Incidental Mutation 'R6805:Srcin1'
ID |
533547 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Srcin1
|
Ensembl Gene |
ENSMUSG00000038453 |
Gene Name |
SRC kinase signaling inhibitor 1 |
Synonyms |
p140Cap, P140 |
MMRRC Submission |
044918-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R6805 (G1)
|
Quality Score |
115.008 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
97400166-97466059 bp(-) (GRCm39) |
Type of Mutation |
critical splice acceptor site |
DNA Base Change (assembly) |
T to A
at 97442806 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000146591
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000107590]
[ENSMUST00000107590]
[ENSMUST00000107590]
[ENSMUST00000107593]
[ENSMUST00000107593]
[ENSMUST00000107593]
[ENSMUST00000107596]
[ENSMUST00000107596]
[ENSMUST00000107596]
[ENSMUST00000126287]
[ENSMUST00000126287]
[ENSMUST00000126287]
[ENSMUST00000207653]
[ENSMUST00000207653]
[ENSMUST00000207653]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably null
Transcript: ENSMUST00000107590
|
SMART Domains |
Protein: ENSMUSP00000103216 Gene: ENSMUSG00000038453
Domain | Start | End | E-Value | Type |
low complexity region
|
26 |
45 |
N/A |
INTRINSIC |
low complexity region
|
66 |
75 |
N/A |
INTRINSIC |
Blast:THAP
|
113 |
142 |
1e-9 |
BLAST |
low complexity region
|
332 |
366 |
N/A |
INTRINSIC |
low complexity region
|
489 |
501 |
N/A |
INTRINSIC |
low complexity region
|
516 |
538 |
N/A |
INTRINSIC |
low complexity region
|
558 |
575 |
N/A |
INTRINSIC |
low complexity region
|
655 |
679 |
N/A |
INTRINSIC |
low complexity region
|
699 |
712 |
N/A |
INTRINSIC |
coiled coil region
|
751 |
784 |
N/A |
INTRINSIC |
low complexity region
|
1034 |
1051 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000107590
|
SMART Domains |
Protein: ENSMUSP00000103216 Gene: ENSMUSG00000038453
Domain | Start | End | E-Value | Type |
low complexity region
|
26 |
45 |
N/A |
INTRINSIC |
low complexity region
|
66 |
75 |
N/A |
INTRINSIC |
Blast:THAP
|
113 |
142 |
1e-9 |
BLAST |
low complexity region
|
332 |
366 |
N/A |
INTRINSIC |
low complexity region
|
489 |
501 |
N/A |
INTRINSIC |
low complexity region
|
516 |
538 |
N/A |
INTRINSIC |
low complexity region
|
558 |
575 |
N/A |
INTRINSIC |
low complexity region
|
655 |
679 |
N/A |
INTRINSIC |
low complexity region
|
699 |
712 |
N/A |
INTRINSIC |
coiled coil region
|
751 |
784 |
N/A |
INTRINSIC |
low complexity region
|
1034 |
1051 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000107590
|
SMART Domains |
Protein: ENSMUSP00000103216 Gene: ENSMUSG00000038453
Domain | Start | End | E-Value | Type |
low complexity region
|
26 |
45 |
N/A |
INTRINSIC |
low complexity region
|
66 |
75 |
N/A |
INTRINSIC |
Blast:THAP
|
113 |
142 |
1e-9 |
BLAST |
low complexity region
|
332 |
366 |
N/A |
INTRINSIC |
low complexity region
|
489 |
501 |
N/A |
INTRINSIC |
low complexity region
|
516 |
538 |
N/A |
INTRINSIC |
low complexity region
|
558 |
575 |
N/A |
INTRINSIC |
