Incidental Mutation 'R1809:Naip1'
ID |
203731 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Naip1
|
Ensembl Gene |
ENSMUSG00000021640 |
Gene Name |
NLR family, apoptosis inhibitory protein 1 |
Synonyms |
Naip, Birc1a, D13Lsd1 |
MMRRC Submission |
039838-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1809 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
13 |
Chromosomal Location |
100544272-100589372 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 100562747 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Lysine
at position 806
(T806K)
|
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: T806K
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000022142 Gene: ENSMUSG00000021640 AA Change: T806K
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: T806K
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.8%
- 10x: 94.9%
- 20x: 91.2%
|
Validation Efficiency |
96% (107/111) |
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: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim2 |
A |
G |
5: 36,000,614 (GRCm39) |
|
probably benign |
Het |
Adamts20 |
C |
T |
15: 94,238,968 (GRCm39) |
S750N |
probably damaging |
Het |
Adh6a |
G |
A |
3: 138,036,722 (GRCm39) |
R370H |
possibly damaging |
Het |
Akr1b7 |
A |
G |
6: 34,396,046 (GRCm39) |
N183D |
probably damaging |
Het |
Aktip |
A |
T |
8: 91,856,348 (GRCm39) |
I43N |
probably damaging |
Het |
Ankrd26 |
A |
T |
6: 118,502,883 (GRCm39) |
|
probably benign |
Het |
Ano9 |
G |
A |
7: 140,688,717 (GRCm39) |
T144I |
possibly damaging |
Het |
Anpep |
G |
T |
7: 79,491,571 (GRCm39) |
D143E |
probably benign |
Het |
Aox1 |
C |
A |
1: 58,333,484 (GRCm39) |
Q234K |
probably benign |
Het |
Ap1g1 |
C |
G |
8: 110,559,814 (GRCm39) |
|
probably benign |
Het |
Arhgef4 |
G |
A |
1: 34,849,636 (GRCm39) |
|
probably null |
Het |
Arsj |
A |
G |
3: 126,231,944 (GRCm39) |
Y230C |
possibly damaging |
Het |
Asmt |
C |
T |
X: 169,109,480 (GRCm39) |
|
probably benign |
Het |
Astl |
A |
T |
2: 127,187,405 (GRCm39) |
K72N |
probably damaging |
Het |
Atp2b2 |
G |
A |
6: 113,780,704 (GRCm39) |
|
probably benign |
Het |
Baiap2l1 |
A |
C |
5: 144,261,365 (GRCm39) |
|
probably null |
Het |
C7 |
A |
T |
15: 5,063,821 (GRCm39) |
N193K |
probably damaging |
Het |
Cacna2d4 |
G |
T |
6: 119,247,785 (GRCm39) |
R362L |
probably damaging |
Het |
Cct4 |
T |
A |
11: 22,947,615 (GRCm39) |
D189E |
probably benign |
Het |
Cd300lg |
G |
A |
11: 101,933,938 (GRCm39) |
G62S |
probably benign |
Het |
Cdk14 |
T |
A |
5: 5,060,901 (GRCm39) |
M307L |
probably damaging |
Het |
Cfi |
G |
A |
3: 129,666,768 (GRCm39) |
|
probably null |
Het |
Clec2g |
G |
T |
6: 128,957,273 (GRCm39) |
|
probably null |
Het |
Cntnap2 |
T |
C |
6: 46,965,609 (GRCm39) |
S807P |
probably damaging |
Het |
Col6a3 |
T |
A |
1: 90,755,671 (GRCm39) |
H206L |
probably damaging |
Het |
Ct55 |
A |
G |
X: 52,735,716 (GRCm39) |
E99G |
probably benign |
Het |
Cyp2c23 |
A |
T |
19: 44,009,997 (GRCm39) |
|
probably benign |
Het |
Degs1l |
T |
C |
1: 180,887,252 (GRCm39) |
