Incidental Mutation 'IGL01025:Rtn3'
| ID |
60421 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Rtn3
|
| Ensembl Gene |
ENSMUSG00000024758 |
| Gene Name |
reticulon 3 |
| Synonyms |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.172)
|
| Stock # |
IGL01025
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
19 |
| Chromosomal Location |
7403266-7460646 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 7460406 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 15
(S15P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000085496
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000025667]
[ENSMUST00000065304]
[ENSMUST00000088169]
[ENSMUST00000088171]
|
| AlphaFold |
Q9ES97 |
| Predicted Effect |
unknown
Transcript: ENSMUST00000025667
AA Change: S15P
|
| SMART Domains |
Protein: ENSMUSP00000025667
Gene: ENSMUSG00000024758
AA Change: S15P
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
40 |
N/A |
INTRINSIC |
|
Pfam:Reticulon
|
49 |
219 |
8.7e-58 |
PFAM |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000065304
AA Change: S15P
|
| SMART Domains |
Protein: ENSMUSP00000065810
Gene: ENSMUSG00000024758
AA Change: S15P
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
40 |
N/A |
INTRINSIC |
|
low complexity region
|
42 |
66 |
N/A |
INTRINSIC |
|
low complexity region
|
80 |
91 |
N/A |
INTRINSIC |
|
low complexity region
|
119 |
131 |
N/A |
INTRINSIC |
|
low complexity region
|
516 |
527 |
N/A |
INTRINSIC |
|
low complexity region
|
639 |
650 |
N/A |
INTRINSIC |
|
Pfam:Reticulon
|
776 |
940 |
9.1e-45 |
PFAM |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000088169
AA Change: S15P
|
| SMART Domains |
Protein: ENSMUSP00000085494
Gene: ENSMUSG00000024758
AA Change: S15P
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
40 |
N/A |
INTRINSIC |
|
low complexity region
|
42 |
66 |
N/A |
INTRINSIC |
|
Pfam:Reticulon
|
68 |
238 |
1.1e-57 |
PFAM |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000088171
AA Change: S15P
|
| SMART Domains |
Protein: ENSMUSP00000085496
Gene: ENSMUSG00000024758
AA Change: S15P
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
56 |
N/A |
INTRINSIC |
|
low complexity region
|
61 |
72 |
N/A |
INTRINSIC |
|
low complexity region
|
100 |
112 |
N/A |
INTRINSIC |
|
low complexity region
|
497 |
508 |
N/A |
INTRINSIC |
|
low complexity region
|
620 |
631 |
N/A |
INTRINSIC |
|
Pfam:Reticulon
|
757 |
927 |
1.8e-56 |
PFAM |
|
| Coding Region Coverage |
|
| 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 reticulon family of highly conserved genes that are preferentially expressed in neuroendocrine tissues. This family of proteins interact with, and modulate the activity of beta-amyloid converting enzyme 1 (BACE1), and the production of amyloid-beta. An increase in the expression of any reticulon protein substantially reduces the production of amyloid-beta, suggesting that reticulon proteins are negative modulators of BACE1 in cells. Alternatively spliced transcript variants encoding different isoforms have been found for this gene, and pseudogenes of this gene are located on chromosomes 4 and 12. [provided by RefSeq, May 2012]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 55 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acap3 |
G |
A |
4: 155,986,676 (GRCm39) |
V335M |
probably damaging |
Het |
| Apex1 |
C |
T |
14: 51,163,711 (GRCm39) |
L113F |
possibly damaging |
Het |
| Bltp1 |
T |
A |
3: 37,100,429 (GRCm39) |
H1218Q |
possibly damaging |
Het |
| Cd33 |
C |
T |
7: 43,182,329 (GRCm39) |
V39M |
probably damaging |
Het |
| Chek2 |
A |
G |
5: 110,996,536 (GRCm39) |
D166G |
probably damaging |
Het |
| Col2a1 |
T |
C |
15: 97,874,054 (GRCm39) |
K1376R |
unknown |
Het |
| Cpd |
C |
T |
11: 76,686,439 (GRCm39) |
