Incidental Mutation 'R7792:Arid2'
| ID |
599986 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Arid2
|
| Ensembl Gene |
ENSMUSG00000033237 |
| Gene Name |
AT-rich interaction domain 2 |
| Synonyms |
1700124K17Rik, zipzap/p200, 4432409D24Rik |
| MMRRC Submission |
045848-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R7792 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
15 |
| Chromosomal Location |
96185399-96302873 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 96267256 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 579
(T579A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000093969
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000096250]
|
| AlphaFold |
E9Q7E2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000096250
AA Change: T579A
PolyPhen 2
Score 0.054 (Sensitivity: 0.94; Specificity: 0.84)
|
| SMART Domains |
Protein: ENSMUSP00000093969
Gene: ENSMUSG00000033237
AA Change: T579A
| Domain | Start | End | E-Value | Type |
|---|
|
ARID
|
10 |
101 |
9.67e-36 |
SMART |
|
BRIGHT
|
14 |
106 |
3.67e-34 |
SMART |
|
Pfam:RFX_DNA_binding
|
521 |
603 |
1.7e-26 |
PFAM |
|
internal_repeat_1
|
767 |
843 |
3.29e-6 |
PROSPERO |
|
low complexity region
|
902 |
942 |
N/A |
INTRINSIC |
|
low complexity region
|
965 |
986 |
N/A |
INTRINSIC |
|
low complexity region
|
1012 |
1054 |
N/A |
INTRINSIC |
|
low complexity region
|
1118 |
1131 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
1132 |
1215 |
3.29e-6 |
PROSPERO |
|
low complexity region
|
1453 |
1468 |
N/A |
INTRINSIC |
|
low complexity region
|
1590 |
1614 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
1626 |
1651 |
4.34e0 |
SMART |
|
ZnF_C2H2
|
1659 |
1684 |
4.74e1 |
SMART |
|
| Meta Mutation Damage Score |
0.1183 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
| Validation Efficiency |
100% (97/97) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the AT-rich interactive domain (ARID)-containing family of DNA-binding proteins. Members of the ARID family have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation and chromatin structure modification. This protein functions as a subunit of the polybromo- and BRG1-associated factor or PBAF (SWI/SNF-B) chromatin remodeling complex which facilitates ligand-dependent transcriptional activation by nuclear receptors. Mutations in this gene are associated with hepatocellular carcinomas. A pseudogene of this gene is found on chromosome1. [provided by RefSeq, Dec 2016]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit embryonic lethality between E12.5 and E14.5, congenital heart defects, impaired coronary artery development, subcutaneous edema and hemorrhage. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 99 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aars1 |
G |
T |
8: 111,769,896 (GRCm39) |
V332F |
possibly damaging |
Het |
| Abhd15 |
T |
A |
11: 77,409,560 (GRCm39) |
S425T |
probably benign |
Het |
| Acads |
A |
T |
5: 115,250,840 (GRCm39) |
F152L |
probably damaging |
Het |
| Acp3 |
T |
A |
9: 104,204,165 (GRCm39) |
H43L |
probably damaging |
Het |
| Adora2a |
A |
G |
10: 75,169,480 (GRCm39) |
S315G |
probably benign |
Het |
| Agxt2 |
A |
T |
15: 10,381,472 (GRCm39) |
D242V |
probably damaging |
Het |
| Alx4 |
A |
G |
2: 93,473,056 (GRCm39) |
D18G |
probably damaging |
Het |
| Ankrd11 |
A |
G |
8: 123,610,970 (GRCm39) |
S2639P |
probably damaging |
Het |
| Arhgap35 |
A |
T |
7: 16,295,453 (GRCm39) |
V1204D |
possibly damaging |
Het |
| B4galt1 |
C |
T |
4: 40,809,373 (GRCm39) |
G332S |
probably benign |
Het |
| B4galt4 |
C |
A |
16: 38,578,172 (GRCm39) |
Y206* |
probably null |
Het |
| Bcl2l14 |
A |
T |
