Incidental Mutation 'IGL01366:2310002L09Rik'
ID 75956
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 2310002L09Rik
Ensembl Gene ENSMUSG00000028396
Gene Name RIKEN cDNA 2310002L09 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.053) question?
Stock # IGL01366
Quality Score
Status
Chromosome 4
Chromosomal Location 73857608-73869083 bp(-) (GRCm39)
Type of Mutation utr 5 prime
DNA Base Change (assembly) A to T at 73868937 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000092633 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030101] [ENSMUST00000095023]
AlphaFold Q9D7L5
Predicted Effect probably benign
Transcript: ENSMUST00000030101
SMART Domains Protein: ENSMUSP00000030101
Gene: ENSMUSG00000028396

DomainStartEndE-ValueType
transmembrane domain 173 195 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000095023
SMART Domains Protein: ENSMUSP00000092633
Gene: ENSMUSG00000028396

DomainStartEndE-ValueType
transmembrane domain 174 196 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts2 T C 11: 50,687,295 (GRCm39) Y1041H probably damaging Het
Adck5 A C 15: 76,479,816 (GRCm39) *568C probably null Het
AK157302 T A 13: 21,679,471 (GRCm39) probably benign Het
Bmpr2 G T 1: 59,852,836 (GRCm39) G56W probably damaging Het
Capn11 A C 17: 45,964,126 (GRCm39) I146S probably damaging Het
Ccdc162 A T 10: 41,456,302 (GRCm39) D1613E possibly damaging Het
Ccdc167 T C 17: 29,924,286 (GRCm39) E50G probably damaging Het
Col5a2 G T 1: 45,431,048 (GRCm39) P864Q possibly damaging Het
Col7a1 C T 9: 108,806,187 (GRCm39) probably benign Het
Crebbp T A 16: 3,944,370 (GRCm39) H556L probably damaging Het
Dcpp1 T A 17: 24,101,710 (GRCm39) I153N possibly damaging Het
Dgke C T 11: 88,946,212 (GRCm39) R196H probably benign Het
Efr3a T A 15: 65,722,999 (GRCm39) I459K probably benign Het
Espl1 T A 15: 102,228,271 (GRCm39) C1682S probably benign Het
Exosc3 C T 4: 45,317,747 (GRCm39) R185H probably damaging Het
Fgd6 T C 10: 93,879,338 (GRCm39) V64A possibly damaging Het
Fhip2b G A 14: 70,822,813 (GRCm39) R688C probably damaging Het
Gata3 A G 2: 9,882,276 (GRCm39) L42P probably damaging Het
Ggta1 C A 2: 35,292,462 (GRCm39) E282* probably null Het
Ghr T C 15: 3,349,669 (GRCm39) D503G probably damaging Het
Gls C T 1: 52,207,558 (GRCm39) G602D probably damaging Het
Gm2058 A G 7: 39,238,658 (GRCm39) noncoding transcript Het
Grb7 T C 11: 98,343,100 (GRCm39) probably benign Het
Ifngr1 A T 10: 19,485,348 (GRCm39) H449L probably damaging Het
Ighg2b T G 12: 113,270,656 (GRCm39) D158A possibly damaging Het
Nphs2 T C 1: 156,138,605 (GRCm39) V83A probably benign Het
Parp6 T A 9: 59,543,996 (GRCm39) M390K possibly damaging Het
Pask T C 1: 93,238,574 (GRCm39) K1304E probably benign Het
Scai A G 2: 38,996,973 (GRCm39) S274P probably benign Het
Sik2 A G 9: 50,818,763 (GRCm39) S404P probably damaging Het
Slc7a8 A T 14: 55,018,645 (GRCm39) I47N probably damaging Het
Tas2r113 A T 6: 132,870,760 (GRCm39) I263F probably benign Het
Tdrd1 T A 19: 56,843,734 (GRCm39) D737E probably benign Het
Trio T C 15: 27,732,954 (GRCm39) T2976A possibly damaging Het
Ttc28 T C 5: 111,233,037 (GRCm39) probably null Het
Vmn1r21 A G 6: 57,820,799 (GRCm39) I215T probably benign Het
Other mutations in 2310002L09Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00561:2310002L09Rik APN 4 73,860,956 (GRCm39) missense possibly damaging 0.66
IGL02596:2310002L09Rik APN 4 73,868,904 (GRCm39) missense possibly damaging 0.94
R0841:2310002L09Rik UTSW 4 73,860,986 (GRCm39) missense probably benign
R2919:2310002L09Rik UTSW 4 73,868,845 (GRCm39) missense probably damaging 1.00
R6056:2310002L09Rik UTSW 4 73,861,115 (GRCm39) missense probably benign 0.00
R6795:2310002L09Rik UTSW 4 73,869,065 (GRCm39) start gained probably benign
R6889:2310002L09Rik UTSW 4 73,861,290 (GRCm39) missense probably benign 0.19
R7709:2310002L09Rik UTSW 4 73,861,091 (GRCm39) missense possibly damaging 0.52
R7793:2310002L09Rik UTSW 4 73,861,172 (GRCm39) missense probably benign 0.05
R8517:2310002L09Rik UTSW 4 73,861,206 (GRCm39) missense probably damaging 1.00
R8671:2310002L09Rik UTSW 4 73,861,166 (GRCm39) missense probably damaging 1.00
R8867:2310002L09Rik UTSW 4 73,861,087 (GRCm39) missense probably damaging 1.00
R8938:2310002L09Rik UTSW 4 73,861,424 (GRCm39) missense probably damaging 1.00
R9618:2310002L09Rik UTSW 4 73,868,934 (GRCm39) start codon destroyed probably null 0.46
Posted On 2013-10-07