Incidental Mutation 'R6500:Xpo6'
| ID |
519676 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Xpo6
|
| Ensembl Gene |
ENSMUSG00000000131 |
| Gene Name |
exportin 6 |
| Synonyms |
Ranbp20, 2610005L19Rik, C230091E20Rik |
| MMRRC Submission |
044632-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.807)
|
| Stock # |
R6500 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
7 |
| Chromosomal Location |
125700887-125799673 bp(-) (GRCm39) |
| Type of Mutation |
intron |
| DNA Base Change (assembly) |
T to C
at 125770262 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000132462
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000009344]
[ENSMUST00000163959]
[ENSMUST00000167147]
[ENSMUST00000168189]
|
| AlphaFold |
Q924Z6 |
| Predicted Effect |
silent
Transcript: ENSMUST00000009344
|
| SMART Domains |
Protein: ENSMUSP00000009344
Gene: ENSMUSG00000000131
| Domain | Start | End | E-Value | Type |
|---|
|
IBN_N
|
31 |
97 |
4.04e-6 |
SMART |
|
Pfam:Xpo1
|
103 |
290 |
1.4e-29 |
PFAM |
|
low complexity region
|
469 |
484 |
N/A |
INTRINSIC |
|
low complexity region
|
672 |
684 |
N/A |
INTRINSIC |
|
low complexity region
|
1022 |
1034 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000163959
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000164106
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000165729
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000166368
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000167147
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000167268
|
| Predicted Effect |
silent
Transcript: ENSMUST00000168189
|
| SMART Domains |
Protein: ENSMUSP00000130527
Gene: ENSMUSG00000000131
| Domain | Start | End | E-Value | Type |
|---|
|
IBN_N
|
31 |
97 |
4.04e-6 |
SMART |
|
Pfam:Xpo1
|
103 |
290 |
1.1e-25 |
PFAM |
|
low complexity region
|
469 |
485 |
N/A |
INTRINSIC |
|
low complexity region
|
673 |
685 |
N/A |
INTRINSIC |
|
low complexity region
|
1023 |
1035 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000169059
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.2%
- 20x: 95.0%
|
| Validation Efficiency |
98% (53/54) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the importin-beta family. Members of this family are regulated by the GTPase Ran to mediate transport of cargo across the nuclear envelope. This protein has been shown to mediate nuclear export of profilin-actin complexes. A pseudogene of this gene is located on the long arm of chromosome 14. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Aug 2012]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 54 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam21 |
A |
G |
12: 81,606,380 (GRCm39) |
F461L |
probably benign |
Het |
| Adamtsl3 |
C |
A |
7: 82,227,818 (GRCm39) |
H1334Q |
probably benign |
Het |
| Adgrf1 |
A |
G |
17: 43,621,263 (GRCm39) |
N500S |
probably damaging |
Het |
| Afdn |
A |
G |
17: 14,042,634 (GRCm39) |
D335G |
possibly damaging |
Het |
| Arhgap19 |
G |
A |
19: 41,775,077 (GRCm39) |
T178M |
probably damaging |
Het |
| Chac2 |
T |
C |
11: 30,927,625 (GRCm39) |
D86G |
probably damaging |
Het |
| Clhc1 |
T |
C |
11: 29,510,542 (GRCm39) |
S209P |
possibly damaging |
Het |
| Col1a2 |
G |
A |
6: 4,515,517 (GRCm39) |
G127S |
unknown |
Het |
| Coro2b |
A |
G |
9: 62,396,606 (GRCm39) |
F51L |
probably benign |
Het |
| Cux2 |
A |
G |
5: 122,002,789 (GRCm39) |
S1139P |
probably benign |
Het |
| Cyth3 |
A |
T |
5: 143,693,595 (GRCm39) |
I379F |
probably damaging |
Het |
| Dock2 |
A |
T |
11: 34,312,822 (GRCm39) |
L240H |
possibly damaging |
Het |
| Ercc6 |
A |
G |
14: 32,248,780 (GRCm39) |
K444E |
probably damaging |
Het |
| Fam3b |
