Incidental Mutation 'IGL03355:Rbm33'
ID 419902
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rbm33
Ensembl Gene ENSMUSG00000048271
Gene Name RNA binding motif protein 33
Synonyms 3200001K10Rik, 6430512A10Rik, Prr8
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # IGL03355
Quality Score
Status
Chromosome 5
Chromosomal Location 28522119-28624237 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) C to A at 28596059 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000059644] [ENSMUST00000114884]
AlphaFold Q9CXK9
Predicted Effect unknown
Transcript: ENSMUST00000059644
AA Change: P794T
SMART Domains Protein: ENSMUSP00000062449
Gene: ENSMUSG00000048271
AA Change: P794T

DomainStartEndE-ValueType
low complexity region 2 14 N/A INTRINSIC
low complexity region 36 55 N/A INTRINSIC
low complexity region 59 81 N/A INTRINSIC
low complexity region 109 124 N/A INTRINSIC
low complexity region 191 202 N/A INTRINSIC
low complexity region 241 253 N/A INTRINSIC
low complexity region 282 301 N/A INTRINSIC
low complexity region 307 327 N/A INTRINSIC
low complexity region 362 407 N/A INTRINSIC
low complexity region 444 460 N/A INTRINSIC
low complexity region 625 707 N/A INTRINSIC
low complexity region 817 837 N/A INTRINSIC
coiled coil region 846 891 N/A INTRINSIC
RRM 1160 1227 1.12e-3 SMART
Predicted Effect unknown
Transcript: ENSMUST00000114884
AA Change: P754T
SMART Domains Protein: ENSMUSP00000110534
Gene: ENSMUSG00000048271
AA Change: P754T

DomainStartEndE-ValueType
low complexity region 2 14 N/A INTRINSIC
low complexity region 36 55 N/A INTRINSIC
low complexity region 59 81 N/A INTRINSIC
low complexity region 109 124 N/A INTRINSIC
low complexity region 201 213 N/A INTRINSIC
low complexity region 242 261 N/A INTRINSIC
low complexity region 267 287 N/A INTRINSIC
low complexity region 322 367 N/A INTRINSIC
low complexity region 404 420 N/A INTRINSIC
low complexity region 585 667 N/A INTRINSIC
low complexity region 777 797 N/A INTRINSIC
coiled coil region 806 851 N/A INTRINSIC
RRM 1120 1187 4.7e-6 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000144967
SMART Domains Protein: ENSMUSP00000121879
Gene: ENSMUSG00000048271

DomainStartEndE-ValueType
RRM 119 186 1.12e-3 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actrt1 T C X: 45,418,624 (GRCm39) V213A probably benign Het
Adam28 A T 14: 68,872,252 (GRCm39) probably benign Het
Apeh T C 9: 107,963,644 (GRCm39) H557R probably benign Het
Atmin T A 8: 117,684,164 (GRCm39) L608* probably null Het
B3gnt5 A T 16: 19,587,903 (GRCm39) M41L probably benign Het
Best3 T C 10: 116,829,010 (GRCm39) F97L possibly damaging Het
Chmp1b2 C A X: 106,831,889 (GRCm39) V180F possibly damaging Het
Col7a1 G A 9: 108,807,228 (GRCm39) V2486M unknown Het
Crym T C 7: 119,798,536 (GRCm39) probably null Het
Cubn T C 2: 13,482,868 (GRCm39) probably null Het
