Incidental Mutation 'R5909:Srrm2'
| ID |
460883 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Srrm2
|
| Ensembl Gene |
ENSMUSG00000039218 |
| Gene Name |
serine/arginine repetitive matrix 2 |
| Synonyms |
5033413A03Rik, SRm300 |
| MMRRC Submission |
044106-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.949)
|
| Stock # |
R5909 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
17 |
| Chromosomal Location |
24009506-24043715 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 24040291 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 2408
(S2408P)
|
| 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 |
probably benign
Transcript: ENSMUST00000088621
AA Change: S2312P
PolyPhen 2
Score 0.268 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000085993
Gene: ENSMUSG00000039218
AA Change: S2312P
| 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: ENSMUST00000189977
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000190568
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000190686
AA Change: S2408P
PolyPhen 2
Score 0.268 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000139842
Gene: ENSMUSG00000039218
AA Change: S2408P
| 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 |
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.5%
- 10x: 97.8%
- 20x: 93.6%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 61 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adamts8 |
T |
C |
9: 30,873,224 (GRCm39) |
S810P |
probably benign |
Het |
| Adcy7 |
A |
T |
8: 89,052,124 (GRCm39) |
I931F |
probably damaging |
Het |
| Alcam |
G |
T |
16: 52,111,356 (GRCm39) |
Q248K |
probably benign |
Het |
| Astn1 |
A |
C |
1: 158,429,507 (GRCm39) |
R750S |
probably damaging |
Het |
| Atp1a2 |
A |
T |
1: 172,114,797 (GRCm39) |
N329K |
probably damaging |
Het |
| Bcl6 |
A |
G |
16: 23,791,556 (GRCm39) |
V266A |
probably benign |
Het |
| Bdp1 |
A |
G |
13: 100,228,794 (GRCm39) |
V278A |
probably benign |
Het |
| Ccdc162 |
T |
C |
10: 41,437,111 (GRCm39) |
E493G |
probably damaging |
Het |
| Cpvl |
T |
C |
6: 53,909,413 (GRCm39) |
Y241C |
probably damaging |
Het |
| Ddx55 |
T |
C |
5: 124,704,913 (GRCm39) |
M390T |
probably benign |
Het |
| Ero1b |
A |
G |
13: 12,594,139 (GRCm39) |
E102G |
probably benign |
Het |
| Etnk1 |
A |
G |
6: 143,143,164 (GRCm39) |
D273G |
probably benign |
Het |
| Exoc3 |
A |
G |
13: 74,347,643 (GRCm39) |
V109A |
probably damaging |
Het |
| F830016B08Rik |
T |
A |
18: 60,433,091 (GRCm39) |
I58N |
probably damaging |
Het |
| Fancd2 |
T |
A |
6: 113,538,672 (GRCm39) |
V589E |
probably benign |
Het |
| Fbll1 |
G |
A |
11: 35,689,159 (GRCm39) |
R35C |
unknown |
Het |
| Fnbp1 |
A |
G |
2: 30,938,211 (GRCm39) |
|
probably null |
Het |
| Glce |
G |
T |
9: 61,967,426 (GRCm39) |
A575D |
probably damaging |
Het |
| Ift20 |
T |
A |
11: 78,430,867 (GRCm39) |
M70K |
possibly damaging |
Het |
| Impg2 |
T |
C |
16: 56,078,499 (GRCm39) |
V487A |
probably damaging |
Het |
| Isx |
A |
G |
8: 75,619,426 (GRCm39) |
D206G |
probably benign |
Het |
| Jak3 |
A |
G |
8: 72,136,875 (GRCm39) |
I684V |
possibly damaging |
Het |
| Kdm5d |
G |
A |
Y: 941,306 (GRCm39) |
S1169N |
probably benign |
Het |
| Krt35 |
A |
T |
11: 99,986,639 (GRCm39) |
L125Q |
probably damaging |
Het |
| Lama4 |
G |
A |
