Incidental Mutation 'IGL02183:Ighg2b'
ID 284301
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ighg2b
Ensembl Gene ENSMUSG00000076613
Gene Name immunoglobulin heavy constant gamma 2B
Synonyms IgG2b, gamma2b
Accession Numbers
Essential gene? Probably non essential (E-score: 0.057) question?
Stock # IGL02183
Quality Score
Status
Chromosome 12
Chromosomal Location 113267934-113271553 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 113271449 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 35 (S35P)
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000103418
AA Change: S35P
SMART Domains Protein: ENSMUSP00000100214
Gene: ENSMUSG00000076613
AA Change: S35P

DomainStartEndE-ValueType
IGc1 22 92 6.9e-16 SMART
low complexity region 108 121 N/A INTRINSIC
IG_like 145 220 4.02e-2 SMART
IGc1 251 324 1.64e-31 SMART
Predicted Effect unknown
Transcript: ENSMUST00000192188
AA Change: S35P
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ace2 T A X: 162,960,465 (GRCm39) probably benign Het
Acsm4 A T 7: 119,293,075 (GRCm39) probably null Het
Apcdd1 T C 18: 63,084,925 (GRCm39) M374T probably damaging Het
Arid4b A G 13: 14,344,575 (GRCm39) E551G possibly damaging Het
Bag4 A T 8: 26,258,058 (GRCm39) L423Q probably damaging Het
Celf1 C T 2: 90,831,831 (GRCm39) P96S probably damaging Het
Cracdl G A 1: 37,664,459 (GRCm39) P480S possibly damaging Het
Cry2 G A 2: 92,243,384 (GRCm39) R486W probably damaging Het
Csn1s1 G A 5: 87,825,477 (GRCm39) S228N possibly damaging Het
Ctnnd2 A G 15: 31,020,886 (GRCm39) Y1124C probably damaging Het
Cyp2j7 T C 4: 96,118,384 (GRCm39) probably benign Het
Dock7 A T 4: 98,847,228 (GRCm39) C1695S possibly damaging Het
Elmo3 T C 8: 106,034,955 (GRCm39) L415P probably benign Het
Entpd5 A G 12: 84,427,154 (GRCm39) probably benign Het
Gpatch11 T C 17: 79,149,660 (GRCm39) probably null Het
Gprin3 C A 6: 59,330,147 (GRCm39) R720I possibly damaging Het
Gria4 T G 9: 4,502,460 (GRCm39) T358P probably damaging Het
Hcn2 T C 10: 79,560,647 (GRCm39) probably null Het
Hivep3 A G 4: 119,989,221 (GRCm39) T1891A probably benign Het
Hmgcr A G 13: 96,799,635 (GRCm39) V153A probably damaging Het
Ifnar1 T C 16: 91,302,034 (GRCm39) V503A possibly damaging Het
Igf2r G A 17: 12,917,403 (GRCm39) probably benign Het
Jmy T C 13: 93,635,750 (GRCm39) D22G possibly damaging Het
Kdm5b T C 1: 134,552,669 (GRCm39) I1215T probably benign Het
Krt84 T C 15: 101,440,791 (GRCm39) I134V unknown Het
Magi3 T A 3: 103,992,663 (GRCm39) M270L probably benign Het
Maneal G A 4: 124,754,209 (GRCm39) T198I probably benign Het
Map7d3 A G X: 55,867,591 (GRCm39) probably benign Het
Myh7 T A 14: 55,212,188 (GRCm39) T1519S probably benign Het
Myo5a T C 9: 75,074,518 (GRCm39) probably benign Het
Naip5 T C 13: 100,358,150 (GRCm39) S1029G probably benign Het
Or14j1 G T 17: 38,146,304 (GRCm39) C138F probably damaging Het
Or4c11c A T 2: 88,662,372 (GRCm39) I304F probably benign Het
Or4g16 T A 2: 111,136,763 (GRCm39) V71E probably damaging Het
Or5d14 T C 2: 87,880,333 (GRCm39) T212A possibly damaging Het
Or5k15 T A 16: 58,710,184 (GRCm39) Q133L probably benign Het
Pald1 A T 10: 61,182,920 (GRCm39) probably benign Het
Pan2 T A 10: 128,144,944 (GRCm39) H230Q possibly damaging Het
Pcdh9 T C 14: 94,123,720 (GRCm39) I817V probably benign Het
