Incidental Mutation 'IGL01751:1700018F24Rik'
ID 153141
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700018F24Rik
Ensembl Gene ENSMUSG00000029620
Gene Name RIKEN cDNA 1700018F24 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # IGL01751
Quality Score
Status
Chromosome 5
Chromosomal Location 144979800-144982491 bp(+) (GRCm39)
Type of Mutation splice site (3 bp from exon)
DNA Base Change (assembly) A to G at 144979981 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000031624 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031624] [ENSMUST00000151196]
AlphaFold B2RW27
Predicted Effect probably null
Transcript: ENSMUST00000031624
SMART Domains Protein: ENSMUSP00000031624
Gene: ENSMUSG00000029620

DomainStartEndE-ValueType
Pfam:RasGEF_N 62 153 2.9e-10 PFAM
low complexity region 166 186 N/A INTRINSIC
low complexity region 230 241 N/A INTRINSIC
low complexity region 260 286 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000151196
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abtb3 C A 10: 85,490,366 (GRCm39) Q1011K probably damaging Het
Aoc1l2 A T 6: 48,907,522 (GRCm39) H174L possibly damaging Het
Auts2 G T 5: 131,501,198 (GRCm39) Q72K probably damaging Het
Ccdc7b A T 8: 129,863,049 (GRCm39) probably benign Het
Frem3 A G 8: 81,342,372 (GRCm39) E1555G probably benign Het
Gm5263 T G 1: 146,296,302 (GRCm39) noncoding transcript Het
Gm5828 A G 1: 16,840,208 (GRCm39) noncoding transcript Het
Gm6605 T C 7: 38,147,630 (GRCm39) noncoding transcript Het
Gvin3 T A 7: 106,201,516 (GRCm39) N576I possibly damaging Het
Hps3 T C 3: 20,065,130 (GRCm39) D638G probably damaging Het
Igdcc4 A T 9: 65,039,014 (GRCm39) N887I probably damaging Het
Itpkc G A 7: 26,912,491 (GRCm39) probably benign Het
Mfge8 A G 7: 78,786,403 (GRCm39) probably null Het
Mrc2 G T 11: 105,216,560 (GRCm39) L116F probably benign Het
Necab1 T C 4: 14,978,171 (GRCm39) D226G probably damaging Het
Neurod2 T C 11: 98,218,201 (GRCm39) E321G possibly damaging Het
Obp2b G T 2: 25,627,760 (GRCm39) V59L possibly damaging Het
Olr1 T C 6: 129,465,811 (GRCm39) N65S possibly damaging Het
Or14c39 A T 7: 86,343,997 (GRCm39) Q111L probably benign Het
Or2n1 G T 17: 38,486,577 (GRCm39) V201L probably benign Het
Or5d43 A T 2: 88,104,977 (GRCm39) C139S possibly damaging Het
Or8b48 C T 9: 38,492,809 (GRCm39) P79S probably damaging Het
Rock1 A G 18: 10,079,113 (GRCm39) probably null Het
Scn3a T A 2: 65,291,596 (GRCm39) M1717L possibly damaging Het
Smg7 T C 1: 152,719,812 (GRCm39) D903G possibly damaging Het
Tlr1 A T 5: 65,083,290 (GRCm39) L429* probably null Het
Ttll9 A T 2: 152,825,025 (GRCm39) N68I probably damaging Het
Ttn A G 2: 76,567,943 (GRCm39) V25904A possibly damaging Het
Uaca G A 9: 60,777,139 (GRCm39) V507M probably damaging Het
Vmn1r195 G T 13: 22,463,421 (GRCm39) C297F probably benign Het
Zdhhc2 G A 8: 40,926,042 (GRCm39) A346T probably benign Het
Other mutations in 1700018F24Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01625:1700018F24Rik APN 5 144,979,957 (GRCm39) missense possibly damaging 0.83
IGL02928:1700018F24Rik APN 5 144,980,327 (GRCm39) missense probably damaging 1.00
IGL03324:1700018F24Rik APN 5 144,982,261 (GRCm39) missense probably benign 0.01
PIT4486001:1700018F24Rik UTSW 5 144,980,914 (GRCm39) missense probably damaging 1.00
R0359:1700018F24Rik UTSW 5 144,982,181 (GRCm39) nonsense probably null
R0554:1700018F24Rik UTSW 5 144,982,181 (GRCm39) nonsense probably null
R0724:1700018F24Rik UTSW 5 144,981,573 (GRCm39) missense probably benign 0.10
R1774:1700018F24Rik UTSW 5 144,982,351 (GRCm39) missense probably damaging 0.99
R2041:1700018F24Rik UTSW 5 144,982,211 (GRCm39) missense probably damaging 0.99
R4625:1700018F24Rik UTSW 5 144,981,693 (GRCm39) missense possibly damaging 0.95
R5043:1700018F24Rik UTSW 5 144,980,910 (GRCm39) nonsense probably null
R5610:1700018F24Rik UTSW 5 144,982,156 (GRCm39) missense possibly damaging 0.92
R5712:1700018F24Rik UTSW 5 144,981,563 (GRCm39) missense probably benign 0.32
R6163:1700018F24Rik UTSW 5 144,982,098 (GRCm39) nonsense probably null
R6799:1700018F24Rik UTSW 5 144,981,624 (GRCm39) missense probably damaging 1.00
R7174:1700018F24Rik UTSW 5 144,981,627 (GRCm39) missense probably benign 0.27
R8127:1700018F24Rik UTSW 5 144,980,249 (GRCm39) missense possibly damaging 0.93
R8688:1700018F24Rik UTSW 5 144,982,183 (GRCm39) missense probably damaging 0.98
R8975:1700018F24Rik UTSW 5 144,980,192 (GRCm39) missense probably damaging 0.97
R9289:1700018F24Rik UTSW 5 144,982,333 (GRCm39) missense probably benign 0.00
R9473:1700018F24Rik UTSW 5 144,980,912 (GRCm39) missense probably benign 0.01
Posted On 2014-02-04