10: 38,948,855 (GRCm39) |
A873T |
probably benign |
Het |
| Lrch4 |
T |
C |
5: 137,632,127 (GRCm39) |
S74P |
possibly damaging |
Het |
| Maneal |
A |
T |
4: 124,750,966 (GRCm39) |
Y263* |
probably null |
Het |
| Mcat |
C |
T |
15: 83,432,116 (GRCm39) |
A251T |
probably benign |
Het |
| Mup3 |
T |
G |
4: 62,004,244 (GRCm39) |
T90P |
probably benign |
Het |
| Mybpc2 |
G |
A |
7: 44,156,515 (GRCm39) |
A812V |
probably damaging |
Het |
| Naa15 |
T |
C |
3: 51,367,485 (GRCm39) |
F503L |
probably damaging |
Het |
| Nudt8 |
T |
C |
19: 4,050,727 (GRCm39) |
L25S |
possibly damaging |
Het |
| Oas1e |
A |
T |
5: 120,926,972 (GRCm39) |
V245D |
probably damaging |
Het |
| Ofcc1 |
A |
G |
13: 40,417,054 (GRCm39) |
M109T |
possibly damaging |
Het |
| Or4c58 |
A |
G |
2: 89,674,735 (GRCm39) |
V194A |
possibly damaging |
Het |
| Or4p18 |
A |
T |
2: 88,232,535 (GRCm39) |
F248I |
probably damaging |
Het |
| Phkb |
G |
T |
8: 86,748,076 (GRCm39) |
|
probably null |
Het |
| Pidd1 |
A |
C |
7: 141,021,183 (GRCm39) |
L365R |
probably damaging |
Het |
| Pira12 |
G |
A |
7: 3,900,621 (GRCm39) |
T43I |
probably damaging |
Het |
| Pkd1l2 |
G |
A |
8: 117,750,795 (GRCm39) |
R1739C |
probably benign |
Het |
| Pkdrej |
A |
T |
15: 85,702,497 (GRCm39) |
D1146E |
possibly damaging |
Het |
| Pkhd1l1 |
G |
T |
15: 44,390,159 (GRCm39) |
W1425L |
probably damaging |
Het |
| Plxna4 |
A |
G |
6: 32,494,181 (GRCm39) |
L145P |
probably damaging |
Het |
| Plxnd1 |
G |
T |
6: 115,945,649 (GRCm39) |
D941E |
probably benign |
Het |
| Prdm13 |
G |
T |
4: 21,683,894 (GRCm39) |
Q126K |
unknown |
Het |
| Rbm25 |
T |
A |
12: 83,728,362 (GRCm39) |
V837E |
probably damaging |
Het |
| Rcc2 |
T |
A |
4: 140,444,379 (GRCm39) |
Y357N |
probably damaging |
Het |
| Siglec1 |
A |
T |
2: 130,919,884 (GRCm39) |
N882K |
probably damaging |
Het |
| Sox13 |
A |
G |
1: 133,311,627 (GRCm39) |
I535T |
probably benign |
Het |
| Stat3 |
G |
A |
11: 100,794,556 (GRCm39) |
T251I |
probably benign |
Het |
| Sulf1 |
A |
T |
1: 12,929,039 (GRCm39) |
D102V |
possibly damaging |
Het |
| Tbc1d2 |
C |
T |
4: 46,629,912 (GRCm39) |
G252R |
probably benign |
Het |
| Tmem145 |
G |
T |
7: 25,007,618 (GRCm39) |
L208F |
possibly damaging |
Het |
| Trim17 |
A |
T |
11: 58,859,506 (GRCm39) |
E240V |
probably damaging |
Het |
| Trim43b |
A |
T |
9: 88,967,451 (GRCm39) |
I395K |
possibly damaging |
Het |
| Trmt61a |
C |
A |
12: 111,647,292 (GRCm39) |
H130N |
probably damaging |
Het |
| Unc5b |
A |
C |
10: 60,608,138 (GRCm39) |
L654R |
probably damaging |
Het |
| Vmn1r66 |
A |
T |
7: 10,008,269 (GRCm39) |
S255T |
probably benign |
Het |
| Ylpm1 |
C |
T |
12: 85,087,660 (GRCm39) |
P1148L |
probably damaging |
Het |
| Zbtb10 |
T |
C |
3: 9,345,109 (GRCm39) |
F677S |
probably benign |
Het |
| Zfp493 |
T |
A |
13: 67,934,717 (GRCm39) |
C223* |
probably null |
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 |
|
|
R4943:Srrm2
|
UTSW |
17 |
24,041,389 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
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 |
|
|
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'- GATCGTGTTAGTGGCAGAACC -3'
(R):5'- CAGCCAATGTAGAAGGCTGC -3'
Sequencing Primer
(F):5'- GTGGCAGAACCTCACCTTTAATG -3'
(R):5'- CAATGTAGAAGGCTGCTGGGC -3'
|
| Posted On |
2017-02-28 |
Incidental Mutation