6: 134,409,277 (GRCm39) |
T284S |
possibly damaging |
Het |
| Bop1 |
C |
T |
15: 76,338,548 (GRCm39) |
V465M |
probably damaging |
Het |
| Cacna1b |
A |
T |
2: 24,567,977 (GRCm39) |
L1037H |
probably damaging |
Het |
| Cadm2 |
G |
A |
16: 66,568,523 (GRCm39) |
T254M |
probably benign |
Het |
| Ccdc180 |
T |
C |
4: 45,890,389 (GRCm39) |
|
probably null |
Het |
| Ccdc7a |
A |
T |
8: 129,618,918 (GRCm39) |
D875E |
possibly damaging |
Het |
| Cenpu |
A |
G |
8: 47,015,502 (GRCm39) |
D139G |
possibly damaging |
Het |
| Cep57l1 |
A |
T |
10: 41,598,936 (GRCm39) |
C292* |
probably null |
Het |
| Cep89 |
G |
A |
7: 35,129,353 (GRCm39) |
R630H |
probably damaging |
Het |
| Chst14 |
A |
G |
2: 118,758,256 (GRCm39) |
H350R |
probably benign |
Het |
| Clca3a1 |
T |
A |
3: 144,455,492 (GRCm39) |
I434F |
possibly damaging |
Het |
| Crispld2 |
A |
G |
8: 120,757,809 (GRCm39) |
T385A |
probably benign |
Het |
| Crmp1 |
A |
C |
5: 37,441,439 (GRCm39) |
N507T |
probably damaging |
Het |
| Cyp4f40 |
T |
A |
17: 32,890,143 (GRCm39) |
I271N |
probably damaging |
Het |
| D630003M21Rik |
G |
T |
2: 158,052,082 (GRCm39) |
Q670K |
possibly damaging |
Het |
| Ddx42 |
T |
C |
11: 106,127,822 (GRCm39) |
I342T |
probably damaging |
Het |
| Dnah9 |
T |
A |
11: 65,740,839 (GRCm39) |
I4116F |
probably damaging |
Het |
| Ehd2 |
T |
C |
7: 15,684,683 (GRCm39) |
H372R |
probably benign |
Het |
| Gja8 |
C |
A |
3: 96,827,092 (GRCm39) |
C190F |
probably damaging |
Het |
| Gm8297 |
A |
T |
14: 16,165,939 (GRCm39) |
D72V |
possibly damaging |
Het |
| Golgb1 |
A |
G |
16: 36,739,092 (GRCm39) |
D2518G |
probably benign |
Het |
| Hsd17b12 |
C |
A |
2: 93,863,986 (GRCm39) |
M285I |
probably benign |
Het |
| Hus1 |
T |
C |
11: 8,950,133 (GRCm39) |
E196G |
probably damaging |
Het |
| Ift70a2 |
T |
C |
2: 75,807,273 (GRCm39) |
N413S |
probably benign |
Het |
| Irf2 |
G |
A |
8: 47,260,314 (GRCm39) |
R82Q |
probably damaging |
Het |
| Irx2 |
A |
G |
13: 72,779,493 (GRCm39) |
D259G |
possibly damaging |
Het |
| Jph1 |
T |
A |
1: 17,074,602 (GRCm39) |
Q472L |
probably benign |
Het |
| Kif2a |
T |
C |
13: 107,124,490 (GRCm39) |
Q142R |
probably benign |
Het |
| Lonp1 |
T |
C |
17: 56,929,515 (GRCm39) |
Y174C |
probably damaging |
Het |
| Mapk14 |
T |
C |
17: 28,965,271 (GRCm39) |
F348L |
probably damaging |
Het |
| Marchf10 |
G |
T |
11: 105,281,054 (GRCm39) |
D410E |
probably benign |
Het |
| Mff |
A |
T |
1: 82,724,802 (GRCm39) |
|
probably null |
Het |
| Mtrex |
A |
T |
13: 113,009,443 (GRCm39) |
D985E |
probably benign |
Het |
| Necab3 |
G |
A |
2: 154,388,200 (GRCm39) |
R271C |
probably damaging |
Het |
| Nlrp4e |
T |
A |
7: 23,021,182 (GRCm39) |
F556L |
possibly damaging |
Het |
| Nt5c2 |
T |
C |
19: 46,878,385 (GRCm39) |
K425E |
probably benign |
Het |
| Ofcc1 |
A |
T |
13: 40,296,302 (GRCm39) |
W511R |
probably damaging |
Het |
| Or1j18 |
A |
C |
2: 36,624,342 (GRCm39) |
E3A |
probably benign |
Het |
| Or2v1 |
T |
A |
11: 49,025,496 (GRCm39) |
I159N |
possibly damaging |
Het |
| Or4k77 |
T |
C |
2: 111,199,748 (GRCm39) |
I257T |
probably benign |
Het |
| Or52p2 |
T |
A |
7: 102,238,090 (GRCm39) |
|
probably benign |
Het |
| P2rx2 |
G |
C |
5: 110,488,210 (GRCm39) |
A448G |
possibly damaging |
Het |
| Pcnx2 |
A |
T |
8: 126,618,757 (GRCm39) |
N56K |
possibly damaging |
Het |
| Pdzd7 |
A |
C |
19: 45,028,657 (GRCm39) |
M162R |
possibly damaging |
Het |
| Phyhd1 |
A |
G |
2: 30,156,782 (GRCm39) |
M1V |
probably null |
Het |
| Plaat3 |
T |
C |
19: 7,556,660 (GRCm39) |
C154R |
probably benign |
Het |
| Plekha5 |
A |
G |
6: 140,534,950 (GRCm39) |
E1126G |
possibly damaging |
Het |
| Plekhm1 |
A |
T |
11: 103,287,886 (GRCm39) |
V87D |
