Incidental Mutation 'R8018:AI429214'
ID617221
Institutional Source Beutler Lab
Gene Symbol AI429214
Ensembl Gene ENSMUSG00000074384
Gene Nameexpressed sequence AI429214
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.070) question?
Stock #R8018 (G1)
Quality Score225.009
Status Not validated
Chromosome8
Chromosomal Location36993604-36995533 bp(+) (GRCm38)
Type of Mutationstart gained
DNA Base Change (assembly) A to T at 36993666 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000096424 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098825]
Predicted Effect probably benign
Transcript: ENSMUST00000098825
SMART Domains Protein: ENSMUSP00000096424
Gene: ENSMUSG00000074384

DomainStartEndE-ValueType
low complexity region 72 86 N/A INTRINSIC
Pfam:DUF4606 175 277 3.7e-48 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930563M21Rik G A 9: 55,973,707 T146I unknown Het
Abca16 A G 7: 120,533,643 E1265G probably benign Het
Adar T C 3: 89,747,575 S924P probably damaging Het
Adgrv1 A T 13: 81,440,225 V4414E possibly damaging Het
Ankmy1 A T 1: 92,886,281 L392Q probably benign Het
Anxa3 A T 5: 96,820,429 I114F probably damaging Het
Ccdc158 T C 5: 92,623,401 D985G possibly damaging Het
Cndp2 C T 18: 84,668,602 V432I probably benign Het
Ctbp2 T C 7: 133,014,366 K280R probably benign Het
Dao AGG AG 5: 114,015,209 probably benign Het
Dynap T C 18: 70,242,022 T41A possibly damaging Het
Elfn2 A G 15: 78,673,768 L193P probably damaging Het
Fam129a A T 1: 151,717,255 K564* probably null Het
Fcrls A T 3: 87,259,626 L20* probably null Het
Flcn T C 11: 59,794,122 D501G probably damaging Het
Gm3147 T C 5: 94,613,980 N244S probably benign Het
Gmip A G 8: 69,815,493 E399G probably benign Het
Grm7 A G 6: 111,207,776 E356G probably benign Het
Hs3st2 A G 7: 121,500,416 probably null Het
Kcnh2 G A 5: 24,320,016 S1158L probably damaging Het
Lancl2 A G 6: 57,713,093 T104A probably damaging Het
Ldlrad4 G T 18: 68,235,669 A66S possibly damaging Het
Mthfd2l T A 5: 90,959,813 I178N probably damaging Het
Nipal3 C T 4: 135,447,348 R364H possibly damaging Het
Olfr124 A G 17: 37,805,147 M1V probably null Het
Oxa1l A G 14: 54,363,300 I77V not run Het
Phf10 T A 17: 14,954,116 Q233H possibly damaging Het
Pias2 T A 18: 77,128,958 N288K probably benign Het
Prm3 CTCTTCTTCTTCTTC CTCTTCTTCTTC 16: 10,790,701 probably benign Het
Ptprd T C 4: 76,085,520 T1010A probably damaging Het
Ralgapa2 T C 2: 146,340,391 D1676G probably damaging Het
Rapgefl1 T G 11: 98,840,340 probably null Het
Rrp7a C T 15: 83,116,924 E269K possibly damaging Het
Ryr3 A C 2: 112,678,432 M3399R probably damaging Het
Secisbp2l C A 2: 125,745,909 R762L probably damaging Het
Smad7 T G 18: 75,369,284 L110R possibly damaging Het
St6gal1 G A 16: 23,357,835 A393T probably benign Het
Tdrd9 T C 12: 112,032,746 V765A probably benign Het
Tdrd9 C T 12: 112,044,388 R1130W probably damaging Het
Tia1 C T 6: 86,425,052 P189S probably benign Het
Tubg1 G T 11: 101,124,028 A199S not run Het
Ubxn8 A G 8: 33,623,215 C204R probably damaging Het
Vmn1r76 A G 7: 11,930,883 S135P probably damaging Het
Vps18 T A 2: 119,294,011 L473H probably damaging Het
Zfp444 A G 7: 6,188,143 T108A probably benign Het
Other mutations in AI429214
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01962:AI429214 APN 8 36994229 missense probably damaging 0.98
IGL02508:AI429214 APN 8 36994086 missense probably benign
R0973:AI429214 UTSW 8 36994319 missense probably benign 0.29
R0973:AI429214 UTSW 8 36994319 missense probably benign 0.29
R0974:AI429214 UTSW 8 36994319 missense probably benign 0.29
R2007:AI429214 UTSW 8 36993769 missense probably benign 0.29
R2113:AI429214 UTSW 8 36994000 nonsense probably null
R2126:AI429214 UTSW 8 36994208 missense probably benign 0.00
R2254:AI429214 UTSW 8 36993766 missense possibly damaging 0.91
R3409:AI429214 UTSW 8 36993917 missense probably benign 0.00
R3411:AI429214 UTSW 8 36993917 missense probably benign 0.00
R3852:AI429214 UTSW 8 36994442 missense probably damaging 1.00
R4657:AI429214 UTSW 8 36994391 missense probably damaging 1.00
R5766:AI429214 UTSW 8 36994229 frame shift probably null
R5767:AI429214 UTSW 8 36994229 frame shift probably null
R6248:AI429214 UTSW 8 36994124 missense probably damaging 1.00
R6888:AI429214 UTSW 8 36993833 missense possibly damaging 0.85
Predicted Primers PCR Primer
(F):5'- TTACACACAGCAGCCTGAGG -3'
(R):5'- TGATGGAACCAGAACTCAGTACC -3'

Sequencing Primer
(F):5'- TTAAAAGCTGTTGAACGGGCTCC -3'
(R):5'- TCAGTACCTCATCTGCACAGG -3'
Posted On2020-01-23