Incidental Mutation 'R5576:Snx2'
| ID |
437238 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Snx2
|
| Ensembl Gene |
ENSMUSG00000034484 |
| Gene Name |
sorting nexin 2 |
| Synonyms |
0610030A03Rik |
| MMRRC Submission |
043131-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R5576 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
18 |
| Chromosomal Location |
53309388-53353937 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 53343822 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Lysine to Glutamic Acid
at position 322
(K322E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000039243
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000037850]
|
| AlphaFold |
Q9CWK8 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000037850
AA Change: K322E
PolyPhen 2
Score 0.332 (Sensitivity: 0.90; Specificity: 0.89)
|
| SMART Domains |
Protein: ENSMUSP00000039243
Gene: ENSMUSG00000034484
AA Change: K322E
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Sorting_nexin
|
2 |
134 |
1.6e-29 |
PFAM |
|
PX
|
138 |
265 |
1.4e-38 |
SMART |
|
Pfam:Vps5
|
281 |
514 |
2.2e-90 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.4%
- 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 belongs to the sorting nexin family whose members contain the phosphoinositide-binding phox (PX) domain. The encoded protein is a component of the retromer complex which plays a role in protein sorting in the endocytic pathway. This protein may form oligomeric complexes with other family members. Alternate splicing results in multiple transcript variants of this gene. Pseudogenes associated with this gene are located on chromosomes 1 and 7. [provided by RefSeq, May 2013]
PHENOTYPE: Homozygous mutant mice are viable and fertile and do not exhibit any apparent abnormalities. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 45 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930522L14Rik |
G |
A |
5: 109,885,570 (GRCm39) |
T96I |
probably benign |
Het |
| Add2 |
G |
T |
6: 86,084,457 (GRCm39) |
|
probably null |
Het |
| Agbl1 |
C |
T |
7: 75,984,985 (GRCm39) |
T134M |
probably benign |
Het |
| Agfg1 |
T |
A |
1: 82,848,445 (GRCm39) |
S32T |
probably benign |
Het |
| Ankrd17 |
A |
C |
5: 90,391,083 (GRCm39) |
S2087A |
probably benign |
Het |
| Apob |
A |
T |
12: 8,048,662 (GRCm39) |
E1012V |
probably damaging |
Het |
| Baiap2 |
T |
A |
11: 119,887,737 (GRCm39) |
V297E |
probably benign |
Het |
| BC034090 |
T |
G |
1: 155,117,214 (GRCm39) |
K301N |
probably benign |
Het |
| Bhlha9 |
T |
C |
11: 76,563,595 (GRCm39) |
I74T |
probably damaging |
Het |
| Btnl9 |
T |
C |
11: 49,069,712 (GRCm39) |
H189R |
probably benign |
Het |
| Ccdc122 |
G |
A |
14: 77,329,317 (GRCm39) |
M123I |
probably benign |
Het |
| Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
| Dnah9 |
T |
C |
11: 65,724,922 (GRCm39) |
|
probably null |
Het |
| Dnaja2 |
A |
T |
8: 86,266,033 (GRCm39) |
L351I |
possibly damaging |
Het |
| Efcab6 |
C |
A |
15: 83,834,201 (GRCm39) |
S469I |
probably benign |
Het |
| Esp15 |
C |
A |
17: 39,953,564 (GRCm39) |
T17K |
probably damaging |
Het |
| Fads1 |
A |
G |
19: 10,163,238 (GRCm39) |
T172A |
probably benign |
Het |
| Fbp2 |
A |
T |
13: 62,985,005 (GRCm39) |
D305E |
probably benign |
Het |
| Golga4 |
A |
G |
9: 118,382,602 (GRCm39) |
T541A |
probably benign |
Het |
| Herc3 |
T |
C |
6: 58,865,710 (GRCm39) |
Y768H |
probably benign |
Het |
| Kmt2a |
A |
G |
9: 44,753,931 (GRCm39) |
V514A |
possibly damaging |
Het |
| Melk |
A |
G |
4: 44,312,255 (GRCm39) |
E141G |
probably null |
Het |
| Nln |
A |
G |
13: 104,195,338 (GRCm39) |
Y245H |
probably damaging |
Het |
| Nrap |
C |
T |
19: 56,310,414 (GRCm39) |
R1563H |
probably damaging |
Het |
| Or7g34 |
T |
A |
9: 19,478,369 (GRCm39) |
M101L |
probably benign |
Het |
| Or8b44 |
A |
C |
9: 38,410,204 (GRCm39) |
K80Q |
probably damaging |
Het |
| Pde4b |
T |
A |
4: 102,287,359 (GRCm39) |
I34N |
probably damaging |
Het |
| Pex11g |
A |
G |
8: 3,515,875 (GRCm39) |
S53P |
probably damaging |
Het |
| Pole |
A |
T |
5: 110,459,931 (GRCm39) |
K1112* |
probably null |
Het |
| Ppfia4 |
T |
G |
1: 134,250,788 (GRCm39) |
D184A |
possibly damaging |
Het |
| Rpp30 |
T |
A |
19: 36,079,251 (GRCm39) |
D216E |
probably benign |
Het |
| Sbno2 |
C |
T |
