Incidental Mutation 'R4791:Prrc2b'
ID |
368534 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Prrc2b
|
Ensembl Gene |
ENSMUSG00000039262 |
Gene Name |
proline-rich coiled-coil 2B |
Synonyms |
5830434P21Rik, Bat2l |
MMRRC Submission |
041976-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R4791 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
2 |
Chromosomal Location |
32041094-32124549 bp(+) (GRCm39) |
Type of Mutation |
splice site (4 bp from exon) |
DNA Base Change (assembly) |
A to G
at 32107351 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000036691]
[ENSMUST00000069817]
|
AlphaFold |
Q7TPM1 |
Predicted Effect |
probably null
Transcript: ENSMUST00000036691
|
SMART Domains |
Protein: ENSMUSP00000035734 Gene: ENSMUSG00000039262
Domain | Start | End | E-Value | Type |
Pfam:BAT2_N
|
1 |
194 |
2.7e-85 |
PFAM |
low complexity region
|
359 |
374 |
N/A |
INTRINSIC |
low complexity region
|
388 |
394 |
N/A |
INTRINSIC |
low complexity region
|
413 |
424 |
N/A |
INTRINSIC |
coiled coil region
|
494 |
544 |
N/A |
INTRINSIC |
low complexity region
|
600 |
621 |
N/A |
INTRINSIC |
low complexity region
|
638 |
656 |
N/A |
INTRINSIC |
low complexity region
|
885 |
900 |
N/A |
INTRINSIC |
low complexity region
|
992 |
1007 |
N/A |
INTRINSIC |
low complexity region
|
1112 |
1126 |
N/A |
INTRINSIC |
low complexity region
|
1218 |
1233 |
N/A |
INTRINSIC |
low complexity region
|
1257 |
1275 |
N/A |
INTRINSIC |
low complexity region
|
1402 |
1421 |
N/A |
INTRINSIC |
low complexity region
|
1425 |
1437 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000069817
|
SMART Domains |
Protein: ENSMUSP00000064892 Gene: ENSMUSG00000039262
Domain | Start | End | E-Value | Type |
Pfam:BAT2_N
|
1 |
191 |
3.1e-65 |
PFAM |
low complexity region
|
359 |
374 |
N/A |
INTRINSIC |
low complexity region
|
388 |
394 |
N/A |
INTRINSIC |
low complexity region
|
413 |
424 |
N/A |
INTRINSIC |
coiled coil region
|
494 |
544 |
N/A |
INTRINSIC |
low complexity region
|
600 |
621 |
N/A |
INTRINSIC |
low complexity region
|
638 |
656 |
N/A |
INTRINSIC |
low complexity region
|
960 |
977 |
N/A |
INTRINSIC |
low complexity region
|
1004 |
1018 |
N/A |
INTRINSIC |
low complexity region
|
1070 |
1094 |
N/A |
INTRINSIC |
low complexity region
|
1307 |
1325 |
N/A |
INTRINSIC |
low complexity region
|
1388 |
1401 |
N/A |
INTRINSIC |
low complexity region
|
1413 |
1426 |
N/A |
INTRINSIC |
low complexity region
|
1572 |
1587 |
N/A |
INTRINSIC |
low complexity region
|
1678 |
1693 |
N/A |
INTRINSIC |
low complexity region
|
1798 |
1812 |
N/A |
INTRINSIC |
low complexity region
|
1904 |
1919 |
N/A |
INTRINSIC |
low complexity region
|
1943 |
1961 |
N/A |
INTRINSIC |
low complexity region
|
2088 |
2107 |
N/A |
INTRINSIC |
low complexity region
|
2111 |
2123 |
N/A |
INTRINSIC |
low complexity region
|
2161 |
2174 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000123270
|
Predicted Effect |
probably null
Transcript: ENSMUST00000128936
|
SMART Domains |
Protein: ENSMUSP00000121664 Gene: ENSMUSG00000039262
Domain | Start | End | E-Value | Type |
low complexity region
|
53 |
68 |
N/A |
INTRINSIC |
low complexity region
|
159 |
174 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000128936
|
SMART Domains |
Protein: ENSMUSP00000121664 Gene: ENSMUSG00000039262
Domain | Start | End | E-Value | Type |
low complexity region
|
53 |
68 |
N/A |
INTRINSIC |
low complexity region
|
159 |
