Incidental Mutation 'R4043:Srrm1'
| ID |
313914 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Srrm1
|
| Ensembl Gene |
ENSMUSG00000028809 |
| Gene Name |
serine/arginine repetitive matrix 1 |
| Synonyms |
SRm160 |
| MMRRC Submission |
041615-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R4043 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
135047795-135080632 bp(-) (GRCm39) |
| Type of Mutation |
unclassified |
| DNA Base Change (assembly) |
C to T
at 135068242 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000124450
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030613]
[ENSMUST00000084846]
[ENSMUST00000105861]
[ENSMUST00000131373]
[ENSMUST00000136342]
[ENSMUST00000136409]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
unknown
Transcript: ENSMUST00000030613
AA Change: R277Q
|
| SMART Domains |
Protein: ENSMUSP00000030613
Gene: ENSMUSG00000028809
AA Change: R277Q
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
20 |
29 |
N/A |
INTRINSIC |
|
PWI
|
40 |
115 |
2.25e-42 |
SMART |
|
low complexity region
|
124 |
141 |
N/A |
INTRINSIC |
|
low complexity region
|
148 |
227 |
N/A |
INTRINSIC |
|
low complexity region
|
248 |
407 |
N/A |
INTRINSIC |
|
internal_repeat_2
|
409 |
455 |
4.31e-5 |
PROSPERO |
|
internal_repeat_1
|
427 |
456 |
3.46e-6 |
PROSPERO |
|
low complexity region
|
476 |
500 |
N/A |
INTRINSIC |
|
low complexity region
|
517 |
534 |
N/A |
INTRINSIC |
|
low complexity region
|
555 |
661 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
666 |
700 |
3.46e-6 |
PROSPERO |
|
internal_repeat_3
|
670 |
693 |
4.31e-5 |
PROSPERO |
|
internal_repeat_4
|
684 |
698 |
4.31e-5 |
PROSPERO |
|
internal_repeat_2
|
689 |
734 |
4.31e-5 |
PROSPERO |
|
internal_repeat_3
|
719 |
740 |
4.31e-5 |
PROSPERO |
|
internal_repeat_5
|
730 |
740 |
8.09e-5 |
PROSPERO |
|
low complexity region
|
746 |
795 |
N/A |
INTRINSIC |
|
internal_repeat_4
|
799 |
813 |
4.31e-5 |
PROSPERO |
|
internal_repeat_5
|
808 |
818 |
8.09e-5 |
PROSPERO |
|
low complexity region
|
827 |
851 |
N/A |
INTRINSIC |
|
low complexity region
|
854 |
886 |
N/A |
INTRINSIC |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000084846
AA Change: R277Q
|
| SMART Domains |
Protein: ENSMUSP00000081906
Gene: ENSMUSG00000028809
AA Change: R277Q
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
20 |
29 |
N/A |
INTRINSIC |
|
PWI
|
40 |
115 |
2.25e-42 |
SMART |
|
low complexity region
|
124 |
141 |
N/A |
INTRINSIC |
|
low complexity region
|
148 |
227 |
N/A |
INTRINSIC |
|
low complexity region
|
248 |
402 |
N/A |
INTRINSIC |
|
internal_repeat_2
|
404 |
450 |
3.57e-5 |
PROSPERO |
|
internal_repeat_1
|
422 |
451 |
2.79e-6 |
PROSPERO |
|
low complexity region
|
471 |
495 |
N/A |
INTRINSIC |
|
low complexity region
|
512 |
529 |
N/A |
INTRINSIC |
|
low complexity region
|
550 |
656 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
661 |
695 |
2.79e-6 |
PROSPERO |
|
internal_repeat_3
|
665 |
688 |
3.57e-5 |
PROSPERO |
|
internal_repeat_4
|
679 |
693 |
3.57e-5 |
PROSPERO |
|
internal_repeat_2
|
684 |
729 |
3.57e-5 |
PROSPERO |
|
internal_repeat_3
|
714 |
735 |
3.57e-5 |
PROSPERO |
|
internal_repeat_5
|
725 |
735 |
6.75e-5 |
PROSPERO |
|
low complexity region
|
741 |
790 |
N/A |
INTRINSIC |
|
internal_repeat_4
|
794 |
808 |
3.57e-5 |
PROSPERO |
|
internal_repeat_5
|
803 |
813 |
6.75e-5 |
PROSPERO |
|
low complexity region
|
822 |
846 |
N/A |
INTRINSIC |
|
low complexity region
|
849 |
886 |
N/A |
INTRINSIC |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000105861
AA Change: R277Q
|
| SMART Domains |
Protein: ENSMUSP00000101487
Gene: ENSMUSG00000028809
AA Change: R277Q
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
20 |
