Incidental Mutation 'IGL02183:Rnf150'
ID 284325
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rnf150
Ensembl Gene ENSMUSG00000047747
Gene Name ring finger protein 150
Synonyms Greul5, A630007N06Rik, C030044C12Rik
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.496) question?
Stock # IGL02183
Quality Score
Status
Chromosome 8
Chromosomal Location 83589985-83817897 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 83730234 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 255 (I255F)
Ref Sequence ENSEMBL: ENSMUSP00000077610 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078525]
AlphaFold Q5DTZ6
Predicted Effect probably damaging
Transcript: ENSMUST00000078525
AA Change: I255F

PolyPhen 2 Score 0.962 (Sensitivity: 0.78; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000077610
Gene: ENSMUSG00000047747
AA Change: I255F

DomainStartEndE-ValueType
signal peptide 1 34 N/A INTRINSIC
low complexity region 54 64 N/A INTRINSIC
Pfam:PA 84 180 2.1e-12 PFAM
transmembrane domain 207 229 N/A INTRINSIC
RING 277 317 1.29e-7 SMART
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
Ighg2b A G 12: 113,271,449 (GRCm39) S35P unknown 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
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 Rnf150
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0512:Rnf150 UTSW 8 83,590,807 (GRCm39) missense probably benign 0.01
R1848:Rnf150 UTSW 8 83,590,639 (GRCm39) start codon destroyed possibly damaging 0.67
R2078:Rnf150 UTSW 8 83,730,234 (GRCm39) missense probably damaging 0.96
R2192:Rnf150 UTSW 8 83,591,020 (GRCm39) missense probably damaging 0.98
R3918:Rnf150 UTSW 8 83,591,090 (GRCm39) missense probably benign 0.25
R4365:Rnf150 UTSW 8 83,590,744 (GRCm39) missense probably benign 0.05
R4781:Rnf150 UTSW 8 83,590,781 (GRCm39) missense probably damaging 1.00
R4810:Rnf150 UTSW 8 83,716,991 (GRCm39) missense possibly damaging 0.66
R4859:Rnf150 UTSW 8 83,590,712 (GRCm39) missense probably damaging 1.00
R5677:Rnf150 UTSW 8 83,730,228 (GRCm39) nonsense probably null
R6022:Rnf150 UTSW 8 83,769,358 (GRCm39) missense probably benign 0.00
R6241:Rnf150 UTSW 8 83,591,093 (GRCm39) missense possibly damaging 0.82
R6283:Rnf150 UTSW 8 83,717,183 (GRCm39) missense probably damaging 1.00
R6306:Rnf150 UTSW 8 83,810,131 (GRCm39) missense possibly damaging 0.90
R7014:Rnf150 UTSW 8 83,769,292 (GRCm39) missense probably benign
R7023:Rnf150 UTSW 8 83,590,706 (GRCm39) missense probably damaging 0.97
R7394:Rnf150 UTSW 8 83,717,100 (GRCm39) nonsense probably null
R7710:Rnf150 UTSW 8 83,590,781 (GRCm39) missense probably damaging 1.00
R7771:Rnf150 UTSW 8 83,590,832 (GRCm39) missense probably benign 0.00
R8073:Rnf150 UTSW 8 83,590,546 (GRCm39) start gained probably benign
R8856:Rnf150 UTSW 8 83,762,715 (GRCm39) missense probably damaging 1.00
R8980:Rnf150 UTSW 8 83,717,087 (GRCm39) missense probably benign 0.19
R9139:Rnf150 UTSW 8 83,590,588 (GRCm39) start gained probably benign
R9289:Rnf150 UTSW 8 83,716,982 (GRCm39) missense probably benign
R9410:Rnf150 UTSW 8 83,762,722 (GRCm39) missense possibly damaging 0.91
R9594:Rnf150 UTSW 8 83,717,144 (GRCm39) missense probably damaging 1.00
R9603:Rnf150 UTSW 8 83,717,208 (GRCm39) missense possibly damaging 0.64
R9763:Rnf150 UTSW 8 83,732,968 (GRCm39) missense probably benign
Posted On 2015-04-16