Incidental Mutation 'R9025:Gm15821'
ID 686517
Institutional Source Beutler Lab
Gene Symbol Gm15821
Ensembl Gene ENSMUSG00000081512
Gene Name predicted gene 15821
Synonyms
MMRRC Submission 068854-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.520) question?
Stock # R9025 (G1)
Quality Score 225.009
Status Validated
Chromosome 17
Chromosomal Location 34430286-34433433 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 34433235 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Valine at position 28 (E28V)
Ref Sequence ENSEMBL: ENSMUSP00000112395 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025197] [ENSMUST00000121995]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000025197
SMART Domains Protein: ENSMUSP00000025197
Gene: ENSMUSG00000024339

DomainStartEndE-ValueType
signal peptide 1 28 N/A INTRINSIC
transmembrane domain 55 77 N/A INTRINSIC
transmembrane domain 97 119 N/A INTRINSIC
Pfam:ABC_membrane 151 419 1.8e-62 PFAM
AAA 494 678 2.58e-19 SMART
Predicted Effect unknown
Transcript: ENSMUST00000121995
AA Change: E28V
SMART Domains Protein: ENSMUSP00000112395
Gene: ENSMUSG00000081512
AA Change: E28V

DomainStartEndE-ValueType
low complexity region 124 136 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency 99% (80/81)
Allele List at MGI
Other mutations in this stock
Total: 82 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2ml1 G T 6: 128,534,545 (GRCm39) N837K possibly damaging Het
Adam29 A T 8: 56,325,196 (GRCm39) C419* probably null Het
Adamts7 C A 9: 90,067,848 (GRCm39) S446* probably null Het
Ager A G 17: 34,819,594 (GRCm39) R371G probably damaging Het
Apobr T A 7: 126,185,629 (GRCm39) V380E possibly damaging Het
Arhgap26 T C 18: 39,379,898 (GRCm39) S105P Het
Atrip A G 9: 108,902,906 (GRCm39) F56S probably damaging Het
Bag2 T C 1: 33,785,905 (GRCm39) Y139C Het
Bccip C T 7: 133,319,346 (GRCm39) Q146* probably null Het
Btbd10 G A 7: 112,951,031 (GRCm39) R20W possibly damaging Het
Catsperd T A 17: 56,962,156 (GRCm39) N443K probably damaging Het
Cdh26 G A 2: 178,104,409 (GRCm39) E265K probably benign Het
Cep76 T C 18: 67,767,885 (GRCm39) R216G probably damaging Het
Cgas C A 9: 78,349,787 (GRCm39) V192L probably benign Het
Cnot1 T A 8: 96,475,660 (GRCm39) M1000L probably benign Het
Cyp1a1 A G 9: 57,610,070 (GRCm39) T495A possibly damaging Het
Cyp2w1 T A 5: 139,342,470 (GRCm39) M421K probably benign Het
Dlg5 T C 14: 24,199,546 (GRCm39) T1453A probably benign Het
Dnah5 G T 15: 28,409,412 (GRCm39) W3610L probably damaging Het
Dnah9 T C 11: 65,896,651 (GRCm39) D2391G probably damaging Het
Dnajc10 G A 2: 80,179,637 (GRCm39) G724R probably damaging Het
Dst T A 1: 34,227,585 (GRCm39) I1726N possibly damaging Het
Dync2h1 A T 9: 7,139,462 (GRCm39) L1391* probably null Het
Dzank1 T C 2: 144,318,012 (GRCm39) S718G probably benign Het
E230025N22Rik T C 18: 36,819,890 (GRCm39) D300G probably damaging Het
Ebf3 T C 7: 136,914,098 (GRCm39) I131V possibly damaging Het
Eif3g T C 9: 20,807,426 (GRCm39) I131V probably benign Het
Eppk1 T A 15: 75,990,503 (GRCm39) Q2126L possibly damaging Het
Fam83h T C 15: 75,874,182 (GRCm39) R1052G probably benign Het
Fry A T 5: 150,219,273 (GRCm39) probably benign Het
Ggt6 C T 11: 72,328,123 (GRCm39) H208Y possibly damaging Het
Gprin2 T C 14: 33,916,957 (GRCm39) Q271R probably damaging Het
Gsdmd T C 15: 75,739,053 (GRCm39) F477L probably benign Het
Hes7 T C 11: 69,013,782 (GRCm39) S214P probably benign Het
