Incidental Mutation 'R4943:Srrm2'
ID |
383305 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Srrm2
|
Ensembl Gene |
ENSMUSG00000039218 |
Gene Name |
serine/arginine repetitive matrix 2 |
Synonyms |
5033413A03Rik, SRm300 |
MMRRC Submission |
042540-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.949)
|
Stock # |
R4943 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
17 |
Chromosomal Location |
24009506-24043715 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 24041389 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Alanine
at position 2533
(V2533A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000139842
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000069579]
[ENSMUST00000088621]
[ENSMUST00000190686]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000069579
|
SMART Domains |
Protein: ENSMUSP00000066210 Gene: ENSMUSG00000055839
Domain | Start | End | E-Value | Type |
UBQ
|
3 |
80 |
5.1e-11 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000088621
AA Change: V2437A
PolyPhen 2
Score 0.936 (Sensitivity: 0.80; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000085993 Gene: ENSMUSG00000039218 AA Change: V2437A
Domain | Start | End | E-Value | Type |
low complexity region
|
82 |
157 |
N/A |
INTRINSIC |
low complexity region
|
161 |
188 |
N/A |
INTRINSIC |
low complexity region
|
223 |
238 |
N/A |
INTRINSIC |
internal_repeat_4
|
248 |
305 |
2.93e-5 |
PROSPERO |
internal_repeat_5
|
259 |
388 |
2.93e-5 |
PROSPERO |
low complexity region
|
407 |
423 |
N/A |
INTRINSIC |
CTD
|
464 |
584 |
5.25e-14 |
SMART |
low complexity region
|
652 |
682 |
N/A |
INTRINSIC |
low complexity region
|
689 |
721 |
N/A |
INTRINSIC |
internal_repeat_6
|
732 |
778 |
4.88e-5 |
PROSPERO |
low complexity region
|
779 |
795 |
N/A |
INTRINSIC |
low complexity region
|
802 |
824 |
N/A |
INTRINSIC |
low complexity region
|
839 |
853 |
N/A |
INTRINSIC |
internal_repeat_2
|
859 |
1124 |
6.34e-6 |
PROSPERO |
internal_repeat_1
|
1055 |
1183 |
3.81e-6 |
PROSPERO |
internal_repeat_4
|
1113 |
1166 |
2.93e-5 |
PROSPERO |
internal_repeat_6
|
1169 |
1213 |
4.88e-5 |
PROSPERO |
low complexity region
|
1236 |
1244 |
N/A |
INTRINSIC |
low complexity region
|
1275 |
1286 |
N/A |
INTRINSIC |
low complexity region
|
1290 |
1312 |
N/A |
INTRINSIC |
internal_repeat_2
|
1313 |
1485 |
6.34e-6 |
PROSPERO |
low complexity region
|
1493 |
1525 |
N/A |
INTRINSIC |
low complexity region
|
1545 |
1555 |
N/A |
INTRINSIC |
low complexity region
|
1559 |
1720 |
N/A |
INTRINSIC |
low complexity region
|
1734 |
1919 |
N/A |
INTRINSIC |
low complexity region
|
1926 |
1951 |
N/A |
INTRINSIC |
low complexity region
|
1966 |
1980 |
N/A |
INTRINSIC |
low complexity region
|
2079 |
2105 |
N/A |
INTRINSIC |
internal_repeat_3
|
2107 |
2118 |
1.06e-5 |
PROSPERO |
internal_repeat_3
|
2135 |
2146 |
1.06e-5 |
PROSPERO |
low complexity region
|
2153 |
2172 |
N/A |
INTRINSIC |
internal_repeat_5
