Incidental Mutation 'R7443:Ighe'
ID577114
Institutional Source Beutler Lab
Gene Symbol Ighe
Ensembl Gene ENSMUSG00000087642
Gene NameImmunoglobulin heavy constant epsilon
SynonymsGm900, LOC380792
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.054) question?
Stock #R7443 (G1)
Quality Score225.009
Status Not validated
Chromosome12
Chromosomal Location113271174-113273248 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) G to T at 113272165 bp
ZygosityHeterozygous
Amino Acid Change Cysteine to Stop codon at position 180 (C180*)
Gene Model predicted gene model for transcript(s):
Predicted Effect probably null
Transcript: ENSMUST00000137336
AA Change: C180*
SMART Domains Protein: ENSMUSP00000118012
Gene: ENSMUSG00000087642
AA Change: C180*

DomainStartEndE-ValueType
IGc1 18 85 2.5e-6 SMART
IG_like 116 190 2.3e-5 SMART
IG_like 221 295 3e-4 SMART
low complexity region 310 323 N/A INTRINSIC
IGc1 325 402 7.4e-35 SMART
Predicted Effect probably null
Transcript: ENSMUST00000223335
AA Change: C180*
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 72 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700042G07Rik G A 4: 116,173,467 G23R probably benign Het
Abl2 T C 1: 156,625,381 I162T probably damaging Het
Acaca G A 11: 84,315,793 S1493N probably benign Het
Arf2 T A 11: 103,969,150 M18K probably benign Het
Bag5 A G 12: 111,710,727 S221P probably damaging Het
Bcr T C 10: 75,143,136 probably null Het
Btg2 T A 1: 134,077,695 K51* probably null Het
C530008M17Rik T C 5: 76,856,638 V282A unknown Het
Chrne A G 11: 70,618,266 V130A probably benign Het
Cubn T A 2: 13,455,509 D714V probably damaging Het
Cyp4a29 A T 4: 115,248,559 I153F probably damaging Het
D730001G18Rik T C 15: 74,775,400 E32G Het
Dph7 C A 2: 24,962,493 H5Q probably benign Het
Epha6 T C 16: 59,775,625 N901S possibly damaging Het
Exosc9 C A 3: 36,553,841 P66Q probably damaging Het
Foxn3 T C 12: 99,388,779 D42G possibly damaging Het
Gbp11 A G 5: 105,330,950 probably null Het
Gm3264 A T 14: 4,871,265 Y37F probably damaging Het
Gm4951 A T 18: 60,246,050 N219I probably benign Het
H2-M10.2 T A 17: 36,286,053 I44F probably benign Het
Hemgn A T 4: 46,396,145 F364I probably damaging Het
Hnf4a A G 2: 163,559,012 I184V probably benign Het
Klk1b22 T A 7: 44,116,110 I162K probably benign Het
Lmo3 C T 6: 138,377,222 A104T probably damaging Het
Lsm14a A G 7: 34,353,838 V263A probably benign Het
Ltbp1 T C 17: 75,364,437 Y1538H probably damaging Het
Map9 A G 3: 82,371,356 E221G possibly damaging Het
Mccc2 G A 13: 99,993,636 A71V possibly damaging Het
Mdc1 T A 17: 35,850,820 V875E probably damaging Het
Mier2 A T 10: 79,540,455 I212N unknown Het
Mitd1 T C 1: 37,881,036 T164A probably benign Het
Myh1 T C 11: 67,220,505 I1590T probably benign Het
Mylk2 T G 2: 152,911,426 probably benign Het
Ncapg T A 5: 45,672,310 V118E probably benign Het
Nynrin G A 14: 55,871,416 V1327I probably benign Het
Oas1c C A 5: 120,805,419 K218N probably damaging Het
Olfr1253 T A 2: 89,751,941 M296L probably benign Het
Olfr154 T A 2: 85,663,568 I289F probably damaging Het
