Incidental Mutation 'R9321:Gm1110'
ID 706211
Institutional Source Beutler Lab
Gene Symbol Gm1110
Ensembl Gene ENSMUSG00000079644
Gene Name predicted gene 1110
Synonyms LOC382064
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.069) question?
Stock # R9321 (G1)
Quality Score 225.009
Status Not validated
Chromosome 9
Chromosomal Location 26790863-26834407 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 26831891 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Leucine at position 87 (M87L)
Ref Sequence ENSEMBL: ENSMUSP00000110916 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115261]
AlphaFold F6Y113
Predicted Effect probably benign
Transcript: ENSMUST00000115261
AA Change: M87L

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
SMART Domains Protein: ENSMUSP00000110916
Gene: ENSMUSG00000079644
AA Change: M87L

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
Pfam:Glyco_hydro_35 55 368 2e-93 PFAM
Pfam:Glyco_hydro_42 70 229 1e-12 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 A G 11: 9,460,475 (GRCm39) S4162G probably benign Het
Acvr2b T C 9: 119,257,351 (GRCm39) I152T probably benign Het
Adam15 T A 3: 89,254,794 (GRCm39) probably null Het
Adam34 C T 8: 44,105,243 (GRCm39) G134D probably damaging Het
Aifm2 C T 10: 61,571,410 (GRCm39) Q315* probably null Het
Akap10 A G 11: 61,791,235 (GRCm39) F408S probably damaging Het
Ap3b2 T C 7: 81,114,252 (GRCm39) probably null Het
Btbd2 A C 10: 80,483,675 (GRCm39) V181G probably damaging Het
Carmil3 G T 14: 55,741,425 (GRCm39) G1070V Het
Ceacam2 G T 7: 25,230,089 (GRCm39) D172E possibly damaging Het
Crtc3 G A 7: 80,259,650 (GRCm39) A203V probably benign Het
Dclre1a A G 19: 56,531,100 (GRCm39) S749P probably damaging Het
Dnah2 C T 11: 69,338,939 (GRCm39) probably null Het
Eif2ak4 G A 2: 118,292,798 (GRCm39) V1341M possibly damaging Het
Enpp5 T C 17: 44,393,689 (GRCm39) V295A possibly damaging Het
Gm57858 A T 3: 36,073,139 (GRCm39) V381E probably damaging Het
H2-Ab1 T C 17: 34,486,969 (GRCm39) L241P probably damaging Het
Hmx2 A G 7: 131,157,320 (GRCm39) T145A probably benign Het
Irag1 A G 7: 110,524,534 (GRCm39) S138P probably benign Het
Itpripl1 T C 2: 126,984,000 (GRCm39) S41G probably benign Het
Kcnb2 G A 1: 15,779,793 (GRCm39) D222N possibly damaging Het
Ldb3 C A 14: 34,266,099 (GRCm39) G499* probably null Het
Lig1 T C 7: 13,034,935 (GRCm39) F577S probably damaging Het
Lnx1 T C 5: 74,780,991 (GRCm39) I177V probably damaging Het
Mark4 G T 7: 19,170,901 (GRCm39) T323K probably benign Het
Mroh5 A G 15: 73,661,113 (GRCm39) V301A probably benign Het
Mtx3 T A 13: 92,984,097 (GRCm39) W125R probably damaging Het
Myo18a G A 11: 77,733,370 (GRCm39) G1404R probably damaging Het
Myom2 C T 8: 15,172,464 (GRCm39) P1188S possibly damaging Het
Nars1 C T 18: 64,637,950 (GRCm39) E335K probably damaging Het
Nfya A T 17: 48,707,494 (GRCm39) V16E unknown Het
Nicn1 C T 9: 108,171,708 (GRCm39) R163C possibly damaging Het
Nlrp4e C G 7: 23,020,755 (GRCm39) A414G probably benign Het
