Incidental Mutation 'IGL00825:Clec2g'
ID |
12535 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Clec2g
|
Ensembl Gene |
ENSMUSG00000000248 |
Gene Name |
C-type lectin domain family 2, member g |
Synonyms |
Ocilrp1, 4632413B12Rik |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.091)
|
Stock # |
IGL00825
|
Quality Score |
|
Status
|
|
Chromosome |
6 |
Chromosomal Location |
128911344-128961670 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
C to A
at 128957144 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000144879
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000000254]
[ENSMUST00000075789]
[ENSMUST00000142388]
[ENSMUST00000203405]
[ENSMUST00000204259]
|
AlphaFold |
Q9D676 |
Predicted Effect |
probably null
Transcript: ENSMUST00000000254
|
SMART Domains |
Protein: ENSMUSP00000000254 Gene: ENSMUSG00000000248
Domain | Start | End | E-Value | Type |
Pfam:Lectin_C
|
3 |
108 |
2.4e-6 |
PFAM |
low complexity region
|
114 |
126 |
N/A |
INTRINSIC |
CLECT
|
143 |
254 |
9.36e-25 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000075789
|
SMART Domains |
Protein: ENSMUSP00000075192 Gene: ENSMUSG00000000248
Domain | Start | End | E-Value | Type |
low complexity region
|
9 |
20 |
N/A |
INTRINSIC |
low complexity region
|
52 |
64 |
N/A |
INTRINSIC |
CLECT
|
81 |
192 |
9.36e-25 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000127246
|
Predicted Effect |
probably null
Transcript: ENSMUST00000142388
|
SMART Domains |
Protein: ENSMUSP00000115140 Gene: ENSMUSG00000000248
Domain | Start | End | E-Value | Type |
low complexity region
|
9 |
20 |
N/A |
INTRINSIC |
low complexity region
|
52 |
64 |
N/A |
INTRINSIC |
CLECT
|
81 |
192 |
9.36e-25 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000203405
|
SMART Domains |
Protein: ENSMUSP00000144788 Gene: ENSMUSG00000000248
Domain | Start | End | E-Value | Type |
low complexity region
|
14 |
25 |
N/A |
INTRINSIC |
transmembrane domain
|
48 |
70 |
N/A |
INTRINSIC |
CLECT
|
86 |
197 |
4.7e-27 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000204259
|
SMART Domains |
Protein: ENSMUSP00000144879 Gene: ENSMUSG00000000248
Domain | Start | End | E-Value | Type |
low complexity region
|
20 |
31 |
N/A |
INTRINSIC |
low complexity region
|
63 |
75 |
N/A |
INTRINSIC |
CLECT
|
92 |
203 |
9.36e-25 |
SMART |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 23 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd3 |
C |
T |
18: 10,704,657 (GRCm39) |
V129M |
probably benign |
Het |
Casp8 |
G |
A |
1: 58,868,165 (GRCm39) |
S202N |
probably benign |
Het |
Cimap1c |
A |
G |
9: 56,758,975 (GRCm39) |
I60T |
probably benign |
Het |
Dnah7b |
T |
C |
1: 46,263,811 (GRCm39) |
Y2098H |
probably damaging |
Het |
Dzip3 |
T |
C |
16: 48,748,778 (GRCm39) |
K1053E |
probably damaging |
Het |
Ern1 |
T |
C |
11: 106,312,793 (GRCm39) |
K196R |
probably benign |
Het |
Jcad |
A |
T |
18: 4,673,516 (GRCm39) |
Y426F |
probably damaging |
Het |
Kansl1l |
T |
C |
1: 66,840,671 (GRCm39) |
T210A |
probably benign |
Het |
Map2k2 |
G |
A |
10: 80,954,052 (GRCm39) |
V173I |
probably benign |
Het |
P3h2 |
A |
G |
16: 25,811,548 (GRCm39) |
I225T |
probably damaging |
Het |
Pld2 |
G |
A |
11: 70,442,006 (GRCm39) |
