Incidental Mutation 'R7514:Nup210l'
ID |
582285 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nup210l
|
Ensembl Gene |
ENSMUSG00000027939 |
Gene Name |
nucleoporin 210-like |
Synonyms |
4930548O11Rik |
MMRRC Submission |
045587-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.427)
|
Stock # |
R7514 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
3 |
Chromosomal Location |
90011439-90119355 bp(+) (GRCm39) |
Type of Mutation |
critical splice donor site (1 bp from exon) |
DNA Base Change (assembly) |
G to C
at 90117766 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000029548
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029548]
[ENSMUST00000107373]
[ENSMUST00000170122]
[ENSMUST00000195998]
[ENSMUST00000196205]
[ENSMUST00000197361]
[ENSMUST00000200410]
|
AlphaFold |
Q9D2F7 |
Predicted Effect |
probably null
Transcript: ENSMUST00000029548
|
SMART Domains |
Protein: ENSMUSP00000029548 Gene: ENSMUSG00000027939
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: ENSMUST00000107373
|
SMART Domains |
Protein: ENSMUSP00000102996 Gene: ENSMUSG00000027935
Domain | Start | End | E-Value | Type |
Pfam:Miro
|
1 |
43 |
3.5e-6 |
PFAM |
Pfam:Arf
|
1 |
88 |
1.8e-5 |
PFAM |
Pfam:Ras
|
1 |
90 |
2.5e-30 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000170122
|
SMART Domains |
Protein: ENSMUSP00000132102 Gene: ENSMUSG00000090733
Domain | Start | End | E-Value | Type |
low complexity region
|
13 |
23 |
N/A |
INTRINSIC |
Pfam:Ribosomal_S27e
|
28 |
82 |
9.8e-34 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000195998
|
SMART Domains |
Protein: ENSMUSP00000142942 Gene: ENSMUSG00000090733
Domain | Start | End | E-Value | Type |
Pfam:Ribosomal_S27e
|
1 |
50 |
3e-30 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000196205
|
SMART Domains |
Protein: ENSMUSP00000142536 Gene: ENSMUSG00000090733
Domain | Start | End | E-Value | Type |
low complexity region
|
11 |
21 |
N/A |
INTRINSIC |
Pfam:Ribosomal_S27e
|
26 |
80 |
7.5e-34 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000197361
|
SMART Domains |
Protein: ENSMUSP00000143402 Gene: ENSMUSG00000090733
Domain | Start | End | E-Value | Type |
low complexity region
|
13 |
23 |
N/A |
INTRINSIC |
Pfam:Ribosomal_S27e
|
28 |
80 |
5.7e-28 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000200410
|
SMART Domains |
Protein: ENSMUSP00000143368 Gene: ENSMUSG00000027939
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: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.4%
|
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: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933427D14Rik |
A |
G |
11: 72,086,628 (GRCm39) |
L261P |
probably damaging |
Het |
A4gnt |
A |
G |
9: 99,502,598 (GRCm39) |
I253V |
probably benign |
Het |
AAdacl4fm3 |
A |
T |
4: 144,429,798 (GRCm39) |
V397D |
possibly damaging |
Het |
Acap2 |
A |
T |
16: 30,973,385 (GRCm39) |
|
probably null |
Het |
Adora2b |
G |
T |
11: 62,156,146 (GRCm39) |
M198I |
probably damaging |
Het |
Akap5 |
C |
A |
12: 76,375,303 (GRCm39) |
T245K |
probably benign |
Het |
Aldh1a2 |
T |
C |
9: 71,192,245 (GRCm39) |
I399T |
probably damaging |
Het |
Ank2 |
G |
A |
3: 126,819,252 (GRCm39) |
S473L |
probably benign |
Het |
Anln |
A |
T |
9: 22,272,153 (GRCm39) |
D655E |
probably damaging |
Het |
Arhgef10 |
T |
C |
8: 15,025,956 (GRCm39) |
V820A |
probably benign |
Het |
Arid1b |
A |
G |
17: 5,391,989 (GRCm39) |
K1787E |
probably benign |
Het |
Art4 |
T |
C |
6: 136,831,739 (GRCm39) |
H134R |
probably benign |
Het |
Borcs6 |
G |
A |
11: 68,951,410 (GRCm39) |
V263M |
