Incidental Mutation 'IGL02456:Iho1'
ID 294179
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Iho1
Ensembl Gene ENSMUSG00000047220
Gene Name interactor of HORMAD1 1
Synonyms Ccdc36, Iho1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.072) question?
Stock # IGL02456
Quality Score
Status
Chromosome 9
Chromosomal Location 108280810-108305683 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 108283820 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Lysine at position 208 (T208K)
Ref Sequence ENSEMBL: ENSMUSP00000075898 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076592] [ENSMUST00000192995]
AlphaFold Q6PDM4
Predicted Effect probably benign
Transcript: ENSMUST00000076592
AA Change: T208K

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000075898
Gene: ENSMUSG00000047220
AA Change: T208K

DomainStartEndE-ValueType
Pfam:DUF4700 19 572 4.7e-274 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000192995
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921511C20Rik T A X: 126,302,584 (GRCm39) Y174* probably null Het
Apc C A 18: 34,446,935 (GRCm39) S1243* probably null Het
Atp8b5 A G 4: 43,365,578 (GRCm39) T731A probably benign Het
Bcl2a1c T A 9: 114,159,458 (GRCm39) F79I probably damaging Het
Brip1 G T 11: 85,955,925 (GRCm39) L863I possibly damaging Het
Cbx4 T A 11: 118,972,938 (GRCm39) K146* probably null Het
Ces1a C T 8: 93,766,126 (GRCm39) V163I possibly damaging Het
Ces5a C T 8: 94,255,272 (GRCm39) probably benign Het
Cfhr1 A C 1: 139,484,131 (GRCm39) N128K possibly damaging Het
Clcn3 T C 8: 61,394,391 (GRCm39) D46G probably damaging Het
Cntnap1 T G 11: 101,068,955 (GRCm39) I166S probably benign Het
Cntnap3 A T 13: 64,946,872 (GRCm39) probably benign Het
Cntnap5c T A 17: 58,714,739 (GRCm39) probably benign Het
Ddx23 A T 15: 98,545,430 (GRCm39) V626E probably damaging Het
Dele1 T A 18: 38,394,177 (GRCm39) L458Q probably damaging Het
Gcm2 T C 13: 41,256,477 (GRCm39) Y424C probably benign Het
Gm9964 A G 11: 79,187,196 (GRCm39) F84L probably damaging Het
Grn T A 11: 102,326,930 (GRCm39) D509E probably benign Het
Kdm5c G A X: 151,029,314 (GRCm39) D343N probably damaging Het
Ly75 C T 2: 60,124,125 (GRCm39) M1717I probably benign Het
Map1a C A 2: 121,129,134 (GRCm39) P133T probably damaging Het
Mpp2 C A 11: 101,950,199 (GRCm39) A552S possibly damaging Het
Mtr T C 13: 12,213,980 (GRCm39) I897M probably damaging Het
Npas3 A T 12: 54,095,550 (GRCm39) I337F probably damaging Het
Nup85 T C 11: 115,472,691 (GRCm39) probably benign Het
Or10a49 A G 7: 108,468,257 (GRCm39) Y35H probably benign Het
Or10al2 T A 17: 37,983,340 (GRCm39) M142K possibly damaging Het
Or2t46 T A 11: 58,472,024 (GRCm39) L118H possibly damaging Het
Or51l4 T A 7: 103,404,700 (GRCm39) I31F possibly damaging Het
Or56a5 T C 7: 104,792,966 (GRCm39) N178S probably damaging Het
Pdia4 A T 6: 47,780,429 (GRCm39) D301E probably benign Het
Phf2 C A 13: 48,982,322 (GRCm39) G134C unknown Het
Polr2h T A 16: 20,539,352 (GRCm39) L76H probably damaging Het
Rbm47 G A 5: 66,184,364 (GRCm39) R80C probably damaging Het
Sfmbt1 T C 14: 30,507,837 (GRCm39) S286P probably damaging Het
Slc5a12 T C 2: 110,447,179 (GRCm39) probably benign Het
Tacc2 T C 7: 130,227,991 (GRCm39) S1559P probably benign Het
Tbc1d16 T G 11: 119,101,372 (GRCm39) H46P probably damaging Het
Tbck A G 3: 132,440,475 (GRCm39) probably benign Het
Tmtc4 A T 14: 123,163,374 (GRCm39) probably null Het
Ttc13 T C 8: 125,417,100 (GRCm39) probably null Het
Ttc17 T C 2: 94,193,130 (GRCm39) probably benign Het
Vmn1r121 T A 7: 20,832,438 (GRCm39) M1L possibly damaging Het
Vps13c T C 9: 67,860,258 (GRCm39) S2825P probably damaging Het
Zan A C 5: 137,445,106 (GRCm39) S1718A unknown Het
Zfp39 G T 11: 58,793,626 (GRCm39) Y37* probably null Het
Zfp407 T C 18: 84,576,766 (GRCm39) N1449S probably damaging Het
Zhx2 C A 15: 57,687,035 (GRCm39) D801E possibly damaging Het
Other mutations in Iho1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01956:Iho1 APN 9 108,294,518 (GRCm39) splice site probably benign
IGL02138:Iho1 APN 9 108,283,820 (GRCm39) missense probably benign 0.00
IGL02305:Iho1 APN 9 108,283,031 (GRCm39) missense possibly damaging 0.82
IGL02936:Iho1 APN 9 108,289,702 (GRCm39) missense possibly damaging 0.69
IGL03150:Iho1 APN 9 108,282,155 (GRCm39) missense probably damaging 0.98
IGL03163:Iho1 APN 9 108,282,132 (GRCm39) missense probably benign 0.00
IGL03280:Iho1 APN 9 108,282,099 (GRCm39) missense possibly damaging 0.92
R0139:Iho1 UTSW 9 108,289,695 (GRCm39) missense probably damaging 1.00
R0276:Iho1 UTSW 9 108,305,639 (GRCm39) missense possibly damaging 0.84
R0744:Iho1 UTSW 9 108,282,000 (GRCm39) missense probably benign
R0836:Iho1 UTSW 9 108,282,000 (GRCm39) missense probably benign
R1792:Iho1 UTSW 9 108,282,111 (GRCm39) missense possibly damaging 0.84
R1918:Iho1 UTSW 9 108,290,184 (GRCm39) missense probably benign 0.16
R2284:Iho1 UTSW 9 108,298,672 (GRCm39) missense probably damaging 1.00
R2401:Iho1 UTSW 9 108,290,205 (GRCm39) missense possibly damaging 0.53
R4731:Iho1 UTSW 9 108,282,584 (GRCm39) missense probably benign 0.00
R4819:Iho1 UTSW 9 108,283,877 (GRCm39) missense probably benign 0.10
R4950:Iho1 UTSW 9 108,298,709 (GRCm39) missense probably damaging 1.00
R4968:Iho1 UTSW 9 108,289,713 (GRCm39) missense probably benign 0.11
R7131:Iho1 UTSW 9 108,294,619 (GRCm39) missense probably benign 0.01
R7201:Iho1 UTSW 9 108,281,974 (GRCm39) missense probably damaging 0.98
R7950:Iho1 UTSW 9 108,282,870 (GRCm39) missense probably benign
R8778:Iho1 UTSW 9 108,282,807 (GRCm39) missense probably damaging 0.97
R9316:Iho1 UTSW 9 108,298,726 (GRCm39) missense possibly damaging 0.60
R9501:Iho1 UTSW 9 108,282,500 (GRCm39) missense probably benign 0.05
Posted On 2015-04-16