Incidental Mutation 'IGL03390:2810004N23Rik'
ID 421043
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 2810004N23Rik
Ensembl Gene ENSMUSG00000031984
Gene Name RIKEN cDNA 2810004N23 gene
Synonyms GtAyu21-55, Ayu21-55, Gt(Ayu21)55Imeg
Accession Numbers
Essential gene? Possibly essential (E-score: 0.717) question?
Stock # IGL03390
Quality Score
Status
Chromosome 8
Chromosomal Location 125566094-125589768 bp(-) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) A to G at 125566564 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000034465 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034465]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000034465
SMART Domains Protein: ENSMUSP00000034465
Gene: ENSMUSG00000031984

DomainStartEndE-ValueType
low complexity region 39 49 N/A INTRINSIC
Pfam:DUF4602 119 243 1e-32 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000161868
Predicted Effect noncoding transcript
Transcript: ENSMUST00000211971
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ccdc18 A G 5: 108,359,997 (GRCm39) Y1127C probably damaging Het
Cdnf T A 2: 3,524,863 (GRCm39) L134* probably null Het
Col11a1 A G 3: 113,883,902 (GRCm39) D257G unknown Het
Cthrc1 T A 15: 38,940,529 (GRCm39) I44N probably benign Het
Dlec1 T C 9: 118,952,288 (GRCm39) Y545H probably benign Het
Drosha T G 15: 12,885,069 (GRCm39) probably null Het
Ebf2 A G 14: 67,661,558 (GRCm39) N562S probably benign Het
Fem1b G A 9: 62,704,246 (GRCm39) A338V probably benign Het
Gga3 A T 11: 115,477,820 (GRCm39) probably null Het
Gm7247 A T 14: 51,760,914 (GRCm39) H161L probably benign Het
Gm7367 A G 7: 59,805,517 (GRCm39) noncoding transcript Het
Inpp5a T G 7: 139,105,664 (GRCm39) V213G probably benign Het
Kcns3 T C 12: 11,141,233 (GRCm39) T489A probably benign Het
Kifc3 G A 8: 95,835,241 (GRCm39) A211V probably damaging Het
Krt71 T C 15: 101,642,987 (GRCm39) D507G possibly damaging Het
Lama5 T C 2: 179,849,011 (GRCm39) Y224C probably damaging Het
Lrrc37a A G 11: 103,386,857 (GRCm39) L2421P unknown Het
Mtch2 C T 2: 90,689,894 (GRCm39) T205I probably benign Het
Or1o11 T C 17: 37,757,255 (GRCm39) V281A probably benign Het
Prkdc T A 16: 15,488,490 (GRCm39) C537* probably null Het
Prl2a1 T C 13: 27,985,699 (GRCm39) V5A probably benign Het
Prob1 T C 18: 35,787,192 (GRCm39) Y354C probably benign Het
Rimklb C T 6: 122,433,280 (GRCm39) S347N possibly damaging Het
Rnase2a T C 14: 51,492,945 (GRCm39) D140G probably damaging Het
Ryr2 G A 13: 11,787,302 (GRCm39) P1017S probably benign Het
Slc3a1 A G 17: 85,340,205 (GRCm39) D209G probably damaging Het
Sntn T A 14: 13,682,205 (GRCm38) probably benign Het
Tal2 G T 4: 53,785,994 (GRCm39) L58F probably damaging Het
Trim39 T C 17: 36,571,463 (GRCm39) K432E probably damaging Het
Trmt5 A T 12: 73,329,501 (GRCm39) M219K probably benign Het
Vmn2r3 T A 3: 64,182,767 (GRCm39) I311L possibly damaging Het
Wfdc17 A T 11: 83,595,611 (GRCm39) probably benign Het
Zbtb6 T G 2: 37,319,584 (GRCm39) I115L probably damaging Het
Zfp750 A T 11: 121,402,770 (GRCm39) C659* probably null Het
Other mutations in 2810004N23Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02977:2810004N23Rik APN 8 125,587,930 (GRCm39) missense probably benign 0.01
FR4342:2810004N23Rik UTSW 8 125,566,572 (GRCm39) frame shift probably null
R0519:2810004N23Rik UTSW 8 125,566,668 (GRCm39) missense possibly damaging 0.90
R1302:2810004N23Rik UTSW 8 125,566,607 (GRCm39) missense probably damaging 1.00
R1349:2810004N23Rik UTSW 8 125,587,992 (GRCm39) missense possibly damaging 0.93
R1640:2810004N23Rik UTSW 8 125,566,584 (GRCm39) missense probably damaging 1.00
R6614:2810004N23Rik UTSW 8 125,587,986 (GRCm39) splice site probably null
R7150:2810004N23Rik UTSW 8 125,589,653 (GRCm39) missense possibly damaging 0.81
R7806:2810004N23Rik UTSW 8 125,569,143 (GRCm39) missense probably benign
R9450:2810004N23Rik UTSW 8 125,567,215 (GRCm39) missense probably damaging 1.00
RF061:2810004N23Rik UTSW 8 125,566,570 (GRCm39) frame shift probably null
Posted On 2016-08-02