Incidental Mutation 'R9300:Arid1b'
ID |
704901 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Arid1b
|
Ensembl Gene |
ENSMUSG00000069729 |
Gene Name |
AT-rich interaction domain 1B |
Synonyms |
9330189K18Rik, B230217J03Rik |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.783)
|
Stock # |
R9300 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
17 |
Chromosomal Location |
5044607-5397931 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 5293274 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Threonine
at position 731
(P731T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000090398
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000092723]
[ENSMUST00000115797]
[ENSMUST00000115799]
[ENSMUST00000232180]
|
AlphaFold |
E9Q4N7 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000092723
AA Change: P731T
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000090398 Gene: ENSMUSG00000069729 AA Change: P731T
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
51 |
N/A |
INTRINSIC |
low complexity region
|
69 |
132 |
N/A |
INTRINSIC |
low complexity region
|
139 |
150 |
N/A |
INTRINSIC |
low complexity region
|
201 |
224 |
N/A |
INTRINSIC |
low complexity region
|
232 |
247 |
N/A |
INTRINSIC |
low complexity region
|
257 |
276 |
N/A |
INTRINSIC |
low complexity region
|
301 |
371 |
N/A |
INTRINSIC |
low complexity region
|
379 |
407 |
N/A |
INTRINSIC |
low complexity region
|
438 |
476 |
N/A |
INTRINSIC |
low complexity region
|
485 |
499 |
N/A |
INTRINSIC |
low complexity region
|
538 |
558 |
N/A |
INTRINSIC |
low complexity region
|
574 |
591 |
N/A |
INTRINSIC |
low complexity region
|
596 |
611 |
N/A |
INTRINSIC |
low complexity region
|
615 |
640 |
N/A |
INTRINSIC |
low complexity region
|
691 |
707 |
N/A |
INTRINSIC |
low complexity region
|
719 |
740 |
N/A |
INTRINSIC |
low complexity region
|
743 |
773 |
N/A |
INTRINSIC |
low complexity region
|
805 |
816 |
N/A |
INTRINSIC |
low complexity region
|
912 |
930 |
N/A |
INTRINSIC |
low complexity region
|
936 |
952 |
N/A |
INTRINSIC |
low complexity region
|
974 |
985 |
N/A |
INTRINSIC |
low complexity region
|
1036 |
1045 |
N/A |
INTRINSIC |
ARID
|
1057 |
1147 |
9.9e-33 |
SMART |
BRIGHT
|
1061 |
1152 |
7.62e-41 |
SMART |
low complexity region
|
1166 |
1177 |
N/A |
INTRINSIC |
low complexity region
|
1257 |
1268 |
N/A |
INTRINSIC |
low complexity region
|
1336 |
1364 |
N/A |
INTRINSIC |
low complexity region
|
1426 |
1456 |
N/A |
INTRINSIC |
low complexity region
|
1473 |
1486 |
N/A |
INTRINSIC |
low complexity region
|
1579 |
1595 |
N/A |
INTRINSIC |
coiled coil region
|
1724 |
1745 |
N/A |
INTRINSIC |
low complexity region
|
1835 |
1843 |
N/A |
INTRINSIC |
Pfam:DUF3518
|
1933 |
2189 |
1.5e-152 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000115797
AA Change: P679T
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000111463 Gene: ENSMUSG00000069729 AA Change: P679T
Domain | Start | End | E-Value | Type |
low complexity region
|
17 |
80 |
N/A |
INTRINSIC |
low complexity region
|
87 |
98 |
N/A |
INTRINSIC |
low complexity region
|
149 |
172 |
N/A |
INTRINSIC |
low complexity region
|
180 |
195 |
N/A |
INTRINSIC |
low complexity region
|
205 |
224 |
N/A |
INTRINSIC |
low complexity region