29 |
N/A |
INTRINSIC |
|
PWI
|
40 |
115 |
2.25e-42 |
SMART |
|
low complexity region
|
124 |
141 |
N/A |
INTRINSIC |
|
low complexity region
|
148 |
227 |
N/A |
INTRINSIC |
|
low complexity region
|
248 |
407 |
N/A |
INTRINSIC |
|
internal_repeat_2
|
409 |
455 |
1.99e-5 |
PROSPERO |
|
internal_repeat_1
|
427 |
456 |
1.45e-6 |
PROSPERO |
|
low complexity region
|
476 |
500 |
N/A |
INTRINSIC |
|
low complexity region
|
517 |
534 |
N/A |
INTRINSIC |
|
low complexity region
|
539 |
647 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
652 |
686 |
1.45e-6 |
PROSPERO |
|
internal_repeat_3
|
656 |
679 |
1.99e-5 |
PROSPERO |
|
internal_repeat_4
|
670 |
684 |
1.99e-5 |
PROSPERO |
|
internal_repeat_2
|
675 |
720 |
1.99e-5 |
PROSPERO |
|
internal_repeat_3
|
705 |
726 |
1.99e-5 |
PROSPERO |
|
internal_repeat_5
|
716 |
726 |
3.82e-5 |
PROSPERO |
|
low complexity region
|
732 |
781 |
N/A |
INTRINSIC |
|
internal_repeat_4
|
785 |
799 |
1.99e-5 |
PROSPERO |
|
internal_repeat_5
|
794 |
804 |
3.82e-5 |
PROSPERO |
|
low complexity region
|
813 |
837 |
N/A |
INTRINSIC |
|
low complexity region
|
840 |
877 |
N/A |
INTRINSIC |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000131301
AA Change: R66Q
|
| SMART Domains |
Protein: ENSMUSP00000125477
Gene: ENSMUSG00000028809
AA Change: R66Q
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
17 |
N/A |
INTRINSIC |
|
low complexity region
|
38 |
61 |
N/A |
INTRINSIC |
|
low complexity region
|
63 |
135 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
182 |
196 |
7.32e-5 |
PROSPERO |
|
internal_repeat_1
|
195 |
209 |
7.32e-5 |
PROSPERO |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000131373
|
| SMART Domains |
Protein: ENSMUSP00000122754
Gene: ENSMUSG00000028809
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
20 |
29 |
N/A |
INTRINSIC |
|
PWI
|
40 |
115 |
2.25e-42 |
SMART |
|
low complexity region
|
124 |
141 |
N/A |
INTRINSIC |
|
low complexity region
|
145 |
197 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134019
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134854
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000136342
AA Change: R277Q
|
| SMART Domains |
Protein: ENSMUSP00000125003
Gene: ENSMUSG00000028809
AA Change: R277Q
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
20 |
29 |
N/A |
INTRINSIC |
|
PWI
|
40 |
115 |
2.25e-42 |
SMART |
|
low complexity region
|
124 |
141 |
N/A |
INTRINSIC |
|
low complexity region
|
148 |
227 |
N/A |
INTRINSIC |
|
low complexity region
|
248 |
407 |
N/A |
INTRINSIC |
|
internal_repeat_2
|
409 |
455 |
3.36e-5 |
PROSPERO |
|
internal_repeat_1
|
427 |
456 |
2.61e-6 |
PROSPERO |
|
low complexity region
|
476 |
500 |
N/A |
INTRINSIC |
|
low complexity region
|
517 |
534 |
N/A |
INTRINSIC |
|
low complexity region
|
555 |
661 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
666 |
700 |
2.61e-6 |
PROSPERO |
|
internal_repeat_3
|
670 |
693 |
3.36e-5 |
PROSPERO |
|
internal_repeat_4
|
684 |
698 |
3.36e-5 |
PROSPERO |
|
internal_repeat_2
|
689 |
734 |
3.36e-5 |
PROSPERO |
|
internal_repeat_3
|
719 |
740 |
3.36e-5 |
PROSPERO |
|
internal_repeat_5
|
730 |
740 |
6.37e-5 |
PROSPERO |
|
low complexity region
|
746 |
795 |
N/A |
INTRINSIC |
|
internal_repeat_4
|
799 |
813 |
3.36e-5 |
PROSPERO |
|
internal_repeat_5
|
808 |
818 |
6.37e-5 |
PROSPERO |
|
low complexity region
|
827 |
851 |
N/A |
INTRINSIC |
|
low complexity region
|
854 |
891 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000154788
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000150619
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000151251
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000136409
|
| SMART Domains |
