Incidental Mutation 'R9251:Gm45861'
ID 701550
Institutional Source Beutler Lab
Gene Symbol Gm45861
Ensembl Gene ENSMUSG00000110333
Gene Name predicted gene 45861
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.102) question?
Stock # R9251 (G1)
Quality Score 225.009
Status Validated
Chromosome 8
Chromosomal Location 27937128-28110945 bp(+) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) T to C at 28032589 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000147714 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000209669] [ENSMUST00000210427]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000209669
Predicted Effect probably benign
Transcript: ENSMUST00000210427
Meta Mutation Damage Score 0.9756 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency 100% (59/59)
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap31 G T 16: 38,423,218 (GRCm39) N949K probably benign Het
Arv1 T A 8: 125,452,062 (GRCm39) I76N probably damaging Het
Cfap44 G A 16: 44,229,276 (GRCm39) A189T probably damaging Het
Ch25h T C 19: 34,451,769 (GRCm39) Y253C probably damaging Het
Cnot11 T C 1: 39,581,587 (GRCm39) M376T probably damaging Het
Cnot7 T C 8: 40,964,622 (GRCm39) probably benign Het
Dnah17 G A 11: 118,012,618 (GRCm39) S481F probably benign Het
Dnah2 C T 11: 69,406,619 (GRCm39) R541Q probably damaging Het
Dnah7a C T 1: 53,621,671 (GRCm39) M1151I probably damaging Het
Dpf2 T C 19: 5,957,166 (GRCm39) D19G probably damaging Het
Eefsec A T 6: 88,332,574 (GRCm39) M212K probably damaging Het
Elp6 G A 9: 110,134,666 (GRCm39) V12I unknown Het
Enox1 G A 14: 77,852,997 (GRCm39) probably null Het
Epha1 G T 6: 42,341,777 (GRCm39) N424K probably damaging Het
Fam171a1 T C 2: 3,226,525 (GRCm39) S553P probably benign Het
Fbxw21 A G 9: 108,974,687 (GRCm39) S278P probably damaging Het
Gm4846 T A 1: 166,311,307 (GRCm39) R517S probably benign Het
Gnrhr A G 5: 86,345,221 (GRCm39) L155P possibly damaging Het
Igfn1 C T 1: 135,894,409 (GRCm39) probably benign Het
Ik T A 18: 36,880,495 (GRCm39) probably null Het
Insrr A T 3: 87,717,391 (GRCm39) Q763L probably benign Het
Klf5 G T 14: 99,538,824 (GRCm39) C79F possibly damaging Het
Lrrcc1 A T 3: 14,623,454 (GRCm39) R760S probably damaging Het
Map3k7 T A 4: 32,002,080 (GRCm39) probably benign Het
Mapkbp1 C T 2: 119,853,671 (GRCm39) A1159V probably benign Het
Mgst3 C T 1: 167,205,860 (GRCm39) probably null Het
Mtch2 T A 2: 90,679,980 (GRCm39) F71I probably damaging Het
Myo1e A G 9: 70,276,076 (GRCm39) I764V probably benign Het
Myo3b T A 2: 70,088,425 (GRCm39) L896* probably null Het
Ndufs5 T G 4: 123,606,628 (GRCm39) E103A probably benign Het
Nfe2l1 G A 11: 96,710,421 (GRCm39) P603S probably damaging Het
Or6c211 T A 10: 129,505,980 (GRCm39) N136I possibly damaging Het
Or8g34 A T 9: 39,373,668 (GRCm39) M311L probably benign Het
Piezo1 T C 8: 123,219,354 (GRCm39) N1093S Het
Pitpnb G A 5: 111,533,390 (GRCm39) R258H probably benign Het
Pla2g4d T C 2: 120,099,378 (GRCm39) E708G possibly damaging Het
Plppr4 T A 3: 117,115,608 (GRCm39) T750S probably benign Het
Prrg4 T G 2: 104,675,399 (GRCm39) E68A probably damaging Het
Rcan2 C T 17: 44,328,701 (GRCm39) T90M possibly damaging Het
Rlbp1 T C 7: 79,027,093 (GRCm39) E189G probably damaging Het
Satb1 A G 17: 52,112,293 (GRCm39) F107S probably damaging Het
