Incidental Mutation 'R1513:Naip5'
ID |
168557 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Naip5
|
Ensembl Gene |
ENSMUSG00000071203 |
Gene Name |
NLR family, apoptosis inhibitory protein 5 |
Synonyms |
Birc1e, Naip-rs3, Lgn1 |
MMRRC Submission |
039560-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.079)
|
Stock # |
R1513 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
13 |
Chromosomal Location |
100348247-100382831 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 100358714 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tryptophan to Arginine
at position 841
(W841R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000058611
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000049789]
|
AlphaFold |
Q9R016 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000049789
AA Change: W841R
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000058611 Gene: ENSMUSG00000071203 AA Change: W841R
Domain | Start | End | E-Value | Type |
low complexity region
|
36 |
51 |
N/A |
INTRINSIC |
BIR
|
58 |
129 |
1.08e-19 |
SMART |
BIR
|
157 |
229 |
1.06e-36 |
SMART |
BIR
|
276 |
347 |
2.14e-32 |
SMART |
Pfam:NACHT
|
464 |
618 |
1.7e-36 |
PFAM |
low complexity region
|
851 |
862 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 98.9%
- 3x: 97.9%
- 10x: 94.7%
- 20x: 87.2%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: This locus controls resistance to Legionella pneumophila, the organism responsible for Legionnaire's disease. Cultured peritoneal macrophages from A/J mice are susceptible, supporting bacterial proliferation; other strains, e.g., C57BL/6 are resistant. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 107 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1500011B03Rik |
A |
T |
5: 114,947,334 (GRCm39) |
C64* |
probably null |
Het |
1700003H04Rik |
A |
C |
3: 124,368,985 (GRCm39) |
Y109D |
possibly damaging |
Het |
Abca15 |
A |
T |
7: 119,939,322 (GRCm39) |
I239F |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,741,167 (GRCm39) |
V99A |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,705,076 (GRCm39) |
I1578K |
probably damaging |
Het |
Ap4e1 |
G |
T |
2: 126,903,475 (GRCm39) |
K792N |
probably null |
Het |
Ap5b1 |
G |
A |
19: 5,619,892 (GRCm39) |
W437* |
probably null |
Het |
Arhgef17 |
A |
G |
7: 100,580,069 (GRCm39) |
L293P |
probably benign |
Het |
Arhgef33 |
A |
C |
17: 80,678,818 (GRCm39) |
M505L |
probably benign |
Het |
Arih1 |
T |
A |
9: 59,310,663 (GRCm39) |
R320S |
probably damaging |
Het |
Atp1b3 |
A |
T |
9: 96,246,206 (GRCm39) |
M1K |
probably null |
Het |
Bbs2 |
T |
C |
8: 94,816,472 (GRCm39) |
D130G |
possibly damaging |
Het |
Bscl2 |
G |
A |
19: 8,818,509 (GRCm39) |
R38H |
probably damaging |
Het |
Cad |
A |
G |
5: 31,226,106 (GRCm39) |
Y1102C |
probably damaging |
Het |
Cc2d1b |
G |
A |
4: 108,490,423 (GRCm39) |
R825Q |
probably damaging |
Het |
Ccdc39 |
A |
G |
3: 33,893,294 (GRCm39) |
V97A |
possibly damaging |
Het |
Ccr1 |
T |
C |
9: 123,764,510 (GRCm39) |
T7A |
probably benign |
Het |
Cd33 |
A |
G |
7: 43,181,618 (GRCm39) |
S181P |
probably damaging |
Het |
Cdc20 |
A |
C |
4: 118,290,304 (GRCm39) |
S452R |
probably damaging |
Het |
Cdk8 |
A |
T |
5: 146,233,188 (GRCm39) |
I229F |
possibly damaging |
Het |
Ces3a |
A |
T |
8: 105,776,909 (GRCm39) |
N131Y |
probably damaging |
Het |
Cgnl1 |
A |
G |
9: 71,631,872 (GRCm39) |
I493T |
probably benign |
Het |
Chia1 |
G |
A |
3: 106,039,220 (GRCm39) |
V437M |
probably benign |
Het |