W337* |
probably null |
Het |
Ppp2r2b |
C |
T |
18: 42,778,840 (GRCm39) |
V429M |
probably damaging |
Het |
Pprc1 |
G |
T |
19: 46,059,845 (GRCm39) |
|
probably benign |
Het |
Ptpn4 |
A |
G |
1: 119,587,655 (GRCm39) |
|
probably benign |
Het |
Rap1gds1 |
T |
A |
3: 138,689,588 (GRCm39) |
I135F |
possibly damaging |
Het |
Rasa2 |
A |
T |
9: 96,452,772 (GRCm39) |
N371K |
probably benign |
Het |
Rbbp8 |
A |
G |
18: 11,855,664 (GRCm39) |
T604A |
probably benign |
Het |
Safb2 |
A |
G |
17: 56,878,208 (GRCm39) |
|
probably null |
Het |
Sec23ip |
C |
A |
7: 128,369,333 (GRCm39) |
L686I |
probably damaging |
Het |
Slc22a6 |
T |
C |
19: 8,595,721 (GRCm39) |
V21A |
possibly damaging |
Het |
Slco1c1 |
A |
T |
6: 141,487,868 (GRCm39) |
N79Y |
probably damaging |
Het |
Tbl1xr1 |
G |
T |
3: 22,243,950 (GRCm39) |
|
probably null |
Het |
Zfp961 |
T |
A |
8: 72,721,888 (GRCm39) |
C134S |
possibly damaging |
Het |
|
Other mutations in Clec2g |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00901:Clec2g
|
APN |
6 |
128,925,655 (GRCm39) |
splice site |
probably benign |
|
IGL01367:Clec2g
|
APN |
6 |
128,925,699 (GRCm39) |
missense |
unknown |
|
IGL01514:Clec2g
|
APN |
6 |
128,925,736 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02742:Clec2g
|
APN |
6 |
128,957,224 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0069:Clec2g
|
UTSW |
6 |
128,957,274 (GRCm39) |
critical splice donor site |
probably null |
|
R0069:Clec2g
|
UTSW |
6 |
128,925,716 (GRCm39) |
missense |
probably benign |
0.02 |
R0368:Clec2g
|
UTSW |
6 |
128,957,224 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1809:Clec2g
|
UTSW |
6 |
128,957,273 (GRCm39) |
critical splice donor site |
probably null |
|
R1813:Clec2g
|
UTSW |
6 |
128,925,660 (GRCm39) |
missense |
unknown |
|
R2866:Clec2g
|
UTSW |
6 |
128,925,719 (GRCm39) |
missense |
probably benign |
|
R4080:Clec2g
|
UTSW |
6 |
128,958,287 (GRCm39) |
missense |
probably damaging |
0.96 |
R4732:Clec2g
|
UTSW |
6 |
128,958,842 (GRCm39) |
nonsense |
probably null |
|
R4733:Clec2g
|
UTSW |
6 |
128,958,842 (GRCm39) |
nonsense |
probably null |
|
R4906:Clec2g
|
UTSW |
6 |
128,956,411 (GRCm39) |
missense |
probably benign |
|
R5014:Clec2g
|
UTSW |
6 |
128,925,765 (GRCm39) |
missense |
probably benign |
0.00 |
R5220:Clec2g
|
UTSW |
6 |
128,958,269 (GRCm39) |
missense |
probably benign |
0.00 |
R5342:Clec2g
|
UTSW |
6 |
128,925,714 (GRCm39) |
missense |
probably benign |
0.04 |
R6155:Clec2g
|
UTSW |
6 |
128,957,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R6353:Clec2g
|
UTSW |
6 |
128,959,895 (GRCm39) |
splice site |
probably null |
|
R6372:Clec2g
|
UTSW |
6 |
128,925,726 (GRCm39) |
missense |
probably benign |
0.00 |
R7678:Clec2g
|
UTSW |
6 |
128,956,400 (GRCm39) |
missense |
probably damaging |
0.96 |
R7821:Clec2g
|
UTSW |
6 |
128,925,740 (GRCm39) |
missense |
probably benign |
0.00 |
R8252:Clec2g
|
UTSW |
6 |
128,958,335 (GRCm39) |
missense |
probably benign |
0.09 |
R8909:Clec2g
|
UTSW |
6 |
128,958,195 (GRCm39) |
missense |
probably benign |
0.09 |
R9010:Clec2g
|
UTSW |
6 |
128,925,688 (GRCm39) |
missense |
unknown |
|
R9781:Clec2g
|
UTSW |
6 |
128,960,012 (GRCm39) |
missense |
probably benign |
0.03 |
|
Posted On |
2012-12-06 |