|
249 |
319 |
N/A |
INTRINSIC |
low complexity region
|
327 |
355 |
N/A |
INTRINSIC |
low complexity region
|
386 |
424 |
N/A |
INTRINSIC |
low complexity region
|
433 |
447 |
N/A |
INTRINSIC |
low complexity region
|
486 |
506 |
N/A |
INTRINSIC |
low complexity region
|
522 |
539 |
N/A |
INTRINSIC |
low complexity region
|
544 |
559 |
N/A |
INTRINSIC |
low complexity region
|
563 |
588 |
N/A |
INTRINSIC |
low complexity region
|
639 |
655 |
N/A |
INTRINSIC |
low complexity region
|
667 |
688 |
N/A |
INTRINSIC |
low complexity region
|
691 |
721 |
N/A |
INTRINSIC |
low complexity region
|
753 |
764 |
N/A |
INTRINSIC |
low complexity region
|
860 |
878 |
N/A |
INTRINSIC |
low complexity region
|
884 |
900 |
N/A |
INTRINSIC |
low complexity region
|
922 |
933 |
N/A |
INTRINSIC |
Blast:ARID
|
981 |
1028 |
1e-8 |
BLAST |
low complexity region
|
1029 |
1054 |
N/A |
INTRINSIC |
ARID
|
1058 |
1148 |
9.9e-33 |
SMART |
BRIGHT
|
1062 |
1153 |
7.62e-41 |
SMART |
low complexity region
|
1167 |
1178 |
N/A |
INTRINSIC |
low complexity region
|
1258 |
1269 |
N/A |
INTRINSIC |
low complexity region
|
1337 |
1365 |
N/A |
INTRINSIC |
low complexity region
|
1427 |
1457 |
N/A |
INTRINSIC |
low complexity region
|
1474 |
1487 |
N/A |
INTRINSIC |
low complexity region
|
1580 |
1596 |
N/A |
INTRINSIC |
coiled coil region
|
1725 |
1746 |
N/A |
INTRINSIC |
low complexity region
|
1836 |
1844 |
N/A |
INTRINSIC |
Pfam:DUF3518
|
1935 |
2190 |
6.3e-121 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000115799
AA Change: P227T
PolyPhen 2
Score 0.665 (Sensitivity: 0.86; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000111465 Gene: ENSMUSG00000069729 AA Change: P227T
Domain | Start | End | E-Value | Type |
low complexity region
|
34 |
54 |
N/A |
INTRINSIC |
low complexity region
|
70 |
87 |
N/A |
INTRINSIC |
low complexity region
|
92 |
107 |
N/A |
INTRINSIC |
low complexity region
|
111 |
136 |
N/A |
INTRINSIC |
low complexity region
|
187 |
203 |
N/A |
INTRINSIC |
low complexity region
|
215 |
236 |
N/A |
INTRINSIC |
low complexity region
|
271 |
282 |
N/A |
INTRINSIC |
low complexity region
|
378 |
396 |
N/A |
INTRINSIC |
low complexity region
|
402 |
418 |
N/A |
INTRINSIC |
low complexity region
|
440 |
451 |
N/A |
INTRINSIC |
Blast:ARID
|
499 |
546 |
1e-8 |
BLAST |
low complexity region
|
547 |
572 |
N/A |
INTRINSIC |
ARID
|
576 |
666 |
9.9e-33 |
SMART |
BRIGHT
|
580 |
671 |
7.62e-41 |
SMART |
low complexity region
|
685 |
696 |
N/A |
INTRINSIC |
low complexity region
|
776 |
787 |
N/A |
INTRINSIC |
low complexity region
|
855 |
883 |
N/A |
INTRINSIC |
low complexity region
|
945 |
975 |
N/A |
INTRINSIC |
low complexity region
|
992 |
1005 |
N/A |
INTRINSIC |
low complexity region
|
1098 |
1114 |
N/A |
INTRINSIC |
coiled coil region
|
1243 |
1264 |
N/A |
INTRINSIC |
low complexity region
|
1354 |
1362 |
N/A |
INTRINSIC |
Pfam:DUF3518
|
1452 |
1708 |
1.1e-152 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000232180
AA Change: P731T