Chrna2 |
G |
A |
14: 66,380,878 (GRCm39) |
R49H |
probably benign |
Het |
Clec12b |
A |
G |
6: 129,353,265 (GRCm39) |
C241R |
probably damaging |
Het |
Col11a1 |
A |
G |
3: 113,890,803 (GRCm39) |
D380G |
unknown |
Het |
Crebbp |
A |
G |
16: 3,933,749 (GRCm39) |
S948P |
probably damaging |
Het |
Dchs1 |
G |
A |
7: 105,421,278 (GRCm39) |
R381* |
probably null |
Het |
Defb19 |
A |
T |
2: 152,418,085 (GRCm39) |
*84R |
probably null |
Het |
Dnah8 |
T |
C |
17: 30,892,862 (GRCm39) |
F816L |
probably benign |
Het |
Dync2h1 |
T |
A |
9: 7,103,663 (GRCm39) |
I371F |
possibly damaging |
Het |
Ezhip |
GTCATCATCATCATC |
GTCATCATCATCATCATC |
X: 5,994,645 (GRCm39) |
|
probably benign |
Het |
Fggy |
T |
C |
4: 95,790,295 (GRCm39) |
|
probably benign |
Het |
Galnt12 |
G |
A |
4: 47,117,956 (GRCm39) |
C125Y |
probably damaging |
Het |
Gm4952 |
A |
T |
19: 12,602,039 (GRCm39) |
D149V |
probably damaging |
Het |
Gm6309 |
A |
T |
5: 146,107,393 (GRCm39) |
H37Q |
possibly damaging |
Het |
Gmnn |
A |
G |
13: 24,940,615 (GRCm39) |
L78P |
possibly damaging |
Het |
Golga4 |
C |
A |
9: 118,384,800 (GRCm39) |
Q613K |
probably benign |
Het |
Iqgap2 |
A |
T |
13: 95,766,518 (GRCm39) |
I1495K |
probably damaging |
Het |
Junb |
T |
C |
8: 85,704,758 (GRCm39) |
T101A |
probably damaging |
Het |
Kif21b |
T |
C |
1: 136,083,849 (GRCm39) |
Y699H |
probably damaging |
Het |
Klf17 |
T |
C |
4: 117,618,132 (GRCm39) |
E75G |
probably damaging |
Het |
Klra17 |
T |
C |
6: 129,849,277 (GRCm39) |
E99G |
possibly damaging |
Het |
Knop1 |
CTCTTCTTCTTCTTCTTCTTCTTC |
CTCTTCTTCTTCTTCTTCTTC |
7: 118,451,672 (GRCm39) |
|
probably benign |
Het |
Krt87 |
C |
T |
15: 101,387,538 (GRCm39) |
V167M |
probably benign |
Het |
Lce1m |
A |
G |
3: 92,925,932 (GRCm39) |
|
probably benign |
Het |
Lpin3 |
A |
T |
2: 160,746,468 (GRCm39) |
Y709F |
probably damaging |
Het |
Ltbp2 |
T |
A |
12: 84,838,718 (GRCm39) |
D1080V |
probably damaging |
Het |
Mycbp2 |
G |
A |
14: 103,441,825 (GRCm39) |
T1980I |
probably damaging |
Het |
Myo1g |
T |
A |
11: 6,465,140 (GRCm39) |
K435M |
probably damaging |
Het |
Mypn |
T |
A |
10: 63,005,147 (GRCm39) |
N320I |
probably damaging |
Het |
Ncapd2 |
A |
T |
6: 125,147,955 (GRCm39) |
M1124K |
probably damaging |
Het |
Ncf4 |
A |
G |
15: 78,146,560 (GRCm39) |
D330G |
probably benign |
Het |
Ndst3 |
C |
T |
3: 123,395,104 (GRCm39) |
V509M |
possibly damaging |
Het |
Neb |
A |
T |
2: 52,117,256 (GRCm39) |
D4105E |
probably damaging |
Het |
Nfix |
G |
A |
8: 85,453,155 (GRCm39) |
R300C |
probably damaging |
Het |
Nsrp1 |
A |
T |
11: 76,937,445 (GRCm39) |
F250L |
probably benign |
Het |
Or11g7 |
A |
G |
14: 50,691,138 (GRCm39) |
I210V |
probably benign |
Het |
Or4l15 |
T |
C |
14: 50,198,558 (GRCm39) |
|
probably null |
Het |
Or52d1 |
C |
T |
7: 103,755,671 (GRCm39) |
L62F |
probably benign |
Het |
Or52k2 |
G |
T |
7: 102,254,509 (GRCm39) |
G316V |
probably benign |
Het |
Or5m12 |
A |
T |
2: 85,735,015 (GRCm39) |
Y128N |
probably damaging |
Het |
Or8k3b |
C |
T |
2: 86,521,141 (GRCm39) |
M59I |
possibly damaging |
Het |
Oxr1 |
A |
G |
15: 41,660,870 (GRCm39) |
D67G |
probably damaging |
Het |
P2ry12 |
A |
T |
3: 59,125,498 (GRCm39) |
I59N |
probably damaging |
Het |
Pcdhb12 |
G |
T |
18: 37,570,111 (GRCm39) |
G419V |
probably damaging |
Het |
Pdzd2 |
G |
T |
15: 12,373,915 (GRCm39) |
S2073R |
possibly damaging |
Het |
Pex5l |
C |
A |
3: 33,069,162 (GRCm39) |
E112* |
probably null |
Het |
Plaur |
A |
G |
7: 24,172,016 (GRCm39) |
D163G |
