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, Lgn1, Naip-rs3 |
| MMRRC Submission |
039560-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.101)
|
| Stock # |
R1513 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
13 |
| Chromosomal Location |
100211739-100246323 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 100222206 bp (GRCm38)
|
| 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: 114,809,273 (GRCm38) |
C64* |
probably null |
Het |
| 1700003H04Rik |
A |
C |
3: 124,575,336 (GRCm38) |
Y109D |
possibly damaging |
Het |
| Abca15 |
A |
T |
7: 120,340,099 (GRCm38) |
I239F |
probably damaging |
Het |
| Adgrv1 |
A |
T |
13: 81,556,957 (GRCm38) |
I1578K |
probably damaging |
Het |
| Adgrv1 |
A |
G |
13: 81,593,048 (GRCm38) |
V99A |
probably damaging |
Het |
| Ap4e1 |
G |
T |
2: 127,061,555 (GRCm38) |
K792N |
probably null |
Het |
| Ap5b1 |
G |
A |
19: 5,569,864 (GRCm38) |
W437* |
probably null |
Het |
| Arhgef17 |
A |
G |
7: 100,930,862 (GRCm38) |
L293P |
probably benign |
Het |
| Arhgef33 |
A |
C |
17: 80,371,389 (GRCm38) |
M505L |
probably benign |
Het |
| Arih1 |
T |
A |
9: 59,403,380 (GRCm38) |
R320S |
probably damaging |
Het |
| Atp1b3 |
A |
T |
9: 96,364,153 (GRCm38) |
M1K |
probably null |
Het |
| Bbs2 |
T |
C |
8: 94,089,844 (GRCm38) |
D130G |
possibly damaging |
Het |
| Bscl2 |
G |
A |
19: 8,841,145 (GRCm38) |
R38H |
probably damaging |
Het |
| Cad |
A |
G |
5: 31,068,762 (GRCm38) |
Y1102C |
probably damaging |
Het |
| Cc2d1b |
G |
A |
4: 108,633,226 (GRCm38) |
R825Q |
probably damaging |
Het |
| Ccdc39 |
A |
G |
3: 33,839,145 (GRCm38) |
V97A |
possibly damaging |
Het |
| Ccr1 |
T |
C |
9: 123,964,473 (GRCm38) |
T7A |
probably benign |
Het |
| Cd33 |
A |
G |
7: 43,532,194 (GRCm38) |
S181P |
probably damaging |
Het |
| Cdc20 |
A |
C |
4: 118,433,107 (GRCm38) |
S452R |
probably damaging |
Het |
| Cdk8 |
A |
T |
5: 146,296,378 (GRCm38) |
I229F |
possibly damaging |
Het |
| Ces3a |
A |
T |
8: 105,050,277 (GRCm38) |
N131Y |
probably damaging |
Het |
| Cgnl1 |
A |
G |
9: 71,724,590 (GRCm38) |
I493T |
probably benign |
Het |
| Chia1 |
G |
A |
3: 106,131,904 (GRCm38) |
V437M |
probably benign |
Het |
| Chrna2 |
G |
A |
14: 66,143,429 (GRCm38) |
R49H |
probably benign |
Het |
| Clec12b |
A |
G |
6: 129,376,302 (GRCm38) |
C241R |
probably damaging |
Het |
| Col11a1 |
A |
G |
3: 114,097,154 (GRCm38) |
D380G |
unknown |
Het |
| Crebbp |
A |
G |
16: 4,115,885 (GRCm38) |
S948P |
probably damaging |
Het |
| Dchs1 |
G |
A |
7: 105,772,071 (GRCm38) |
R381* |
probably null |
Het |
| Defb19 |
A |
T |
2: 152,576,165 (GRCm38) |
*84R |
probably null |
Het |
| Dnah8 |
T |
C |
17: 30,673,888 (GRCm38) |
F816L |
probably benign |
Het |
| Dync2h1 |
T |
A |
9: 7,103,663 (GRCm38) |
I371F |
possibly damaging |
Het |
| Ezhip |
GTCATCATCATCATC |
GTCATCATCATCATCATC |
X: 6,082,591 (GRCm38) |
|
probably benign |
Het |
| Fggy |
T |
C |
4: 95,902,058 (GRCm38) |
|
probably benign |
Het |
| Galnt12 |
G |
A |
4: 47,117,956 (GRCm38) |
C125Y |
probably damaging |
Het |
| Gm4952 |
A |
T |
19: 12,624,675 (GRCm38) |
D149V |
probably damaging |
Het |
| Gm6309 |
A |
T |
5: 146,170,583 (GRCm38) |
H37Q |
possibly damaging |
Het |
| Gmnn |
A |
G |
13: 24,756,632 (GRCm38) |
L78P |
possibly damaging |
Het |
| Golga4 |
C |
A |
9: 118,555,732 (GRCm38) |
