Incidental Mutation 'IGL01329:Ifnar2'
| ID |
74450 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Ifnar2
|
| Ensembl Gene |
ENSMUSG00000022971 |
| Gene Name |
interferon (alpha and beta) receptor 2 |
| Synonyms |
Ifnar-2 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.148)
|
| Stock # |
IGL01329
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
16 |
| Chromosomal Location |
91169671-91202477 bp(+) (GRCm39) |
| Type of Mutation |
unclassified |
| DNA Base Change (assembly) |
T to A
at 91188599 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000023693]
[ENSMUST00000089042]
[ENSMUST00000117836]
[ENSMUST00000134491]
[ENSMUST00000139503]
|
| AlphaFold |
O35664 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000023693
|
| SMART Domains |
Protein: ENSMUSP00000023693
Gene: ENSMUSG00000022971
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Tissue_fac
|
9 |
118 |
8.9e-18 |
PFAM |
|
Pfam:Interfer-bind
|
132 |
231 |
9.2e-19 |
PFAM |
|
low complexity region
|
315 |
326 |
N/A |
INTRINSIC |
|
low complexity region
|
361 |
389 |
N/A |
INTRINSIC |
|
low complexity region
|
476 |
485 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000089042
|
| SMART Domains |
Protein: ENSMUSP00000086443
Gene: ENSMUSG00000022971
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Tissue_fac
|
9 |
118 |
2.9e-18 |
PFAM |
|
Pfam:Interfer-bind
|
132 |
231 |
1.5e-17 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000117836
|
| SMART Domains |
Protein: ENSMUSP00000113358
Gene: ENSMUSG00000022971
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Tissue_fac
|
9 |
118 |
2.9e-18 |
PFAM |
|
Pfam:Interfer-bind
|
132 |
231 |
1.5e-17 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000134491
|
| SMART Domains |
Protein: ENSMUSP00000134796
Gene: ENSMUSG00000022971
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Interfer-bind
|
30 |
117 |
3.6e-16 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000139503
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000160764
|
| SMART Domains |
Protein: ENSMUSP00000123997
Gene: ENSMUSG00000093701
| Domain | Start | End | E-Value | Type |
|---|
|
FN3
|
2 |
92 |
5.1e1 |
SMART |
|
FN3
|
110 |
187 |
9.09e0 |
SMART |
|
FN3
|
201 |
291 |
1.39e0 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000161517
|
| SMART Domains |
Protein: ENSMUSP00000125579
Gene: ENSMUSG00000093701
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Interfer-bind
|
1 |
100 |
7.5e-20 |
PFAM |
|
| 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 a type I membrane protein that forms one of the two chains of a receptor for interferons alpha and beta. Binding and activation of the receptor stimulates Janus protein kinases, which in turn phosphorylate several proteins, including STAT1 and STAT2. Multiple transcript variants encoding at least two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice with mutations of this gene have defects in immune responses involving, variously, NK cells, CD4+ and CD8+ T cells and B cells in response to induced and transplanted tumors, viruses, and double stranded DNA. These defects include diminished secretion of type I and type II interferons. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcb4 |
T |
C |
5: 8,944,166 (GRCm39) |
|
probably null |
Het |
| Ankib1 |
A |
T |
5: 3,784,194 (GRCm39) |
|
probably benign |
Het |
| Birc2 |
T |
C |
9: 7,860,733 (GRCm39) |
Y195C |
probably damaging |
Het |
| Cand2 |
T |
C |
6: 115,759,755 (GRCm39) |
I142T |
probably benign |
Het |
| Cdh15 |
T |
C |
8: 123,592,062 (GRCm39) |
|
probably benign |
Het |
| Ceacam5 |
G |
A |
7: 17,479,534 (GRCm39) |
G217D |
probably damaging |
Het |
| Cfap54 |
T |
A |
10: 92,917,385 (GRCm39) |
H25L |
unknown |
Het |
| Cfap95 |
A |
G |
19: 23,630,100 (GRCm39) |
|
probably benign |
Het |
| Col22a1 |
A |
G |
15: 71,778,889 (GRCm39) |
V266A |
probably benign |
Het |
| D3Ertd751e |
A |
G |
3: 41,703,132 (GRCm39) |
D69G |
probably benign |
Het |
| Dnah3 |
T |
C |
7: 119,622,164 (GRCm39) |
I1518V |
probably damaging |
Het |
| Entpd8 |
A |
G |
2: 24,974,358 (GRCm39) |
K381R |
probably benign |
Het |
| Fli1 |
T |
A |
9: 32,335,397 (GRCm39) |
K345I |
probably damaging |
Het |
| G6pd2 |
T |
C |
5: 61,967,281 (GRCm39) |
V352A |
probably damaging |
Het |
| Gbp11 |
C |
T |
5: 105,475,482 (GRCm39) |
|
probably null |
Het |
| Gm11992 |
A |
G |
11: 9,018,383 (GRCm39) |