probably benign |
Het |
Plk2 |
A |
G |
13: 110,536,622 (GRCm39) |
Y638C |
probably benign |
Het |
Ppp1r15b |
A |
G |
1: 133,061,088 (GRCm39) |
N535S |
probably benign |
Het |
Ppp2r1b |
T |
C |
9: 50,781,445 (GRCm39) |
L21P |
probably damaging |
Het |
Prkar2a |
G |
A |
9: 108,605,469 (GRCm39) |
V176I |
possibly damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Rag1 |
A |
G |
2: 101,473,336 (GRCm39) |
M602T |
possibly damaging |
Het |
Rb1 |
A |
G |
14: 73,559,524 (GRCm39) |
V60A |
probably benign |
Het |
Rgs20 |
T |
A |
1: 4,982,560 (GRCm39) |
I303F |
probably damaging |
Het |
Rnf43 |
T |
A |
11: 87,620,257 (GRCm39) |
I240N |
probably damaging |
Het |
Romo1 |
G |
A |
2: 155,986,433 (GRCm39) |
V19M |
probably benign |
Het |
Ryr1 |
A |
G |
7: 28,770,046 (GRCm39) |
S2676P |
probably damaging |
Het |
Ryr3 |
G |
A |
2: 112,539,542 (GRCm39) |
Q3233* |
probably null |
Het |
Skic2 |
G |
T |
17: 35,066,420 (GRCm39) |
P188T |
probably damaging |
Het |
Slc26a6 |
A |
G |
9: 108,733,035 (GRCm39) |
R5G |
probably benign |
Het |
Slc33a1 |
A |
G |
3: 63,871,376 (GRCm39) |
L79P |
probably damaging |
Het |
Snx31 |
G |
A |
15: 36,545,745 (GRCm39) |
R91C |
probably damaging |
Het |
Tecpr2 |
T |
C |
12: 110,921,234 (GRCm39) |
I1269T |
possibly damaging |
Het |
Tjap1 |
G |
T |
17: 46,572,368 (GRCm39) |
D89E |
probably benign |
Het |
Tmem53 |
A |
T |
4: 117,123,090 (GRCm39) |
Q39L |
probably damaging |
Het |
Tmod1 |
G |
T |
4: 46,083,549 (GRCm39) |
V95F |
possibly damaging |
Het |
Trim30c |
A |
C |
7: 104,031,896 (GRCm39) |
H306Q |
probably benign |
Het |
Trpm3 |
A |
T |
19: 22,964,236 (GRCm39) |
M1244L |
possibly damaging |
Het |
Tspan32 |
A |
G |
7: 142,558,886 (GRCm39) |
I14V |
probably null |
Het |
Ube4b |
A |
G |
4: 149,436,035 (GRCm39) |
V695A |
probably benign |
Het |
Ubxn11 |
G |
A |
4: 133,851,452 (GRCm39) |
|
probably null |
Het |
Ugt3a1 |
A |
G |
15: 9,361,610 (GRCm39) |
I129V |
probably benign |
Het |
Vmn1r45 |
A |
G |
6: 89,910,058 (GRCm39) |
V304A |
probably damaging |
Het |
Vmn2r124 |
A |
T |
17: 18,283,535 (GRCm39) |
S410C |
probably damaging |
Het |
Vmn2r15 |
T |
A |
5: 109,441,195 (GRCm39) |
D221V |
probably damaging |
Het |
Vmn2r79 |
G |
A |
7: 86,686,652 (GRCm39) |
V678I |
probably benign |
Het |
Vps13b |
A |
T |
15: 35,438,876 (GRCm39) |
R319* |
probably null |
Het |
Wdr95 |
G |
A |
5: 149,522,759 (GRCm39) |
R639Q |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,341,874 (GRCm39) |
I1372V |
probably benign |
Het |
Xpo5 |
T |
A |
17: 46,537,906 (GRCm39) |
M611K |
probably benign |
Het |
Zfat |
A |
G |
15: 68,084,529 (GRCm39) |
C121R |
probably damaging |
Het |
Zfp382 |
A |
T |
7: 29,832,721 (GRCm39) |
Y124F |
probably benign |
Het |
Zfp512b |
A |
G |
2: 181,230,982 (GRCm39) |
F371S |
probably benign |
Het |
Zfy2 |
A |
G |
Y: 2,116,185 (GRCm39) |
V285A |
probably benign |
Het |
|
Other mutations in Naip5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00096:Naip5
|
APN |
13 |
100,382,683 (GRCm39) |
nonsense |
probably null |
|
IGL00493:Naip5
|
APN |
13 |
100,367,279 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01294:Naip5
|
APN |
13 |
100,353,588 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01405:Naip5
|
APN |
13 |
100,358,453 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01568:Naip5
|
APN |
13 |
100,353,609 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01804:Naip5
|
APN |
13 |
100,358,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02012:Naip5
|
APN |
13 |
