Incidental Mutation 'IGL02132:4921513I03Rik'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4921513I03Rik
Ensembl Gene ENSMUSG00000044544
Gene NameRIKEN cDNA 4921513I03 gene
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL02132
Quality Score
Chromosomal Location120765774-120778886 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) G to A at 120778730 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000089781 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092143]
Predicted Effect noncoding transcript
Transcript: ENSMUST00000056994
SMART Domains Protein: ENSMUSP00000059458
Gene: ENSMUSG00000044544

low complexity region 62 74 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000092143
SMART Domains Protein: ENSMUSP00000089781
Gene: ENSMUSG00000051236

Pfam:SelR 41 161 1.9e-56 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000219219
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930432E11Rik C T 7: 29,563,279 noncoding transcript Het
Adcy10 T C 1: 165,572,543 V1507A probably damaging Het
Ap3b2 T A 7: 81,460,998 M1010L unknown Het
Bmp10 T C 6: 87,434,148 S308P probably benign Het
Cnih3 C A 1: 181,454,709 Y169* probably null Het
Cpsf4l A G 11: 113,699,859 S222P possibly damaging Het
Cyp2d10 G A 15: 82,404,607 probably benign Het
Dcstamp A T 15: 39,754,532 E112D probably damaging Het
Fras1 C T 5: 96,781,637 Q3967* probably null Het
Gcm1 C A 9: 78,064,839 P354H possibly damaging Het
Gen1 A G 12: 11,241,866 S706P probably benign Het
Glb1l3 G T 9: 26,825,170 T532N probably benign Het
Gm5069 T A 1: 180,327,307 probably benign Het
Gzmc A C 14: 56,233,965 F40V probably benign Het
Itgb2 G T 10: 77,550,061 C286F probably damaging Het
Jak3 A G 8: 71,678,480 Y48C probably damaging Het
Lrp2 G A 2: 69,537,616 S184L probably benign Het
Myo1f T A 17: 33,579,971 N203K probably benign Het
Nrxn2 G A 19: 6,472,276 G182R probably damaging Het
Olfr1000 A C 2: 85,608,320 L197V probably benign Het
Olfr1208 A G 2: 88,897,159 V146A probably benign Het
Olfr726 T C 14: 50,084,486 N65S probably damaging Het
Otog C T 7: 46,305,479 S2692L probably damaging Het
Pde9a C T 17: 31,453,470 T34I probably benign Het
Phip T C 9: 82,881,341 T1295A possibly damaging Het
Pik3cb A G 9: 99,071,377 V451A probably benign Het
Psd2 T G 18: 36,004,756 probably benign Het
Pycr2 T C 1: 180,906,197 I118T probably damaging Het
Rnf17 T G 14: 56,421,166 M104R probably benign Het
Rp1l1 T C 14: 64,028,810 V615A probably benign Het
Sel1l3 T A 5: 53,170,405 R511W possibly damaging Het
Sis T C 3: 72,947,471 N478D probably benign Het
Trps1 T A 15: 50,822,278 S584C probably damaging Het
Vmn2r124 T C 17: 18,064,229 probably benign Het
Vmn2r9 G A 5: 108,843,636 L620F probably damaging Het
Zc3h13 T C 14: 75,330,347 S1027P probably benign Het
Zfp644 A T 5: 106,635,894 I929K probably benign Het
Other mutations in 4921513I03Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0062:4921513I03Rik UTSW 10 120778606 unclassified probably benign
R0062:4921513I03Rik UTSW 10 120778606 unclassified probably benign
R1694:4921513I03Rik UTSW 10 120778628 unclassified probably benign
R5740:4921513I03Rik UTSW 10 120778508 unclassified probably benign
R5923:4921513I03Rik UTSW 10 120778770 unclassified probably benign
X0022:4921513I03Rik UTSW 10 120778800 unclassified probably benign
Posted On2015-04-16