Incidental Mutation 'IGL01909:1700111E14Rik'
ID 179758
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700111E14Rik
Ensembl Gene ENSMUSG00000029837
Gene Name RIKEN cDNA 1700111E14 gene
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL01909
Quality Score
Status
Chromosome 6
Chromosomal Location 36913983-36962719 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) A to T at 36914152 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000138457 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042075] [ENSMUST00000090314] [ENSMUST00000101532] [ENSMUST00000138286] [ENSMUST00000150300]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000031863
SMART Domains Protein: ENSMUSP00000031863
Gene: ENSMUSG00000029837

DomainStartEndE-ValueType
SCOP:d1dj8a_ 101 140 4e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000042075
SMART Domains Protein: ENSMUSP00000047858
Gene: ENSMUSG00000038665

DomainStartEndE-ValueType
C1 22 76 3.67e-1 SMART
C1 95 153 5.92e-4 SMART
DAGKc 220 344 6.73e-58 SMART
DAGKa 370 527 2.29e-92 SMART
ANK 792 822 5.53e-3 SMART
ANK 828 857 2.07e-2 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000090314
SMART Domains Protein: ENSMUSP00000087788
Gene: ENSMUSG00000038665

DomainStartEndE-ValueType
low complexity region 10 34 N/A INTRINSIC
low complexity region 36 50 N/A INTRINSIC
low complexity region 54 116 N/A INTRINSIC
C1 173 227 3.67e-1 SMART
C1 246 304 5.92e-4 SMART
DAGKc 371 495 6.73e-58 SMART
DAGKa 521 678 2.29e-92 SMART
ANK 943 973 5.53e-3 SMART
ANK 979 1008 2.07e-2 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000101532
SMART Domains Protein: ENSMUSP00000099071
Gene: ENSMUSG00000038665

DomainStartEndE-ValueType
low complexity region 10 34 N/A INTRINSIC
low complexity region 36 50 N/A INTRINSIC
low complexity region 54 116 N/A INTRINSIC
C1 173 227 3.67e-1 SMART
C1 246 304 5.92e-4 SMART
DAGKc 371 495 6.73e-58 SMART
DAGKa 521 678 2.29e-92 SMART
ANK 964 994 5.53e-3 SMART
ANK 1000 1029 2.07e-2 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000138286
SMART Domains Protein: ENSMUSP00000138628
Gene: ENSMUSG00000038665

DomainStartEndE-ValueType
low complexity region 10 34 N/A INTRINSIC
low complexity region 36 50 N/A INTRINSIC
low complexity region 54 116 N/A INTRINSIC
C1 173 227 1.8e-3 SMART
C1 246 304 2.9e-6 SMART
DAGKc 371 495 3.2e-60 SMART
DAGKa 521 678 1.1e-94 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000143046
Predicted Effect probably benign
Transcript: ENSMUST00000150300
SMART Domains Protein: ENSMUSP00000138457
Gene: ENSMUSG00000038665

DomainStartEndE-ValueType
low complexity region 10 34 N/A INTRINSIC
low complexity region 36 50 N/A INTRINSIC
low complexity region 54 116 N/A INTRINSIC
C1 173 227 3.67e-1 SMART
C1 246 304 5.92e-4 SMART
DAGKc 371 495 6.73e-58 SMART
DAGKa 521 591 1.43e-6 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actn2 A T 13: 12,324,479 (GRCm39) probably null Het
Apom C T 17: 35,350,208 (GRCm39) A78T probably benign Het
Bambi A G 18: 3,508,229 (GRCm39) Y7C possibly damaging Het
Cdc42bpb T C 12: 111,289,576 (GRCm39) M418V probably benign Het
Clptm1 T C 7: 19,389,701 (GRCm39) N43D probably benign Het
Cspp1 T C 1: 10,136,886 (GRCm39) V241A probably benign Het
Ctnna3 T A 10: 63,339,910 (GRCm39) I32N probably benign Het
Elp2 A G 18: 24,752,576 (GRCm39) probably benign Het
Frmd4a A G 2: 4,608,844 (GRCm39) D893G probably benign Het
Gm10718 A T 9: 3,025,118 (GRCm39) Y194F probably benign Het
Gm21738 G A 14: 19,416,979 (GRCm38) S144L probably benign Het
Gm5862 A C 5: 26,227,769 (GRCm39) W41G probably benign Het
H2-M10.1 C A 17: 36,635,971 (GRCm39) G154* probably null Het
Igdcc3 C T 9: 65,051,819 (GRCm39) R141W probably damaging Het
Igkv14-130 A G 6: 67,768,323 (GRCm39) K60E possibly damaging Het
Kcnmb2 A G 3: 32,252,512 (GRCm39) probably benign Het
Lrp4 T C 2: 91,324,529 (GRCm39) L1288P possibly damaging Het
Mavs T A 2: 131,087,441 (GRCm39) M313K probably benign Het
Mia2 A G 12: 59,154,731 (GRCm39) E148G possibly damaging Het
Or6c76b A T 10: 129,692,950 (GRCm39) T188S probably damaging Het
Or8b12b T A 9: 37,684,159 (GRCm39) I68K possibly damaging Het
Or8d1 T A 9: 38,767,013 (GRCm39) Y218* probably null Het
Plekha3 C T 2: 76,517,047 (GRCm39) T133M probably damaging Het
Plxna1 A T 6: 89,309,066 (GRCm39) probably null Het
Septin2 A G 1: 93,426,823 (GRCm39) N144S probably damaging Het
Slc9a4 T C 1: 40,651,451 (GRCm39) probably benign Het
Slco1b2 T A 6: 141,594,312 (GRCm39) I59K probably damaging Het
Sp140l2 A G 1: 85,231,907 (GRCm39) probably benign Het
Tnrc6b A G 15: 80,786,184 (GRCm39) S1243G possibly damaging Het
Unc13a T A 8: 72,091,854 (GRCm39) probably benign Het
Vmn2r105 T C 17: 20,444,918 (GRCm39) R525G probably damaging Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Vmn2r37 T A 7: 9,219,032 (GRCm39) K451* probably null Het
Vmn2r71 C T 7: 85,270,001 (GRCm39) T504I probably benign Het
Zfp668 A T 7: 127,465,994 (GRCm39) C397S probably damaging Het
Posted On 2014-05-07