100,359,847 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02183:Naip5
|
APN |
13 |
100,358,150 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02449:Naip5
|
APN |
13 |
100,358,683 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02815:Naip5
|
APN |
13 |
100,359,239 (GRCm39) |
missense |
probably benign |
|
IGL02992:Naip5
|
APN |
13 |
100,359,536 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03027:Naip5
|
APN |
13 |
100,359,524 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03234:Naip5
|
APN |
13 |
100,349,135 (GRCm39) |
missense |
probably damaging |
1.00 |
inwood2
|
UTSW |
13 |
100,359,522 (GRCm39) |
nonsense |
probably null |
|
inwood3
|
UTSW |
13 |
100,358,411 (GRCm39) |
nonsense |
probably null |
|
Nuchal
|
UTSW |
13 |
100,351,171 (GRCm39) |
missense |
possibly damaging |
0.82 |
PIT4131001:Naip5
|
UTSW |
13 |
100,356,268 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4131001:Naip5
|
UTSW |
13 |
100,356,247 (GRCm39) |
missense |
probably benign |
|
R0001:Naip5
|
UTSW |
13 |
100,359,622 (GRCm39) |
missense |
probably benign |
|
R0001:Naip5
|
UTSW |
13 |
100,351,158 (GRCm39) |
critical splice donor site |
probably null |
|
R0462:Naip5
|
UTSW |
13 |
100,358,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R0636:Naip5
|
UTSW |
13 |
100,356,196 (GRCm39) |
missense |
probably benign |
|
R0674:Naip5
|
UTSW |
13 |
100,359,707 (GRCm39) |
missense |
probably benign |
0.04 |
R0764:Naip5
|
UTSW |
13 |
100,353,613 (GRCm39) |
missense |
probably benign |
0.03 |
R0837:Naip5
|
UTSW |
13 |
100,367,251 (GRCm39) |
missense |
probably benign |
|
R1179:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R1302:Naip5
|
UTSW |
13 |
100,358,099 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1441:Naip5
|
UTSW |
13 |
100,356,225 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1638:Naip5
|
UTSW |
13 |
100,349,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R1651:Naip5
|
UTSW |
13 |
100,358,419 (GRCm39) |
missense |
probably benign |
0.41 |
R1707:Naip5
|
UTSW |
13 |
100,379,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Naip5
|
UTSW |
13 |
100,359,726 (GRCm39) |
nonsense |
probably null |
|
R1836:Naip5
|
UTSW |
13 |
100,356,195 (GRCm39) |
missense |
probably benign |
0.18 |
R1972:Naip5
|
UTSW |
13 |
100,349,278 (GRCm39) |
missense |
probably damaging |
0.98 |
R2080:Naip5
|
UTSW |
13 |
100,358,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R2333:Naip5
|
UTSW |
13 |
100,359,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R2348:Naip5
|
UTSW |
13 |
100,356,246 (GRCm39) |
missense |
probably benign |
0.01 |
R3055:Naip5
|
UTSW |
13 |
100,358,386 (GRCm39) |
missense |
probably benign |
0.23 |
R3401:Naip5
|
UTSW |
13 |
100,358,411 (GRCm39) |
nonsense |
probably null |
|
R3723:Naip5
|
UTSW |
13 |
100,359,522 (GRCm39) |
nonsense |
probably null |
|
R3775:Naip5
|
UTSW |
13 |
100,359,883 (GRCm39) |
missense |
probably benign |
0.00 |
R3775:Naip5
|
UTSW |
13 |
100,359,902 (GRCm39) |
missense |
probably benign |
0.00 |
R4019:Naip5
|
UTSW |
13 |
100,359,883 (GRCm39) |
missense |
probably benign |
0.00 |
R4019:Naip5
|
UTSW |
13 |
100,359,902 (GRCm39) |
missense |
probably benign |
0.00 |
R4020:Naip5
|
UTSW |
13 |
100,359,902 (GRCm39) |
missense |
probably benign |
0.00 |
R4020:Naip5
|
UTSW |
13 |
100,359,883 (GRCm39) |
missense |
probably benign |
0.00 |
R4074:Naip5
|
UTSW |
13 |
100,382,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R4082:Naip5
|
UTSW |
13 |