probably damaging |
Het |
C8a |
A |
T |
4: 104,703,247 (GRCm39) |
M314K |
possibly damaging |
Het |
Cbfa2t3 |
T |
G |
8: 123,361,865 (GRCm39) |
M386L |
probably damaging |
Het |
Ccdc170 |
T |
A |
10: 4,496,839 (GRCm39) |
V459E |
probably benign |
Het |
Cdh4 |
T |
A |
2: 179,532,636 (GRCm39) |
N699K |
possibly damaging |
Het |
Cdk12 |
T |
C |
11: 98,113,484 (GRCm39) |
L756P |
unknown |
Het |
Chsy1 |
A |
G |
7: 65,821,868 (GRCm39) |
D701G |
probably damaging |
Het |
Cnot9 |
A |
G |
1: 74,567,921 (GRCm39) |
T270A |
probably benign |
Het |
Crat |
C |
T |
2: 30,294,577 (GRCm39) |
R497Q |
probably benign |
Het |
Csnk2a1-ps3 |
A |
G |
1: 156,352,324 (GRCm39) |
D175G |
probably benign |
Het |
Cyb5r1 |
A |
G |
1: 134,338,268 (GRCm39) |
E228G |
probably damaging |
Het |
D630003M21Rik |
A |
G |
2: 158,059,273 (GRCm39) |
L209P |
probably damaging |
Het |
Dennd2c |
T |
A |
3: 103,070,378 (GRCm39) |
D791E |
probably benign |
Het |
Dnah14 |
T |
C |
1: 181,455,632 (GRCm39) |
I919T |
probably damaging |
Het |
Dpp8 |
T |
C |
9: 64,986,036 (GRCm39) |
L842S |
probably damaging |
Het |
Ern1 |
A |
G |
11: 106,300,719 (GRCm39) |
|
probably null |
Het |
Exo1 |
T |
C |
1: 175,734,232 (GRCm39) |
|
probably null |
Het |
Fam161b |
T |
G |
12: 84,404,512 (GRCm39) |
E56A |
possibly damaging |
Het |
Fbrsl1 |
T |
C |
5: 110,580,799 (GRCm39) |
T153A |
probably benign |
Het |
Fcgr3 |
T |
G |
1: 170,886,912 (GRCm39) |
D4A |
probably benign |
Het |
Gltp |
C |
T |
5: 114,808,521 (GRCm39) |
A193T |
probably benign |
Het |
Gm3159 |
A |
T |
14: 4,399,690 (GRCm38) |
S142C |
probably damaging |
Het |
Gphn |
T |
C |
12: 78,672,939 (GRCm39) |
V485A |
probably damaging |
Het |
Grik2 |
A |
T |
10: 49,399,904 (GRCm39) |
N275K |
probably damaging |
Het |
Gstt3 |
G |
T |
10: 75,612,625 (GRCm39) |
Q102K |
probably damaging |
Het |
Hivep3 |
T |
A |
4: 119,954,052 (GRCm39) |
F789L |
possibly damaging |
Het |
Ing5 |
A |
G |
1: 93,744,164 (GRCm39) |
N157D |
possibly damaging |
Het |
Itga3 |
C |
T |
11: 94,956,722 (GRCm39) |
W177* |
probably null |
Het |
Jag2 |
T |
C |
12: 112,892,672 (GRCm39) |
T83A |
probably benign |
Het |
Krt90 |
G |
A |
15: 101,461,605 (GRCm39) |
T532I |
unknown |
Het |
Lcn2 |
A |
G |
2: 32,277,861 (GRCm39) |
|
probably null |
Het |
Lrig2 |
A |
G |
3: 104,373,076 (GRCm39) |
S602P |
probably damaging |
Het |
Lsm1 |
A |
C |
8: 26,282,237 (GRCm39) |
R33S |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,923,934 (GRCm39) |
Y492* |
probably null |
Het |
Mcm3 |
A |
T |
1: 20,876,120 (GRCm39) |
L658Q |
probably benign |
Het |
Myh4 |
G |
A |
11: 67,134,148 (GRCm39) |
|
probably null |
Het |
Nck2 |
T |
C |
1: 43,608,381 (GRCm39) |
V341A |
probably benign |
Het |
Nucb1 |
T |
C |
7: 45,151,142 (GRCm39) |
|
probably null |
Het |
Or1j1 |
A |
G |
2: 36,702,651 (GRCm39) |
I151T |
probably benign |
Het |
Or5al5 |
A |
T |
2: 85,961,972 (GRCm39) |
F12I |
probably damaging |
Het |
Or7g22 |
A |
T |
9: 19,049,161 (GRCm39) |
S291C |
possibly damaging |
Het |
Or8b48 |
T |
A |
9: 38,493,347 (GRCm39) |
M258K |
probably damaging |
Het |
Or8b54 |
G |
A |
9: 38,686,974 (GRCm39) |
C141Y |
probably damaging |
Het |
Pla2g4a |
G |
A |
1: 149,727,113 (GRCm39) |
P556S |
probably damaging |
Het |
Plat |
T |
C |
8: 23,265,658 (GRCm39) |
C234R |
probably damaging |
Het |
Ppfia1 |
T |
C |
7: 144,071,450 (GRCm39) |
I321V |
probably benign |
Het |
Prrc1 |
T |
A |
18: 57,496,325 (GRCm39) |
V92E |
probably benign |
Het |
Prss3 |
A |
G |
6: 41,350,848 (GRCm39) |
V214A |
probably damaging |
Het |
Ptprg |
G |
T |
14: 12,179,342 (GRCm38) |
K786N |
possibly damaging |