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This locus encodes an AT-rich DNA interacting domain-containing protein. The encoded protein is a component of the SWI/SNF chromatin remodeling complex and may play a role in cell-cycle activation. The protein encoded by this locus is similar to AT-rich interactive domain-containing protein 1A. These two proteins function as alternative, mutually exclusive ARID-subunits of the SWI/SNF complex. The associated complexes play opposing roles. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]
|
Allele List at MGI |
All alleles(61) : Targeted(2) Gene trapped(59)
|
Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
G |
A |
5: 8,875,614 (GRCm39) |
V596I |
probably benign |
Het |
Acad8 |
A |
T |
9: 26,888,928 (GRCm39) |
H371Q |
probably damaging |
Het |
Actn3 |
G |
T |
19: 4,921,656 (GRCm39) |
R175S |
probably benign |
Het |
Adamts9 |
G |
T |
6: 92,864,371 (GRCm39) |
D780E |
probably benign |
Het |
AK157302 |
C |
A |
13: 21,679,537 (GRCm39) |
T21K |
probably benign |
Het |
Ank3 |
A |
T |
10: 69,706,872 (GRCm39) |
H329L |
unknown |
Het |
Ankrd36 |
A |
G |
11: 5,519,979 (GRCm39) |
H18R |
possibly damaging |
Het |
Anks1b |
T |
A |
10: 90,412,966 (GRCm39) |
V38D |
possibly damaging |
Het |
Apbb2 |
A |
T |
5: 66,470,677 (GRCm39) |
L520H |
probably damaging |
Het |
Atp1a4 |
A |
G |
1: 172,067,398 (GRCm39) |
F578S |
probably damaging |
Het |
Atp6v0a2 |
A |
T |
5: 124,789,312 (GRCm39) |
I360F |
probably damaging |
Het |
Bcas3 |
A |
T |
11: 85,448,184 (GRCm39) |
I600F |
probably damaging |
Het |
C1qtnf7 |
T |
G |
5: 43,766,441 (GRCm39) |
C20W |
possibly damaging |
Het |
Cadm1 |
A |
T |
9: 47,708,821 (GRCm39) |
K184* |
probably null |
Het |
Ccdc138 |
A |
T |
10: 58,343,448 (GRCm39) |
H101L |
probably benign |
Het |
Cep120 |
T |
A |
18: 53,852,369 (GRCm39) |
N503I |
probably damaging |
Het |
Chil4 |
T |
C |
3: 106,109,874 (GRCm39) |
T380A |
probably benign |
Het |
Clip2 |
A |
G |
5: 134,526,942 (GRCm39) |
|
probably null |
Het |
Cyp3a11 |
G |
A |
5: 145,799,164 (GRCm39) |
P341L |
possibly damaging |
Het |
Cyp3a41a |
G |
C |
5: 145,656,906 (GRCm39) |
|
probably benign |
Het |
Dcaf1 |
A |
G |
9: 106,725,042 (GRCm39) |
I509M |
possibly damaging |
Het |
Dcaf13 |
T |
C |
15: 39,010,102 (GRCm39) |
S429P |
probably damaging |
Het |
Eln |
A |
G |
5: 134,758,220 (GRCm39) |
V151A |
unknown |
Het |
Endou |
T |
G |
15: 97,610,954 (GRCm39) |
M377L |
probably benign |
Het |
Etfa |
A |
G |
9: 55,396,152 (GRCm39) |
I138T |
probably damaging |
Het |
Fbxw10 |
T |
A |
11: 62,768,109 (GRCm39) |
S982T |
probably benign |
Het |
Gm9602 |
A |
T |
14: 15,933,435 (GRCm39) |
R47* |
probably null |
Het |
Hectd4 |
G |
A |
5: 121,486,952 (GRCm39) |
V3316I |
probably benign |
Het |
Hif1a |
T |
C |
12: 73,987,302 (GRCm39) |
L477S |
probably benign |
Het |
Icam5 |
G |
C |
9: 20,946,846 (GRCm39) |
G458A |
probably benign |
Het |
Itm2b |
A |
T |
14: 73,603,896 (GRCm39) |
D106E |
probably benign |
Het |
Kdm4d |
G |
A |
9: 14,375,336 (GRCm39) |
T174M |
probably damaging |
Het |
Kif16b |
G |
T |
2: 142,541,207 (GRCm39) |
D1364E |
probably benign |
Het |
Lbhd1 |
G |
A |
19: 8,861,550 (GRCm39) |
V61M |
probably damaging |
Het |
Lclat1 |
T |
A |
17: 73,546,919 (GRCm39) |
S279T |
probably benign |
Het |
Lhx4 |
G |
A |
1: 155,580,956 (GRCm39) |
L190F |
probably damaging |
Het |
Lima1 |
C |
T |
15: 99,704,320 (GRCm39) |
S283N |
probably benign |
Het |
Magi1 |
C |
A |
6: 93,724,209 (GRCm39) |
D496Y |
probably damaging |
