Incidental Mutation 'R1419:Gm16380'
ID 159996
Institutional Source Beutler Lab
Gene Symbol Gm16380
Ensembl Gene ENSMUSG00000059830
Gene Name predicted pseudogene 16380
Synonyms
MMRRC Submission 039475-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.295) question?
Stock # R1419 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 53884082-53884561 bp(+) (GRCm38)
Type of Mutation exon
DNA Base Change (assembly) C to T at 53884187 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000077997
SMART Domains Protein: ENSMUSP00000129245
Gene: ENSMUSG00000059830

DomainStartEndE-ValueType
Pfam:Siva 1 152 6.6e-65 PFAM
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 98.0%
  • 10x: 95.5%
  • 20x: 90.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca15 T A 7: 120,374,902 M894K probably benign Het
Ablim1 C A 19: 57,134,633 C173F probably damaging Het
Abtb2 G T 2: 103,709,420 R710L probably benign Het
AI481877 T C 4: 59,064,457 T826A possibly damaging Het
Arap3 T C 18: 37,978,432 T1144A possibly damaging Het
Arhgef12 A T 9: 43,027,220 V92D probably damaging Het
Ash1l T G 3: 88,984,897 M1361R probably damaging Het
Atm A C 9: 53,457,489 N2337K probably benign Het
Cog7 T C 7: 121,955,992 E316G probably damaging Het
Dsp A G 13: 38,186,695 Y858C probably damaging Het
Enc1 G T 13: 97,246,184 G401C probably damaging Het
Gata6 T C 18: 11,064,706 V506A probably benign Het
H2-Ke6 G A 17: 34,027,643 R89C probably benign Het
Hsh2d G A 8: 72,200,460 D229N probably benign Het
Ift80 T A 3: 68,940,198 N322Y probably damaging Het
Igsf9 T A 1: 172,498,011 V1082E probably damaging Het
Katnal2 A T 18: 76,977,432 L481Q possibly damaging Het
Kcnma1 T C 14: 23,367,642 T713A probably damaging Het
Kif13a T C 13: 46,825,235 T230A probably damaging Het
Klhl14 C A 18: 21,652,193 R59L probably damaging Het
Mecom A G 3: 29,980,889 C213R probably damaging Het
Mrpl13 T A 15: 55,534,321 M178L probably benign Het
Myof T C 19: 37,901,911 E1971G probably damaging Het
Naa10 A G X: 73,917,916 V133A probably damaging Het
Nlrp4g G A 9: 124,349,434 noncoding transcript Het
Ofcc1 C T 13: 40,208,829 G206R probably benign Het
Olfr1042 A G 2: 86,159,429 *314Q probably null Het
Olfr1234 T C 2: 89,363,322 T36A probably damaging Het
Olfr1297 A T 2: 111,621,295 F260I probably benign Het
Oplah T C 15: 76,297,920 I1047V probably benign Het
Paip1 A G 13: 119,457,017 D189G probably damaging Het
Pkn1 A G 8: 83,673,522 F624L probably damaging Het
Plxnb1 C A 9: 109,114,386 P1899H probably damaging Het
Rpa3 T A 6: 8,257,720 E47D probably benign Het
Snai2 C T 16: 14,708,180 H232Y possibly damaging Het
Spint5 T C 2: 164,715,411 S23P possibly damaging Het
St8sia2 G A 7: 73,966,994 Q78* probably null Het
Tktl2 A G 8: 66,513,038 N416S probably damaging Het
Tm7sf3 T A 6: 146,603,977 I494F possibly damaging Het
Trf C T 9: 103,226,108 V119M probably damaging Het
Other mutations in Gm16380
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02207:Gm16380 APN 9 53884539 exon noncoding transcript
R0386:Gm16380 UTSW 9 53884443 exon noncoding transcript
R0398:Gm16380 UTSW 9 53884169 exon noncoding transcript
R0512:Gm16380 UTSW 9 53884245 exon noncoding transcript
R2301:Gm16380 UTSW 9 53884200 exon noncoding transcript
R3697:Gm16380 UTSW 9 53884452 exon noncoding transcript
R5128:Gm16380 UTSW 9 53884113 exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- ATCTAGTGACGTGTGCTCGGCG -3'
(R):5'- TCCACAGATCTCATGCACGATGAAC -3'

Sequencing Primer
(F):5'- TGTGTGATACCCGCTACCAT -3'
(R):5'- TCATGCACGATGAACAAGCG -3'
Posted On 2014-03-14