Incidental Mutation 'R5024:Ppp1r12b'
ID |
391192 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ppp1r12b
|
Ensembl Gene |
ENSMUSG00000073557 |
Gene Name |
protein phosphatase 1, regulatory subunit 12B |
Synonyms |
1810037O03Rik, 9530009M10Rik |
MMRRC Submission |
042615-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.265)
|
Stock # |
R5024 (G1)
|
Quality Score |
142 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
134682396-134883680 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 134883471 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Alanine to Glutamic Acid
at position 17
(A17E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000131406
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000045665]
[ENSMUST00000086444]
[ENSMUST00000112163]
[ENSMUST00000168381]
|
AlphaFold |
Q8BG95 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000045665
AA Change: A17E
PolyPhen 2
Score 0.209 (Sensitivity: 0.92; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000047463 Gene: ENSMUSG00000073557 AA Change: A17E
Domain | Start | End | E-Value | Type |
low complexity region
|
11 |
27 |
N/A |
INTRINSIC |
ANK
|
56 |
86 |
8.36e1 |
SMART |
ANK
|
90 |
119 |
5.32e-5 |
SMART |
ANK
|
123 |
152 |
1.08e-5 |
SMART |
ANK
|
216 |
245 |
1.51e-4 |
SMART |
ANK
|
249 |
278 |
3.85e-2 |
SMART |
low complexity region
|
351 |
379 |
N/A |
INTRINSIC |
low complexity region
|
411 |
423 |
N/A |
INTRINSIC |
low complexity region
|
465 |
477 |
N/A |
INTRINSIC |
internal_repeat_3
|
539 |
576 |
2.45e-5 |
PROSPERO |
PDB:2KJY|A
|
608 |
663 |
3e-12 |
PDB |
internal_repeat_3
|
729 |
766 |
2.45e-5 |
PROSPERO |
low complexity region
|
790 |
800 |
N/A |
INTRINSIC |
low complexity region
|
840 |
864 |
N/A |
INTRINSIC |
coiled coil region
|
867 |
974 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000086444
AA Change: A17E
PolyPhen 2
Score 0.209 (Sensitivity: 0.92; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000083633 Gene: ENSMUSG00000073557 AA Change: A17E
Domain | Start | End | E-Value | Type |
low complexity region
|
11 |
27 |
N/A |
INTRINSIC |
ANK
|
56 |
86 |
8.36e1 |
SMART |
ANK
|
90 |
119 |
5.32e-5 |
SMART |
ANK
|
123 |
152 |
1.08e-5 |
SMART |
ANK
|
216 |
245 |
1.51e-4 |
SMART |
ANK
|
249 |
278 |
3.85e-2 |
SMART |
low complexity region
|
351 |
379 |
N/A |
INTRINSIC |
low complexity region
|
411 |
423 |
N/A |
INTRINSIC |
low complexity region
|
465 |
477 |
N/A |
INTRINSIC |
internal_repeat_3
|
539 |
576 |
1.9e-5 |
PROSPERO |
PDB:2KJY|A
|
608 |
663 |
3e-12 |
PDB |
internal_repeat_3
|
729 |
766 |
1.9e-5 |
PROSPERO |
low complexity region
|
790 |
800 |
N/A |
INTRINSIC |
low complexity region
|
840 |
864 |
N/A |
INTRINSIC |
Pfam:PRKG1_interact
|
875 |
982 |
4.6e-31 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000112163
AA Change: A17E
PolyPhen 2
Score 0.209 (Sensitivity: 0.92; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000107788 Gene: ENSMUSG00000073557 AA Change: A17E
