Incidental Mutation 'R1672:Naip1'
ID |
187738 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Naip1
|
Ensembl Gene |
ENSMUSG00000021640 |
Gene Name |
NLR family, apoptosis inhibitory protein 1 |
Synonyms |
Naip, Birc1a, D13Lsd1 |
MMRRC Submission |
039708-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1672 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
13 |
Chromosomal Location |
100544272-100589372 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 100559657 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Asparagine
at position 1116
(D1116N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000152583
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022142]
[ENSMUST00000221727]
[ENSMUST00000221943]
[ENSMUST00000222155]
|
AlphaFold |
Q9QWK5 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000022142
AA Change: D1116N
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000022142 Gene: ENSMUSG00000021640 AA Change: D1116N
Domain | Start | End | E-Value | Type |
low complexity region
|
36 |
51 |
N/A |
INTRINSIC |
BIR
|
58 |
129 |
1.18e-20 |
SMART |
BIR
|
157 |
229 |
1.06e-36 |
SMART |
BIR
|
276 |
347 |
7.82e-26 |
SMART |
AAA
|
462 |
603 |
1.14e-2 |
SMART |
low complexity region
|
908 |
919 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000221727
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000221943
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000222155
AA Change: D1116N
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.4%
- 20x: 92.7%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Mice homozygous for disruptions in this gene display a normal phenotype. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310079G19Rik |
G |
A |
16: 88,424,096 (GRCm39) |
Q132* |
probably null |
Het |
Aadacl4 |
T |
A |
4: 144,349,889 (GRCm39) |
L382* |
probably null |
Het |
Afg3l2 |
A |
G |
18: 67,540,493 (GRCm39) |
I672T |
probably benign |
Het |
Aftph |
A |
T |
11: 20,676,762 (GRCm39) |
D282E |
probably benign |
Het |
Agpat5 |
A |
G |
8: 18,920,930 (GRCm39) |
N161S |
probably benign |
Het |
Alpk2 |
C |
T |
18: 65,414,030 (GRCm39) |
E1562K |
probably damaging |
Het |
Anxa2 |
TCCC |
TCC |
9: 69,397,036 (GRCm39) |
|
probably null |
Het |
Apobr |
A |
G |
7: 126,186,723 (GRCm39) |
R745G |
probably benign |
Het |
Arrdc5 |
T |
C |
17: 56,607,144 (GRCm39) |
T34A |
possibly damaging |
Het |
Astl |
T |
C |
2: 127,189,163 (GRCm39) |
L163P |
probably damaging |
Het |
Atf7ip2 |
A |
T |
16: 10,027,005 (GRCm39) |
H91L |
probably damaging |
Het |
Atp13a3 |
A |
T |
16: 30,151,092 (GRCm39) |
S1073T |
possibly damaging |
Het |
Bcl2a1a |
A |
T |
9: 88,839,503 (GRCm39) |
I134L |
probably damaging |
Het |
Brinp1 |
T |
C |
4: 68,747,520 (GRCm39) |
|
probably null |
Het |
Capn9 |
A |
G |
8: 125,340,570 (GRCm39) |
N578S |
probably benign |
Het |
Casp2 |
T |
A |
6: 42,245,842 (GRCm39) |
D166E |
probably damaging |
Het |
Ccr1l1 |
A |
T |
9: 123,777,544 (GRCm39) |
I301N |
probably damaging |
Het |
Chtop |
T |
A |
3: 90,414,874 (GRCm39) |
T15S |
probably damaging |