174 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000129626
|
Predicted Effect |
probably null
Transcript: ENSMUST00000132459
|
SMART Domains |
Protein: ENSMUSP00000116429 Gene: ENSMUSG00000039262
Domain | Start | End | E-Value | Type |
Pfam:BAT2_N
|
1 |
119 |
9.8e-24 |
PFAM |
low complexity region
|
287 |
302 |
N/A |
INTRINSIC |
low complexity region
|
316 |
322 |
N/A |
INTRINSIC |
low complexity region
|
341 |
352 |
N/A |
INTRINSIC |
coiled coil region
|
421 |
471 |
N/A |
INTRINSIC |
low complexity region
|
528 |
549 |
N/A |
INTRINSIC |
low complexity region
|
566 |
584 |
N/A |
INTRINSIC |
low complexity region
|
813 |
828 |
N/A |
INTRINSIC |
low complexity region
|
920 |
935 |
N/A |
INTRINSIC |
low complexity region
|
1040 |
1054 |
N/A |
INTRINSIC |
low complexity region
|
1146 |
1161 |
N/A |
INTRINSIC |
low complexity region
|
1185 |
1203 |
N/A |
INTRINSIC |
low complexity region
|
1330 |
1349 |
N/A |
INTRINSIC |
low complexity region
|
1353 |
1365 |
N/A |
INTRINSIC |
low complexity region
|
1403 |
1416 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000140015
|
Predicted Effect |
probably null
Transcript: ENSMUST00000156313
|
SMART Domains |
Protein: ENSMUSP00000114994 Gene: ENSMUSG00000039262
Domain | Start | End | E-Value | Type |
low complexity region
|
125 |
140 |
N/A |
INTRINSIC |
low complexity region
|
231 |
246 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000156313
|
SMART Domains |
Protein: ENSMUSP00000114994 Gene: ENSMUSG00000039262
Domain | Start | End | E-Value | Type |
low complexity region
|
125 |
140 |
N/A |
INTRINSIC |
low complexity region
|
231 |
246 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142219
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000175128
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141053
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.3%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
C |
T |
7: 45,631,584 (GRCm39) |
V1231M |
probably benign |
Het |
Agl |
A |
G |
3: 116,580,177 (GRCm39) |
|
probably null |
Het |
Ak7 |
T |
C |
12: 105,676,404 (GRCm39) |
F35L |
probably benign |
Het |
Aldh1a1 |
A |
G |
19: 20,597,349 (GRCm39) |
N110S |
probably damaging |
Het |
Arhgef5 |
C |
T |
6: 43,260,117 (GRCm39) |
L1368F |
probably damaging |
Het |
Atp5mf |
T |
C |
5: 145,121,365 (GRCm39) |
Y72C |
possibly damaging |
Het |
Atp6v0a2 |
T |
G |
5: 124,784,667 (GRCm39) |
F317V |
probably benign |
Het |
Bank1 |
A |
T |
3: 135,960,690 (GRCm39) |
S56T |
probably benign |
Het |
Cachd1 |
T |
A |
4: 100,775,282 (GRCm39) |
C166S |
probably damaging |
Het |
Cand1 |
A |
G |
10: 119,046,607 (GRCm39) |
I961T |
probably benign |
Het |
Ccdc73 |
G |
A |
2: 104,811,450 (GRCm39) |
|
probably null |
Het |
Cct6b |
A |
T |
11: 82,632,830 (GRCm39) |
|
probably null |
Het |
Chd2 |
A |
C |
7: 73,118,325 (GRCm39) |
S1098A |
probably benign |
Het |
Col6a4 |
A |
T |
9: 105,957,401 (GRCm39) |
V141E |
possibly damaging |
Het |
Col6a5 |
T |
C |
9: 105,807,983 (GRCm39) |
T1022A |
unknown |
Het |
Cr2 |
A |
T |
1: 194,838,243 (GRCm39) |
C698S |
probably damaging |
Het |
Dnaaf5 |
C |
A |
5: 139,170,405 (GRCm39) |
Q786K |
possibly damaging |
Het |
Dnah6 |
T |
C |
6: 73,072,057 (GRCm39) |
D2423G |
probably benign |
Het |
Dnhd1 |
T |
C |
7: 105,370,324 (GRCm39) |
F4583S |
probably damaging |
Het |
Duoxa2 |
A |
T |
2: 122,131,679 (GRCm39) |
T123S |
probably damaging |
Het |
Edem1 |
T |
G |
6: 108,818,595 (GRCm39) |
V201G |
