Incidental Mutation 'R8946:Irag1'
| ID |
681304 |
| 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 |
068784-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.070)
|
| Stock # |
R8946 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
7 |
| Chromosomal Location |
110467473-110581668 bp(-) (GRCm39) |
| Type of Mutation |
critical splice donor site (2 bp from exon) |
| DNA Base Change (assembly) |
A to T
at 110477347 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000120045
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000005751]
[ENSMUST00000125758]
[ENSMUST00000127935]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000005751
|
| SMART Domains |
Protein: ENSMUSP00000005751
Gene: ENSMUSG00000005611
| 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
|
| SMART Domains |
Protein: ENSMUSP00000114578
Gene: ENSMUSG00000005611
| 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 null
Transcript: ENSMUST00000127935
|
| SMART Domains |
Protein: ENSMUSP00000120045
Gene: ENSMUSG00000005611
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:MRVI1
|
124 |
715 |
7.9e-228 |
PFAM |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.4%
|
| Validation Efficiency |
97% (65/67) |
| 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: 66 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Akap12 |
A |
G |
10: 4,304,368 (GRCm39) |
S393G |
probably damaging |
Het |
| Ankrd28 |
A |
G |
14: 31,430,083 (GRCm39) |
F862L |
probably damaging |
Het |
| Ankrd31 |
T |
C |
13: 97,046,037 (GRCm39) |
*1546Q |
probably null |
Het |
| Ankrd33b |
T |
C |
15: 31,297,894 (GRCm39) |
T288A |
probably benign |
Het |
| Aox1 |
T |
C |
1: 58,145,227 (GRCm39) |
I1331T |
possibly damaging |
Het |
| Atp13a5 |
A |
G |
16: 29,146,601 (GRCm39) |
L231P |
probably damaging |
Het |
| C1qtnf12 |
T |
C |
4: 156,050,882 (GRCm39) |
F284L |
probably damaging |
Het |
| Caprin1 |
A |
T |
2: 103,608,378 (GRCm39) |
H250Q |
probably damaging |
Het |
| Cd2bp2 |
A |
C |
7: 126,793,923 (GRCm39) |
I122S |
probably damaging |
Het |
| Cd300lf |
T |
A |
11: 115,024,738 (GRCm39) |
|
probably benign |
Het |
| Ceacam14 |
A |
G |
7: 17,547,999 (GRCm39) |
I30V |
probably benign |
Het |
| Chchd1 |
T |
A |
14: 20,753,385 (GRCm39) |
*56R |
probably null |
Het |
| Ckap5 |
A |
G |
2: 91,409,861 (GRCm39) |
T948A |
probably benign |
Het |
| Clec12a |
A |
T |
6: 129,340,949 (GRCm39) |
N243I |
possibly damaging |
Het |
| Col11a2 |
A |
G |
17: 34,270,757 (GRCm39) |
M462V |
probably benign |
Het |
| Col6a5 |
C |
T |
9: 105,822,833 (GRCm39) |
E175K |
unknown |
Het |
| Csnka2ip |
T |
C |
16: 64,300,667 (GRCm39) |
|
probably benign |
Het |
| D130040H23Rik |
C |
A |
8: 69,755,033 (GRCm39) |
T146N |
possibly damaging |
Het |
| Dennd5b |
T |
C |
6: 148,943,485 (GRCm39) |
|
probably benign |
Het |
| Fanci |
A |
G |
7: 79,045,726 (GRCm39) |
T23A |
probably benign |
Het |
| Fmnl1 |
T |
C |
11: 103,071,741 (GRCm39) |
Y83H |
probably damaging |
Het |
| Galnt13 |
C |
A |
2: 54,770,075 (GRCm39) |
T289N |
probably benign |
Het |
| Gcn1 |
A |
G |
5: 115,733,404 (GRCm39) |
D1074G |
probably benign |
Het |
| Gm10801 |
ATTTTCAGTTTTCTTGCCATATTCCACGTCCTGCACTGGACATTTCTAAATTTTCCACCTTTTTCAGTTTTC |
ATTTTCAGTTTTC |
2: 98,492,669 (GRCm39) |
|
probably null |
Het |
| Gnl1 |
T |
C |
17: 36,294,479 (GRCm39) |
I366T |
probably benign |
Het |
| Gtf2ird2 |
A |
T |
5: 134,245,161 (GRCm39) |
Y473F |
probably damaging |
Het |
| Ikzf1 |
T |
A |
11: 11,719,485 (GRCm39) |
D397E |
