Incidental Mutation 'R1478:Srrm2'
| ID |
165663 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Srrm2
|
| Ensembl Gene |
ENSMUSG00000039218 |
| Gene Name |
serine/arginine repetitive matrix 2 |
| Synonyms |
5033413A03Rik, SRm300 |
| MMRRC Submission |
039531-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.949)
|
| Stock # |
R1478 (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 24034876 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 507
(S507P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000085993
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000088621]
[ENSMUST00000190686]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000088621
AA Change: S507P
PolyPhen 2
Score 0.226 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000085993
Gene: ENSMUSG00000039218
AA Change: S507P
| 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 |
probably benign
Transcript: ENSMUST00000186045
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000186914
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000189977
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000190686
AA Change: S603P
|
| SMART Domains |
Protein: ENSMUSP00000139842
Gene: ENSMUSG00000039218
AA Change: S603P
| 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: 99.1%
- 3x: 98.2%
- 10x: 95.7%
- 20x: 90.6%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 63 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aacs |
T |
A |
5: 125,580,287 (GRCm39) |
I204N |
possibly damaging |
Het |
| Acaca |
A |
G |
11: 84,263,453 (GRCm39) |
T2025A |
probably damaging |
Het |
| B4galt3 |
C |
T |
1: 171,103,938 (GRCm39) |
R170C |
probably benign |
Het |
| BC028528 |
T |
C |
3: 95,799,271 (GRCm39) |
|
probably null |
Het |
| Ccdc73 |
A |
T |
2: 104,737,955 (GRCm39) |
Q17L |
possibly damaging |
Het |
| Ccdc73 |
A |
G |
2: 104,745,012 (GRCm39) |
T50A |
possibly damaging |
Het |
| Ccdc83 |
T |
C |
7: 89,908,677 (GRCm39) |
D19G |
probably damaging |
Het |
| Ccn6 |
G |
A |
10: 39,029,239 (GRCm39) |
R230W |
probably damaging |
Het |
| Cct8l1 |
T |
C |
5: 25,722,767 (GRCm39) |
V494A |
probably benign |
Het |
| Chd1 |
T |
C |
17: 15,959,769 (GRCm39) |
F663L |
probably damaging |
Het |
| Chn2 |
A |
T |
6: 54,270,065 (GRCm39) |
E319V |
probably damaging |
Het |
| Cnnm1 |
T |
C |
19: 43,460,295 (GRCm39) |
V679A |
probably damaging |
Het |
| Cntn6 |
C |
T |
6: 104,753,389 (GRCm39) |
T447I |
probably benign |
Het |
| Cyp3a11 |
G |
T |
5: 145,795,581 (GRCm39) |
L457I |
probably benign |
Het |
| Dera |
T |
A |
6: 137,807,193 (GRCm39) |
S214T |
possibly damaging |
Het |
| Dmtf1 |
A |
G |
5: 9,171,404 (GRCm39) |
V501A |
possibly damaging |
Het |
| Dnpep |
A |
G |
1: 75,292,671 (GRCm39) |
V114A |
probably damaging |
Het |
| Dscam |
C |
T |
16: 96,592,110 (GRCm39) |
V722M |
probably benign |
Het |
| Dsp |
A |
G |
13: 38,365,114 (GRCm39) |
N499S |
probably damaging |
Het |
| Ecd |
A |
T |
14: 20,396,725 (GRCm39) |
Y53* |
probably null |
Het |
| Esyt3 |
T |
C |
9: 99,200,119 (GRCm39) |
T692A |
probably benign |
Het |
| Fat1 |
T |
A |
8: 45,478,659 (GRCm39) |
N2545K |
probably damaging |
Het |
| Fndc3a |
A |
G |
14: 72,795,072 (GRCm39) |
|
probably null |
Het |
| Fscn3 |
A |
G |
6: 28,430,567 (GRCm39) |
M246V |
probably benign |
Het |
| Gde1 |
G |
T |
