Incidental Mutation 'IGL02375:Epn2'
| ID |
291073 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Epn2
|
| Ensembl Gene |
ENSMUSG00000001036 |
| Gene Name |
epsin 2 |
| Synonyms |
Ibp2, 9530051D10Rik |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL02375
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
61408075-61470513 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 61410497 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 512
(V512A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000136553
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000001063]
[ENSMUST00000108711]
[ENSMUST00000108712]
[ENSMUST00000108713]
[ENSMUST00000178202]
[ENSMUST00000179936]
|
| AlphaFold |
Q8CHU3 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000001063
AA Change: V512A
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000001063
Gene: ENSMUSG00000001036
AA Change: V512A
| Domain | Start | End | E-Value | Type |
|---|
|
ENTH
|
18 |
144 |
1.03e-65 |
SMART |
|
UIM
|
218 |
237 |
3.37e-1 |
SMART |
|
UIM
|
255 |
274 |
2.48e1 |
SMART |
|
low complexity region
|
449 |
461 |
N/A |
INTRINSIC |
|
low complexity region
|
493 |
517 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000108711
AA Change: V494A
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000104351
Gene: ENSMUSG00000001036
AA Change: V494A
| Domain | Start | End | E-Value | Type |
|---|
|
ENTH
|
18 |
144 |
1.03e-65 |
SMART |
|
UIM
|
218 |
237 |
6.29e-1 |
SMART |
|
UIM
|
243 |
262 |
2.48e1 |
SMART |
|
low complexity region
|
431 |
443 |
N/A |
INTRINSIC |
|
low complexity region
|
475 |
499 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000108712
AA Change: V551A
PolyPhen 2
Score 0.969 (Sensitivity: 0.77; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000104352
Gene: ENSMUSG00000001036
AA Change: V551A
| Domain | Start | End | E-Value | Type |
|---|
|
ENTH
|
18 |
144 |
1.03e-65 |
SMART |
|
UIM
|
275 |
294 |
6.29e-1 |
SMART |
|
UIM
|
300 |
319 |
2.48e1 |
SMART |
|
low complexity region
|
488 |
500 |
N/A |
INTRINSIC |
|
low complexity region
|
532 |
556 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000108713
AA Change: V500A
PolyPhen 2
Score 0.406 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000104353
Gene: ENSMUSG00000001036
AA Change: V500A
| Domain | Start | End | E-Value | Type |
|---|
|
ENTH
|
18 |
144 |
1.03e-65 |
SMART |
|
UIM
|
218 |
237 |
6.29e-1 |
SMART |
|
UIM
|
243 |
262 |
2.48e1 |
SMART |
|
low complexity region
|
437 |
449 |
N/A |
INTRINSIC |
|
low complexity region
|
481 |
505 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000148956
|
| SMART Domains |
Protein: ENSMUSP00000122514
Gene: ENSMUSG00000001036
| Domain | Start | End | E-Value | Type |
|---|
|
SCOP:d1eyha_
|
2 |
35 |
1e-9 |
SMART |
|
PDB:1EDU|A
|
2 |
37 |
5e-8 |
PDB |
|
UIM
|
152 |
171 |
6.29e-1 |
SMART |
|
UIM
|
177 |
196 |
2.48e1 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000178202
AA Change: V512A
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000136553
Gene: ENSMUSG00000001036
AA Change: V512A
| Domain | Start | End | E-Value | Type |
|---|
|
ENTH
|
18 |
144 |
1.03e-65 |
SMART |
|
UIM
|
218 |
237 |
3.37e-1 |
SMART |
|
UIM
|
255 |
274 |
2.48e1 |
SMART |
|
low complexity region
|
449 |
461 |
N/A |
INTRINSIC |
|
low complexity region
|
493 |
517 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000179936
AA Change: V557A
PolyPhen 2
Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000136950
Gene: ENSMUSG00000001036
AA Change: V557A
| Domain | Start | End | E-Value | Type |
|---|
|
ENTH
|
18 |
144 |
1.03e-65 |
SMART |
|
UIM
