Incidental Mutation 'R1471:Nup210l'
| ID |
164862 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Nup210l
|
| Ensembl Gene |
ENSMUSG00000027939 |
| Gene Name |
nucleoporin 210-like |
| Synonyms |
4930548O11Rik |
| MMRRC Submission |
039524-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.432)
|
| Stock # |
R1471 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
3 |
| Chromosomal Location |
90011439-90119355 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to C
at 90077869 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Leucine
at position 914
(I914L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000143368
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029548]
[ENSMUST00000200410]
|
| AlphaFold |
Q9D2F7 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000029548
AA Change: I914L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000029548
Gene: ENSMUSG00000027939
AA Change: I914L
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
13 |
32 |
N/A |
INTRINSIC |
|
BID_2
|
457 |
536 |
2.05e1 |
SMART |
|
Blast:S1
|
949 |
1023 |
2e-16 |
BLAST |
|
BID_2
|
1077 |
1152 |
4.51e-11 |
SMART |
|
Blast:BID_2
|
1468 |
1550 |
7e-15 |
BLAST |
|
transmembrane domain
|
1807 |
1829 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000200410
AA Change: I914L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000143368
Gene: ENSMUSG00000027939
AA Change: I914L
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
32 |
N/A |
INTRINSIC |
|
BID_2
|
457 |
536 |
6.9e-2 |
SMART |
|
Blast:S1
|
938 |
1023 |
9e-17 |
BLAST |
|
BID_2
|
1077 |
1152 |
1.5e-13 |
SMART |
|
Blast:BID_2
|
1468 |
1550 |
7e-15 |
BLAST |
|
transmembrane domain
|
1807 |
1829 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.6%
- 10x: 96.8%
- 20x: 94.4%
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Mice homozygous for a transgene insertion exhibit male infertility, asthenozoospermia, teratozoospermia, azoospermia, and seminiferous tubule degeneration. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 96 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930486L24Rik |
C |
A |
13: 61,001,336 (GRCm39) |
K130N |
probably damaging |
Het |
| Adam6a |
T |
A |
12: 113,508,013 (GRCm39) |
S129T |
probably damaging |
Het |
| Adamts10 |
T |
A |
17: 33,772,112 (GRCm39) |
F1087I |
probably damaging |
Het |
| Afp |
T |
A |
5: 90,651,541 (GRCm39) |
N385K |
possibly damaging |
Het |
| Ahnak |
T |
G |
19: 8,990,296 (GRCm39) |
|
probably benign |
Het |
| Akap6 |
A |
G |
12: 53,188,279 (GRCm39) |
T1898A |
probably benign |
Het |
| Antxr2 |
C |
A |
5: 98,123,199 (GRCm39) |
V283F |
possibly damaging |
Het |
| Asgr1 |
T |
C |
11: 69,946,919 (GRCm39) |
V55A |
possibly damaging |
Het |
| Asxl3 |
A |
G |
18: 22,649,411 (GRCm39) |
K467E |
probably damaging |
Het |
| Atp5f1a |
C |
A |
18: 77,868,969 (GRCm39) |
Q398K |
probably damaging |
Het |
| Atxn2 |
T |
A |
5: 121,924,437 (GRCm39) |
D455E |
probably damaging |
Het |
| B4galt6 |
C |
T |
18: 20,878,410 (GRCm39) |
A39T |
possibly damaging |
Het |
| C130073F10Rik |
C |
T |
4: 101,747,535 (GRCm39) |
E165K |
probably benign |
Het |
| Cabin1 |
A |
G |
10: 75,530,626 (GRCm39) |
C1519R |
probably damaging |
Het |
| Casp8ap2 |
C |
T |
4: 32,639,386 (GRCm39) |
R147* |
probably null |
Het |
| Ccdc88b |
A |
G |
19: 6,831,391 (GRCm39) |
L517P |
probably benign |
Het |
| Cd109 |
G |
A |