Q613K |
probably benign |
Het |
| Iqgap2 |
A |
T |
13: 95,630,010 (GRCm38) |
I1495K |
probably damaging |
Het |
| Junb |
T |
C |
8: 84,978,129 (GRCm38) |
T101A |
probably damaging |
Het |
| Kif21b |
T |
C |
1: 136,156,111 (GRCm38) |
Y699H |
probably damaging |
Het |
| Klf17 |
T |
C |
4: 117,760,935 (GRCm38) |
E75G |
probably damaging |
Het |
| Klra17 |
T |
C |
6: 129,872,314 (GRCm38) |
E99G |
possibly damaging |
Het |
| Knop1 |
CTCTTCTTCTTCTTCTTCTTCTTC |
CTCTTCTTCTTCTTCTTCTTC |
7: 118,852,449 (GRCm38) |
|
probably benign |
Het |
| Krt83 |
C |
T |
15: 101,489,657 (GRCm38) |
V167M |
probably benign |
Het |
| Lce1m |
A |
G |
3: 93,018,625 (GRCm38) |
|
probably benign |
Het |
| Lpin3 |
A |
T |
2: 160,904,548 (GRCm38) |
Y709F |
probably damaging |
Het |
| Ltbp2 |
T |
A |
12: 84,791,944 (GRCm38) |
D1080V |
probably damaging |
Het |
| Mycbp2 |
G |
A |
14: 103,204,389 (GRCm38) |
T1980I |
probably damaging |
Het |
| Myo1g |
T |
A |
11: 6,515,140 (GRCm38) |
K435M |
probably damaging |
Het |
| Mypn |
T |
A |
10: 63,169,368 (GRCm38) |
N320I |
probably damaging |
Het |
| Ncapd2 |
A |
T |
6: 125,170,992 (GRCm38) |
M1124K |
probably damaging |
Het |
| Ncf4 |
A |
G |
15: 78,262,360 (GRCm38) |
D330G |
probably benign |
Het |
| Ndst3 |
C |
T |
3: 123,601,455 (GRCm38) |
V509M |
possibly damaging |
Het |
| Neb |
A |
T |
2: 52,227,244 (GRCm38) |
D4105E |
probably damaging |
Het |
| Nfix |
G |
A |
8: 84,726,526 (GRCm38) |
R300C |
probably damaging |
Het |
| Nsrp1 |
A |
T |
11: 77,046,619 (GRCm38) |
F250L |
probably benign |
Het |
| Or11g7 |
A |
G |
14: 50,453,681 (GRCm38) |
I210V |
probably benign |
Het |
| Or4l15 |
T |
C |
14: 49,961,101 (GRCm38) |
|
probably null |
Het |
| Or52d1 |
C |
T |
7: 104,106,464 (GRCm38) |
L62F |
probably benign |
Het |
| Or52k2 |
G |
T |
7: 102,605,302 (GRCm38) |
G316V |
probably benign |
Het |
| Or5m12 |
A |
T |
2: 85,904,671 (GRCm38) |
Y128N |
probably damaging |
Het |
| Or8k3b |
C |
T |
2: 86,690,797 (GRCm38) |
M59I |
possibly damaging |
Het |
| Oxr1 |
A |
G |
15: 41,797,474 (GRCm38) |
D67G |
probably damaging |
Het |
| P2ry12 |
A |
T |
3: 59,218,077 (GRCm38) |
I59N |
probably damaging |
Het |
| Pcdhb12 |
G |
T |
18: 37,437,058 (GRCm38) |
G419V |
probably damaging |
Het |
| Pdzd2 |
G |
T |
15: 12,373,829 (GRCm38) |
S2073R |
possibly damaging |
Het |
| Pex5l |
C |
A |
3: 33,015,013 (GRCm38) |
E112* |
probably null |
Het |
| Plaur |
A |
G |
7: 24,472,591 (GRCm38) |
D163G |
probably benign |
Het |
| Plk2 |
A |
G |
13: 110,400,088 (GRCm38) |
Y638C |
probably benign |
Het |
| Ppp1r15b |
A |
G |
1: 133,133,350 (GRCm38) |
N535S |
probably benign |
Het |
| Ppp2r1b |
T |
C |
9: 50,870,145 (GRCm38) |
L21P |
probably damaging |
Het |
| Prkar2a |
G |
A |
9: 108,728,270 (GRCm38) |
V176I |
possibly damaging |
Het |
| Ptpro |
T |
A |
6: 137,443,594 (GRCm38) |
V1007D |
probably damaging |
Het |
| Rag1 |
A |
G |
2: 101,642,991 (GRCm38) |
M602T |
possibly damaging |
Het |
| Rb1 |
A |
G |
14: 73,322,084 (GRCm38) |
V60A |
probably benign |
Het |
| Rgs20 |
T |
A |
1: 4,912,337 (GRCm38) |
I303F |
probably damaging |
Het |
| Rnf43 |
T |
A |
11: 87,729,431 (GRCm38) |
I240N |
probably damaging |
Het |
| Romo1 |
G |
A |
2: 156,144,513 (GRCm38) |
V19M |
probably benign |
Het |
| Ryr1 |
A |
G |
7: 29,070,621 (GRCm38) |
S2676P |