|
275 |
294 |
6.29e-1 |
SMART |
|
UIM
|
300 |
319 |
2.48e1 |
SMART |
|
low complexity region
|
494 |
506 |
N/A |
INTRINSIC |
|
low complexity region
|
538 |
562 |
N/A |
INTRINSIC |
|
| 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 encodes a protein which interacts with clathrin and adaptor-related protein complex 2, alpha 1 subunit. The protein is found in a brain-derived clathrin-coated vesicle fraction and localizes to the peri-Golgi region and the cell periphery. The protein is thought to be involved in clathrin-mediated endocytosis. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a null mutation are viable and fertile with no gross abnormalities. Mice homozygous null for both Epn1 and Epn2 display defects in angiogenic vascular remodeling, impaired somitogenesis and extensive cell death in the nervous tissue, resulting in lethality during organogenesis. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 40 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700034J05Rik |
T |
A |
6: 146,854,813 (GRCm39) |
K76N |
possibly damaging |
Het |
| Agxt |
A |
G |
1: 93,063,425 (GRCm39) |
E109G |
probably damaging |
Het |
| Alcam |
T |
C |
16: 52,109,299 (GRCm39) |
T325A |
probably benign |
Het |
| Apol7c |
T |
C |
15: 77,413,049 (GRCm39) |
E67G |
probably damaging |
Het |
| Bco1 |
C |
A |
8: 117,840,178 (GRCm39) |
S232Y |
probably benign |
Het |
| Cacna1c |
A |
T |
6: 118,652,884 (GRCm39) |
V763D |
probably damaging |
Het |
| Ccdc15 |
T |
C |
9: 37,215,628 (GRCm39) |
D618G |
probably damaging |
Het |
| Cimip1 |
A |
G |
2: 173,364,496 (GRCm39) |
M14V |
probably benign |
Het |
| Col6a5 |
T |
C |
9: 105,783,312 (GRCm39) |
N1603S |
unknown |
Het |
| Cyp4v3 |
A |
G |
8: 45,761,411 (GRCm39) |
|
probably null |
Het |
| Eml5 |
A |
T |
12: 98,810,346 (GRCm39) |
V870E |
probably damaging |
Het |
| Farp2 |
A |
G |
1: 93,504,185 (GRCm39) |
R321G |
probably damaging |
Het |
| Garin3 |
G |
T |
11: 46,297,379 (GRCm39) |
V228L |
probably damaging |
Het |
| Gprasp1 |
T |
C |
X: 134,701,552 (GRCm39) |
S582P |
probably damaging |
Het |
| Grhl2 |
T |
C |
15: 37,291,821 (GRCm39) |
V303A |
probably damaging |
Het |
| Grik1 |
A |
T |
16: 87,743,444 (GRCm39) |
F594L |
probably damaging |
Het |
| Hivep1 |
A |
G |
13: 42,309,925 (GRCm39) |
K722E |
probably benign |
Het |
| Htr5b |
G |
A |
1: 121,455,564 (GRCm39) |
R119C |
probably damaging |
Het |
| Ifit2 |
T |
C |
19: 34,551,737 (GRCm39) |
S426P |
probably benign |
Het |
| Kif13a |
T |
C |
13: 46,978,698 (GRCm39) |
Y234C |
probably damaging |
Het |
| Mios |
T |
A |
6: 8,222,598 (GRCm39) |
F511I |
probably benign |
Het |
| Mtfmt |
T |
C |
9: 65,346,849 (GRCm39) |
W148R |
probably damaging |
Het |
| Myo1c |
C |
A |
11: 75,552,400 (GRCm39) |
T391N |
probably benign |
Het |
| Nlrp1a |
A |
T |
11: 71,004,339 (GRCm39) |
L710* |
probably null |
Het |
| Nlrp1b |
A |
G |
11: 71,052,506 (GRCm39) |
I971T |
probably damaging |
Het |
| Nup43 |
A |
G |
10: 7,549,358 (GRCm39) |
D171G |
probably damaging |
Het |
| Or5b12b |
A |
G |
19: 12,861,305 (GRCm39) |
E20G |
probably benign |
Het |
| P2rx7 |
T |
C |
5: 122,811,719 (GRCm39) |
|
probably benign |
Het |
| Pgap6 |
T |
A |
17: 26,338,473 (GRCm39) |
Y512N |
probably benign |
Het |
| Poli |
C |
T |
18: 70,656,363 (GRCm39) |
G155R |
probably damaging |
Het |
| Rad9b |
T |
C |
5: 122,471,405 (GRCm39) |
S220G |
possibly damaging |
Het |
| Rgn |
C |
T |
X: 20,416,700 (GRCm39) |
S28L |
probably damaging |
Het |
| Tcp11l2 |
G |
A |
10: 84,440,932 (GRCm39) |
|
probably null |
Het |
| Tenm4 |
G |
A |
7: 96,353,344 (GRCm39) |
V379I |
possibly damaging |
Het |
| Thsd7a |