R963H |
probably damaging |
Het |
| Cracd |
A |
G |
5: 76,805,921 (GRCm39) |
|
probably benign |
Het |
| Cyp2c67 |
A |
C |
19: 39,628,376 (GRCm39) |
Y189* |
probably null |
Het |
| Dock6 |
T |
C |
9: 21,723,103 (GRCm39) |
E1606G |
possibly damaging |
Het |
| Dusp4 |
A |
T |
8: 35,285,666 (GRCm39) |
E309V |
probably benign |
Het |
| Dync2h1 |
A |
G |
9: 7,162,789 (GRCm39) |
I600T |
probably damaging |
Het |
| Fer1l4 |
A |
G |
2: 155,894,105 (GRCm39) |
V66A |
probably benign |
Het |
| Fktn |
T |
C |
4: 53,737,568 (GRCm39) |
L269P |
possibly damaging |
Het |
| Ftsj3 |
A |
G |
11: 106,141,185 (GRCm39) |
I645T |
probably damaging |
Het |
| Fxr2 |
A |
G |
11: 69,534,713 (GRCm39) |
H198R |
probably damaging |
Het |
| Fzd7 |
T |
C |
1: 59,523,539 (GRCm39) |
V474A |
probably damaging |
Het |
| Gm10295 |
T |
A |
7: 71,000,406 (GRCm39) |
D58V |
unknown |
Het |
| Hdlbp |
T |
C |
1: 93,357,891 (GRCm39) |
I337V |
probably benign |
Het |
| Hydin |
T |
C |
8: 111,053,033 (GRCm39) |
V235A |
probably benign |
Het |
| Igfbp4 |
C |
T |
11: 98,939,069 (GRCm39) |
H30Y |
probably damaging |
Het |
| Kcna4 |
T |
C |
2: 107,126,736 (GRCm39) |
V490A |
probably damaging |
Het |
| Kcnj13 |
T |
G |
1: 87,314,700 (GRCm39) |
D174A |
probably benign |
Het |
| Krt7 |
T |
A |
15: 101,321,302 (GRCm39) |
L373Q |
probably benign |
Het |
| Lama3 |
G |
A |
18: 12,614,094 (GRCm39) |
V1288I |
probably benign |
Het |
| Mroh9 |
T |
C |
1: 162,875,435 (GRCm39) |
D488G |
possibly damaging |
Het |
| Myh7 |
T |
C |
14: 55,216,994 (GRCm39) |
E1121G |
probably damaging |
Het |
| Myom1 |
A |
G |
17: 71,384,912 (GRCm39) |
N768D |
probably damaging |
Het |
| Naa16 |
T |
C |
14: 79,622,196 (GRCm39) |
T48A |
probably damaging |
Het |
| Naglu |
C |
T |
11: 100,964,773 (GRCm39) |
P287S |
probably benign |
Het |
| Nipbl |
A |
G |
15: 8,379,939 (GRCm39) |
V951A |
possibly damaging |
Het |
| Nlrp3 |
T |
A |
11: 59,442,713 (GRCm39) |
M755K |
probably benign |
Het |
| Nlrp4e |
T |
C |
7: 23,052,586 (GRCm39) |
|
probably benign |
Het |
| Nt5dc1 |
C |
T |
10: 34,283,553 (GRCm39) |
A79T |
possibly damaging |
Het |
| Or10aa3 |
T |
C |
1: 173,878,251 (GRCm39) |
F104S |
probably damaging |
Het |
| Or6c205 |
A |
T |
10: 129,086,609 (GRCm39) |
I69F |
possibly damaging |
Het |
| Or8b47 |
A |
G |
9: 38,435,029 (GRCm39) |
|
probably benign |
Het |
| Otof |
A |
G |
5: 30,541,597 (GRCm39) |
L774P |
possibly damaging |
Het |
| Phf20l1 |
C |
T |
15: 66,484,981 (GRCm39) |
R322C |
probably damaging |
Het |
| Pkhd1 |
C |
T |
1: 20,279,400 (GRCm39) |
G2973R |
probably benign |
Het |
| Plekhg5 |
G |
T |
4: 152,192,983 (GRCm39) |
D613Y |
probably damaging |
Het |
| Ppm1h |
T |
A |
10: 122,714,534 (GRCm39) |
|
probably null |
Het |
| Pramel31 |
T |
A |
4: 144,089,947 (GRCm39) |
L329Q |
probably damaging |
Het |
| Prpf39 |
T |
C |
12: 65,089,255 (GRCm39) |
|
probably benign |
Het |
| Slc22a28 |
G |
T |
19: 8,094,272 (GRCm39) |
|
probably benign |
Het |
| Slc4a5 |
T |
A |
6: 83,239,515 (GRCm39) |
L143Q |
probably damaging |
Het |
| Sox17 |
T |
C |
1: 4,562,426 (GRCm39) |
D130G |
possibly damaging |
Het |
| Stag1 |
A |
G |
9: 100,833,710 (GRCm39) |
T1108A |
possibly damaging |
Het |
| Sugp2 |
G |
A |
8: 70,695,185 (GRCm39) |
D53N |
probably damaging |
Het |
| Trim33 |
G |
A |
3: 103,261,234 (GRCm39) |
|
probably benign |
Het |
| Ttn |
A |
G |
2: 76,629,568 (GRCm39) |
I14291T |
probably damaging |
Het |
| Ttn |
A |
G |
2: 76,619,869 (GRCm39) |
V15933A |
probably damaging |
Het |
| Tulp3 |
A |
C |
6: 128,302,847 (GRCm39) |
I324S |
probably damaging |
Het |
| Zfhx2 |
T |
C |
14: 55,301,717 (GRCm39) |
E2089G |
probably damaging |
Het |
| Zhx1 |
T |
C |
15: 57,918,075 (GRCm39) |
D57G |
probably benign |
Het |
|
| Other mutations in Rtn3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00791:Rtn3