Protein: ENSMUSP00000124450
Gene: ENSMUSG00000028809
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
13 |
22 |
N/A |
INTRINSIC |
|
Pfam:PWI
|
38 |
95 |
4.4e-17 |
PFAM |
|
low complexity region
|
119 |
131 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.0724 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.7%
- 20x: 92.9%
|
| Validation Efficiency |
97% (64/66) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 64 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgrf3 |
T |
C |
5: 30,409,360 (GRCm39) |
N44D |
probably benign |
Het |
| AU018091 |
A |
G |
7: 3,208,962 (GRCm39) |
F375L |
probably damaging |
Het |
| Bsph1 |
G |
T |
7: 13,192,201 (GRCm39) |
|
probably null |
Het |
| Casp1 |
A |
G |
9: 5,302,444 (GRCm39) |
D122G |
probably benign |
Het |
| Ccdc146 |
C |
T |
5: 21,521,941 (GRCm39) |
C361Y |
probably benign |
Het |
| Cdc37l1 |
T |
C |
19: 28,968,028 (GRCm39) |
S31P |
possibly damaging |
Het |
| Cdca2 |
A |
T |
14: 67,941,455 (GRCm39) |
M249K |
probably benign |
Het |
| Cfap73 |
C |
T |
5: 120,768,030 (GRCm39) |
|
probably null |
Het |
| Cgnl1 |
A |
G |
9: 71,612,575 (GRCm39) |
L749S |
probably damaging |
Het |
| Cmtr2 |
C |
A |
8: 110,948,462 (GRCm39) |
C257* |
probably null |
Het |
| Col6a4 |
A |
T |
9: 105,949,610 (GRCm39) |
L675* |
probably null |
Het |
| Cpne8 |
A |
T |
15: 90,456,204 (GRCm39) |
D186E |
probably damaging |
Het |
| Csmd3 |
A |
G |
15: 47,619,362 (GRCm39) |
|
probably null |
Het |
| Daglb |
T |
A |
5: 143,472,906 (GRCm39) |
Y354N |
possibly damaging |
Het |
| Dlgap1 |
T |
C |
17: 71,068,075 (GRCm39) |
S549P |
probably damaging |
Het |
| Dnah11 |
T |
C |
12: 117,843,678 (GRCm39) |
D4389G |
probably damaging |
Het |
| Dst |
T |
A |
1: 34,229,765 (GRCm39) |
C2631S |
probably benign |
Het |
| Gimap1 |
T |
A |
6: 48,720,176 (GRCm39) |
W263R |
probably damaging |
Het |
| Gne |
A |
C |
4: 44,040,383 (GRCm39) |
C594G |
possibly damaging |
Het |
| Gtf2a1 |
T |
C |
12: 91,542,441 (GRCm39) |
H47R |
probably benign |
Het |
| Hdac6 |
T |
C |
X: 7,797,731 (GRCm39) |
T993A |
probably benign |
Het |
| Helz2 |
T |
C |
2: 180,871,503 (GRCm39) |
D2703G |
probably benign |
Het |
| Jmjd1c |
G |
A |
10: 67,055,245 (GRCm39) |
V222I |
possibly damaging |
Het |
| Katnip |
A |
G |
7: 125,467,913 (GRCm39) |
I1366V |
probably benign |
Het |
| Kndc1 |
A |
G |
7: 139,504,044 (GRCm39) |
E1116G |
probably benign |
Het |
| Krt10 |
C |
T |
11: 99,277,819 (GRCm39) |
|
probably null |
Het |
| Lrrc37a |
T |
G |
11: 103,389,479 (GRCm39) |
H1982P |
possibly damaging |
Het |
| Med13l |
T |
A |
5: 118,731,528 (GRCm39) |
L68Q |
probably damaging |
Het |
| Megf10 |
C |
A |
18: 57,392,870 (GRCm39) |
D422E |
probably damaging |
Het |
| Mpz |
C |
T |
1: 170,987,340 (GRCm39) |
|
probably benign |
Het |
| Muc5ac |
A |
T |
7: 141,361,215 (GRCm39) |
T1508S |
possibly damaging |
Het |
| Myo3a |
C |
T |
2: 22,338,350 (GRCm39) |
|
probably benign |
Het |
| Ndnf |
A |
T |
6: 65,680,920 (GRCm39) |
N400Y |
possibly damaging |
Het |
| Or5h24 |
G |
A |
16: 58,919,124 (GRCm39) |
T77I |
unknown |
Het |
| Or6p1 |
T |
C |
1: 174,258,657 (GRCm39) |
I221T |
probably damaging |
Het |
| Or7g35 |
G |
T |
9: 19,496,291 (GRCm39) |
V153F |
probably benign |
Het |
| Otol1 |
A |
G |
3: 69,935,112 (GRCm39) |
D368G |
probably damaging |
Het |
| Pappa |
A |
G |
4: 65,232,824 (GRCm39) |
N1321S |
probably benign |
Het |
| Patl1 |
T |
A |
19: 11,920,314 (GRCm39) |
L756Q |
probably damaging |
Het |
| Plcg2 |
A |
G |
8: 118,339,717 (GRCm39) |
M1043V |
probably benign |
Het |
| Plekhg2 |
G |
A |
7: 28,064,144 (GRCm39) |
|
probably benign |
Het |
| Ppp2r2d |
G |
A |
7: 138,484,145 (GRCm39) |
W265* |
probably null |
Het |
| Ppp4r3c1 |
A |
G |