Nme5 T G 18: 34,704,597 (GRCm39) I83L probably benign Het
Nos1 G C 5: 118,017,402 (GRCm39) R255P probably benign Het
Nptx1 A G 11: 119,438,378 (GRCm39) L13P unknown Het
Or11g27 G A 14: 50,771,471 (GRCm39) V201I probably benign Het
Or13c25 G T 4: 52,911,314 (GRCm39) T160N probably damaging Het
Or13m2-ps1 T A 6: 42,777,792 (GRCm39) V39D possibly damaging Het
Or4k44 A G 2: 111,368,434 (GRCm39) S67P probably damaging Het
Or5j3 A T 2: 86,128,297 (GRCm39) I46F probably benign Het
Or6d13 T C 6: 116,518,370 (GRCm39) Y319H probably benign Het
Pdzd2 T C 15: 12,386,023 (GRCm39) T916A probably benign Het
Plekha6 A G 1: 133,209,549 (GRCm39) N615S probably damaging Het
Prorp A G 12: 55,351,434 (GRCm39) I248V possibly damaging Het
Rad52 T C 6: 119,889,969 (GRCm39) Y32H probably damaging Het
Slc22a16 T A 10: 40,450,047 (GRCm39) I161N probably damaging Het
Slx4 A G 16: 3,804,654 (GRCm39) M720T probably benign Het
Spem1 T C 11: 69,712,661 (GRCm39) H58R probably benign Het
Spg7 C A 8: 123,803,688 (GRCm39) D239E probably benign Het
Tas2r123 A T 6: 132,825,095 (GRCm39) M331L probably benign Het
Tcaf1 T C 6: 42,656,290 (GRCm39) T229A probably benign Het
Tdrd1 T C 19: 56,848,767 (GRCm39) L939P probably damaging Het
Timd2 T C 11: 46,577,916 (GRCm39) T72A probably benign Het
Tmem179 G T 12: 112,477,390 (GRCm39) N31K probably damaging Het
Tpd52l1 T C 10: 31,214,189 (GRCm39) S165G Het
Tubgcp6 T C 15: 88,992,186 (GRCm39) T600A probably damaging Het
Txlna T A 4: 129,528,246 (GRCm39) E230D probably damaging Het
Ush2a A T 1: 188,089,148 (GRCm39) I368F probably damaging Het
Vmn1r76 A T 7: 11,665,094 (GRCm39) M40K possibly damaging Het
Zfp592 C T 7: 80,691,226 (GRCm39) S1135L possibly damaging Het
Zfp606 A G 7: 12,226,610 (GRCm39) T244A possibly damaging Het
Other mutations in Gm1110
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00591:Gm1110 APN 9 26,792,170 (GRCm39) nonsense probably null
IGL01089:Gm1110 APN 9 26,793,156 (GRCm39) missense probably benign
IGL01631:Gm1110 APN 9 26,809,212 (GRCm39) critical splice donor site probably null
IGL02008:Gm1110 APN 9 26,794,526 (GRCm39) missense probably benign 0.09
IGL02331:Gm1110 APN 9 26,824,583 (GRCm39) critical splice donor site probably null
IGL02335:Gm1110 APN 9 26,793,059 (GRCm39) missense probably benign 0.00
IGL02550:Gm1110 APN 9 26,793,130 (GRCm39) missense probably benign 0.09
IGL02614:Gm1110 APN 9 26,832,010 (GRCm39) missense probably benign 0.11
IGL03409:Gm1110 APN 9 26,807,916 (GRCm39) missense probably benign 0.21
PIT4458001:Gm1110 UTSW 9 26,792,124 (GRCm39) missense probably benign 0.00
R0189:Gm1110 UTSW 9 26,794,514 (GRCm39) missense probably null 0.99
R0271:Gm1110 UTSW 9 26,831,962 (GRCm39) missense probably damaging 1.00
R1034:Gm1110 UTSW 9 26,832,646 (GRCm39) missense probably damaging 1.00
R1229:Gm1110 UTSW 9 26,793,102 (GRCm39) missense probably benign
R1355:Gm1110 UTSW 9 26,795,057 (GRCm39) missense probably benign 0.01
R1566:Gm1110 UTSW 9 26,792,166 (GRCm39) missense probably damaging 1.00