A |
G |
16: 97,302,101 (GRCm39) |
L52P |
possibly damaging |
Het |
| Fat4 |
T |
G |
3: 39,035,418 (GRCm39) |
Y3023* |
probably null |
Het |
| Gad1 |
A |
T |
2: 70,423,780 (GRCm39) |
N396Y |
probably damaging |
Het |
| Gbp2b |
A |
G |
3: 142,317,252 (GRCm39) |
E536G |
probably benign |
Het |
| Gm11564 |
G |
A |
11: 99,706,061 (GRCm39) |
T123I |
unknown |
Het |
| Herc2 |
G |
T |
7: 55,796,393 (GRCm39) |
E1922* |
probably null |
Het |
| Hrh4 |
G |
T |
18: 13,155,525 (GRCm39) |
V355F |
probably damaging |
Het |
| Isyna1 |
A |
G |
8: 71,047,339 (GRCm39) |
I21V |
probably damaging |
Het |
| Jak1 |
T |
C |
4: 101,039,130 (GRCm39) |
D165G |
probably benign |
Het |
| Klhl38 |
C |
A |
15: 58,185,809 (GRCm39) |
G307* |
probably null |
Het |
| Krt77 |
T |
C |
15: 101,772,772 (GRCm39) |
N269S |
probably damaging |
Het |
| Lrp4 |
T |
A |
2: 91,322,765 (GRCm39) |
I1118N |
possibly damaging |
Het |
| Ly6i |
T |
C |
15: 74,853,833 (GRCm39) |
Y30C |
probably damaging |
Het |
| Magi2 |
A |
G |
5: 20,807,345 (GRCm39) |
E620G |
possibly damaging |
Het |
| Mbl2 |
A |
G |
19: 30,216,839 (GRCm39) |
D217G |
possibly damaging |
Het |
| Mogat2 |
T |
A |
7: 98,871,553 (GRCm39) |
I253F |
probably benign |
Het |
| Mpped2 |
T |
C |
2: 106,691,925 (GRCm39) |
L210P |
probably damaging |
Het |
| Nav3 |
C |
A |
10: 109,600,617 (GRCm39) |
A1337S |
probably damaging |
Het |
| Ncaph2 |
T |
A |
15: 89,248,407 (GRCm39) |
V206E |
probably benign |
Het |
| Nlgn1 |
T |
C |
3: 25,488,094 (GRCm39) |
E747G |
possibly damaging |
Het |
| Nlrc3 |
C |
T |
16: 3,770,308 (GRCm39) |
G237D |
possibly damaging |
Het |
| Nsun7 |
A |
G |
5: 66,452,827 (GRCm39) |
D514G |
probably benign |
Het |
| Or10al5 |
C |
G |
17: 38,063,577 (GRCm39) |
D277E |
probably damaging |
Het |
| Pals2 |
A |
G |
6: 50,175,146 (GRCm39) |
K500E |
possibly damaging |
Het |
| Pcnx2 |
C |
A |
8: 126,480,224 (GRCm39) |
V2028F |
probably damaging |
Het |
| Pdx1 |
G |
T |
5: 147,207,440 (GRCm39) |
W131L |
probably damaging |
Het |
| Pkdrej |
C |
T |
15: 85,703,747 (GRCm39) |
V730I |
probably damaging |
Het |
| Plcg1 |
T |
A |
2: 160,596,487 (GRCm39) |
Y669N |
probably damaging |
Het |
| Plpp1 |
G |
T |
13: 113,003,454 (GRCm39) |
W226L |
probably damaging |
Het |
| Sfxn1 |
G |
A |
13: 54,242,918 (GRCm39) |
V59I |
probably benign |
Het |
| Shank1 |
T |
C |
7: 43,976,645 (GRCm39) |
I581T |
unknown |
Het |
| Slc35f6 |
A |
C |
5: 30,814,164 (GRCm39) |
K150N |
possibly damaging |
Het |
| Slc5a7 |
A |
T |
17: 54,591,231 (GRCm39) |
S234T |
probably benign |
Het |
| Smg6 |
C |
T |
11: 74,821,331 (GRCm39) |
T534I |
possibly damaging |
Het |
| Ush2a |
C |
T |
1: 188,573,724 (GRCm39) |
T3649I |
probably benign |
Het |
| Vmn1r158 |
T |
C |
7: 22,490,078 (GRCm39) |
T44A |
possibly damaging |
Het |
| Vmn1r217 |
A |
T |
13: 23,298,073 (GRCm39) |
Y276* |
probably null |
Het |
| Vmn2r100 |
T |
A |
17: 19,742,355 (GRCm39) |
I243N |
probably damaging |
Het |
| Vwde |
T |
C |
6: 13,208,404 (GRCm39) |
|
probably null |
Het |
| Washc4 |
C |
A |
10: 83,394,687 (GRCm39) |
P306T |
probably damaging |
Het |
| Wdhd1 |
C |
T |
14: 47,488,217 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Xpo6 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01111:Xpo6
|
APN |
7 |
125,728,740 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL01432:Xpo6
|
APN |
7 |
125,723,553 (GRCm39) |
missense |
probably benign |
0.31 |
|
IGL01627:Xpo6
|
APN |
7 |
125,748,506 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01878:Xpo6
|
APN |
7 |
125,773,365 (GRCm39) |
missense |
probably benign |
0.35 |
|
IGL02185:Xpo6
|
APN |
7 |
125,712,980 (GRCm39) |
splice site |
probably benign |
|
|
IGL02744:Xpo6
|
APN |