X: 88,975,909 (GRCm39) |
F96S |
probably damaging |
Het |
| Prss40 |
G |
T |
1: 34,599,960 (GRCm39) |
S9* |
probably null |
Het |
| Radil |
T |
A |
5: 142,479,988 (GRCm39) |
I471F |
probably benign |
Het |
| Radx |
C |
T |
X: 138,407,752 (GRCm39) |
S364L |
probably damaging |
Het |
| Rpl10l |
A |
T |
12: 66,330,977 (GRCm39) |
M52K |
probably damaging |
Het |
| Scn1a |
A |
T |
2: 66,156,380 (GRCm39) |
S510T |
possibly damaging |
Het |
| Sdad1 |
T |
G |
5: 92,450,553 (GRCm39) |
N194T |
probably damaging |
Het |
| Sel1l3 |
A |
T |
5: 53,345,396 (GRCm39) |
Y259* |
probably null |
Het |
| Slc22a26 |
T |
C |
19: 7,765,694 (GRCm39) |
|
probably null |
Het |
| Snap91 |
C |
T |
9: 86,659,102 (GRCm39) |
G477D |
probably damaging |
Het |
| Spata6l |
A |
T |
19: 28,923,183 (GRCm39) |
C80S |
possibly damaging |
Het |
| Srr |
T |
C |
11: 74,799,947 (GRCm39) |
T202A |
probably benign |
Het |
| Trp53bp2 |
T |
A |
1: 182,276,626 (GRCm39) |
L869Q |
possibly damaging |
Het |
| Ttbk1 |
T |
A |
17: 46,757,688 (GRCm39) |
D982V |
probably benign |
Het |
| Ttn |
T |
C |
2: 76,624,501 (GRCm39) |
T15324A |
probably benign |
Het |
| Ush1c |
T |
C |
7: 45,870,952 (GRCm39) |
E276G |
probably damaging |
Het |
| Vcan |
T |
A |
13: 89,840,662 (GRCm39) |
L1627F |
probably benign |
Het |
| Vps8 |
A |
C |
16: 21,345,146 (GRCm39) |
D823A |
probably damaging |
Het |
| Zfp616 |
T |
A |
11: 73,976,108 (GRCm39) |
N792K |
possibly damaging |
Het |
| Zfpm2 |
A |
T |
15: 40,734,023 (GRCm39) |
D2V |
possibly damaging |
Het |
| Zfyve16 |
A |
C |
13: 92,650,271 (GRCm39) |
|
probably null |
Het |
| Zmym2 |
T |
A |
14: 57,195,765 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Srrm1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02063:Srrm1
|
APN |
4 |
135,074,518 (GRCm39) |
splice site |
probably null |
|
|
IGL02070:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02073:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02193:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02232:Srrm1
|
APN |
4 |
135,080,427 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
IGL02377:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02379:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02380:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02382:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02386:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02387:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02393:Srrm1
|
APN |
4 |
135,048,725 (GRCm39) |
unclassified |
probably benign |
|
|
IGL02436:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02438:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02439:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02440:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02500:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02561:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02562:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02566:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02567:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02568:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02569:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02570:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02572:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02583:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02584:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02585:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02586:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02587:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02588:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02589:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