9: 78,561,869 (GRCm39) |
V220I |
probably damaging |
Het |
| Cd2ap |
T |
C |
17: 43,131,488 (GRCm39) |
K369R |
probably benign |
Het |
| Cd300c |
A |
G |
11: 114,850,614 (GRCm39) |
V63A |
probably benign |
Het |
| Cnot10 |
A |
G |
9: 114,420,619 (GRCm39) |
V741A |
probably benign |
Het |
| Col18a1 |
G |
T |
10: 76,932,040 (GRCm39) |
Q350K |
unknown |
Het |
| Crnkl1 |
T |
C |
2: 145,774,236 (GRCm39) |
K76E |
possibly damaging |
Het |
| Cryzl2 |
A |
G |
1: 157,298,291 (GRCm39) |
K227E |
probably benign |
Het |
| Cts6 |
G |
A |
13: 61,344,194 (GRCm39) |
T286I |
probably benign |
Het |
| Cul1 |
T |
C |
6: 47,491,820 (GRCm39) |
V392A |
probably damaging |
Het |
| Dcaf7 |
T |
A |
11: 105,937,573 (GRCm39) |
F65L |
probably benign |
Het |
| Dgke |
A |
C |
11: 88,946,320 (GRCm39) |
V160G |
possibly damaging |
Het |
| Dock8 |
C |
A |
19: 25,178,400 (GRCm39) |
Q2098K |
possibly damaging |
Het |
| Efhb |
T |
A |
17: 53,706,140 (GRCm39) |
D799V |
possibly damaging |
Het |
| Ephb2 |
T |
C |
4: 136,386,262 (GRCm39) |
D829G |
probably benign |
Het |
| Exosc1 |
A |
T |
19: 41,913,157 (GRCm39) |
S117R |
probably damaging |
Het |
| Fga |
T |
C |
3: 82,935,925 (GRCm39) |
S51P |
probably benign |
Het |
| Fmn1 |
T |
C |
2: 113,523,439 (GRCm39) |
F1141L |
possibly damaging |
Het |
| Foxm1 |
C |
T |
6: 128,350,837 (GRCm39) |
L713F |
probably damaging |
Het |
| Galnt4 |
A |
G |
10: 98,944,536 (GRCm39) |
E87G |
probably benign |
Het |
| Gamt |
T |
C |
10: 80,096,692 (GRCm39) |
D15G |
probably benign |
Het |
| Gm15557 |
C |
A |
2: 155,784,174 (GRCm39) |
D154E |
possibly damaging |
Het |
| Gnptab |
A |
G |
10: 88,281,625 (GRCm39) |
I1211V |
probably benign |
Het |
| Greb1 |
A |
T |
12: 16,761,775 (GRCm39) |
M535K |
probably damaging |
Het |
| Grm8 |
C |
A |
6: 27,363,308 (GRCm39) |
A736S |
possibly damaging |
Het |
| Hspa14 |
T |
C |
2: 3,492,645 (GRCm39) |
I373M |
probably benign |
Het |
| Ifi207 |
T |
A |
1: 173,557,629 (GRCm39) |
T370S |
unknown |
Het |
| Igf1r |
A |
G |
7: 67,653,585 (GRCm39) |
N41S |
probably damaging |
Het |
| Ikzf5 |
A |
T |
7: 130,993,496 (GRCm39) |
V224D |
probably damaging |
Het |
| Il10 |
C |
A |
1: 130,949,110 (GRCm39) |
Y90* |
probably null |
Het |
| Itga4 |
A |
G |
2: 79,117,376 (GRCm39) |
D394G |
probably benign |
Het |
| Kif21a |
A |
T |
15: 90,840,622 (GRCm39) |
S1165T |
probably benign |
Het |
| Krtap14 |
A |
G |
16: 88,622,515 (GRCm39) |
S155P |
probably damaging |
Het |
| Loxl2 |
A |
G |
14: 69,930,546 (GRCm39) |
N770S |
probably benign |
Het |
| Man2b1 |
A |
G |
8: 85,813,474 (GRCm39) |
D222G |
probably damaging |
Het |
| Mcub |
T |
A |
3: 129,709,464 (GRCm39) |
Y283F |
probably damaging |
Het |
| Meis3 |
T |
A |
7: 15,911,496 (GRCm39) |
Y64* |
probably null |
Het |
| Mfsd6 |
T |
A |
1: 52,748,716 (GRCm39) |
I50F |
probably benign |
Het |
| Micu2 |
T |
C |
14: 58,182,854 (GRCm39) |
T165A |
probably damaging |
Het |
| Mtcl1 |
T |
C |
17: 66,686,143 (GRCm39) |
E921G |
probably damaging |
Het |
| Muc5b |
A |
T |
7: 141,396,971 (GRCm39) |
N215Y |
unknown |
Het |
| Muc6 |
A |
G |
7: 141,234,176 (GRCm39) |
F772L |
possibly damaging |
Het |
| Myt1 |
A |
G |
2: 181,438,904 (GRCm39) |
D142G |
probably benign |
Het |
| Nol6 |
C |
T |
4: 41,120,281 (GRCm39) |
V479I |
probably benign |
Het |
| Nsun7 |
A |
G |
5: 66,441,572 (GRCm39) |
K414E |
probably benign |
Het |
| Obox3 |
G |
A |
7: 15,360,875 (GRCm39) |
P88L |
