Incidental Mutation 'IGL01068:Rnf225'
ID 51445
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rnf225
Ensembl Gene ENSMUSG00000033967
Gene Name ring finger protein 225
Synonyms 2310014L17Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01068
Quality Score
Status
Chromosome 7
Chromosomal Location 12927416-12931072 bp(+) (GRCm38)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 12928900 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000118798 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000004554] [ENSMUST00000045870] [ENSMUST00000108539] [ENSMUST00000137329] [ENSMUST00000147435]
AlphaFold Q9D7D1
Predicted Effect probably benign
Transcript: ENSMUST00000004554
SMART Domains Protein: ENSMUSP00000004554
Gene: ENSMUSG00000012848

DomainStartEndE-ValueType
Pfam:Ribosomal_S7 49 204 3.5e-44 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000045870
SMART Domains Protein: ENSMUSP00000042816
Gene: ENSMUSG00000033967

DomainStartEndE-ValueType
low complexity region 14 27 N/A INTRINSIC
low complexity region 35 47 N/A INTRINSIC
RING 63 110 2.91e-6 SMART
low complexity region 150 170 N/A INTRINSIC
low complexity region 175 196 N/A INTRINSIC
transmembrane domain 202 224 N/A INTRINSIC
low complexity region 266 278 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000083072
Predicted Effect probably benign
Transcript: ENSMUST00000108539
SMART Domains Protein: ENSMUSP00000104179
Gene: ENSMUSG00000012848

DomainStartEndE-ValueType
Pfam:Ribosomal_S7 51 204 1.8e-40 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000137329
SMART Domains Protein: ENSMUSP00000121961
Gene: ENSMUSG00000012848

DomainStartEndE-ValueType
Pfam:Ribosomal_S7 49 182 1.2e-34 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139349
Predicted Effect probably benign
Transcript: ENSMUST00000147435
SMART Domains Protein: ENSMUSP00000118798
Gene: ENSMUSG00000012848

DomainStartEndE-ValueType
Pfam:Ribosomal_S7 49 182 1.2e-34 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931406B18Rik T C 7: 43,504,175 probably benign Het
Adgra1 A G 7: 139,845,625 E18G probably damaging Het
Aen G A 7: 78,907,302 M299I probably damaging Het
Atg16l1 C T 1: 87,774,824 S269L probably damaging Het
Atp8a1 A G 5: 67,667,337 V853A probably benign Het
Bicral T C 17: 46,825,391 I298V probably damaging Het
Cad A G 5: 31,061,770 probably benign Het
Chd9 A T 8: 91,042,116 Y2448F probably benign Het
Clstn3 A G 6: 124,462,139 L16S probably damaging Het
Cmtr2 G A 8: 110,222,869 V604M possibly damaging Het
Ctcf A T 8: 105,681,485 probably benign Het
Eif2ak2 A G 17: 78,865,371 I295T probably damaging Het
Foxm1 G A 6: 128,370,967 R284H possibly damaging Het
Gabra2 T C 5: 70,962,072 I362M probably benign Het
Hivep1 C A 13: 42,159,984 P1900Q probably benign Het
Klhl25 G T 7: 75,866,149 E268* probably null Het
Klk1b16 T C 7: 44,140,678 L124P probably damaging Het
Ltf A T 9: 111,035,812 probably null Het
Mpped2 T A 2: 106,864,746 H248Q probably damaging Het
Mrpl1 T A 5: 96,224,036 probably benign Het
Mthfd1l T A 10: 4,028,428 S429R probably damaging Het
Myl2 G A 5: 122,106,704 V146I probably benign Het
Myo10 T A 15: 25,739,309 I527N possibly damaging Het
Ncoa3 T C 2: 166,052,795 S333P probably damaging Het
Olfr1297 T G 2: 111,621,340 T245P probably damaging Het
Olfr350 T G 2: 36,850,270 S75A probably damaging Het
Oxct1 T C 15: 4,053,764 F155S probably damaging Het
P4ha1 T C 10: 59,339,335 V39A probably damaging Het
Padi6 G T 4: 140,730,953 T514N possibly damaging Het
Pgm1 G A 5: 64,107,796 V387I probably damaging Het
Ppt1 G A 4: 122,844,007 C46Y probably damaging Het
Rpl26 T C 11: 68,902,398 Y42H probably benign Het
Rundc1 A G 11: 101,434,142 N558S probably damaging Het
Sema3e T G 5: 14,233,718 probably null Het
Slc8a1 T C 17: 81,388,942 I888V probably benign Het
Thsd7b T C 1: 129,596,146 C306R probably damaging Het
Tmem209 A C 6: 30,502,086 L197R probably benign Het
Tmem38b T G 4: 53,849,024 V119G probably damaging Het
Trpc1 T C 9: 95,726,494 D82G probably damaging Het
Zfp292 A G 4: 34,806,763 F2094L probably damaging Het
Zfp638 C T 6: 83,934,994 R453W probably damaging Het
Other mutations in Rnf225
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0033:Rnf225 UTSW 7 12928158 missense probably damaging 1.00
R4541:Rnf225 UTSW 7 12928593 splice site probably null
R4741:Rnf225 UTSW 7 12927930 missense probably benign 0.02
R5388:Rnf225 UTSW 7 12928005 missense probably damaging 1.00
R7128:Rnf225 UTSW 7 12927984 missense probably benign 0.03
Z1177:Rnf225 UTSW 7 12928245 missense probably damaging 0.99
Posted On 2013-06-21