Incidental Mutation 'R4447:3930402G23Rik'
ID 328799
Institutional Source Beutler Lab
Gene Symbol 3930402G23Rik
Ensembl Gene ENSMUSG00000038917
Gene Name RIKEN cDNA 3930402G23 gene
Synonyms
MMRRC Submission 041708-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.231) question?
Stock # R4447 (G1)
Quality Score 225
Status Validated
Chromosome 8
Chromosomal Location 10974427-10978457 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to A at 10976129 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000040608
SMART Domains Protein: ENSMUSP00000044199
Gene: ENSMUSG00000038917

DomainStartEndE-ValueType
low complexity region 12 23 N/A INTRINSIC
low complexity region 62 68 N/A INTRINSIC
low complexity region 81 91 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207377
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208615
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.3%
Validation Efficiency 100% (32/32)
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsf2 G T 11: 94,460,185 (GRCm39) P389Q possibly damaging Het
Aldh6a1 A G 12: 84,486,483 (GRCm39) V120A possibly damaging Het
Alg11 C A 8: 22,558,095 (GRCm39) A469E probably benign Het
Ankar A G 1: 72,726,948 (GRCm39) S415P possibly damaging Het
Ano3 A T 2: 110,591,923 (GRCm39) probably null Het
Asic4 A T 1: 75,447,014 (GRCm39) probably benign Het
Atp1a4 A C 1: 172,061,998 (GRCm39) I709S probably damaging Het
Cyp11b2 T C 15: 74,727,412 (GRCm39) I90V probably benign Het
Galnt2 A G 8: 125,022,116 (GRCm39) D14G probably benign Het
Iqcm T C 8: 76,356,394 (GRCm39) S176P probably damaging Het
Irf5 T A 6: 29,535,941 (GRCm39) D318E probably damaging Het
Map2k3 A T 11: 60,837,997 (GRCm39) S253C probably damaging Het
Mgst1 G T 6: 138,118,662 (GRCm39) probably benign Het
Mipol1 G T 12: 57,399,534 (GRCm39) probably benign Het
Niban1 A T 1: 151,512,153 (GRCm39) probably null Het
Or7c19 T A 8: 85,957,995 (GRCm39) Y290* probably null Het
Pomgnt1 G T 4: 116,010,120 (GRCm39) V161L possibly damaging Het
Rnpc3 T C 3: 113,404,786 (GRCm39) probably benign Het
Rxfp1 C T 3: 79,559,434 (GRCm39) probably benign Het
Scn5a T C 9: 119,379,693 (GRCm39) D197G probably damaging Het
Spata31d1e T C 13: 59,890,012 (GRCm39) T603A probably benign Het
Thsd7a G A 6: 12,324,634 (GRCm39) T1479I probably damaging Het
Twsg1 C T 17: 66,236,782 (GRCm39) D83N possibly damaging Het
Ubqln3 C T 7: 103,792,021 (GRCm39) R23Q probably benign Het
Vmn1r228 T C 17: 20,997,369 (GRCm39) I50V probably damaging Het
Wnk4 T A 11: 101,159,277 (GRCm39) S565T possibly damaging Het
Wwc2 A G 8: 48,321,702 (GRCm39) Y471H unknown Het
Zfp407 A T 18: 84,580,819 (GRCm39) V98D possibly damaging Het
Zfp598 T A 17: 24,895,529 (GRCm39) V73E probably damaging Het
Zscan29 T A 2: 121,000,367 (GRCm39) probably null Het
Other mutations in 3930402G23Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0113:3930402G23Rik UTSW 8 10,976,126 (GRCm39) unclassified noncoding transcript
R4448:3930402G23Rik UTSW 8 10,976,129 (GRCm39) unclassified noncoding transcript
R4450:3930402G23Rik UTSW 8 10,976,129 (GRCm39) unclassified noncoding transcript
R4653:3930402G23Rik UTSW 8 10,976,075 (GRCm39) unclassified noncoding transcript
Predicted Primers PCR Primer
(F):5'- TAATCCTCTCGGGCATGTGAG -3'
(R):5'- GTTAGCACAAGAGGTCCTGC -3'

Sequencing Primer
(F):5'- AGCTAACTCTGGCCCGGTATTTG -3'
(R):5'- TCCTGCGGAGGAAGCACTAG -3'
Posted On 2015-07-21