Incidental Mutation 'R4523:Irag1'
| ID |
334308 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Irag1
|
| Ensembl Gene |
ENSMUSG00000005611 |
| Gene Name |
inositol 1,4,5-triphosphate receptor associated 1 |
| Synonyms |
Ris1, Mrvi1 |
| MMRRC Submission |
042004-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.070)
|
| Stock # |
R4523 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
7 |
| Chromosomal Location |
110467473-110581668 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 110523048 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Valine
at position 338
(M338V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000114578
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000005751]
[ENSMUST00000125758]
[ENSMUST00000127935]
[ENSMUST00000154466]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000005751
AA Change: M273V
PolyPhen 2
Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)
|
| SMART Domains |
Protein: ENSMUSP00000005751
Gene: ENSMUSG00000005611
AA Change: M273V
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
98 |
113 |
N/A |
INTRINSIC |
|
low complexity region
|
138 |
160 |
N/A |
INTRINSIC |
|
Pfam:MRVI1
|
265 |
856 |
1.8e-227 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000125758
AA Change: M338V
PolyPhen 2
Score 0.023 (Sensitivity: 0.95; Specificity: 0.81)
|
| SMART Domains |
Protein: ENSMUSP00000114578
Gene: ENSMUSG00000005611
AA Change: M338V
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
163 |
178 |
N/A |
INTRINSIC |
|
low complexity region
|
203 |
225 |
N/A |
INTRINSIC |
|
Pfam:MRVI1
|
336 |
921 |
1.5e-202 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000127935
AA Change: M132V
PolyPhen 2
Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)
|
| SMART Domains |
Protein: ENSMUSP00000120045
Gene: ENSMUSG00000005611
AA Change: M132V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:MRVI1
|
124 |
715 |
7.9e-228 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000135590
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142368
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000149923
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000154466
|
| SMART Domains |
Protein: ENSMUSP00000120765
Gene: ENSMUSG00000005611
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
98 |
113 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.2%
|
| Validation Efficiency |
100% (61/61) |
| MGI Phenotype |
FUNCTION: This gene is a putative tumor suppressor gene that is frequently disrupted by mouse AIDS-related virus (MRV). The encoded protein participates in signaling by nitric oxide (NO) to inhibit intracellular calcium release and platelet aggregation in cardiovascular tissue. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2013]
PHENOTYPE: Mice homozygous for a knock-out allele show lower blood pressure, a slightly reduced heart rate, and failure of cGMP-mediated relaxation of receptor-triggered smooth muscle contraction; 50% of mice die prematurely with an enlarged stomach, a dilated cecum, pyloric stenosis and impaired GI motility. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 54 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Atp8a1 |
G |
T |
5: 67,824,943 (GRCm39) |
T796K |
probably benign |
Het |
| Atr |
T |
C |
9: 95,744,916 (GRCm39) |
S78P |
probably damaging |
Het |
| Calb2 |
C |
T |
8: 110,875,141 (GRCm39) |
|
probably null |
Het |
| Ccdc88c |
G |
T |
12: 100,879,591 (GRCm39) |
S1843R |
possibly damaging |
Het |
| Cdca7 |
A |
G |
2: 72,310,042 (GRCm39) |
S77G |
probably damaging |
Het |
| Cfap47 |
A |
T |
X: 78,553,601 (GRCm39) |
N291K |
possibly damaging |
Het |
| Cnot2 |
C |
T |
10: 116,417,379 (GRCm39) |
|
probably benign |
Het |
| Cstf2t |
T |
A |
19: 31,060,482 (GRCm39) |
V6D |
possibly damaging |
Het |
| Cybc1 |
A |
G |
11: 121,114,934 (GRCm39) |
|
probably benign |
Het |
| Dido1 |
T |
C |
