Incidental Mutation 'R4802:Itpr2'
ID |
472776 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Itpr2
|
Ensembl Gene |
ENSMUSG00000030287 |
Gene Name |
inositol 1,4,5-triphosphate receptor 2 |
Synonyms |
Ip3r2, Itpr5 |
MMRRC Submission |
042424-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4802 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
6 |
Chromosomal Location |
146009797-146403721 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 146272829 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Alanine
at position 855
(T855A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000078526
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053273]
[ENSMUST00000079573]
[ENSMUST00000131890]
[ENSMUST00000139732]
|
AlphaFold |
no structure available at present |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000053273
AA Change: T888A
PolyPhen 2
Score 0.953 (Sensitivity: 0.79; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000049584 Gene: ENSMUSG00000030287 AA Change: T888A
Domain | Start | End | E-Value | Type |
low complexity region
|
68 |
80 |
N/A |
INTRINSIC |
MIR
|
112 |
166 |
1.1e-5 |
SMART |
MIR
|
173 |
223 |
8.9e-6 |
SMART |
MIR
|
231 |
287 |
5.11e-6 |
SMART |
MIR
|
294 |
402 |
3.73e-8 |
SMART |
Pfam:RYDR_ITPR
|
473 |
670 |
1.5e-62 |
PFAM |
low complexity region
|
882 |
890 |
N/A |
INTRINSIC |
Pfam:RYDR_ITPR
|
1183 |
1346 |
1.6e-16 |
PFAM |
low complexity region
|
1773 |
1785 |
N/A |
INTRINSIC |
low complexity region
|
1897 |
1908 |
N/A |
INTRINSIC |
Pfam:RIH_assoc
|
1912 |
2022 |
4.6e-34 |
PFAM |
low complexity region
|
2088 |
2098 |
N/A |
INTRINSIC |
transmembrane domain
|
2228 |
2250 |
N/A |
INTRINSIC |
Pfam:Ion_trans
|
2260 |
2552 |
5.1e-20 |
PFAM |
coiled coil region
|
2631 |
2686 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000079573
AA Change: T855A
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000078526 Gene: ENSMUSG00000030287 AA Change: T855A
Domain | Start | End | E-Value | Type |
low complexity region
|
68 |
80 |
N/A |
INTRINSIC |
MIR
|
112 |
166 |
1.1e-5 |
SMART |
MIR
|
198 |
254 |
5.11e-6 |
SMART |
MIR
|
261 |
369 |
3.73e-8 |
SMART |
Pfam:RYDR_ITPR
|
438 |
644 |
5.4e-75 |
PFAM |
low complexity region
|
849 |
857 |
N/A |
INTRINSIC |
Pfam:RYDR_ITPR
|
1148 |
1322 |
7.2e-60 |
PFAM |
low complexity region
|
1740 |
1752 |
N/A |
INTRINSIC |
Pfam:RIH_assoc
|
1875 |
1994 |
5.8e-35 |
PFAM |
low complexity region
|
2055 |
2065 |
N/A |
INTRINSIC |
transmembrane domain
|
2195 |
2217 |
N/A |
INTRINSIC |
transmembrane domain
|
2230 |
2249 |
N/A |
INTRINSIC |
low complexity region
|
2268 |
2279 |
N/A |
INTRINSIC |
Pfam:Ion_trans
|
2281 |
2507 |
2.4e-12 |
PFAM |
coiled coil region
|
2598 |
2653 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000131890
AA Change: T530A
PolyPhen 2
Score 0.806 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000121773 Gene: ENSMUSG00000030287 AA Change: T530A
Domain | Start | End | E-Value | Type |
Pfam:MIR
|
1 |
74 |
4.8e-22 |
PFAM |
Pfam:RYDR_ITPR
|
113 |
319 |
1.9e-76 |
PFAM |
low complexity region
|
524 |
532 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000139732
|
SMART Domains |
Protein: ENSMUSP00000119110 Gene: ENSMUSG00000030287
Domain | Start | End | E-Value | Type |
low complexity region
|
21 |
33 |
N/A |
INTRINSIC |
MIR
|
65 |
119 |
1.1e-5 |
SMART |
MIR
|
126 |
176 |
8.9e-6 |
SMART |
MIR
|
184 |
240 |
5.11e-6 |
SMART |
MIR
|
247 |
355 |
3.73e-8 |
SMART |
Pfam:RYDR_ITPR
|
424 |
630 |
3e-76 |
PFAM |
|
Meta Mutation Damage Score |
0.0737 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.3%
|
Validation Efficiency |