Het |
Map1a |
T |
C |
2: 121,133,446 (GRCm39) |
S1421P |
probably damaging |
Het |
Map3k20 |
C |
T |
2: 72,202,257 (GRCm39) |
H163Y |
probably damaging |
Het |
Mier3 |
T |
G |
13: 111,822,890 (GRCm39) |
|
probably null |
Het |
Mllt3 |
G |
A |
4: 87,692,284 (GRCm39) |
Q560* |
probably null |
Het |
Mmp25 |
T |
A |
17: 23,851,728 (GRCm39) |
D327V |
probably benign |
Het |
Nckap5 |
G |
A |
1: 125,909,423 (GRCm39) |
Q1603* |
probably null |
Het |
Nell1 |
G |
A |
7: 49,712,368 (GRCm39) |
V63I |
probably benign |
Het |
Or10al3 |
C |
T |
17: 38,011,815 (GRCm39) |
P85S |
probably damaging |
Het |
Or2ag2b |
A |
T |
7: 106,418,111 (GRCm39) |
I274F |
probably benign |
Het |
Or8a1 |
A |
C |
9: 37,641,578 (GRCm39) |
S234A |
probably benign |
Het |
Pde12 |
C |
T |
14: 26,386,931 (GRCm39) |
E526K |
probably damaging |
Het |
Pfn4 |
T |
C |
12: 4,825,442 (GRCm39) |
V93A |
possibly damaging |
Het |
Poglut2 |
A |
G |
1: 44,156,362 (GRCm39) |
I75T |
possibly damaging |
Het |
Ppp2r3d |
A |
G |
9: 124,423,977 (GRCm38) |
S60P |
unknown |
Het |
Prelp |
T |
C |
1: 133,842,257 (GRCm39) |
H296R |
probably damaging |
Het |
Prickle1 |
T |
C |
15: 93,398,749 (GRCm39) |
E693G |
possibly damaging |
Het |
Rars1 |
A |
G |
11: 35,706,488 (GRCm39) |
L477P |
probably damaging |
Het |
Rasal1 |
G |
A |
5: 120,802,172 (GRCm39) |
R328H |
probably damaging |
Het |
Rasef |
A |
G |
4: 73,659,393 (GRCm39) |
F220S |
probably benign |
Het |
Rif1 |
C |
T |
2: 52,001,151 (GRCm39) |
S1535L |
probably damaging |
Het |
Rnf17 |
T |
C |
14: 56,697,495 (GRCm39) |
I463T |
possibly damaging |
Het |
Ryr3 |
A |
T |
2: 112,690,695 (GRCm39) |
D1138E |
probably benign |
Het |
Scn9a |
T |
A |
2: 66,335,236 (GRCm39) |
Y1251F |
probably benign |
Het |
Sdk2 |
A |
G |
11: 113,715,856 (GRCm39) |
W1568R |
possibly damaging |
Het |
Senp6 |
A |
G |
9: 80,049,433 (GRCm39) |
E1019G |
probably damaging |
Het |
Shh |
A |
G |
5: 28,663,461 (GRCm39) |
Y236H |
probably damaging |
Het |
Sin3a |
A |
G |
9: 57,014,744 (GRCm39) |
D655G |
probably damaging |
Het |
Slc35a4 |
C |
T |
18: 36,815,274 (GRCm39) |
P35S |
probably damaging |
Het |
Slc35g1 |
T |
C |
19: 38,384,633 (GRCm39) |
L24P |
probably benign |
Het |
Slc39a4 |
G |
T |
15: 76,498,759 (GRCm39) |
Q312K |
probably damaging |
Het |
Slc6a5 |
A |
T |
7: 49,601,175 (GRCm39) |
I659F |
probably damaging |
Het |
Slc7a4 |
T |
C |
16: 17,392,399 (GRCm39) |
Y345C |
probably benign |
Het |
Slco6c1 |
G |
T |
1: 96,993,809 (GRCm39) |
R645S |
probably benign |
Het |
Soat1 |
T |
C |
1: 156,268,923 (GRCm39) |
Y209C |
probably benign |
Het |
Tbc1d9b |
T |
C |
11: 50,054,714 (GRCm39) |
S953P |
probably benign |
Het |
Tgm1 |
G |
A |
14: 55,942,303 (GRCm39) |
H683Y |
probably benign |
Het |
Tmem98 |
G |
A |
11: 80,708,432 (GRCm39) |
R134Q |
probably damaging |
Het |
Trpm3 |
A |
C |
19: 22,955,745 (GRCm39) |
M1107L |
possibly damaging |
Het |
Vmn1r11 |
G |
A |
6: 57,114,872 (GRCm39) |
V179I |
probably benign |
Het |
Vmn1r119 |
G |
T |
7: 20,745,638 (GRCm39) |
T248K |
probably damaging |
Het |
Vmn1r236 |
T |
A |
17: 21,506,945 (GRCm39) |
I21N |
possibly damaging |
Het |
Vmn2r24 |
A |
G |
6: 123,793,030 (GRCm39) |
T786A |
possibly damaging |
Het |
Vstm5 |
A |
T |
9: 15,168,585 (GRCm39) |
I50F |
probably damaging |
Het |