probably benign |
Het |
| Or10ag57 |
A |
G |
2: 87,218,862 (GRCm39) |
Y271C |
probably damaging |
Het |
| Or4f4b |
T |
C |
2: 111,314,351 (GRCm39) |
L192P |
probably damaging |
Het |
| Or8h8 |
C |
T |
2: 86,752,922 (GRCm39) |
|
probably null |
Het |
| Or8w1 |
T |
C |
2: 87,466,014 (GRCm39) |
T26A |
probably benign |
Het |
| Pclo |
T |
C |
5: 14,730,441 (GRCm39) |
|
probably benign |
Het |
| Pcsk5 |
T |
C |
19: 17,545,688 (GRCm39) |
N745D |
probably damaging |
Het |
| Pdzrn3 |
T |
A |
6: 101,128,473 (GRCm39) |
N731I |
possibly damaging |
Het |
| Pkdrej |
T |
A |
15: 85,701,334 (GRCm39) |
Q1534L |
probably benign |
Het |
| Pramel28 |
T |
C |
4: 143,691,523 (GRCm39) |
N400S |
probably benign |
Het |
| Rell1 |
T |
A |
5: 64,093,428 (GRCm39) |
D109V |
probably damaging |
Het |
| Rplp0 |
C |
T |
5: 115,701,403 (GRCm39) |
T285I |
probably damaging |
Het |
| Sanbr |
A |
T |
11: 23,565,222 (GRCm39) |
M255K |
probably damaging |
Het |
| Sema3g |
C |
T |
14: 30,950,002 (GRCm39) |
R728C |
probably damaging |
Het |
| Slc15a2 |
A |
G |
16: 36,574,153 (GRCm39) |
Y536H |
probably damaging |
Het |
| Slc26a5 |
T |
A |
5: 22,021,962 (GRCm39) |
Y488F |
probably benign |
Het |
| Slc5a4a |
A |
T |
10: 76,022,362 (GRCm39) |
S566C |
probably damaging |
Het |
| Spink7 |
C |
T |
18: 62,729,275 (GRCm39) |
E21K |
possibly damaging |
Het |
| Src |
C |
T |
2: 157,299,107 (GRCm39) |
Q35* |
probably null |
Het |
| Srrm2 |
T |
A |
17: 24,039,770 (GRCm39) |
V2234E |
probably damaging |
Het |
| Stk36 |
A |
T |
1: 74,650,314 (GRCm39) |
Q282L |
probably benign |
Het |
| Tas2r118 |
T |
G |
6: 23,969,170 (GRCm39) |
E297A |
probably damaging |
Het |
| Terf1 |
A |
G |
1: 15,913,194 (GRCm39) |
Y385C |
probably damaging |
Het |
| Tmc3 |
T |
C |
7: 83,247,498 (GRCm39) |
S198P |
probably damaging |
Het |
| Tmprss11b |
C |
T |
5: 86,808,355 (GRCm39) |
R407H |
possibly damaging |
Het |
| Tspyl4 |
G |
A |
10: 34,174,107 (GRCm39) |
E200K |
probably damaging |
Het |
| Ttc21a |
T |
C |
9: 119,771,707 (GRCm39) |
Y169H |
probably damaging |
Het |
| Ugt2b36 |
C |
T |
5: 87,239,930 (GRCm39) |
D152N |
probably damaging |
Het |
| Unk |
T |
C |
11: 115,940,235 (GRCm39) |
I196T |
probably benign |
Het |
| Uroc1 |
T |
G |
6: 90,321,153 (GRCm39) |
V243G |
probably damaging |
Het |
| Usp34 |
C |
A |
11: 23,438,862 (GRCm39) |
Q3475K |
probably benign |
Het |
| Vmn2r117 |
T |
A |
17: 23,697,447 (GRCm39) |
I82L |
probably benign |
Het |
| Vmn2r44 |
A |
T |
7: 8,380,882 (GRCm39) |
V337E |
probably damaging |
Het |
| Zbtb14 |
C |
A |
17: 69,695,497 (GRCm39) |
F398L |
probably damaging |
Het |
| Zfp362 |
T |
C |
4: 128,680,993 (GRCm39) |
T111A |
probably benign |
Het |
| Zfp598 |
T |
C |
17: 24,899,046 (GRCm39) |
V615A |
probably benign |
Het |
|
| Other mutations in Nup210l |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00780:Nup210l
|
APN |
3 |
90,098,156 (GRCm39) |
splice site |
probably benign |
|
|
IGL00813:Nup210l
|
APN |
3 |
90,039,725 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01375:Nup210l
|
APN |
3 |
90,067,200 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL01731:Nup210l
|
APN |
3 |
90,061,873 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01786:Nup210l
|
APN |
3 |
90,030,083 (GRCm39) |
nonsense |
probably null |
|
|
IGL01958:Nup210l
|
APN |
3 |
90,111,231 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
IGL02094:Nup210l
|
