Incidental Mutation 'R1706:Igsf8'
ID |
190045 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Igsf8
|
Ensembl Gene |
ENSMUSG00000038034 |
Gene Name |
immunoglobulin superfamily, member 8 |
Synonyms |
KCT-4, PGRL, PG regulatory-like protein, EWI-2, ESTM34 |
MMRRC Submission |
039739-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1706 (G1)
|
Quality Score |
148 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
172139934-172147410 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 172144972 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Cysteine
at position 100
(R100C)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000134280
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000039506]
[ENSMUST00000062387]
[ENSMUST00000085912]
[ENSMUST00000128508]
[ENSMUST00000139528]
[ENSMUST00000194204]
[ENSMUST00000195659]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000039506
AA Change: R163C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000041232 Gene: ENSMUSG00000038034 AA Change: R163C
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
IG
|
32 |
147 |
1.38e-6 |
SMART |
low complexity region
|
155 |
166 |
N/A |
INTRINSIC |
IG
|
169 |
285 |
2.3e-3 |
SMART |
IG
|
309 |
433 |
9.49e-5 |
SMART |
IG
|
445 |
571 |
3.59e-5 |
SMART |
transmembrane domain
|
578 |
600 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000062387
|
SMART Domains |
Protein: ENSMUSP00000060110 Gene: ENSMUSG00000038026
Domain | Start | End | E-Value | Type |
low complexity region
|
9 |
21 |
N/A |
INTRINSIC |
Pfam:IRK
|
25 |
350 |
3.1e-142 |
PFAM |
low complexity region
|
362 |
377 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000085912
AA Change: R163C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000083076 Gene: ENSMUSG00000038034 AA Change: R163C
Domain | Start | End | E-Value | Type |
low complexity region
|
4 |
19 |
N/A |
INTRINSIC |
IG
|
32 |
147 |
1.38e-6 |
SMART |
low complexity region
|
155 |
166 |
N/A |
INTRINSIC |
IG
|
169 |
285 |
2.3e-3 |
SMART |
IG
|
309 |
433 |
9.49e-5 |
SMART |
IG
|
445 |
571 |
3.59e-5 |
SMART |
transmembrane domain
|
578 |
600 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000128508
|
SMART Domains |
Protein: ENSMUSP00000122611 Gene: ENSMUSG00000038034
Domain | Start | End | E-Value | Type |
low complexity region
|
4 |
19 |
N/A |
INTRINSIC |
IG
|
32 |
147 |
1.38e-6 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000139528
AA Change: R100C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000134280 Gene: ENSMUSG00000038034 AA Change: R100C
Domain | Start | End | E-Value | Type |
IG_like
|
19 |
84 |
3.66e1 |
SMART |
low complexity region
|
92 |
103 |
N/A |
INTRINSIC |
IG
|
106 |
222 |
2.3e-3 |
SMART |
IG
|
246 |
370 |
9.49e-5 |
SMART |
IG
|
382 |
508 |
3.59e-5 |
SMART |
transmembrane domain
|
515 |
537 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000150598
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000194204
|
SMART Domains |
Protein: ENSMUSP00000141633 Gene: ENSMUSG00000038026
Domain | Start | End | E-Value | Type |
low complexity region
|
9 |
21 |
N/A |
INTRINSIC |
Pfam:IRK
|
25 |
361 |
7.4e-165 |
PFAM |
low complexity region
|
362 |
377 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000194505
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000195659
|
SMART Domains |
Protein: ENSMUSP00000141313 Gene: ENSMUSG00000038034
Domain | Start | End | E-Value | Type |
Blast:IG
|
1 |
67 |
2e-42 |
BLAST |
SCOP:d1nkr_1
|
6 |
64 |
1e-3 |
SMART |
transmembrane domain
|
74 |
96 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.3583 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.7%