Het |
Rabgap1 |
G |
T |
2: 37,427,354 (GRCm39) |
G645V |
probably damaging |
Het |
Rfx4 |
T |
C |
10: 84,716,090 (GRCm39) |
S470P |
probably damaging |
Het |
Rin3 |
C |
T |
12: 102,335,909 (GRCm39) |
Q607* |
probably null |
Het |
Sema3a |
A |
G |
5: 13,573,093 (GRCm39) |
H207R |
probably benign |
Het |
Serpinb12 |
G |
A |
1: 106,878,534 (GRCm39) |
E181K |
probably damaging |
Het |
Serpinb6c |
G |
A |
13: 34,081,386 (GRCm39) |
Q88* |
probably null |
Het |
Shmt1 |
A |
C |
11: 60,692,812 (GRCm39) |
C90W |
probably damaging |
Het |
Slc16a13 |
C |
T |
11: 70,109,710 (GRCm39) |
V264M |
probably damaging |
Het |
Slc17a8 |
G |
T |
10: 89,427,969 (GRCm39) |
P286Q |
probably damaging |
Het |
Slc27a6 |
C |
T |
18: 58,745,293 (GRCm39) |
Q576* |
probably null |
Het |
Slc30a9 |
T |
C |
5: 67,505,421 (GRCm39) |
S470P |
possibly damaging |
Het |
Slc44a2 |
G |
T |
9: 21,253,768 (GRCm39) |
K136N |
possibly damaging |
Het |
Smarca5 |
A |
T |
8: 81,444,163 (GRCm39) |
H534Q |
probably damaging |
Het |
Son |
T |
G |
16: 91,451,748 (GRCm39) |
L165R |
probably damaging |
Het |
Sox10 |
G |
A |
15: 79,040,421 (GRCm39) |
P373L |
probably benign |
Het |
Sp100 |
C |
T |
1: 85,608,860 (GRCm39) |
R330* |
probably null |
Het |
Srrm4 |
A |
G |
5: 116,584,570 (GRCm39) |
L500P |
probably damaging |
Het |
Tap1 |
T |
C |
17: 34,415,639 (GRCm39) |
L689P |
probably damaging |
Het |
Tfg |
A |
G |
16: 56,525,972 (GRCm39) |
|
probably null |
Het |
Tjp2 |
C |
T |
19: 24,088,886 (GRCm39) |
V677I |
probably benign |
Het |
Tmprss11g |
T |
G |
5: 86,645,176 (GRCm39) |
D85A |
probably damaging |
Het |
Tnfsf9 |
T |
C |
17: 57,414,238 (GRCm39) |
S222P |
probably damaging |
Het |
Trank1 |
A |
G |
9: 111,193,824 (GRCm39) |
N616S |
probably damaging |
Het |
Tubgcp6 |
C |
A |
15: 89,004,728 (GRCm39) |
W297L |
probably damaging |
Het |
Twist1 |
T |
C |
12: 34,008,355 (GRCm39) |
S127P |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,179,966 (GRCm39) |
I247T |
unknown |
Het |
Ubr5 |
G |
A |
15: 37,988,481 (GRCm39) |
T2153M |
|
Het |
Utrn |
A |
G |
10: 12,573,833 (GRCm39) |
V1079A |
probably benign |
Het |
Vcan |
T |
C |
13: 89,852,237 (GRCm39) |
T908A |
probably damaging |
Het |
Vmn2r104 |
A |
G |
17: 20,249,791 (GRCm39) |
F827L |
probably damaging |
Het |
Vmn2r111 |
T |
A |
17: 22,767,380 (GRCm39) |
T706S |
probably benign |
Het |
Vmn2r114 |
T |
C |
17: 23,527,035 (GRCm39) |
D499G |
probably null |
Het |
Vmn2r92 |
T |
C |
17: 18,391,533 (GRCm39) |
S512P |
probably damaging |
Het |
Vps4b |
A |
T |
1: 106,708,232 (GRCm39) |
|
probably null |
Het |
Vwa8 |
A |
C |
14: 79,219,674 (GRCm39) |
|
probably null |
Het |
Wnt10b |
T |
C |
15: 98,672,045 (GRCm39) |
Q224R |
probably benign |
Het |
Ylpm1 |
C |
T |
12: 85,077,268 (GRCm39) |
P1331L |
possibly damaging |
Het |
Zfhx4 |
G |
A |
3: 5,307,267 (GRCm39) |
M164I |
possibly damaging |
Het |
Zfp51 |
A |
G |
17: 21,683,762 (GRCm39) |
T126A |
probably benign |
Het |
Zfp609 |
A |
G |
9: 65,613,418 (GRCm39) |
V339A |
probably benign |
Het |
Zfp687 |
C |
T |
3: 94,914,841 (GRCm39) |
R1220H |
probably damaging |
Het |
Zfyve21 |
C |
T |
12: 111,790,249 (GRCm39) |
L84F |
probably damaging |
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 |
R1471:Nup210l
|
UTSW |
3 |
90,077,869 (GRCm39) |
missense |
probably benign |
|
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 |
|
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'- TATGCTAGGATTACAGATGCATGC -3'
(R):5'- AGTCAGAAGTATACACATGCCG -3'
Sequencing Primer
(F):5'- CAGATGCATGCCAATATTCTTAAGC -3'
(R):5'- GAGAACCCCTGTCTCAAA -3'
|
Posted On |
2019-10-17 |