Incidental Mutation 'IGL02021:1110002L01Rik'
List |< first << previous [record 7 of 32981] next >> last >|
ID183972
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1110002L01Rik
Ensembl Gene ENSMUSG00000071456
Gene NameRIKEN cDNA 1110002L01 gene
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL02021
Quality Score
Status
Chromosome12
Chromosomal Location3403878-3427011 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) G to A at 3407890 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000151286 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020999] [ENSMUST00000219895] [ENSMUST00000220210]
Predicted Effect probably benign
Transcript: ENSMUST00000020999
SMART Domains Protein: ENSMUSP00000020999
Gene: ENSMUSG00000020668

DomainStartEndE-ValueType
KISc 8 375 5.43e-171 SMART
low complexity region 404 421 N/A INTRINSIC
low complexity region 435 443 N/A INTRINSIC
low complexity region 486 505 N/A INTRINSIC
Blast:KISc 508 579 3e-8 BLAST
low complexity region 580 602 N/A INTRINSIC
Blast:KISc 603 666 1e-16 BLAST
Predicted Effect noncoding transcript
Transcript: ENSMUST00000095903
SMART Domains Protein: ENSMUSP00000093591
Gene: ENSMUSG00000071456

DomainStartEndE-ValueType
transmembrane domain 51 68 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000168012
SMART Domains Protein: ENSMUSP00000130978
Gene: ENSMUSG00000071456

DomainStartEndE-ValueType
transmembrane domain 51 68 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000179637
SMART Domains Protein: ENSMUSP00000136462
Gene: ENSMUSG00000071456

DomainStartEndE-ValueType
transmembrane domain 51 68 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180149
SMART Domains Protein: ENSMUSP00000137142
Gene: ENSMUSG00000071456

DomainStartEndE-ValueType
transmembrane domain 51 68 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217891
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217965
Predicted Effect noncoding transcript
Transcript: ENSMUST00000218952
Predicted Effect probably benign
Transcript: ENSMUST00000219895
Predicted Effect probably benign
Transcript: ENSMUST00000220210
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam10 C T 9: 70,743,909 T72I possibly damaging Het
Adam26b T A 8: 43,519,872 M698L probably benign Het
Ankrd27 A T 7: 35,614,456 H404L probably damaging Het
Atp1a1 T C 3: 101,594,208 S60G probably benign Het
Bcat1 T C 6: 145,047,289 probably benign Het
Cd177 G A 7: 24,745,206 A650V probably benign Het
Cmya5 T C 13: 93,094,549 N1344D probably benign Het
Ctsd G T 7: 142,385,476 L71I probably damaging Het
Dctn2 T C 10: 127,275,057 probably null Het
Ddr1 G A 17: 35,683,480 A801V probably damaging Het
Duoxa1 A G 2: 122,304,646 F251S probably benign Het
Fcho1 A C 8: 71,721,275 S2A probably benign Het
Gm4861 T C 3: 137,552,110 probably null Het
Gm4922 C A 10: 18,784,477 G166W probably damaging Het
Hic2 A G 16: 17,258,753 E482G probably benign Het
Hoxa5 C T 6: 52,202,657 R246K probably damaging Het
Ipo11 A T 13: 106,857,237 F721I probably damaging Het
Lama1 A T 17: 67,821,626 S2993C probably damaging Het
Lonp2 T A 8: 86,708,971 S612T probably benign Het
Lpar5 T G 6: 125,081,992 Y225* probably null Het
Map4k3 A G 17: 80,609,826 Y574H probably damaging Het
Msantd4 A G 9: 4,385,163 E296G probably damaging Het
Ncs1 A G 2: 31,284,165 D109G probably damaging Het
Nnt T C 13: 119,336,247 probably benign Het
Nr1h5 T C 3: 102,947,742 probably benign Het
Olfr1288 A G 2: 111,479,480 D232G probably benign Het
Olfr704 A T 7: 106,865,489 K170* probably null Het
Plk4 A G 3: 40,810,708 D595G probably damaging Het
Rbm17 C A 2: 11,595,438 probably benign Het
Slc24a3 T A 2: 145,518,916 I193N probably damaging Het
St5 T C 7: 109,557,372 Y57C probably damaging Het
Stat5a G T 11: 100,883,889 V759F probably damaging Het
Tgfbi T A 13: 56,631,353 L463Q probably damaging Het
Tigar G T 6: 127,089,290 A95E probably damaging Het
Tph1 A G 7: 46,656,997 I180T possibly damaging Het
Usp22 T A 11: 61,154,499 Y517F probably damaging Het
Vmn2r105 A C 17: 20,227,895 I222M possibly damaging Het
Wapl A G 14: 34,722,336 I582V probably benign Het
Zfp217 A G 2: 170,115,149 V643A probably benign Het
Other mutations in 1110002L01Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02621:1110002L01Rik APN 12 3426688 unclassified probably benign
Posted On2014-05-07