97% (93/96) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the inositol 1,4,5-triphosphate receptor family, whose members are second messenger intracellular calcium release channels. These proteins mediate a rise in cytoplasmic calcium in response to receptor activated production of inositol triphosphate. Inositol triphosphate receptor-mediated signaling is involved in many processes including cell migration, cell division, smooth muscle contraction, and neuronal signaling. This protein is a type 2 receptor that consists of a cytoplasmic amino-terminus that binds inositol triphosphate, six membrane-spanning helices that contribute to the ion pore, and a short cytoplasmic carboxy-terminus. A mutation in this gene has been associated with anhidrosis, suggesting that intracellular calcium release mediated by this protein is required for eccrine sweat production. [provided by RefSeq, Apr 2015] PHENOTYPE: Homozygotes for a knock-out allele are viable and fertile but show decreased sweating and disturbed calcium signaling in sweat glands. Mice homozygous for a different knock-out allele have atrial myocytes that are significantly less prone to develop proarrhythmic disturbances in calcium signaling. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 167 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057J18Rik |
A |
G |
10: 28,859,922 (GRCm39) |
|
probably null |
Het |
4932416K20Rik |
T |
A |
8: 105,523,664 (GRCm39) |
|
noncoding transcript |
Het |
Aadacl3 |
A |
G |
4: 144,182,802 (GRCm39) |
I222T |
probably damaging |
Het |
Abca13 |
G |
T |
11: 9,472,341 (GRCm39) |
G4249V |
possibly damaging |
Het |
Abcb10 |
A |
G |
8: 124,693,266 (GRCm39) |
V346A |
probably benign |
Het |
Abcc2 |
A |
T |
19: 43,807,800 (GRCm39) |
I814F |
probably damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Ankrd28 |
A |
C |
14: 31,458,787 (GRCm39) |
D335E |
probably damaging |
Het |
Ankrd44 |
T |
C |
1: 54,801,475 (GRCm39) |
H284R |
probably damaging |
Het |
Arfgef3 |
G |
T |
10: 18,467,654 (GRCm39) |
Q1849K |
probably benign |
Het |
Bach1 |
T |
A |
16: 87,519,340 (GRCm39) |
D543E |
probably damaging |
Het |
Bahcc1 |
G |
A |
11: 120,173,051 (GRCm39) |
V1558I |
probably benign |
Het |
Bbs5 |
T |
A |
2: 69,485,958 (GRCm39) |
W168R |
probably damaging |
Het |
Bcar3 |
A |
T |
3: 122,323,243 (GRCm39) |
D766V |
probably benign |
Het |
C1ra |
A |
G |
6: 124,490,727 (GRCm39) |
D40G |
probably benign |
Het |
Cbr4 |
T |
C |
8: 61,943,113 (GRCm39) |
|
probably benign |
Het |
Ccdc138 |
G |
A |
10: 58,409,465 (GRCm39) |
C598Y |
probably damaging |
Het |
Cd200r3 |
T |
A |
16: 44,778,188 (GRCm39) |
N197K |
possibly damaging |
Het |
Cenpf |
T |
A |
1: 189,383,417 (GRCm39) |
E2634D |
probably damaging |
Het |
Cisd2 |
T |
C |
3: 135,116,902 (GRCm39) |
K63R |
probably damaging |
Het |
Clca3a2 |
A |
T |
3: 144,513,112 (GRCm39) |
S478T |
possibly damaging |
Het |
Clptm1l |
T |
C |
13: 73,755,981 (GRCm39) |
M199T |
possibly damaging |
Het |
Cntnap4 |
T |
A |
8: 113,500,222 (GRCm39) |
S505T |
possibly damaging |
Het |
Cr2 |
C |
T |
1: 194,845,619 (GRCm39) |
G112D |
probably damaging |
Het |
Crb2 |
T |
A |
2: 37,683,768 (GRCm39) |
I1090N |
probably benign |
Het |
Csmd3 |
G |
T |
15: 47,484,688 (GRCm39) |
P3057Q |
probably damaging |
Het |
Ctso |
G |
A |
3: 81,861,547 (GRCm39) |
V307I |
probably damaging |
Het |
Cyp3a41b |
T |
A |
5: 145,510,461 (GRCm39) |
T138S |
probably benign |
Het |
Dctn3 |
G |
T |
4: 41,719,904 (GRCm39) |
Y67* |
probably null |
Het |
Dennd4c |
C |
A |
4: 86,738,121 (GRCm39) |
Y918* |
probably null |
Het |
Dlg5 |
C |
T |
14: 24,204,757 (GRCm39) |
G1262D |
probably damaging |
Het |
Dnaaf1 |
G |
A |
8: 120,304,100 (GRCm39) |
G46D |
probably benign |
Het |
Dnah6 |
A |
G |
6: 73,066,681 (GRCm39) |
V2563A |
probably damaging |
Het |
Dnajc13 |
A |
G |
9: 104,052,926 (GRCm39) |
Y1679H |
probably benign |
Het |
Eif2ak3 |
T |
C |
6: 70,864,877 (GRCm39) |
Y578H |
probably benign |
Het |
Endod1 |
C |
T |
9: 14,268,319 (GRCm39) |
V389M |
probably benign |
Het |
Entpd2 |
T |
G |
2: 25,289,776 (GRCm39) |
|
probably null |
Het |
Ephb4 |
T |
C |
5: 137,363,768 (GRCm39) |
L582P |
probably damaging |
Het |
Eps15 |
T |
C |
4: 109,181,414 (GRCm39) |
L316S |
possibly damaging |
Het |
Erbb4 |
G |
T |
1: 68,369,405 (GRCm39) |
T412K |
probably damaging |
Het |
Fam117a |
T |
A |
11: 95,254,896 (GRCm39) |
F90I |
probably damaging |
Het |
Fam187b |
T |
G |
7: 30,676,515 (GRCm39) |
V8G |
possibly damaging |
Het |
Far1 |
T |
A |
7: 113,138,660 (GRCm39) |
I59N |
possibly damaging |
Het |
Fbxo34 |
T |
A |
14: 47,768,326 (GRCm39) |
L562Q |
probably damaging |
Het |
Frem1 |
T |
A |
4: 82,834,865 (GRCm39) |
|
probably benign |
Het |