probably damaging |
Het |
Eef1d |
C |
T |
15: 75,775,531 (GRCm39) |
A43T |
possibly damaging |
Het |
Elavl3 |
T |
C |
9: 21,935,974 (GRCm39) |
K249E |
probably damaging |
Het |
Epg5 |
G |
T |
18: 77,992,211 (GRCm39) |
E303* |
probably null |
Het |
Fam83h |
T |
C |
15: 75,874,217 (GRCm39) |
D1040G |
probably damaging |
Het |
Fndc7 |
A |
T |
3: 108,783,975 (GRCm39) |
F211L |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,812,452 (GRCm39) |
T2924A |
possibly damaging |
Het |
Gm5616 |
T |
C |
9: 48,361,983 (GRCm39) |
|
noncoding transcript |
Het |
Gpr135 |
T |
A |
12: 72,116,642 (GRCm39) |
D375V |
probably benign |
Het |
Hgd |
A |
G |
16: 37,452,187 (GRCm39) |
*446W |
probably null |
Het |
Hivep2 |
C |
A |
10: 14,004,713 (GRCm39) |
T437K |
probably benign |
Het |
Htra2 |
A |
G |
6: 83,028,798 (GRCm39) |
L379P |
probably damaging |
Het |
Hypk |
G |
T |
2: 121,288,136 (GRCm39) |
|
probably null |
Het |
Ica1l |
A |
G |
1: 60,049,360 (GRCm39) |
F198L |
probably damaging |
Het |
Igsf11 |
G |
A |
16: 38,845,226 (GRCm39) |
S319N |
probably damaging |
Het |
Il12rb1 |
T |
C |
8: 71,266,012 (GRCm39) |
S213P |
possibly damaging |
Het |
Katnal1 |
C |
T |
5: 148,841,460 (GRCm39) |
V135M |
probably damaging |
Het |
Kcnc4 |
G |
A |
3: 107,354,859 (GRCm39) |
P530S |
probably benign |
Het |
Kcnu1 |
T |
C |
8: 26,403,780 (GRCm39) |
Y24H |
probably damaging |
Het |
Kdm5b |
A |
G |
1: 134,558,538 (GRCm39) |
E1515G |
possibly damaging |
Het |
Kif18a |
A |
T |
2: 109,118,220 (GRCm39) |
M12L |
probably benign |
Het |
Klre1 |
T |
C |
6: 129,561,118 (GRCm39) |
S160P |
probably damaging |
Het |
Lama2 |
A |
T |
10: 27,343,267 (GRCm39) |
H68Q |
probably damaging |
Het |
Lgals8 |
T |
C |
13: 12,468,203 (GRCm39) |
K49R |
possibly damaging |
Het |
Lmf1 |
G |
A |
17: 25,873,445 (GRCm39) |
V317M |
probably damaging |
Het |
Lsr |
T |
C |
7: 30,657,977 (GRCm39) |
T328A |
probably damaging |
Het |
Mark4 |
C |
T |
7: 19,185,582 (GRCm39) |
E51K |
probably benign |
Het |
Mindy2 |
T |
C |
9: 70,541,283 (GRCm39) |
|
probably null |
Het |
Mkks |
G |
A |
2: 136,718,082 (GRCm39) |
T400I |
probably benign |
Het |
Mon2 |
T |
A |
10: 122,841,962 (GRCm39) |
M1544L |
probably benign |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Myo5c |
T |
G |
9: 75,198,198 (GRCm39) |
L1341R |
probably damaging |
Het |
Nin |
T |
C |
12: 70,090,581 (GRCm39) |
R945G |
possibly damaging |
Het |
Nox4 |
T |
C |
7: 86,954,055 (GRCm39) |
V120A |
probably benign |
Het |
Or1s2 |
T |
A |
19: 13,758,706 (GRCm39) |
C243* |
probably null |
Het |
Or2aj4 |
G |
T |
16: 19,385,413 (GRCm39) |
H73Q |
possibly damaging |
Het |
Or2z2 |
A |
T |
11: 58,346,370 (GRCm39) |
V135E |
possibly damaging |
Het |
Or4a66 |
C |
T |
2: 88,531,242 (GRCm39) |
V144I |
probably benign |
Het |
Or7g29 |
T |
C |
9: 19,287,105 (GRCm39) |
E24G |
probably benign |
Het |
Plekha2 |
T |
A |
8: 25,532,778 (GRCm39) |
R398W |
probably damaging |
Het |
Pradc1 |
A |
G |
6: 85,424,173 (GRCm39) |
W58R |
probably damaging |
Het |
Pramel20 |
A |
G |
4: 143,297,559 (GRCm39) |
|
probably benign |
Het |
Psg19 |
T |
A |
7: 18,528,071 (GRCm39) |
N224I |
probably damaging |
Het |
Ranbp17 |
A |
C |
11: 33,437,746 (GRCm39) |
V164G |
probably benign |
Het |
Rasgrp3 |
A |
G |
17: 75,807,168 (GRCm39) |
S211G |
probably benign |
Het |
Rcc1l |
G |
A |
5: 134,192,615 (GRCm39) |
P270S |
possibly damaging |
Het |
Rfx6 |
T |
A |
10: 51,596,040 (GRCm39) |
|
probably null |
Het |
Rnf222 |
A |
T |