probably damaging |
Het |
| Ryr3 |
G |
A |
2: 112,709,197 (GRCm38) |
Q3233* |
probably null |
Het |
| Skic2 |
G |
T |
17: 34,847,444 (GRCm38) |
P188T |
probably damaging |
Het |
| Slc26a6 |
A |
G |
9: 108,855,836 (GRCm38) |
R5G |
probably benign |
Het |
| Slc33a1 |
A |
G |
3: 63,963,955 (GRCm38) |
L79P |
probably damaging |
Het |
| Snx31 |
G |
A |
15: 36,545,600 (GRCm38) |
R91C |
probably damaging |
Het |
| Tecpr2 |
T |
C |
12: 110,954,800 (GRCm38) |
I1269T |
possibly damaging |
Het |
| Tjap1 |
G |
T |
17: 46,261,442 (GRCm38) |
D89E |
probably benign |
Het |
| Tmem53 |
A |
T |
4: 117,265,893 (GRCm38) |
Q39L |
probably damaging |
Het |
| Tmod1 |
G |
T |
4: 46,083,549 (GRCm38) |
V95F |
possibly damaging |
Het |
| Trim30c |
A |
C |
7: 104,382,689 (GRCm38) |
H306Q |
probably benign |
Het |
| Trpm3 |
A |
T |
19: 22,986,872 (GRCm38) |
M1244L |
possibly damaging |
Het |
| Tspan32 |
A |
G |
7: 143,005,149 (GRCm38) |
I14V |
probably null |
Het |
| Ube4b |
A |
G |
4: 149,351,578 (GRCm38) |
V695A |
probably benign |
Het |
| Ubxn11 |
G |
A |
4: 134,124,141 (GRCm38) |
|
probably null |
Het |
| Ugt3a2 |
A |
G |
15: 9,361,524 (GRCm38) |
I129V |
probably benign |
Het |
| Vmn1r45 |
A |
G |
6: 89,933,076 (GRCm38) |
V304A |
probably damaging |
Het |
| Vmn2r124 |
A |
T |
17: 18,063,273 (GRCm38) |
S410C |
probably damaging |
Het |
| Vmn2r15 |
T |
A |
5: 109,293,329 (GRCm38) |
D221V |
probably damaging |
Het |
| Vmn2r79 |
G |
A |
7: 87,037,444 (GRCm38) |
V678I |
probably benign |
Het |
| Vps13b |
A |
T |
15: 35,438,730 (GRCm38) |
R319* |
probably null |
Het |
| Wdr95 |
G |
A |
5: 149,599,294 (GRCm38) |
R639Q |
probably benign |
Het |
| Xirp2 |
A |
G |
2: 67,511,530 (GRCm38) |
I1372V |
probably benign |
Het |
| Xpo5 |
T |
A |
17: 46,226,980 (GRCm38) |
M611K |
probably benign |
Het |
| Zfat |
A |
G |
15: 68,212,680 (GRCm38) |
C121R |
probably damaging |
Het |
| Zfp382 |
A |
T |
7: 30,133,296 (GRCm38) |
Y124F |
probably benign |
Het |
| Zfp512b |
A |
G |
2: 181,589,189 (GRCm38) |
F371S |
probably benign |
Het |
| Zfy2 |
A |
G |
Y: 2,116,185 (GRCm38) |
V285A |
probably benign |
Het |
|
| Other mutations in Naip5 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00096:Naip5
|
APN |
13 |
100,246,175 (GRCm38) |
nonsense |
probably null |
|
|
IGL00493:Naip5
|
APN |
13 |
100,230,771 (GRCm38) |
missense |
probably damaging |
0.96 |
|
IGL01294:Naip5
|
APN |
13 |
100,217,080 (GRCm38) |
missense |
probably damaging |
0.99 |
|
IGL01405:Naip5
|
APN |
13 |
100,221,945 (GRCm38) |
missense |
probably benign |
0.11 |
|
IGL01568:Naip5
|
APN |
13 |
100,217,101 (GRCm38) |
missense |
probably benign |
0.26 |
|
IGL01804:Naip5
|
APN |
13 |
100,221,584 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02012:Naip5
|
APN |
13 |
100,223,339 (GRCm38) |
missense |
probably benign |
0.01 |
|
IGL02183:Naip5
|
APN |
13 |
100,221,642 (GRCm38) |
missense |
probably benign |
0.41 |
|
IGL02449:Naip5
|
APN |
13 |
100,222,175 (GRCm38) |
missense |
probably benign |
0.34 |
|
IGL02815:Naip5
|
APN |
13 |
100,222,731 (GRCm38) |
missense |
probably benign |
|
|
IGL02992:Naip5
|
APN |
13 |
100,223,028 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL03027:Naip5
|
APN |
13 |
100,223,016 (GRCm38) |
missense |
probably benign |
0.00 |
|
IGL03234:Naip5
|
APN |
13 |
100,212,627 (GRCm38) |
missense |