low complexity region
|
655 |
679 |
N/A |
INTRINSIC |
low complexity region
|
699 |
712 |
N/A |
INTRINSIC |
coiled coil region
|
751 |
784 |
N/A |
INTRINSIC |
low complexity region
|
1034 |
1051 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000107593
|
SMART Domains |
Protein: ENSMUSP00000103219 Gene: ENSMUSG00000038453
Domain | Start | End | E-Value | Type |
low complexity region
|
26 |
45 |
N/A |
INTRINSIC |
low complexity region
|
66 |
75 |
N/A |
INTRINSIC |
Blast:THAP
|
113 |
142 |
1e-9 |
BLAST |
low complexity region
|
332 |
366 |
N/A |
INTRINSIC |
low complexity region
|
489 |
501 |
N/A |
INTRINSIC |
low complexity region
|
516 |
538 |
N/A |
INTRINSIC |
low complexity region
|
558 |
575 |
N/A |
INTRINSIC |
low complexity region
|
655 |
679 |
N/A |
INTRINSIC |
low complexity region
|
699 |
712 |
N/A |
INTRINSIC |
coiled coil region
|
751 |
784 |
N/A |
INTRINSIC |
low complexity region
|
1034 |
1051 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000107593
|
SMART Domains |
Protein: ENSMUSP00000103219 Gene: ENSMUSG00000038453
Domain | Start | End | E-Value | Type |
low complexity region
|
26 |
45 |
N/A |
INTRINSIC |
low complexity region
|
66 |
75 |
N/A |
INTRINSIC |
Blast:THAP
|
113 |
142 |
1e-9 |
BLAST |
low complexity region
|
332 |
366 |
N/A |
INTRINSIC |
low complexity region
|
489 |
501 |
N/A |
INTRINSIC |
low complexity region
|
516 |
538 |
N/A |
INTRINSIC |
low complexity region
|
558 |
575 |
N/A |
INTRINSIC |
low complexity region
|
655 |
679 |
N/A |
INTRINSIC |
low complexity region
|
699 |
712 |
N/A |
INTRINSIC |
coiled coil region
|
751 |
784 |
N/A |
INTRINSIC |
low complexity region
|
1034 |
1051 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000107593
|
SMART Domains |
Protein: ENSMUSP00000103219 Gene: ENSMUSG00000038453
Domain | Start | End | E-Value | Type |
low complexity region
|
26 |
45 |
N/A |
INTRINSIC |
low complexity region
|
66 |
75 |
N/A |
INTRINSIC |
Blast:THAP
|
113 |
142 |
1e-9 |
BLAST |
low complexity region
|
332 |
366 |
N/A |
INTRINSIC |
low complexity region
|
489 |
501 |
N/A |
INTRINSIC |
low complexity region
|
516 |
538 |
N/A |
INTRINSIC |
low complexity region
|
558 |
575 |
N/A |
INTRINSIC |
low complexity region
|
655 |
679 |
N/A |
INTRINSIC |
low complexity region
|
699 |
712 |
N/A |
INTRINSIC |
coiled coil region
|
751 |
784 |
N/A |
INTRINSIC |
low complexity region
|
1034 |
1051 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000107596
|
SMART Domains |
Protein: ENSMUSP00000103222 Gene: ENSMUSG00000038453
Domain | Start | End | E-Value | Type |
low complexity region
|
32 |
41 |
N/A |
INTRINSIC |
Blast:THAP
|
79 |
108 |
8e-10 |
BLAST |
low complexity region
|
118 |
128 |
N/A |
INTRINSIC |
Pfam:AIP3
|
218 |
330 |
2e-11 |
PFAM |
low complexity region
|
331 |
365 |
N/A |
INTRINSIC |
low complexity region
|
488 |
500 |
N/A |
INTRINSIC |
low complexity region
|
515 |
537 |
N/A |
INTRINSIC |
low complexity region
|
557 |
574 |
N/A |
INTRINSIC |
