Incidental Mutation 'R6931:2900092C05Rik'
ID 540021
Institutional Source Beutler Lab
Gene Symbol 2900092C05Rik
Ensembl Gene ENSMUSG00000030385
Gene Name RIKEN cDNA 2900092C05 gene
Synonyms
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.059) question?
Stock # R6931 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 12512517-12556323 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to A at 12512596 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Serine to Arginine at position 6 (S6R)
Ref Sequence ENSEMBL: ENSMUSP00000032541 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032541]
AlphaFold Q5I0V9
Predicted Effect unknown
Transcript: ENSMUST00000032541
AA Change: S6R
SMART Domains Protein: ENSMUSP00000032541
Gene: ENSMUSG00000030385
AA Change: S6R

DomainStartEndE-ValueType
signal peptide 1 25 N/A INTRINSIC
transmembrane domain 96 118 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.4%
  • 20x: 98.0%
Validation Efficiency 99% (77/78)
Allele List at MGI
Other mutations in this stock
Total: 79 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700123L14Rik T C 6: 96,165,548 T172A possibly damaging Het
2310003L06Rik T A 5: 87,970,702 I15N probably damaging Het
Abca6 T A 11: 110,244,328 L210F probably benign Het
Abcc4 T C 14: 118,527,988 Q919R probably damaging Het
Adcy1 A G 11: 7,150,884 D811G possibly damaging Het
Akna A G 4: 63,387,102 S476P probably benign Het
Ankrd49 T C 9: 14,782,826 N15S probably benign Het
Apcdd1 A G 18: 62,933,908 D31G probably damaging Het
Aplp1 G T 7: 30,443,200 R106S probably damaging Het
Arhgap40 T C 2: 158,531,218 L132S probably benign Het
Atp8b5 G T 4: 43,364,108 probably null Het
Axl T C 7: 25,761,433 D717G probably damaging Het
Bub1 T A 2: 127,801,382 D1014V probably damaging Het
Cacna2d4 T A 6: 119,282,234 V603E possibly damaging Het
Cnot11 G C 1: 39,539,921 C289S probably damaging Het
Coasy A G 11: 101,083,581 H191R probably benign Het
Cyp11a1 A T 9: 58,025,120 N341Y possibly damaging Het
Cyp1a2 T C 9: 57,682,156 N125S probably benign Het
Cyp2j8 A T 4: 96,444,781 probably null Het
Dnah9 A T 11: 66,117,626 I791K possibly damaging Het
Ecm2 A T 13: 49,529,011 Q505H probably benign Het
Fam135a T A 1: 24,085,487 M1L probably damaging Het
Fam171a2 A G 11: 102,438,434 S500P possibly damaging Het
Fat3 A G 9: 15,959,942 S3718P possibly damaging Het
Frem1 G A 4: 82,970,677 P1085S probably damaging Het
Gcfc2 A G 6: 81,942,985 I390V probably benign Het
Gemin4 A G 11: 76,210,956 L993P probably damaging Het
Ggnbp2 T A 11: 84,833,167 D647V probably damaging Het
Gm7534 A T 4: 134,193,153 M567K probably benign Het
Gpr84 A C 15: 103,309,014 L212R probably damaging Het
Hnrnpu T C 1: 178,331,432 probably benign Het
Hspg2 G T 4: 137,540,720 C2116F probably damaging Het
Icam4 T A 9: 21,030,451 V249E probably damaging Het
Itga1 T C 13: 115,001,563 N429D probably benign Het
Kcns1 T C 2: 164,164,838 T402A probably damaging Het
Ky T A 9: 102,537,627 V246E probably damaging Het
March1 A G 8: 66,468,492 T529A probably benign Het
Med18 C G 4: 132,459,883 V102L probably damaging Het
Mlst8 T C 17: 24,477,275 D160G probably damaging Het
Mthfd1 T C 12: 76,303,698 I470T probably benign Het
Muc1 C T 3: 89,229,159 probably benign Het
Mup8 G A 4: 60,220,322 L137F probably damaging Het
Mybpc1 A T 10: 88,542,330 L341* probably null Het
Nacad A G 11: 6,601,877 F438S probably benign Het
Necap2 C A 4: 141,078,212 probably null Het
Nifk T C 1: 118,332,348 L163S possibly damaging Het
Npsr1 A G 9: 24,289,997 I73V probably benign Het