R1574:Gm1110 UTSW 9 26,792,422 (GRCm39) splice site probably benign
R1916:Gm1110 UTSW 9 26,800,934 (GRCm39) missense probably damaging 1.00
R2011:Gm1110 UTSW 9 26,805,554 (GRCm39) missense probably benign 0.01
R2214:Gm1110 UTSW 9 26,813,786 (GRCm39) missense probably benign 0.37
R2567:Gm1110 UTSW 9 26,831,992 (GRCm39) missense probably benign
R2967:Gm1110 UTSW 9 26,792,339 (GRCm39) missense probably benign 0.05
R4271:Gm1110 UTSW 9 26,806,944 (GRCm39) critical splice donor site probably null
R4683:Gm1110 UTSW 9 26,831,890 (GRCm39) missense probably damaging 0.99
R4945:Gm1110 UTSW 9 26,831,891 (GRCm39) missense possibly damaging 0.46
R5015:Gm1110 UTSW 9 26,793,162 (GRCm39) missense probably benign 0.01
R5089:Gm1110 UTSW 9 26,793,683 (GRCm39) missense probably damaging 0.96
R5225:Gm1110 UTSW 9 26,813,774 (GRCm39) missense probably damaging 1.00
R5239:Gm1110 UTSW 9 26,804,866 (GRCm39) missense probably benign 0.00
R5395:Gm1110 UTSW 9 26,800,928 (GRCm39) missense probably benign
R5783:Gm1110 UTSW 9 26,793,632 (GRCm39) missense probably benign
R6045:Gm1110 UTSW 9 26,794,505 (GRCm39) critical splice donor site probably null
R6245:Gm1110 UTSW 9 26,832,043 (GRCm39) missense probably benign 0.04
R6357:Gm1110 UTSW 9 26,825,424 (GRCm39) splice site probably null
R6863:Gm1110 UTSW 9 26,792,360 (GRCm39) missense probably damaging 1.00
R7336:Gm1110 UTSW 9 26,825,653 (GRCm39) missense probably damaging 0.99
R7454:Gm1110 UTSW 9 26,831,945 (GRCm39) missense probably benign
R7555:Gm1110 UTSW 9 26,804,924 (GRCm39) missense probably benign 0.05
R7579:Gm1110 UTSW 9 26,795,122 (GRCm39) missense possibly damaging 0.93
R7990:Gm1110 UTSW 9 26,792,137 (GRCm39) missense possibly damaging 0.66
R8062:Gm1110 UTSW 9 26,793,117 (GRCm39) missense probably damaging 0.99
R8108:Gm1110 UTSW 9 26,831,957 (GRCm39) missense probably damaging 1.00
R8323:Gm1110 UTSW 9 26,813,719 (GRCm39) critical splice donor site probably null
R8354:Gm1110 UTSW 9 26,794,577 (GRCm39) missense probably benign 0.00
R8354:Gm1110 UTSW 9 26,794,576 (GRCm39) missense probably benign 0.01
R8454:Gm1110 UTSW 9 26,794,577 (GRCm39) missense probably benign 0.00
R8454:Gm1110 UTSW 9 26,794,576 (GRCm39) missense probably benign 0.01
R8494:Gm1110 UTSW 9 26,792,154 (GRCm39) missense probably benign 0.04
R8978:Gm1110 UTSW 9 26,807,095 (GRCm39) splice site probably benign
R9513:Gm1110 UTSW 9 26,795,083 (GRCm39) missense possibly damaging 0.95
R9545:Gm1110 UTSW 9 26,800,977 (GRCm39) missense probably benign 0.00
R9758:Gm1110 UTSW 9 26,800,894 (GRCm39) nonsense probably null
RF002:Gm1110 UTSW 9 26,831,936 (GRCm39) missense probably damaging 1.00
X0063:Gm1110 UTSW 9 26,805,576 (GRCm39) missense probably benign 0.01
Z1088:Gm1110 UTSW 9 26,824,606 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- ATGTCTGCTCCTTTAGGTAATCCTG -3'
(R):5'- TGAACACTCATTCATCCTGTGC -3'

Sequencing Primer
(F):5'- GGTAATCCTGACTAATAAGTTGGC -3'
(R):5'- CCTGTGCTATAGAAATCATATGCCC -3'
Posted On 2022-04-18