100,382,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R4105:Naip5
|
UTSW |
13 |
100,356,247 (GRCm39) |
missense |
probably benign |
|
R4227:Naip5
|
UTSW |
13 |
100,349,276 (GRCm39) |
missense |
probably damaging |
0.99 |
R4639:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4640:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4641:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4644:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4645:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4700:Naip5
|
UTSW |
13 |
100,359,922 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4727:Naip5
|
UTSW |
13 |
100,358,378 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4729:Naip5
|
UTSW |
13 |
100,358,639 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4816:Naip5
|
UTSW |
13 |
100,356,189 (GRCm39) |
missense |
probably benign |
0.32 |
R4816:Naip5
|
UTSW |
13 |
100,356,195 (GRCm39) |
missense |
probably benign |
0.01 |
R4816:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R4869:Naip5
|
UTSW |
13 |
100,381,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5162:Naip5
|
UTSW |
13 |
100,359,914 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5244:Naip5
|
UTSW |
13 |
100,382,170 (GRCm39) |
missense |
probably benign |
0.08 |
R5411:Naip5
|
UTSW |
13 |
100,382,254 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5632:Naip5
|
UTSW |
13 |
100,367,170 (GRCm39) |
splice site |
probably null |
|
R5760:Naip5
|
UTSW |
13 |
100,379,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R5916:Naip5
|
UTSW |
13 |
100,359,209 (GRCm39) |
missense |
probably benign |
0.02 |
R6302:Naip5
|
UTSW |
13 |
100,359,674 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6304:Naip5
|
UTSW |
13 |
100,359,674 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6411:Naip5
|
UTSW |
13 |
100,359,913 (GRCm39) |
missense |
probably benign |
0.01 |
R6474:Naip5
|
UTSW |
13 |
100,351,171 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6499:Naip5
|
UTSW |
13 |
100,358,102 (GRCm39) |
missense |
probably benign |
|
R6544:Naip5
|
UTSW |
13 |
100,359,652 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6827:Naip5
|
UTSW |
13 |
100,382,437 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6954:Naip5
|
UTSW |
13 |
100,359,922 (GRCm39) |
missense |
probably damaging |
0.99 |
R7052:Naip5
|
UTSW |
13 |
100,358,855 (GRCm39) |
missense |
probably benign |
0.01 |
R7138:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R7141:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R7375:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7375:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7401:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7401:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7447:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7447:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7466:Naip5
|
UTSW |
13 |
100,358,494 (GRCm39) |
nonsense |
probably null |
|
R7491:Naip5
|
UTSW |
13 |
100,353,579 (GRCm39) |
missense |
probably benign |
0.18 |
R7559:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7559:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7562:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7562:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7588:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7588:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7589:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7589:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7590:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7590:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7742:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R7886:Naip5