low complexity region
|
654 |
678 |
N/A |
INTRINSIC |
low complexity region
|
698 |
711 |
N/A |
INTRINSIC |
coiled coil region
|
750 |
783 |
N/A |
INTRINSIC |
low complexity region
|
1033 |
1050 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000107596
|
SMART Domains |
Protein: ENSMUSP00000103222 Gene: ENSMUSG00000038453
Domain | Start | End | E-Value | Type |
low complexity region
|
32 |
41 |
N/A |
INTRINSIC |
Blast:THAP
|
79 |
108 |
8e-10 |
BLAST |
low complexity region
|
118 |
128 |
N/A |
INTRINSIC |
Pfam:AIP3
|
218 |
330 |
2e-11 |
PFAM |
low complexity region
|
331 |
365 |
N/A |
INTRINSIC |
low complexity region
|
488 |
500 |
N/A |
INTRINSIC |
low complexity region
|
515 |
537 |
N/A |
INTRINSIC |
low complexity region
|
557 |
574 |
N/A |
INTRINSIC |
low complexity region
|
654 |
678 |
N/A |
INTRINSIC |
low complexity region
|
698 |
711 |
N/A |
INTRINSIC |
coiled coil region
|
750 |
783 |
N/A |
INTRINSIC |
low complexity region
|
1033 |
1050 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000107596
|
SMART Domains |
Protein: ENSMUSP00000103222 Gene: ENSMUSG00000038453
Domain | Start | End | E-Value | Type |
low complexity region
|
32 |
41 |
N/A |
INTRINSIC |
Blast:THAP
|
79 |
108 |
8e-10 |
BLAST |
low complexity region
|
118 |
128 |
N/A |
INTRINSIC |
Pfam:AIP3
|
218 |
330 |
2e-11 |
PFAM |
low complexity region
|
331 |
365 |
N/A |
INTRINSIC |
low complexity region
|
488 |
500 |
N/A |
INTRINSIC |
low complexity region
|
515 |
537 |
N/A |
INTRINSIC |
low complexity region
|
557 |
574 |
N/A |
INTRINSIC |
low complexity region
|
654 |
678 |
N/A |
INTRINSIC |
low complexity region
|
698 |
711 |
N/A |
INTRINSIC |
coiled coil region
|
750 |
783 |
N/A |
INTRINSIC |
low complexity region
|
1033 |
1050 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000126287
|
SMART Domains |
Protein: ENSMUSP00000116444 Gene: ENSMUSG00000038453
Domain | Start | End | E-Value | Type |
low complexity region
|
26 |
45 |
N/A |
INTRINSIC |
low complexity region
|
66 |
75 |
N/A |
INTRINSIC |
Blast:THAP
|
113 |
142 |
7e-10 |
BLAST |
low complexity region
|
152 |
162 |
N/A |
INTRINSIC |
Pfam:AIP3
|
244 |
339 |
9.7e-10 |
PFAM |
low complexity region
|
357 |
391 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000126287
|
SMART Domains |
Protein: ENSMUSP00000116444 Gene: ENSMUSG00000038453
Domain | Start | End | E-Value | Type |
low complexity region
|
26 |
45 |
N/A |
INTRINSIC |
low complexity region
|
66 |
75 |
N/A |
INTRINSIC |
Blast:THAP
|
113 |
142 |
7e-10 |
BLAST |
low complexity region
|
152 |
162 |
N/A |
INTRINSIC |
Pfam:AIP3
|
244 |
339 |
9.7e-10 |
PFAM |
low complexity region
|
357 |
391 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000126287
|
SMART Domains |
Protein: ENSMUSP00000116444 Gene: ENSMUSG00000038453
Domain | Start | End | E-Value | Type |
low complexity region
|
26 |
45 |
N/A |
INTRINSIC |
low complexity region
|
66 |
75 |
N/A |
INTRINSIC |
Blast:THAP
|
113 |
142 |
7e-10 |
BLAST |
low complexity region
|
152 |
