Incidental Mutation 'IGL01745:1700125H20Rik'
ID152998
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700125H20Rik
Ensembl Gene ENSMUSG00000018479
Gene NameRIKEN cDNA 1700125H20 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.078) question?
Stock #IGL01745
Quality Score
Status
Chromosome11
Chromosomal Location85170404-85181145 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 85172870 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Alanine at position 30 (T30A)
Ref Sequence ENSEMBL: ENSMUSP00000018623 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000018623] [ENSMUST00000100681]
Predicted Effect probably benign
Transcript: ENSMUST00000018623
AA Change: T30A

PolyPhen 2 Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
SMART Domains Protein: ENSMUSP00000018623
Gene: ENSMUSG00000018479
AA Change: T30A

DomainStartEndE-ValueType
DUF4208 31 134 1.43e-35 SMART
low complexity region 211 230 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000100681
SMART Domains Protein: ENSMUSP00000098248
Gene: ENSMUSG00000018479

DomainStartEndE-ValueType
Blast:DUF4208 1 24 1e-7 BLAST
low complexity region 101 120 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 13 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ccdc153 T G 9: 44,243,111 S56R possibly damaging Het
D630045J12Rik T C 6: 38,191,720 K965E probably damaging Het
F2rl1 A G 13: 95,513,753 V207A probably benign Het
Matn4 A G 2: 164,400,743 V145A probably damaging Het
Mllt6 T G 11: 97,676,928 L757R probably damaging Het
Olfr1033 T A 2: 86,042,037 S241T possibly damaging Het
Olfr154 T C 2: 85,663,577 N286D possibly damaging Het
Olfr520 A G 7: 99,735,388 T82A probably damaging Het
Prrc2c A G 1: 162,724,728 S30P probably damaging Het
Setd2 T C 9: 110,594,711 V2278A probably damaging Het
Slco4a1 G A 2: 180,464,679 C218Y probably damaging Het
Vps35 A T 8: 85,273,463 probably benign Het
Zfp593 A G 4: 134,245,044 S82P probably damaging Het
Other mutations in 1700125H20Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01490:1700125H20Rik APN 11 85178312 missense probably damaging 0.97
R0178:1700125H20Rik UTSW 11 85178438 missense probably benign 0.09
R1614:1700125H20Rik UTSW 11 85172864 missense possibly damaging 0.46
R3161:1700125H20Rik UTSW 11 85173284 missense probably damaging 0.98
R5707:1700125H20Rik UTSW 11 85173312 missense probably benign 0.39
R5796:1700125H20Rik UTSW 11 85173275 missense probably null 0.77
R6033:1700125H20Rik UTSW 11 85178372 missense probably damaging 1.00
R6033:1700125H20Rik UTSW 11 85178372 missense probably damaging 1.00
X0066:1700125H20Rik UTSW 11 85178349 missense probably benign 0.05
Posted On2014-02-04