Incidental Mutation 'R2108:Nrp2'
ID |
232221 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nrp2
|
Ensembl Gene |
ENSMUSG00000025969 |
Gene Name |
neuropilin 2 |
Synonyms |
1110048P06Rik, NP-2, Npn-2, NP2, Npn2 |
MMRRC Submission |
040112-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.958)
|
Stock # |
R2108 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
62742476-62857851 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 62783436 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Asparagine
at position 179
(I179N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000109794
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027112]
[ENSMUST00000063594]
[ENSMUST00000075144]
[ENSMUST00000102822]
[ENSMUST00000114155]
[ENSMUST00000114157]
|
AlphaFold |
O35375 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000027112
AA Change: I179N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000027112 Gene: ENSMUSG00000025969 AA Change: I179N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
CUB
|
28 |
142 |
3.4e-45 |
SMART |
CUB
|
149 |
267 |
1.04e-40 |
SMART |
FA58C
|
276 |
427 |
1.63e-45 |
SMART |
FA58C
|
433 |
592 |
9.33e-14 |
SMART |
MAM
|
641 |
802 |
2.31e-60 |
SMART |
Pfam:DUF3481
|
822 |
906 |
1.4e-35 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000063594
AA Change: I179N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000069379 Gene: ENSMUSG00000025969 AA Change: I179N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
CUB
|
28 |
142 |
3.4e-45 |
SMART |
CUB
|
149 |
267 |
1.04e-40 |
SMART |
FA58C
|
276 |
427 |
1.63e-45 |
SMART |
FA58C
|
433 |
592 |
9.33e-14 |
SMART |
MAM
|
641 |
802 |
2.31e-60 |
SMART |
low complexity region
|
816 |
831 |
N/A |
INTRINSIC |
Pfam:DUF3481
|
839 |
923 |
1.6e-25 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000075144
AA Change: I179N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000074642 Gene: ENSMUSG00000025969 AA Change: I179N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
CUB
|
28 |
142 |
3.4e-45 |
SMART |
CUB
|
149 |
267 |
1.04e-40 |
SMART |
FA58C
|
276 |
427 |
1.63e-45 |
SMART |
FA58C
|
433 |
592 |
9.33e-14 |
SMART |
MAM
|
641 |
802 |
2.31e-60 |
SMART |
Pfam:DUF3481
|
827 |
911 |
2.3e-25 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000102822
AA Change: I179N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000099886 Gene: ENSMUSG00000025969 AA Change: I179N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
CUB
|
28 |
142 |
3.4e-45 |
SMART |
CUB
|
149 |
267 |
1.04e-40 |
SMART |
FA58C
|
276 |
427 |
1.63e-45 |
SMART |
FA58C
|
433 |
592 |
9.33e-14 |
SMART |
MAM
|
641 |
802 |
2.31e-60 |
SMART |
Pfam:DUF3481
|
822 |
906 |
2.3e-25 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000114155
AA Change: I179N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000109792 Gene: ENSMUSG00000025969 AA Change: I179N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
CUB
|
28 |
142 |
3.4e-45 |
SMART |
CUB
|
149 |
267 |
1.04e-40 |
SMART |
FA58C
|
276 |
427 |
1.63e-45 |
SMART |
FA58C
|
433 |
592 |
9.33e-14 |
SMART |
MAM
|
641 |
802 |
2.31e-60 |
SMART |
Pfam:DUF3481
|
817 |
901 |
9.4e-36 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000114157
AA Change: I179N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000109794 Gene: ENSMUSG00000025969 AA Change: I179N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
CUB
|
28 |
142 |
3.4e-45 |
SMART |
CUB
|
149 |
267 |
1.04e-40 |
SMART |