Domain | Start | End | E-Value | Type |
low complexity region
|
11 |
27 |
N/A |
INTRINSIC |
Pfam:Ank_5
|
45 |
97 |
1.3e-8 |
PFAM |
Pfam:Ank_3
|
59 |
86 |
9.2e-6 |
PFAM |
Pfam:Ank_4
|
60 |
97 |
6.2e-9 |
PFAM |
Pfam:Ank
|
63 |
89 |
1.4e-4 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000132025
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000168381
AA Change: A17E
PolyPhen 2
Score 0.209 (Sensitivity: 0.92; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000131406 Gene: ENSMUSG00000073557 AA Change: A17E
Domain | Start | End | E-Value | Type |
low complexity region
|
11 |
27 |
N/A |
INTRINSIC |
ANK
|
56 |
86 |
8.36e1 |
SMART |
ANK
|
90 |
119 |
5.32e-5 |
SMART |
ANK
|
123 |
152 |
1.08e-5 |
SMART |
ANK
|
216 |
245 |
1.51e-4 |
SMART |
ANK
|
249 |
278 |
3.85e-2 |
SMART |
low complexity region
|
351 |
379 |
N/A |
INTRINSIC |
low complexity region
|
411 |
423 |
N/A |
INTRINSIC |
low complexity region
|
465 |
477 |
N/A |
INTRINSIC |
internal_repeat_3
|
539 |
576 |
1.9e-5 |
PROSPERO |
PDB:2KJY|A
|
608 |
663 |
3e-12 |
PDB |
internal_repeat_3
|
729 |
766 |
1.9e-5 |
PROSPERO |
low complexity region
|
790 |
800 |
N/A |
INTRINSIC |
low complexity region
|
840 |
864 |
N/A |
INTRINSIC |
coiled coil region
|
867 |
986 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.4%
|
Validation Efficiency |
99% (95/96) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrd1 |
A |
G |
5: 129,248,959 (GRCm39) |
N575S |
probably damaging |
Het |
Akap6 |
C |
T |
12: 53,189,345 (GRCm39) |
T2253M |
probably benign |
Het |
Arhgef37 |
A |
C |
18: 61,639,511 (GRCm39) |
N289K |
probably damaging |
Het |
Atad2b |
A |
C |
12: 4,987,534 (GRCm39) |
T121P |
probably benign |
Het |
Atp4a |
A |
C |
7: 30,415,289 (GRCm39) |
D303A |
possibly damaging |
Het |
Calu |
A |
T |
6: 29,374,518 (GRCm39) |
|
probably benign |
Het |
Ccdc141 |
A |
C |
2: 76,885,047 (GRCm39) |
N531K |
probably benign |
Het |
Ccdc146 |
T |
C |
5: 21,604,612 (GRCm39) |
|
probably null |
Het |
Cd207 |
G |
A |
6: 83,651,301 (GRCm39) |
T218I |
probably damaging |
Het |
Cd2ap |
A |
C |
17: 43,116,236 (GRCm39) |
|
probably null |
Het |
Ceacam23 |
A |
G |
7: 17,644,607 (GRCm39) |
I575V |
probably benign |
Het |
Clip3 |
G |
A |
7: 29,991,644 (GRCm39) |
|
probably benign |
Het |
Clstn1 |
G |
A |
4: 149,719,751 (GRCm39) |
R432H |
possibly damaging |
Het |
Csmd2 |
A |
G |
4: 128,215,141 (GRCm39) |
Y521C |
possibly damaging |
Het |
Dnah8 |
A |
T |
17: 30,955,070 (GRCm39) |
E2033V |
probably damaging |
Het |
Eng |
T |
G |
2: 32,563,404 (GRCm39) |
V319G |
probably benign |
Het |
Erp44 |
C |
T |
4: 48,241,296 (GRCm39) |
W57* |
probably null |
Het |
Etv1 |
T |
A |
12: 38,904,233 (GRCm39) |
|
probably null |
Het |
Eva1c |
T |
C |
16: 90,673,081 (GRCm39) |
|
probably null |
Het |
Fam221b |
T |
A |
4: 43,659,674 (GRCm39) |
N482I |
probably damaging |
