Incidental Mutation 'R8221:E330034G19Rik'
ID652039
Institutional Source Beutler Lab
Gene Symbol E330034G19Rik
Ensembl Gene ENSMUSG00000038925
Gene NameRIKEN cDNA E330034G19 gene
Synonyms
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.154) question?
Stock #R8221 (G1)
Quality Score225.009
Status Validated
Chromosome14
Chromosomal Location24293214-24309966 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) A to C at 24296067 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000123912 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000161740] [ENSMUST00000162224] [ENSMUST00000163055]
Predicted Effect noncoding transcript
Transcript: ENSMUST00000041413
SMART Domains Protein: ENSMUSP00000040386
Gene: ENSMUSG00000038925

DomainStartEndE-ValueType
coiled coil region 78 131 N/A INTRINSIC
low complexity region 154 172 N/A INTRINSIC
coiled coil region 207 325 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160710
SMART Domains Protein: ENSMUSP00000125673
Gene: ENSMUSG00000038925

DomainStartEndE-ValueType
coiled coil region 96 149 N/A INTRINSIC
low complexity region 172 190 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000161740
SMART Domains Protein: ENSMUSP00000124917
Gene: ENSMUSG00000038925

DomainStartEndE-ValueType
coiled coil region 100 153 N/A INTRINSIC
low complexity region 176 194 N/A INTRINSIC
coiled coil region 229 347 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000162224
SMART Domains Protein: ENSMUSP00000124926
Gene: ENSMUSG00000038925

DomainStartEndE-ValueType
coiled coil region 13 66 N/A INTRINSIC
low complexity region 89 107 N/A INTRINSIC
coiled coil region 136 256 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000163055
SMART Domains Protein: ENSMUSP00000123912
Gene: ENSMUSG00000038925

