Incidental Mutation 'IGL02298:4922502D21Rik'
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ID290228
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4922502D21Rik
Ensembl Gene ENSMUSG00000047720
Gene NameRIKEN cDNA 4922502D21 gene
SynonymsLOC381816
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.026) question?
Stock #IGL02298
Quality Score
Status
Chromosome6
Chromosomal Location129322164-129331796 bp(-) (GRCm38)
Type of Mutationstart codon destroyed
DNA Base Change (assembly) T to A at 129331564 bp
ZygosityHeterozygous
Amino Acid Change Methionine to Leucine at position 1 (M1L)
Ref Sequence ENSEMBL: ENSMUSP00000062024 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000051283]
Predicted Effect probably benign
Transcript: ENSMUST00000051283
AA Change: M1L

PolyPhen 2 Score 0.090 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000062024
Gene: ENSMUSG00000047720
AA Change: M1L

DomainStartEndE-ValueType
low complexity region 31 44 N/A INTRINSIC
CLECT 71 183 1.32e-19 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000203159
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 15 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ahctf1 A G 1: 179,752,479 S2053P probably benign Het
Alkbh2 C T 5: 114,125,572 E125K probably benign Het
Cd226 A T 18: 89,207,051 D24V probably damaging Het
Dync1h1 G A 12: 110,640,888 E2638K probably damaging Het
Fbxw5 G A 2: 25,504,444 W143* probably null Het
Galk2 T C 2: 125,859,370 S5P probably benign Het
Gm8890 T G 5: 11,257,191 L12R probably damaging Het
Gtf2h2 A G 13: 100,481,039 V205A probably damaging Het
Helb C A 10: 120,101,526 Q604H probably damaging Het
Ifih1 A G 2: 62,610,439 probably null Het
Map7d1 T C 4: 126,233,921 E675G unknown Het
Olfr912 C T 9: 38,581,513 P79S probably damaging Het
Shc4 T C 2: 125,649,154 H488R probably damaging Het
Zfhx4 G A 3: 5,244,304 probably null Het
Zfp451 A T 1: 33,772,921 N904K probably damaging Het
Other mutations in 4922502D21Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02053:4922502D21Rik APN 6 129326762 missense probably benign 0.00
IGL03350:4922502D21Rik APN 6 129331023 missense probably benign 0.07
R0178:4922502D21Rik UTSW 6 129326823 missense probably benign 0.01
R0270:4922502D21Rik UTSW 6 129325608 nonsense probably null
R0414:4922502D21Rik UTSW 6 129326850 unclassified probably benign
R0648:4922502D21Rik UTSW 6 129330969 missense probably benign 0.03
R1065:4922502D21Rik UTSW 6 129323050 missense possibly damaging 0.83
R2075:4922502D21Rik UTSW 6 129326703 missense probably benign 0.01
R6163:4922502D21Rik UTSW 6 129326747 missense probably benign 0.00
X0026:4922502D21Rik UTSW 6 129326693 missense probably benign 0.03
Posted On2015-04-16