possibly damaging |
Het |
| Ints15 |
C |
G |
5: 143,300,795 (GRCm39) |
E19Q |
probably benign |
Het |
| Intu |
C |
T |
3: 40,637,789 (GRCm39) |
A425V |
possibly damaging |
Het |
| Jakmip1 |
G |
A |
5: 37,343,084 (GRCm39) |
|
probably null |
Het |
| Lif |
C |
A |
11: 4,219,225 (GRCm39) |
P168Q |
possibly damaging |
Het |
| Myh11 |
A |
C |
16: 14,048,580 (GRCm39) |
S576A |
probably benign |
Het |
| Neb |
A |
G |
2: 52,041,425 (GRCm39) |
V6559A |
probably damaging |
Het |
| Nphs1 |
A |
G |
7: 30,162,625 (GRCm39) |
N368S |
probably damaging |
Het |
| Npsr1 |
G |
A |
9: 24,224,525 (GRCm39) |
V148I |
probably benign |
Het |
| Or51f1 |
C |
A |
7: 102,505,725 (GRCm39) |
G255* |
probably null |
Het |
| Or52ab4 |
T |
C |
7: 102,987,573 (GRCm39) |
F104S |
probably damaging |
Het |
| Or56a5 |
T |
A |
7: 104,792,832 (GRCm39) |
I223F |
probably damaging |
Het |
| Or5b111 |
A |
T |
19: 13,291,502 (GRCm39) |
L49Q |
probably damaging |
Het |
| Or7e166 |
C |
T |
9: 19,624,885 (GRCm39) |
T254I |
probably damaging |
Het |
| Patz1 |
T |
C |
11: 3,241,856 (GRCm39) |
C415R |
probably damaging |
Het |
| Pcdha9 |
A |
T |
18: 37,131,546 (GRCm39) |
N205I |
possibly damaging |
Het |
| Pcdhga12 |
A |
T |
18: 37,899,711 (GRCm39) |
E181V |
probably benign |
Het |
| Pcnx1 |
T |
C |
12: 82,018,158 (GRCm39) |
Y1333H |
probably damaging |
Het |
| Phf7 |
A |
T |
14: 30,970,106 (GRCm39) |
|
probably benign |
Het |
| Pomc |
T |
G |
12: 4,010,298 (GRCm39) |
S180A |
probably benign |
Het |
| Ppp1r7 |
T |
A |
1: 93,288,536 (GRCm39) |
|
probably null |
Het |
| Prrc2c |
A |
T |
1: 162,536,478 (GRCm39) |
|
probably benign |
Het |
| Rsf1 |
GGC |
GGCCACGGCCGC |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
| Semp2l1 |
C |
T |
1: 32,585,685 (GRCm39) |
R75Q |
probably benign |
Het |
| Senp1 |
T |
C |
15: 97,940,782 (GRCm39) |
K664E |
probably damaging |
Het |
| Skint7 |
A |
G |
4: 111,839,198 (GRCm39) |
N164S |
possibly damaging |
Het |
| Smg1 |
C |
A |
7: 117,751,900 (GRCm39) |
R2775M |
probably null |
Het |
| Snrnp27 |
C |
T |
6: 86,653,226 (GRCm39) |
V131M |
probably damaging |
Het |
| Spire1 |
C |
A |
18: 67,629,686 (GRCm39) |
R357L |
probably damaging |
Het |
| Sspo |
G |
A |
6: 48,434,071 (GRCm39) |
V959I |
probably damaging |
Het |
| St6galnac2 |
T |
C |
11: 116,568,458 (GRCm39) |
H335R |
probably damaging |
Het |
| Stard13 |
C |
T |
5: 150,984,267 (GRCm39) |
R623H |
probably damaging |
Het |
| Syde1 |
T |
A |
10: 78,424,683 (GRCm39) |
E383V |
probably damaging |
Het |
| Taf10 |
A |
G |
7: 105,393,524 (GRCm39) |
M1T |
probably null |
Het |
| Traf3ip3 |
A |
G |
1: 192,869,415 (GRCm39) |
C257R |
probably damaging |
Het |
| Trpm8 |
G |
A |
1: 88,276,061 (GRCm39) |
|
probably benign |
Het |
| Veph1 |
A |
G |
3: 66,171,301 (GRCm39) |
|
probably null |
Het |
| Vmn1r169 |
A |
T |
7: 23,276,640 (GRCm39) |
T11S |
possibly damaging |
Het |
| Wdhd1 |
A |
T |
14: 47,482,752 (GRCm39) |
S961T |
probably benign |
Het |
| Zfp773 |
T |
C |
7: 7,135,469 (GRCm39) |
T376A |
possibly 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 |
|
R4523:Irag1
|
UTSW |
7 |
110,523,048 (GRCm39) |
missense |
probably benign |
0.02 |
|
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 |
|
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 |
PCR Primer
(F):5'- TTAGATATTCCTAGGCAGCAGCATC -3'
(R):5'- AGATGTGCAGTCTCTCCCTG -3'
Sequencing Primer
(F):5'- AGGAGTCTAGTCAAGTCTAGCCATTG -3'
(R):5'- AGTCTCTCCCTGCAATGACG -3'
|
| Posted On |
2021-08-31 |
Incidental Mutation