|
2182 |
2320 |
2.93e-5 |
PROSPERO |
internal_repeat_1
|
2224 |
2368 |
3.81e-6 |
PROSPERO |
low complexity region
|
2390 |
2425 |
N/A |
INTRINSIC |
low complexity region
|
2518 |
2539 |
N/A |
INTRINSIC |
low complexity region
|
2541 |
2550 |
N/A |
INTRINSIC |
low complexity region
|
2552 |
2571 |
N/A |
INTRINSIC |
low complexity region
|
2594 |
2607 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000175240
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000186259
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000186914
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000190568
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000190686
AA Change: V2533A
PolyPhen 2
Score 0.936 (Sensitivity: 0.80; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000139842 Gene: ENSMUSG00000039218 AA Change: V2533A
Domain | Start | End | E-Value | Type |
Pfam:cwf21
|
58 |
102 |
1.5e-13 |
PFAM |
low complexity region
|
178 |
253 |
N/A |
INTRINSIC |
low complexity region
|
257 |
284 |
N/A |
INTRINSIC |
low complexity region
|
319 |
334 |
N/A |
INTRINSIC |
internal_repeat_4
|
344 |
401 |
3.07e-5 |
PROSPERO |
internal_repeat_5
|
355 |
484 |
3.07e-5 |
PROSPERO |
low complexity region
|
503 |
519 |
N/A |
INTRINSIC |
CTD
|
560 |
680 |
5.25e-14 |
SMART |
low complexity region
|
748 |
778 |
N/A |
INTRINSIC |
low complexity region
|
785 |
817 |
N/A |
INTRINSIC |
internal_repeat_6
|
828 |
874 |
5.11e-5 |
PROSPERO |
low complexity region
|
875 |
891 |
N/A |
INTRINSIC |
low complexity region
|
898 |
920 |
N/A |
INTRINSIC |
low complexity region
|
935 |
949 |
N/A |
INTRINSIC |
internal_repeat_2
|
955 |
1220 |
6.62e-6 |
PROSPERO |
internal_repeat_1
|
1151 |
1279 |
3.97e-6 |
PROSPERO |
internal_repeat_4
|
1209 |
1262 |
3.07e-5 |
PROSPERO |
internal_repeat_6
|
1265 |
1309 |
5.11e-5 |
PROSPERO |
low complexity region
|
1332 |
1340 |
N/A |
INTRINSIC |
low complexity region
|
1371 |
1382 |
N/A |
INTRINSIC |
low complexity region
|
1386 |
1408 |
N/A |
INTRINSIC |
internal_repeat_2
|
1409 |
1581 |
6.62e-6 |
PROSPERO |
low complexity region
|
1589 |
1621 |
N/A |
INTRINSIC |
low complexity region
|
1641 |
1651 |
N/A |
INTRINSIC |
low complexity region
|
1655 |
1816 |
N/A |
INTRINSIC |
low complexity region
|
1830 |
2015 |
N/A |
INTRINSIC |
low complexity region
|
2022 |
2047 |
N/A |
INTRINSIC |
low complexity region
|
2062 |
2076 |
N/A |
INTRINSIC |
low complexity region
|
2175 |
2201 |
N/A |
INTRINSIC |
internal_repeat_3
|
2203 |
2214 |
1.1e-5 |
PROSPERO |
internal_repeat_3
|
2231 |
2242 |
1.1e-5 |
PROSPERO |
low complexity region
|
2249 |
2268 |
N/A |
INTRINSIC |
internal_repeat_5
|
2278 |
2416 |
3.07e-5 |
PROSPERO |
internal_repeat_1
|
2320 |
2464 |
3.97e-6 |
PROSPERO |
low complexity region
|
2486 |
2521 |
N/A |
INTRINSIC |
low complexity region
|
2614 |
2635 |
N/A |
INTRINSIC |
low complexity region
|
2637 |
2646 |
N/A |
INTRINSIC |
low complexity region