7: 118,291,007 (GRCm39) |
T106K |
probably benign |
Het |
| Gjc2 |
A |
G |
11: 59,068,434 (GRCm39) |
I16T |
possibly damaging |
Het |
| Hacd4 |
A |
T |
4: 88,341,260 (GRCm39) |
M168K |
probably damaging |
Het |
| Hmx3 |
A |
G |
7: 131,145,826 (GRCm39) |
E178G |
probably damaging |
Het |
| Htt |
A |
G |
5: 34,961,171 (GRCm39) |
Y266C |
probably damaging |
Het |
| Jkampl |
A |
T |
6: 73,446,039 (GRCm39) |
L170Q |
probably damaging |
Het |
| Kif27 |
G |
T |
13: 58,451,359 (GRCm39) |
R990S |
probably damaging |
Het |
| Krtap22-2 |
A |
T |
16: 88,807,534 (GRCm39) |
Y21* |
probably null |
Het |
| Lrrc41 |
T |
A |
4: 115,952,405 (GRCm39) |
L661* |
probably null |
Het |
| Lrrc63 |
T |
C |
14: 75,363,424 (GRCm39) |
T236A |
probably benign |
Het |
| Mmp13 |
T |
C |
9: 7,272,892 (GRCm39) |
L84P |
probably damaging |
Het |
| Myh8 |
T |
C |
11: 67,183,551 (GRCm39) |
I754T |
probably benign |
Het |
| Neb |
A |
C |
2: 52,065,619 (GRCm39) |
D5961E |
probably benign |
Het |
| Nlrx1 |
T |
C |
9: 44,175,374 (GRCm39) |
H134R |
probably benign |
Het |
| Npepps |
A |
T |
11: 97,117,673 (GRCm39) |
M542K |
probably benign |
Het |
| Nup160 |
C |
T |
2: 90,509,743 (GRCm39) |
|
probably benign |
Het |
| Or3a1c |
T |
A |
11: 74,045,963 (GRCm39) |
|
probably null |
Het |
| Or8g33 |
T |
A |
9: 39,337,888 (GRCm39) |
T160S |
possibly damaging |
Het |
| Pikfyve |
T |
C |
1: 65,302,136 (GRCm39) |
|
probably null |
Het |
| Ppp6r1 |
A |
T |
7: 4,643,377 (GRCm39) |
|
probably null |
Het |
| Prss33 |
A |
G |
17: 24,054,072 (GRCm39) |
W45R |
probably damaging |
Het |
| Ptprf |
A |
T |
4: 118,069,302 (GRCm39) |
Y980* |
probably null |
Het |
| Qrich1 |
T |
C |
9: 108,436,531 (GRCm39) |
V743A |
probably benign |
Het |
| Rev3l |
G |
A |
10: 39,659,329 (GRCm39) |
|
probably null |
Het |
| Samd9l |
A |
T |
6: 3,376,369 (GRCm39) |
N297K |
probably benign |
Het |
| Sap130 |
A |
G |
18: 31,813,527 (GRCm39) |
H528R |
possibly damaging |
Het |
| Slc9b2 |
T |
C |
3: 135,031,863 (GRCm39) |
V241A |
probably benign |
Het |
| Snx14 |
A |
T |
9: 88,276,581 (GRCm39) |
V577E |
probably benign |
Het |
| Stat2 |
A |
G |
10: 128,117,969 (GRCm39) |
|
probably null |
Het |
| Susd5 |
T |
C |
9: 113,925,752 (GRCm39) |
F545S |
probably benign |
Het |
| Tafa2 |
T |
A |
10: 123,429,401 (GRCm39) |
M5K |
possibly damaging |
Het |
| Tnnt2 |
A |
G |
1: 135,775,764 (GRCm39) |
T107A |
probably benign |
Het |
| Trappc6b |
T |
A |
12: 59,094,953 (GRCm39) |
I41F |
possibly damaging |
Het |
| Ttn |
T |
A |
2: 76,682,417 (GRCm39) |
|
probably benign |
Het |
| Vmn1r88 |
A |
C |
7: 12,911,878 (GRCm39) |
D78A |
probably damaging |
Het |
| Xpc |
C |
T |
6: 91,485,510 (GRCm39) |
D122N |
possibly damaging |
Het |
| Xpo1 |
C |
T |
11: 23,241,623 (GRCm39) |
A890V |
probably damaging |
Het |
| Zfp493 |
A |
G |
13: 67,934,680 (GRCm39) |
H211R |
probably damaging |
Het |
| Zfp958 |
A |
T |
8: 4,679,190 (GRCm39) |
H405L |
probably damaging |
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 |
|
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 |
|
|
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'- TGGTCCAGGAGCAGAAATACCCAG -3'
(R):5'- TACTTCGAGATCGTCGTCGTGCTG -3'
Sequencing Primer
(F):5'- TACCCAGAGAAGAGGCAGGTC -3'
(R):5'- CGTTCTAGACCGAGATCGAG -3'
|
| Posted On |
2014-03-28 |
Incidental Mutation