Het |
Coq5 |
T |
A |
5: 115,417,975 (GRCm39) |
|
probably null |
Het |
Crbn |
G |
A |
6: 106,772,886 (GRCm39) |
P34L |
probably damaging |
Het |
Crisp1 |
G |
T |
17: 40,619,760 (GRCm39) |
D59E |
possibly damaging |
Het |
Cyp4f14 |
A |
T |
17: 33,128,210 (GRCm39) |
D268E |
probably benign |
Het |
D5Ertd579e |
T |
C |
5: 36,770,621 (GRCm39) |
D1258G |
possibly damaging |
Het |
Dcp1b |
T |
C |
6: 119,194,872 (GRCm39) |
S531P |
probably benign |
Het |
Defb25 |
T |
C |
2: 152,464,410 (GRCm39) |
M45V |
probably benign |
Het |
Dffa |
T |
C |
4: 149,190,702 (GRCm39) |
L77P |
probably damaging |
Het |
Dixdc1 |
T |
C |
9: 50,601,164 (GRCm39) |
Q361R |
probably damaging |
Het |
Dnah1 |
A |
G |
14: 30,998,157 (GRCm39) |
L2560P |
probably damaging |
Het |
Fabp5 |
A |
G |
3: 10,080,601 (GRCm39) |
T108A |
probably benign |
Het |
Fam149a |
T |
G |
8: 45,792,411 (GRCm39) |
|
probably null |
Het |
Fam20c |
A |
G |
5: 138,793,056 (GRCm39) |
Y430C |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,489,872 (GRCm39) |
T3595A |
probably damaging |
Het |
Fbp1 |
A |
G |
13: 63,015,245 (GRCm39) |
Y245H |
probably damaging |
Het |
Frem1 |
C |
T |
4: 82,917,128 (GRCm39) |
R605H |
probably benign |
Het |
Fscb |
A |
G |
12: 64,518,292 (GRCm39) |
I1058T |
unknown |
Het |
Fyb2 |
A |
G |
4: 104,808,059 (GRCm39) |
K373R |
probably benign |
Het |
Ggta1 |
A |
T |
2: 35,292,145 (GRCm39) |
Y387* |
probably null |
Het |
Gm18856 |
T |
C |
13: 14,140,342 (GRCm39) |
|
probably benign |
Het |
Gm572 |
T |
C |
4: 148,752,966 (GRCm39) |
S282P |
possibly damaging |
Het |
Gpd2 |
A |
T |
2: 57,247,712 (GRCm39) |
I552F |
probably damaging |
Het |
Grk5 |
T |
C |
19: 61,074,653 (GRCm39) |
|
probably null |
Het |
Hivep1 |
T |
C |
13: 42,313,760 (GRCm39) |
V2000A |
probably damaging |
Het |
Ipo5 |
C |
T |
14: 121,170,714 (GRCm39) |
L466F |
probably damaging |
Het |
Itgb1 |
G |
A |
8: 129,458,526 (GRCm39) |
S785N |
probably damaging |
Het |
Itpr3 |
G |
A |
17: 27,307,987 (GRCm39) |
R258K |
probably benign |
Het |
Kcnk12 |
A |
G |
17: 88,053,747 (GRCm39) |
V305A |
probably benign |
Het |
Klf5 |
C |
T |
14: 99,538,986 (GRCm39) |
T133I |
probably damaging |
Het |
Lrig2 |
A |
G |
3: 104,399,128 (GRCm39) |
I178T |
probably damaging |
Het |
Lyrm4 |
A |
T |
13: 36,276,907 (GRCm39) |
M30K |
probably benign |
Het |
Mpv17 |
A |
G |
5: 31,311,063 (GRCm39) |
Y7H |
probably damaging |
Het |
Mrps22 |
T |
C |
9: 98,478,869 (GRCm39) |
|
probably null |
Het |
Myof |
A |
T |
19: 37,931,927 (GRCm39) |
W967R |
probably damaging |
Het |
Or1e33 |
T |
C |
11: 73,738,781 (GRCm39) |
T57A |
probably benign |
Het |
Or6c66b |
C |
A |
10: 129,376,561 (GRCm39) |
H52N |
probably benign |
Het |
Or8g50 |
G |
A |
9: 39,648,492 (GRCm39) |
C127Y |
probably damaging |
Het |
Or9k2b |
T |
C |
10: 130,016,261 (GRCm39) |
T163A |
probably benign |
Het |
Ovol2 |
T |
C |
2: 144,147,710 (GRCm39) |
Y180C |
probably damaging |
Het |
Pacs1 |
T |
C |
19: 5,202,337 (GRCm39) |
S418G |
probably benign |
Het |
Pcdh1 |
T |
C |
18: 38,325,233 (GRCm39) |
E903G |
