Incidental Mutation 'IGL00961:4921522P10Rik'
ID 306594
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4921522P10Rik
Ensembl Gene ENSMUSG00000040467
Gene Name RIKEN cDNA 4921522P10 gene
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL00961
Quality Score
Status
Chromosome 8
Chromosomal Location 8711801-8714728 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) C to A at 8713425 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000146939 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000001319] [ENSMUST00000048545] [ENSMUST00000207817]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000001319
SMART Domains Protein: ENSMUSP00000001319
Gene: ENSMUSG00000001300

DomainStartEndE-ValueType
Pfam:Ephrin 32 167 4.6e-53 PFAM
transmembrane domain 231 253 N/A INTRINSIC
low complexity region 267 277 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000048545
SMART Domains Protein: ENSMUSP00000039493
Gene: ENSMUSG00000040459

DomainStartEndE-ValueType
low complexity region 3 75 N/A INTRINSIC
low complexity region 95 113 N/A INTRINSIC
Pfam:ARGLU 117 267 8.2e-55 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000048606
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207070
Predicted Effect probably benign
Transcript: ENSMUST00000207817
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208252
Predicted Effect noncoding transcript
Transcript: ENSMUST00000209169
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arfgef3 T A 10: 18,486,985 (GRCm39) I1350F probably damaging Het
Arfip1 A G 3: 84,405,095 (GRCm39) V236A probably benign Het
Bicc1 A G 10: 70,796,987 (GRCm39) I124T probably damaging Het
Cacnb4 T A 2: 52,367,724 (GRCm39) I82F possibly damaging Het
Card11 A T 5: 140,885,464 (GRCm39) M365K probably damaging Het
Chd2 A G 7: 73,093,997 (GRCm39) S1560P probably damaging Het
Depdc1a T A 3: 159,229,451 (GRCm39) N594K possibly damaging Het
Dmbx1 A T 4: 115,777,203 (GRCm39) V215E probably benign Het
Farp2 A T 1: 93,549,035 (GRCm39) E1047V possibly damaging Het
Gm21759 A T 5: 8,229,731 (GRCm39) probably benign Het
Gpr182 C T 10: 127,586,559 (GRCm39) V131I probably benign Het
Irx1 T C 13: 72,108,076 (GRCm39) D202G probably damaging Het
Lrp6 T C 6: 134,484,609 (GRCm39) D338G probably damaging Het
Nrxn3 A T 12: 90,171,320 (GRCm39) I241L possibly damaging Het
Parp6 A G 9: 59,540,242 (GRCm39) Y265C probably damaging Het
Prex1 G T 2: 166,427,656 (GRCm39) Q999K probably damaging Het
Rad54b T C 4: 11,599,699 (GRCm39) I301T probably damaging Het
Rnf213 A T 11: 119,331,669 (GRCm39) I2294F possibly damaging Het
Ska3 T C 14: 58,059,581 (GRCm39) I81M possibly damaging Het
Smap1 T C 1: 23,887,355 (GRCm39) N308S probably benign Het
Stag3 A G 5: 138,296,611 (GRCm39) K490E probably benign Het
Stk11ip C T 1: 75,506,910 (GRCm39) R664C probably damaging Het
Tmem176b T A 6: 48,811,004 (GRCm39) I259F possibly damaging Het
Usp37 T C 1: 74,529,314 (GRCm39) T122A probably benign Het
Vmn2r7 T C 3: 64,623,234 (GRCm39) E453G possibly damaging Het
Posted On 2015-04-16