FA58C
|
276 |
427 |
1.63e-45 |
SMART |
FA58C
|
433 |
592 |
9.33e-14 |
SMART |
MAM
|
641 |
802 |
2.31e-60 |
SMART |
low complexity region
|
821 |
836 |
N/A |
INTRINSIC |
Pfam:DUF3481
|
844 |
928 |
2.4e-25 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126344
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.4%
- 20x: 95.5%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the neuropilin family of receptor proteins. The encoded transmembrane protein binds to SEMA3C protein {sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C} and SEMA3F protein {sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F}, and interacts with vascular endothelial growth factor (VEGF). This protein may play a role in cardiovascular development, axon guidance, and tumorigenesis. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008] PHENOTYPE: Nullizygous mice may exhibit pre- or postnatal lethality, reduced fertility, hydrocephalus, aberrant sensory innervation, reduced interneuron count, seizure susceptibility and abnormal lymphangiogenesis. Homozygotes for a gene trap allele show abnormal neuronal development and axonal trajectories. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd10 |
A |
G |
16: 45,552,303 (GRCm39) |
M190T |
probably benign |
Het |
Abhd5 |
A |
G |
9: 122,207,005 (GRCm39) |
Y250C |
probably damaging |
Het |
Ace2 |
A |
G |
X: 162,923,728 (GRCm39) |
N24S |
probably benign |
Het |
Adamtsl2 |
A |
G |
2: 26,985,570 (GRCm39) |
M485V |
probably benign |
Het |
Adamtsl4 |
G |
T |
3: 95,588,357 (GRCm39) |
P577H |
probably damaging |
Het |
Akap8l |
C |
T |
17: 32,551,457 (GRCm39) |
R511H |
probably damaging |
Het |
Apc |
T |
C |
18: 34,402,282 (GRCm39) |
Y141H |
probably damaging |
Het |
Arsi |
A |
T |
18: 61,049,443 (GRCm39) |
T109S |
possibly damaging |
Het |
Asb3 |
G |
A |
11: 31,031,355 (GRCm39) |
|
probably null |
Het |
Atm |
T |
C |
9: 53,355,297 (GRCm39) |
D2899G |
probably damaging |
Het |
Bcas3 |
G |
A |
11: 85,348,704 (GRCm39) |
V199I |
probably damaging |
Het |
Bub1 |
T |
C |
2: 127,661,255 (GRCm39) |
K279E |
probably damaging |
Het |
C3 |
A |
T |
17: 57,530,974 (GRCm39) |
|
probably null |
Het |
Cabcoco1 |
T |
C |
10: 68,267,153 (GRCm39) |
K185E |
probably benign |
Het |
Cadm2 |
A |
T |
16: 66,528,357 (GRCm39) |
I326N |
probably benign |
Het |
Ccr3 |
T |
C |
9: 123,829,336 (GRCm39) |
S224P |
possibly damaging |
Het |
Cdhr4 |
A |
G |
9: 107,874,843 (GRCm39) |
T638A |
probably damaging |
Het |
Cfap46 |
T |
C |
7: 139,263,677 (GRCm39) |
I4V |
probably benign |
Het |
Csf2rb2 |
A |
T |
15: 78,176,744 (GRCm39) |
V216E |
probably damaging |
Het |
Csmd3 |
A |
T |
15: 47,868,257 (GRCm39) |
D754E |
possibly damaging |
Het |
Dnaaf1 |
T |
C |
8: 120,309,471 (GRCm39) |
|
probably null |
Het |
Dnah11 |
A |
C |
12: 117,984,088 (GRCm39) |
Y2466D |
probably damaging |
Het |
Dtx2 |
C |
T |
5: 136,059,431 (GRCm39) |
S493F |
probably damaging |
Het |
E2f7 |
T |
C |
10: 110,616,763 (GRCm39) |
Y668H |
probably benign |
Het |
Ehmt1 |
A |
T |
2: 24,727,630 (GRCm39) |
S735T |
probably damaging |
Het |
Eomes |
T |
C |
9: 118,307,920 (GRCm39) |
F65L |
probably benign |
Het |
Ercc6l2 |
T |
C |
13: 64,019,802 (GRCm39) |
|
probably benign |
Het |
Fbrsl1 |
A |
T |
5: 110,526,300 (GRCm39) |
L439Q |
probably damaging |
Het |
Fyco1 |
C |
T |
9: 123,626,581 (GRCm39) |
|
probably null |
Het |
Gfm2 |
A |
G |
13: 97,291,950 (GRCm39) |
T229A |
probably benign |
Het |
Gm7735 |
G |
A |
16: 88,966,433 (GRCm39) |