probably damaging |
Het |
Pcdhb15 |
A |
T |
18: 37,607,713 (GRCm39) |
Y315F |
probably damaging |
Het |
Pex1 |
T |
C |
5: 3,676,085 (GRCm39) |
L891P |
probably damaging |
Het |
Potefam1 |
T |
A |
2: 111,051,119 (GRCm39) |
M226L |
probably benign |
Het |
Ppfia2 |
G |
A |
10: 106,666,429 (GRCm39) |
M378I |
possibly damaging |
Het |
Ppp1r9a |
T |
A |
6: 5,143,491 (GRCm39) |
|
probably null |
Het |
Prm3 |
T |
C |
16: 10,608,563 (GRCm39) |
E64G |
possibly damaging |
Het |
Prmt6 |
T |
C |
3: 110,157,887 (GRCm39) |
D134G |
possibly damaging |
Het |
Prss42 |
G |
A |
9: 110,629,996 (GRCm39) |
G250D |
probably damaging |
Het |
Pwwp2b |
G |
A |
7: 138,834,747 (GRCm39) |
V63I |
probably benign |
Het |
Rbm17 |
T |
C |
2: 11,590,530 (GRCm39) |
D375G |
possibly damaging |
Het |
Rhbdl1 |
A |
T |
17: 26,055,383 (GRCm39) |
|
probably null |
Het |
Rims2 |
T |
A |
15: 39,155,584 (GRCm39) |
D128E |
probably benign |
Het |
Rock2 |
A |
G |
12: 17,015,653 (GRCm39) |
K850R |
probably benign |
Het |
Rreb1 |
T |
C |
13: 38,114,513 (GRCm39) |
I624T |
probably benign |
Het |
Rrp36 |
A |
T |
17: 46,983,340 (GRCm39) |
D91E |
probably damaging |
Het |
Scn7a |
C |
T |
2: 66,527,944 (GRCm39) |
D849N |
possibly damaging |
Het |
Sec24a |
A |
T |
11: 51,634,775 (GRCm39) |
Y50* |
probably null |
Het |
Sh2d4b |
A |
G |
14: 40,614,921 (GRCm39) |
M1T |
probably null |
Het |
Slc4a7 |
A |
G |
14: 14,760,247 (GRCm38) |
I561V |
possibly damaging |
Het |
Slc7a12 |
T |
C |
3: 14,564,337 (GRCm39) |
V70A |
possibly damaging |
Het |
Slfnl1 |
A |
T |
4: 120,392,972 (GRCm39) |
I355F |
probably damaging |
Het |
Spata2 |
C |
T |
2: 167,325,439 (GRCm39) |
R460H |
probably damaging |
Het |
Stk11ip |
C |
T |
1: 75,505,629 (GRCm39) |
Q433* |
probably null |
Het |
Susd1 |
T |
C |
4: 59,411,395 (GRCm39) |
Y146C |
probably damaging |
Het |
Susd5 |
A |
T |
9: 113,897,890 (GRCm39) |
D115V |
probably damaging |
Het |
Tas2r110 |
T |
A |
6: 132,845,029 (GRCm39) |
V20E |
probably damaging |
Het |
Tbc1d4 |
T |
C |
14: 101,712,651 (GRCm39) |
Y694C |
possibly damaging |
Het |
Tmem131 |
T |
C |
1: 36,863,840 (GRCm39) |
E640G |
probably damaging |
Het |
Togaram1 |
A |
G |
12: 65,068,342 (GRCm39) |
T1782A |
probably benign |
Het |
Trim24 |
T |
C |
6: 37,892,214 (GRCm39) |
L249P |
probably damaging |
Het |
Ttf1 |
T |
C |
2: 28,957,164 (GRCm39) |
I478T |
probably damaging |
Het |
Upf2 |
T |
A |
2: 6,044,908 (GRCm39) |
|
probably null |
Het |
Urb1 |
A |
T |
16: 90,584,285 (GRCm39) |
C566S |
probably damaging |
Het |
Vmn1r191 |
T |
C |
13: 22,363,262 (GRCm39) |
N164S |
probably benign |
Het |
Vmn2r81 |
T |
A |
10: 79,104,112 (GRCm39) |
V245E |
probably damaging |
Het |
Vwce |
T |
A |
19: 10,630,459 (GRCm39) |
F506Y |
possibly damaging |
Het |
Wnt8b |
T |
C |
19: 44,499,715 (GRCm39) |
F155L |
probably damaging |
Het |
Xrra1 |
A |
T |
7: 99,547,647 (GRCm39) |
I279F |
probably benign |
Het |
Zfp229 |
T |
C |
17: 21,964,828 (GRCm39) |
S353P |
probably damaging |
Het |
Zfp607b |
C |
T |
7: 27,391,948 (GRCm39) |
H8Y |
possibly damaging |
Het |
Zfp933 |
A |
T |