Dnah7b A G 1: 46,158,464 (GRCm39) D349G probably benign Het
Eea1 T C 10: 95,878,074 (GRCm39) probably benign Het
Emc1 C T 4: 139,098,904 (GRCm39) probably benign Het
Eps8 T C 6: 137,489,143 (GRCm39) probably benign Het
Ereg A G 5: 91,236,440 (GRCm39) probably benign Het
Faah G A 4: 115,859,725 (GRCm39) P369S probably benign Het
Fam135a A T 1: 24,068,249 (GRCm39) N703K possibly damaging Het
Frmpd1 T C 4: 45,279,140 (GRCm39) S622P probably damaging Het
Gm10030 A G 9: 110,835,841 (GRCm39) noncoding transcript Het
Gpr179 A T 11: 97,228,434 (GRCm39) S1240R possibly damaging Het
Hax1 A T 3: 89,904,754 (GRCm39) H146Q possibly damaging Het
Ift46 A G 9: 44,693,445 (GRCm39) N31D possibly damaging Het
Kel C T 6: 41,675,821 (GRCm39) probably null Het
Khk A T 5: 31,086,904 (GRCm39) I108L probably benign Het
Morc4 T C X: 138,750,431 (GRCm39) N375S probably null Het
Mta3 A T 17: 84,107,474 (GRCm39) probably benign Het
Nacc2 T C 2: 25,952,249 (GRCm39) K369R probably damaging Het
Nkap T C X: 36,403,323 (GRCm39) probably benign Het
Obscn A T 11: 58,928,618 (GRCm39) L6016Q probably damaging Het
Or52e2 T C 7: 102,804,408 (GRCm39) E182G probably damaging Het
Or8c9 A T 9: 38,240,952 (GRCm39) Q20L probably benign Het
Pde4c T A 8: 71,199,244 (GRCm39) L182Q probably damaging Het
Pla2g10 G T 16: 13,548,284 (GRCm39) probably null Het
Rap1gap2 T A 11: 74,303,170 (GRCm39) I426F probably damaging Het
Rnf139 C A 15: 58,771,881 (GRCm39) D635E probably benign Het
Sar1a T C 10: 61,520,718 (GRCm39) V15A possibly damaging Het
Scarb1 A C 5: 125,366,766 (GRCm39) S56A probably benign Het
Scn3a T C 2: 65,290,912 (GRCm39) K1945E possibly damaging Het
Sec62 G A 3: 30,864,071 (GRCm39) G118R unknown Het
Sgce T A 6: 4,689,738 (GRCm39) Q356L probably damaging Het
Slco4c1 A T 1: 96,770,232 (GRCm39) Y277* probably null Het
Smarca4 C T 9: 21,547,132 (GRCm39) T219I probably benign Het
Sphkap A T 1: 83,258,224 (GRCm39) I173N probably damaging Het
Spred3 C T 7: 28,860,997 (GRCm39) C394Y unknown Het
Stra6l A G 4: 45,873,689 (GRCm39) D283G probably benign Het
Tipin A T 9: 64,195,406 (GRCm39) Q4L probably benign Het
Tmprss11c T A 5: 86,379,730 (GRCm39) I380F probably benign Het
Tymp T C 15: 89,259,219 (GRCm39) D195G possibly damaging Het
Ugt2b34 T A 5: 87,054,544 (GRCm39) Y79F probably benign Het
Vmn2r16 T A 5: 109,511,580 (GRCm39) S596T possibly damaging Het
Wdhd1 A G 14: 47,481,346 (GRCm39) S1024P possibly damaging Het
Other mutations in Rbm33
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01284:Rbm33 APN 5 28,615,707 (GRCm39) missense probably damaging 0.98
IGL01470:Rbm33 APN 5 28,592,846 (GRCm39) missense probably damaging 1.00
IGL01565:Rbm33 APN 5 28,596,077 (GRCm39) unclassified probably benign
IGL02119:Rbm33 APN 5 28,544,015 (GRCm39) missense probably damaging 1.00
IGL02740:Rbm33 APN 5 28,536,121 (GRCm39) missense probably damaging 1.00