probably damaging |
1.00 |
|
inwood2
|
UTSW |
13 |
100,223,014 (GRCm38) |
nonsense |
probably null |
|
|
inwood3
|
UTSW |
13 |
100,221,903 (GRCm38) |
nonsense |
probably null |
|
|
Nuchal
|
UTSW |
13 |
100,214,663 (GRCm38) |
missense |
possibly damaging |
0.82 |
|
PIT4131001:Naip5
|
UTSW |
13 |
100,219,760 (GRCm38) |
missense |
probably benign |
0.00 |
|
PIT4131001:Naip5
|
UTSW |
13 |
100,219,739 (GRCm38) |
missense |
probably benign |
|
|
R0001:Naip5
|
UTSW |
13 |
100,223,114 (GRCm38) |
missense |
probably benign |
|
|
R0001:Naip5
|
UTSW |
13 |
100,214,650 (GRCm38) |
critical splice donor site |
probably null |
|
|
R0462:Naip5
|
UTSW |
13 |
100,221,732 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0636:Naip5
|
UTSW |
13 |
100,219,688 (GRCm38) |
missense |
probably benign |
|
|
R0674:Naip5
|
UTSW |
13 |
100,223,199 (GRCm38) |
missense |
probably benign |
0.04 |
|
R0764:Naip5
|
UTSW |
13 |
100,217,105 (GRCm38) |
missense |
probably benign |
0.03 |
|
R0837:Naip5
|
UTSW |
13 |
100,230,743 (GRCm38) |
missense |
probably benign |
|
|
R1179:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R1302:Naip5
|
UTSW |
13 |
100,221,591 (GRCm38) |
missense |
possibly damaging |
0.91 |
|
R1441:Naip5
|
UTSW |
13 |
100,219,717 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R1638:Naip5
|
UTSW |
13 |
100,212,669 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1651:Naip5
|
UTSW |
13 |
100,221,911 (GRCm38) |
missense |
probably benign |
0.41 |
|
R1707:Naip5
|
UTSW |
13 |
100,242,855 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1835:Naip5
|
UTSW |
13 |
100,223,218 (GRCm38) |
nonsense |
probably null |
|
|
R1836:Naip5
|
UTSW |
13 |
100,219,687 (GRCm38) |
missense |
probably benign |
0.18 |
|
R1972:Naip5
|
UTSW |
13 |
100,212,770 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R2080:Naip5
|
UTSW |
13 |
100,221,533 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2333:Naip5
|
UTSW |
13 |
100,223,171 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2348:Naip5
|
UTSW |
13 |
100,219,738 (GRCm38) |
missense |
probably benign |
0.01 |
|
R3055:Naip5
|
UTSW |
13 |
100,221,878 (GRCm38) |
missense |
probably benign |
0.23 |
|
R3401:Naip5
|
UTSW |
13 |
100,221,903 (GRCm38) |
nonsense |
probably null |
|
|
R3723:Naip5
|
UTSW |
13 |
100,223,014 (GRCm38) |
nonsense |
probably null |
|
|
R3775:Naip5
|
UTSW |
13 |
100,223,375 (GRCm38) |
missense |
probably benign |
0.00 |
|
R3775:Naip5
|
UTSW |
13 |
100,223,394 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4019:Naip5
|
UTSW |
13 |
100,223,375 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4019:Naip5
|
UTSW |
13 |
100,223,394 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4020:Naip5
|
UTSW |
13 |
100,223,394 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4020:Naip5
|
UTSW |
13 |
100,223,375 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4074:Naip5
|
UTSW |
13 |
100,246,064 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4082:Naip5
|
UTSW |
13 |
100,245,830 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4105:Naip5
|
UTSW |
13 |
100,219,739 (GRCm38) |
missense |
probably benign |
|
|
R4227:Naip5
|
UTSW |
13 |