G19D |
unknown |
Het |
Gnpda1 |
T |
C |
18: 38,466,243 (GRCm39) |
|
probably null |
Het |
Gpr6 |
T |
A |
10: 40,946,649 (GRCm39) |
Y311F |
possibly damaging |
Het |
Gprc6a |
A |
T |
10: 51,491,304 (GRCm39) |
V744E |
probably damaging |
Het |
Grin3a |
C |
T |
4: 49,665,510 (GRCm39) |
D1042N |
possibly damaging |
Het |
Gstm3 |
A |
G |
3: 107,873,450 (GRCm39) |
C174R |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,471,487 (GRCm39) |
E2670G |
possibly damaging |
Het |
Hsd3b6 |
A |
T |
3: 98,713,503 (GRCm39) |
Y265* |
probably null |
Het |
Hus1 |
T |
A |
11: 8,961,110 (GRCm39) |
M1L |
probably null |
Het |
Idi2l |
G |
A |
13: 8,991,764 (GRCm39) |
P221S |
possibly damaging |
Het |
Ifi213 |
T |
G |
1: 173,396,668 (GRCm39) |
|
probably null |
Het |
Igf2r |
A |
C |
17: 12,917,138 (GRCm39) |
N1587K |
probably benign |
Het |
Ints1 |
A |
T |
5: 139,753,505 (GRCm39) |
V709E |
probably damaging |
Het |
Ints8 |
C |
A |
4: 11,235,552 (GRCm39) |
R359L |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lrp1b |
C |
T |
2: 41,000,769 (GRCm39) |
E2152K |
probably damaging |
Het |
Lrp2 |
A |
T |
2: 69,336,968 (GRCm39) |
V1268D |
possibly damaging |
Het |
Mpo |
T |
C |
11: 87,686,901 (GRCm39) |
Y177H |
probably damaging |
Het |
Mpp4 |
G |
A |
1: 59,182,941 (GRCm39) |
P322L |
possibly damaging |
Het |
Mprip |
A |
G |
11: 59,660,717 (GRCm39) |
K2166R |
probably damaging |
Het |
Myo15a |
T |
C |
11: 60,382,636 (GRCm39) |
Y1544H |
probably damaging |
Het |
Neu1 |
G |
A |
17: 35,153,374 (GRCm39) |
R299Q |
probably benign |
Het |
Nfxl1 |
C |
A |
5: 72,671,675 (GRCm39) |
|
probably null |
Het |
Nup153 |
A |
G |
13: 46,846,986 (GRCm39) |
|
probably null |
Het |
Or1j4 |
C |
A |
2: 36,740,355 (GRCm39) |
A99E |
possibly damaging |
Het |
Or2g7 |
G |
T |
17: 38,378,746 (GRCm39) |
R228L |
possibly damaging |
Het |
Or5p54 |
A |
T |
7: 107,554,709 (GRCm39) |
H287L |
probably benign |
Het |
Or6c6c |
A |
T |
10: 129,541,490 (GRCm39) |
I248L |
probably benign |
Het |
Or8g27 |
A |
T |
9: 39,129,318 (GRCm39) |
I222F |
probably damaging |
Het |
P2ry12 |
A |
T |
3: 59,124,774 (GRCm39) |
D300E |
probably damaging |
Het |
Pkhd1 |
C |
A |
1: 20,623,798 (GRCm39) |
G766* |
probably null |
Het |
Plagl1 |
A |
C |
10: 13,004,391 (GRCm39) |
|
probably benign |
Het |
Prkcq |
A |
T |
2: 11,237,380 (GRCm39) |
Y53F |
probably damaging |
Het |
Psg18 |
T |
C |
7: 18,084,799 (GRCm39) |
E99G |
probably damaging |
Het |
Ptprz1 |
T |
A |
6: 23,033,476 (GRCm39) |
H1921Q |
probably damaging |
Het |
Rcc1l |
A |
G |
5: 134,184,629 (GRCm39) |
V391A |
probably benign |
Het |
Sdr42e1 |
C |
T |
8: 118,391,763 (GRCm39) |
V11I |
probably damaging |
Het |
Slc12a3 |
C |
A |
8: 95,067,158 (GRCm39) |
N404K |
probably damaging |
Het |
Slc38a4 |
T |
C |
15: 96,906,878 (GRCm39) |
M287V |
probably benign |
Het |
Slc6a8 |
A |
T |
X: 72,720,492 (GRCm39) |
I96F |
possibly damaging |
Het |
Smyd2 |
A |
G |
1: 189,629,623 (GRCm39) |
S136P |
probably damaging |
Het |
Sox11 |
A |
G |
12: 27,391,702 (GRCm39) |
Y236H |
probably damaging |
Het |
Tbc1d2 |
G |
A |
4: 46,637,652 (GRCm39) |
P198L |
possibly damaging |
Het |
Tcof1 |
G |
T |
18: 60,968,845 (GRCm39) |
A256E |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,555,497 (GRCm39) |
Y2726C |
probably damaging |
Het |
Tnfsf14 |
T |
A |
17: 57,497,867 (GRCm39) |
R122W |
probably damaging |
Het |
Tril |
T |
C |
6: 53,796,068 (GRCm39) |
T385A |
probably damaging |
Het |
Trrap |
A |
G |
5: 144,762,684 (GRCm39) |