11: 68,783,845 (GRCm39) |
E137D |
probably damaging |
Het |
Selenof |
T |
G |
3: 144,302,584 (GRCm39) |
Y120D |
probably damaging |
Het |
Sema3b |
G |
T |
9: 107,481,012 (GRCm39) |
D108E |
probably damaging |
Het |
Shank3 |
T |
A |
15: 89,384,557 (GRCm39) |
L143Q |
probably damaging |
Het |
Shtn1 |
G |
C |
19: 59,039,305 (GRCm39) |
R45G |
probably damaging |
Het |
Sirt4 |
T |
C |
5: 115,618,373 (GRCm39) |
T234A |
possibly damaging |
Het |
Slc25a30 |
C |
A |
14: 76,000,806 (GRCm39) |
W266L |
probably benign |
Het |
Spata20 |
A |
T |
11: 94,375,412 (GRCm39) |
N127K |
probably damaging |
Het |
Spmip4 |
G |
T |
6: 50,572,817 (GRCm39) |
P32Q |
probably damaging |
Het |
St14 |
C |
T |
9: 31,006,918 (GRCm39) |
G636D |
probably benign |
Het |
Stat5a |
G |
A |
11: 100,756,289 (GRCm39) |
E170K |
probably damaging |
Het |
Sugp2 |
C |
T |
8: 70,695,440 (GRCm39) |
R138C |
probably damaging |
Het |
Sult1e1 |
C |
A |
5: 87,734,589 (GRCm39) |
W119L |
possibly damaging |
Het |
Sv2a |
T |
C |
3: 96,099,874 (GRCm39) |
V608A |
possibly damaging |
Het |
Syne2 |
T |
C |
12: 75,956,018 (GRCm39) |
Y575H |
possibly damaging |
Het |
Taok2 |
G |
A |
7: 126,467,304 (GRCm39) |
S167L |
possibly damaging |
Het |
Thoc6 |
T |
C |
17: 23,889,041 (GRCm39) |
H151R |
possibly damaging |
Het |
Tm9sf2 |
T |
C |
14: 122,377,062 (GRCm39) |
S197P |
probably benign |
Het |
Tmem260 |
CAGGGACCGGCATAG |
CAG |
14: 48,749,451 (GRCm39) |
|
probably benign |
Het |
Tmx2 |
G |
A |
2: 84,508,340 (GRCm39) |
P15L |
probably damaging |
Het |
Top1mt |
C |
T |
15: 75,540,474 (GRCm39) |
|
probably null |
Het |
Trpm6 |
T |
A |
19: 18,845,345 (GRCm39) |
S1682T |
probably benign |
Het |
Trrap |
C |
T |
5: 144,740,087 (GRCm39) |
R1171W |
probably damaging |
Het |
Ugt3a1 |
A |
G |
15: 9,361,665 (GRCm39) |
D147G |
probably damaging |
Het |
Utp25 |
G |
A |
1: 192,810,575 (GRCm39) |
H143Y |
probably benign |
Het |
Vnn3 |
A |
G |
10: 23,740,519 (GRCm39) |
H274R |
probably benign |
Het |
Vwf |
C |
A |
6: 125,620,326 (GRCm39) |
T1668K |
|
Het |
Zfp568 |
T |
C |
7: 29,714,608 (GRCm39) |
S162P |
probably damaging |
Het |
Zfp658 |
T |
A |
7: 43,223,890 (GRCm39) |
C722S |
possibly damaging |
Het |
Zfp808 |
T |
A |
13: 62,319,045 (GRCm39) |
H91Q |
probably damaging |
Het |
|
Other mutations in Prrc2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00156:Prrc2b
|
APN |
2 |
32,098,731 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00846:Prrc2b
|
APN |
2 |
32,089,109 (GRCm39) |
splice site |
probably benign |
|
IGL00977:Prrc2b
|
APN |
2 |
32,103,822 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01372:Prrc2b
|
APN |
2 |
32,113,942 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01993:Prrc2b
|
APN |
2 |
32,114,057 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02097:Prrc2b
|
APN |
2 |
32,081,513 (GRCm39) |
splice site |
probably benign |
|
IGL02165:Prrc2b
|
APN |
2 |
32,104,652 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02184:Prrc2b
|
APN |
2 |
32,111,467 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02238:Prrc2b
|
APN |
2 |
32,103,429 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02338:Prrc2b
|
APN |
2 |
32,104,047 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02399:Prrc2b
|
APN |
2 |
32,116,973 (GRCm39) |
nonsense |
probably null |
|
IGL02597:Prrc2b
|
APN |
2 |
32,109,625 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02729:Prrc2b
|
APN |
2 |
