Incidental Mutation 'IGL01565:Rbm33'
ID 90961
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 # IGL01565
Quality Score
Status
Chromosome 5
Chromosomal Location 28522119-28624237 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 28596077 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: S800P
SMART Domains Protein: ENSMUSP00000062449
Gene: ENSMUSG00000048271
AA Change: S800P

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: S760P
SMART Domains Protein: ENSMUSP00000110534
Gene: ENSMUSG00000048271
AA Change: S760P

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: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017N19Rik A G 10: 100,439,222 (GRCm39) T36A probably damaging Het
Ankrd35 A G 3: 96,592,101 (GRCm39) M796V probably damaging Het
Brpf1 A T 6: 113,293,611 (GRCm39) Q560L probably damaging Het
Dbil5 T G 11: 76,109,091 (GRCm39) probably benign Het
Dnah9 T C 11: 65,924,655 (GRCm39) K2200E possibly damaging Het
Gtf2i T C 5: 134,284,767 (GRCm39) I471V probably damaging Het
Has3 T A 8: 107,601,077 (GRCm39) W180R probably benign Het
Lrfn1 T C 7: 28,158,194 (GRCm39) C38R probably damaging Het
Lrsam1 C T 2: 32,826,507 (GRCm39) A455T probably damaging Het
Mettl2 C A 11: 105,017,364 (GRCm39) D14E probably benign Het
Mocs1 G A 17: 49,759,348 (GRCm39) R364Q probably benign Het
Ndst2 A T 14: 20,778,274 (GRCm39) V435E probably damaging Het
Pi4ka A T 16: 17,207,306 (GRCm39) probably benign Het
Pigr A C 1: 130,772,211 (GRCm39) D143A possibly damaging Het
Polq A C 16: 36,833,475 (GRCm39) N56T probably benign Het
Prmt7 T G 8: 106,977,041 (GRCm39) D584E probably damaging Het
R3hdm1 A T 1: 128,114,553 (GRCm39) Q511H probably damaging Het
Rdh19 T G 10: 127,695,464 (GRCm39) M226R probably benign Het
Rock2 G A 12: 17,003,318 (GRCm39) D386N possibly damaging Het
Slc7a2 A G 8: 41,352,275 (GRCm39) T96A possibly damaging Het
Spata2 A G 2: 167,326,214 (GRCm39) S202P probably damaging Het
Swsap1 T A 9: 21,868,524 (GRCm39) D265E possibly damaging Het
Tdrd3 A T 14: 87,709,668 (GRCm39) I117L probably benign Het
Ticrr A G 7: 79,344,296 (GRCm39) D1387G probably benign Het
Tnfaip6 A G 2: 51,945,846 (GRCm39) S231G probably damaging Het
Trim50 T A 5: 135,396,355 (GRCm39) D434E probably benign Het
Tyw5 T C 1: 57,433,240 (GRCm39) Y105C probably damaging Het
Usp50 G T 2: 126,619,888 (GRCm39) C141* probably null Het
Zfp647 A T 15: 76,795,870 (GRCm39) C263* probably null 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
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
IGL03355:Rbm33 APN 5 28,596,059 (GRCm39) unclassified probably benign
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 2013-12-09