probably damaging |
Het |
| Pole |
G |
A |
5: 110,445,332 (GRCm39) |
|
probably null |
Het |
| Pramel22 |
A |
G |
4: 143,381,123 (GRCm39) |
L300P |
probably benign |
Het |
| R3hcc1 |
T |
C |
14: 69,942,957 (GRCm39) |
M207V |
probably benign |
Het |
| R3hcc1l |
T |
A |
19: 42,552,403 (GRCm39) |
S467T |
probably damaging |
Het |
| Rasgrp4 |
G |
T |
7: 28,842,527 (GRCm39) |
R267L |
probably damaging |
Het |
| Rbm20 |
T |
C |
19: 53,838,567 (GRCm39) |
I848T |
probably benign |
Het |
| Rims2 |
T |
C |
15: 39,061,923 (GRCm39) |
S56P |
possibly damaging |
Het |
| Rmc1 |
G |
A |
18: 12,314,656 (GRCm39) |
D289N |
probably damaging |
Het |
| Sacs |
T |
A |
14: 61,447,222 (GRCm39) |
D3089E |
probably benign |
Het |
| Sall2 |
C |
T |
14: 52,553,521 (GRCm39) |
G16R |
probably damaging |
Het |
| Scgb1b19 |
G |
A |
7: 32,987,912 (GRCm39) |
C93Y |
probably damaging |
Het |
| Scn3a |
T |
A |
2: 65,297,334 (GRCm39) |
K1442* |
probably null |
Het |
| Sepsecs |
A |
G |
5: 52,801,391 (GRCm39) |
S424P |
probably damaging |
Het |
| Set |
G |
T |
2: 29,960,323 (GRCm39) |
V219F |
probably benign |
Het |
| Sh3tc1 |
A |
T |
5: 35,868,295 (GRCm39) |
F390I |
probably damaging |
Het |
| Simc1 |
G |
A |
13: 54,695,143 (GRCm39) |
V1269M |
probably damaging |
Het |
| Ska3 |
T |
G |
14: 58,047,512 (GRCm39) |
D341A |
probably damaging |
Het |
| Slc16a10 |
A |
T |
10: 39,913,411 (GRCm39) |
|
probably null |
Het |
| Srgap1 |
T |
A |
10: 121,761,872 (GRCm39) |
N92I |
probably damaging |
Het |
| Sspo |
T |
C |
6: 48,431,624 (GRCm39) |
V639A |
probably damaging |
Het |
| Stk11 |
A |
T |
10: 79,961,271 (GRCm39) |
|
probably benign |
Het |
| Sult5a1 |
G |
A |
8: 123,872,180 (GRCm39) |
H221Y |
probably benign |
Het |
| Sytl3 |
T |
A |
17: 7,003,977 (GRCm39) |
M559K |
probably benign |
Het |
| Tab2 |
A |
C |
10: 7,794,897 (GRCm39) |
D528E |
possibly damaging |
Het |
| Tbc1d15 |
A |
G |
10: 115,057,492 (GRCm39) |
I218T |
possibly damaging |
Het |
| Tenm4 |
T |
A |
7: 96,423,221 (GRCm39) |
M672K |
possibly damaging |
Het |
| Tent4b |
A |
T |
8: 88,979,182 (GRCm39) |
Q561L |
probably benign |
Het |
| Tfrc |
A |
G |
16: 32,437,985 (GRCm39) |
K346R |
probably benign |
Het |
| Thsd1 |
G |
T |
8: 22,733,114 (GRCm39) |
G54W |
probably damaging |
Het |
| Tmprss15 |
A |
T |
16: 78,800,275 (GRCm39) |
L618I |
probably damaging |
Het |
| Top3a |
T |
C |
11: 60,633,790 (GRCm39) |
S769G |
probably benign |
Het |
| Trp63 |
C |
A |
16: 25,686,974 (GRCm39) |
P396Q |
possibly damaging |
Het |
| Uggt1 |
T |
C |
1: 36,247,065 (GRCm39) |
S311G |
probably damaging |
Het |
| Usp10 |
G |
A |
8: 120,678,740 (GRCm39) |
E574K |
possibly damaging |
Het |
| Wfdc6b |
T |
A |
2: 164,459,822 (GRCm39) |
I148K |
probably damaging |
Het |
| Zcchc2 |
T |
G |
1: 105,945,982 (GRCm39) |
I474R |
probably damaging |
Het |
| Zdhhc2 |
A |
G |
8: 40,900,182 (GRCm39) |
K82R |
probably benign |
Het |
| Zfp273 |
A |
G |
13: 67,974,135 (GRCm39) |
D421G |
possibly damaging |
Het |
| Zfp280d |
T |
C |
9: 72,238,601 (GRCm39) |
I639T |
probably damaging |
Het |
| Zfp429 |
A |
T |
13: 67,538,558 (GRCm39) |
C295* |
probably null |
Het |
|
| Other mutations in Arid2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00091:Arid2
|
APN |
15 |
96,270,183 (GRCm39) |
missense |
probably benign |
|
|
IGL00321:Arid2
|
APN |
15 |
96,186,970 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL00434:Arid2
|
APN |
15 |
96,269,181 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL00576:Arid2
|
APN |
15 |
96,254,639 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL00766:Arid2
|
APN |
15 |
96,268,286 (GRCm39) |
missense |
probably benign |
0.09 |
|
IGL01563:Arid2
|
APN |
15 |
