Incidental Mutation 'IGL02388:4930597O21Rik'
ID 291637
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4930597O21Rik
Ensembl Gene ENSMUSG00000053442
Gene Name RIKEN cDNA 4930597O21 gene
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL02388
Quality Score
Status
Chromosome 6
Chromosomal Location 66871636-66873505 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to T at 66873097 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000145234 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000043148] [ENSMUST00000114222] [ENSMUST00000114224] [ENSMUST00000114225] [ENSMUST00000114226] [ENSMUST00000114227] [ENSMUST00000204862] [ENSMUST00000204511] [ENSMUST00000114228]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000043148
SMART Domains Protein: ENSMUSP00000046557
Gene: ENSMUSG00000036402

DomainStartEndE-ValueType
G_gamma 7 72 1.12e-28 SMART
GGL 11 72 2.07e-31 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000065878
SMART Domains Protein: ENSMUSP00000087261
Gene: ENSMUSG00000053442

DomainStartEndE-ValueType
low complexity region 4 15 N/A INTRINSIC
low complexity region 18 58 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000114222
SMART Domains Protein: ENSMUSP00000109860
Gene: ENSMUSG00000036402

DomainStartEndE-ValueType
G_gamma 7 72 1.12e-28 SMART
GGL 11 72 2.07e-31 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000114224
SMART Domains Protein: ENSMUSP00000109862
Gene: ENSMUSG00000036402

DomainStartEndE-ValueType
G_gamma 7 72 1.12e-28 SMART
GGL 11 72 2.07e-31 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000114225
SMART Domains Protein: ENSMUSP00000109863
Gene: ENSMUSG00000036402

DomainStartEndE-ValueType
G_gamma 7 72 1.12e-28 SMART
GGL 11 72 2.07e-31 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000114226
SMART Domains Protein: ENSMUSP00000109864
Gene: ENSMUSG00000036402

DomainStartEndE-ValueType
G_gamma 7 72 1.12e-28 SMART
GGL 11 72 2.07e-31 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000114227
SMART Domains Protein: ENSMUSP00000109865
Gene: ENSMUSG00000036402

DomainStartEndE-ValueType
G_gamma 7 72 1.12e-28 SMART
GGL 11 72 2.07e-31 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000204862
SMART Domains Protein: ENSMUSP00000145234
Gene: ENSMUSG00000036402

DomainStartEndE-ValueType
G_gamma 7 65 5.8e-25 SMART
GGL 11 65 7.1e-26 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203383
Predicted Effect probably benign
Transcript: ENSMUST00000204511
SMART Domains Protein: ENSMUSP00000145346
Gene: ENSMUSG00000036402

DomainStartEndE-ValueType
G_gamma 7 83 8e-27 SMART
GGL 11 83 2.9e-27 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000114228
SMART Domains Protein: ENSMUSP00000109866
Gene: ENSMUSG00000036402

DomainStartEndE-ValueType
G_gamma 7 72 1.12e-28 SMART
GGL 11 72 2.07e-31 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8a A G 11: 109,969,641 (GRCm39) probably benign Het
Asphd1 A T 7: 126,545,884 (GRCm39) probably benign Het
Ccdc77 G A 6: 120,308,858 (GRCm39) A301V probably benign Het
Cep350 G T 1: 155,829,499 (GRCm39) T135K probably benign Het
Chrna7 A T 7: 62,757,439 (GRCm39) D153E probably damaging Het
Clec4b2 G T 6: 123,179,187 (GRCm39) probably null Het
Cyp2c67 T C 19: 39,631,799 (GRCm39) N133D probably benign Het
Dglucy T C 12: 100,823,257 (GRCm39) I484T probably damaging Het
Dtna G T 18: 23,730,571 (GRCm39) M319I probably benign Het
E2f5 T A 3: 14,653,340 (GRCm39) M152K probably benign Het
Emsy A T 7: 98,290,873 (GRCm39) M58K probably damaging Het
Epha1 A G 6: 42,341,950 (GRCm39) Y367H probably damaging Het
Etv1 A G 12: 38,831,798 (GRCm39) S32G possibly damaging Het
Fam114a1 A T 5: 65,166,323 (GRCm39) probably benign Het
Fbxo30 T A 10: 11,166,122 (GRCm39) N281K probably benign Het
Galnt12 G T 4: 47,117,941 (GRCm39) R412L probably damaging Het
Gm5786 T A 12: 59,128,382 (GRCm39) noncoding transcript Het
Gm9845 T C 3: 39,412,616 (GRCm39) noncoding transcript Het
Hecw2 A G 1: 53,964,858 (GRCm39) V656A probably benign Het
Hpse2 A T 19: 43,282,692 (GRCm39) V187D probably damaging Het
Itsn2 T A 12: 4,679,557 (GRCm39) M122K possibly damaging Het
Kcnj11 A G 7: 45,749,213 (GRCm39) S37P probably benign Het
Kif13b T C 14: 65,037,807 (GRCm39) I1491T probably damaging Het
Krt36 T A 11: 99,995,990 (GRCm39) K145* probably null Het
Loxhd1 A G 18: 77,456,833 (GRCm39) I499V probably benign Het
Map3k4 G T 17: 12,490,497 (GRCm39) N311K probably damaging Het
Mical2 C A 7: 111,934,620 (GRCm39) H880N probably benign Het
Myo1d A T 11: 80,528,823 (GRCm39) C666* probably null Het
Nlrx1 C T 9: 44,175,302 (GRCm39) R158H probably benign Het
Or10ag53 T A 2: 87,082,295 (GRCm39) Y5N probably benign Het
Or10q1 C A 19: 13,726,994 (GRCm39) H175N possibly damaging Het
Or13a17 A G 7: 140,271,024 (GRCm39) T69A probably benign Het
Or1e21 A T 11: 73,344,106 (GRCm39) L311I probably benign Het
Or4a78 T C 2: 89,497,316 (GRCm39) S305G probably benign Het
Pdgfrl A G 8: 41,430,094 (GRCm39) R154G probably benign Het
Pitpnb T C 5: 111,478,699 (GRCm39) F7S possibly damaging Het
Ppm1n G A 7: 19,013,097 (GRCm39) R285C probably damaging Het
Prdm11 A T 2: 92,805,957 (GRCm39) I331N possibly damaging Het
Ptprb C T 10: 116,203,426 (GRCm39) P2066L probably damaging Het
Ric8b T C 10: 84,828,135 (GRCm39) probably benign Het
Setx A G 2: 29,063,665 (GRCm39) I2320M probably damaging Het
Skil C A 3: 31,165,787 (GRCm39) S368* probably null Het
Slc1a5 G T 7: 16,519,644 (GRCm39) probably null Het
Trpm7 A C 2: 126,661,811 (GRCm39) V1079G possibly damaging Het
Tulp1 A G 17: 28,577,633 (GRCm39) F2L probably damaging Het
Ulbp3 A T 10: 3,075,050 (GRCm39) noncoding transcript Het
Zbtb17 A G 4: 141,189,224 (GRCm39) Y48C probably damaging Het
Zfp605 T A 5: 110,275,506 (GRCm39) I208N possibly damaging Het
Posted On 2015-04-16