Hmcn2 A G 2: 31,347,967 (GRCm39) H4871R possibly damaging Het
Il15ra G A 2: 11,723,233 (GRCm39) V86I possibly damaging Het
Il17rb C A 14: 29,724,857 (GRCm39) probably benign Het
Itpr3 G A 17: 27,337,651 (GRCm39) probably benign Het
Kcnab2 T C 4: 152,491,635 (GRCm39) Y63C probably damaging Het
Kctd17 A T 15: 78,314,282 (GRCm39) Y84F probably damaging Het
Lama1 T A 17: 68,119,491 (GRCm39) V2656E Het
Lama2 T C 10: 26,860,367 (GRCm39) N3040S probably benign Het
Ldha C T 7: 46,500,433 (GRCm39) R173C unknown Het
Lig1 A G 7: 13,037,746 (GRCm39) I665M probably damaging Het
Lipe G A 7: 25,083,923 (GRCm39) A412V probably damaging Het
Lrrc63 T C 14: 75,322,284 (GRCm39) T607A probably benign Het
Majin G A 19: 6,263,427 (GRCm39) probably null Het
Map3k19 A G 1: 127,758,175 (GRCm39) L335P probably benign Het
Map3k9 A G 12: 81,819,507 (GRCm39) L249P probably damaging Het
Muc5b G T 7: 141,426,209 (GRCm39) D4769Y probably damaging Het
Myh9 T C 15: 77,653,192 (GRCm39) T1382A probably benign Het
Nedd4l T A 18: 65,311,995 (GRCm39) D407E probably damaging Het
Ngp A G 9: 110,251,451 (GRCm39) I160V possibly damaging Het
Nmrk1 A G 19: 18,617,156 (GRCm39) probably benign Het
Nnmt C A 9: 48,503,461 (GRCm39) K188N probably damaging Het
Nup153 T A 13: 46,837,709 (GRCm39) Q1171L probably benign Het
Oplah T A 15: 76,187,417 (GRCm39) E556V probably benign Het
Or9g3 T G 2: 85,589,879 (GRCm39) L280F possibly damaging Het
Otog A G 7: 45,937,520 (GRCm39) D1743G probably benign Het
Otogl T C 10: 107,613,432 (GRCm39) Y2011C probably damaging Het
Pbx4 C T 8: 70,317,097 (GRCm39) P118L probably benign Het
Plekha6 T A 1: 133,212,999 (GRCm39) S757T probably benign Het
Plk5 C G 10: 80,193,830 (GRCm39) R40G probably damaging Het
Polr3a C T 14: 24,519,479 (GRCm39) S643N probably damaging Het
Pwp1 T A 10: 85,718,745 (GRCm39) L304Q probably damaging Het
Qrich2 GCTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTG GCTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTG 11: 116,348,367 (GRCm39) probably benign Het
Rab11fip1 A G 8: 27,644,736 (GRCm39) F350L probably benign Het
Safb2 T C 17: 56,873,614 (GRCm39) E683G probably damaging Het
Scarb1 A T 5: 125,381,414 (GRCm39) N43K probably damaging Het
Serpina3k A G 12: 104,307,230 (GRCm39) E154G probably damaging Het
Sgsm3 T A 15: 80,892,182 (GRCm39) V250D probably damaging Het
Slit1 T A 19: 41,612,968 (GRCm39) I851F probably benign Het
Spag4 G A 2: 155,910,424 (GRCm39) G350E probably damaging Het
Sult2a7 A T 7: 14,225,755 (GRCm39) L77Q probably damaging Het
Tbc1d2 T A 4: 46,607,062 (GRCm39) T783S probably damaging Het
Thoc6 T C 17: 23,888,862 (GRCm39) E182G Het
Tmem132a A T 19: 10,837,525 (GRCm39) I595N probably damaging Het
Trim69 A G 2: 122,003,771 (GRCm39) N240S probably benign Het
Ush1c A T 7: 45,846,614 (GRCm39) probably benign Het
Wnk4 T G 11: 101,153,641 (GRCm39) Y234* probably null Het
Zfp943 A G 17: 22,211,321 (GRCm39) N136D possibly damaging Het
Znhit2 G A 19: 6,111,669 (GRCm39) R138H possibly damaging Het
Other mutations in Gm15821
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02505:Gm15821 APN 17 34,433,259 (GRCm39) intron probably benign
R0032:Gm15821 UTSW 17 34,431,199 (GRCm39) splice site probably benign
Predicted Primers PCR Primer
(F):5'- TGGACCGAAAGCCGAATCTG -3'
(R):5'- GTGGTGATCATACTCGGTCAGG -3'

Sequencing Primer
(F):5'- AGCCGAATCTGCCCCAG -3'
(R):5'- ATCATACTCGGTCAGGGGCTC -3'
Posted On 2021-10-11