96,270,278 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01697:Arid2
|
APN |
15 |
96,259,453 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL01845:Arid2
|
APN |
15 |
96,254,678 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02159:Arid2
|
APN |
15 |
96,256,793 (GRCm39) |
splice site |
probably benign |
|
|
IGL02341:Arid2
|
APN |
15 |
96,270,066 (GRCm39) |
missense |
probably benign |
|
|
IGL02416:Arid2
|
APN |
15 |
96,247,936 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
IGL02578:Arid2
|
APN |
15 |
96,270,116 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02598:Arid2
|
APN |
15 |
96,269,417 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02644:Arid2
|
APN |
15 |
96,266,589 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02653:Arid2
|
APN |
15 |
96,185,583 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03115:Arid2
|
APN |
15 |
96,268,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03137:Arid2
|
APN |
15 |
96,269,199 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL03220:Arid2
|
APN |
15 |
96,259,653 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03249:Arid2
|
APN |
15 |
96,299,846 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03256:Arid2
|
APN |
15 |
96,268,643 (GRCm39) |
missense |
probably benign |
0.18 |
|
IGL03386:Arid2
|
APN |
15 |
96,259,455 (GRCm39) |
missense |
probably damaging |
1.00 |
|
H8562:Arid2
|
UTSW |
15 |
96,267,427 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
I2288:Arid2
|
UTSW |
15 |
96,267,392 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0254:Arid2
|
UTSW |
15 |
96,268,452 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0284:Arid2
|
UTSW |
15 |
96,276,848 (GRCm39) |
splice site |
probably benign |
|
|
R0347:Arid2
|
UTSW |
15 |
96,268,833 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0366:Arid2
|
UTSW |
15 |
96,259,601 (GRCm39) |
splice site |
probably benign |
|
|
R0400:Arid2
|
UTSW |
15 |
96,254,806 (GRCm39) |
unclassified |
probably benign |
|
|
R0650:Arid2
|
UTSW |
15 |
96,299,930 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R0651:Arid2
|
UTSW |
15 |
96,299,930 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R1034:Arid2
|
UTSW |
15 |
96,267,386 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1615:Arid2
|
UTSW |
15 |
96,269,535 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R1696:Arid2
|
UTSW |
15 |
96,268,064 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2024:Arid2
|
UTSW |
15 |
96,259,680 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2046:Arid2
|
UTSW |
15 |
96,267,268 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2069:Arid2
|
UTSW |
15 |
96,260,471 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2149:Arid2
|
UTSW |
15 |
96,268,716 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2300:Arid2
|
UTSW |
15 |
96,299,887 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2336:Arid2
|
UTSW |
15 |
96,260,430 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2359:Arid2
|
UTSW |
15 |
96,259,759 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2368:Arid2
|
UTSW |
15 |
96,247,893 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R2829:Arid2
|
UTSW |
15 |
96,267,335 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R3013:Arid2
|
UTSW |
15 |
96,259,817 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3109:Arid2
|
UTSW |
15 |
96,254,627 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3765:Arid2
|
UTSW |
15 |
96,268,595 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3785:Arid2
|
UTSW |
15 |
96,270,439 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R3811:Arid2
|
UTSW |
15 |
