Incidental Mutation 'IGL02132:4921513I03Rik'
ID281027
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4921513I03Rik
Ensembl Gene ENSMUSG00000044544
Gene NameRIKEN cDNA 4921513I03 gene
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL02132
Quality Score
Status
Chromosome10
Chromosomal Location120765774-120778886 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) G to A at 120778730 bp
ZygosityHeterozygous
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

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

DomainStartEndE-ValueType
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