Incidental Mutation 'IGL03339:Ighg2c'
ID 417136
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ighg2c
Ensembl Gene ENSMUSG00000076612
Gene Name immunoglobulin heavy constant gamma 2C
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.085) question?
Stock # IGL03339
Quality Score
Status
Chromosome 12
Chromosomal Location 113251009-113252552 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 113251614 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glycine at position 171 (V171G)
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000103416
AA Change: V171G
SMART Domains Protein: ENSMUSP00000100212
Gene: ENSMUSG00000076612
AA Change: V171G

DomainStartEndE-ValueType
IGc1 21 91 2.4e-15 SMART
IG_like 143 218 1.64e-2 SMART
IGc1 249 322 1.97e-34 SMART
transmembrane domain 350 372 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000195192
AA Change: V171G
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
6820408C15Rik A G 2: 152,284,376 (GRCm39) E323G probably damaging Het
A4gnt T C 9: 99,502,601 (GRCm39) S254P probably damaging Het
Actn4 A G 7: 28,601,407 (GRCm39) L447P probably damaging Het
Agbl2 C A 2: 90,627,907 (GRCm39) S237R probably damaging Het
Apc G A 18: 34,431,527 (GRCm39) D309N probably damaging Het
Arhgef3 A G 14: 27,123,814 (GRCm39) M492V probably damaging Het
Atp10b T A 11: 43,121,442 (GRCm39) M1035K probably null Het
Cfap69 T A 5: 5,636,436 (GRCm39) probably benign Het
Ctf1 A G 7: 127,313,166 (GRCm39) N24S probably benign Het
Cx3cr1 T A 9: 119,880,503 (GRCm39) K300* probably null Het
Ddx25 A T 9: 35,453,299 (GRCm39) Y484N probably damaging Het
Eif4g1 A G 16: 20,499,734 (GRCm39) E506G possibly damaging Het
Ficd G T 5: 113,876,800 (GRCm39) R325L probably benign Het
G6pc2 A G 2: 69,051,239 (GRCm39) probably benign Het
Gm11168 C A 9: 3,004,767 (GRCm39) P103T probably benign Het
Hbb-y A T 7: 103,501,976 (GRCm39) H98Q probably damaging Het
Hmcn1 A G 1: 150,577,720 (GRCm39) S2014P probably benign Het
Hoxc5 T C 15: 102,922,568 (GRCm39) Y19H probably damaging Het
Igfbpl1 A G 4: 45,813,555 (GRCm39) probably benign Het
Kctd13 A G 7: 126,544,190 (GRCm39) D296G probably benign Het
Mfsd2b A C 12: 4,924,335 (GRCm39) M1R probably null Het
Nipbl A G 15: 8,380,360 (GRCm39) S811P probably benign Het
Or10al2 G A 17: 37,983,448 (GRCm39) C178Y possibly damaging Het
Or10al3 G T 17: 38,011,682 (GRCm39) M40I probably damaging Het
Or52r1 G A 7: 102,536,989 (GRCm39) R124C probably benign Het
Or5b122 T G 19: 13,563,439 (GRCm39) M257R probably damaging Het
Pcolce2 T C 9: 95,560,393 (GRCm39) probably benign Het
Pik3c2a G T 7: 116,017,256 (GRCm39) T167K possibly damaging Het
Ppp1r18 A G 17: 36,178,938 (GRCm39) D271G probably benign Het
Rnf213 T C 11: 119,333,830 (GRCm39) I3013T probably damaging Het
Rock1 A T 18: 10,097,493 (GRCm39) M765K probably benign Het
Sec16a T C 2: 26,325,945 (GRCm39) Y1244C probably benign Het
Taar7d T C 10: 23,903,204 (GRCm39) C29R possibly damaging Het
Tlcd4 C T 3: 121,022,489 (GRCm39) probably benign Het
Ttn A C 2: 76,572,264 (GRCm39) F26210V probably damaging Het
Ube2b A T 11: 51,877,534 (GRCm39) V145D probably damaging Het
Vmn1r219 T G 13: 23,347,580 (GRCm39) S256R possibly damaging Het
Other mutations in Ighg2c
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02087:Ighg2c APN 12 113,248,986 (GRCm39) unclassified probably benign
IGL02560:Ighg2c APN 12 113,251,504 (GRCm39) missense unknown
R0047:Ighg2c UTSW 12 113,251,788 (GRCm39) splice site probably benign
R0047:Ighg2c UTSW 12 113,251,788 (GRCm39) splice site probably benign
R0415:Ighg2c UTSW 12 113,251,530 (GRCm39) missense unknown
R0571:Ighg2c UTSW 12 113,252,382 (GRCm39) nonsense probably null
R0634:Ighg2c UTSW 12 113,251,584 (GRCm39) missense unknown
R0893:Ighg2c UTSW 12 113,251,053 (GRCm39) missense unknown
R1169:Ighg2c UTSW 12 113,249,572 (GRCm39) unclassified probably benign
R3895:Ighg2c UTSW 12 113,251,278 (GRCm39) missense unknown
R5065:Ighg2c UTSW 12 113,251,708 (GRCm39) missense unknown
R6407:Ighg2c UTSW 12 113,252,271 (GRCm39) missense unknown
R6846:Ighg2c UTSW 12 113,251,930 (GRCm39) missense unknown
R7052:Ighg2c UTSW 12 113,252,343 (GRCm39) missense
R7231:Ighg2c UTSW 12 113,251,636 (GRCm39) missense
R7513:Ighg2c UTSW 12 113,252,471 (GRCm39) missense
R8783:Ighg2c UTSW 12 113,252,412 (GRCm39) missense
R9175:Ighg2c UTSW 12 113,252,499 (GRCm39) missense
R9419:Ighg2c UTSW 12 113,251,015 (GRCm39) critical splice donor site probably benign
Z1177:Ighg2c UTSW 12 113,251,300 (GRCm39) missense
Posted On 2016-08-02