Incidental Mutation 'IGL01884:1190005I06Rik'
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Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1190005I06Rik
Ensembl Gene ENSMUSG00000043687
Gene NameRIKEN cDNA 1190005I06 gene
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.059) question?
Stock #IGL01884
Quality Score
Chromosomal Location120608602-120647632 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) G to A at 120609035 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000137785 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000123927] [ENSMUST00000127664] [ENSMUST00000144417] [ENSMUST00000180677] [ENSMUST00000181333]
Predicted Effect probably benign
Transcript: ENSMUST00000123927
SMART Domains Protein: ENSMUSP00000119467
Gene: ENSMUSG00000043687

low complexity region 15 32 N/A INTRINSIC
Pfam:DUF4597 48 110 4.2e-44 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000127664
SMART Domains Protein: ENSMUSP00000118564
Gene: ENSMUSG00000092329

Pfam:Glycos_transf_2 104 287 7.4e-31 PFAM
Pfam:Glyco_transf_7C 261 331 4.9e-8 PFAM
RICIN 406 531 9.28e-27 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000144417
SMART Domains Protein: ENSMUSP00000121882
Gene: ENSMUSG00000043687

low complexity region 15 26 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000180677
SMART Domains Protein: ENSMUSP00000137752
Gene: ENSMUSG00000043687

Pfam:DUF4597 13 75 1.3e-44 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000181333
SMART Domains Protein: ENSMUSP00000137785
Gene: ENSMUSG00000097919

Pfam:UPF0172 1 79 4.9e-29 PFAM
Pfam:DUF4597 93 155 2.5e-43 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 23 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Col11a1 G A 3: 114,066,542 G206R unknown Het
Cyp2e1 T C 7: 140,773,750 Y426H probably benign Het
Fcrl1 A G 3: 87,384,737 K68E probably damaging Het
Gabbr2 A G 4: 46,875,711 V137A probably damaging Het
Gm10718 A T 9: 3,025,118 Y194F probably benign Het
Gm21738 G A 14: 19,416,979 S144L probably benign Het
Hacd1 G A 2: 14,035,782 P221S probably damaging Het
Kndc1 C T 7: 139,914,194 T535I probably damaging Het
Lce1f G T 3: 92,719,301 C16* probably null Het
Lrba C T 3: 86,310,412 A543V possibly damaging Het
Lrp1b A T 2: 41,284,213 C676* probably null Het
Mocos A G 18: 24,683,216 K617E probably damaging Het
Muc5b A G 7: 141,868,083 probably benign Het
Mylk A T 16: 34,988,877 probably benign Het
Naip2 A G 13: 100,188,821 probably benign Het
Olfr809 A G 10: 129,776,828 K320E probably benign Het
Pcdhb5 C T 18: 37,321,334 P256S probably benign Het
Rbl2 A G 8: 91,096,836 E464G probably damaging Het
Rfc1 A T 5: 65,274,460 L769Q possibly damaging Het
Setd7 T C 3: 51,542,711 Y98C possibly damaging Het
Tbc1d8 A G 1: 39,376,445 Y920H probably damaging Het
Tcte1 T C 17: 45,539,809 probably null Het
Vmn2r-ps159 C T 4: 156,338,254 noncoding transcript Het
Other mutations in 1190005I06Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6466:1190005I06Rik UTSW 8 120608996 missense probably damaging 1.00
R7274:1190005I06Rik UTSW 8 120611266 missense possibly damaging 0.71
Posted On2014-05-07