02596:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02597:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02601:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02602:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02609:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02614:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02631:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02632:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02657:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02658:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02659:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02660:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02677:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02683:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02686:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02690:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02713:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02723:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02724:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02725:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02730:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02731:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02732:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02733:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02734:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02743:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02744:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
IGL02752:Srrm1
|
APN |
4 |
135,052,415 (GRCm39) |
missense |
unknown |
|
|
Serious
|
UTSW |
4 |
135,068,237 (GRCm39) |
nonsense |
probably null |
|
|
R0131:Srrm1
|
UTSW |
4 |
135,067,884 (GRCm39) |
nonsense |
probably null |
|
|
R0131:Srrm1
|
UTSW |
4 |
135,067,884 (GRCm39) |
nonsense |
probably null |
|
|
R0132:Srrm1
|
UTSW |
4 |
135,067,884 (GRCm39) |
nonsense |
probably null |
|
|
R0510:Srrm1
|
UTSW |
4 |
135,065,854 (GRCm39) |
intron |
probably benign |
|
|
R0691:Srrm1
|
UTSW |
4 |
135,052,302 (GRCm39) |
nonsense |
probably null |
|
|
R1337:Srrm1
|
UTSW |
4 |
135,074,044 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1397:Srrm1
|
UTSW |
4 |
135,048,742 (GRCm39) |
unclassified |
probably benign |
|
|
R2883:Srrm1
|
UTSW |
4 |
135,048,722 (GRCm39) |
unclassified |
probably benign |
|
|
R4772:Srrm1
|
UTSW |
4 |
135,069,690 (GRCm39) |
unclassified |
probably benign |
|
|
R4837:Srrm1
|
UTSW |
4 |
135,072,823 (GRCm39) |
intron |
probably benign |
|
|
R4975:Srrm1
|
UTSW |
4 |
135,074,031 (GRCm39) |
splice site |
probably benign |
|
|
R5401:Srrm1
|
UTSW |
4 |
135,051,380 (GRCm39) |
splice site |
probably benign |
|
|
R6144:Srrm1
|
UTSW |
4 |
135,065,184 (GRCm39) |
unclassified |
probably benign |
|
|
R6542:Srrm1
|
UTSW |
4 |
135,068,237 (GRCm39) |
nonsense |
probably null |
|
|
R7147:Srrm1
|
UTSW |
4 |
135,074,137 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8054:Srrm1
|
UTSW |
4 |
135,052,326 (GRCm39) |
missense |
unknown |
|
|
R8371:Srrm1
|
UTSW |
4 |
135,052,532 (GRCm39) |
missense |
unknown |
|
|
R8523:Srrm1
|
UTSW |
4 |
135,051,313 (GRCm39) |
missense |
unknown |
|
|
R8767:Srrm1
|
UTSW |
4 |
135,059,532 (GRCm39) |
missense |
unknown |
|
|
Z1177:Srrm1
|
UTSW |
4 |
135,059,052 (GRCm39) |
missense |
unknown |
|
|
Z1177:Srrm1
|
UTSW |
4 |
135,051,309 (GRCm39) |
missense |
unknown |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TGGTACATCACAAAGTGGACTTC -3'
(R):5'- GGGTTCGAGCTTGTACCATAAATAC -3'
Sequencing Primer
(F):5'- TCACAAAGTGGACTTCATTCTTAATG -3'
(R):5'- AGACAGCCAATATTGTTGAATTGGC -3'
|
| Posted On |
2015-04-30 |
Incidental Mutation