Incidental Mutation 'IGL02264:4921504E06Rik'
ID 286861
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4921504E06Rik
Ensembl Gene ENSMUSG00000026734
Gene Name RIKEN cDNA 4921504E06 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.049) question?
Stock # IGL02264
Quality Score
Status
Chromosome 2
Chromosomal Location 19467648-19558721 bp(-) (GRCm39)
Type of Mutation splice site (6 bp from exon)
DNA Base Change (assembly) A to G at 19547180 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000058720 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000062060]
AlphaFold Q8CET2
Predicted Effect probably null
Transcript: ENSMUST00000062060
SMART Domains Protein: ENSMUSP00000058720
Gene: ENSMUSG00000026734

DomainStartEndE-ValueType
low complexity region 2 10 N/A INTRINSIC
Pfam:DUF4709 36 145 1e-45 PFAM
coiled coil region 165 257 N/A INTRINSIC
low complexity region 366 386 N/A INTRINSIC
coiled coil region 417 463 N/A INTRINSIC
Pfam:DUF4724 477 559 3.9e-24 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000131199
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd17b T C 19: 21,655,796 (GRCm39) L26P probably damaging Het
Abtb1 A G 6: 88,813,517 (GRCm39) V407A probably benign Het
Adamts17 C A 7: 66,697,207 (GRCm39) probably null Het
Arhgap21 G T 2: 20,864,850 (GRCm39) probably null Het
Brwd1 T C 16: 95,820,656 (GRCm39) D1290G probably damaging Het
Btbd6 A G 12: 112,940,589 (GRCm39) T49A probably damaging Het
Carmil1 C T 13: 24,259,699 (GRCm39) V702I possibly damaging Het
Cts8 T A 13: 61,398,772 (GRCm39) I245F probably damaging Het
Dclre1a T A 19: 56,532,725 (GRCm39) N623I possibly damaging Het
Dnah9 A T 11: 65,971,314 (GRCm39) probably benign Het
Emc1 T C 4: 139,102,775 (GRCm39) F978S probably damaging Het
Fam185a G A 5: 21,685,392 (GRCm39) V363I possibly damaging Het
Iglc2 G T 16: 19,017,397 (GRCm39) S69R probably damaging Het
Ints5 T C 19: 8,873,076 (GRCm39) V345A probably benign Het
Kif21b T A 1: 136,087,495 (GRCm39) L937Q probably damaging Het
Lrba A G 3: 86,687,569 (GRCm39) R2825G probably damaging Het
Map1a A G 2: 121,137,794 (GRCm39) E2870G probably damaging Het
Or4c125 G T 2: 89,170,028 (GRCm39) T206K probably benign Het
Or4k41 A G 2: 111,280,207 (GRCm39) T241A probably benign Het
Or5aq7 C T 2: 86,937,785 (GRCm39) probably benign Het
Or8b48 C T 9: 38,492,809 (GRCm39) P79S probably damaging Het
Pcsk1 C A 13: 75,254,078 (GRCm39) T210K probably damaging Het
Phaf1 C T 8: 105,961,178 (GRCm39) A71V possibly damaging Het
Slco5a1 A G 1: 12,942,219 (GRCm39) V809A probably benign Het
Synm T C 7: 67,384,144 (GRCm39) T1173A probably damaging Het
Tbc1d9b T C 11: 50,040,584 (GRCm39) I367T probably damaging Het
Tmem169 T A 1: 72,340,114 (GRCm39) Y181* probably null Het
Trp73 G T 4: 154,148,885 (GRCm39) F289L probably null Het
Ttll9 A G 2: 152,842,055 (GRCm39) Y303C probably damaging Het
Ubr4 G T 4: 139,182,939 (GRCm39) E3577* probably null Het
Zbtb3 T G 19: 8,780,729 (GRCm39) V114G probably damaging Het
Other mutations in 4921504E06Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00776:4921504E06Rik APN 2 19,545,182 (GRCm39) missense probably benign 0.06
IGL01590:4921504E06Rik APN 2 19,482,590 (GRCm39) splice site probably benign
IGL02591:4921504E06Rik APN 2 19,485,249 (GRCm39) missense probably benign 0.26
H8786:4921504E06Rik UTSW 2 19,498,905 (GRCm39) missense probably benign 0.04
R0545:4921504E06Rik UTSW 2 19,547,187 (GRCm39) missense probably damaging 1.00
R0762:4921504E06Rik UTSW 2 19,482,667 (GRCm39) missense probably damaging 0.97
R1325:4921504E06Rik UTSW 2 19,499,938 (GRCm39) missense possibly damaging 0.71
R1456:4921504E06Rik UTSW 2 19,485,731 (GRCm39) critical splice donor site probably null
R2013:4921504E06Rik UTSW 2 19,545,124 (GRCm39) missense probably benign 0.01
R2089:4921504E06Rik UTSW 2 19,522,357 (GRCm39) missense probably damaging 1.00
R2091:4921504E06Rik UTSW 2 19,522,357 (GRCm39) missense probably damaging 1.00
R2091:4921504E06Rik UTSW 2 19,522,357 (GRCm39) missense probably damaging 1.00
R3922:4921504E06Rik UTSW 2 19,485,371 (GRCm39) missense probably benign 0.00
R3982:4921504E06Rik UTSW 2 19,547,180 (GRCm39) splice site probably null
R3983:4921504E06Rik UTSW 2 19,547,180 (GRCm39) splice site probably null
R4074:4921504E06Rik UTSW 2 19,485,401 (GRCm39) missense probably damaging 0.96
R4995:4921504E06Rik UTSW 2 19,498,995 (GRCm39) nonsense probably null
R5303:4921504E06Rik UTSW 2 19,521,110 (GRCm39) missense possibly damaging 0.92
R5308:4921504E06Rik UTSW 2 19,528,892 (GRCm39) missense probably damaging 1.00
R6227:4921504E06Rik UTSW 2 19,558,581 (GRCm39) splice site probably null
R6253:4921504E06Rik UTSW 2 19,528,929 (GRCm39) missense possibly damaging 0.53
R6268:4921504E06Rik UTSW 2 19,545,219 (GRCm39) missense probably benign 0.10
R6496:4921504E06Rik UTSW 2 19,545,217 (GRCm39) missense probably benign 0.17
R7196:4921504E06Rik UTSW 2 19,498,806 (GRCm39) missense probably benign 0.00
R7472:4921504E06Rik UTSW 2 19,545,219 (GRCm39) missense probably benign 0.10
R8146:4921504E06Rik UTSW 2 19,498,814 (GRCm39) missense possibly damaging 0.83
R8150:4921504E06Rik UTSW 2 19,538,635 (GRCm39) missense probably benign 0.10
R8534:4921504E06Rik UTSW 2 19,545,153 (GRCm39) missense probably damaging 1.00
R9067:4921504E06Rik UTSW 2 19,522,493 (GRCm39) missense probably damaging 0.98
Z1177:4921504E06Rik UTSW 2 19,485,343 (GRCm39) missense possibly damaging 0.83
Posted On 2015-04-16