Wdr1 |
T |
C |
5: 38,685,255 (GRCm39) |
D572G |
probably damaging |
Het |
Xaf1 |
T |
C |
11: 72,192,517 (GRCm39) |
F5S |
probably benign |
Het |
Zan |
A |
T |
5: 137,468,519 (GRCm39) |
|
probably null |
Het |
Zfp697 |
T |
C |
3: 98,334,979 (GRCm39) |
V248A |
possibly damaging |
Het |
Zftraf1 |
C |
A |
15: 76,530,541 (GRCm39) |
V260L |
probably benign |
Het |
Zkscan3 |
T |
A |
13: 21,577,667 (GRCm39) |
T249S |
unknown |
Het |
Znfx1 |
A |
G |
2: 166,897,860 (GRCm39) |
Y355H |
probably damaging |
Het |
|
Other mutations in Arid1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00325:Arid1b
|
APN |
17 |
5,387,385 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL00340:Arid1b
|
APN |
17 |
5,371,559 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00886:Arid1b
|
APN |
17 |
5,177,254 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01161:Arid1b
|
APN |
17 |
5,392,674 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01391:Arid1b
|
APN |
17 |
5,369,133 (GRCm39) |
splice site |
probably benign |
|
IGL01456:Arid1b
|
APN |
17 |
5,341,510 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02152:Arid1b
|
APN |
17 |
5,364,243 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02288:Arid1b
|
APN |
17 |
5,314,315 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02713:Arid1b
|
APN |
17 |
5,393,286 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02858:Arid1b
|
APN |
17 |
5,392,166 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02885:Arid1b
|
APN |
17 |
5,392,428 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02989:Arid1b
|
APN |
17 |
5,385,322 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4449:Arid1b
|
UTSW |
17 |
5,045,864 (GRCm39) |
small insertion |
probably benign |
|
PIT4142001:Arid1b
|
UTSW |
17 |
5,389,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Arid1b
|
UTSW |
17 |
5,364,309 (GRCm39) |
critical splice donor site |
probably null |
|
R0124:Arid1b
|
UTSW |
17 |
5,389,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R0153:Arid1b
|
UTSW |
17 |
5,393,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R0465:Arid1b
|
UTSW |
17 |
5,046,535 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0825:Arid1b
|
UTSW |
17 |
5,392,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R1172:Arid1b
|
UTSW |
17 |
5,389,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Arid1b
|
UTSW |
17 |
5,293,197 (GRCm39) |
missense |
probably damaging |
0.99 |
R1468:Arid1b
|
UTSW |
17 |
5,293,197 (GRCm39) |
missense |
probably damaging |
0.99 |
R1616:Arid1b
|
UTSW |
17 |
5,389,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R1754:Arid1b
|
UTSW |
17 |
5,329,476 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1760:Arid1b
|
UTSW |
17 |
5,392,088 (GRCm39) |
missense |
probably damaging |
0.97 |
R1812:Arid1b
|
UTSW |
17 |
5,387,304 (GRCm39) |
missense |
probably benign |
0.10 |
R1911:Arid1b
|
UTSW |
17 |
5,393,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R3874:Arid1b
|
UTSW |
17 |
5,386,790 (GRCm39) |
splice site |
probably null |
|
R3913:Arid1b
|
UTSW |
17 |
5,392,532 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3916:Arid1b
|
UTSW |
17 |
5,392,928 (GRCm39) |
missense |
probably benign |
0.25 |
R3922:Arid1b
|
UTSW |
17 |
