Incidental Mutation 'IGL01505:Il15ra'
| ID |
89053 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Il15ra
|
| Ensembl Gene |
ENSMUSG00000023206 |
| Gene Name |
interleukin 15 receptor, alpha chain |
| Synonyms |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.057)
|
| Stock # |
IGL01505
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
11709992-11738796 bp(+) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
T to C
at 11737956 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000132058
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000078834]
[ENSMUST00000114831]
[ENSMUST00000114832]
[ENSMUST00000114833]
[ENSMUST00000114834]
[ENSMUST00000123600]
[ENSMUST00000128156]
[ENSMUST00000148748]
[ENSMUST00000135341]
[ENSMUST00000138349]
|
| AlphaFold |
Q60819 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000078834
|
| SMART Domains |
Protein: ENSMUSP00000077878
Gene: ENSMUSG00000023206
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
28 |
N/A |
INTRINSIC |
|
CCP
|
36 |
96 |
3.87e-8 |
SMART |
|
low complexity region
|
107 |
117 |
N/A |
INTRINSIC |
|
low complexity region
|
118 |
135 |
N/A |
INTRINSIC |
|
low complexity region
|
154 |
172 |
N/A |
INTRINSIC |
|
transmembrane domain
|
206 |
228 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000091456
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000114831
|
| SMART Domains |
Protein: ENSMUSP00000110480
Gene: ENSMUSG00000023206
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
28 |
N/A |
INTRINSIC |
|
CCP
|
36 |
96 |
3.87e-8 |
SMART |
|
low complexity region
|
107 |
117 |
N/A |
INTRINSIC |
|
transmembrane domain
|
173 |
195 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000114832
|
| SMART Domains |
Protein: ENSMUSP00000110481
Gene: ENSMUSG00000023206
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
28 |
N/A |
INTRINSIC |
|
CCP
|
36 |
96 |
3.87e-8 |
SMART |
|
transmembrane domain
|
98 |
120 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000114833
|
| SMART Domains |
Protein: ENSMUSP00000110482
Gene: ENSMUSG00000023206
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
28 |
N/A |
INTRINSIC |
|
CCP
|
36 |
96 |
3.87e-8 |
SMART |
|
transmembrane domain
|
109 |
131 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000114834
|
| SMART Domains |
Protein: ENSMUSP00000110483
Gene: ENSMUSG00000023206
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
28 |
N/A |
INTRINSIC |
|
CCP
|
36 |
96 |
3.87e-8 |
SMART |
|
low complexity region
|
107 |
117 |
N/A |
INTRINSIC |
|
transmembrane domain
|
140 |
162 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000123600
|
| SMART Domains |
Protein: ENSMUSP00000130792
Gene: ENSMUSG00000023206
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
14 |
32 |
N/A |
INTRINSIC |
|
transmembrane domain
|
66 |
88 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000128156
|
| SMART Domains |
Protein: ENSMUSP00000126364
Gene: ENSMUSG00000023206
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
14 |
32 |
N/A |
INTRINSIC |
|
transmembrane domain
|
66 |
88 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000148748
|
| SMART Domains |
Protein: ENSMUSP00000132058
Gene: ENSMUSG00000023206
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
14 |
32 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126394
|
| SMART Domains |
Protein: ENSMUSP00000131640
Gene: ENSMUSG00000023206
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
4 |
26 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000191662
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139774
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000135341
|
| SMART Domains |
Protein: ENSMUSP00000132731
Gene: ENSMUSG00000023206
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
4 |
26 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000138349
|
| SMART Domains |
Protein: ENSMUSP00000131473
Gene: ENSMUSG00000023206
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
