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) question?
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

DomainStartEndE-ValueType
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

DomainStartEndE-ValueType
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

DomainStartEndE-ValueType
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

DomainStartEndE-ValueType
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

DomainStartEndE-ValueType
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
GeneRefVarChr/LocMutationPredicted EffectZygosity
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
AlleleSourceChrCoordTypePredicted EffectPPH 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