96,186,967 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3812:Arid2
|
UTSW |
15 |
96,186,967 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3813:Arid2
|
UTSW |
15 |
96,267,831 (GRCm39) |
missense |
probably benign |
0.26 |
|
R3843:Arid2
|
UTSW |
15 |
96,249,721 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R3978:Arid2
|
UTSW |
15 |
96,261,503 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4279:Arid2
|
UTSW |
15 |
96,269,637 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4569:Arid2
|
UTSW |
15 |
96,290,343 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4597:Arid2
|
UTSW |
15 |
96,268,737 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5020:Arid2
|
UTSW |
15 |
96,269,869 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5154:Arid2
|
UTSW |
15 |
96,299,866 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5303:Arid2
|
UTSW |
15 |
96,290,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5620:Arid2
|
UTSW |
15 |
96,270,387 (GRCm39) |
missense |
probably benign |
0.20 |
|
R5766:Arid2
|
UTSW |
15 |
96,270,086 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6005:Arid2
|
UTSW |
15 |
96,268,853 (GRCm39) |
missense |
probably benign |
|
|
R6169:Arid2
|
UTSW |
15 |
96,266,558 (GRCm39) |
missense |
probably benign |
0.36 |
|
R6216:Arid2
|
UTSW |
15 |
96,254,790 (GRCm39) |
missense |
probably benign |
0.18 |
|
R6392:Arid2
|
UTSW |
15 |
96,259,483 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6430:Arid2
|
UTSW |
15 |
96,261,575 (GRCm39) |
missense |
probably benign |
|
|
R6454:Arid2
|
UTSW |
15 |
96,270,294 (GRCm39) |
missense |
probably benign |
0.20 |
|
R6672:Arid2
|
UTSW |
15 |
96,260,226 (GRCm39) |
missense |
probably benign |
0.30 |
|
R6776:Arid2
|
UTSW |
15 |
96,268,830 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6985:Arid2
|
UTSW |
15 |
96,268,029 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7132:Arid2
|
UTSW |
15 |
96,247,894 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R7133:Arid2
|
UTSW |
15 |
96,276,756 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7453:Arid2
|
UTSW |
15 |
96,268,605 (GRCm39) |
missense |
probably benign |
|
|
R7562:Arid2
|
UTSW |
15 |
96,299,849 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7594:Arid2
|
UTSW |
15 |
96,288,875 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7692:Arid2
|
UTSW |
15 |
96,254,578 (GRCm39) |
nonsense |
probably null |
|
|
R8036:Arid2
|
UTSW |
15 |
96,266,625 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8094:Arid2
|
UTSW |
15 |
96,266,592 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R8327:Arid2
|
UTSW |
15 |
96,260,485 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9065:Arid2
|
UTSW |
15 |
96,269,372 (GRCm39) |
missense |
probably benign |
0.44 |
|
R9143:Arid2
|
UTSW |
15 |
96,259,715 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9320:Arid2
|
UTSW |
15 |
96,269,067 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9346:Arid2
|
UTSW |
15 |
96,185,792 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9519:Arid2
|
UTSW |
15 |
96,186,948 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R9651:Arid2
|
UTSW |
15 |
96,256,822 (GRCm39) |
missense |
probably benign |
0.44 |
|
X0024:Arid2
|
UTSW |
15 |
96,270,371 (GRCm39) |
missense |
probably benign |
0.00 |
|
X0066:Arid2
|
UTSW |
15 |
96,254,685 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Arid2
|
UTSW |
15 |
96,288,867 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- CCAATCGACTCTGTCATGTTGAAG -3'
(R):5'- TGTACAAAGTACAGAGCCAGGC -3'
Sequencing Primer
(F):5'- CGACTCTGTCATGTTGAAGATGTTC -3'
(R):5'- GCCTATAATCCTAGCTTTCAGGAGG -3'
|
| Posted On |
2019-11-26 |
Incidental Mutation