Gfra3 |
G |
T |
18: 34,853,245 (GRCm39) |
P10Q |
probably damaging |
Het |
Gm10619 |
T |
A |
7: 73,459,773 (GRCm39) |
|
noncoding transcript |
Het |
Gm19965 |
T |
A |
1: 116,749,626 (GRCm39) |
Y436N |
probably benign |
Het |
Gm28042 |
T |
C |
2: 119,872,535 (GRCm39) |
|
probably benign |
Het |
Gm4953 |
A |
T |
1: 158,995,988 (GRCm39) |
|
noncoding transcript |
Het |
Gm5799 |
A |
T |
14: 43,782,005 (GRCm39) |
H59L |
probably damaging |
Het |
Gmppb |
T |
A |
9: 107,927,416 (GRCm39) |
V121E |
probably benign |
Het |
Ighv7-4 |
G |
C |
12: 114,186,899 (GRCm39) |
|
probably benign |
Het |
Ipo4 |
A |
G |
14: 55,868,671 (GRCm39) |
S446P |
probably damaging |
Het |
Jaml |
T |
C |
9: 45,012,362 (GRCm39) |
I283T |
possibly damaging |
Het |
Klhl32 |
T |
C |
4: 24,649,698 (GRCm39) |
Y399C |
possibly damaging |
Het |
Lratd2 |
C |
A |
15: 60,695,793 (GRCm39) |
|
probably benign |
Het |
Lrriq1 |
G |
A |
10: 103,057,179 (GRCm39) |
T207I |
probably benign |
Het |
Lrriq3 |
A |
T |
3: 154,893,607 (GRCm39) |
H436L |
probably benign |
Het |
Mad2l1bp |
T |
C |
17: 46,459,189 (GRCm39) |
K114E |
possibly damaging |
Het |
Mamstr |
T |
C |
7: 45,291,842 (GRCm39) |
V64A |
possibly damaging |
Het |
Map4 |
T |
A |
9: 109,864,325 (GRCm39) |
S517T |
probably benign |
Het |
Matn1 |
A |
T |
4: 130,677,336 (GRCm39) |
I182F |
possibly damaging |
Het |
Mcm3 |
A |
G |
1: 20,880,380 (GRCm39) |
I484T |
probably damaging |
Het |
Med13 |
T |
A |
11: 86,169,599 (GRCm39) |
I1922F |
probably damaging |
Het |
Metap2 |
A |
G |
10: 93,704,757 (GRCm39) |
V137A |
probably damaging |
Het |
Mex3d |
A |
G |
10: 80,222,788 (GRCm39) |
V156A |
possibly damaging |
Het |
Mfsd6 |
G |
A |
1: 52,748,755 (GRCm39) |
P37S |
probably benign |
Het |
Mmut |
A |
G |
17: 41,248,242 (GRCm39) |
T90A |
probably benign |
Het |
Mrgprx1 |
A |
C |
7: 47,670,959 (GRCm39) |
S263A |
possibly damaging |
Het |
Mrtfa |
T |
C |
15: 80,989,000 (GRCm39) |
E7G |
probably benign |
Het |
Msantd5f6 |
C |
T |
4: 73,319,504 (GRCm39) |
W80* |
probably null |
Het |
Msl1 |
C |
T |
11: 98,694,795 (GRCm39) |
R505* |
probably null |
Het |
Mta2 |
T |
C |
19: 8,923,215 (GRCm39) |
S96P |
probably damaging |
Het |
Mtr |
A |
T |
13: 12,210,137 (GRCm39) |
N986K |
probably benign |
Het |
Mutyh |
C |
T |
4: 116,674,226 (GRCm39) |
T259I |
probably benign |
Het |
Myof |
T |
C |
19: 37,934,186 (GRCm39) |
T908A |
probably benign |
Het |
Nav2 |
A |
T |
7: 49,195,600 (GRCm39) |
D992V |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,090,715 (GRCm39) |
T1352A |
possibly damaging |
Het |
Nfix |
CAAAAA |
CAAAA |
8: 85,442,876 (GRCm39) |
|
probably null |
Het |
Nudt19 |
T |
C |
7: 35,255,564 (GRCm39) |
|
probably benign |
Het |
Nudt6 |
G |
A |
3: 37,459,503 (GRCm39) |
R161C |
probably benign |
Het |
Olr1 |
A |
G |
6: 129,465,053 (GRCm39) |
F141S |
possibly damaging |
Het |
Oprl1 |
G |
T |
2: 181,361,046 (GRCm39) |
M340I |
probably benign |
Het |
Or10ag57 |
T |
A |
2: 87,218,553 (GRCm39) |
V168E |
probably benign |
Het |
Or10d1 |
T |
G |
9: 39,484,154 (GRCm39) |
M134L |
probably benign |
Het |
Or11g2 |
A |
G |
14: 50,856,479 (GRCm39) |
T267A |
probably benign |
Het |
Or14j1 |
T |
C |
17: 38,146,240 (GRCm39) |
Y117H |
probably damaging |
Het |
Or1e17 |
T |
A |
11: 73,831,696 (GRCm39) |
I208K |
possibly damaging |
Het |
Or2ak6 |
T |
C |
11: 58,592,617 (GRCm39) |
V30A |
probably benign |
Het |
Or2r2 |
A |
T |
6: 42,463,613 (GRCm39) |
N171K |
probably benign |
Het |
Or4f53 |
T |
A |
2: 111,087,497 (GRCm39) |
F12L |
probably damaging |
Het |
Or5d43 |
T |
A |
2: 88,105,223 (GRCm39) |
M57L |
probably damaging |
Het |
Or5g26 |
T |
A |
2: 85,494,622 (GRCm39) |
D52V |
probably damaging |
Het |
Or9s15 |
T |
A |
1: 92,524,720 (GRCm39) |
C160S |
probably benign |
Het |
Otogl |
A |
C |
10: 107,737,197 (GRCm39) |
C72W |
probably damaging |
Het |
Pcdha11 |
T |
A |
18: 37,138,518 (GRCm39) |
I49N |
probably damaging |
Het |
Pcdha4 |
T |
A |
18: 37,087,008 (GRCm39) |
L397* |
probably null |
Het |
Pcdhb14 |
A |
G |
18: 37,581,331 (GRCm39) |
S146G |
probably benign |
Het |
Pclo |
T |
A |
5: 14,725,829 (GRCm39) |
H1562Q |
unknown |
Het |
Pcsk9 |
T |
C |
4: 106,304,766 (GRCm39) |