2: 180,314,085 (GRCm39) |
I852V |
probably damaging |
Het |
| Dmgdh |
C |
T |
13: 93,825,138 (GRCm39) |
Q154* |
probably null |
Het |
| Dnah12 |
T |
C |
14: 26,491,979 (GRCm39) |
F1138S |
probably damaging |
Het |
| Dnah12 |
G |
A |
14: 26,598,915 (GRCm39) |
A998T |
possibly damaging |
Het |
| Dusp5 |
T |
G |
19: 53,526,032 (GRCm39) |
Y225D |
probably damaging |
Het |
| Fam193a |
G |
A |
5: 34,600,715 (GRCm39) |
D601N |
probably benign |
Het |
| Fbxo41 |
A |
G |
6: 85,461,024 (GRCm39) |
I228T |
probably damaging |
Het |
| Fmo2 |
T |
C |
1: 162,715,277 (GRCm39) |
K115R |
probably benign |
Het |
| Gak |
G |
T |
5: 108,724,432 (GRCm39) |
Q1093K |
probably benign |
Het |
| Gm5277 |
G |
T |
3: 78,799,493 (GRCm39) |
|
noncoding transcript |
Het |
| Hgsnat |
A |
G |
8: 26,458,389 (GRCm39) |
|
probably null |
Het |
| Hycc1 |
T |
C |
5: 24,170,120 (GRCm39) |
T410A |
probably benign |
Het |
| Map3k3 |
G |
A |
11: 106,039,694 (GRCm39) |
R278H |
probably damaging |
Het |
| Muc4 |
T |
C |
16: 32,555,154 (GRCm39) |
|
probably benign |
Het |
| Nectin3 |
C |
A |
16: 46,268,953 (GRCm39) |
R483L |
probably benign |
Het |
| Nop2 |
G |
T |
6: 125,110,515 (GRCm39) |
R47L |
probably damaging |
Het |
| Ntng1 |
A |
G |
3: 109,842,312 (GRCm39) |
S154P |
probably damaging |
Het |
| Olfml2b |
T |
C |
1: 170,496,791 (GRCm39) |
I474T |
probably benign |
Het |
| Optc |
G |
T |
1: 133,831,492 (GRCm39) |
T138K |
possibly damaging |
Het |
| Or7g25 |
T |
C |
9: 19,160,525 (GRCm39) |
T57A |
probably damaging |
Het |
| Or8k22 |
C |
G |
2: 86,163,644 (GRCm39) |
D19H |
probably benign |
Het |
| Orc4 |
G |
A |
2: 48,827,501 (GRCm39) |
P31S |
probably benign |
Het |
| Pabir3 |
G |
A |
X: 52,382,376 (GRCm39) |
R94H |
possibly damaging |
Het |
| Pard3 |
C |
T |
8: 128,125,108 (GRCm39) |
P421S |
probably benign |
Het |
| Pcdhb22 |
G |
T |
18: 37,653,474 (GRCm39) |
E647D |
probably benign |
Het |
| Pclo |
A |
G |
5: 14,730,006 (GRCm39) |
|
probably benign |
Het |
| Prkce |
G |
T |
17: 86,798,178 (GRCm39) |
|
probably null |
Het |
| Prr12 |
T |
C |
7: 44,697,947 (GRCm39) |
D656G |
unknown |
Het |
| Ptprk |
A |
T |
10: 28,342,048 (GRCm39) |
D485V |
probably damaging |
Het |
| Ptprn2 |
T |
C |
12: 116,839,620 (GRCm39) |
L381P |
probably damaging |
Het |
| Rnf144b |
T |
C |
13: 47,361,013 (GRCm39) |
I51T |
probably benign |
Het |
| Rpl10l |
T |
C |
12: 66,330,512 (GRCm39) |
D207G |
probably benign |
Het |
| Sh3glb2 |
A |
T |
2: 30,240,711 (GRCm39) |
V118E |
probably damaging |
Het |
| Sipa1l2 |
C |
T |
8: 126,219,163 (GRCm39) |
G58D |
probably damaging |
Het |
| Slc5a4a |
C |
T |
10: 75,984,196 (GRCm39) |
A46V |
probably damaging |
Het |
| Spmip8 |
T |
A |
8: 96,039,638 (GRCm39) |
Y18* |
probably null |
Het |
| Tgm7 |
C |
A |
2: 120,929,069 (GRCm39) |
|
probably null |
Het |
| Tjap1 |
A |
G |
17: 46,569,718 (GRCm39) |
V424A |
probably benign |
Het |
| Trpm6 |
A |
T |
19: 18,773,864 (GRCm39) |
I414F |
probably damaging |
Het |
| Tsr3 |
C |
G |
17: 25,460,723 (GRCm39) |
D196E |
probably benign |
Het |
| Ubqlnl |
C |
T |
7: 103,798,925 (GRCm39) |
V191M |
probably benign |
Het |
| Vmn2r72 |
T |
A |
7: 85,401,134 (GRCm39) |
H95L |
probably benign |
Het |
| Vmn2r97 |
T |
A |
17: 19,149,333 (GRCm39) |
N240K |
probably benign |
Het |
| Xdh |
C |
A |
17: 74,205,339 (GRCm39) |
G1042V |
probably damaging |
Het |
| Zcchc4 |
A |
G |
5: 52,941,409 (GRCm39) |
D68G |
probably damaging |
Het |
|
| Other mutations in Irag1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01079:Irag1
|
APN |
7 |
110,545,174 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
IGL01384:Irag1
|
APN |
7 |
110,525,708 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL01474:Irag1
|
APN |
7 |
110,470,640 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
IGL02081:Irag1
|
APN |
7 |
110,523,281 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL02193:Irag1
|
APN |
7 |