- 20x: 93.6%
|
Validation Efficiency |
100% (60/60) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member the EWI subfamily of the immunoglobulin protein superfamily. Members of this family contain a single transmembrane domain, an EWI (Glu-Trp-Ile)-motif and a variable number of immunoglobulin domains. This protein interacts with the tetraspanins CD81 and CD9 and may regulate their role in certain cellular functions including cell migration and viral infection. The encoded protein may also function as a tumor suppressor by inhibiting the proliferation of certain cancers. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Sep 2011]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524L21Rik |
T |
C |
18: 6,624,059 (GRCm39) |
|
probably benign |
Het |
4931406C07Rik |
G |
A |
9: 15,209,153 (GRCm39) |
T47I |
probably damaging |
Het |
Adcy2 |
T |
A |
13: 68,868,865 (GRCm39) |
N558I |
probably damaging |
Het |
Ago3 |
G |
A |
4: 126,264,085 (GRCm39) |
P374S |
probably damaging |
Het |
Ak8 |
T |
C |
2: 28,650,007 (GRCm39) |
C345R |
possibly damaging |
Het |
Akap8l |
C |
T |
17: 32,551,457 (GRCm39) |
R511H |
probably damaging |
Het |
BC005624 |
T |
C |
2: 30,868,922 (GRCm39) |
E84G |
possibly damaging |
Het |
Cav1 |
T |
C |
6: 17,339,181 (GRCm39) |
F89L |
probably damaging |
Het |
Cfap206 |
G |
A |
4: 34,688,875 (GRCm39) |
P593L |
probably damaging |
Het |
Clcn6 |
G |
A |
4: 148,102,025 (GRCm39) |
T353I |
probably benign |
Het |
Cstl1 |
G |
A |
2: 148,593,079 (GRCm39) |
|
probably null |
Het |
Cyp2d10 |
A |
C |
15: 82,289,783 (GRCm39) |
S140A |
probably damaging |
Het |
D130052B06Rik |
G |
A |
11: 33,566,230 (GRCm39) |
R18H |
unknown |
Het |
Ddi2 |
A |
G |
4: 141,411,308 (GRCm39) |
F535L |
probably benign |
Het |
Dop1a |
C |
T |
9: 86,436,133 (GRCm39) |
T2383M |
possibly damaging |
Het |
Duox1 |
A |
G |
2: 122,149,953 (GRCm39) |
T115A |
probably benign |
Het |
Ercc6l2 |
T |
A |
13: 64,020,272 (GRCm39) |
|
probably benign |
Het |
Gm7052 |
A |
G |
17: 22,258,823 (GRCm39) |
|
probably benign |
Het |
Gm9925 |
G |
A |
18: 74,198,573 (GRCm39) |
|
probably benign |
Het |
Gnas |
T |
A |
2: 174,141,768 (GRCm39) |
S646T |
possibly damaging |
Het |
Gpatch3 |
T |
A |
4: 133,302,484 (GRCm39) |
C138* |
probably null |
Het |
Kcnh3 |
A |
G |
15: 99,135,959 (GRCm39) |
K652R |
possibly damaging |
Het |
Kcnn4 |
T |
A |
7: 24,074,167 (GRCm39) |
V77E |
probably damaging |
Het |
Kif13b |
T |
A |
14: 64,998,115 (GRCm39) |
|
probably benign |
Het |
Lca5l |
T |
C |
16: 95,977,164 (GRCm39) |
N214S |
probably benign |
Het |
Luc7l3 |
T |
C |
11: 94,188,582 (GRCm39) |
|
probably benign |
Het |
Lypd3 |
T |
C |
7: 24,339,755 (GRCm39) |
I274T |
probably benign |
Het |
Macf1 |
A |
G |
4: 123,264,377 (GRCm39) |
|
probably null |
Het |
Mchr1 |
A |
G |
15: 81,121,364 (GRCm39) |
Y38C |
probably damaging |
Het |
Mia2 |
T |
A |
12: 59,191,552 (GRCm39) |
L716* |
probably null |
Het |
Mki67 |
A |
G |
7: 135,302,295 (GRCm39) |
L913P |
probably benign |
Het |
Mug2 |
T |
A |
6: 122,013,191 (GRCm39) |
|
probably benign |
Het |
Neu3 |
A |
G |
7: 99,472,563 (GRCm39) |
L58P |
probably damaging |
Het |
Or4p23 |
G |
A |
2: 88,576,482 (GRCm39) |
P250L |
probably damaging |
Het |
Or8h9 |
A |
T |
2: 86,789,424 (GRCm39) |
I126N |
probably damaging |
Het |
Pak1ip1 |
T |
C |
13: 41,166,164 (GRCm39) |
V363A |
probably benign |
Het |
Pcdhb16 |
A |
G |
18: 37,612,705 (GRCm39) |
D555G |
probably benign |
Het |
Pygb |
G |
A |
2: 150,669,067 (GRCm39) |
G671D |
probably damaging |
Het |
Rab30 |
A |
T |
7: 92,478,875 (GRCm39) |