7 |
125,707,620 (GRCm39) |
unclassified |
probably benign |
|
|
IGL02927:Xpo6
|
APN |
7 |
125,755,901 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL03216:Xpo6
|
APN |
7 |
125,703,985 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Anthracite
|
UTSW |
7 |
125,701,505 (GRCm39) |
nonsense |
probably null |
|
|
Bituminous
|
UTSW |
7 |
125,712,127 (GRCm39) |
splice site |
probably benign |
|
|
Cerise
|
UTSW |
7 |
125,708,016 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Crayola
|
UTSW |
7 |
125,706,250 (GRCm39) |
missense |
probably damaging |
0.98 |
|
pastel
|
UTSW |
7 |
125,707,791 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0845:Xpo6
|
UTSW |
7 |
125,728,715 (GRCm39) |
splice site |
probably benign |
|
|
R1671:Xpo6
|
UTSW |
7 |
125,707,715 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R2349:Xpo6
|
UTSW |
7 |
125,712,875 (GRCm39) |
missense |
probably benign |
0.18 |
|
R3051:Xpo6
|
UTSW |
7 |
125,703,893 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3052:Xpo6
|
UTSW |
7 |
125,703,893 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3053:Xpo6
|
UTSW |
7 |
125,703,893 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3902:Xpo6
|
UTSW |
7 |
125,719,581 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4011:Xpo6
|
UTSW |
7 |
125,739,780 (GRCm39) |
missense |
probably benign |
0.13 |
|
R4231:Xpo6
|
UTSW |
7 |
125,773,354 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R4569:Xpo6
|
UTSW |
7 |
125,727,427 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4604:Xpo6
|
UTSW |
7 |
125,712,924 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R4736:Xpo6
|
UTSW |
7 |
125,739,755 (GRCm39) |
missense |
probably benign |
|
|
R4919:Xpo6
|
UTSW |
7 |
125,752,115 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4953:Xpo6
|
UTSW |
7 |
125,768,443 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5017:Xpo6
|
UTSW |
7 |
125,703,919 (GRCm39) |
missense |
probably benign |
0.31 |
|
R5590:Xpo6
|
UTSW |
7 |
125,706,250 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5856:Xpo6
|
UTSW |
7 |
125,748,674 (GRCm39) |
intron |
probably benign |
|
|
R6077:Xpo6
|
UTSW |
7 |
125,709,124 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R6156:Xpo6
|
UTSW |
7 |
125,708,016 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6256:Xpo6
|
UTSW |
7 |
125,707,791 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6481:Xpo6
|
UTSW |
7 |
125,712,057 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7407:Xpo6
|
UTSW |
7 |
125,770,224 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7480:Xpo6
|
UTSW |
7 |
125,701,505 (GRCm39) |
nonsense |
probably null |
|
|
R7630:Xpo6
|
UTSW |
7 |
125,739,561 (GRCm39) |
splice site |
probably null |
|
|
R7794:Xpo6
|
UTSW |
7 |
125,760,035 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7984:Xpo6
|
UTSW |
7 |
125,719,616 (GRCm39) |
missense |
probably benign |
|
|
R8022:Xpo6
|
UTSW |
7 |
125,768,426 (GRCm39) |
missense |
probably benign |
0.04 |
|
R8283:Xpo6
|
UTSW |
7 |
125,727,421 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R8438:Xpo6
|
UTSW |
7 |
125,760,054 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R8786:Xpo6
|
UTSW |
7 |
125,712,127 (GRCm39) |
splice site |
probably benign |
|
|
R9427:Xpo6
|
UTSW |
7 |
125,748,418 (GRCm39) |
nonsense |
probably null |
|
|
R9674:Xpo6
|
UTSW |
7 |
125,723,700 (GRCm39) |
missense |
probably benign |
0.20 |
|
R9711:Xpo6
|
UTSW |
7 |
125,712,873 (GRCm39) |
missense |
probably benign |
0.00 |
|
X0012:Xpo6
|
UTSW |
7 |
125,768,399 (GRCm39) |
missense |
probably damaging |
0.97 |
|
| Predicted Primers |
|
| Posted On |
2018-06-06 |
Incidental Mutation