|
2648 |
2667 |
N/A |
INTRINSIC |
low complexity region
|
2690 |
2703 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.0594 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.5%
|
Validation Efficiency |
99% (81/82) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
C |
A |
13: 77,393,446 (GRCm39) |
T366K |
possibly damaging |
Het |
2510039O18Rik |
T |
A |
4: 148,029,555 (GRCm39) |
H508Q |
probably damaging |
Het |
Aadacl4fm5 |
T |
A |
4: 144,504,290 (GRCm39) |
E287V |
probably benign |
Het |
Actl9 |
G |
A |
17: 33,652,059 (GRCm39) |
V40M |
possibly damaging |
Het |
Aen |
T |
A |
7: 78,552,109 (GRCm39) |
V23E |
probably damaging |
Het |
Agbl1 |
G |
A |
7: 76,069,764 (GRCm39) |
R432K |
probably benign |
Het |
Akap13 |
T |
A |
7: 75,398,988 (GRCm39) |
F2689I |
probably benign |
Het |
Arhgap45 |
A |
G |
10: 79,862,337 (GRCm39) |
S475G |
probably benign |
Het |
Atg7 |
A |
C |
6: 114,674,045 (GRCm39) |
Q231P |
probably benign |
Het |
Calr3 |
A |
T |
8: 73,185,221 (GRCm39) |
V226D |
probably benign |
Het |
Cldn10 |
G |
A |
14: 119,025,725 (GRCm39) |
G53S |
possibly damaging |
Het |
Cops4 |
A |
T |
5: 100,695,292 (GRCm39) |
M404L |
probably benign |
Het |
Cpne4 |
A |
T |
9: 104,896,972 (GRCm39) |
H375L |
probably damaging |
Het |
D16Ertd472e |
A |
T |
16: 78,372,877 (GRCm39) |
V20D |
probably damaging |
Het |
Dcun1d5 |
T |
C |
9: 7,186,844 (GRCm39) |
F55L |
possibly damaging |
Het |
Dhx8 |
T |
A |
11: 101,628,526 (GRCm39) |
L93* |
probably null |
Het |
Dtx4 |
A |
G |
19: 12,478,424 (GRCm39) |
L53P |
probably damaging |
Het |
Ern2 |
C |
T |
7: 121,772,481 (GRCm39) |
R659H |
possibly damaging |
Het |
Etl4 |
G |
A |
2: 20,812,092 (GRCm39) |
A1392T |
probably benign |
Het |
Fat2 |
T |
C |
11: 55,169,859 (GRCm39) |
R2967G |
probably benign |
Het |
Fat4 |
A |
G |
3: 39,034,322 (GRCm39) |
D2658G |
probably benign |
Het |
Ftsj3 |
A |
G |
11: 106,140,344 (GRCm39) |
V808A |
probably damaging |
Het |
Gm10447 |
A |
T |
11: 53,347,216 (GRCm39) |
Y104* |
probably null |
Het |
Gm27013 |
A |
T |
6: 130,653,163 (GRCm39) |
C766* |
probably null |
Het |
Gm5581 |
A |
G |
6: 131,144,088 (GRCm39) |
|
noncoding transcript |
Het |
Gpr158 |
G |
A |
2: 21,831,968 (GRCm39) |
V1023I |
probably damaging |
Het |
Hectd2 |
T |
G |
19: 36,581,647 (GRCm39) |
|
probably null |
Het |
Hmcn2 |
T |
C |
2: 31,225,504 (GRCm39) |
Y138H |
probably damaging |
Het |
Kif28 |
T |
C |
1: 179,541,516 (GRCm39) |
I369V |
probably benign |
Het |
Kif4-ps |
C |
T |
12: 101,115,476 (GRCm39) |
|
noncoding transcript |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Map3k20 |
G |
A |
2: 72,202,262 (GRCm39) |
M164I |
possibly damaging |
Het |
Map4k4 |
A |
G |
1: 40,058,754 (GRCm39) |
I1050V |
probably damaging |
Het |
Med23 |
T |
A |
10: 24,751,567 (GRCm39) |
V133D |
possibly damaging |
Het |
Mycn |
A |
T |
12: 12,987,080 (GRCm39) |
L439Q |
probably damaging |
Het |
Myh2 |
G |
T |
11: 67,088,143 (GRCm39) |