E434G |
probably benign |
Het |
Phc2 |
A |
G |
4: 128,645,391 (GRCm39) |
K833E |
probably damaging |
Het |
Pja2 |
A |
T |
17: 64,599,857 (GRCm39) |
S480R |
probably damaging |
Het |
Pkd1 |
G |
A |
17: 24,797,070 (GRCm39) |
G2493D |
probably damaging |
Het |
Plk5 |
G |
A |
10: 80,195,138 (GRCm39) |
V179M |
possibly damaging |
Het |
Polr1a |
G |
A |
6: 71,953,054 (GRCm39) |
V1541I |
probably benign |
Het |
Ppard |
C |
G |
17: 28,505,348 (GRCm39) |
R12G |
unknown |
Het |
Ppp1r14a |
A |
G |
7: 28,990,951 (GRCm39) |
D73G |
probably damaging |
Het |
Psd3 |
C |
T |
8: 68,573,800 (GRCm39) |
R127H |
probably benign |
Het |
Pten |
G |
T |
19: 32,735,903 (GRCm39) |
G20V |
possibly damaging |
Het |
Ptprf |
G |
A |
4: 118,067,526 (GRCm39) |
|
probably benign |
Het |
Rad54l |
T |
C |
4: 115,980,121 (GRCm39) |
D21G |
probably null |
Het |
Rgs14 |
T |
C |
13: 55,528,770 (GRCm39) |
Y304H |
probably damaging |
Het |
Rgs9 |
T |
C |
11: 109,131,694 (GRCm39) |
K346R |
probably damaging |
Het |
Rnf169 |
C |
G |
7: 99,575,653 (GRCm39) |
G314A |
probably damaging |
Het |
Rpgrip1l |
T |
A |
8: 91,996,805 (GRCm39) |
T692S |
probably damaging |
Het |
Rtf1 |
T |
C |
2: 119,505,709 (GRCm39) |
V54A |
possibly damaging |
Het |
Rtn4 |
T |
C |
11: 29,658,660 (GRCm39) |
V938A |
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,723,113 (GRCm39) |
T2509A |
probably damaging |
Het |
Ryr2 |
T |
A |
13: 11,702,818 (GRCm39) |
D2890V |
probably damaging |
Het |
Scel |
A |
C |
14: 103,820,536 (GRCm39) |
T348P |
probably benign |
Het |
Scgb1b2 |
G |
T |
7: 30,990,998 (GRCm39) |
L37I |
possibly damaging |
Het |
Sdf4 |
A |
G |
4: 156,085,178 (GRCm39) |
H171R |
possibly damaging |
Het |
Sec31a |
A |
G |
5: 100,541,222 (GRCm39) |
V295A |
probably damaging |
Het |
Semp2l2a |
T |
A |
8: 13,886,970 (GRCm39) |
I374F |
possibly damaging |
Het |
Setx |
T |
A |
2: 29,036,385 (GRCm39) |
S957T |
probably benign |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Six5 |
A |
G |
7: 18,830,894 (GRCm39) |
N507S |
probably benign |
Het |
Slc12a7 |
T |
C |
13: 73,912,011 (GRCm39) |
|
probably null |
Het |
Slc1a7 |
T |
A |
4: 107,850,237 (GRCm39) |
V116E |
probably damaging |
Het |
Slc22a1 |
A |
G |
17: 12,894,422 (GRCm39) |
L42P |
probably damaging |
Het |
Slc25a31 |
A |
T |
3: 40,675,975 (GRCm39) |
I174F |
probably damaging |
Het |
Slc31a2 |
A |
T |
4: 62,210,869 (GRCm39) |
M3L |
probably damaging |
Het |
Slco1a4 |
T |
A |
6: 141,791,223 (GRCm39) |
|
probably benign |
Het |
Smcr8 |
C |
T |
11: 60,669,436 (GRCm39) |
|
probably null |
Het |
Smg5 |
G |
T |
3: 88,262,999 (GRCm39) |
E801* |
probably null |
Het |
Smgc |
C |
A |
15: 91,738,819 (GRCm39) |
H492Q |
probably benign |
Het |
Smyd4 |
G |
T |
11: 75,294,010 (GRCm39) |
G694V |
probably damaging |
Het |
Sorcs3 |
A |
G |
19: 48,387,183 (GRCm39) |
T223A |
possibly damaging |
Het |
Stab1 |
G |
T |
14: 30,863,328 (GRCm39) |
C2119* |
probably null |
Het |
Taar9 |
A |
G |
10: 23,984,741 (GRCm39) |
I231T |
probably damaging |
Het |
Tacr2 |
A |
G |
10: 62,097,327 (GRCm39) |
Y269C |
probably damaging |
Het |
Taf3 |
T |
G |
2: 9,955,934 (GRCm39) |
K744N |
possibly damaging |
Het |
Tarbp1 |
C |
G |
8: 127,201,628 (GRCm39) |
E59D |
possibly damaging |
Het |
Tcstv1b |
T |
A |
13: 120,634,758 (GRCm39) |
S13R |
probably benign |
Het |
Tenm4 |
T |
A |
7: 96,555,452 (GRCm39) |
V2682E |
probably damaging |
Het |
Tet1 |
A |
C |
10: 62,658,442 (GRCm39) |
L1468R |
probably damaging |
Het |
Tgfb2 |
A |
T |
1: 186,361,110 (GRCm39) |
Y380* |
probably null |
Het |
Tgm5 |
T |
G |
2: 120,882,953 (GRCm39) |
K435Q |
probably damaging |
Het |
Themis |
A |
G |
10: 28,637,507 (GRCm39) |
T204A |
probably benign |
Het |
Tm4sf1 |
T |
C |
3: 57,202,100 (GRCm39) |
Y37C |
probably damaging |
Het |
Tnn |
T |
C |
1: 159,972,603 (GRCm39) |
N333S |
possibly damaging |
Het |
Tppp2 |
A |
G |
14: 52,156,805 (GRCm39) |
N61D |
probably benign |
Het |
Treml2 |
A |
G |
17: 48,616,187 (GRCm39) |
T276A |
probably benign |
Het |
Trit1 |
T |
C |
4: 122,910,431 (GRCm39) |
V10A |
probably benign |
Het |
Ttn |
T |
A |
2: 76,794,990 (GRCm39) |
|
probably benign |
Het |
Uba1y |
T |
G |
Y: 825,890 (GRCm39) |
|