Olfr183 T A 16: 58,999,990 F102I probably damaging Het
Olfr382 A T 11: 73,516,848 V117D possibly damaging Het
Olfr46 A G 7: 140,611,048 N286S probably damaging Het
Olfr739 A G 14: 50,425,050 D177G probably damaging Het
Otoa A T 7: 121,132,410 M618L probably benign Het
Plcg2 A T 8: 117,504,289 T37S probably benign Het
Plekhg4 T C 8: 105,380,867 L1010P probably damaging Het
Plxnb1 T C 9: 109,114,607 F1921L probably damaging Het
Prss47 T A 13: 65,049,489 K144N probably damaging Het
Rapgef2 T C 3: 79,081,224 K953E probably damaging Het
Rasip1 T A 7: 45,638,724 I909N probably damaging Het
Rps5 A G 7: 12,922,995 T8A probably benign Het
Rsbn1l T C 5: 20,927,623 K213E possibly damaging Het
Serpinb5 T C 1: 106,881,970 F369L probably benign Het
Slc4a5 T C 6: 83,264,315 V306A probably benign Het
Sox13 C A 1: 133,384,573 K484N probably damaging Het
Sox13 T C 1: 133,384,631 Y465C probably damaging Het
Stx3 A G 19: 11,791,844 I39T possibly damaging Het
Tbc1d5 T C 17: 50,966,735 Y116C probably damaging Het
Tcp11l1 T A 2: 104,684,135 Q429L probably benign Het
Tns3 G A 11: 8,451,442 T952I probably benign Het
Trib3 T C 2: 152,339,772 H176R possibly damaging Het
Trim12a A G 7: 104,300,842 Y297H probably damaging Het
Unc13a A G 8: 71,630,959 V1577A probably damaging Het
Vezf1 C A 11: 88,074,663 P244T probably damaging Het
Vmn1r121 T A 7: 21,098,020 D165V probably damaging Het
Vmn2r117 T A 17: 23,460,133 I706F probably benign Het
Vmn2r117 C T 17: 23,460,345 C635Y probably damaging Het
Vmn2r13 T A 5: 109,192,043 H22L probably benign Het
Vmn2r87 A T 10: 130,472,719 M550K probably damaging Het
Wdr6 A G 9: 108,574,290 L798P probably damaging Het
Wtap C T 17: 12,980,934 G54D probably benign Het
Zfp827 A G 8: 79,190,418 S541G Het
Zkscan3 A T 13: 21,388,438 Y341* probably null Het
Other mutations in Ighe
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00235:Ighe APN 12 113271515 missense unknown
IGL01315:Ighe APN 12 113271352 missense unknown
IGL01415:Ighe APN 12 113271391 missense unknown
Allegra UTSW 12 113271374 nonsense probably null
R0610:Ighe UTSW 12 113271743 missense unknown
R1540:Ighe UTSW 12 113271446 missense unknown
R1838:Ighe UTSW 12 113271850 missense unknown
R2010:Ighe UTSW 12 113271488 missense unknown
R3498:Ighe UTSW 12 113271374 nonsense probably null
R5230:Ighe UTSW 12 113271386 missense unknown
R5288:Ighe UTSW 12 113271472 missense probably benign 0.00
R6713:Ighe UTSW 12 113269288 unclassified probably benign
R7010:Ighe UTSW 12 113273141 missense
R7146:Ighe UTSW 12 113272355 missense
R7324:Ighe UTSW 12 113272334 missense
R7473:Ighe UTSW 12 113271356 missense probably damaging 1.00
R7493:Ighe UTSW 12 113271403 missense
R7862:Ighe UTSW 12 113271808 missense
R7873:Ighe UTSW 12 113271322 missense
R7945:Ighe UTSW 12 113271808 missense
R7956:Ighe UTSW 12 113271322 missense
R8038:Ighe UTSW 12 113269433 missense
Predicted Primers PCR Primer
(F):5'- ACCGTTTTGATACAGGTCCAG -3'
(R):5'- TCCACCATCCAGCTGTACTG -3'

Sequencing Primer
(F):5'- TTGATACAGGTCCAGGGGGC -3'
(R):5'- AGCTGTACTGCTTCATTTATGGC -3'
Posted On2019-10-07