Het |
Fam83h |
T |
C |
15: 75,876,991 (GRCm39) |
H202R |
probably damaging |
Het |
Fbxw13 |
T |
C |
9: 109,008,403 (GRCm39) |
T449A |
probably benign |
Het |
Fbxw25 |
A |
T |
9: 109,492,442 (GRCm39) |
|
probably null |
Het |
Frmd3 |
T |
A |
4: 74,016,381 (GRCm39) |
S99T |
probably benign |
Het |
Gm5174 |
G |
T |
10: 86,492,451 (GRCm39) |
|
noncoding transcript |
Het |
Gm815 |
C |
T |
19: 26,865,175 (GRCm39) |
Q49* |
probably null |
Het |
H2-DMa |
A |
T |
17: 34,357,461 (GRCm39) |
I245F |
possibly damaging |
Het |
Herc1 |
A |
T |
9: 66,377,608 (GRCm39) |
K3458M |
possibly damaging |
Het |
Hirip3 |
A |
G |
7: 126,463,661 (GRCm39) |
|
probably null |
Het |
Hjurp |
A |
T |
1: 88,202,772 (GRCm39) |
Y71N |
possibly damaging |
Het |
Hmcn1 |
T |
A |
1: 150,556,439 (GRCm39) |
E2449V |
possibly damaging |
Het |
Igll1 |
G |
T |
16: 16,681,657 (GRCm39) |
H33N |
probably benign |
Het |
Il6 |
T |
C |
5: 30,224,512 (GRCm39) |
L184P |
probably damaging |
Het |
Impg2 |
T |
A |
16: 56,080,463 (GRCm39) |
S756T |
probably damaging |
Het |
Insyn2a |
A |
G |
7: 134,520,207 (GRCm39) |
S108P |
probably damaging |
Het |
Kank4 |
T |
G |
4: 98,673,898 (GRCm39) |
D5A |
probably damaging |
Het |
Kcna7 |
G |
A |
7: 45,056,015 (GRCm39) |
R77H |
probably damaging |
Het |
Kcns2 |
A |
T |
15: 34,839,683 (GRCm39) |
T349S |
probably benign |
Het |
Keap1 |
A |
G |
9: 21,148,522 (GRCm39) |
Y162H |
probably damaging |
Het |
Kif9 |
T |
C |
9: 110,312,161 (GRCm39) |
F10L |
possibly damaging |
Het |
Klhdc8b |
ACACGCACGCACGCACGCACGCACGCACGCACGCACGCAC |
ACACGCACGCACGCACGCACGCACGCACGCACGCACGCACGCAC |
9: 108,326,184 (GRCm39) |
|
probably benign |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Lpar6 |
A |
G |
14: 73,476,809 (GRCm39) |
T257A |
probably damaging |
Het |
Lpin1 |
A |
T |
12: 16,604,007 (GRCm39) |
L608Q |
probably benign |
Het |
Lyst |
T |
C |
13: 13,808,989 (GRCm39) |
S220P |
probably benign |
Het |
M1ap |
A |
G |
6: 83,005,339 (GRCm39) |
|
probably benign |
Het |
Mbd6 |
C |
T |
10: 127,122,310 (GRCm39) |
V173I |
probably benign |
Het |
Myo5b |
A |
T |
18: 74,849,105 (GRCm39) |
T1115S |
possibly damaging |
Het |
Mysm1 |
C |
A |
4: 94,839,253 (GRCm39) |
V683F |
possibly damaging |
Het |
Nlrp4g |
T |
A |
9: 124,350,155 (GRCm38) |
|
noncoding transcript |
Het |
Odad2 |
T |
C |
18: 7,088,555 (GRCm39) |
M1005V |
probably benign |
Het |
Or14c39 |
A |
T |
7: 86,344,089 (GRCm39) |
M142L |
probably benign |
Het |
Or2ak5 |
T |
A |
11: 58,611,776 (GRCm39) |
I33F |
probably benign |
Het |
Or5al6 |
G |
T |
2: 85,976,877 (GRCm39) |
A67E |
probably damaging |
Het |
Or8j3c |
C |
T |
2: 86,253,805 (GRCm39) |
G72S |
possibly damaging |
Het |
Otud6b |
T |
A |
4: 14,826,293 (GRCm39) |
Q34L |
probably damaging |
Het |
Parp11 |
C |
T |
6: 127,448,599 (GRCm39) |
T72I |
probably damaging |
Het |
Pbx1 |
T |
A |
1: 168,011,158 (GRCm39) |
D343V |
possibly damaging |
Het |
Phf11 |