Olfr1179 G A 2: 88,402,064 T290I probably benign Het
Olfr1186 T A 2: 88,526,194 C204S possibly damaging Het
Olfr142 A T 2: 90,252,777 C70* probably null Het
Olfr715 A G 7: 107,128,901 L164P probably damaging Het
Oog3 C T 4: 144,159,353 C225Y probably benign Het
Plagl2 C A 2: 153,235,943 K39N probably benign Het
Plcg2 T A 8: 117,557,319 D118E probably benign Het
Ppp4r3b A T 11: 29,211,786 K720I possibly damaging Het
Prmt3 A T 7: 49,829,016 T442S probably benign Het
Prr14l G A 5: 32,830,691 H487Y probably damaging Het
Psmb3 G A 11: 97,703,971 V63I probably benign Het
Psmc6 T A 14: 45,343,725 I326K possibly damaging Het
Ptcd1 T C 5: 145,155,075 T405A probably benign Het
Rbm33 G A 5: 28,410,745 V29M probably damaging Het
Rsrc1 C T 3: 66,994,649 P44L unknown Het
Scarb1 T A 5: 125,284,719 I107F probably damaging Het
Slc39a12 A G 2: 14,389,375 S19G probably benign Het
Slc44a5 T C 3: 154,258,506 V503A probably benign Het
Slc9a9 T C 9: 94,670,086 S9P possibly damaging Het
Snrnp35 A C 5: 124,490,701 R192S possibly damaging Het
Tbx15 T C 3: 99,352,151 L446P probably damaging Het
Tlnrd1 A G 7: 83,882,597 F209L probably benign Het
Tmprss12 C T 15: 100,285,268 R164C probably damaging Het
Tnfsf4 T A 1: 161,417,073 F111Y possibly damaging Het
Trib2 A T 12: 15,793,639 M198K probably benign Het
Ttll8 A G 15: 88,914,304 S743P possibly damaging Het
Ush2a A T 1: 188,728,383 N2614Y probably benign Het
Usp6nl G A 2: 6,430,458 V343I possibly damaging Het
Vrtn C A 12: 84,650,242 Q589K probably benign Het
Zbed5 T A 5: 129,903,329 Y706* probably null Het
Zc3h10 A G 10: 128,544,684 V268A probably damaging Het
Zfp442 C T 2: 150,410,940 probably null Het
Other mutations in 2900092C05Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00714:2900092C05Rik APN 7 12556004 splice site probably benign
IGL01744:2900092C05Rik APN 7 12550532 missense possibly damaging 0.92
IGL03047:2900092C05Rik UTSW 7 12512641 missense possibly damaging 0.92
R0001:2900092C05Rik UTSW 7 12554607 splice site probably benign
R0607:2900092C05Rik UTSW 7 12554698 missense probably benign 0.19
R0831:2900092C05Rik UTSW 7 12550596 splice site probably benign
R1468:2900092C05Rik UTSW 7 12512580 start codon destroyed probably null 0.83
R1468:2900092C05Rik UTSW 7 12512580 start codon destroyed probably null 0.83
R1846:2900092C05Rik UTSW 7 12512882 missense probably benign 0.38
R1852:2900092C05Rik UTSW 7 12512702 splice site probably null
R1912:2900092C05Rik UTSW 7 12554655 missense probably benign 0.01
R3442:2900092C05Rik UTSW 7 12512656 nonsense probably null
R3694:2900092C05Rik UTSW 7 12550516 missense possibly damaging 0.46
R3751:2900092C05Rik UTSW 7 12556046 missense probably benign 0.02
R5977:2900092C05Rik UTSW 7 12554737 missense probably benign 0.17
R6158:2900092C05Rik UTSW 7 12512672 missense probably benign 0.37
R6777:2900092C05Rik UTSW 7 12512829 missense probably benign 0.00
R7284:2900092C05Rik UTSW 7 12512678 nonsense probably null
R7406:2900092C05Rik UTSW 7 12515464 missense possibly damaging 0.66
R8472:2900092C05Rik UTSW 7 12512641 missense possibly damaging 0.92
R8802:2900092C05Rik UTSW 7 12515488 missense possibly damaging 0.66
R8877:2900092C05Rik UTSW 7 12554777 critical splice donor site probably null
R9175:2900092C05Rik UTSW 7 12515485 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TGCCCAAGTTCTGTGAAGGG -3'
(R):5'- CTGTCTACTCCCTTGAAAAGAAAAC -3'

Sequencing Primer
(F):5'- CCCAAGTTCTGTGAAGGGATTCC -3'
(R):5'- CTCCCTTGAAAAGAAAACTTGTAGC -3'
Posted On 2018-11-06