A1920S |
probably damaging |
Het |
Myom3 |
T |
C |
4: 135,541,585 (GRCm39) |
V1392A |
possibly damaging |
Het |
Nktr |
T |
A |
9: 121,549,020 (GRCm39) |
|
probably benign |
Het |
Nme3 |
A |
G |
17: 25,115,697 (GRCm39) |
K48E |
probably damaging |
Het |
Nt5dc1 |
T |
C |
10: 34,186,387 (GRCm39) |
R58G |
probably damaging |
Het |
Nup205 |
A |
G |
6: 35,201,574 (GRCm39) |
E1270G |
probably damaging |
Het |
Or12d16-ps1 |
G |
T |
17: 37,705,916 (GRCm39) |
A162S |
probably benign |
Het |
Or4e2 |
C |
G |
14: 52,688,051 (GRCm39) |
Y60* |
probably null |
Het |
Or51l4 |
A |
T |
7: 103,404,503 (GRCm39) |
F96L |
probably benign |
Het |
Or8c20 |
C |
T |
9: 38,260,924 (GRCm39) |
H176Y |
probably damaging |
Het |
Pclo |
T |
C |
5: 14,762,651 (GRCm39) |
L3708P |
unknown |
Het |
Pde4dip |
A |
T |
3: 97,662,827 (GRCm39) |
N590K |
probably damaging |
Het |
Prokr1 |
A |
C |
6: 87,558,806 (GRCm39) |
I193S |
possibly damaging |
Het |
Pxdc1 |
C |
A |
13: 34,822,989 (GRCm39) |
|
probably null |
Het |
Rapgef2 |
A |
T |
3: 78,971,854 (GRCm39) |
S1494T |
probably benign |
Het |
Rbms3 |
G |
C |
9: 116,507,573 (GRCm39) |
|
probably benign |
Het |
Reep3 |
T |
A |
10: 66,932,042 (GRCm39) |
|
probably benign |
Het |
Rwdd2b |
T |
C |
16: 87,231,422 (GRCm39) |
K244R |
possibly damaging |
Het |
Stab2 |
T |
C |
10: 86,790,026 (GRCm39) |
Y580C |
probably damaging |
Het |
Stac2 |
G |
T |
11: 97,932,398 (GRCm39) |
S198R |
probably benign |
Het |
Tdp2 |
T |
A |
13: 25,022,248 (GRCm39) |
N222K |
probably benign |
Het |
Tex21 |
A |
G |
12: 76,268,474 (GRCm39) |
S103P |
probably damaging |
Het |
Thbs1 |
A |
T |
2: 117,943,930 (GRCm39) |
I183F |
probably damaging |
Het |
Tm9sf1 |
T |
C |
14: 55,878,625 (GRCm39) |
I256V |
probably damaging |
Het |
Tmem207 |
C |
T |
16: 26,336,603 (GRCm39) |
W50* |
probably null |
Het |
Trpm2 |
C |
A |
10: 77,801,841 (GRCm39) |
V75L |
probably damaging |
Het |
Vmn1r227 |
A |
T |
17: 20,955,623 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r13 |
C |
A |
5: 109,322,915 (GRCm39) |
V125L |
probably benign |
Het |
Vmn2r75 |
A |
T |
7: 85,814,705 (GRCm39) |
S263T |
probably damaging |
Het |
Wdr64 |
G |
A |
1: 175,547,882 (GRCm39) |
V140I |
probably benign |
Het |
Xpo4 |
T |
C |
14: 57,875,697 (GRCm39) |
I145M |
possibly damaging |
Het |
Zan |
G |
A |
5: 137,456,152 (GRCm39) |
T1336I |
unknown |
Het |
Zdbf2 |
G |
T |
1: 63,342,073 (GRCm39) |
V151F |
possibly damaging |
Het |
Zfhx3 |
T |
C |
8: 109,674,949 (GRCm39) |
S2000P |
probably damaging |
Het |
Zfp65 |
T |
A |
13: 67,859,099 (GRCm39) |
I12F |
probably damaging |
Het |
Zfp703 |
C |
A |
8: 27,469,619 (GRCm39) |
Q428K |
probably benign |
Het |
Zfp947 |
A |
C |
17: 22,364,813 (GRCm39) |
M287R |
probably benign |
Het |
Zfp976 |
A |
T |
7: 42,261,846 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Srrm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00421:Srrm2
|
APN |
17 |
24,031,452 (GRCm39) |