4: 147,910,476 (GRCm39) |
H373Q |
probably damaging |
Het |
Zfp938 |
A |
G |
10: 82,060,982 (GRCm39) |
L546P |
probably benign |
Het |
Zfp988 |
C |
T |
4: 147,415,739 (GRCm39) |
R58C |
probably benign |
Het |
Zkscan14 |
C |
T |
5: 145,138,464 (GRCm39) |
V8I |
probably benign |
Het |
|
Other mutations in Naip1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01115:Naip1
|
APN |
13 |
100,580,228 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01145:Naip1
|
APN |
13 |
100,545,629 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01356:Naip1
|
APN |
13 |
100,559,722 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01414:Naip1
|
APN |
13 |
100,545,681 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01505:Naip1
|
APN |
13 |
100,562,441 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01573:Naip1
|
APN |
13 |
100,563,890 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01931:Naip1
|
APN |
13 |
100,545,540 (GRCm39) |
nonsense |
probably null |
|
IGL02043:Naip1
|
APN |
13 |
100,563,304 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02097:Naip1
|
APN |
13 |
100,562,096 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02331:Naip1
|
APN |
13 |
100,563,304 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02627:Naip1
|
APN |
13 |
100,562,156 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02675:Naip1
|
APN |
13 |
100,545,626 (GRCm39) |
missense |
probably benign |
|
IGL02801:Naip1
|
APN |
13 |
100,580,876 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02851:Naip1
|
APN |
13 |
100,569,770 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03038:Naip1
|
APN |
13 |
100,573,841 (GRCm39) |
nonsense |
probably null |
|
IGL03399:Naip1
|
APN |
13 |
100,545,426 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4340:Naip1
|
UTSW |
13 |
100,559,584 (GRCm39) |
missense |
probably benign |
|
FR4342:Naip1
|
UTSW |
13 |
100,561,979 (GRCm39) |
missense |
probably benign |
0.00 |
R0051:Naip1
|
UTSW |
13 |
100,547,509 (GRCm39) |
missense |
probably damaging |
0.96 |
R0095:Naip1
|
UTSW |
13 |
100,559,591 (GRCm39) |
missense |
probably benign |
0.24 |
R0147:Naip1
|
UTSW |
13 |
100,563,418 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0375:Naip1
|
UTSW |
13 |
100,545,656 (GRCm39) |
missense |
probably benign |
0.21 |
R0442:Naip1
|
UTSW |
13 |
100,581,024 (GRCm39) |
missense |
probably benign |
0.00 |
R0455:Naip1
|
UTSW |
13 |
100,559,727 (GRCm39) |
missense |
probably benign |
0.00 |
R0491:Naip1
|
UTSW |
13 |
100,559,727 (GRCm39) |
missense |
probably benign |
0.00 |
R0614:Naip1
|
UTSW |
13 |
100,580,708 (GRCm39) |
missense |
probably benign |
0.00 |
R0785:Naip1
|
UTSW |
13 |
100,559,593 (GRCm39) |
missense |
probably benign |
0.00 |
R0785:Naip1
|
UTSW |
13 |
100,559,584 (GRCm39) |
missense |
probably benign |
|
R0787:Naip1
|
UTSW |
13 |
100,562,604 (GRCm39) |
missense |
probably benign |
0.22 |
R1081:Naip1
|
UTSW |
13 |
100,559,578 (GRCm39) |
missense |
probably benign |
0.21 |
R1177:Naip1
|
UTSW |
13 |
100,563,572 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1476:Naip1
