Incidental Mutation 'IGL02441:Ppp6r3'
| ID |
293975 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Ppp6r3
|
| Ensembl Gene |
ENSMUSG00000024908 |
| Gene Name |
protein phosphatase 6, regulatory subunit 3 |
| Synonyms |
4930528G08Rik, Pptcs3, Saps3, D19Bwg1430e, D19Ertd703e, Pp6r3, 9130026N02Rik |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.876)
|
| Stock # |
IGL02441
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
19 |
| Chromosomal Location |
3504928-3625749 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 3514693 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Proline to Serine
at position 141
(P141S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000153575
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000025846]
[ENSMUST00000113997]
[ENSMUST00000172362]
[ENSMUST00000225475]
|
| AlphaFold |
Q922D4 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000025846
AA Change: P739S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000025846
Gene: ENSMUSG00000024908
AA Change: P739S
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
25 |
52 |
N/A |
INTRINSIC |
|
Pfam:SAPS
|
128 |
365 |
2.7e-69 |
PFAM |
|
Pfam:SAPS
|
360 |
513 |
1.4e-44 |
PFAM |
|
low complexity region
|
609 |
627 |
N/A |
INTRINSIC |
|
low complexity region
|
743 |
758 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000113997
AA Change: P768S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000109630
Gene: ENSMUSG00000024908
AA Change: P768S
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
25 |
52 |
N/A |
INTRINSIC |
|
Pfam:SAPS
|
128 |
365 |
5.8e-69 |
PFAM |
|
Pfam:SAPS
|
363 |
513 |
2.7e-44 |
PFAM |
|
low complexity region
|
638 |
656 |
N/A |
INTRINSIC |
|
low complexity region
|
772 |
787 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000172362
AA Change: P722S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000131084
Gene: ENSMUSG00000024908
AA Change: P722S
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
25 |
52 |
N/A |
INTRINSIC |
|
Pfam:SAPS
|
128 |
365 |
2.6e-69 |
PFAM |
|
Pfam:SAPS
|
360 |
513 |
1.3e-44 |
PFAM |
|
low complexity region
|
592 |
610 |
N/A |
INTRINSIC |
|
low complexity region
|
726 |
741 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000225475
AA Change: P141S
PolyPhen 2
Score 0.143 (Sensitivity: 0.92; Specificity: 0.86)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000225624
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Protein phosphatase regulatory subunits, such as SAPS3, modulate the activity of protein phosphatase catalytic subunits by restricting substrate specificity, recruiting substrates, and determining the intracellular localization of the holoenzyme. SAPS3 is a regulatory subunit for the protein phosphatase-6 catalytic subunit (PPP6C; MIM 612725) (Stefansson and Brautigan, 2006 [PubMed 16769727]).[supplied by OMIM, Nov 2010]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 58 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Alg8 |
C |
T |
7: 97,029,504 (GRCm39) |
R179C |
probably benign |
Het |
| Als2 |
A |
G |
1: 59,254,631 (GRCm39) |
M242T |
probably damaging |
Het |
| Atad1 |
C |
T |
19: 32,684,348 (GRCm39) |
V17I |
probably benign |
Het |
| Bag4 |
A |
G |
8: 26,258,136 (GRCm39) |
V397A |
probably damaging |
Het |
| Brd7 |
A |
G |
8: 89,070,218 (GRCm39) |
V396A |
probably damaging |
Het |
| Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
| Cdhr4 |
T |
A |
9: 107,870,466 (GRCm39) |
I123N |
possibly damaging |
Het |
| Cep68 |
A |
G |
11: 20,189,186 (GRCm39) |
F609L |
probably benign |
Het |
| Clec3b |
C |
A |
9: 122,980,178 (GRCm39) |
P24T |
possibly damaging |
Het |
| Ctsg |
T |
A |
14: 56,339,869 (GRCm39) |
T9S |
probably benign |
Het |
| Dalrd3 |
A |
T |
9: 108,448,725 (GRCm39) |
|
probably benign |
Het |
| Dock6 |
A |
T |
9: 21,753,222 (GRCm39) |
V286E |
possibly damaging |
Het |
| Dpep2 |
G |
A |
8: 106,711,723 (GRCm39) |
A568V |
probably benign |
Het |
| Dph5 |
A |
C |