T |
C |
14: 59,495,932 (GRCm39) |
|
probably null |
Het |
Pramel15 |
C |
A |
4: 144,099,878 (GRCm39) |
E296* |
probably null |
Het |
Ranbp9 |
A |
T |
13: 43,588,331 (GRCm39) |
I67N |
probably damaging |
Het |
Rasgrp4 |
A |
G |
7: 28,847,832 (GRCm39) |
E414G |
probably damaging |
Het |
Rbbp5 |
A |
G |
1: 132,418,226 (GRCm39) |
H15R |
possibly damaging |
Het |
Scd2 |
A |
G |
19: 44,289,710 (GRCm39) |
Y235C |
probably benign |
Het |
Sdr16c5 |
C |
T |
4: 4,010,365 (GRCm39) |
G170S |
probably damaging |
Het |
Sh3bp4 |
G |
T |
1: 89,073,317 (GRCm39) |
G722C |
probably damaging |
Het |
Shmt1 |
A |
T |
11: 60,688,305 (GRCm39) |
|
probably benign |
Het |
Slc12a1 |
A |
G |
2: 125,008,057 (GRCm39) |
I206V |
probably benign |
Het |
Slc26a3 |
A |
G |
12: 31,503,907 (GRCm39) |
D304G |
probably benign |
Het |
Slc26a7 |
T |
A |
4: 14,532,572 (GRCm39) |
D434V |
possibly damaging |
Het |
Slc6a16 |
G |
T |
7: 44,909,390 (GRCm39) |
M185I |
probably benign |
Het |
Stat4 |
A |
G |
1: 52,121,729 (GRCm39) |
I363V |
possibly damaging |
Het |
Tgfb1i1 |
G |
T |
7: 127,847,389 (GRCm39) |
M1I |
probably null |
Het |
Thoc2l |
A |
G |
5: 104,670,124 (GRCm39) |
K1549E |
possibly damaging |
Het |
Tmem225 |
T |
C |
9: 40,060,639 (GRCm39) |
V66A |
probably benign |
Het |
Tmtc4 |
T |
C |
14: 123,178,714 (GRCm39) |
|
probably null |
Het |
Trpc4 |
T |
A |
3: 54,102,217 (GRCm39) |
N38K |
probably benign |
Het |
Ttll12 |
A |
T |
15: 83,471,314 (GRCm39) |
Y218N |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,778,769 (GRCm39) |
|
probably null |
Het |
Tulp1 |
A |
C |
17: 28,570,969 (GRCm39) |
Y178* |
probably null |
Het |
Vmn2r58 |
A |
G |
7: 41,513,746 (GRCm39) |
V299A |
probably damaging |
Het |
Washc4 |
C |
A |
10: 83,419,200 (GRCm39) |
Q911K |
possibly damaging |
Het |
Wdr3 |
T |
C |
3: 100,062,252 (GRCm39) |
D221G |
probably benign |
Het |
Zan |
A |
T |
5: 137,460,155 (GRCm39) |
C1245* |
probably null |
Het |
Zfyve9 |
A |
C |
4: 108,548,866 (GRCm39) |
S773A |
probably benign |
Het |
|
Other mutations in Ppp1r12b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01358:Ppp1r12b
|
APN |
1 |
134,819,897 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01788:Ppp1r12b
|
APN |
1 |
134,821,245 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01880:Ppp1r12b
|
APN |
1 |
134,814,159 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02109:Ppp1r12b
|
APN |
1 |
134,800,543 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02247:Ppp1r12b
|
APN |
1 |
134,763,721 (GRCm39) |
missense |
probably benign |
|
IGL02336:Ppp1r12b
|
APN |
1 |
134,814,244 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02903:Ppp1r12b
|
APN |
1 |
134,883,387 (GRCm39) |
missense |
probably benign |
|
IGL02963:Ppp1r12b
|
APN |
1 |
134,814,286 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03074:Ppp1r12b
|
APN |
1 |
134,763,758 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03302:Ppp1r12b
