Incidental Mutation 'R0020:Rimoc1'
ID 201381
Institutional Source Beutler Lab
Gene Symbol Rimoc1
Ensembl Gene ENSMUSG00000041935
Gene Name RAB7A interacting MON1-CCZ1 complex subunit 1
Synonyms AW549877
MMRRC Submission 038315-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R0020 (G1)
Quality Score 33
Status Validated
Chromosome 15
Chromosomal Location 4011517-4025226 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 4021350 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000038476 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000046633]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000046633
SMART Domains Protein: ENSMUSP00000038476
Gene: ENSMUSG00000041935

DomainStartEndE-ValueType
low complexity region 44 57 N/A INTRINSIC
low complexity region 119 131 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180518
Predicted Effect noncoding transcript
Transcript: ENSMUST00000228184
Predicted Effect noncoding transcript
Transcript: ENSMUST00000228421
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.9%
  • 10x: 97.9%
  • 20x: 96.4%
Validation Efficiency 99% (67/68)
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ado T C 10: 67,383,927 (GRCm39) D226G probably benign Het
Agfg2 C T 5: 137,652,064 (GRCm39) V432M probably benign Het
Atf2 T C 2: 73,676,628 (GRCm39) D122G possibly damaging Het
Brd10 A T 19: 29,693,597 (GRCm39) D2032E probably damaging Het
Cd2bp2 G A 7: 126,792,996 (GRCm39) T342M probably damaging Het
Cip2a A T 16: 48,821,975 (GRCm39) H201L probably damaging Het
Col6a3 T A 1: 90,739,272 (GRCm39) I319F probably damaging Het
Cst11 T A 2: 148,613,253 (GRCm39) Y24F probably damaging Het
Cstb T A 10: 78,263,170 (GRCm39) V65E probably benign Het
Cyp2j11 G A 4: 96,195,641 (GRCm39) H352Y probably benign Het
D130043K22Rik T A 13: 25,038,475 (GRCm39) probably benign Het
Dbh A G 2: 27,060,584 (GRCm39) probably benign Het
Dhdh T C 7: 45,137,528 (GRCm39) K53R probably benign Het
Drc3 A G 11: 60,261,371 (GRCm39) Y174C probably damaging Het
Ezr G T 17: 7,010,126 (GRCm39) Q308K probably damaging Het
F3 A T 3: 121,525,265 (GRCm39) N169Y probably damaging Het
Fbn2 G T 18: 58,238,236 (GRCm39) T587K probably damaging Het
Fhl5 A T 4: 25,200,054 (GRCm39) V260E probably benign Het
Glyr1 A G 16: 4,854,913 (GRCm39) I55T probably damaging Het
Gm12695 G C 4: 96,657,972 (GRCm39) P66A probably damaging Het
Gon4l G T 3: 88,766,244 (GRCm39) V428L probably damaging Het
Ighv6-5 T C 12: 114,380,241 (GRCm39) D92G probably null Het
Inhba A C 13: 16,200,949 (GRCm39) K170N possibly damaging Het
Kng2 A G 16: 22,816,046 (GRCm39) V317A probably benign Het
Larp1 T A 11: 57,940,849 (GRCm39) D658E probably damaging Het
Map3k14 T C 11: 103,118,500 (GRCm39) E562G probably damaging Het
Megf10 G T 18: 57,420,965 (GRCm39) V868F possibly damaging Het
Nap1l1 A C 10: 111,326,884 (GRCm39) E148D probably benign Het
Nlrp4a A T 7: 26,149,797 (GRCm39) H468L probably damaging Het
Nphs1 G T 7: 30,162,633 (GRCm39) V357L probably benign Het
Or10aa3 T A 1: 173,878,413 (GRCm39) V158E probably damaging Het
Pclo A G 5: 14,719,687 (GRCm39) T1275A unknown Het
Pde4d T A 13: 110,091,104 (GRCm39) C35S possibly damaging Het
Pkd1l1 A G 11: 8,825,765 (GRCm39) probably benign Het
Pkd2 A G 5: 104,651,382 (GRCm39) E910G probably damaging Het
Pot1b T A 17: 55,960,429 (GRCm39) M634L probably benign Het
Ppp2r5c C T 12: 110,541,257 (GRCm39) Q469* probably null Het
Ppp6r2 T A 15: 89,143,342 (GRCm39) M163K probably damaging Het
Prss43 C A 9: 110,657,580 (GRCm39) probably benign Het
Rb1cc1 C A 1: 6,334,772 (GRCm39) N1444K possibly damaging Het
Scube2 A G 7: 109,430,095 (GRCm39) probably benign Het
Slamf9 T C 1: 172,303,082 (GRCm39) S7P possibly damaging Het
Slc35b2 T A 17: 45,877,782 (GRCm39) M303K probably damaging Het
Slc4a7 T A 14: 14,796,108 (GRCm38) F1116I probably benign Het
Slco1a8 A T 6: 141,918,076 (GRCm39) V600E possibly damaging Het
Smarcad1 T A 6: 65,060,991 (GRCm39) probably benign Het
Tamalin T C 15: 101,128,433 (GRCm39) V157A probably damaging Het
Tns3 A C 11: 8,495,227 (GRCm39) probably null Het
Zfp282 T G 6: 47,856,943 (GRCm39) W59G probably damaging Het
Zfp746 C A 6: 48,041,641 (GRCm39) A362S probably benign Het
Other mutations in Rimoc1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00578:Rimoc1 APN 15 4,018,118 (GRCm39) missense probably damaging 1.00
IGL01527:Rimoc1 APN 15 4,018,165 (GRCm39) missense probably damaging 1.00
IGL02170:Rimoc1 APN 15 4,015,848 (GRCm39) missense probably benign
IGL03188:Rimoc1 APN 15 4,018,187 (GRCm39) missense probably damaging 0.99
R0020:Rimoc1 UTSW 15 4,021,350 (GRCm39) splice site probably benign
R0123:Rimoc1 UTSW 15 4,015,776 (GRCm39) missense probably damaging 0.98
R0134:Rimoc1 UTSW 15 4,015,776 (GRCm39) missense probably damaging 0.98
R0225:Rimoc1 UTSW 15 4,015,776 (GRCm39) missense probably damaging 0.98
R0631:Rimoc1 UTSW 15 4,015,971 (GRCm39) splice site probably benign
R1070:Rimoc1 UTSW 15 4,015,848 (GRCm39) missense probably benign 0.22
R4437:Rimoc1 UTSW 15 4,021,318 (GRCm39) missense probably damaging 1.00
R6186:Rimoc1 UTSW 15 4,015,851 (GRCm39) missense possibly damaging 0.67
R7663:Rimoc1 UTSW 15 4,018,165 (GRCm39) missense probably damaging 1.00
R8027:Rimoc1 UTSW 15 4,015,694 (GRCm39) missense probably benign 0.00
R9293:Rimoc1 UTSW 15 4,021,336 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GGAAGTGTTAAGTTCTCTTCCACCACC -3'
(R):5'- ATGTGAGAAATGCGCCTTCGCC -3'

Sequencing Primer
(F):5'- gcctcgaactcagaaagatcc -3'
(R):5'- TCGCCTGCCACCACTTC -3'
Posted On 2014-06-02