162 |
N/A |
INTRINSIC |
Pfam:AIP3
|
244 |
339 |
9.7e-10 |
PFAM |
low complexity region
|
357 |
391 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000207653
|
Predicted Effect |
probably null
Transcript: ENSMUST00000207653
|
Predicted Effect |
probably null
Transcript: ENSMUST00000207653
|
Meta Mutation Damage Score |
0.9503 |
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.7%
- 10x: 98.8%
- 20x: 97.1%
|
Validation Efficiency |
98% (62/63) |
MGI Phenotype |
PHENOTYPE: Mice homozygous for a knock-out allele display abnormalities in object recognition memory and motor learning, dendritic spine disorganization, impaired synaptic plasticity, and reduced long term potentiation and long term depression. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930407I10Rik |
A |
G |
15: 81,946,744 (GRCm39) |
T214A |
possibly damaging |
Het |
A930009A15Rik |
G |
T |
10: 115,415,810 (GRCm39) |
|
probably benign |
Het |
Aadac |
A |
C |
3: 59,944,757 (GRCm39) |
D143A |
probably benign |
Het |
Acot10 |
T |
G |
15: 20,665,452 (GRCm39) |
T430P |
probably benign |
Het |
Adgrb3 |
T |
C |
1: 25,865,253 (GRCm39) |
T197A |
possibly damaging |
Het |
Bbs1 |
A |
G |
19: 4,950,643 (GRCm39) |
I200T |
probably damaging |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Cadps |
G |
A |
14: 12,467,103 (GRCm38) |
A943V |
probably damaging |
Het |
Cc2d2a |
A |
G |
5: 43,838,673 (GRCm39) |
E48G |
probably damaging |
Het |
Clca3a1 |
A |
T |
3: 144,724,428 (GRCm39) |
C211S |
probably damaging |
Het |
Col18a1 |
A |
G |
10: 76,890,073 (GRCm39) |
L1429P |
probably damaging |
Het |
Cplane1 |
T |
C |
15: 8,273,790 (GRCm39) |
V2591A |
probably benign |
Het |
Cul2 |
T |
G |
18: 3,421,263 (GRCm39) |
Y196D |
probably damaging |
Het |
D630023F18Rik |
T |
C |
1: 65,156,365 (GRCm39) |
S43G |
probably benign |
Het |
Ddx39a |
G |
A |
8: 84,449,766 (GRCm39) |
R427Q |
probably damaging |
Het |
Def6 |
A |
G |
17: 28,442,691 (GRCm39) |
T285A |
probably damaging |
Het |
Defb21 |
T |
A |
2: 152,416,789 (GRCm39) |
D88E |
probably benign |
Het |
Defb6 |
A |
G |
8: 19,278,117 (GRCm39) |
K63R |
probably benign |
Het |
Dnph1 |
T |
C |
17: 46,809,670 (GRCm39) |
S112P |
probably damaging |
Het |
Dock10 |
T |
A |
1: 80,564,407 (GRCm39) |
I467L |
probably benign |
Het |
Dspp |
C |
A |
5: 104,323,716 (GRCm39) |
H286Q |
probably benign |
Het |
Eya1 |
T |
A |
1: 14,253,501 (GRCm39) |
T459S |
probably benign |
Het |
Faf1 |
T |
C |
4: 109,719,049 (GRCm39) |
L385P |
probably damaging |
Het |
Fbxw21 |
C |
A |
9: 108,986,633 (GRCm39) |
R82L |
probably damaging |
Het |
Fryl |
A |
G |
5: 73,222,437 (GRCm39) |
V2048A |
probably benign |
Het |
Galnt5 |
A |
T |
2: 57,925,311 (GRCm39) |
D864V |
possibly damaging |
Het |
Gata6 |
T |
G |
18: 11,054,460 (GRCm39) |
S130A |
possibly damaging |
Het |
Gbf1 |
G |
T |
19: 46,250,946 (GRCm39) |
R434L |
probably damaging |
Het |
Gga3 |
A |
G |
11: 115,476,588 (GRCm39) |
F709L |
probably damaging |
Het |
Hcar1 |
A |
G |
5: 124,017,193 (GRCm39) |