missense |
probably benign |
0.23 |
IGL00484:Srrm2
|
APN |
17 |
24,037,492 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01413:Srrm2
|
APN |
17 |
24,034,999 (GRCm39) |
unclassified |
probably benign |
|
IGL02272:Srrm2
|
APN |
17 |
24,034,756 (GRCm39) |
unclassified |
probably benign |
|
IGL02279:Srrm2
|
APN |
17 |
24,034,306 (GRCm39) |
unclassified |
probably benign |
|
IGL02325:Srrm2
|
APN |
17 |
24,029,453 (GRCm39) |
unclassified |
probably benign |
|
IGL02947:Srrm2
|
APN |
17 |
24,029,720 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03002:Srrm2
|
APN |
17 |
24,034,708 (GRCm39) |
unclassified |
probably benign |
|
BB009:Srrm2
|
UTSW |
17 |
24,037,501 (GRCm39) |
missense |
probably benign |
0.23 |
BB019:Srrm2
|
UTSW |
17 |
24,037,501 (GRCm39) |
missense |
probably benign |
0.23 |
R0173:Srrm2
|
UTSW |
17 |
24,034,103 (GRCm39) |
unclassified |
probably benign |
|
R1018:Srrm2
|
UTSW |
17 |
24,041,514 (GRCm39) |
missense |
probably damaging |
0.98 |
R1109:Srrm2
|
UTSW |
17 |
24,038,591 (GRCm39) |
unclassified |
probably benign |
|
R1199:Srrm2
|
UTSW |
17 |
24,036,725 (GRCm39) |
unclassified |
probably benign |
|
R1471:Srrm2
|
UTSW |
17 |
24,039,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R1478:Srrm2
|
UTSW |
17 |
24,034,876 (GRCm39) |
missense |
probably benign |
0.23 |
R1618:Srrm2
|
UTSW |
17 |
24,037,906 (GRCm39) |
unclassified |
probably benign |
|
R1678:Srrm2
|
UTSW |
17 |
24,037,960 (GRCm39) |
missense |
probably benign |
0.23 |
R1853:Srrm2
|
UTSW |
17 |
24,039,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R1968:Srrm2
|
UTSW |
17 |
24,040,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R2094:Srrm2
|
UTSW |
17 |
24,031,403 (GRCm39) |
unclassified |
probably benign |
|
R2102:Srrm2
|
UTSW |
17 |
24,036,722 (GRCm39) |
unclassified |
probably benign |
|
R2156:Srrm2
|
UTSW |
17 |
24,037,237 (GRCm39) |
missense |
probably benign |
0.23 |
R2214:Srrm2
|
UTSW |
17 |
24,035,719 (GRCm39) |
unclassified |
probably benign |
|
R2913:Srrm2
|
UTSW |
17 |
24,034,658 (GRCm39) |
unclassified |
probably benign |
|
R3721:Srrm2
|
UTSW |
17 |
24,041,549 (GRCm39) |
small deletion |
probably benign |
|
R4411:Srrm2
|
UTSW |
17 |
24,029,442 (GRCm39) |
unclassified |
probably benign |
|
R4412:Srrm2
|
UTSW |
17 |
24,029,442 (GRCm39) |
unclassified |
probably benign |
|
R4413:Srrm2
|
UTSW |
17 |
24,029,442 (GRCm39) |
unclassified |
probably benign |
|
R4583:Srrm2
|
UTSW |
17 |
24,038,593 (GRCm39) |
unclassified |
probably benign |
|
R4682:Srrm2
|
UTSW |
17 |
24,034,666 (GRCm39) |
missense |
probably benign |
0.23 |
R4910:Srrm2
|
UTSW |
17 |
24,034,362 (GRCm39) |
unclassified |
probably benign |
|
R5023:Srrm2
|
UTSW |
17 |
24,038,291 (GRCm39) |
unclassified |
probably benign |
|
R5033:Srrm2
|
UTSW |
17 |
24,039,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5163:Srrm2
|
UTSW |
17 |
24,038,524 (GRCm39) |
unclassified |
probably benign |
|
R5186:Srrm2