APN |
3 |
90,087,520 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02120:Nup210l
|
APN |
3 |
90,044,169 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02313:Nup210l
|
APN |
3 |
90,030,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02336:Nup210l
|
APN |
3 |
90,088,859 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02348:Nup210l
|
APN |
3 |
90,011,471 (GRCm39) |
utr 5 prime |
probably benign |
|
|
IGL02372:Nup210l
|
APN |
3 |
90,109,278 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
IGL02557:Nup210l
|
APN |
3 |
90,031,537 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02559:Nup210l
|
APN |
3 |
90,067,260 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02738:Nup210l
|
APN |
3 |
90,044,157 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
IGL03231:Nup210l
|
APN |
3 |
90,096,852 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03257:Nup210l
|
APN |
3 |
90,087,455 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL03388:Nup210l
|
APN |
3 |
90,077,351 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03134:Nup210l
|
UTSW |
3 |
90,098,194 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R0003:Nup210l
|
UTSW |
3 |
90,027,218 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0040:Nup210l
|
UTSW |
3 |
90,089,212 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0083:Nup210l
|
UTSW |
3 |
90,096,882 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0090:Nup210l
|
UTSW |
3 |
90,119,086 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0108:Nup210l
|
UTSW |
3 |
90,096,882 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0142:Nup210l
|
UTSW |
3 |
90,079,420 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0306:Nup210l
|
UTSW |
3 |
90,114,675 (GRCm39) |
missense |
probably benign |
0.13 |
|
R0332:Nup210l
|
UTSW |
3 |
90,039,616 (GRCm39) |
splice site |
probably benign |
|
|
R0346:Nup210l
|
UTSW |
3 |
90,096,745 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0463:Nup210l
|
UTSW |
3 |
90,087,518 (GRCm39) |
missense |
probably null |
1.00 |
|
R0622:Nup210l
|
UTSW |
3 |
90,075,047 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0765:Nup210l
|
UTSW |
3 |
90,027,184 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0990:Nup210l
|
UTSW |
3 |
90,119,232 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1014:Nup210l
|
UTSW |
3 |
90,077,355 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R1036:Nup210l
|
UTSW |
3 |
90,100,247 (GRCm39) |
splice site |
probably benign |
|
|
R1177:Nup210l
|
UTSW |
3 |
90,109,310 (GRCm39) |
missense |
probably benign |
0.11 |
|
R1183:Nup210l
|
UTSW |
3 |
90,067,252 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1188:Nup210l
|
UTSW |
3 |
90,105,486 (GRCm39) |
missense |
probably benign |
0.16 |
|
R1457:Nup210l
|
UTSW |
3 |
90,098,279 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R1627:Nup210l
|
UTSW |
3 |
90,051,476 (GRCm39) |
missense |
probably benign |
0.15 |
|
R1778:Nup210l
|
UTSW |
3 |
90,096,793 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1827:Nup210l
|
UTSW |
3 |
90,061,864 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1843:Nup210l
|
UTSW |
3 |
90,079,393 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1858:Nup210l
|
UTSW |
3 |
90,061,806 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1942:Nup210l
|
UTSW |
3 |
90,058,544 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2015:Nup210l