5,393,316 (GRCm39) |
missense |
probably damaging |
0.97 |
R4119:Arid1b
|
UTSW |
17 |
5,046,069 (GRCm39) |
unclassified |
probably benign |
|
R4290:Arid1b
|
UTSW |
17 |
5,090,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R4291:Arid1b
|
UTSW |
17 |
5,090,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R4352:Arid1b
|
UTSW |
17 |
5,147,859 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4386:Arid1b
|
UTSW |
17 |
5,045,247 (GRCm39) |
unclassified |
probably benign |
|
R4458:Arid1b
|
UTSW |
17 |
5,293,191 (GRCm39) |
missense |
probably damaging |
0.99 |
R4524:Arid1b
|
UTSW |
17 |
5,147,895 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4622:Arid1b
|
UTSW |
17 |
5,045,325 (GRCm39) |
unclassified |
probably benign |
|
R4723:Arid1b
|
UTSW |
17 |
5,387,565 (GRCm39) |
missense |
probably benign |
0.01 |
R4782:Arid1b
|
UTSW |
17 |
5,389,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R4799:Arid1b
|
UTSW |
17 |
5,389,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R4910:Arid1b
|
UTSW |
17 |
5,392,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R4946:Arid1b
|
UTSW |
17 |
5,393,118 (GRCm39) |
missense |
probably damaging |
0.99 |
R5083:Arid1b
|
UTSW |
17 |
5,364,293 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5204:Arid1b
|
UTSW |
17 |
5,393,316 (GRCm39) |
missense |
probably damaging |
0.97 |
R5347:Arid1b
|
UTSW |
17 |
5,341,332 (GRCm39) |
nonsense |
probably null |
|
R5553:Arid1b
|
UTSW |
17 |
5,364,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R5713:Arid1b
|
UTSW |
17 |
5,387,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R5820:Arid1b
|
UTSW |
17 |
5,046,529 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5992:Arid1b
|
UTSW |
17 |
5,045,231 (GRCm39) |
unclassified |
probably benign |
|
R6038:Arid1b
|
UTSW |
17 |
5,386,957 (GRCm39) |
missense |
probably benign |
0.07 |
R6038:Arid1b
|
UTSW |
17 |
5,386,957 (GRCm39) |
missense |
probably benign |
0.07 |
R6153:Arid1b
|
UTSW |
17 |
5,293,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R6222:Arid1b
|
UTSW |
17 |
5,377,922 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6249:Arid1b
|
UTSW |
17 |
5,329,636 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6279:Arid1b
|
UTSW |
17 |
5,392,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R6329:Arid1b
|
UTSW |
17 |
5,387,538 (GRCm39) |
nonsense |
probably null |
|
R6368:Arid1b
|
UTSW |
17 |
5,382,808 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6466:Arid1b
|
UTSW |
17 |
5,377,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R6861:Arid1b
|
UTSW |
17 |
5,377,961 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7008:Arid1b
|
UTSW |
17 |
5,341,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R7270:Arid1b
|
UTSW |
17 |
5,046,318 (GRCm39) |
missense |
unknown |
|
R7514:Arid1b
|
UTSW |
17 |
5,391,989 (GRCm39) |
missense |
probably benign |
0.28 |
R7519:Arid1b
|
UTSW |
17 |
5,046,128 (GRCm39) |
small insertion |
probably benign |
|
R7519:Arid1b
|
UTSW |
17 |
5,046,119 (GRCm39) |
small insertion |
probably benign |
|
R7521:Arid1b
|
UTSW |
17 |
5,392,865 (GRCm39) |
missense |
probably benign |
0.06 |
R7521:Arid1b
|
UTSW |
17 |
5,046,119 (GRCm39) |
small insertion |
probably benign |
|
R7521:Arid1b
|
UTSW |
17 |