T2386A |
probably benign |
Het |
Tspear |
T |
A |
10: 77,706,253 (GRCm39) |
L341H |
possibly damaging |
Het |
Uba7 |
A |
G |
9: 107,856,487 (GRCm39) |
M595V |
probably benign |
Het |
Usp43 |
GC |
G |
11: 67,746,566 (GRCm39) |
|
probably null |
Het |
Utrn |
C |
A |
10: 12,312,108 (GRCm39) |
D616Y |
probably damaging |
Het |
Vmn2r69 |
T |
C |
7: 85,059,404 (GRCm39) |
I502V |
probably benign |
Het |
Vps13d |
C |
A |
4: 144,801,617 (GRCm39) |
G419C |
probably damaging |
Het |
Zbtb25 |
A |
T |
12: 76,396,880 (GRCm39) |
M114K |
probably benign |
Het |
Zcchc4 |
A |
G |
5: 52,953,474 (GRCm39) |
Y161C |
probably damaging |
Het |
Zfp292 |
A |
T |
4: 34,808,593 (GRCm39) |
F1484I |
possibly damaging |
Het |
Zfp326 |
A |
G |
5: 106,062,646 (GRCm39) |
|
probably benign |
Het |
Zfp395 |
T |
A |
14: 65,630,565 (GRCm39) |
S372T |
probably benign |
Het |
Zfp423 |
T |
A |
8: 88,507,806 (GRCm39) |
E825V |
possibly damaging |
Het |
Zfp445 |
A |
T |
9: 122,681,305 (GRCm39) |
Y879N |
probably benign |
Het |
Zfp451 |
A |
G |
1: 33,818,248 (GRCm39) |
I77T |
possibly damaging |
Het |
Zfp85 |
A |
T |
13: 67,897,003 (GRCm39) |
S356R |
probably benign |
Het |
|
Other mutations in Nrp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00765:Nrp2
|
APN |
1 |
62,743,410 (GRCm39) |
nonsense |
probably null |
|
IGL01912:Nrp2
|
APN |
1 |
62,810,896 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01996:Nrp2
|
APN |
1 |
62,788,419 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02184:Nrp2
|
APN |
1 |
62,758,099 (GRCm39) |
nonsense |
probably null |
|
IGL02682:Nrp2
|
APN |
1 |
62,810,996 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02928:Nrp2
|
APN |
1 |
62,854,605 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03024:Nrp2
|
APN |
1 |
62,810,893 (GRCm39) |
missense |
probably damaging |
1.00 |
Euphorbia
|
UTSW |
1 |
62,801,972 (GRCm39) |
missense |
probably benign |
0.02 |
Sabra
|
UTSW |
1 |
62,822,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Nrp2
|
UTSW |
1 |
62,784,536 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0068:Nrp2
|
UTSW |
1 |
62,784,536 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0683:Nrp2
|
UTSW |
1 |
62,783,477 (GRCm39) |
missense |
probably benign |
0.41 |
R0789:Nrp2
|
UTSW |
1 |
62,784,609 (GRCm39) |
missense |
probably benign |
0.44 |
R1418:Nrp2
|
UTSW |
1 |
62,822,491 (GRCm39) |
nonsense |
probably null |
|
R1468:Nrp2
|
UTSW |
1 |
62,777,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Nrp2
|
UTSW |
1 |
62,777,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R1544:Nrp2
|
UTSW |
1 |
62,802,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R1645:Nrp2
|
UTSW |
1 |
62,824,283 (GRCm39) |
missense |
probably damaging |
0.97 |
R1677:Nrp2
|
UTSW |
1 |
62,822,479 (GRCm39) |
missense |
probably benign |
0.18 |
R1752:Nrp2
|
UTSW |
1 |
62,777,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Nrp2
|
UTSW |
1 |
62,777,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R1916:Nrp2
|
UTSW |
1 |
62,801,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R1962:Nrp2
|
UTSW |
1 |
62,758,090 (GRCm39) |
missense |
probably benign |
0.03 |
R2164:Nrp2
|
UTSW |
1 |
62,783,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R2216:Nrp2
|
UTSW |
1 |
62,802,077 (GRCm39) |
nonsense |
probably null |
|
R2679:Nrp2
|
UTSW |
1 |
62,824,237 (GRCm39) |
missense |
probably benign |
0.00 |
R4349:Nrp2
|
UTSW |
1 |
62,777,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R4351:Nrp2