probably null |
Het |
Vcam1 |
C |
G |
3: 115,909,584 (GRCm39) |
G581A |
probably damaging |
Het |
Vmn1r16 |
G |
A |
6: 57,300,175 (GRCm39) |
T149I |
probably benign |
Het |
Vmn1r209 |
T |
C |
13: 22,989,826 (GRCm39) |
D288G |
probably damaging |
Het |
Vmn1r78 |
T |
A |
7: 11,886,891 (GRCm39) |
Y167* |
probably null |
Het |
Vmn2r103 |
T |
A |
17: 20,015,338 (GRCm39) |
S493T |
probably benign |
Het |
Vmn2r105 |
T |
A |
17: 20,447,556 (GRCm39) |
M423L |
probably benign |
Het |
Vps13c |
T |
C |
9: 67,871,564 (GRCm39) |
F3244L |
probably damaging |
Het |
Zfp119b |
A |
T |
17: 56,246,642 (GRCm39) |
D149E |
probably damaging |
Het |
Zfp345 |
T |
C |
2: 150,315,228 (GRCm39) |
Y103C |
possibly damaging |
Het |
Zmym6 |
C |
T |
4: 127,017,009 (GRCm39) |
T930I |
probably benign |
Het |
|
Other mutations in Itpr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Itpr2
|
APN |
6 |
146,298,510 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00163:Itpr2
|
APN |
6 |
146,292,334 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00229:Itpr2
|
APN |
6 |
146,045,683 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00712:Itpr2
|
APN |
6 |
146,133,934 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL00952:Itpr2
|
APN |
6 |
146,060,459 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00983:Itpr2
|
APN |
6 |
146,212,479 (GRCm39) |
splice site |
probably benign |
|
IGL01012:Itpr2
|
APN |
6 |
146,246,659 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01289:Itpr2
|
APN |
6 |
146,014,033 (GRCm39) |
nonsense |
probably null |
|
IGL01411:Itpr2
|
APN |
6 |
146,277,560 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01557:Itpr2
|
APN |
6 |
146,060,474 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01669:Itpr2
|
APN |
6 |
146,081,727 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01809:Itpr2
|
APN |
6 |
146,129,079 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01814:Itpr2
|
APN |
6 |
146,134,044 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02198:Itpr2
|
APN |
6 |
146,224,725 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02218:Itpr2
|
APN |
6 |
146,141,760 (GRCm39) |
splice site |
probably benign |
|
IGL02332:Itpr2
|
APN |
6 |
146,328,040 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02425:Itpr2
|
APN |
6 |
146,292,819 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02432:Itpr2
|
APN |
6 |
146,226,671 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02726:Itpr2
|
APN |
6 |
146,277,419 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02851:Itpr2
|
APN |
6 |
146,287,477 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02933:Itpr2
|
APN |
6 |
146,214,402 (GRCm39) |
missense |
probably benign |
|
IGL03015:Itpr2
|
APN |
6 |
146,277,435 (GRCm39) |
missense |
probably benign |
|
IGL03067:Itpr2
|
APN |
6 |
146,226,680 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03093:Itpr2
|
APN |
6 |
146,281,008 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03214:Itpr2
|
APN |
6 |
146,081,742 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03275:Itpr2
|
APN |
6 |
146,060,375 (GRCm39) |
splice site |
probably benign |
|
IGL03332:Itpr2
|
APN |
6 |
146,045,647 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03352:Itpr2
|
APN |
6 |
146,058,602 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03377:Itpr2
|
APN |
6 |
146,231,256 (GRCm39) |
missense |
probably benign |
|
IGL03377:Itpr2
|
APN |
6 |
146,231,213 (GRCm39) |
missense |
probably damaging |
0.96 |
dollar_short
|
UTSW |
6 |
146,298,517 (GRCm39) |
nonsense |
probably null |
|
enfermos
|
UTSW |
6 |
146,135,504 (GRCm39) |
missense |
probably damaging |
0.98 |
Hopla
|
UTSW |
6 |
146,096,096 (GRCm39) |
missense |
probably damaging |
0.98 |
P0029:Itpr2
|
UTSW |
6 |
146,280,987 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4431001:Itpr2
|
UTSW |
6 |
146,256,218 (GRCm39) |
missense |
probably benign |
|
PIT4453001:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4504001:Itpr2
|
UTSW |
6 |
146,131,369 (GRCm39) |
missense |
probably damaging |
0.99 |
R0040:Itpr2
|
UTSW |
6 |
146,246,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Itpr2
|