3: 115,720,390 (GRCm39) |
Q192P |
possibly damaging |
Het |
| Eppin |
T |
A |
2: 164,433,698 (GRCm39) |
R37* |
probably null |
Het |
| Esyt1 |
A |
G |
10: 128,348,293 (GRCm39) |
L865P |
possibly damaging |
Het |
| Exoc6b |
A |
G |
6: 84,981,990 (GRCm39) |
L102P |
probably damaging |
Het |
| Foxo6 |
A |
G |
4: 120,125,232 (GRCm39) |
I521T |
possibly damaging |
Het |
| Guca1a |
A |
T |
17: 47,705,578 (GRCm39) |
|
probably benign |
Het |
| Hpx |
A |
G |
7: 105,241,430 (GRCm39) |
F327S |
probably damaging |
Het |
| Hspa12b |
A |
G |
2: 130,980,515 (GRCm39) |
M145V |
probably null |
Het |
| Hspa4 |
A |
T |
11: 53,161,809 (GRCm39) |
S448T |
probably benign |
Het |
| Kbtbd6 |
T |
C |
14: 79,690,759 (GRCm39) |
Y422H |
probably benign |
Het |
| Lama4 |
A |
T |
10: 38,937,441 (GRCm39) |
D677V |
probably benign |
Het |
| Ldb1 |
C |
T |
19: 46,024,195 (GRCm39) |
E111K |
probably damaging |
Het |
| Macf1 |
A |
G |
4: 123,281,029 (GRCm39) |
S3823P |
probably damaging |
Het |
| Man1a2 |
G |
A |
3: 100,499,189 (GRCm39) |
T415I |
probably benign |
Het |
| Map3k2 |
T |
C |
18: 32,333,099 (GRCm39) |
|
probably benign |
Het |
| Morn5 |
T |
A |
2: 35,945,038 (GRCm39) |
Y87* |
probably null |
Het |
| Mpp3 |
T |
C |
11: 101,900,501 (GRCm39) |
D326G |
probably benign |
Het |
| Mrgprx1 |
T |
C |
7: 47,671,336 (GRCm39) |
H137R |
probably benign |
Het |
| Nav2 |
C |
A |
7: 49,102,260 (GRCm39) |
P292T |
probably damaging |
Het |
| Nlrp2 |
C |
A |
7: 5,338,566 (GRCm39) |
|
probably null |
Het |
| Noxo1 |
G |
A |
17: 24,918,030 (GRCm39) |
S112N |
probably damaging |
Het |
| Nudt9 |
G |
T |
5: 104,212,885 (GRCm39) |
K319N |
probably benign |
Het |
| Or8b38 |
A |
T |
9: 37,973,233 (GRCm39) |
I206L |
probably benign |
Het |
| Osbpl7 |
C |
A |
11: 96,958,528 (GRCm39) |
Q728K |
probably damaging |
Het |
| Pcsk1 |
A |
T |
13: 75,280,282 (GRCm39) |
E702D |
probably benign |
Het |
| Piezo2 |
T |
C |
18: 63,205,933 (GRCm39) |
D1492G |
probably damaging |
Het |
| Plekhg1 |
A |
G |
10: 3,908,103 (GRCm39) |
K1007E |
possibly damaging |
Het |
| Prrt3 |
T |
C |
6: 113,473,977 (GRCm39) |
T354A |
probably damaging |
Het |
| Ptk2 |
C |
A |
15: 73,192,675 (GRCm39) |
W181L |
probably benign |
Het |
| Rif1 |
T |
A |
2: 51,995,527 (GRCm39) |
H915Q |
probably benign |
Het |
| Selenbp2 |
G |
T |
3: 94,611,371 (GRCm39) |
V361L |
probably benign |
Het |
| Slamf7 |
A |
G |
1: 171,468,625 (GRCm39) |
L89P |
probably damaging |
Het |
| Slc6a21 |
G |
A |
7: 44,937,505 (GRCm39) |
V599M |
probably damaging |
Het |
| Sltm |
G |
T |
9: 70,494,467 (GRCm39) |
S921I |
probably damaging |
Het |
| Smc4 |
C |
A |
3: 68,913,544 (GRCm39) |
A44E |
probably damaging |
Het |
| Tdrd5 |
A |
T |
1: 156,087,513 (GRCm39) |
|
probably benign |
Het |
| Tead2 |
T |
A |
7: 44,866,845 (GRCm39) |
I68N |
probably damaging |
Het |
| Tnks1bp1 |
T |
A |
2: 84,902,143 (GRCm39) |
S1680T |
probably damaging |
Het |
| Topbp1 |
T |
C |
9: 103,197,438 (GRCm39) |
V386A |
possibly damaging |
Het |
| Tpx2 |
C |
A |
2: 152,724,207 (GRCm39) |
P328T |
possibly damaging |
Het |
| Ttn |
T |
A |
2: 76,576,332 (GRCm39) |
I24854F |
probably damaging |
Het |
| Zbtb11 |
G |
A |
16: 55,794,552 (GRCm39) |
R43H |
possibly damaging |
Het |
| Zfp609 |
A |
G |
9: 65,610,611 (GRCm39) |
L784S |
possibly damaging |
Het |
| Zfp703 |
T |
C |
8: 27,470,036 (GRCm39) |
S567P |
probably damaging |
Het |
| Zfp750 |
A |
G |
11: 121,404,455 (GRCm39) |
I140T |
probably benign |
Het |
|
| Other mutations in Ppp6r3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00332:Ppp6r3
|
APN |
19 |
3,564,729 (GRCm39) |
splice site |
probably null |
|
|
IGL00340:Ppp6r3
|
APN |
19 |
3,568,324 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00585:Ppp6r3
|
APN |
19 |
3,540,826 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01304:Ppp6r3
|
APN |
19 |
3,517,261 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02048:Ppp6r3
|
APN |
19 |
3,523,848 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
IGL02055:Ppp6r3