DomainStartEndE-ValueType
coiled coil region 13 66 N/A INTRINSIC
low complexity region 89 107 N/A INTRINSIC
coiled coil region 142 181 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.8%
Validation Efficiency 100% (74/74)
Allele List at MGI
Other mutations in this stock
Total: 77 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acly A G 11: 100,519,750 F134S probably damaging Het
Acsl5 T C 19: 55,268,830 probably null Het
Adam29 G T 8: 55,872,428 N330K probably benign Het
Adgrv1 A G 13: 81,528,914 S1933P probably benign Het
Afap1l2 T C 19: 56,914,392 H785R probably damaging Het
Ahnak T A 19: 9,010,436 L3028* probably null Het
Ajuba T C 14: 54,570,390 T462A possibly damaging Het
Ankrd36 A G 11: 5,584,016 N289S possibly damaging Het
Ankrd46 A T 15: 36,485,855 L84Q probably damaging Het
Ankrd54 T G 15: 79,056,070 D163A probably damaging Het
Arhgef28 A G 13: 98,145,556 L10P probably benign Het
Atm A T 9: 53,455,988 probably null Het
Azin1 G C 15: 38,492,328 F312L probably damaging Het
BC080695 T G 4: 143,571,960 Y158D probably benign Het
C2cd4c A G 10: 79,612,648 S222P probably damaging Het
Cdyl A G 13: 35,816,164 T143A probably benign Het
Clhc1 G A 11: 29,553,751 V56I possibly damaging Het
Cntn4 T C 6: 106,509,510 S300P probably benign Het
Col12a1 A G 9: 79,643,942 Y2131H probably damaging Het
Cyp3a41b A G 5: 145,569,380 S287P probably benign Het
Dctn4 A G 18: 60,556,329 D424G probably benign Het
Dnajb8 C T 6: 88,222,958 R159C possibly damaging Het
Dopey2 A G 16: 93,749,959 T284A probably benign Het
Ehhadh G A 16: 21,762,623 P540S possibly damaging Het
Emsy T C 7: 98,647,904 E24G probably damaging Het
F930015N05Rik A C 11: 64,435,592 L74W unknown Het
Fat1 A G 8: 44,953,353 D1047G Het
Galnt7 A G 8: 57,552,566 V211A possibly damaging Het
Gdap2 T C 3: 100,202,295 C543R unknown Het
Ghr A C 15: 3,333,419 D190E probably benign Het
Glrx A G 13: 75,847,227 M89V probably benign Het
Gm10323 A C 13: 66,852,795 Y91* noncoding transcript Het
Gnb4 A T 3: 32,590,035 D153E possibly damaging Het
Gnptab G T 10: 88,440,392 probably null Het
Grip2 T C 6: 91,785,684 D193G possibly damaging Het
Igsf3 T C 3: 101,439,722 W658R probably damaging Het
Ip6k1 T A 9: 108,045,916 F416I probably benign Het
Klhl1 T G 14: 96,280,110 T377P possibly damaging Het
Lrrc38 G A 4: 143,350,733 G189R probably damaging Het
Lrrfip1 T C 1: 91,115,156 S428P probably benign Het
Megf10 A G 18: 57,283,821 D754G probably benign Het
Mrgprx2 T A 7: 48,482,779 Y97F probably benign Het
Msantd2 T G 9: 37,489,388 V22G probably damaging Het
Myl6b T C 10: 128,497,340 K11R unknown Het
Nab2 C A 10: 127,662,776 V475L probably benign Het
Npas1 T C 7: 16,455,965 E552G probably damaging Het
Pknox2 T C 9: 36,909,744 N274S possibly damaging Het
Pmepa1 A T 2: 173,227,907 L247Q probably damaging Het
Poll T C 19: 45,553,608 K420E probably damaging Het
Polr2a A G 11: 69,737,518 V1283A probably benign Het
Ppil4 A T 10: 7,795,680 Y36F probably benign Het
Psd2 C T 18: 35,980,425 R317W probably damaging Het
Pspc1 T A 14: 56,778,159 M1L probably benign Het
Qrsl1 A T 10: 43,882,084 F338I possibly damaging Het
Rcor3 A G 1: 192,130,449 Y77H unknown Het
Sbno2 G A 10: 80,070,011 P157L probably benign Het
Scn10a C T 9: 119,617,763 V1400I probably damaging Het
Setd3 C G 12: 108,107,353 G555A possibly damaging Het
Slc12a4 A T 8: 105,951,969 M245K probably benign Het
Slc1a5 T A 7: 16,781,977 L26Q probably benign Het
Slc38a3 T G 9: 107,657,709 M156L probably damaging Het
Slc45a2 A T 15: 11,001,147 I111F probably benign Het
Slc4a3 T A 1: 75,552,166 M491K probably benign Het
Son A G 16: 91,656,846 D827G probably damaging Het
Sppl2c A T 11: 104,186,884 H170L probably damaging Het
St6gal2 T A 17: 55,490,934 probably null Het
Taf4b T A 18: 14,898,049 L830H probably damaging Het
Tex22 A G 12: 113,075,076 probably null Het
Tiam2 C T 17: 3,518,585 R1669C probably damaging Het
Tmprss15 T A 16: 79,024,335 N506I probably damaging Het
Topors A T 4: 40,260,686 I866K unknown Het
Trip12 G T 1: 84,766,050 T512K possibly damaging Het
Ubr1 T A 2: 120,961,104 H133L probably damaging Het
Wwtr1 T C 3: 57,459,020 D422G probably damaging Het
Zfp689 A C 7: 127,444,586 C291G probably damaging Het
Zfyve9 A G 4: 108,719,680 L68P possibly damaging Het
Zswim5 G T 4: 116,878,022 R188L probably benign Het
Other mutations in E330034G19Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02515:E330034G19Rik APN 14 24297984 missense possibly damaging 0.89
R0565:E330034G19Rik UTSW 14 24306917 missense probably benign 0.27
R1507:E330034G19Rik UTSW 14 24306987 missense possibly damaging 0.46
R1819:E330034G19Rik UTSW 14 24298013 missense probably damaging 0.99
R3158:E330034G19Rik UTSW 14 24296897 missense possibly damaging 0.79
R3966:E330034G19Rik UTSW 14 24306871 missense unknown
R4621:E330034G19Rik UTSW 14 24296002 utr 5 prime probably benign
R4992:E330034G19Rik UTSW 14 24306996 missense unknown
R5567:E330034G19Rik UTSW 14 24296824 missense possibly damaging 0.94
R5570:E330034G19Rik UTSW 14 24296824 missense possibly damaging 0.94
R5630:E330034G19Rik UTSW 14 24308268 unclassified probably benign
R6062:E330034G19Rik UTSW 14 24293380 intron probably benign
R6550:E330034G19Rik UTSW 14 24296818 missense probably benign 0.12
R6799:E330034G19Rik UTSW 14 24296110 missense probably benign 0.03
R6831:E330034G19Rik UTSW 14 24296095 missense probably benign 0.16
R6920:E330034G19Rik UTSW 14 24308242 missense unknown
R7457:E330034G19Rik UTSW 14 24309514 missense unknown
R8097:E330034G19Rik UTSW 14 24306852 missense unknown
R8210:E330034G19Rik UTSW 14 24296036 missense
R8243:E330034G19Rik UTSW 14 24308292 missense
R8830:E330034G19Rik UTSW 14 24309508 missense unknown
Predicted Primers PCR Primer
(F):5'- ATAGAATGTGGCATCCCCTGG -3'
(R):5'- CTGGGAGGGATGACAATCTC -3'

Sequencing Primer
(F):5'- GCATCCCCTGGTTTGGG -3'
(R):5'- CCATGCTGATAGCTAAGAGGC -3'
Posted On2020-09-24