UTSW |
6 |
146,246,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Itpr2
|
UTSW |
6 |
146,133,789 (GRCm39) |
splice site |
probably null |
|
R0048:Itpr2
|
UTSW |
6 |
146,133,789 (GRCm39) |
splice site |
probably null |
|
R0055:Itpr2
|
UTSW |
6 |
146,224,631 (GRCm39) |
missense |
probably benign |
0.42 |
R0055:Itpr2
|
UTSW |
6 |
146,224,631 (GRCm39) |
missense |
probably benign |
0.42 |
R0088:Itpr2
|
UTSW |
6 |
146,142,683 (GRCm39) |
missense |
probably benign |
|
R0089:Itpr2
|
UTSW |
6 |
146,251,520 (GRCm39) |
critical splice donor site |
probably null |
|
R0114:Itpr2
|
UTSW |
6 |
146,214,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Itpr2
|
UTSW |
6 |
146,141,951 (GRCm39) |
missense |
probably benign |
0.00 |
R0144:Itpr2
|
UTSW |
6 |
146,228,653 (GRCm39) |
missense |
probably damaging |
0.98 |
R0180:Itpr2
|
UTSW |
6 |
146,403,407 (GRCm39) |
start gained |
probably benign |
|
R0211:Itpr2
|
UTSW |
6 |
146,096,111 (GRCm39) |
missense |
probably benign |
0.17 |
R0305:Itpr2
|
UTSW |
6 |
146,212,601 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0367:Itpr2
|
UTSW |
6 |
146,135,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R0374:Itpr2
|
UTSW |
6 |
146,260,890 (GRCm39) |
missense |
probably benign |
0.00 |
R0391:Itpr2
|
UTSW |
6 |
146,131,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R0450:Itpr2
|
UTSW |
6 |
146,319,477 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0464:Itpr2
|
UTSW |
6 |
146,277,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R0510:Itpr2
|
UTSW |
6 |
146,319,477 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0532:Itpr2
|
UTSW |
6 |
146,013,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R0625:Itpr2
|
UTSW |
6 |
146,068,149 (GRCm39) |
missense |
probably benign |
|
R0633:Itpr2
|
UTSW |
6 |
146,275,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R0636:Itpr2
|
UTSW |
6 |
146,072,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R1086:Itpr2
|
UTSW |
6 |
146,251,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1352:Itpr2
|
UTSW |
6 |
146,013,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R1631:Itpr2
|
UTSW |
6 |
146,081,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R1655:Itpr2
|
UTSW |
6 |
146,277,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R1767:Itpr2
|
UTSW |
6 |
146,251,566 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1779:Itpr2
|
UTSW |
6 |
146,060,399 (GRCm39) |
nonsense |
probably null |
|
R1796:Itpr2
|
UTSW |
6 |
146,198,171 (GRCm39) |
missense |
probably benign |
|
R1815:Itpr2
|
UTSW |
6 |
146,260,914 (GRCm39) |
missense |
probably benign |
0.08 |
R1827:Itpr2
|
UTSW |
6 |
146,229,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R1828:Itpr2
|
UTSW |
6 |
146,229,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R1884:Itpr2
|
UTSW |
6 |
146,287,469 (GRCm39) |
missense |
probably benign |
0.16 |
R1902:Itpr2
|
UTSW |
6 |
146,131,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R1931:Itpr2
|
UTSW |
6 |
146,141,852 (GRCm39) |
missense |
probably benign |
0.41 |
R1964:Itpr2
|
UTSW |
6 |
146,013,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R2010:Itpr2
|
UTSW |
6 |
146,129,022 (GRCm39) |
splice site |
probably null |
|
R2168:Itpr2
|
UTSW |
6 |
146,013,176 (GRCm39) |
missense |
probably benign |
0.05 |
R2179:Itpr2
|
UTSW |
6 |
146,277,464 (GRCm39) |
missense |
probably benign |
|
R2290:Itpr2
|
UTSW |
6 |
146,324,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R2874:Itpr2
|
UTSW |
6 |
146,327,996 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2888:Itpr2
|
UTSW |
6 |
146,072,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R2897:Itpr2
|
UTSW |
6 |
146,224,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R2897:Itpr2
|
UTSW |
6 |
146,074,839 (GRCm39) |
missense |
probably benign |
0.03 |
R2898:Itpr2
|
UTSW |
6 |
146,224,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R2898:Itpr2
|
UTSW |
6 |
146,074,839 (GRCm39) |
missense |
probably benign |
0.03 |
R3024:Itpr2
|
UTSW |
6 |
146,081,808 (GRCm39) |
missense |
probably benign |
0.35 |
R3104:Itpr2
|
UTSW |
6 |
146,214,335 (GRCm39) |
critical splice donor site |
probably null |