A |
T |
6: 12,343,264 (GRCm39) |
C1118S |
probably damaging |
Het |
| Trpm7 |
A |
G |
2: 126,667,664 (GRCm39) |
Y776H |
probably damaging |
Het |
| Trpv4 |
T |
C |
5: 114,774,418 (GRCm39) |
N222S |
probably benign |
Het |
| Tut1 |
C |
T |
19: 8,941,403 (GRCm39) |
R397C |
probably damaging |
Het |
| Vmn1r72 |
T |
A |
7: 11,403,672 (GRCm39) |
T259S |
probably benign |
Het |
| Wdr17 |
A |
G |
8: 55,149,423 (GRCm39) |
S2P |
possibly damaging |
Het |
|
| Other mutations in Epn2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01478:Epn2
|
APN |
11 |
61,413,912 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01582:Epn2
|
APN |
11 |
61,412,695 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03213:Epn2
|
APN |
11 |
61,410,510 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Ipanema
|
UTSW |
11 |
61,410,384 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0400:Epn2
|
UTSW |
11 |
61,423,522 (GRCm39) |
splice site |
probably null |
|
|
R0458:Epn2
|
UTSW |
11 |
61,437,281 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R0471:Epn2
|
UTSW |
11 |
61,426,134 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0833:Epn2
|
UTSW |
11 |
61,410,317 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0836:Epn2
|
UTSW |
11 |
61,410,317 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1418:Epn2
|
UTSW |
11 |
61,413,912 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1699:Epn2
|
UTSW |
11 |
61,414,014 (GRCm39) |
nonsense |
probably null |
|
|
R1743:Epn2
|
UTSW |
11 |
61,437,237 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R4039:Epn2
|
UTSW |
11 |
61,437,348 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4696:Epn2
|
UTSW |
11 |
61,426,129 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4752:Epn2
|
UTSW |
11 |
61,437,197 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4913:Epn2
|
UTSW |
11 |
61,425,402 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6053:Epn2
|
UTSW |
11 |
61,437,323 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6302:Epn2
|
UTSW |
11 |
61,437,312 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6455:Epn2
|
UTSW |
11 |
61,424,467 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6669:Epn2
|
UTSW |
11 |
61,410,384 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7032:Epn2
|
UTSW |
11 |
61,437,528 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7439:Epn2
|
UTSW |
11 |
61,437,674 (GRCm39) |
start gained |
probably benign |
|
|
R8008:Epn2
|
UTSW |
11 |
61,437,492 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8128:Epn2
|
UTSW |
11 |
61,413,321 (GRCm39) |
splice site |
probably null |
|
|
R9114:Epn2
|
UTSW |
11 |
61,437,446 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9546:Epn2
|
UTSW |
11 |
61,437,407 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9548:Epn2
|
UTSW |
11 |
61,436,988 (GRCm39) |
missense |
probably benign |
0.31 |
|
Z1177:Epn2
|
UTSW |
11 |
61,437,250 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1186:Epn2
|
UTSW |
11 |
61,470,460 (GRCm39) |
start gained |
probably benign |
|
|
Z1187:Epn2
|
UTSW |
11 |
61,470,460 (GRCm39) |
start gained |
probably benign |
|
|
Z1188:Epn2
|
UTSW |
11 |
61,470,460 (GRCm39) |
start gained |
probably benign |
|
|
Z1189:Epn2
|
UTSW |
11 |
61,470,460 (GRCm39) |
start gained |
probably benign |
|
|
Z1190:Epn2
|
UTSW |
11 |
61,470,460 (GRCm39) |
start gained |
probably benign |
|
|
Z1191:Epn2
|
UTSW |
11 |
61,470,460 (GRCm39) |
start gained |
probably benign |
|
|
Z1192:Epn2
|
UTSW |
11 |
61,470,460 (GRCm39) |
start gained |
probably benign |
|
|
| Posted On |
2015-04-16 |
Incidental Mutation