5,046,135 (GRCm39) |
small insertion |
probably benign |
|
R7616:Arid1b
|
UTSW |
17 |
5,045,661 (GRCm39) |
missense |
unknown |
|
R7654:Arid1b
|
UTSW |
17 |
5,341,360 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7711:Arid1b
|
UTSW |
17 |
5,387,095 (GRCm39) |
missense |
probably benign |
0.28 |
R7828:Arid1b
|
UTSW |
17 |
5,147,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R7864:Arid1b
|
UTSW |
17 |
5,392,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R7998:Arid1b
|
UTSW |
17 |
5,377,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R8105:Arid1b
|
UTSW |
17 |
5,341,518 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8260:Arid1b
|
UTSW |
17 |
5,382,788 (GRCm39) |
missense |
probably benign |
0.03 |
R8374:Arid1b
|
UTSW |
17 |
5,392,919 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8779:Arid1b
|
UTSW |
17 |
5,391,809 (GRCm39) |
missense |
probably benign |
0.03 |
R8801:Arid1b
|
UTSW |
17 |
5,387,103 (GRCm39) |
missense |
probably benign |
0.05 |
R8894:Arid1b
|
UTSW |
17 |
5,377,668 (GRCm39) |
missense |
probably damaging |
0.98 |
R8982:Arid1b
|
UTSW |
17 |
5,293,316 (GRCm39) |
missense |
probably damaging |
0.98 |
R9034:Arid1b
|
UTSW |
17 |
5,387,180 (GRCm39) |
missense |
probably benign |
0.01 |
R9272:Arid1b
|
UTSW |
17 |
5,386,879 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9332:Arid1b
|
UTSW |
17 |
5,045,584 (GRCm39) |
missense |
unknown |
|
R9481:Arid1b
|
UTSW |
17 |
5,369,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R9493:Arid1b
|
UTSW |
17 |
5,046,423 (GRCm39) |
missense |
unknown |
|
R9512:Arid1b
|
UTSW |
17 |
5,391,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9548:Arid1b
|
UTSW |
17 |
5,385,262 (GRCm39) |
missense |
probably damaging |
1.00 |
RF007:Arid1b
|
UTSW |
17 |
5,045,869 (GRCm39) |
small insertion |
probably benign |
|
RF008:Arid1b
|
UTSW |
17 |
5,045,870 (GRCm39) |
small insertion |
probably benign |
|
RF008:Arid1b
|
UTSW |
17 |
5,045,869 (GRCm39) |
small insertion |
probably benign |
|
RF025:Arid1b
|
UTSW |
17 |
5,045,871 (GRCm39) |
small insertion |
probably benign |
|
RF025:Arid1b
|
UTSW |
17 |
5,045,863 (GRCm39) |
small insertion |
probably benign |
|
RF028:Arid1b
|
UTSW |
17 |
5,045,873 (GRCm39) |
small insertion |
probably benign |
|
RF032:Arid1b
|
UTSW |
17 |
5,045,863 (GRCm39) |
small insertion |
probably benign |
|
RF033:Arid1b
|
UTSW |
17 |
5,045,860 (GRCm39) |
small insertion |
probably benign |
|
RF041:Arid1b
|
UTSW |
17 |
5,045,870 (GRCm39) |
small insertion |
probably benign |
|
RF045:Arid1b
|
UTSW |
17 |
5,045,858 (GRCm39) |
small insertion |
probably benign |
|
RF046:Arid1b
|
UTSW |
17 |
5,045,865 (GRCm39) |
small insertion |
probably benign |
|
RF058:Arid1b
|
UTSW |
17 |
5,045,858 (GRCm39) |
small insertion |
probably benign |
|
X0023:Arid1b
|
UTSW |
17 |
5,392,668 (GRCm39) |
missense |
probably benign |
0.39 |
X0027:Arid1b
|
UTSW |
17 |
5,392,647 (GRCm39) |
nonsense |
probably null |
|
Z1177:Arid1b
|
UTSW |
17 |
5,046,603 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
Predicted Primers |
PCR Primer
(F):5'- TTTCTCAGGACCTGTCTGGC -3'
(R):5'- CCTAATATGTAAACATGCCCATGG -3'
Sequencing Primer
(F):5'- GTCTGGCTCCATCGATGAC -3'
(R):5'- ACATGCCCATGGTTTTAAGGAG -3'
|
Posted On |
2022-03-25 |