Incidental Mutation 'IGL02182:1700017D01Rik'
ID283297
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700017D01Rik
Ensembl Gene ENSMUSG00000024729
Gene NameRIKEN cDNA 1700017D01 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.094) question?
Stock #IGL02182
Quality Score
Status
Chromosome19
Chromosomal Location11096816-11130876 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) A to T at 11097072 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000025635 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025635]
Predicted Effect probably benign
Transcript: ENSMUST00000025635
SMART Domains Protein: ENSMUSP00000025635
Gene: ENSMUSG00000024729

DomainStartEndE-ValueType
Pfam:CD20 18 118 2.4e-8 PFAM
transmembrane domain 130 152 N/A INTRINSIC
low complexity region 169 185 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000186376
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam34 T A 8: 43,651,753 N285I probably benign Het
Adprh T C 16: 38,447,476 H149R probably benign Het
Ahctf1 A G 1: 179,753,078 V1853A probably benign Het
Ank1 T C 8: 23,113,852 V905A possibly damaging Het
Atp10b T G 11: 43,248,947 L1234R probably damaging Het
Bco1 G A 8: 117,133,066 A503T probably damaging Het
Cpz T A 5: 35,517,722 Y61F probably damaging Het
Dnah8 T A 17: 30,794,763 M3826K possibly damaging Het
Dtd2 A G 12: 51,999,709 S116P probably benign Het
Efcab1 T A 16: 14,920,795 D163E probably damaging Het
Eml5 T C 12: 98,802,322 D1498G probably damaging Het
Fat4 T C 3: 38,890,546 V1196A probably damaging Het
Gm15557 T C 2: 155,941,817 D405G probably damaging Het
Lpp C T 16: 24,762,145 R204W probably damaging Het
Mfsd11 T A 11: 116,873,914 V388E possibly damaging Het
Olfr512 A G 7: 108,713,868 T160A probably benign Het
Olfr547 A G 7: 102,535,568 I274V probably benign Het
Pik3cg A T 12: 32,205,273 D238E possibly damaging Het
Plcb3 T C 19: 6,969,620 H9R probably benign Het
Ppp3cc A C 14: 70,225,024 V388G probably benign Het
Ranbp2 T A 10: 58,485,760 C2626* probably null Het
Resp18 T C 1: 75,273,971 T155A probably benign Het
Ror2 C T 13: 53,110,728 S764N probably damaging Het
Scarb2 C T 5: 92,454,054 S327N probably damaging Het
Secisbp2l T A 2: 125,747,577 I684F probably damaging Het
Slc39a6 T C 18: 24,601,290 D114G probably damaging Het
Smap1 T A 1: 23,859,099 E85D probably damaging Het
Tas2r121 T A 6: 132,700,170 I280F probably damaging Het
Uhrf2 T C 19: 30,039,209 V86A probably benign Het
Vip A T 10: 5,643,561 Y91F probably benign Het
Zfp318 C T 17: 46,396,810 R265* probably null Het
Zfp618 G A 4: 63,095,561 probably benign Het
Other mutations in 1700017D01Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02142:1700017D01Rik APN 19 11110331 nonsense probably null
IGL03156:1700017D01Rik APN 19 11105750 missense possibly damaging 0.80
R0189:1700017D01Rik UTSW 19 11096947 missense possibly damaging 0.46
R0218:1700017D01Rik UTSW 19 11116437 nonsense probably null
R0464:1700017D01Rik UTSW 19 11112437 missense probably damaging 1.00
R0617:1700017D01Rik UTSW 19 11112400 missense probably damaging 1.00
R1171:1700017D01Rik UTSW 19 11112377 missense probably damaging 0.97
R2341:1700017D01Rik UTSW 19 11105793 missense probably benign
R5099:1700017D01Rik UTSW 19 11112461 critical splice acceptor site probably null
R5330:1700017D01Rik UTSW 19 11091858 unclassified probably benign
R5331:1700017D01Rik UTSW 19 11091858 unclassified probably benign
R5341:1700017D01Rik UTSW 19 11110381 intron probably benign
R6109:1700017D01Rik UTSW 19 11101912 missense possibly damaging 0.66
R6177:1700017D01Rik UTSW 19 11105750 missense possibly damaging 0.53
R6970:1700017D01Rik UTSW 19 11112314 critical splice donor site probably null
R7038:1700017D01Rik UTSW 19 11110311 missense probably benign
X0019:1700017D01Rik UTSW 19 11105792 missense probably benign 0.00
Posted On2015-04-16