14 |
32 |
N/A |
INTRINSIC |
|
transmembrane domain
|
66 |
88 |
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 cytokine receptor that specifically binds interleukin 15 (IL15) with high affinity. The receptors of IL15 and IL2 share two subunits, IL2R beta and IL2R gamma. This forms the basis of many overlapping biological activities of IL15 and IL2. The protein encoded by this gene is structurally related to IL2R alpha, an additional IL2-specific alpha subunit necessary for high affinity IL2 binding. Unlike IL2RA, IL15RA is capable of binding IL15 with high affinity independent of other subunits, which suggests distinct roles between IL15 and IL2. This receptor is reported to enhance cell proliferation and expression of apoptosis inhibitor BCL2L1/BCL2-XL and BCL2. Multiple alternatively spliced transcript variants of this gene have been reported.[provided by RefSeq, Apr 2010]
PHENOTYPE: Mutation of this gene results in absence of NK cell production in spleen and bone marrow. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 59 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930546C10Rik |
T |
C |
18: 69,080,418 (GRCm39) |
|
probably null |
Het |
| A2m |
A |
G |
6: 121,653,906 (GRCm39) |
N1413S |
possibly damaging |
Het |
| Aadacl4fm4 |
C |
T |
4: 144,401,188 (GRCm39) |
V99M |
probably damaging |
Het |
| Arhgap45 |
A |
T |
10: 79,862,376 (GRCm39) |
N488Y |
probably benign |
Het |
| Arid4a |
G |
A |
12: 71,083,889 (GRCm39) |
D94N |
probably damaging |
Het |
| Atp7a |
A |
G |
X: 105,153,436 (GRCm39) |
K1114E |
probably damaging |
Het |
| Atp8a2 |
C |
T |
14: 60,265,512 (GRCm39) |
V275M |
probably benign |
Het |
| Ceacam12 |
T |
C |
7: 17,801,357 (GRCm39) |
V112A |
probably damaging |
Het |
| Cep295 |
T |
A |
9: 15,229,345 (GRCm39) |
D2256V |
probably benign |
Het |
| Chid1 |
A |
T |
7: 141,093,807 (GRCm39) |
|
probably null |
Het |
| Clcn5 |
A |
T |
X: 7,036,678 (GRCm39) |
L268* |
probably null |
Het |
| Cldn17 |
A |
G |
16: 88,303,591 (GRCm39) |
I46T |
possibly damaging |
Het |
| Cnot1 |
A |
T |
8: 96,455,346 (GRCm39) |
I2025N |
probably damaging |
Het |
| Cntn5 |
C |
T |
9: 9,706,092 (GRCm39) |
V574M |
probably damaging |
Het |
| Col14a1 |
T |
A |
15: 55,318,619 (GRCm39) |
C1373S |
unknown |
Het |
| Col9a1 |
A |
G |
1: 24,224,205 (GRCm39) |
N129S |
unknown |
Het |
| Cp |
C |
T |
3: 20,031,356 (GRCm39) |
P598S |
possibly damaging |
Het |
| Cpb1 |
G |
A |
3: 20,320,410 (GRCm39) |
R150C |
probably damaging |
Het |
| Cyp2j7 |
T |
A |
4: 96,115,917 (GRCm39) |
|
probably null |
Het |
| Dnajb7 |
T |
C |
15: 81,291,692 (GRCm39) |
E215G |
possibly damaging |
Het |
| Dock1 |
G |
A |
7: 134,760,239 (GRCm39) |
R1634Q |
possibly damaging |
Het |
| Dop1b |
A |
G |
16: 93,554,004 (GRCm39) |
T313A |
possibly damaging |
Het |
| Fgd2 |
T |
A |
17: 29,585,971 (GRCm39) |
V185E |
probably damaging |
Het |
| Flnb |
T |
C |
14: 7,902,003 (GRCm38) |
|
probably null |
Het |
| Fzd7 |
A |
G |
1: 59,523,062 (GRCm39) |
E315G |
probably benign |
Het |
| Gjd3 |
T |
A |
11: 102,691,552 (GRCm39) |
K150N |
probably benign |
Het |
| Gpihbp1 |
C |
T |
15: 75,469,977 (GRCm39) |
|
probably benign |
Het |
| Gpr160 |
T |
C |
3: 30,950,002 (GRCm39) |
S25P |
possibly damaging |
Het |
| Grsf1 |
G |
A |
5: 88,820,608 (GRCm39) |
R58* |
probably null |
Het |
| Ifit1 |
T |
A |
19: 34,625,854 (GRCm39) |
M330K |
probably benign |
Het |
| Igkv1-122 |
T |
C |
6: 67,994,178 (GRCm39) |
V22A |
probably benign |
Het |
| Ikbke |
A |
T |
1: 131,183,048 (GRCm39) |
D692E |
probably benign |
Het |
| Il18rap |
A |
G |
1: 40,576,244 (GRCm39) |
I252V |
probably damaging |
Het |
| Klra10 |
C |
T |
6: 130,249,680 (GRCm39) |
G202R |
probably damaging |
Het |
| Kpna7 |
A |
G |
5: 144,929,661 (GRCm39) |
V388A |
probably damaging |
Het |
| L2hgdh |
A |
G |
12: 69,768,175 (GRCm39) |
S108P |
probably damaging |
Het |
| Msto1 |
G |
A |
3: 88,818,050 (GRCm39) |
T388M |
probably benign |
Het |