I279T |
probably damaging |
Het |
Dlec1 |
T |
C |
9: 118,965,767 (GRCm39) |
V1058A |
probably benign |
Het |
Dpp9 |
A |
G |
17: 56,506,038 (GRCm39) |
Y454H |
probably damaging |
Het |
Drosha |
G |
A |
15: 12,890,198 (GRCm39) |
G920R |
probably null |
Het |
Duox2 |
A |
G |
2: 122,114,378 (GRCm39) |
S1142P |
possibly damaging |
Het |
Fam13a |
C |
T |
6: 58,942,045 (GRCm39) |
|
probably null |
Het |
Filip1l |
A |
G |
16: 57,327,023 (GRCm39) |
R18G |
probably benign |
Het |
Foxa1 |
A |
G |
12: 57,589,527 (GRCm39) |
V231A |
probably damaging |
Het |
Gm4787 |
A |
T |
12: 81,425,303 (GRCm39) |
M285K |
possibly damaging |
Het |
Gm5084 |
T |
A |
13: 60,360,320 (GRCm39) |
|
noncoding transcript |
Het |
Gm6788 |
G |
A |
19: 28,740,586 (GRCm39) |
|
noncoding transcript |
Het |
Gm9922 |
G |
T |
14: 101,966,841 (GRCm39) |
|
probably benign |
Het |
Gtf3c4 |
A |
T |
2: 28,723,988 (GRCm39) |
Y440* |
probably null |
Het |
Helq |
A |
G |
5: 100,921,820 (GRCm39) |
S795P |
probably damaging |
Het |
Helz |
T |
A |
11: 107,489,997 (GRCm39) |
S151T |
possibly damaging |
Het |
Irgm1 |
T |
C |
11: 48,757,440 (GRCm39) |
T124A |
probably benign |
Het |
Itgam |
C |
T |
7: 127,670,109 (GRCm39) |
P134S |
possibly damaging |
Het |
Kdm6a |
T |
C |
X: 18,102,923 (GRCm39) |
Y217H |
probably benign |
Het |
Kif6 |
T |
C |
17: 50,208,812 (GRCm39) |
L744P |
probably benign |
Het |
Kmt2c |
C |
T |
5: 25,489,190 (GRCm39) |
R1203H |
probably damaging |
Het |
Ksr2 |
A |
G |
5: 117,693,535 (GRCm39) |
T328A |
probably damaging |
Het |
Lig1 |
T |
C |
7: 13,034,281 (GRCm39) |
|
probably benign |
Het |
Lpar3 |
G |
A |
3: 145,946,303 (GRCm39) |
|
probably benign |
Het |
Lrrk2 |
T |
C |
15: 91,584,095 (GRCm39) |
F285S |
possibly damaging |
Het |
Marchf7 |
A |
G |
2: 60,062,637 (GRCm39) |
D148G |
probably benign |
Het |
Mcee |
T |
C |
7: 64,050,049 (GRCm39) |
L60S |
probably damaging |
Het |
Mob2 |
A |
G |
7: 141,570,111 (GRCm39) |
I81T |
probably damaging |
Het |
Mphosph8 |
T |
A |
14: 56,909,909 (GRCm39) |
D87E |
probably damaging |
Het |
Msantd5f9 |
A |
G |
4: 73,835,754 (GRCm39) |
F237L |
probably benign |
Het |
Myo1g |
T |
C |
11: 6,462,283 (GRCm39) |
T560A |
probably benign |
Het |
Nagk |
C |
T |
6: 83,774,169 (GRCm39) |
T42I |
probably benign |
Het |
Ncor2 |
A |
G |
5: 125,195,857 (GRCm39) |
|
probably benign |
Het |
Ocln |
G |
T |
13: 100,647,967 (GRCm39) |
Y401* |
probably null |
Het |
Odad2 |
T |
A |
18: 7,211,630 (GRCm39) |
Y748F |
probably benign |
Het |
Oma1 |
T |
A |
4: 103,182,374 (GRCm39) |
N292K |
probably damaging |
Het |
Or8b55 |
G |
A |
9: 38,727,443 (GRCm39) |
V215I |
probably benign |
Het |
Ovch2 |
T |
A |
7: 107,389,412 (GRCm39) |
|
probably null |
Het |
Pcdhb16 |
T |
C |
18: 37,611,441 (GRCm39) |
F134L |
probably damaging |
Het |
Pipox |
A |
T |
11: 77,772,360 (GRCm39) |
Y337N |
probably benign |
Het |
Polr3b |
A |
G |
10: 84,528,865 (GRCm39) |
D763G |
probably damaging |
Het |
Pygo1 |
T |
A |
9: 72,852,078 (GRCm39) |
N88K |
probably damaging |
Het |
Rab3gap1 |
T |
C |