|
UTSW |
1 |
62,777,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R4352:Nrp2
|
UTSW |
1 |
62,777,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R4353:Nrp2
|
UTSW |
1 |
62,777,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R4811:Nrp2
|
UTSW |
1 |
62,758,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R5362:Nrp2
|
UTSW |
1 |
62,808,221 (GRCm39) |
missense |
probably benign |
0.01 |
R5387:Nrp2
|
UTSW |
1 |
62,801,972 (GRCm39) |
missense |
probably benign |
0.02 |
R5461:Nrp2
|
UTSW |
1 |
62,786,370 (GRCm39) |
nonsense |
probably null |
|
R5704:Nrp2
|
UTSW |
1 |
62,824,267 (GRCm39) |
missense |
probably benign |
0.00 |
R6143:Nrp2
|
UTSW |
1 |
62,799,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R6303:Nrp2
|
UTSW |
1 |
62,784,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R6304:Nrp2
|
UTSW |
1 |
62,784,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R6376:Nrp2
|
UTSW |
1 |
62,758,176 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6945:Nrp2
|
UTSW |
1 |
62,799,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R7347:Nrp2
|
UTSW |
1 |
62,784,663 (GRCm39) |
missense |
probably benign |
0.04 |
R7393:Nrp2
|
UTSW |
1 |
62,784,583 (GRCm39) |
missense |
probably damaging |
0.98 |
R7593:Nrp2
|
UTSW |
1 |
62,758,203 (GRCm39) |
missense |
probably damaging |
0.96 |
R7881:Nrp2
|
UTSW |
1 |
62,810,990 (GRCm39) |
missense |
probably benign |
0.42 |
R7882:Nrp2
|
UTSW |
1 |
62,822,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R7948:Nrp2
|
UTSW |
1 |
62,784,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R7958:Nrp2
|
UTSW |
1 |
62,784,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R7959:Nrp2
|
UTSW |
1 |
62,784,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R7960:Nrp2
|
UTSW |
1 |
62,784,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R7961:Nrp2
|
UTSW |
1 |
62,784,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R8009:Nrp2
|
UTSW |
1 |
62,784,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:Nrp2
|
UTSW |
1 |
62,784,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R8014:Nrp2
|
UTSW |
1 |
62,784,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R8015:Nrp2
|
UTSW |
1 |
62,784,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R8068:Nrp2
|
UTSW |
1 |
62,784,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R8069:Nrp2
|
UTSW |
1 |
62,784,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R8070:Nrp2
|
UTSW |
1 |
62,784,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R8071:Nrp2
|
UTSW |
1 |
62,784,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R8206:Nrp2
|
UTSW |
1 |
62,786,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R8791:Nrp2
|
UTSW |
1 |
62,788,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R9090:Nrp2
|
UTSW |
1 |
62,784,670 (GRCm39) |
missense |
probably benign |
0.21 |
R9271:Nrp2
|
UTSW |
1 |
62,784,670 (GRCm39) |
missense |
probably benign |
0.21 |
R9287:Nrp2
|
UTSW |
1 |
62,835,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R9469:Nrp2
|
UTSW |
1 |
62,804,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R9646:Nrp2
|
UTSW |
1 |
62,777,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R9752:Nrp2
|
UTSW |
1 |
62,851,726 (GRCm39) |
missense |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- CATTTAAATAACCCAAAGGCAGAGG -3'
(R):5'- TCAAGTCCAGTCACTTTGGC -3'
Sequencing Primer
(F):5'- GCAGAGAAAGGCTACTCTCTAATAAC -3'
(R):5'- AGAGACAGTCCTCTGGGTATATCTC -3'
|
Posted On |
2014-09-18 |