Incidental Mutation 'IGL01349:Arih2'
| ID |
75262 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Arih2
|
| Ensembl Gene |
ENSMUSG00000064145 |
| Gene Name |
ariadne RBR E3 ubiquitin protein ligase 2 |
| Synonyms |
TRIAD1 |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL01349
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
108480141-108526585 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 108482609 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Cysteine
at position 444
(Y444C)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000013338
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000013338]
[ENSMUST00000193190]
[ENSMUST00000193197]
[ENSMUST00000193552]
|
| AlphaFold |
Q9Z1K6 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000013338
AA Change: Y444C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000013338
Gene: ENSMUSG00000064145
AA Change: Y444C
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
14 |
36 |
N/A |
INTRINSIC |
|
RING
|
138 |
171 |
1.21e-1 |
SMART |
|
IBR
|
207 |
269 |
7.29e-23 |
SMART |
|
ZnF_C2HC
|
255 |
271 |
2.03e0 |
SMART |
|
IBR
|
277 |
339 |
1.81e-9 |
SMART |
|
RING
|
299 |
339 |
5.86e-1 |
SMART |
|
low complexity region
|
421 |
432 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000192686
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000192853
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000193190
|
| SMART Domains |
Protein: ENSMUSP00000141914
Gene: ENSMUSG00000064145
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
14 |
36 |
N/A |
INTRINSIC |
|
RING
|
138 |
171 |
5.7e-4 |
SMART |
|
IBR
|
207 |
269 |
2.5e-25 |
SMART |
|
ZnF_C2HC
|
255 |
271 |
8.4e-3 |
SMART |
|
Blast:IBR
|
277 |
317 |
2e-17 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000193197
|
| SMART Domains |
Protein: ENSMUSP00000141911
Gene: ENSMUSG00000064145
| Domain | Start | End | E-Value | Type |
|---|
|
IBR
|
1 |
36 |
1.5e-3 |
SMART |
|
ZnF_C2HC
|
22 |
38 |
8.4e-3 |
SMART |
|
Blast:IBR
|
44 |
79 |
1e-18 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000193552
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000193923
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000194073
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| 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 an E3 ubiquitin-protein ligase that polyubiquitinates some proteins, tagging them for degradation. The encoded protein upregulates p53 in some cancer cells and may inhibit myelopoiesis. Several transcript variants encoding different isoforms have been found for this gene, although the full-length nature of some of them have not been determined yet. [provided by RefSeq, Nov 2015]
PHENOTYPE: Homozygous inactivation of this gene causes altered dendritic cell physiology, enhanced liver apoptosis, and complete fetal lethality that is partially modified by genetic background. On a mixed genetic background, mice that survive past weaning succumb to a severe multiorgan inflammatory response. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 46 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca13 |
C |
T |
11: 9,242,076 (GRCm39) |
S1313L |
probably benign |
Het |
| Adam28 |
T |
C |
14: 68,848,455 (GRCm39) |
H667R |
probably benign |
Het |
| Arap1 |
T |
C |
7: 101,036,359 (GRCm39) |
V382A |
possibly damaging |
Het |
| Asxl3 |
T |
G |
18: 22,657,294 (GRCm39) |
V1768G |
probably benign |
Het |
| Bbs9 |
T |
A |
9: 22,798,979 (GRCm39) |
M869K |
probably benign |
Het |
| C4bp |
A |
G |
1: 130,570,665 (GRCm39) |
|
probably benign |
Het |
| Cc2d2a |
A |
T |
5: 43,881,126 (GRCm39) |
Y1167F |
probably benign |
Het |
| Cgn |
T |
A |
3: 94,674,486 (GRCm39) |
K884* |
probably null |
Het |
| Chd1l |
T |
C |
3: 97,498,550 (GRCm39) |
Y283C |
probably benign |
Het |
| Cry1 |
A |
G |
10: 84,984,603 (GRCm39) |
V157A |
probably benign |
Het |
| Dcc |
T |
A |
18: 71,503,808 (GRCm39) |
D950V |
probably damaging |
Het |
| Dlc1 |
A |
G |
8: 37,050,978 (GRCm39) |
F918L |
probably damaging |
Het |
| Dnah2 |
T |
C |
11: 69,366,432 (GRCm39) |
N1890S |
probably damaging |
Het |
| Dnah5 |
A |
G |
15: 28,295,059 (GRCm39) |
|
probably benign |
Het |
| Eif4b |
C |
T |
15: 101,999,858 (GRCm39) |
T412I |
probably benign |
Het |
| Eloa |
A |
C |
4: 135,741,758 (GRCm39) |
Y29D |
probably benign |
Het |
| Erbb4 |
A |
G |
1: 68,385,752 (GRCm39) |
F279S |
probably benign |
Het |
| Etl4 |
A |
G |
2: 20,718,207 (GRCm39) |
D316G |
probably damaging |
Het |
| Gm5114 |
T |
C |
7: 39,058,531 (GRCm39) |
S363G |
probably benign |
Het |
| Gpam |
A |
G |
19: 55,084,551 (GRCm39) |
|
probably null |
Het |
| Il17rd |
T |
A |
14: 26,817,901 (GRCm39) |
S197T |
probably damaging |
Het |
| Iqsec3 |
T |
C |
6: 121,450,083 (GRCm39) |
E147G |
possibly damaging |
Het |
| Itk |
T |
A |
11: 46,232,027 (GRCm39) |
T303S |
possibly damaging |
Het |
| Kcnh6 |
A |
G |
11: 105,914,743 (GRCm39) |
D716G |
possibly damaging |
Het |
| Lca5 |
A |
G |
9: 83,308,670 (GRCm39) |
S59P |
probably damaging |
Het |
| Lrrc40 |
T |
C |