100,212,768 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4639:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R4640:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R4641:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R4644:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R4645:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R4700:Naip5
|
UTSW |
13 |
100,223,414 (GRCm38) |
missense |
possibly damaging |
0.62 |
|
R4727:Naip5
|
UTSW |
13 |
100,221,870 (GRCm38) |
missense |
possibly damaging |
0.81 |
|
R4729:Naip5
|
UTSW |
13 |
100,222,131 (GRCm38) |
missense |
possibly damaging |
0.75 |
|
R4816:Naip5
|
UTSW |
13 |
100,219,681 (GRCm38) |
missense |
probably benign |
0.32 |
|
R4816:Naip5
|
UTSW |
13 |
100,219,687 (GRCm38) |
missense |
probably benign |
0.01 |
|
R4816:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4869:Naip5
|
UTSW |
13 |
100,245,131 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5162:Naip5
|
UTSW |
13 |
100,223,406 (GRCm38) |
missense |
possibly damaging |
0.78 |
|
R5244:Naip5
|
UTSW |
13 |
100,245,662 (GRCm38) |
missense |
probably benign |
0.08 |
|
R5411:Naip5
|
UTSW |
13 |
100,245,746 (GRCm38) |
missense |
possibly damaging |
0.54 |
|
R5632:Naip5
|
UTSW |
13 |
100,230,662 (GRCm38) |
splice site |
probably null |
|
|
R5760:Naip5
|
UTSW |
13 |
100,242,838 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5916:Naip5
|
UTSW |
13 |
100,222,701 (GRCm38) |
missense |
probably benign |
0.02 |
|
R6302:Naip5
|
UTSW |
13 |
100,223,166 (GRCm38) |
missense |
possibly damaging |
0.76 |
|
R6304:Naip5
|
UTSW |
13 |
100,223,166 (GRCm38) |
missense |
possibly damaging |
0.76 |
|
R6411:Naip5
|
UTSW |
13 |
100,223,405 (GRCm38) |
missense |
probably benign |
0.01 |
|
R6474:Naip5
|
UTSW |
13 |
100,214,663 (GRCm38) |
missense |
possibly damaging |
0.82 |
|
R6499:Naip5
|
UTSW |
13 |
100,221,594 (GRCm38) |
missense |
probably benign |
|
|
R6544:Naip5
|
UTSW |
13 |
100,223,144 (GRCm38) |
missense |
possibly damaging |
0.50 |
|
R6827:Naip5
|
UTSW |
13 |
100,245,929 (GRCm38) |
missense |
possibly damaging |
0.48 |
|
R6954:Naip5
|
UTSW |
13 |
100,223,414 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7052:Naip5
|
UTSW |
13 |
100,222,347 (GRCm38) |
missense |
probably benign |
0.01 |
|
R7138:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R7141:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R7375:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7375:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
|
R7401:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7401:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
|
R7447:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7447:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
|
R7466:Naip5
|
UTSW |
13 |
100,221,986 (GRCm38) |
nonsense |
probably null |
|
|
R7491:Naip5
|
UTSW |
13 |
100,217,071 (GRCm38) |
missense |
probably benign |
0.18 |
|
R7559:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
|
R7559:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7562:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
|
R7562:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7588:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
|
R7588:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7589:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
|
R7589:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7590:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