|
APN |
19 |
3,571,781 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02108:Ppp6r3
|
APN |
19 |
3,542,494 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02227:Ppp6r3
|
APN |
19 |
3,568,245 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
IGL02427:Ppp6r3
|
APN |
19 |
3,516,580 (GRCm39) |
missense |
probably null |
|
|
IGL02805:Ppp6r3
|
APN |
19 |
3,542,428 (GRCm39) |
missense |
probably benign |
0.15 |
|
IGL03298:Ppp6r3
|
APN |
19 |
3,571,829 (GRCm39) |
missense |
probably damaging |
0.97 |
|
PIT1430001:Ppp6r3
|
UTSW |
19 |
3,521,059 (GRCm39) |
nonsense |
probably null |
|
|
R0324:Ppp6r3
|
UTSW |
19 |
3,514,693 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0362:Ppp6r3
|
UTSW |
19 |
3,528,285 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1876:Ppp6r3
|
UTSW |
19 |
3,521,971 (GRCm39) |
splice site |
probably benign |
|
|
R2860:Ppp6r3
|
UTSW |
19 |
3,571,782 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R2861:Ppp6r3
|
UTSW |
19 |
3,571,782 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R2862:Ppp6r3
|
UTSW |
19 |
3,571,782 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R3958:Ppp6r3
|
UTSW |
19 |
3,546,583 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4158:Ppp6r3
|
UTSW |
19 |
3,562,037 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4160:Ppp6r3
|
UTSW |
19 |
3,562,037 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4473:Ppp6r3
|
UTSW |
19 |
3,561,978 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4901:Ppp6r3
|
UTSW |
19 |
3,517,229 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4996:Ppp6r3
|
UTSW |
19 |
3,523,833 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5139:Ppp6r3
|
UTSW |
19 |
3,514,610 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5414:Ppp6r3
|
UTSW |
19 |
3,557,330 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5776:Ppp6r3
|
UTSW |
19 |
3,576,901 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R6290:Ppp6r3
|
UTSW |
19 |
3,544,011 (GRCm39) |
missense |
probably benign |
|
|
R6525:Ppp6r3
|
UTSW |
19 |
3,543,936 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6797:Ppp6r3
|
UTSW |
19 |
3,564,719 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6977:Ppp6r3
|
UTSW |
19 |
3,517,272 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7176:Ppp6r3
|
UTSW |
19 |
3,521,989 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7178:Ppp6r3
|
UTSW |
19 |
3,568,337 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7239:Ppp6r3
|
UTSW |
19 |
3,543,981 (GRCm39) |
missense |
probably benign |
0.38 |
|
R7326:Ppp6r3
|
UTSW |
19 |
3,557,325 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7536:Ppp6r3
|
UTSW |
19 |
3,557,341 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R7583:Ppp6r3
|
UTSW |
19 |
3,540,790 (GRCm39) |
missense |
probably benign |
|
|
R7991:Ppp6r3
|
UTSW |
19 |
3,509,750 (GRCm39) |
missense |
probably benign |
|
|
R8486:Ppp6r3
|
UTSW |
19 |
3,537,072 (GRCm39) |
missense |
probably benign |
|
|
R8699:Ppp6r3
|
UTSW |
19 |
3,546,587 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8818:Ppp6r3
|
UTSW |
19 |
3,517,216 (GRCm39) |
missense |
probably benign |
0.31 |
|
R8826:Ppp6r3
|
UTSW |
19 |
3,521,984 (GRCm39) |
missense |
|
|
|
R8846:Ppp6r3
|
UTSW |
19 |
3,564,654 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8863:Ppp6r3
|
UTSW |
19 |
3,521,030 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8869:Ppp6r3
|
UTSW |
19 |
3,561,927 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8895:Ppp6r3
|
UTSW |
19 |
3,544,017 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8909:Ppp6r3
|
UTSW |
19 |
3,509,461 (GRCm39) |
missense |
probably benign |
0.17 |
|
R9147:Ppp6r3
|
UTSW |
19 |
3,543,974 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9148:Ppp6r3
|
UTSW |
19 |
3,543,974 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9200:Ppp6r3
|
UTSW |
19 |
3,519,748 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2015-04-16 |
Incidental Mutation