|
R3607:Itpr2
|
UTSW |
6 |
146,129,099 (GRCm39) |
missense |
probably damaging |
0.98 |
R3732:Itpr2
|
UTSW |
6 |
146,284,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Itpr2
|
UTSW |
6 |
146,284,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R3733:Itpr2
|
UTSW |
6 |
146,284,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R3792:Itpr2
|
UTSW |
6 |
146,316,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R3806:Itpr2
|
UTSW |
6 |
146,133,789 (GRCm39) |
splice site |
probably null |
|
R3821:Itpr2
|
UTSW |
6 |
146,319,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R3929:Itpr2
|
UTSW |
6 |
146,275,857 (GRCm39) |
splice site |
probably null |
|
R3958:Itpr2
|
UTSW |
6 |
146,327,008 (GRCm39) |
missense |
probably damaging |
0.97 |
R3959:Itpr2
|
UTSW |
6 |
146,327,008 (GRCm39) |
missense |
probably damaging |
0.97 |
R3960:Itpr2
|
UTSW |
6 |
146,327,008 (GRCm39) |
missense |
probably damaging |
0.97 |
R3960:Itpr2
|
UTSW |
6 |
146,131,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R4074:Itpr2
|
UTSW |
6 |
146,274,742 (GRCm39) |
splice site |
probably null |
|
R4085:Itpr2
|
UTSW |
6 |
146,045,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R4114:Itpr2
|
UTSW |
6 |
146,327,008 (GRCm39) |
missense |
probably damaging |
0.97 |
R4115:Itpr2
|
UTSW |
6 |
146,327,008 (GRCm39) |
missense |
probably damaging |
0.97 |
R4588:Itpr2
|
UTSW |
6 |
146,142,694 (GRCm39) |
missense |
probably benign |
0.33 |
R4663:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4673:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4684:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4686:Itpr2
|
UTSW |
6 |
146,131,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R4713:Itpr2
|
UTSW |
6 |
146,298,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R4713:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4729:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Itpr2
|
UTSW |
6 |
146,274,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Itpr2
|
UTSW |
6 |
146,272,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R4877:Itpr2
|
UTSW |
6 |
146,226,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R4970:Itpr2
|
UTSW |
6 |
146,135,489 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4986:Itpr2
|
UTSW |
6 |
146,141,840 (GRCm39) |
missense |
probably damaging |
0.96 |
R5112:Itpr2
|
UTSW |
6 |
146,135,489 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5200:Itpr2
|
UTSW |
6 |
146,045,605 (GRCm39) |
critical splice donor site |
probably null |
|
R5224:Itpr2
|
UTSW |
6 |
146,068,149 (GRCm39) |
missense |
probably benign |
|
R5243:Itpr2
|
UTSW |
6 |
146,089,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R5348:Itpr2
|
UTSW |
6 |
146,378,191 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5393:Itpr2
|
UTSW |
6 |
146,277,653 (GRCm39) |
nonsense |
probably null |
|
R5552:Itpr2
|
UTSW |
6 |
146,195,578 (GRCm39) |
missense |
probably benign |
|
R5579:Itpr2
|
UTSW |
6 |
146,074,864 (GRCm39) |
nonsense |
probably null |
|
R5744:Itpr2
|
UTSW |
6 |
146,277,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R5825:Itpr2
|
UTSW |
6 |
146,045,647 (GRCm39) |
missense |
probably damaging |
0.98 |
R5910:Itpr2
|
UTSW |
6 |
146,231,069 (GRCm39) |
missense |
probably benign |
0.10 |
R5911:Itpr2
|
UTSW |
6 |
146,214,441 (GRCm39) |
missense |
probably benign |
0.42 |
R6044:Itpr2
|
UTSW |
6 |
146,298,449 (GRCm39) |
missense |
probably null |
0.98 |
R6072:Itpr2
|
UTSW |
6 |
146,248,609 (GRCm39) |
missense |
probably damaging |
0.98 |
R6191:Itpr2
|
UTSW |
6 |
146,229,833 (GRCm39) |
missense |
probably benign |
0.01 |
R6483:Itpr2
|
UTSW |
6 |
146,013,975 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6511:Itpr2
|
UTSW |
6 |
146,231,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R6524:Itpr2
|
UTSW |
6 |
146,246,709 (GRCm39) |
missense |
probably benign |
0.01 |
R6561:Itpr2
|
UTSW |
6 |
146,135,504 (GRCm39) |
missense |
probably damaging |
0.98 |
R6594:Itpr2
|
UTSW |
6 |
146,091,978 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6603:Itpr2
|
UTSW |
6 |
146,248,669 (GRCm39) |
missense |
probably damaging |
0.98 |
R6736:Itpr2
|
UTSW |