V166A |
probably benign |
Het |
Hexa |
T |
A |
9: 59,471,220 (GRCm39) |
N491K |
possibly damaging |
Het |
Hpse2 |
A |
T |
19: 43,282,760 (GRCm39) |
C164* |
probably null |
Het |
Ifi202b |
T |
C |
1: 173,802,555 (GRCm39) |
Y93C |
probably damaging |
Het |
Iftap |
T |
C |
2: 101,396,804 (GRCm39) |
K192E |
probably benign |
Het |
Iscu |
T |
A |
5: 113,913,304 (GRCm39) |
I79N |
probably damaging |
Het |
Jmjd7 |
T |
A |
2: 119,861,804 (GRCm39) |
Y182* |
probably null |
Het |
Jup |
A |
T |
11: 100,274,284 (GRCm39) |
D135E |
probably benign |
Het |
Kit |
T |
A |
5: 75,813,468 (GRCm39) |
I881N |
probably damaging |
Het |
Llgl1 |
T |
A |
11: 60,593,691 (GRCm39) |
S55T |
probably benign |
Het |
Lonp2 |
G |
A |
8: 87,435,724 (GRCm39) |
M653I |
probably benign |
Het |
Lrp8 |
T |
C |
4: 107,711,517 (GRCm39) |
Y307H |
probably damaging |
Het |
Med13 |
A |
T |
11: 86,169,622 (GRCm39) |
M1914K |
possibly damaging |
Het |
Ms4a1 |
A |
G |
19: 11,230,537 (GRCm39) |
|
probably null |
Het |
Naip1 |
A |
G |
13: 100,563,849 (GRCm39) |
S439P |
probably benign |
Het |
Nrg1 |
T |
C |
8: 32,311,292 (GRCm39) |
R476G |
probably damaging |
Het |
Or10ag59 |
T |
A |
2: 87,405,262 (GRCm39) |
|
probably null |
Het |
Or7g20 |
G |
T |
9: 18,946,597 (GRCm39) |
M59I |
probably damaging |
Het |
Pds5b |
T |
A |
5: 150,729,026 (GRCm39) |
|
probably null |
Het |
Phf12 |
G |
A |
11: 77,918,199 (GRCm39) |
G804R |
probably damaging |
Het |
Pou6f2 |
T |
C |
13: 18,414,074 (GRCm39) |
T234A |
|
Het |
Prune2 |
A |
T |
19: 17,097,954 (GRCm39) |
I1153L |
probably benign |
Het |
Ptprc |
C |
T |
1: 137,995,623 (GRCm39) |
|
probably null |
Het |
Qpctl |
T |
C |
7: 18,883,079 (GRCm39) |
Q11R |
probably benign |
Het |
Rfx4 |
A |
G |
10: 84,676,092 (GRCm39) |
K103E |
possibly damaging |
Het |
St6galnac1 |
G |
T |
11: 116,659,770 (GRCm39) |
A181D |
probably damaging |
Het |
Stk36 |
T |
C |
1: 74,661,398 (GRCm39) |
V475A |
probably benign |
Het |
Tbc1d21 |
T |
C |
9: 58,268,571 (GRCm39) |
T263A |
possibly damaging |
Het |
Tex24 |
A |
T |
8: 27,835,028 (GRCm39) |
K185N |
probably damaging |
Het |
Tnxb |
T |
A |
17: 34,917,127 (GRCm39) |
V2174E |
possibly damaging |
Het |
Tollip |
A |
G |
7: 141,444,582 (GRCm39) |
S57P |
probably benign |
Het |
Zbtb49 |
A |
G |
5: 38,370,585 (GRCm39) |
|
probably benign |
Het |
Zfp758 |
A |
G |
17: 22,580,650 (GRCm39) |
T30A |
probably benign |
Het |
|
Other mutations in Srcin1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01874:Srcin1
|
APN |
11 |
97,423,924 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03347:Srcin1
|
APN |
11 |
97,416,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R1619:Srcin1
|
UTSW |
11 |
97,416,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R1678:Srcin1
|
UTSW |
11 |
97,409,470 (GRCm39) |
missense |
probably damaging |
0.99 |
R1733:Srcin1
|
UTSW |
11 |
97,424,327 (GRCm39) |
missense |
probably benign |
|
R2023:Srcin1
|
UTSW |
11 |
97,416,872 (GRCm39) |
missense |
probably benign |
|
