Incidental Mutation 'IGL01745:1700125H20Rik'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700125H20Rik
Ensembl Gene ENSMUSG00000018479
Gene NameRIKEN cDNA 1700125H20 gene
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.078) question?
Stock #IGL01745
Quality Score
Chromosomal Location85170404-85181145 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 85172870 bp
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

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

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