32,098,770 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02743:Prrc2b
|
APN |
2 |
32,084,441 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02815:Prrc2b
|
APN |
2 |
32,094,265 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03159:Prrc2b
|
APN |
2 |
32,084,498 (GRCm39) |
missense |
probably damaging |
0.98 |
BB002:Prrc2b
|
UTSW |
2 |
32,094,127 (GRCm39) |
missense |
probably damaging |
1.00 |
BB012:Prrc2b
|
UTSW |
2 |
32,094,127 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Prrc2b
|
UTSW |
2 |
32,111,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R0082:Prrc2b
|
UTSW |
2 |
32,102,310 (GRCm39) |
splice site |
probably benign |
|
R0105:Prrc2b
|
UTSW |
2 |
32,103,323 (GRCm39) |
nonsense |
probably null |
|
R0276:Prrc2b
|
UTSW |
2 |
32,109,666 (GRCm39) |
missense |
probably damaging |
0.97 |
R0325:Prrc2b
|
UTSW |
2 |
32,089,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R0436:Prrc2b
|
UTSW |
2 |
32,120,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R0595:Prrc2b
|
UTSW |
2 |
32,073,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:Prrc2b
|
UTSW |
2 |
32,103,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R0650:Prrc2b
|
UTSW |
2 |
32,119,267 (GRCm39) |
splice site |
probably benign |
|
R1282:Prrc2b
|
UTSW |
2 |
32,113,456 (GRCm39) |
missense |
probably damaging |
0.96 |
R1421:Prrc2b
|
UTSW |
2 |
32,090,990 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1452:Prrc2b
|
UTSW |
2 |
32,084,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R1535:Prrc2b
|
UTSW |
2 |
32,094,301 (GRCm39) |
missense |
probably benign |
0.06 |
R1709:Prrc2b
|
UTSW |
2 |
32,084,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R1710:Prrc2b
|
UTSW |
2 |
32,102,234 (GRCm39) |
missense |
probably damaging |
0.99 |
R2094:Prrc2b
|
UTSW |
2 |
32,072,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R2202:Prrc2b
|
UTSW |
2 |
32,113,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R2203:Prrc2b
|
UTSW |
2 |
32,113,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R2204:Prrc2b
|
UTSW |
2 |
32,113,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R2428:Prrc2b
|
UTSW |
2 |
32,106,067 (GRCm39) |
missense |
probably benign |
0.00 |
R2435:Prrc2b
|
UTSW |
2 |
32,109,741 (GRCm39) |
missense |
probably damaging |
0.99 |
R3439:Prrc2b
|
UTSW |
2 |
32,096,359 (GRCm39) |
missense |
probably benign |
0.01 |
R4175:Prrc2b
|
UTSW |
2 |
32,108,820 (GRCm39) |
intron |
probably benign |
|
R4710:Prrc2b
|
UTSW |
2 |
32,083,869 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4728:Prrc2b
|
UTSW |
2 |
32,120,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R4876:Prrc2b
|
UTSW |
2 |
32,104,212 (GRCm39) |
missense |
probably benign |
0.00 |
R4908:Prrc2b
|
UTSW |
2 |
32,116,330 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4997:Prrc2b
|
UTSW |
2 |
32,112,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R5240:Prrc2b
|
UTSW |
2 |
32,096,408 (GRCm39) |
missense |
probably benign |
0.01 |
R5276:Prrc2b
|
UTSW |
2 |
32,104,734 (GRCm39) |
missense |
probably benign |
0.09 |
R5455:Prrc2b
|
UTSW |
2 |
32,111,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5821:Prrc2b
|
UTSW |
2 |
32,102,144 (GRCm39) |
missense |
probably damaging |
0.99 |
R5835:Prrc2b
|
UTSW |
2 |
32,096,485 (GRCm39) |
missense |
probably benign |
0.18 |
R5958:Prrc2b
|
UTSW |
2 |
32,102,092 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6052:Prrc2b
|
UTSW |
2 |
32,102,297 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6218:Prrc2b