1: 127,862,251 (GRCm39) |
M674T |
probably damaging |
Het |
Rbm25 |
T |
C |
12: 83,719,501 (GRCm39) |
|
probably benign |
Het |
Rbm26 |
C |
T |
14: 105,354,542 (GRCm39) |
|
probably benign |
Het |
Rbms2 |
G |
A |
10: 127,974,055 (GRCm39) |
T187I |
possibly damaging |
Het |
Rnase11 |
T |
A |
14: 51,287,184 (GRCm39) |
R123S |
probably benign |
Het |
Rngtt |
A |
G |
4: 33,443,614 (GRCm39) |
N485D |
probably benign |
Het |
Rp1l1 |
A |
T |
14: 64,265,415 (GRCm39) |
M334L |
probably benign |
Het |
Rps9 |
T |
A |
7: 3,707,726 (GRCm39) |
L56Q |
probably damaging |
Het |
Saysd1 |
C |
A |
14: 20,133,170 (GRCm39) |
|
probably benign |
Het |
Sema4d |
C |
T |
13: 51,867,727 (GRCm39) |
|
probably null |
Het |
Shisa5 |
A |
T |
9: 108,869,998 (GRCm39) |
D34V |
probably damaging |
Het |
Skil |
A |
G |
3: 31,171,655 (GRCm39) |
D547G |
probably damaging |
Het |
Slc2a5 |
T |
A |
4: 150,227,514 (GRCm39) |
F444L |
probably damaging |
Het |
Slc9b2 |
T |
G |
3: 135,022,892 (GRCm39) |
C10G |
possibly damaging |
Het |
Sorcs2 |
G |
T |
5: 36,386,564 (GRCm39) |
|
probably benign |
Het |
Stk17b |
T |
G |
1: 53,805,140 (GRCm39) |
K140N |
possibly damaging |
Het |
Stradb |
T |
A |
1: 59,033,549 (GRCm39) |
L404Q |
possibly damaging |
Het |
Synj2 |
T |
C |
17: 6,076,826 (GRCm39) |
M432T |
possibly damaging |
Het |
Tanc1 |
G |
T |
2: 59,630,441 (GRCm39) |
R800L |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,522,987 (GRCm39) |
M1473V |
probably benign |
Het |
Tesc |
A |
G |
5: 118,199,667 (GRCm39) |
I190V |
probably benign |
Het |
Tex15 |
T |
C |
8: 34,064,262 (GRCm39) |
F1231L |
probably benign |
Het |
Thrsp |
T |
C |
7: 97,066,332 (GRCm39) |
I127V |
probably benign |
Het |
Tlr6 |
A |
T |
5: 65,111,055 (GRCm39) |
C617* |
probably null |
Het |
Trank1 |
A |
T |
9: 111,221,893 (GRCm39) |
I2877F |
probably benign |
Het |
Tut4 |
T |
A |
4: 108,406,552 (GRCm39) |
H1373Q |
probably damaging |
Het |
Ucp1 |
T |
C |
8: 84,024,496 (GRCm39) |
S274P |
probably damaging |
Het |
Ucp2 |
T |
A |
7: 100,147,606 (GRCm39) |
V195E |
probably damaging |
Het |
Vars2 |
T |
C |
17: 35,973,108 (GRCm39) |
T394A |
probably damaging |
Het |
Vmn1r1 |
A |
G |
1: 181,985,371 (GRCm39) |
V98A |
possibly damaging |
Het |
Vmn1r225 |
A |
G |
17: 20,722,918 (GRCm39) |
I120V |
probably benign |
Het |
Vmn2r102 |
A |
T |
17: 19,897,881 (GRCm39) |
M299L |
probably benign |
Het |
Vmn2r25 |
A |
G |
6: 123,802,337 (GRCm39) |
V522A |
probably benign |
Het |
Vmn2r70 |
T |
C |
7: 85,215,130 (GRCm39) |
I135V |
probably benign |
Het |
Vwf |
T |
C |
6: 125,567,138 (GRCm39) |
|
probably benign |
Het |
Zfp446 |
T |
C |
7: 12,713,048 (GRCm39) |
F29L |
probably damaging |
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 |
R1672:Naip1
|
UTSW |
13 |
100,559,657 (GRCm39) |
missense |
probably benign |
0.00 |
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'- GGAGAACATTCAGCAACAGTGTTG -3'
(R):5'- AGGAGTTTCTTGCTGCCATG -3'
Sequencing Primer
(F):5'- GAGCAATGCGCAATAAATGTTCTG -3'
(R):5'- GCCATGAGACTGACTGAACTTCTG -3'
|
Posted On |
2014-06-23 |