IGL02869:Rbm33 APN 5 28,615,753 (GRCm39) missense probably damaging 0.99
IGL03381:Rbm33 APN 5 28,599,390 (GRCm39) missense unknown
FR4449:Rbm33 UTSW 5 28,599,166 (GRCm39) small deletion probably benign
FR4548:Rbm33 UTSW 5 28,599,199 (GRCm39) small deletion probably benign
R0091:Rbm33 UTSW 5 28,557,604 (GRCm39) missense possibly damaging 0.94
R0725:Rbm33 UTSW 5 28,599,481 (GRCm39) missense unknown
R1522:Rbm33 UTSW 5 28,542,002 (GRCm39) missense probably damaging 1.00
R1918:Rbm33 UTSW 5 28,592,915 (GRCm39) missense probably damaging 1.00
R2186:Rbm33 UTSW 5 28,599,228 (GRCm39) missense unknown
R2448:Rbm33 UTSW 5 28,547,415 (GRCm39) missense probably benign 0.01
R4151:Rbm33 UTSW 5 28,592,938 (GRCm39) missense probably damaging 1.00
R4685:Rbm33 UTSW 5 28,613,280 (GRCm39) unclassified probably benign
R4787:Rbm33 UTSW 5 28,547,435 (GRCm39) splice site probably null
R4954:Rbm33 UTSW 5 28,544,274 (GRCm39) missense probably damaging 1.00
R5013:Rbm33 UTSW 5 28,547,409 (GRCm39) missense probably benign 0.05
R5141:Rbm33 UTSW 5 28,557,687 (GRCm39) missense probably damaging 1.00
R5248:Rbm33 UTSW 5 28,542,050 (GRCm39) critical splice donor site probably null
R5259:Rbm33 UTSW 5 28,557,772 (GRCm39) splice site probably null
R5695:Rbm33 UTSW 5 28,544,010 (GRCm39) missense probably damaging 1.00
R5790:Rbm33 UTSW 5 28,544,296 (GRCm39) missense probably damaging 1.00
R6591:Rbm33 UTSW 5 28,557,544 (GRCm39) missense probably damaging 0.99
R6668:Rbm33 UTSW 5 28,547,498 (GRCm39) missense probably benign 0.01
R6691:Rbm33 UTSW 5 28,557,544 (GRCm39) missense probably damaging 0.99
R6930:Rbm33 UTSW 5 28,557,504 (GRCm39) missense probably benign 0.09
R6931:Rbm33 UTSW 5 28,615,743 (GRCm39) missense probably damaging 1.00
R7034:Rbm33 UTSW 5 28,599,496 (GRCm39) missense unknown
R7056:Rbm33 UTSW 5 28,599,001 (GRCm39) unclassified probably benign
R7224:Rbm33 UTSW 5 28,599,322 (GRCm39) missense
R7579:Rbm33 UTSW 5 28,573,264 (GRCm39) missense probably damaging 1.00
R7839:Rbm33 UTSW 5 28,573,397 (GRCm39) splice site probably null
R7961:Rbm33 UTSW 5 28,599,606 (GRCm39) missense
R8009:Rbm33 UTSW 5 28,599,606 (GRCm39) missense
R8051:Rbm33 UTSW 5 28,557,623 (GRCm39) missense probably damaging 0.99
R8265:Rbm33 UTSW 5 28,599,322 (GRCm39) missense
R8461:Rbm33 UTSW 5 28,592,970 (GRCm39) missense probably damaging 1.00
R8734:Rbm33 UTSW 5 28,557,874 (GRCm39) intron probably benign
R9206:Rbm33 UTSW 5 28,557,584 (GRCm39) missense probably damaging 1.00
R9233:Rbm33 UTSW 5 28,544,239 (GRCm39) missense probably benign 0.00
R9376:Rbm33 UTSW 5 28,544,164 (GRCm39) missense probably damaging 1.00
R9731:Rbm33 UTSW 5 28,544,242 (GRCm39) missense probably damaging 1.00
RF011:Rbm33 UTSW 5 28,599,179 (GRCm39) small deletion probably benign
RF026:Rbm33 UTSW 5 28,599,179 (GRCm39) small deletion probably benign
RF047:Rbm33 UTSW 5 28,599,160 (GRCm39) small insertion probably benign
Posted On 2016-08-02