|
APN |
1 |
134,765,788 (GRCm39) |
splice site |
probably benign |
|
R0102:Ppp1r12b
|
UTSW |
1 |
134,763,637 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0102:Ppp1r12b
|
UTSW |
1 |
134,763,637 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0189:Ppp1r12b
|
UTSW |
1 |
134,793,514 (GRCm39) |
critical splice donor site |
probably null |
|
R0556:Ppp1r12b
|
UTSW |
1 |
134,705,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R0594:Ppp1r12b
|
UTSW |
1 |
134,704,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R0690:Ppp1r12b
|
UTSW |
1 |
134,803,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R1354:Ppp1r12b
|
UTSW |
1 |
134,763,721 (GRCm39) |
missense |
probably benign |
0.42 |
R1676:Ppp1r12b
|
UTSW |
1 |
134,705,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R1775:Ppp1r12b
|
UTSW |
1 |
134,821,086 (GRCm39) |
critical splice donor site |
probably null |
|
R1839:Ppp1r12b
|
UTSW |
1 |
134,765,719 (GRCm39) |
missense |
probably benign |
0.32 |
R1946:Ppp1r12b
|
UTSW |
1 |
134,820,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R1971:Ppp1r12b
|
UTSW |
1 |
134,793,651 (GRCm39) |
missense |
probably benign |
0.00 |
R1997:Ppp1r12b
|
UTSW |
1 |
134,774,093 (GRCm39) |
intron |
probably benign |
|
R3110:Ppp1r12b
|
UTSW |
1 |
134,800,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R3112:Ppp1r12b
|
UTSW |
1 |
134,800,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R3908:Ppp1r12b
|
UTSW |
1 |
134,770,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R3912:Ppp1r12b
|
UTSW |
1 |
134,815,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R3977:Ppp1r12b
|
UTSW |
1 |
134,693,713 (GRCm39) |
missense |
probably benign |
0.00 |
R4243:Ppp1r12b
|
UTSW |
1 |
134,709,846 (GRCm39) |
intron |
probably benign |
|
R4835:Ppp1r12b
|
UTSW |
1 |
134,883,471 (GRCm39) |
missense |
probably benign |
0.21 |
R4836:Ppp1r12b
|
UTSW |
1 |
134,883,471 (GRCm39) |
missense |
probably benign |
0.21 |
R4843:Ppp1r12b
|
UTSW |
1 |
134,883,471 (GRCm39) |
missense |
probably benign |
0.21 |
R4854:Ppp1r12b
|
UTSW |
1 |
134,801,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R4870:Ppp1r12b
|
UTSW |
1 |
134,876,771 (GRCm39) |
missense |
probably benign |
0.00 |
R4881:Ppp1r12b
|
UTSW |
1 |
134,883,471 (GRCm39) |
missense |
probably benign |
0.21 |
R5054:Ppp1r12b
|
UTSW |
1 |
134,883,471 (GRCm39) |
missense |
probably benign |
0.21 |
R5055:Ppp1r12b
|
UTSW |
1 |
134,883,471 (GRCm39) |
missense |
probably benign |
0.21 |
R5056:Ppp1r12b
|
UTSW |
1 |
134,883,471 (GRCm39) |
missense |
probably benign |
0.21 |
R5056:Ppp1r12b
|
UTSW |
1 |
134,762,130 (GRCm39) |
intron |
probably benign |
|
R5158:Ppp1r12b
|
UTSW |
1 |
134,814,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R5599:Ppp1r12b
|
UTSW |
1 |
134,793,645 (GRCm39) |
missense |
probably benign |
0.08 |
R5771:Ppp1r12b
|
UTSW |
1 |
134,701,162 (GRCm39) |