I79L |
possibly damaging |
Het |
Rab44 |
C |
A |
17: 29,357,080 (GRCm39) |
T70K |
probably damaging |
Het |
Rccd1 |
C |
G |
7: 79,970,411 (GRCm39) |
G69R |
possibly damaging |
Het |
Sema5b |
T |
C |
16: 35,470,125 (GRCm39) |
V329A |
probably damaging |
Het |
Setd2 |
A |
G |
9: 110,378,932 (GRCm39) |
S632G |
probably benign |
Het |
Slc22a14 |
T |
C |
9: 119,010,050 (GRCm39) |
N15S |
probably benign |
Het |
Smurf2 |
G |
A |
11: 106,715,573 (GRCm39) |
H632Y |
probably damaging |
Het |
Syt10 |
C |
T |
15: 89,674,979 (GRCm39) |
D456N |
probably damaging |
Het |
Tex10 |
C |
T |
4: 48,456,800 (GRCm39) |
R637Q |
probably benign |
Het |
Tgm6 |
T |
C |
2: 129,987,079 (GRCm39) |
C516R |
possibly damaging |
Het |
Tmprss9 |
T |
C |
10: 80,734,021 (GRCm39) |
|
probably benign |
Het |
Trim67 |
A |
G |
8: 125,521,160 (GRCm39) |
N174S |
probably damaging |
Het |
Ttc8 |
C |
A |
12: 98,910,142 (GRCm39) |
T123K |
probably benign |
Het |
Ugt1a7c |
T |
A |
1: 88,023,447 (GRCm39) |
M202K |
probably damaging |
Het |
Vmn2r7 |
T |
A |
3: 64,598,880 (GRCm39) |
H559L |
possibly damaging |
Het |
Zfp511 |
A |
G |
7: 139,617,192 (GRCm39) |
D96G |
probably benign |
Het |
Zfp868 |
A |
G |
8: 70,065,060 (GRCm39) |
Y92H |
probably benign |
Het |
Zzz3 |
T |
A |
3: 152,154,735 (GRCm39) |
D633E |
probably damaging |
Het |
|
Other mutations in Igsf8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00495:Igsf8
|
APN |
1 |
172,145,111 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02090:Igsf8
|
APN |
1 |
172,140,156 (GRCm39) |
intron |
probably benign |
|
IGL02523:Igsf8
|
APN |
1 |
172,146,980 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03092:Igsf8
|
APN |
1 |
172,140,096 (GRCm39) |
intron |
probably benign |
|
IGL03184:Igsf8
|
APN |
1 |
172,146,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R0398:Igsf8
|
UTSW |
1 |
172,145,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R0468:Igsf8
|
UTSW |
1 |
172,146,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Igsf8
|
UTSW |
1 |
172,146,265 (GRCm39) |
missense |
probably benign |
0.06 |
R0612:Igsf8
|
UTSW |
1 |
172,146,974 (GRCm39) |
makesense |
probably null |
|
R0613:Igsf8
|
UTSW |
1 |
172,145,156 (GRCm39) |
missense |
probably benign |
0.00 |
R0883:Igsf8
|
UTSW |
1 |
172,143,826 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0941:Igsf8
|
UTSW |
1 |
172,143,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R1689:Igsf8
|
UTSW |
1 |
172,146,504 (GRCm39) |
missense |
probably damaging |
0.99 |
R2050:Igsf8
|
UTSW |
1 |
172,146,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R2182:Igsf8
|
UTSW |
1 |
172,118,295 (GRCm39) |
critical splice donor site |
probably null |
|
R3625:Igsf8
|
UTSW |
1 |
172,145,336 (GRCm39) |
missense |
probably benign |
0.18 |
R3833:Igsf8
|
UTSW |
1 |
172,145,837 (GRCm39) |
missense |
probably benign |
0.00 |
R4674:Igsf8
|
UTSW |
1 |
172,146,479 (GRCm39) |
nonsense |
probably null |
|
R4796:Igsf8
|
UTSW |
1 |
172,143,889 (GRCm39) |
missense |
probably benign |
0.07 |
R6768:Igsf8
|
UTSW |
1 |
172,145,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R7519:Igsf8
|
UTSW |
1 |
172,143,874 (GRCm39) |
missense |
probably benign |
0.38 |
R9515:Igsf8
|
UTSW |
1 |
172,146,525 (GRCm39) |
missense |
|
|
R9667:Igsf8
|
UTSW |
1 |
172,145,319 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1176:Igsf8
|
UTSW |
1 |
172,145,921 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TGCCATCAAGCCAGTCTTTCCAGC -3'
(R):5'- ACTACTTCCTGTAGAGTGGCTCGC -3'
Sequencing Primer
(F):5'- gcccttgaacttgactcttctg -3'
(R):5'- TGTTTTGGTCTGAGCCAGGC -3'
|
Posted On |
2014-05-14 |