3: 157,764,302 (GRCm39) |
|
probably benign |
Het |
| Mmp7 |
T |
C |
9: 7,699,335 (GRCm39) |
|
probably benign |
Het |
| Mycbp2 |
T |
C |
14: 103,359,983 (GRCm39) |
T4427A |
probably damaging |
Het |
| Nf2 |
T |
C |
11: 4,734,472 (GRCm39) |
D513G |
possibly damaging |
Het |
| Or2y1b |
T |
A |
11: 49,209,127 (GRCm39) |
Y251* |
probably null |
Het |
| Pde7a |
C |
T |
3: 19,283,843 (GRCm39) |
|
probably benign |
Het |
| Pira2 |
T |
C |
7: 3,847,138 (GRCm39) |
T135A |
probably damaging |
Het |
| Rb1 |
T |
C |
14: 73,506,558 (GRCm39) |
Y397C |
probably damaging |
Het |
| Ros1 |
A |
T |
10: 51,927,122 (GRCm39) |
M2187K |
probably damaging |
Het |
| Ryr2 |
T |
A |
13: 11,602,125 (GRCm39) |
I4586F |
possibly damaging |
Het |
| Serpinb3c |
A |
T |
1: 107,200,513 (GRCm39) |
M210K |
probably damaging |
Het |
| Slc22a19 |
C |
A |
19: 7,651,792 (GRCm39) |
V472F |
probably benign |
Het |
| Slc4a11 |
A |
G |
2: 130,528,863 (GRCm39) |
I462T |
probably benign |
Het |
| Spag11b |
A |
T |
8: 19,191,492 (GRCm39) |
H55L |
probably damaging |
Het |
| Trpv5 |
G |
T |
6: 41,652,309 (GRCm39) |
N125K |
possibly damaging |
Het |
| Ubr4 |
G |
T |
4: 139,208,039 (GRCm39) |
R4940L |
unknown |
Het |
| Vcan |
T |
A |
13: 89,852,062 (GRCm39) |
H966L |
probably damaging |
Het |
| Vmn1r204 |
T |
A |
13: 22,740,504 (GRCm39) |
I45K |
probably damaging |
Het |
| Vnn3 |
A |
T |
10: 23,727,814 (GRCm39) |
I75F |
probably damaging |
Het |
| Vps13b |
A |
T |
15: 35,794,091 (GRCm39) |
M2256L |
probably benign |
Het |
| Zfc3h1 |
T |
A |
10: 115,259,353 (GRCm39) |
L1642M |
probably damaging |
Het |
|
| Other mutations in Arih2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL03213:Arih2
|
APN |
9 |
108,484,546 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0009:Arih2
|
UTSW |
9 |
108,488,926 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0009:Arih2
|
UTSW |
9 |
108,488,926 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0314:Arih2
|
UTSW |
9 |
108,485,878 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0413:Arih2
|
UTSW |
9 |
108,493,916 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0450:Arih2
|
UTSW |
9 |
108,482,291 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R0469:Arih2
|
UTSW |
9 |
108,482,291 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R0865:Arih2
|
UTSW |
9 |
108,526,499 (GRCm39) |
utr 5 prime |
probably benign |
|
|
R2099:Arih2
|
UTSW |
9 |
108,493,937 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2913:Arih2
|
UTSW |
9 |
108,521,275 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4383:Arih2
|
UTSW |
9 |
108,521,476 (GRCm39) |
start codon destroyed |
probably benign |
0.41 |
|
R4636:Arih2
|
UTSW |
9 |
108,491,013 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5033:Arih2
|
UTSW |
9 |
108,488,859 (GRCm39) |
unclassified |
probably benign |
|
|
R5562:Arih2
|
UTSW |
9 |
108,484,546 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5976:Arih2
|
UTSW |
9 |
108,485,172 (GRCm39) |
makesense |
probably null |
|
|
R6248:Arih2
|
UTSW |
9 |
108,488,841 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8312:Arih2
|
UTSW |
9 |
108,521,473 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8349:Arih2
|
UTSW |
9 |
108,488,872 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R8449:Arih2
|
UTSW |
9 |
108,488,872 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R8883:Arih2
|
UTSW |
9 |
108,486,992 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8911:Arih2
|
UTSW |
9 |
108,488,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8912:Arih2
|
UTSW |
9 |
108,488,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8914:Arih2
|
UTSW |
9 |
108,488,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9091:Arih2
|
UTSW |
9 |
108,493,890 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9270:Arih2
|
UTSW |
9 |
108,493,890 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9348:Arih2
|
UTSW |
9 |
108,488,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9349:Arih2
|
UTSW |
9 |
108,488,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9350:Arih2
|
UTSW |
9 |
108,488,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9409:Arih2
|
UTSW |
9 |
108,488,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9410:Arih2
|
UTSW |
9 |
108,488,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9411:Arih2
|
UTSW |
9 |
108,488,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9415:Arih2
|
UTSW |
9 |
108,486,986 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9465:Arih2
|
UTSW |
9 |
108,488,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9466:Arih2
|
UTSW |
9 |
108,488,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9478:Arih2
|
UTSW |
9 |
108,488,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9479:Arih2
|
UTSW |
9 |
108,488,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9536:Arih2
|
UTSW |
9 |
108,488,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9776:Arih2
|
UTSW |
9 |
108,484,504 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-10-07 |
Incidental Mutation