Incidental Mutation 'R6245:Gm1110'
ID 505531
Institutional Source Beutler Lab
Gene Symbol Gm1110
Ensembl Gene ENSMUSG00000079644
Gene Name predicted gene 1110
Synonyms LOC382064
MMRRC Submission 044403-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.069) question?
Stock # R6245 (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 G at 26832043 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Proline at position 36 (H36P)
Ref Sequence ENSEMBL: ENSMUSP00000110916 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115261]
AlphaFold F6Y113
Predicted Effect probably benign
Transcript: ENSMUST00000115261
AA Change: H36P

PolyPhen 2 Score 0.036 (Sensitivity: 0.94; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000110916
Gene: ENSMUSG00000079644
AA Change: H36P

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
Predicted Effect noncoding transcript
Transcript: ENSMUST00000214461
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217197
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.6%
  • 20x: 96.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca9 A G 11: 110,026,249 (GRCm39) I937T probably damaging Het
Adgrl3 T A 5: 81,836,403 (GRCm39) N720K probably benign Het
Akr1c21 T G 13: 4,625,231 (GRCm39) V54G possibly damaging Het
Alpi G T 1: 87,028,556 (GRCm39) D111E probably damaging Het
Armc3 C T 2: 19,253,516 (GRCm39) T219M probably damaging Het
Bms1 T A 6: 118,373,797 (GRCm39) E780V probably damaging Het
Ccdc159 T C 9: 21,846,864 (GRCm39) S244P probably damaging Het
Cdon T C 9: 35,388,235 (GRCm39) W737R probably damaging Het
Chdh T A 14: 29,757,262 (GRCm39) V395D probably damaging Het
Col22a1 C A 15: 71,845,665 (GRCm39) D366Y probably damaging Het
Cplane1 T C 15: 8,207,902 (GRCm39) Y218H probably benign Het
Crnkl1 T A 2: 145,770,051 (GRCm39) N264I probably benign Het
Ctnnd2 T C 15: 30,905,894 (GRCm39) L847P probably damaging Het
Cyp4a31 A C 4: 115,428,545 (GRCm39) T382P possibly damaging Het
Dcaf8 A T 1: 171,993,434 (GRCm39) M1L probably benign Het
Ddx31 T A 2: 28,734,994 (GRCm39) F52I probably benign Het
Dynlt5 A G 4: 102,845,864 (GRCm39) N32S probably benign Het
Efcab3 A T 11: 104,675,834 (GRCm39) Y1542F probably benign Het
Eps15 G A 4: 109,240,063 (GRCm39) S852N possibly damaging Het
Fchsd1 A T 18: 38,095,828 (GRCm39) L552Q probably damaging Het
Fetub C T 16: 22,751,081 (GRCm39) R143C probably damaging Het
Frem2 T C 3: 53,563,245 (GRCm39) M421V probably benign Het
Hadha C T 5: 30,325,042 (GRCm39) probably null Het
Hspa4 C T 11: 53,153,766 (GRCm39) E702K probably benign Het
Intu C A 3: 40,629,756 (GRCm39) T362K probably damaging Het
Jaml C T 9: 45,009,217 (GRCm39) T248I probably damaging Het
Kcnj1 A T 9: 32,308,163 (GRCm39) S176C probably damaging Het
Kcnj9 A G 1: 172,153,704 (GRCm39) L140P probably damaging Het
Kif7 T C 7: 79,351,891 (GRCm39) K957R probably damaging Het
Klc4 T A 17: 46,947,605 (GRCm39) I366F probably damaging Het
Lamb2 A G 9: 108,365,398 (GRCm39) probably null Het
Madd T C 2: 91,008,449 (GRCm39) D151G probably benign Het
Man2a1 C A 17: 65,017,821 (GRCm39) A689E probably damaging Het
Mapk8ip1 C A 2: 92,219,589 (GRCm39) G81C probably damaging Het
Msmp T C 4: 43,583,909 (GRCm39) Y48C probably damaging Het
Muc6 T C 7: 141,235,086 (GRCm39) N567S probably damaging Het
Nrap A G 19: 56,342,653 (GRCm39) Y748H probably damaging Het
Nrap C T 19: 56,368,307 (GRCm39) A192T possibly damaging Het
Or2p2 T A 13: 21,256,860 (GRCm39) T204S possibly damaging Het
Or2y14 T A 11: 49,404,992 (GRCm39) F176I possibly damaging Het
Or5w15 G C 2: 87,568,240 (GRCm39) Q143E possibly damaging Het
Pcdhb8 T G 18: 37,490,222 (GRCm39) D633E possibly damaging Het
Pcdhb9 G A 18: 37,536,207 (GRCm39) V734M probably damaging Het
Plscr1 T C 9: 92,141,374 (GRCm39) Y21H unknown Het
Ptk2b G T 14: 66,400,515 (GRCm39) P767T probably damaging Het
Ptprz1 T C 6: 23,051,989 (GRCm39) Y1424H probably damaging Het
Sec31a T A 5: 100,534,043 (GRCm39) Q118L probably benign Het
Selenop A G 15: 3,304,216 (GRCm39) S21G probably damaging Het
Shank1 G A 7: 44,001,677 (GRCm39) S1132N unknown Het
Slf1 A G 13: 77,232,502 (GRCm39) L534P probably damaging Het
Sparcl1 T A 5: 104,233,013 (GRCm39) H596L probably damaging Het
Spocd1 C T 4: 129,850,901 (GRCm39) probably null Het
Tbc1d24 A T 17: 24,404,967 (GRCm39) I59N probably damaging Het
Tjp3 G A 10: 81,113,110 (GRCm39) T580I probably benign Het
Tmem154 C T 3: 84,591,603 (GRCm39) T51M possibly damaging Het
Tmem8b G A 4: 43,690,246 (GRCm39) V894I probably benign Het
Trbv20 A T 6: 41,165,840 (GRCm39) L88F possibly damaging Het
Tssk2 A C 16: 17,716,812 (GRCm39) I72L possibly damaging Het
Tub T A 7: 108,626,265 (GRCm39) I267N probably damaging Het
Vmn2r104 A T 17: 20,261,829 (GRCm39) F434I possibly damaging Het
Vmn2r42 T C 7: 8,195,733 (GRCm39) N471S probably damaging Het
Vmn2r94 C G 17: 18,478,385 (GRCm39) G121R probably damaging Het
Wdr72 T C 9: 74,055,505 (GRCm39) S245P probably damaging Het
Zbtb42 A G 12: 112,645,969 (GRCm39) Y48C probably damaging Het
Zdbf2 T C 1: 63,343,592 (GRCm39) V657A possibly damaging Het
Zfp768 A T 7: 126,943,263 (GRCm39) C288* probably null Het
Zfp988 T A 4: 147,416,470 (GRCm39) C301* probably null 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
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
R9321:Gm1110 UTSW 9 26,831,891 (GRCm39) missense probably benign 0.00
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'- TAAGAGTATTGAAGCCACCGG -3'
(R):5'- ACAAATTGATCCCTGTCCCTAG -3'

Sequencing Primer
(F):5'- GCCTGCATCTTCCTCAAACTGAG -3'
(R):5'- ATTGATCCCTGTCCCTAGATTCTTTC -3'
Posted On 2018-02-28