Piezo2 A G 18: 63,153,705 (GRCm39) S2547P probably benign Het
Ppargc1b T A 18: 61,442,167 (GRCm39) probably null Het
Prdm6 T C 18: 53,597,749 (GRCm39) probably benign Het
Prr5l A T 2: 101,602,465 (GRCm39) probably benign Het
Rab3gap2 T A 1: 185,003,665 (GRCm39) L1020* probably null Het
Rhbdf1 T C 11: 32,160,543 (GRCm39) H669R probably damaging Het
Rnf150 A T 8: 83,730,234 (GRCm39) I255F probably damaging Het
Rnf17 T A 14: 56,745,325 (GRCm39) D1360E probably null Het
Sag T C 1: 87,756,197 (GRCm39) probably null Het
Scn2a C T 2: 65,501,947 (GRCm39) T90I probably benign Het
Scn9a T A 2: 66,314,955 (GRCm39) probably benign Het
Serpinb13 T C 1: 106,926,640 (GRCm39) M212T probably damaging Het
Slc39a14 C T 14: 70,544,134 (GRCm39) G484E possibly damaging Het
Slco1a1 A T 6: 141,867,669 (GRCm39) probably benign Het
Slitrk3 A T 3: 72,957,312 (GRCm39) Y487N probably damaging Het
Stkld1 T C 2: 26,836,671 (GRCm39) M279T probably benign Het
Tmem161b T C 13: 84,420,373 (GRCm39) Y125H probably damaging Het
Tmem71 A G 15: 66,426,874 (GRCm39) probably benign Het
Ubxn7 T C 16: 32,188,201 (GRCm39) F142L probably damaging Het
Vmn2r22 A G 6: 123,614,963 (GRCm39) L209P probably damaging Het
Wdr73 A T 7: 80,543,508 (GRCm39) W136R probably damaging Het
Wif1 C T 10: 120,911,181 (GRCm39) R107C probably damaging Het
Ythdf2 G T 4: 131,932,885 (GRCm39) L92M probably benign Het
Zfp53 T A 17: 21,720,512 (GRCm39) I34N possibly damaging Het
Zpld2 A G 4: 133,929,291 (GRCm39) L338S probably benign Het
Other mutations in Ighg2b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01366:Ighg2b APN 12 113,270,656 (GRCm39) missense possibly damaging 0.79
IGL01837:Ighg2b APN 12 113,270,065 (GRCm39) missense unknown
IGL01973:Ighg2b APN 12 113,271,305 (GRCm39) missense unknown
IGL01998:Ighg2b APN 12 113,270,709 (GRCm39) missense unknown
IGL02147:Ighg2b APN 12 113,270,011 (GRCm39) makesense probably null
IGL03089:Ighg2b APN 12 113,270,298 (GRCm39) missense probably damaging 1.00
PIT4453001:Ighg2b UTSW 12 113,270,492 (GRCm39) missense unknown
R4199:Ighg2b UTSW 12 113,270,907 (GRCm39) missense probably damaging 0.96
R4459:Ighg2b UTSW 12 113,270,578 (GRCm39) missense unknown
R4577:Ighg2b UTSW 12 113,270,512 (GRCm39) missense unknown
R4589:Ighg2b UTSW 12 113,270,104 (GRCm39) missense unknown
R4807:Ighg2b UTSW 12 113,267,965 (GRCm39) unclassified probably benign
R4822:Ighg2b UTSW 12 113,270,011 (GRCm39) makesense probably null
R5424:Ighg2b UTSW 12 113,271,550 (GRCm39) missense unknown
R5641:Ighg2b UTSW 12 113,270,767 (GRCm39) missense unknown
R6297:Ighg2b UTSW 12 113,270,512 (GRCm39) missense unknown
R6701:Ighg2b UTSW 12 113,270,699 (GRCm39) missense unknown
R6703:Ighg2b UTSW 12 113,268,653 (GRCm39) unclassified probably benign
R6880:Ighg2b UTSW 12 113,270,726 (GRCm39) missense
R7342:Ighg2b UTSW 12 113,270,050 (GRCm39) missense
R7505:Ighg2b UTSW 12 113,268,600 (GRCm39) missense
R7908:Ighg2b UTSW 12 113,270,074 (GRCm39) missense
R8543:Ighg2b UTSW 12 113,270,552 (GRCm39) missense probably damaging 1.00
R8951:Ighg2b UTSW 12 113,270,926 (GRCm39) missense probably benign
R9237:Ighg2b UTSW 12 113,270,217 (GRCm39) missense
R9539:Ighg2b UTSW 12 113,270,498 (GRCm39) missense
R9789:Ighg2b UTSW 12 113,270,304 (GRCm39) missense
Posted On 2015-04-16