|
UTSW |
13 |
100,563,378 (GRCm39) |
missense |
probably benign |
0.35 |
R1809:Naip1
|
UTSW |
13 |
100,562,747 (GRCm39) |
missense |
probably benign |
|
R2057:Naip1
|
UTSW |
13 |
100,562,081 (GRCm39) |
missense |
probably damaging |
0.96 |
R2182:Naip1
|
UTSW |
13 |
100,550,188 (GRCm39) |
missense |
probably benign |
0.01 |
R2395:Naip1
|
UTSW |
13 |
100,559,614 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2518:Naip1
|
UTSW |
13 |
100,559,727 (GRCm39) |
missense |
probably benign |
0.00 |
R3033:Naip1
|
UTSW |
13 |
100,568,966 (GRCm39) |
missense |
probably benign |
0.01 |
R3122:Naip1
|
UTSW |
13 |
100,545,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R3439:Naip1
|
UTSW |
13 |
100,559,727 (GRCm39) |
missense |
probably benign |
0.00 |
R4167:Naip1
|
UTSW |
13 |
100,580,794 (GRCm39) |
missense |
probably benign |
0.04 |
R4179:Naip1
|
UTSW |
13 |
100,562,684 (GRCm39) |
missense |
probably damaging |
0.99 |
R4212:Naip1
|
UTSW |
13 |
100,563,383 (GRCm39) |
splice site |
probably null |
|
R4639:Naip1
|
UTSW |
13 |
100,580,791 (GRCm39) |
missense |
probably benign |
0.31 |
R4674:Naip1
|
UTSW |
13 |
100,580,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R4736:Naip1
|
UTSW |
13 |
100,581,034 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4740:Naip1
|
UTSW |
13 |
100,581,034 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4778:Naip1
|
UTSW |
13 |
100,563,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:Naip1
|
UTSW |
13 |
100,562,129 (GRCm39) |
missense |
probably benign |
0.00 |
R4855:Naip1
|
UTSW |
13 |
100,559,728 (GRCm39) |
splice site |
probably null |
|
R5740:Naip1
|
UTSW |
13 |
100,569,009 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5797:Naip1
|
UTSW |
13 |
100,581,034 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5806:Naip1
|
UTSW |
13 |
100,581,243 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R5895:Naip1
|
UTSW |
13 |
100,559,636 (GRCm39) |
missense |
probably benign |
0.00 |
R5896:Naip1
|
UTSW |
13 |
100,559,636 (GRCm39) |
missense |
probably benign |
0.00 |
R6023:Naip1
|
UTSW |
13 |
100,562,694 (GRCm39) |
missense |
probably benign |
0.00 |
R6109:Naip1
|
UTSW |
13 |
100,563,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R6117:Naip1
|
UTSW |
13 |
100,581,245 (GRCm39) |
start codon destroyed |
probably damaging |
0.99 |
R6133:Naip1
|
UTSW |
13 |
100,581,151 (GRCm39) |
missense |
probably benign |
0.10 |
R6241:Naip1
|
UTSW |
13 |
100,562,169 (GRCm39) |
missense |
probably damaging |
0.99 |
R6335:Naip1
|
UTSW |
13 |
100,563,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R6404:Naip1
|
UTSW |
13 |
100,559,727 (GRCm39) |
missense |
probably benign |
0.00 |
R6475:Naip1
|
UTSW |
13 |
100,545,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R6508:Naip1
|
UTSW |
13 |
100,572,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R6580:Naip1
|
UTSW |
13 |
100,581,157 (GRCm39) |
missense |
probably damaging |
0.99 |
R6600:Naip1
|
UTSW |
13 |
100,559,666 (GRCm39) |
missense |
probably benign |