| Naip1 |
T |
C |
13: 100,562,441 (GRCm39) |
E908G |
probably damaging |
Het |
| Neto1 |
C |
A |
18: 86,491,814 (GRCm39) |
D238E |
possibly damaging |
Het |
| Nlrp5 |
T |
A |
7: 23,117,159 (GRCm39) |
D294E |
probably benign |
Het |
| Nr3c2 |
T |
C |
8: 77,635,816 (GRCm39) |
S306P |
probably damaging |
Het |
| Or8b41 |
T |
A |
9: 38,055,167 (GRCm39) |
C240* |
probably null |
Het |
| Pard3 |
T |
A |
8: 128,050,544 (GRCm39) |
L202H |
probably damaging |
Het |
| Pdzd2 |
T |
C |
15: 12,458,293 (GRCm39) |
N190S |
probably damaging |
Het |
| Pi4ka |
T |
C |
16: 17,127,222 (GRCm39) |
D1077G |
probably benign |
Het |
| Pmfbp1 |
A |
C |
8: 110,240,543 (GRCm39) |
L208F |
probably damaging |
Het |
| Pms1 |
C |
T |
1: 53,246,130 (GRCm39) |
D470N |
probably benign |
Het |
| Prdm10 |
T |
C |
9: 31,238,578 (GRCm39) |
F108L |
probably benign |
Het |
| Rab11fip1 |
A |
T |
8: 27,644,804 (GRCm39) |
M327K |
possibly damaging |
Het |
| Slc37a4 |
T |
A |
9: 44,311,261 (GRCm39) |
L184Q |
probably damaging |
Het |
| Smdt1 |
T |
C |
15: 82,232,094 (GRCm39) |
|
probably benign |
Het |
| Smg6 |
A |
G |
11: 75,047,117 (GRCm39) |
Y1270C |
probably damaging |
Het |
| Speer4f2 |
T |
A |
5: 17,581,565 (GRCm39) |
V169E |
possibly damaging |
Het |
| Stpg2 |
C |
T |
3: 139,023,214 (GRCm39) |
A410V |
probably benign |
Het |
| Tnrc6b |
T |
A |
15: 80,764,164 (GRCm39) |
D555E |
probably benign |
Het |
| Tsg101 |
A |
G |
7: 46,558,808 (GRCm39) |
Y46H |
probably damaging |
Het |
| Vmn2r111 |
G |
A |
17: 22,767,553 (GRCm39) |
S648L |
probably benign |
Het |
| Vmn2r73 |
T |
A |
7: 85,507,267 (GRCm39) |
R682* |
probably null |
Het |
| Xkr5 |
A |
T |
8: 18,983,514 (GRCm39) |
I676N |
probably damaging |
Het |
|
| Other mutations in Il15ra |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
R0105:Il15ra
|
UTSW |
2 |
11,735,459 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0105:Il15ra
|
UTSW |
2 |
11,735,459 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0945:Il15ra
|
UTSW |
2 |
11,723,138 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1863:Il15ra
|
UTSW |
2 |
11,728,247 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R1975:Il15ra
|
UTSW |
2 |
11,728,334 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R2172:Il15ra
|
UTSW |
2 |
11,728,382 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R2202:Il15ra
|
UTSW |
2 |
11,723,155 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3709:Il15ra
|
UTSW |
2 |
11,735,458 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3710:Il15ra
|
UTSW |
2 |
11,735,458 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4621:Il15ra
|
UTSW |
2 |
11,723,140 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4701:Il15ra
|
UTSW |
2 |
11,723,156 (GRCm39) |
splice site |
probably null |
|
|
R4779:Il15ra
|
UTSW |
2 |
11,723,117 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4844:Il15ra
|
UTSW |
2 |
11,723,082 (GRCm39) |
start gained |
probably benign |
|
|
R5237:Il15ra
|
UTSW |
2 |
11,738,016 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5810:Il15ra
|
UTSW |
2 |
11,738,063 (GRCm39) |
splice site |
probably null |
|
|
R5880:Il15ra
|
UTSW |
2 |
11,735,426 (GRCm39) |
makesense |
probably null |
|
|
R6160:Il15ra
|
UTSW |
2 |
11,724,827 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7291:Il15ra
|
UTSW |
2 |
11,723,192 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7788:Il15ra
|
UTSW |
2 |
11,728,404 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8941:Il15ra
|
UTSW |
2 |
11,737,995 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R9013:Il15ra
|
UTSW |
2 |
11,732,576 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9025:Il15ra
|
UTSW |
2 |
11,723,233 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R9481:Il15ra
|
UTSW |
2 |
11,724,854 (GRCm39) |
missense |
probably benign |
0.35 |
|
R9756:Il15ra
|
UTSW |
2 |
11,728,259 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Posted On |
2013-12-03 |
Incidental Mutation