Incidental Mutation 'R0334:Igsf23'
ID 26118
Institutional Source Beutler Lab
Gene Symbol Igsf23
Ensembl Gene ENSMUSG00000040498
Gene Name immunoglobulin superfamily, member 23
Synonyms 2210010C17Rik
MMRRC Submission 038543-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.119) question?
Stock # R0334 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 19671230-19684681 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 19675678 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Glycine at position 143 (S143G)
Ref Sequence ENSEMBL: ENSMUSP00000147077 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000043440] [ENSMUST00000208974]
AlphaFold B2RTN2
Predicted Effect probably benign
Transcript: ENSMUST00000043440
AA Change: S181G

PolyPhen 2 Score 0.271 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000047914
Gene: ENSMUSG00000040498
AA Change: S181G

DomainStartEndE-ValueType
signal peptide 1 34 N/A INTRINSIC
IG 107 181 2.71e0 SMART
low complexity region 182 195 N/A INTRINSIC
transmembrane domain 213 235 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207513
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208210
Predicted Effect probably benign
Transcript: ENSMUST00000208974
AA Change: S143G

PolyPhen 2 Score 0.271 (Sensitivity: 0.91; Specificity: 0.88)
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.4%
  • 20x: 93.6%
Validation Efficiency 99% (68/69)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that has one immunoglobulin (Ig) domain and is a member of the immunoglobulin superfamily. Proteins in this superfamily are usually found on or in cell membranes and act as receptors in immune response pathways. [provided by RefSeq, Nov 2011]
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aggf1 T C 13: 95,508,105 (GRCm39) N87S probably benign Het
Ap2b1 T C 11: 83,258,700 (GRCm39) probably benign Het
Arfgef3 A G 10: 18,468,029 (GRCm39) Y1724H probably damaging Het
Arhgef10l G A 4: 140,311,237 (GRCm39) Q243* probably null Het
Atp8a2 A T 14: 59,928,961 (GRCm39) F1031Y probably damaging Het
Bmp8b A G 4: 123,008,553 (GRCm39) probably null Het
Brinp2 G T 1: 158,123,155 (GRCm39) T37K probably benign Het
Bsph1 T A 7: 13,184,864 (GRCm39) L9* probably null Het
C6 T G 15: 4,784,849 (GRCm39) N238K probably benign Het
Cbs T C 17: 31,838,130 (GRCm39) D373G probably damaging Het
Clec4a3 T C 6: 122,946,329 (GRCm39) F191S possibly damaging Het
Cpz A G 5: 35,661,025 (GRCm39) V530A probably damaging Het
Ctsc G T 7: 87,927,550 (GRCm39) S47I possibly damaging Het
Cyp7b1 T G 3: 18,157,960 (GRCm39) Y53S probably damaging Het
Dach1 C T 14: 98,406,184 (GRCm39) G188R probably damaging Het
Defb4 T C 8: 19,251,220 (GRCm39) I29T probably benign Het
Disc1 A T 8: 125,987,836 (GRCm39) probably null Het
Dnah2 A G 11: 69,327,662 (GRCm39) M3429T probably damaging Het
Dnah7a A T 1: 53,472,213 (GRCm39) I3518N possibly damaging Het
Dnah8 A T 17: 31,090,325 (GRCm39) H4609L probably damaging Het
Evi5 C A 5: 107,968,401 (GRCm39) C182F probably damaging Het
Fam149b G A 14: 20,413,492 (GRCm39) R237H probably damaging Het
Fut8 T A 12: 77,440,536 (GRCm39) D174E possibly damaging Het
Ghr T C 15: 3,370,580 (GRCm39) probably benign Het
Gm10801 G C 2: 98,494,352 (GRCm39) R143T possibly damaging Het
Gpr176 T C 2: 118,110,189 (GRCm39) S357G probably benign Het
Grwd1 A T 7: 45,476,601 (GRCm39) probably null Het
H2-T24 A G 17: 36,325,772 (GRCm39) V273A possibly damaging Het