|
UTSW |
3 |
90,092,739 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2113:Nup210l
|
UTSW |
3 |
90,098,281 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R2944:Nup210l
|
UTSW |
3 |
90,088,852 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3736:Nup210l
|
UTSW |
3 |
90,027,320 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3740:Nup210l
|
UTSW |
3 |
90,114,701 (GRCm39) |
missense |
probably benign |
0.08 |
|
R3741:Nup210l
|
UTSW |
3 |
90,114,701 (GRCm39) |
missense |
probably benign |
0.08 |
|
R3742:Nup210l
|
UTSW |
3 |
90,114,701 (GRCm39) |
missense |
probably benign |
0.08 |
|
R3771:Nup210l
|
UTSW |
3 |
90,027,201 (GRCm39) |
nonsense |
probably null |
|
|
R3773:Nup210l
|
UTSW |
3 |
90,027,201 (GRCm39) |
nonsense |
probably null |
|
|
R3879:Nup210l
|
UTSW |
3 |
90,092,780 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3882:Nup210l
|
UTSW |
3 |
90,031,517 (GRCm39) |
missense |
probably benign |
0.19 |
|
R3953:Nup210l
|
UTSW |
3 |
90,100,361 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R3954:Nup210l
|
UTSW |
3 |
90,100,361 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R3955:Nup210l
|
UTSW |
3 |
90,100,361 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R3956:Nup210l
|
UTSW |
3 |
90,100,361 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R4200:Nup210l
|
UTSW |
3 |
90,027,218 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4290:Nup210l
|
UTSW |
3 |
90,114,633 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4328:Nup210l
|
UTSW |
3 |
90,083,142 (GRCm39) |
splice site |
probably null |
|
|
R4629:Nup210l
|
UTSW |
3 |
90,098,181 (GRCm39) |
nonsense |
probably null |
|
|
R4629:Nup210l
|
UTSW |
3 |
90,075,182 (GRCm39) |
missense |
probably benign |
0.21 |
|
R4897:Nup210l
|
UTSW |
3 |
90,100,378 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4906:Nup210l
|
UTSW |
3 |
90,077,337 (GRCm39) |
missense |
probably benign |
0.06 |
|
R4966:Nup210l
|
UTSW |
3 |
90,014,208 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5004:Nup210l
|
UTSW |
3 |
90,087,472 (GRCm39) |
nonsense |
probably null |
|
|
R5237:Nup210l
|
UTSW |
3 |
90,087,505 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5499:Nup210l
|
UTSW |
3 |
90,081,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5522:Nup210l
|
UTSW |
3 |
90,061,972 (GRCm39) |
missense |
probably benign |
0.10 |
|
R5627:Nup210l
|
UTSW |
3 |
90,051,557 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5678:Nup210l
|
UTSW |
3 |
90,098,266 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5726:Nup210l
|
UTSW |
3 |
90,036,514 (GRCm39) |
splice site |
probably null |
|
|
R5792:Nup210l
|
UTSW |
3 |
90,107,164 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6129:Nup210l
|
UTSW |
3 |
90,011,483 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6272:Nup210l
|
UTSW |
3 |
90,077,331 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R6290:Nup210l
|
UTSW |
3 |
90,027,216 (GRCm39) |
nonsense |
probably null |
|
|
R6293:Nup210l
|
UTSW |
3 |
90,022,371 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6446:Nup210l
|
UTSW |
3 |
90,079,375 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6698:Nup210l
|
UTSW |
3 |
90,089,815 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R6855:Nup210l
|
UTSW |
3 |
90,044,231 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6895:Nup210l