R2238:Srcin1
|
UTSW |
11 |
97,425,645 (GRCm39) |
missense |
probably benign |
0.00 |
R3983:Srcin1
|
UTSW |
11 |
97,416,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R4572:Srcin1
|
UTSW |
11 |
97,425,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R4628:Srcin1
|
UTSW |
11 |
97,439,752 (GRCm39) |
missense |
probably benign |
0.12 |
R4946:Srcin1
|
UTSW |
11 |
97,442,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R5175:Srcin1
|
UTSW |
11 |
97,464,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R5424:Srcin1
|
UTSW |
11 |
97,427,885 (GRCm39) |
nonsense |
probably null |
|
R5705:Srcin1
|
UTSW |
11 |
97,439,777 (GRCm39) |
missense |
probably benign |
0.42 |
R5918:Srcin1
|
UTSW |
11 |
97,424,323 (GRCm39) |
splice site |
probably null |
|
R6563:Srcin1
|
UTSW |
11 |
97,425,600 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6613:Srcin1
|
UTSW |
11 |
97,424,653 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6756:Srcin1
|
UTSW |
11 |
97,425,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R7060:Srcin1
|
UTSW |
11 |
97,464,711 (GRCm39) |
missense |
probably damaging |
0.99 |
R7271:Srcin1
|
UTSW |
11 |
97,442,715 (GRCm39) |
missense |
probably damaging |
0.99 |
R7304:Srcin1
|
UTSW |
11 |
97,442,519 (GRCm39) |
missense |
probably benign |
0.01 |
R7469:Srcin1
|
UTSW |
11 |
97,425,435 (GRCm39) |
missense |
probably damaging |
0.98 |
R7567:Srcin1
|
UTSW |
11 |
97,425,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R7846:Srcin1
|
UTSW |
11 |
97,416,926 (GRCm39) |
nonsense |
probably null |
|
R7994:Srcin1
|
UTSW |
11 |
97,422,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R8203:Srcin1
|
UTSW |
11 |
97,457,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R8377:Srcin1
|
UTSW |
11 |
97,442,804 (GRCm39) |
missense |
probably damaging |
0.99 |
R8488:Srcin1
|
UTSW |
11 |
97,416,686 (GRCm39) |
splice site |
probably null |
|
R8559:Srcin1
|
UTSW |
11 |
97,427,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R8690:Srcin1
|
UTSW |
11 |
97,414,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R8794:Srcin1
|
UTSW |
11 |
97,439,803 (GRCm39) |
missense |
probably benign |
0.00 |
R8982:Srcin1
|
UTSW |
11 |
97,426,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R9061:Srcin1
|
UTSW |
11 |
97,427,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R9253:Srcin1
|
UTSW |
11 |
97,416,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R9632:Srcin1
|
UTSW |
11 |
97,442,648 (GRCm39) |
missense |
probably benign |
0.11 |
X0024:Srcin1
|
UTSW |
11 |
97,427,294 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Srcin1
|
UTSW |
11 |
97,409,553 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1177:Srcin1
|
UTSW |
11 |
97,417,687 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Predicted Primers |
PCR Primer
(F):5'- CATGAACGCATCTCGCTTGC -3'
(R):5'- CCCCAACTTGCAATTCTAAGTTCAC -3'
Sequencing Primer
(F):5'- TTTCTGGAGCCCGCTGAG -3'
(R):5'- GCAATTCTAAGTTCACCTCATATACC -3'
|
Posted On |
2018-09-12 |