a
|
UTSW |
15 |
99,841,351 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R8087:Fam186a
|
UTSW |
15 |
99,839,725 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R8130:Fam186a
|
UTSW |
15 |
99,841,914 (GRCm39) |
frame shift |
probably null |
|
|
R8239:Fam186a
|
UTSW |
15 |
99,839,191 (GRCm39) |
missense |
unknown |
|
|
R8246:Fam186a
|
UTSW |
15 |
99,838,428 (GRCm39) |
missense |
unknown |
|
|
R8446:Fam186a
|
UTSW |
15 |
99,845,335 (GRCm39) |
missense |
unknown |
|
|
R8469:Fam186a
|
UTSW |
15 |
99,845,186 (GRCm39) |
missense |
unknown |
|
|
R8676:Fam186a
|
UTSW |
15 |
99,845,023 (GRCm39) |
missense |
unknown |
|
|
R8790:Fam186a
|
UTSW |
15 |
99,841,024 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R8808:Fam186a
|
UTSW |
15 |
99,842,604 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R8848:Fam186a
|
UTSW |
15 |
99,838,034 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R9083:Fam186a
|
UTSW |
15 |
99,843,079 (GRCm39) |
missense |
probably benign |
0.27 |
|
R9106:Fam186a
|
UTSW |
15 |
99,844,107 (GRCm39) |
small deletion |
probably benign |
|
|
R9116:Fam186a
|
UTSW |
15 |
99,840,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9156:Fam186a
|
UTSW |
15 |
99,841,159 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R9227:Fam186a
|
UTSW |
15 |
99,853,384 (GRCm39) |
missense |
unknown |
|
|
R9250:Fam186a
|
UTSW |
15 |
99,845,330 (GRCm39) |
missense |
unknown |
|
|
R9282:Fam186a
|
UTSW |
15 |
99,839,879 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9495:Fam186a
|
UTSW |
15 |
99,844,766 (GRCm39) |
missense |
unknown |
|
|
R9514:Fam186a
|
UTSW |
15 |
99,844,766 (GRCm39) |
missense |
unknown |
|
|
R9521:Fam186a
|
UTSW |
15 |
99,841,471 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9553:Fam186a
|
UTSW |
15 |
99,844,561 (GRCm39) |
missense |
unknown |
|
|
R9641:Fam186a
|
UTSW |
15 |
99,838,244 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9655:Fam186a
|
UTSW |
15 |
99,840,973 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9661:Fam186a
|
UTSW |
15 |
99,842,492 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R9673:Fam186a
|
UTSW |
15 |
99,841,024 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R9762:Fam186a
|
UTSW |
15 |
99,842,393 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
X0021:Fam186a
|
UTSW |
15 |
99,843,316 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1088:Fam186a
|
UTSW |
15 |
99,843,875 (GRCm39) |
missense |
unknown |
|
|
| Predicted Primers |
PCR Primer
(F):5'- CCTGCTCAGAGGTCAGACTTAAACG -3'
(R):5'- TCAGGACCTGGGGATCACTCTCAC -3'
Sequencing Primer
(F):5'- GGTAGAAGCTATTCCCAGATCCTG -3'
(R):5'- GGGATCACTCTCACCCCTG -3'
|
| Posted On |
2014-05-14 |
Incidental Mutation