|
UTSW |
17 |
24,035,561 (GRCm39) |
missense |
probably benign |
0.23 |
R5197:Srrm2
|
UTSW |
17 |
24,036,358 (GRCm39) |
missense |
probably benign |
0.23 |
R5366:Srrm2
|
UTSW |
17 |
24,037,678 (GRCm39) |
missense |
probably benign |
0.23 |
R5483:Srrm2
|
UTSW |
17 |
24,040,246 (GRCm39) |
missense |
probably damaging |
0.96 |
R5551:Srrm2
|
UTSW |
17 |
24,037,450 (GRCm39) |
unclassified |
probably benign |
|
R5602:Srrm2
|
UTSW |
17 |
24,038,311 (GRCm39) |
unclassified |
probably benign |
|
R5733:Srrm2
|
UTSW |
17 |
24,040,360 (GRCm39) |
missense |
probably damaging |
0.98 |
R5774:Srrm2
|
UTSW |
17 |
24,037,249 (GRCm39) |
unclassified |
probably benign |
|
R5909:Srrm2
|
UTSW |
17 |
24,040,291 (GRCm39) |
missense |
probably benign |
0.27 |
R5961:Srrm2
|
UTSW |
17 |
24,039,083 (GRCm39) |
unclassified |
probably benign |
|
R6122:Srrm2
|
UTSW |
17 |
24,039,330 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6906:Srrm2
|
UTSW |
17 |
24,039,337 (GRCm39) |
missense |
probably damaging |
0.97 |
R7084:Srrm2
|
UTSW |
17 |
24,039,290 (GRCm39) |
missense |
probably damaging |
0.99 |
R7177:Srrm2
|
UTSW |
17 |
24,035,747 (GRCm39) |
missense |
unknown |
|
R7197:Srrm2
|
UTSW |
17 |
24,037,198 (GRCm39) |
missense |
unknown |
|
R7442:Srrm2
|
UTSW |
17 |
24,039,091 (GRCm39) |
missense |
unknown |
|
R7644:Srrm2
|
UTSW |
17 |
24,038,294 (GRCm39) |
missense |
unknown |
|
R7664:Srrm2
|
UTSW |
17 |
24,039,955 (GRCm39) |
missense |
probably damaging |
0.99 |
R7874:Srrm2
|
UTSW |
17 |
24,034,652 (GRCm39) |
missense |
unknown |
|
R7932:Srrm2
|
UTSW |
17 |
24,037,501 (GRCm39) |
missense |
probably benign |
0.23 |
R7950:Srrm2
|
UTSW |
17 |
24,027,084 (GRCm39) |
missense |
unknown |
|
R7958:Srrm2
|
UTSW |
17 |
24,040,286 (GRCm39) |
missense |
probably benign |
0.25 |
R8081:Srrm2
|
UTSW |
17 |
24,039,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R8118:Srrm2
|
UTSW |
17 |
24,027,057 (GRCm39) |
missense |
unknown |
|
R8174:Srrm2
|
UTSW |
17 |
24,034,297 (GRCm39) |
missense |
unknown |
|
R8191:Srrm2
|
UTSW |
17 |
24,039,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R8334:Srrm2
|
UTSW |
17 |
24,027,330 (GRCm39) |
missense |
unknown |
|
R8523:Srrm2
|
UTSW |
17 |
24,027,489 (GRCm39) |
unclassified |
probably benign |
|
R8728:Srrm2
|
UTSW |
17 |
24,038,831 (GRCm39) |
missense |
unknown |
|
R8912:Srrm2
|
UTSW |
17 |
24,038,575 (GRCm39) |
missense |
probably benign |
0.23 |
R9209:Srrm2
|
UTSW |
17 |
24,039,880 (GRCm39) |
missense |
probably benign |
0.05 |
RF006:Srrm2
|
UTSW |
17 |
24,031,562 (GRCm39) |
missense |
unknown |
|
Z1176:Srrm2
|
UTSW |
17 |
24,036,157 (GRCm39) |
missense |
unknown |
|
Z1177:Srrm2
|
UTSW |
17 |
24,036,484 (GRCm39) |
missense |
unknown |
|
|
Predicted Primers |
PCR Primer
(F):5'- TTTGGTCAGCTCTGTGCCAC -3'
(R):5'- CCTTTCTGGAGAACTCACCC -3'
Sequencing Primer
(F):5'- TGTGCCACTGCTCCAGAGAAG -3'
(R):5'- TGAGGGCCAGGCTTAGCAG -3'
|
Posted On |
2016-04-27 |