Incidental Mutation 'R4023:1110038F14Rik'
ID 313366
Institutional Source Beutler Lab
Gene Symbol 1110038F14Rik
Ensembl Gene ENSMUSG00000063236
Gene Name RIKEN cDNA 1110038F14 gene
Synonyms
MMRRC Submission 040957-MU
Accession Numbers
Essential gene? Not available question?
Stock # R4023 (G1)
Quality Score 153
Status Not validated
Chromosome 15
Chromosomal Location 76832706-76835179 bp(+) (GRCm39)
Type of Mutation small insertion (1 aa in frame mutation)
DNA Base Change (assembly) CGGG to CGGGGGG at 76833863 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000154907 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071792] [ENSMUST00000229229] [ENSMUST00000230274]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000071792
SMART Domains Protein: ENSMUSP00000071698
Gene: ENSMUSG00000063236

DomainStartEndE-ValueType
low complexity region 2 17 N/A INTRINSIC
low complexity region 21 39 N/A INTRINSIC
Pfam:DUF4615 102 221 4e-41 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000229229
Predicted Effect probably benign
Transcript: ENSMUST00000230274
Predicted Effect noncoding transcript
Transcript: ENSMUST00000231058
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 93.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acad8 T C 9: 26,890,481 (GRCm39) I276V probably benign Het
Adgrg7 A T 16: 56,550,661 (GRCm39) Y684N probably damaging Het
Akap9 C T 5: 4,042,077 (GRCm39) T1370I possibly damaging Het
Akna C G 4: 63,292,627 (GRCm39) G1094A probably benign Het
Catsperb C A 12: 101,568,942 (GRCm39) Y871* probably null Het
Clcn4 T G 7: 7,293,427 (GRCm39) Y443S probably damaging Het
Clcn6 T A 4: 148,098,740 (GRCm39) T463S possibly damaging Het
Colec10 A G 15: 54,325,947 (GRCm39) D259G probably damaging Het
Ctnna2 A T 6: 77,613,827 (GRCm39) D254E possibly damaging Het
Depdc1a G A 3: 159,221,786 (GRCm39) probably null Het
Dlec1 T C 9: 118,966,408 (GRCm39) Y1126H probably damaging Het
Fezf2 A T 14: 12,343,986 (GRCm38) C302S probably damaging Het
Flnc T C 6: 29,451,634 (GRCm39) I1591T possibly damaging Het
Kidins220 A G 12: 25,107,143 (GRCm39) probably null Het
Mctp2 C A 7: 71,739,987 (GRCm39) C801F possibly damaging Het
Myo1e A G 9: 70,232,157 (GRCm39) I229V probably benign Het
Or5t17 A T 2: 86,833,266 (GRCm39) K318* probably null Het
Or8c17 G A 9: 38,180,757 (GRCm39) C308Y possibly damaging Het
Ppp3r1 T C 11: 17,144,786 (GRCm39) V133A probably damaging Het
Rif1 T A 2: 52,011,099 (GRCm39) Y2389N probably benign Het
Sidt1 A G 16: 44,102,249 (GRCm39) S304P possibly damaging Het
Siglecf T A 7: 43,004,995 (GRCm39) S408R possibly damaging Het
Stat5a T A 11: 100,765,752 (GRCm39) C279* probably null Het
Tas2r105 A G 6: 131,663,789 (GRCm39) V213A probably benign Het
Tasor2 T C 13: 3,634,554 (GRCm39) D751G probably damaging Het
Tektl1 T C 10: 78,588,727 (GRCm39) T28A probably benign Het
Top2b T G 14: 16,409,189 (GRCm38) I777M probably damaging Het
Ugcg C T 4: 59,207,798 (GRCm39) P46S probably benign Het
Usp46 A G 5: 74,193,136 (GRCm39) Y47H probably damaging Het
Vmn1r34 T A 6: 66,614,688 (GRCm39) M17L probably benign Het
Vmn2r120 T A 17: 57,843,718 (GRCm39) D42V possibly damaging Het
Wdr20 A G 12: 110,759,950 (GRCm39) T279A probably benign Het
Zfyve1 A G 12: 83,641,296 (GRCm39) V120A probably benign Het
Other mutations in 1110038F14Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01060:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL01063:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL01065:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL01066:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL01067:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL01069:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL01070:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL01128:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL01131:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL01132:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL01133:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL01134:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL01135:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL01154:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL01155:1110038F14Rik APN 15 76,834,475 (GRCm39) missense probably damaging 1.00
IGL02472:1110038F14Rik APN 15 76,834,578 (GRCm39) missense probably damaging 0.98
ANU05:1110038F14Rik UTSW 15 76,834,475 (GRCm39) missense probably damaging 1.00
R1845:1110038F14Rik UTSW 15 76,833,863 (GRCm39) small insertion probably benign
Predicted Primers PCR Primer
(F):5'- AACGGTGACAGTTCTGTGGTC -3'
(R):5'- CCTCTGTCCCCTAAGAGAGAATAC -3'

Sequencing Primer
(F):5'- TGGAATTCAGAGATCCGCCTG -3'
(R):5'- AGAATACTTTCTCCCCACTTACATC -3'
Posted On 2015-04-30