6 |
146,226,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R6783:Itpr2
|
UTSW |
6 |
146,287,371 (GRCm39) |
critical splice donor site |
probably null |
|
R6831:Itpr2
|
UTSW |
6 |
146,013,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R6857:Itpr2
|
UTSW |
6 |
146,298,517 (GRCm39) |
nonsense |
probably null |
|
R7103:Itpr2
|
UTSW |
6 |
146,226,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R7111:Itpr2
|
UTSW |
6 |
146,226,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R7126:Itpr2
|
UTSW |
6 |
146,259,294 (GRCm39) |
nonsense |
probably null |
|
R7165:Itpr2
|
UTSW |
6 |
146,195,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R7184:Itpr2
|
UTSW |
6 |
146,212,585 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7249:Itpr2
|
UTSW |
6 |
146,212,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:Itpr2
|
UTSW |
6 |
146,060,447 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7342:Itpr2
|
UTSW |
6 |
146,228,685 (GRCm39) |
missense |
probably damaging |
0.98 |
R7392:Itpr2
|
UTSW |
6 |
146,260,838 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7414:Itpr2
|
UTSW |
6 |
146,274,706 (GRCm39) |
missense |
probably benign |
0.06 |
R7448:Itpr2
|
UTSW |
6 |
146,231,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R7492:Itpr2
|
UTSW |
6 |
146,292,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R7515:Itpr2
|
UTSW |
6 |
146,228,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R7529:Itpr2
|
UTSW |
6 |
146,096,096 (GRCm39) |
missense |
probably damaging |
0.98 |
R7558:Itpr2
|
UTSW |
6 |
146,292,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R7650:Itpr2
|
UTSW |
6 |
146,135,492 (GRCm39) |
missense |
probably benign |
0.36 |
R7678:Itpr2
|
UTSW |
6 |
146,089,048 (GRCm39) |
missense |
probably benign |
0.00 |
R7790:Itpr2
|
UTSW |
6 |
146,126,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R7798:Itpr2
|
UTSW |
6 |
146,287,513 (GRCm39) |
missense |
probably benign |
0.06 |
R7831:Itpr2
|
UTSW |
6 |
146,193,082 (GRCm39) |
missense |
probably benign |
0.04 |
R8023:Itpr2
|
UTSW |
6 |
146,088,988 (GRCm39) |
missense |
probably damaging |
0.97 |
R8046:Itpr2
|
UTSW |
6 |
146,327,957 (GRCm39) |
missense |
probably damaging |
0.96 |
R8236:Itpr2
|
UTSW |
6 |
146,292,281 (GRCm39) |
critical splice donor site |
probably null |
|
R8241:Itpr2
|
UTSW |
6 |
146,320,013 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8245:Itpr2
|
UTSW |
6 |
146,274,604 (GRCm39) |
missense |
probably damaging |
0.98 |
R8324:Itpr2
|
UTSW |
6 |
146,229,896 (GRCm39) |
missense |
probably damaging |
0.97 |
R8339:Itpr2
|
UTSW |
6 |
146,214,396 (GRCm39) |
missense |
probably benign |
0.19 |
R8458:Itpr2
|
UTSW |
6 |
146,135,464 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8506:Itpr2
|
UTSW |
6 |
146,319,914 (GRCm39) |
critical splice donor site |
probably null |
|
R8529:Itpr2
|
UTSW |
6 |
146,231,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R8672:Itpr2
|
UTSW |
6 |
146,276,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R8755:Itpr2
|
UTSW |
6 |
146,133,926 (GRCm39) |
missense |
probably benign |
|
R8816:Itpr2
|
UTSW |
6 |
146,142,710 (GRCm39) |
missense |
probably damaging |
0.98 |
R9160:Itpr2
|
UTSW |
6 |
146,276,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R9273:Itpr2
|
UTSW |
6 |
146,226,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R9284:Itpr2
|
UTSW |
6 |
146,256,174 (GRCm39) |
missense |
probably benign |
0.01 |
R9322:Itpr2
|
UTSW |
6 |
146,226,587 (GRCm39) |
missense |
probably benign |
0.19 |
R9357:Itpr2
|
UTSW |
6 |
146,260,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R9424:Itpr2
|
UTSW |
6 |
146,212,505 (GRCm39) |
missense |
probably damaging |
0.98 |
R9438:Itpr2
|
UTSW |
6 |
146,068,166 (GRCm39) |
missense |
probably benign |
|
R9576:Itpr2
|
UTSW |
6 |
146,212,505 (GRCm39) |
missense |
probably damaging |
0.98 |
V8831:Itpr2
|
UTSW |
6 |
146,287,380 (GRCm39) |
missense |
probably damaging |
1.00 |
X0054:Itpr2
|
UTSW |
6 |
146,224,734 (GRCm39) |
missense |
probably damaging |
1.00 |
X0063:Itpr2
|
UTSW |
6 |
146,081,851 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
|
Posted On |
2017-04-14 |