|
APN |
19 |
7,412,434 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01347:Rtn3
|
APN |
19 |
7,434,645 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01845:Rtn3
|
APN |
19 |
7,435,241 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02217:Rtn3
|
APN |
19 |
7,412,449 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03024:Rtn3
|
APN |
19 |
7,460,455 (GRCm39) |
utr 5 prime |
probably benign |
|
|
R0399:Rtn3
|
UTSW |
19 |
7,435,241 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0633:Rtn3
|
UTSW |
19 |
7,434,958 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0826:Rtn3
|
UTSW |
19 |
7,445,245 (GRCm39) |
intron |
probably benign |
|
|
R1327:Rtn3
|
UTSW |
19 |
7,408,376 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R1735:Rtn3
|
UTSW |
19 |
7,435,276 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R2093:Rtn3
|
UTSW |
19 |
7,434,215 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3116:Rtn3
|
UTSW |
19 |
7,409,355 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3894:Rtn3
|
UTSW |
19 |
7,412,450 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3961:Rtn3
|
UTSW |
19 |
7,435,510 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3962:Rtn3
|
UTSW |
19 |
7,435,510 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3963:Rtn3
|
UTSW |
19 |
7,435,510 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4161:Rtn3
|
UTSW |
19 |
7,460,444 (GRCm39) |
missense |
probably benign |
0.38 |
|
R4960:Rtn3
|
UTSW |
19 |
7,433,886 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5585:Rtn3
|
UTSW |
19 |
7,435,560 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5735:Rtn3
|
UTSW |
19 |
7,434,057 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5796:Rtn3
|
UTSW |
19 |
7,434,832 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R5807:Rtn3
|
UTSW |
19 |
7,434,192 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5864:Rtn3
|
UTSW |
19 |
7,412,476 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6322:Rtn3
|
UTSW |
19 |
7,435,503 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R6703:Rtn3
|
UTSW |
19 |
7,412,410 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6885:Rtn3
|
UTSW |
19 |
7,435,696 (GRCm39) |
missense |
probably benign |
0.31 |
|
R6888:Rtn3
|
UTSW |
19 |
7,434,614 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6989:Rtn3
|
UTSW |
19 |
7,433,856 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6992:Rtn3
|
UTSW |
19 |
7,412,489 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7506:Rtn3
|
UTSW |
19 |
7,407,118 (GRCm39) |
missense |
probably benign |
0.08 |
|
R7610:Rtn3
|
UTSW |
19 |
7,435,294 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7639:Rtn3
|
UTSW |
19 |
7,435,356 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7909:Rtn3
|
UTSW |
19 |
7,433,827 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R7915:Rtn3
|
UTSW |
19 |
7,434,865 (GRCm39) |
missense |
probably benign |
0.06 |
|
R8088:Rtn3
|
UTSW |
19 |
7,412,363 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8549:Rtn3
|
UTSW |
19 |
7,434,624 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8725:Rtn3
|
UTSW |
19 |
7,434,726 (GRCm39) |
missense |
probably benign |
|
|
R8727:Rtn3
|
UTSW |
19 |
7,434,726 (GRCm39) |
missense |
probably benign |
|
|
R8917:Rtn3
|
UTSW |
19 |
7,434,105 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R9225:Rtn3
|
UTSW |
19 |
7,434,854 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9336:Rtn3
|
UTSW |
19 |
7,460,328 (GRCm39) |
missense |
unknown |
|
|
X0060:Rtn3
|
UTSW |
19 |
7,409,936 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
Z1192:Rtn3
|
UTSW |
19 |
7,460,342 (GRCm39) |
missense |
unknown |
|
|
| Posted On |
2013-07-11 |
Incidental Mutation