|
UTSW |
13 |
100,382,689 (GRCm39) |
missense |
probably benign |
0.28 |
R7996:Naip5
|
UTSW |
13 |
100,358,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R8026:Naip5
|
UTSW |
13 |
100,382,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R8046:Naip5
|
UTSW |
13 |
100,358,741 (GRCm39) |
missense |
probably benign |
|
R8319:Naip5
|
UTSW |
13 |
100,358,167 (GRCm39) |
missense |
probably benign |
0.12 |
R8471:Naip5
|
UTSW |
13 |
100,358,153 (GRCm39) |
missense |
probably damaging |
0.99 |
R8480:Naip5
|
UTSW |
13 |
100,358,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R8496:Naip5
|
UTSW |
13 |
100,349,247 (GRCm39) |
missense |
probably benign |
0.00 |
R8500:Naip5
|
UTSW |
13 |
100,359,220 (GRCm39) |
missense |
probably damaging |
0.98 |
R8712:Naip5
|
UTSW |
13 |
100,359,604 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8780:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R8781:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R8788:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R8817:Naip5
|
UTSW |
13 |
100,349,207 (GRCm39) |
missense |
probably benign |
0.01 |
R8833:Naip5
|
UTSW |
13 |
100,359,442 (GRCm39) |
missense |
probably damaging |
0.97 |
R8835:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R8958:Naip5
|
UTSW |
13 |
100,354,117 (GRCm39) |
nonsense |
probably null |
|
R9031:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9032:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9074:Naip5
|
UTSW |
13 |
100,358,264 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9098:Naip5
|
UTSW |
13 |
100,366,127 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9204:Naip5
|
UTSW |
13 |
100,359,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R9223:Naip5
|
UTSW |
13 |
100,364,184 (GRCm39) |
missense |
probably benign |
0.05 |
R9358:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9389:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9403:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9518:Naip5
|
UTSW |
13 |
100,358,367 (GRCm39) |
missense |
probably benign |
|
R9568:Naip5
|
UTSW |
13 |
100,359,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9568:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9569:Naip5
|
UTSW |
13 |
100,359,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9569:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9570:Naip5
|
UTSW |
13 |
100,359,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9572:Naip5
|
UTSW |
13 |
100,359,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9581:Naip5
|
UTSW |
13 |
100,351,194 (GRCm39) |
missense |
probably benign |
0.11 |
R9627:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9725:Naip5
|
UTSW |
13 |
100,358,784 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9763:Naip5
|
UTSW |
13 |
100,367,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R9764:Naip5
|
UTSW |
13 |
100,367,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R9765:Naip5
|
UTSW |
13 |
100,367,269 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Predicted Primers |
PCR Primer
(F):5'- AAGACTTCCATGAGGACCTGGAGC -3'
(R):5'- GACAAATCGACTCACCTCTGAAGGC -3'
Sequencing Primer
(F):5'- CTCAACAGTAACAGGCTTTCTGG -3'
(R):5'- CTCTGAAGGCAATAAACTCCTTTAAC -3'
|
Posted On |
2014-04-13 |