10: 79,903,171 (GRCm39) |
A398T |
probably damaging |
Het |
| Sbp |
T |
A |
17: 24,164,552 (GRCm39) |
S94T |
probably benign |
Het |
| Skp1 |
T |
G |
11: 52,133,415 (GRCm39) |
D33E |
possibly damaging |
Het |
| Slc17a8 |
A |
G |
10: 89,433,364 (GRCm39) |
W220R |
probably damaging |
Het |
| Slfn9 |
A |
T |
11: 82,872,258 (GRCm39) |
M826K |
probably benign |
Het |
| Spata32 |
T |
A |
11: 103,100,653 (GRCm39) |
N38I |
possibly damaging |
Het |
| Sycp1 |
T |
C |
3: 102,726,218 (GRCm39) |
R969G |
probably damaging |
Het |
| Trgc2 |
T |
C |
13: 19,489,301 (GRCm39) |
I144V |
probably benign |
Het |
| Trpc1 |
A |
G |
9: 95,603,377 (GRCm39) |
L385S |
probably damaging |
Het |
| Vmn2r105 |
C |
T |
17: 20,444,836 (GRCm39) |
|
probably null |
Het |
| Xrcc6 |
T |
A |
15: 81,906,693 (GRCm39) |
D79E |
probably damaging |
Het |
| Zan |
A |
T |
5: 137,426,744 (GRCm39) |
C2467* |
probably null |
Het |
| Zfp26 |
A |
G |
9: 20,348,803 (GRCm39) |
V587A |
possibly damaging |
Het |
| Zfp553 |
C |
T |
7: 126,835,875 (GRCm39) |
R477C |
possibly damaging |
Het |
|
| Other mutations in Snx2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00836:Snx2
|
APN |
18 |
53,349,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL00861:Snx2
|
APN |
18 |
53,343,869 (GRCm39) |
splice site |
probably null |
|
|
IGL01116:Snx2
|
APN |
18 |
53,327,495 (GRCm39) |
splice site |
probably benign |
|
|
IGL01642:Snx2
|
APN |
18 |
53,349,519 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02178:Snx2
|
APN |
18 |
53,332,857 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
IGL02368:Snx2
|
APN |
18 |
53,322,793 (GRCm39) |
missense |
probably benign |
|
|
IGL02597:Snx2
|
APN |
18 |
53,343,444 (GRCm39) |
missense |
probably benign |
0.09 |
|
IGL02964:Snx2
|
APN |
18 |
53,327,630 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03372:Snx2
|
APN |
18 |
53,349,463 (GRCm39) |
missense |
probably damaging |
1.00 |
|
blanched
|
UTSW |
18 |
53,327,516 (GRCm39) |
missense |
probably damaging |
0.98 |
|
bleached
|
UTSW |
18 |
53,330,997 (GRCm39) |
splice site |
probably null |
|
|
R0332:Snx2
|
UTSW |
18 |
53,345,983 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0723:Snx2
|
UTSW |
18 |
53,343,444 (GRCm39) |
missense |
probably benign |
0.09 |
|
R0746:Snx2
|
UTSW |
18 |
53,330,961 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0826:Snx2
|
UTSW |
18 |
53,327,594 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0894:Snx2
|
UTSW |
18 |
53,309,488 (GRCm39) |
missense |
probably benign |
|
|
R0970:Snx2
|
UTSW |
18 |
53,343,762 (GRCm39) |
splice site |
probably benign |
|
|
R1897:Snx2
|
UTSW |
18 |
53,330,950 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2049:Snx2
|
UTSW |
18 |
53,327,516 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2910:Snx2
|
UTSW |
18 |
53,332,946 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2911:Snx2
|
UTSW |
18 |
53,332,946 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4460:Snx2
|
UTSW |
18 |
53,309,516 (GRCm39) |
missense |
probably benign |
0.31 |
|
R5225:Snx2
|
UTSW |
18 |
53,322,784 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5352:Snx2
|
UTSW |
18 |
53,330,997 (GRCm39) |
splice site |
probably null |
|
|
R5450:Snx2
|
UTSW |
18 |
53,343,784 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5965:Snx2
|
UTSW |
18 |
53,327,534 (GRCm39) |
nonsense |
probably null |
|
|
R6063:Snx2
|
UTSW |
18 |
53,342,697 (GRCm39) |
nonsense |
probably null |
|
|
R6222:Snx2
|
UTSW |
18 |
53,332,896 (GRCm39) |
nonsense |
probably null |
|
|
R6291:Snx2
|
UTSW |
18 |
53,342,737 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6890:Snx2
|
UTSW |
18 |
53,345,951 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7380:Snx2
|
UTSW |
18 |
53,327,640 (GRCm39) |
missense |
probably benign |
|
|
R8081:Snx2
|
UTSW |
18 |
53,349,459 (GRCm39) |
missense |
probably benign |
0.13 |
|
R8363:Snx2
|
UTSW |
18 |
53,330,936 (GRCm39) |
nonsense |
probably null |
|
|
R9451:Snx2
|
UTSW |
18 |
53,343,415 (GRCm39) |
missense |
probably benign |
0.37 |
|
| Predicted Primers |
PCR Primer
(F):5'- GCTTATTGAGTTCAGTTCTCAGCTAC -3'
(R):5'- TCTGTTTTGAGACAGCCTAGCG -3'
Sequencing Primer
(F):5'- TACATCAGTTGACCACCGTGG -3'
(R):5'- TTTTGAGACAGCCTAGCGTCAGAC -3'
|
| Posted On |
2016-10-26 |
Incidental Mutation