critical splice donor site |
probably null |
|
R5775:Ppp1r12b
|
UTSW |
1 |
134,803,780 (GRCm39) |
missense |
probably benign |
|
R5872:Ppp1r12b
|
UTSW |
1 |
134,704,144 (GRCm39) |
missense |
probably benign |
0.03 |
R5896:Ppp1r12b
|
UTSW |
1 |
134,693,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R6060:Ppp1r12b
|
UTSW |
1 |
134,883,262 (GRCm39) |
missense |
probably benign |
0.02 |
R6129:Ppp1r12b
|
UTSW |
1 |
134,819,990 (GRCm39) |
nonsense |
probably null |
|
R6369:Ppp1r12b
|
UTSW |
1 |
134,814,280 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6868:Ppp1r12b
|
UTSW |
1 |
134,814,176 (GRCm39) |
missense |
probably benign |
0.00 |
R7681:Ppp1r12b
|
UTSW |
1 |
134,793,673 (GRCm39) |
missense |
probably benign |
0.02 |
R7940:Ppp1r12b
|
UTSW |
1 |
134,803,793 (GRCm39) |
missense |
probably benign |
0.00 |
R8057:Ppp1r12b
|
UTSW |
1 |
134,883,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R8070:Ppp1r12b
|
UTSW |
1 |
134,803,807 (GRCm39) |
missense |
probably benign |
0.06 |
R8134:Ppp1r12b
|
UTSW |
1 |
134,814,280 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8147:Ppp1r12b
|
UTSW |
1 |
134,801,680 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8224:Ppp1r12b
|
UTSW |
1 |
134,830,200 (GRCm39) |
missense |
probably benign |
0.19 |
R8270:Ppp1r12b
|
UTSW |
1 |
134,803,886 (GRCm39) |
missense |
probably benign |
0.37 |
R8304:Ppp1r12b
|
UTSW |
1 |
134,824,101 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8803:Ppp1r12b
|
UTSW |
1 |
134,818,492 (GRCm39) |
critical splice donor site |
probably benign |
|
R8826:Ppp1r12b
|
UTSW |
1 |
134,693,730 (GRCm39) |
missense |
probably benign |
0.18 |
R8954:Ppp1r12b
|
UTSW |
1 |
134,762,200 (GRCm39) |
missense |
probably benign |
0.00 |
R9081:Ppp1r12b
|
UTSW |
1 |
134,705,085 (GRCm39) |
missense |
probably benign |
0.18 |
R9171:Ppp1r12b
|
UTSW |
1 |
134,801,725 (GRCm39) |
missense |
probably benign |
0.01 |
R9223:Ppp1r12b
|
UTSW |
1 |
134,807,376 (GRCm39) |
missense |
probably benign |
0.00 |
R9521:Ppp1r12b
|
UTSW |
1 |
134,705,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R9609:Ppp1r12b
|
UTSW |
1 |
134,824,084 (GRCm39) |
nonsense |
probably null |
|
X0022:Ppp1r12b
|
UTSW |
1 |
134,763,611 (GRCm39) |
missense |
probably benign |
0.00 |
X0027:Ppp1r12b
|
UTSW |
1 |
134,824,092 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1187:Ppp1r12b
|
UTSW |
1 |
134,883,262 (GRCm39) |
missense |
probably benign |
0.02 |
Z1189:Ppp1r12b
|
UTSW |
1 |
134,883,262 (GRCm39) |
missense |
probably benign |
0.02 |
Z1190:Ppp1r12b
|
UTSW |
1 |
134,883,262 (GRCm39) |
missense |
probably benign |
0.02 |
Z1192:Ppp1r12b
|
UTSW |
1 |
134,883,262 (GRCm39) |
missense |
probably benign |
0.02 |
|
Predicted Primers |
PCR Primer
(F):5'- GTTGATGTCCGCACCTCTTG -3'
(R):5'- GCAGGTCTCCTACTACAAGTCC -3'
Sequencing Primer
(F):5'- GCACCTCTTGCCAGAAGC -3'
(R):5'- CGTGCGTGCTGAAGCTAAG -3'
|
Posted On |
2016-06-06 |