Sdc3 A T 4: 130,548,513 (GRCm39) probably benign Het
Slc22a3 A T 17: 12,726,093 (GRCm39) V40D probably damaging Het
Slc35d1 A G 4: 103,048,027 (GRCm39) probably null Het
Slfn1 T C 11: 83,012,121 (GRCm39) F79S probably damaging Het
Snrpg G T 6: 86,353,557 (GRCm39) V46L probably benign Het
Tbl1xr1 G A 3: 22,264,569 (GRCm39) C508Y probably benign Het
Thada A T 17: 84,538,564 (GRCm39) D1481E probably benign Het
Tnfsf8 A G 4: 63,779,217 (GRCm39) V27A probably benign Het
Tns1 T C 1: 74,030,855 (GRCm39) H300R probably damaging Het
Ttc13 C A 8: 125,401,992 (GRCm39) G589V probably benign Het
Ttc28 A G 5: 111,040,698 (GRCm39) I29V possibly damaging Het
Tubb4a T A 17: 57,387,778 (GRCm39) N416I possibly damaging Het
Ubr4 T A 4: 139,177,636 (GRCm39) I1884N Het
Usp16 A G 16: 87,266,640 (GRCm39) K175E probably benign Het
Usp24 A G 4: 106,217,715 (GRCm39) I479M probably benign Het
Utrn T C 10: 12,512,531 (GRCm39) T2313A probably benign Het
Ythdc2 T C 18: 44,974,442 (GRCm39) V368A probably benign Het
Zfp628 T C 7: 4,923,880 (GRCm39) S701P probably damaging Het
Other mutations in Gm45861
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6286:Gm45861 UTSW 8 28,019,619 (GRCm39) missense unknown
R6580:Gm45861 UTSW 8 28,034,979 (GRCm39) missense unknown
R6650:Gm45861 UTSW 8 27,995,043 (GRCm39) missense unknown
R6784:Gm45861 UTSW 8 27,990,086 (GRCm39) critical splice acceptor site probably null
R6881:Gm45861 UTSW 8 28,025,279 (GRCm39) splice site probably null
R6909:Gm45861 UTSW 8 28,017,109 (GRCm39) missense unknown
R6929:Gm45861 UTSW 8 28,014,462 (GRCm39) missense unknown
R6959:Gm45861 UTSW 8 28,038,213 (GRCm39) critical splice donor site probably null
R7023:Gm45861 UTSW 8 28,071,034 (GRCm39) missense unknown
R7157:Gm45861 UTSW 8 28,032,537 (GRCm39) missense unknown
R7157:Gm45861 UTSW 8 28,032,536 (GRCm39) nonsense probably null
R7453:Gm45861 UTSW 8 28,031,686 (GRCm39) missense unknown
R7462:Gm45861 UTSW 8 28,024,517 (GRCm39) critical splice donor site probably null
R7545:Gm45861 UTSW 8 28,071,032 (GRCm39) missense unknown
R7674:Gm45861 UTSW 8 28,030,147 (GRCm39) missense unknown
R7840:Gm45861 UTSW 8 28,072,751 (GRCm39) missense unknown
R7938:Gm45861 UTSW 8 28,071,990 (GRCm39) missense unknown
R8092:Gm45861 UTSW 8 28,057,823 (GRCm39) missense unknown
R8242:Gm45861 UTSW 8 28,038,821 (GRCm39) missense unknown
R8856:Gm45861 UTSW 8 28,010,788 (GRCm39) missense unknown
R8900:Gm45861 UTSW 8 28,019,632 (GRCm39) missense unknown
R8988:Gm45861 UTSW 8 28,032,531 (GRCm39) missense unknown
R9067:Gm45861 UTSW 8 27,995,043 (GRCm39) missense unknown
R9266:Gm45861 UTSW 8 28,074,674 (GRCm39) missense unknown
R9455:Gm45861 UTSW 8 28,041,394 (GRCm39) nonsense probably null
R9643:Gm45861 UTSW 8 27,994,083 (GRCm39) missense unknown
R9684:Gm45861 UTSW 8 28,014,601 (GRCm39) missense unknown
R9729:Gm45861 UTSW 8 28,045,436 (GRCm39) missense unknown
Z1176:Gm45861 UTSW 8 28,074,897 (GRCm39) missense unknown
Z1177:Gm45861 UTSW 8 28,059,979 (GRCm39) missense unknown
Z1177:Gm45861 UTSW 8 28,025,397 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- GCTGTCTGCTTGGAGAACAT -3'
(R):5'- AATATGGACGGGTGGATGTG -3'

Sequencing Primer
(F):5'- CTGCTTGGAGAACATTTCAAGG -3'
(R):5'- AGCACAGCATAGGTTACTTGTCCTG -3'
Posted On 2022-03-25