110,498,162 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02537:Irag1
|
APN |
7 |
110,470,680 (GRCm39) |
nonsense |
probably null |
|
|
IGL03084:Irag1
|
APN |
7 |
110,485,036 (GRCm39) |
splice site |
probably benign |
|
|
IGL03264:Irag1
|
APN |
7 |
110,525,553 (GRCm39) |
missense |
probably benign |
0.00 |
|
hurricane
|
UTSW |
7 |
110,523,170 (GRCm39) |
missense |
probably benign |
0.09 |
|
R0346:Irag1
|
UTSW |
7 |
110,498,183 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0401:Irag1
|
UTSW |
7 |
110,476,104 (GRCm39) |
missense |
probably benign |
0.09 |
|
R0731:Irag1
|
UTSW |
7 |
110,476,107 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1168:Irag1
|
UTSW |
7 |
110,495,138 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1342:Irag1
|
UTSW |
7 |
110,487,252 (GRCm39) |
missense |
probably benign |
0.07 |
|
R1887:Irag1
|
UTSW |
7 |
110,523,740 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2183:Irag1
|
UTSW |
7 |
110,498,189 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3417:Irag1
|
UTSW |
7 |
110,476,161 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R3736:Irag1
|
UTSW |
7 |
110,523,170 (GRCm39) |
missense |
probably benign |
0.09 |
|
R4063:Irag1
|
UTSW |
7 |
110,522,984 (GRCm39) |
missense |
probably benign |
0.38 |
|
R4436:Irag1
|
UTSW |
7 |
110,476,124 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4948:Irag1
|
UTSW |
7 |
110,487,236 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5070:Irag1
|
UTSW |
7 |
110,524,519 (GRCm39) |
missense |
probably benign |
|
|
R5085:Irag1
|
UTSW |
7 |
110,470,700 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5605:Irag1
|
UTSW |
7 |
110,545,209 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R6194:Irag1
|
UTSW |
7 |
110,498,901 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6218:Irag1
|
UTSW |
7 |
110,476,112 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6273:Irag1
|
UTSW |
7 |
110,470,790 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6608:Irag1
|
UTSW |
7 |
110,487,758 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6754:Irag1
|
UTSW |
7 |
110,528,719 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6835:Irag1
|
UTSW |
7 |
110,520,541 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7064:Irag1
|
UTSW |
7 |
110,495,061 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7304:Irag1
|
UTSW |
7 |
110,498,931 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R7412:Irag1
|
UTSW |
7 |
110,522,963 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7420:Irag1
|
UTSW |
7 |
110,470,680 (GRCm39) |
nonsense |
probably null |
|
|
R7857:Irag1
|
UTSW |
7 |
110,522,742 (GRCm39) |
nonsense |
probably null |
|
|
R8078:Irag1
|
UTSW |
7 |
110,498,942 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8139:Irag1
|
UTSW |
7 |
110,498,879 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8280:Irag1
|
UTSW |
7 |
110,522,828 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R8733:Irag1
|
UTSW |
7 |
110,477,425 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8946:Irag1
|
UTSW |
7 |
110,477,347 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9150:Irag1
|
UTSW |
7 |
110,498,205 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9321:Irag1
|
UTSW |
7 |
110,524,534 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9373:Irag1
|
UTSW |
7 |
110,545,038 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9445:Irag1
|
UTSW |
7 |
110,545,161 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R9482:Irag1
|
UTSW |
7 |
110,545,259 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9715:Irag1
|
UTSW |
7 |
110,470,640 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
X0065:Irag1
|
UTSW |
7 |
110,523,251 (GRCm39) |
missense |
probably benign |
0.31 |
|
Z1176:Irag1
|
UTSW |
7 |
110,523,206 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
|
| Posted On |
2015-08-18 |
Incidental Mutation