|
UTSW |
3 |
90,067,231 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6899:Nup210l
|
UTSW |
3 |
90,075,204 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R6978:Nup210l
|
UTSW |
3 |
90,061,873 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R6980:Nup210l
|
UTSW |
3 |
90,027,234 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7038:Nup210l
|
UTSW |
3 |
90,067,254 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7273:Nup210l
|
UTSW |
3 |
90,025,854 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7450:Nup210l
|
UTSW |
3 |
90,022,495 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7514:Nup210l
|
UTSW |
3 |
90,117,766 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7658:Nup210l
|
UTSW |
3 |
90,119,300 (GRCm39) |
missense |
probably benign |
0.43 |
|
R7735:Nup210l
|
UTSW |
3 |
90,092,883 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7772:Nup210l
|
UTSW |
3 |
90,067,233 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7800:Nup210l
|
UTSW |
3 |
90,041,904 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7840:Nup210l
|
UTSW |
3 |
90,030,036 (GRCm39) |
missense |
probably benign |
0.08 |
|
R7847:Nup210l
|
UTSW |
3 |
90,058,430 (GRCm39) |
missense |
probably benign |
|
|
R7848:Nup210l
|
UTSW |
3 |
90,111,212 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8084:Nup210l
|
UTSW |
3 |
90,043,365 (GRCm39) |
missense |
probably benign |
0.15 |
|
R8121:Nup210l
|
UTSW |
3 |
90,022,428 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8421:Nup210l
|
UTSW |
3 |
90,111,174 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8458:Nup210l
|
UTSW |
3 |
90,092,874 (GRCm39) |
missense |
probably null |
1.00 |
|
R8701:Nup210l
|
UTSW |
3 |
90,030,121 (GRCm39) |
missense |
probably benign |
0.41 |
|
R8720:Nup210l
|
UTSW |
3 |
90,117,681 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8770:Nup210l
|
UTSW |
3 |
90,025,850 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8896:Nup210l
|
UTSW |
3 |
90,025,932 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9033:Nup210l
|
UTSW |
3 |
90,105,396 (GRCm39) |
missense |
probably benign |
|
|
R9371:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9373:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9381:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9426:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9427:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9501:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9523:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9574:Nup210l
|
UTSW |
3 |
90,117,693 (GRCm39) |
missense |
probably benign |
|
|
R9612:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9654:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9660:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9660:Nup210l
|
UTSW |
3 |
90,105,402 (GRCm39) |
missense |
probably benign |
0.30 |
|
R9662:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9682:Nup210l
|
UTSW |
3 |
90,051,469 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R9729:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9750:Nup210l
|
UTSW |
3 |
90,117,659 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- ACTGTGTCCTCTGTGGCAGTCC -3'
(R):5'- TGACGGCCTGAGAGACAGATCC -3'
Sequencing Primer
(F):5'- AGTCCCACTTTGTCCTCTGTG -3'
(R):5'- cacacacacacacacacacac -3'
|
| Posted On |
2014-03-28 |
Incidental Mutation