*292W |
probably null |
Het |
| Impg1 |
T |
C |
9: 80,230,111 (GRCm39) |
K661R |
probably benign |
Het |
| Inf2 |
G |
T |
12: 112,578,290 (GRCm39) |
E651* |
probably null |
Het |
| Ints1 |
A |
G |
5: 139,753,258 (GRCm39) |
|
probably benign |
Het |
| Iqcf4 |
T |
C |
9: 106,447,832 (GRCm39) |
K26E |
probably benign |
Het |
| Map4k3 |
A |
G |
17: 80,951,613 (GRCm39) |
V289A |
probably benign |
Het |
| Mis18bp1 |
T |
C |
12: 65,205,215 (GRCm39) |
K319R |
possibly damaging |
Het |
| Nubpl |
T |
C |
12: 52,352,638 (GRCm39) |
V291A |
probably damaging |
Het |
| Or4f56 |
A |
G |
2: 111,703,295 (GRCm39) |
F302L |
probably benign |
Het |
| Or4k15c |
C |
T |
14: 50,321,454 (GRCm39) |
R228H |
probably benign |
Het |
| Or8b57 |
A |
G |
9: 40,003,324 (GRCm39) |
S313P |
possibly damaging |
Het |
| Or8k38 |
T |
C |
2: 86,488,551 (GRCm39) |
N84D |
probably benign |
Het |
| Otof |
A |
G |
5: 30,598,723 (GRCm39) |
S29P |
probably benign |
Het |
| Pcca |
A |
G |
14: 122,927,545 (GRCm39) |
D436G |
possibly damaging |
Het |
| Rasef |
T |
A |
4: 73,645,882 (GRCm39) |
T496S |
probably damaging |
Het |
| Saa2 |
A |
G |
7: 46,402,896 (GRCm39) |
D49G |
probably benign |
Het |
| Scart1 |
T |
A |
7: 139,804,552 (GRCm39) |
|
probably null |
Het |
| Scn2a |
A |
G |
2: 65,547,852 (GRCm39) |
I1015V |
probably benign |
Het |
| Sim2 |
T |
C |
16: 93,907,119 (GRCm39) |
Y154H |
possibly damaging |
Het |
| Spag17 |
A |
G |
3: 100,002,865 (GRCm39) |
H1863R |
probably benign |
Het |
| Supt16 |
C |
T |
14: 52,414,489 (GRCm39) |
E438K |
probably benign |
Het |
| Svil |
A |
G |
18: 5,064,501 (GRCm39) |
E1111G |
probably benign |
Het |
| Trabd2b |
T |
C |
4: 114,266,322 (GRCm39) |
V112A |
probably damaging |
Het |
| Vmn1r205 |
T |
C |
13: 22,776,273 (GRCm39) |
I276M |
probably benign |
Het |
| Vps13d |
A |
T |
4: 144,882,776 (GRCm39) |
I939N |
possibly damaging |
Het |
| Zc3h11a |
T |
C |
1: 133,553,600 (GRCm39) |
M515V |
probably benign |
Het |
| Zfp457 |
T |
C |
13: 67,442,330 (GRCm39) |
T82A |
possibly damaging |
Het |
|
| Other mutations in Ifnar2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02817:Ifnar2
|
APN |
16 |
91,184,880 (GRCm39) |
missense |
probably benign |
0.01 |
|
macro-2
|
UTSW |
16 |
91,180,787 (GRCm39) |
start codon destroyed |
probably null |
|
|
R0701:Ifnar2
|
UTSW |
16 |
91,201,117 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R1342:Ifnar2
|
UTSW |
16 |
91,200,809 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R1542:Ifnar2
|
UTSW |
16 |
91,196,153 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1631:Ifnar2
|
UTSW |
16 |
91,188,755 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1913:Ifnar2
|
UTSW |
16 |
91,201,058 (GRCm39) |
missense |
probably benign |
0.33 |
|
R3078:Ifnar2
|
UTSW |
16 |
91,182,889 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R4193:Ifnar2
|
UTSW |
16 |
91,201,232 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4592:Ifnar2
|
UTSW |
16 |
91,188,684 (GRCm39) |
missense |
probably benign |
|
|
R5385:Ifnar2
|
UTSW |
16 |
91,201,086 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R5545:Ifnar2
|
UTSW |
16 |
91,181,913 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5645:Ifnar2
|
UTSW |
16 |
91,201,115 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R6223:Ifnar2
|
UTSW |
16 |
91,184,876 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6371:Ifnar2
|
UTSW |
16 |
91,184,986 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6710:Ifnar2
|
UTSW |
16 |
91,190,771 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6929:Ifnar2
|
UTSW |
16 |
91,190,766 (GRCm39) |
nonsense |
probably null |
|
|
R7530:Ifnar2
|
UTSW |
16 |
91,201,201 (GRCm39) |
missense |
probably benign |
0.18 |
|
R7763:Ifnar2
|
UTSW |
16 |
91,196,181 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8444:Ifnar2
|
UTSW |
16 |
91,200,857 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8529:Ifnar2
|
UTSW |
16 |
91,188,684 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R8969:Ifnar2
|
UTSW |
16 |
91,201,060 (GRCm39) |
missense |
probably benign |
0.18 |
|
R9016:Ifnar2
|
UTSW |
16 |
91,201,073 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R9667:Ifnar2
|
UTSW |
16 |
91,184,984 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9765:Ifnar2
|
UTSW |
16 |
91,184,975 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
| Posted On |
2013-10-07 |
Incidental Mutation