|
UTSW |
2 |
32,098,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R6428:Prrc2b
|
UTSW |
2 |
32,116,508 (GRCm39) |
splice site |
probably null |
|
R6505:Prrc2b
|
UTSW |
2 |
32,112,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R6812:Prrc2b
|
UTSW |
2 |
32,103,153 (GRCm39) |
missense |
probably benign |
0.30 |
R6826:Prrc2b
|
UTSW |
2 |
32,112,300 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6827:Prrc2b
|
UTSW |
2 |
32,090,963 (GRCm39) |
missense |
probably benign |
0.37 |
R7021:Prrc2b
|
UTSW |
2 |
32,111,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R7078:Prrc2b
|
UTSW |
2 |
32,103,531 (GRCm39) |
missense |
probably benign |
0.01 |
R7081:Prrc2b
|
UTSW |
2 |
32,103,075 (GRCm39) |
missense |
probably benign |
0.12 |
R7101:Prrc2b
|
UTSW |
2 |
32,117,005 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7215:Prrc2b
|
UTSW |
2 |
32,119,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R7228:Prrc2b
|
UTSW |
2 |
32,104,318 (GRCm39) |
nonsense |
probably null |
|
R7566:Prrc2b
|
UTSW |
2 |
32,084,402 (GRCm39) |
missense |
probably benign |
0.02 |
R7719:Prrc2b
|
UTSW |
2 |
32,107,280 (GRCm39) |
nonsense |
probably null |
|
R7925:Prrc2b
|
UTSW |
2 |
32,094,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R7999:Prrc2b
|
UTSW |
2 |
32,084,426 (GRCm39) |
missense |
probably damaging |
0.96 |
R8099:Prrc2b
|
UTSW |
2 |
32,098,686 (GRCm39) |
missense |
probably benign |
0.06 |
R8154:Prrc2b
|
UTSW |
2 |
32,108,689 (GRCm39) |
missense |
probably benign |
0.42 |
R8252:Prrc2b
|
UTSW |
2 |
32,109,392 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8379:Prrc2b
|
UTSW |
2 |
32,104,666 (GRCm39) |
missense |
probably damaging |
0.96 |
R8485:Prrc2b
|
UTSW |
2 |
32,102,105 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8845:Prrc2b
|
UTSW |
2 |
32,106,162 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8845:Prrc2b
|
UTSW |
2 |
32,102,105 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8919:Prrc2b
|
UTSW |
2 |
32,104,953 (GRCm39) |
missense |
probably benign |
|
R8982:Prrc2b
|
UTSW |
2 |
32,102,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R9065:Prrc2b
|
UTSW |
2 |
32,109,304 (GRCm39) |
missense |
probably damaging |
0.99 |
R9127:Prrc2b
|
UTSW |
2 |
32,103,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R9217:Prrc2b
|
UTSW |
2 |
32,103,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R9338:Prrc2b
|
UTSW |
2 |
32,098,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R9344:Prrc2b
|
UTSW |
2 |
32,103,600 (GRCm39) |
missense |
probably benign |
0.28 |
R9386:Prrc2b
|
UTSW |
2 |
32,104,125 (GRCm39) |
missense |
probably benign |
|
R9601:Prrc2b
|
UTSW |
2 |
32,090,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R9607:Prrc2b
|
UTSW |
2 |
32,098,794 (GRCm39) |
missense |
probably damaging |
0.99 |
R9670:Prrc2b
|
UTSW |
2 |
32,103,199 (GRCm39) |
missense |
probably benign |
0.00 |
R9706:Prrc2b
|
UTSW |
2 |
32,107,300 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Prrc2b
|
UTSW |
2 |
32,106,744 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Prrc2b
|
UTSW |
2 |
32,104,441 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Prrc2b
|
UTSW |
2 |
32,116,364 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GTGTGCTTAAGCCATGCAGTC -3'
(R):5'- TTCTGCTAGTCTATTGGAGTAGTCC -3'
Sequencing Primer
(F):5'- CATGCAGTCATGGCTTAAGGTG -3'
(R):5'- TCCTGGGGCCAGAGATGTATC -3'
|
Posted On |
2016-02-04 |