0.00 |
R6600:Naip1
|
UTSW |
13 |
100,559,578 (GRCm39) |
missense |
probably benign |
0.21 |
R6603:Naip1
|
UTSW |
13 |
100,559,666 (GRCm39) |
missense |
probably benign |
0.00 |
R6603:Naip1
|
UTSW |
13 |
100,559,578 (GRCm39) |
missense |
probably benign |
0.21 |
R6633:Naip1
|
UTSW |
13 |
100,559,593 (GRCm39) |
missense |
probably benign |
0.00 |
R6633:Naip1
|
UTSW |
13 |
100,559,584 (GRCm39) |
missense |
probably benign |
|
R6720:Naip1
|
UTSW |
13 |
100,559,585 (GRCm39) |
missense |
probably benign |
0.00 |
R6805:Naip1
|
UTSW |
13 |
100,563,849 (GRCm39) |
missense |
probably benign |
0.04 |
R7043:Naip1
|
UTSW |
13 |
100,563,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R7615:Naip1
|
UTSW |
13 |
100,562,284 (GRCm39) |
missense |
probably benign |
0.00 |
R7797:Naip1
|
UTSW |
13 |
100,580,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R7820:Naip1
|
UTSW |
13 |
100,559,578 (GRCm39) |
missense |
probably benign |
0.21 |
R7842:Naip1
|
UTSW |
13 |
100,563,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R8117:Naip1
|
UTSW |
13 |
100,563,509 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8132:Naip1
|
UTSW |
13 |
100,573,883 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8177:Naip1
|
UTSW |
13 |
100,563,911 (GRCm39) |
missense |
probably benign |
0.00 |
R8203:Naip1
|
UTSW |
13 |
100,562,328 (GRCm39) |
missense |
probably benign |
0.02 |
R8283:Naip1
|
UTSW |
13 |
100,563,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R8319:Naip1
|
UTSW |
13 |
100,565,721 (GRCm39) |
missense |
probably benign |
0.13 |
R8377:Naip1
|
UTSW |
13 |
100,562,374 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8864:Naip1
|
UTSW |
13 |
100,562,828 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8871:Naip1
|
UTSW |
13 |
100,580,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R8987:Naip1
|
UTSW |
13 |
100,563,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R9079:Naip1
|
UTSW |
13 |
100,559,727 (GRCm39) |
missense |
probably benign |
0.00 |
R9275:Naip1
|
UTSW |
13 |
100,562,684 (GRCm39) |
missense |
probably damaging |
0.99 |
R9354:Naip1
|
UTSW |
13 |
100,563,994 (GRCm39) |
missense |
probably benign |
0.31 |
R9524:Naip1
|
UTSW |
13 |
100,563,101 (GRCm39) |
missense |
probably benign |
0.06 |
R9617:Naip1
|
UTSW |
13 |
100,569,821 (GRCm39) |
missense |
probably benign |
0.01 |
R9776:Naip1
|
UTSW |
13 |
100,559,584 (GRCm39) |
missense |
probably benign |
|
R9802:Naip1
|
UTSW |
13 |
100,562,713 (GRCm39) |
missense |
probably benign |
|
RF007:Naip1
|
UTSW |
13 |
100,562,642 (GRCm39) |
missense |
probably benign |
0.03 |
X0066:Naip1
|
UTSW |
13 |
100,573,830 (GRCm39) |
missense |
probably damaging |
1.00 |
Y4335:Naip1
|
UTSW |
13 |
100,562,030 (GRCm39) |
missense |
probably benign |
0.00 |
Y4336:Naip1
|
UTSW |
13 |
100,562,030 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TGGAAAGGCAAGTAGCTTTACCAGC -3'
(R):5'- TGTGAGTCTAGAGACCAGCACAGG -3'
Sequencing Primer
(F):5'- CTGAGACATGAGCTGGAGATCAAG -3'
(R):5'- AGCTGGCAGTAACTTCATGC -3'
|
Posted On |
2014-05-09 |