Hdac4 A C 1: 91,883,760 (GRCm39) probably benign Het
Herc3 A G 6: 58,895,802 (GRCm39) T1017A probably damaging Het
Hsd11b1 T C 1: 192,924,476 (GRCm39) probably benign Het
Kbtbd12 T A 6: 88,594,888 (GRCm39) Y314F probably damaging Het
Kcnmb2 A G 3: 32,252,508 (GRCm39) probably null Het
Kdm5b A G 1: 134,532,260 (GRCm39) I479M probably damaging Het
Kidins220 A G 12: 25,058,068 (GRCm39) T600A probably damaging Het
Mrgprb2 A C 7: 48,202,077 (GRCm39) I216S probably damaging Het
Muc21 A G 17: 35,933,614 (GRCm39) probably benign Het
Myo1g A G 11: 6,461,084 (GRCm39) probably benign Het
Nrxn3 T C 12: 89,780,412 (GRCm39) probably null Het
Or2ag2 A G 7: 106,485,622 (GRCm39) V134A probably benign Het
Or8b54 A T 9: 38,686,535 (GRCm39) probably null Het
Or8g26 A G 9: 39,095,980 (GRCm39) I169V probably benign Het
Pdia5 A T 16: 35,284,760 (GRCm39) S66T possibly damaging Het
Plec T C 15: 76,062,206 (GRCm39) E2604G probably damaging Het
Plekha6 G T 1: 133,209,918 (GRCm39) A654S probably benign Het
Pnpla2 G A 7: 141,039,433 (GRCm39) probably null Het
Pramel19 T C 4: 101,798,781 (GRCm39) F251L probably benign Het
Prb1c T A 6: 132,341,021 (GRCm39) Q17L unknown Het
Prkdc A G 16: 15,554,663 (GRCm39) D2128G probably benign Het
Rabggta A T 14: 55,958,268 (GRCm39) L131Q probably damaging Het
Rbks A T 5: 31,781,863 (GRCm39) Y312* probably null Het
Rnf139 A G 15: 58,771,322 (GRCm39) Y449C probably damaging Het
Sanbr A G 11: 23,567,129 (GRCm39) probably benign Het
Sbno1 A G 5: 124,524,931 (GRCm39) V1058A possibly damaging Het
Sema3a A T 5: 13,607,268 (GRCm39) N321I probably damaging Het
Slit3 T A 11: 35,469,928 (GRCm39) V310E probably damaging Het
Slitrk5 T C 14: 111,918,256 (GRCm39) S627P probably benign Het
Stat2 T A 10: 128,113,736 (GRCm39) F172I probably damaging Het
Tchh C A 3: 93,352,923 (GRCm39) R788S unknown Het
Tnks T A 8: 35,320,413 (GRCm39) K753* probably null Het
Trank1 T A 9: 111,194,421 (GRCm39) V815D probably benign Het
Trank1 T A 9: 111,222,008 (GRCm39) I2915N probably damaging Het
Trpc6 T C 9: 8,610,344 (GRCm39) S271P probably damaging Het
Trpm5 T C 7: 142,640,613 (GRCm39) Q213R probably benign Het
Ulk3 C T 9: 57,501,510 (GRCm39) probably benign Het
Usp31 T C 7: 121,258,185 (GRCm39) D694G probably damaging Het
Wnt3a A G 11: 59,147,144 (GRCm39) S181P probably damaging Het
Yipf3 T C 17: 46,559,238 (GRCm39) F22S possibly damaging Het
Zbtb40 A T 4: 136,713,867 (GRCm39) H1094Q probably damaging Het
Other mutations in Igsf23
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01478:Igsf23 APN 7 19,672,161 (GRCm39) utr 3 prime probably benign
R0831:Igsf23 UTSW 7 19,675,662 (GRCm39) splice site probably benign
R2351:Igsf23 UTSW 7 19,678,723 (GRCm39) nonsense probably null
R4835:Igsf23 UTSW 7 19,675,755 (GRCm39) missense possibly damaging 0.80
R4850:Igsf23 UTSW 7 19,687,859 (GRCm39) unclassified probably benign
R6739:Igsf23 UTSW 7 19,678,673 (GRCm39) missense probably damaging 0.97
R6924:Igsf23 UTSW 7 19,675,684 (GRCm39) missense possibly damaging 0.83
R8244:Igsf23 UTSW 7 19,675,798 (GRCm39) missense possibly damaging 0.66
R8285:Igsf23 UTSW 7 19,675,881 (GRCm39) missense possibly damaging 0.90
R9747:Igsf23 UTSW 7 19,675,839 (GRCm39) missense probably benign 0.09
Predicted Primers PCR Primer
(F):5'- GCAGACATTCACGCAGATACACATGAG -3'
(R):5'- CTTCCAAGGGCATAATCTACAGTGACC -3'

Sequencing Primer
(F):5'- GCCTACCAAGTAGAAGAAAACATGG -3'
(R):5'- GGGCATAATCTACAGTGACCTTAAC -3'
Posted On 2013-04-16