Incidental Mutation 'R6131:Gm1818'
ID 487145
Institutional Source Beutler Lab
Gene Symbol Gm1818
Ensembl Gene ENSMUSG00000091277
Gene Name predicted gene 1818
Synonyms LOC217536
MMRRC Submission 044278-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.899) question?
Stock # R6131 (G1)
Quality Score 225.009
Status Validated
Chromosome 12
Chromosomal Location 48602091-48606668 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to A at 48602319 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000169406
SMART Domains Protein: ENSMUSP00000131939
Gene: ENSMUSG00000091277

DomainStartEndE-ValueType
low complexity region 1 22 N/A INTRINSIC
Pfam:RrnaAD 78 377 4.3e-23 PFAM
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.5%
  • 20x: 95.8%
Validation Efficiency 96% (50/52)
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5031439G07Rik A T 15: 84,844,793 (GRCm39) W75R probably damaging Het
Aadacl2fm3 A G 3: 59,776,324 (GRCm39) K165R possibly damaging Het
Abca15 T C 7: 119,939,428 (GRCm39) V274A probably benign Het
Afg3l2 G T 18: 67,554,329 (GRCm39) L458M probably damaging Het
Ap1m2 T C 9: 21,207,797 (GRCm39) Y396C probably damaging Het
Apob T C 12: 8,065,874 (GRCm39) S405P probably benign Het
Arhgap26 G T 18: 39,419,638 (GRCm39) G533* probably null Het
Atxn2l T C 7: 126,102,337 (GRCm39) probably benign Het
Ccdc88c A T 12: 100,907,387 (GRCm39) L995H probably damaging Het
Ccn3 A G 15: 54,612,756 (GRCm39) D255G probably benign Het
Cep192 A G 18: 67,971,068 (GRCm39) H1023R possibly damaging Het
Cog5 T A 12: 31,936,220 (GRCm39) M589K possibly damaging Het
Col25a1 C A 3: 130,329,114 (GRCm39) P337Q probably damaging Het
Cyfip1 T G 7: 55,523,228 (GRCm39) V51G possibly damaging Het
Dnah7b A T 1: 46,292,626 (GRCm39) I3004F probably damaging Het
Dsg3 A T 18: 20,671,569 (GRCm39) D758V probably damaging Het
Dsg3 A G 18: 20,653,534 (GRCm39) probably null Het
Eml5 A T 12: 98,827,510 (GRCm39) H573Q probably damaging Het
Erp27 T C 6: 136,885,201 (GRCm39) D199G probably damaging Het
Flnb A G 14: 7,894,635 (GRCm38) Y811C possibly damaging Het
G6pd2 A T 5: 61,966,593 (GRCm39) S123C probably benign Het
Gm29340 C T 2: 116,798,519 (GRCm39) noncoding transcript Het
H2bc7 C A 13: 23,758,310 (GRCm39) probably benign Het
Hcn2 G T 10: 79,569,742 (GRCm39) G581W probably damaging Het
Kidins220 T C 12: 25,042,313 (GRCm39) probably null Het
Lonp1 T C 17: 56,921,457 (GRCm39) E926G probably benign Het
Lrp1 T C 10: 127,396,026 (GRCm39) I2415V probably benign Het
Mmel1 C T 4: 154,979,475 (GRCm39) H728Y probably damaging Het
Mmp10 A G 9: 7,503,633 (GRCm39) probably null Het
Myo16 T A 8: 10,619,877 (GRCm39) I1476N probably benign Het
Nectin3 G T 16: 46,215,515 (GRCm39) H76N probably damaging Het
Nphs2 G A 1: 156,153,521 (GRCm39) R204Q probably damaging Het
Or5ac15 T C 16: 58,940,256 (GRCm39) Y59C probably damaging Het
Or8b36 ATTGCTGTTT ATTGCTGTTTGCTGTTT 9: 37,937,836 (GRCm39) probably null Het
Or8b53 T A 9: 38,667,362 (GRCm39) I126N probably damaging Het
Otx1 A T 11: 21,949,406 (GRCm39) L24H probably damaging Het
Pate10 T A 9: 35,652,840 (GRCm39) C27* probably null Het
Psme2b T C 11: 48,836,752 (GRCm39) D65G probably damaging Het
Rlf T C 4: 121,012,172 (GRCm39) K214E probably damaging Het
Rnasel A T 1: 153,630,206 (GRCm39) T241S probably damaging Het
Samd9l C G 6: 3,377,252 (GRCm39) G3A probably benign Het
Smg7 A G 1: 152,720,962 (GRCm39) probably null Het
Spag16 A G 1: 70,764,242 (GRCm39) probably null Het
Spata31d1c T A 13: 65,183,485 (GRCm39) D342E probably benign Het
Stab2 A G 10: 86,719,642 (GRCm39) probably null Het
Taar7b A T 10: 23,876,615 (GRCm39) Y260F probably benign Het
Vcpip1 T C 1: 9,817,517 (GRCm39) I289V probably damaging Het
Vmn2r130 C T 17: 23,282,629 (GRCm39) A103V probably benign Het
Vmn2r39 A G 7: 9,017,963 (GRCm39) V791A probably damaging Het
Vmn2r66 T A 7: 84,644,224 (GRCm39) I729F probably damaging Het
Zfp536 T A 7: 37,269,137 (GRCm39) D93V probably damaging Het
Other mutations in Gm1818
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01456:Gm1818 APN 12 48,602,583 (GRCm39) exon noncoding transcript
IGL01472:Gm1818 APN 12 48,603,072 (GRCm39) exon noncoding transcript
IGL01634:Gm1818 APN 12 48,602,992 (GRCm39) exon noncoding transcript
IGL01874:Gm1818 APN 12 48,602,973 (GRCm39) exon noncoding transcript
IGL02287:Gm1818 APN 12 48,602,505 (GRCm39) exon noncoding transcript
IGL02805:Gm1818 APN 12 48,602,518 (GRCm39) exon noncoding transcript
R1174:Gm1818 UTSW 12 48,602,982 (GRCm39) exon noncoding transcript
R1175:Gm1818 UTSW 12 48,602,982 (GRCm39) exon noncoding transcript
R1636:Gm1818 UTSW 12 48,602,550 (GRCm39) exon noncoding transcript
R4797:Gm1818 UTSW 12 48,602,393 (GRCm39) exon noncoding transcript
R4828:Gm1818 UTSW 12 48,602,409 (GRCm39) exon noncoding transcript
R4937:Gm1818 UTSW 12 48,606,607 (GRCm39) exon noncoding transcript
R5022:Gm1818 UTSW 12 48,602,318 (GRCm39) exon noncoding transcript
R5023:Gm1818 UTSW 12 48,602,318 (GRCm39) exon noncoding transcript
R5952:Gm1818 UTSW 12 48,602,719 (GRCm39) exon noncoding transcript
R6057:Gm1818 UTSW 12 48,602,346 (GRCm39) exon noncoding transcript
Z1088:Gm1818 UTSW 12 48,602,907 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- TCCGGGCAGTAGTCATAGATCC -3'
(R):5'- AGTTCCTGCACATGGAACCTTG -3'

Sequencing Primer
(F):5'- GGCAGTAGTCATAGATCCACTTAAAG -3'
(R):5'- ACATGGAACCTTGGTCGTC -3'
Posted On 2017-10-10