|
R7590:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7742:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R7886:Naip5
|
UTSW |
13 |
100,246,181 (GRCm38) |
missense |
probably benign |
0.28 |
|
R7996:Naip5
|
UTSW |
13 |
100,221,656 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8026:Naip5
|
UTSW |
13 |
100,245,898 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8046:Naip5
|
UTSW |
13 |
100,222,233 (GRCm38) |
missense |
probably benign |
|
|
R8319:Naip5
|
UTSW |
13 |
100,221,659 (GRCm38) |
missense |
probably benign |
0.12 |
|
R8471:Naip5
|
UTSW |
13 |
100,221,645 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R8480:Naip5
|
UTSW |
13 |
100,222,235 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8496:Naip5
|
UTSW |
13 |
100,212,739 (GRCm38) |
missense |
probably benign |
0.00 |
|
R8500:Naip5
|
UTSW |
13 |
100,222,712 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R8712:Naip5
|
UTSW |
13 |
100,223,096 (GRCm38) |
missense |
possibly damaging |
0.61 |
|
R8780:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R8781:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R8788:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R8817:Naip5
|
UTSW |
13 |
100,212,699 (GRCm38) |
missense |
probably benign |
0.01 |
|
R8833:Naip5
|
UTSW |
13 |
100,222,934 (GRCm38) |
missense |
probably damaging |
0.97 |
|
R8835:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R8958:Naip5
|
UTSW |
13 |
100,217,609 (GRCm38) |
nonsense |
probably null |
|
|
R9031:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R9032:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R9074:Naip5
|
UTSW |
13 |
100,221,756 (GRCm38) |
missense |
possibly damaging |
0.92 |
|
R9098:Naip5
|
UTSW |
13 |
100,229,619 (GRCm38) |
missense |
possibly damaging |
0.67 |
|
R9204:Naip5
|
UTSW |
13 |
100,222,500 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9223:Naip5
|
UTSW |
13 |
100,227,676 (GRCm38) |
missense |
probably benign |
0.05 |
|
R9358:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R9389:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R9403:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R9518:Naip5
|
UTSW |
13 |
100,221,859 (GRCm38) |
missense |
probably benign |
|
|
R9568:Naip5
|
UTSW |
13 |
100,223,313 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9568:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R9569:Naip5
|
UTSW |
13 |
100,223,313 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9569:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R9570:Naip5
|
UTSW |
13 |
100,223,313 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9572:Naip5
|
UTSW |
13 |
100,223,313 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9581:Naip5
|
UTSW |
13 |
100,214,686 (GRCm38) |
missense |
probably benign |
0.11 |
|
R9627:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
|
R9725:Naip5
|
UTSW |
13 |
100,222,276 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R9763:Naip5
|
UTSW |
13 |
100,230,761 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R9764:Naip5
|
UTSW |
13 |
100,230,761 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R9765:Naip5
|
UTSW |
13 |
100,230,761 (GRCm38) |
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 |
Incidental Mutation