Incidental Mutation 'IGL02951:2610028H24Rik'
ID 366016
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 2610028H24Rik
Ensembl Gene ENSMUSG00000009114
Gene Name RIKEN cDNA 2610028H24 gene
Synonyms ORF67
Accession Numbers
Essential gene? Probably non essential (E-score: 0.057) question?
Stock # IGL02951
Quality Score
Status
Chromosome 10
Chromosomal Location 76284915-76296944 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to A at 76290536 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000101055 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000049185] [ENSMUST00000092406] [ENSMUST00000105415]
AlphaFold G5E8K1
Predicted Effect probably benign
Transcript: ENSMUST00000049185
SMART Domains Protein: ENSMUSP00000045647
Gene: ENSMUSG00000033126

DomainStartEndE-ValueType
Pfam:UPF0054 8 148 7.6e-29 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000092406
SMART Domains Protein: ENSMUSP00000090061
Gene: ENSMUSG00000009114

DomainStartEndE-ValueType
low complexity region 13 27 N/A INTRINSIC
low complexity region 94 140 N/A INTRINSIC
Pfam:DUF4587 145 216 7.6e-33 PFAM
low complexity region 223 235 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000105415
SMART Domains Protein: ENSMUSP00000101055
Gene: ENSMUSG00000009114

DomainStartEndE-ValueType
low complexity region 73 119 N/A INTRINSIC
Pfam:DUF4587 124 195 4.4e-34 PFAM
low complexity region 202 214 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acot10 G A 15: 20,665,868 (GRCm39) T291I probably benign Het
Adam34l T G 8: 44,080,125 (GRCm39) H33P possibly damaging Het
Atp13a3 A G 16: 30,157,439 (GRCm39) probably null Het
Atp2a1 C T 7: 126,049,399 (GRCm39) V548M possibly damaging Het
Bsn G A 9: 107,992,812 (GRCm39) S980L probably damaging Het
Ccdc158 A G 5: 92,797,865 (GRCm39) M425T probably damaging Het
Cdh23 A G 10: 60,147,143 (GRCm39) L2733S probably damaging Het
Chd3 C T 11: 69,251,874 (GRCm39) probably null Het
Cimap1d T C 10: 79,475,811 (GRCm39) N251S probably benign Het
Dock2 T C 11: 34,260,448 (GRCm39) probably benign Het
Elfn2 T C 15: 78,556,082 (GRCm39) K822E probably damaging Het
Eps15l1 G A 8: 73,112,240 (GRCm39) S764L probably benign Het
Etl4 C A 2: 20,806,348 (GRCm39) probably benign Het
Faap24 C A 7: 35,092,376 (GRCm39) K180N probably damaging Het
Fhod1 G A 8: 106,057,862 (GRCm39) R888W probably damaging Het
Fus T C 7: 127,581,009 (GRCm39) probably benign Het
Gm3453 T C 14: 5,976,168 (GRCm38) E201G possibly damaging Het
Gnpat G T 8: 125,597,644 (GRCm39) D69Y probably benign Het
Gpaa1 T A 15: 76,217,019 (GRCm39) probably benign Het
Gsta1 A T 9: 78,149,819 (GRCm39) K211* probably null Het
Lct G T 1: 128,227,948 (GRCm39) Q1182K probably damaging Het
Mroh1 T C 15: 76,311,836 (GRCm39) L523P probably damaging Het
Mrpl46 A G 7: 78,425,200 (GRCm39) probably benign Het
Mst1r G T 9: 107,785,403 (GRCm39) V354F possibly damaging Het
Myo15b A G 11: 115,772,127 (GRCm39) D299G probably damaging Het
Myo6 G A 9: 80,171,516 (GRCm39) V506I possibly damaging Het
Nadk A C 4: 155,671,933 (GRCm39) K271Q probably benign Het
Nbas A G 12: 13,412,542 (GRCm39) R954G probably benign Het
Nbr1 T A 11: 101,462,805 (GRCm39) probably null Het
Nup88 T C 11: 70,835,698 (GRCm39) D587G possibly damaging Het
Oas1a A T 5: 121,043,727 (GRCm39) F135Y probably damaging Het
Obscn A G 11: 58,885,339 (GRCm39) probably benign Het
Or4k42 T G 2: 111,320,465 (GRCm39) I13L probably benign Het
Parp14 G A 16: 35,678,903 (GRCm39) T355I probably benign Het
Pdgfd G T 9: 6,288,494 (GRCm39) L43F probably damaging Het
Pou5f2 T C 13: 78,173,237 (GRCm39) S60P probably benign Het
Prp2 A G 6: 132,576,788 (GRCm39) N25S unknown Het
Ptprq A T 10: 107,503,321 (GRCm39) F779Y probably benign Het
Rims2 C T 15: 39,398,334 (GRCm39) R1078C probably damaging Het
Rnf38 G T 4: 44,129,619 (GRCm39) S425* probably null Het
Rps21 T A 2: 179,899,840 (GRCm39) I59N probably damaging Het
Scn5a A T 9: 119,324,751 (GRCm39) F1359Y probably damaging Het
Slc35b2 A G 17: 45,875,694 (GRCm39) E67G probably damaging Het
Slc37a2 A G 9: 37,166,611 (GRCm39) F15L probably benign Het
Snapc4 A C 2: 26,260,847 (GRCm39) N465K probably benign Het
Spata31f1a C T 4: 42,850,696 (GRCm39) E487K probably benign Het
Stxbp2 A T 8: 3,691,971 (GRCm39) I538F probably benign Het
Taco1 A G 11: 105,960,353 (GRCm39) N98S probably benign Het
Tcea3 T C 4: 135,985,299 (GRCm39) probably null Het
Thada T C 17: 84,751,456 (GRCm39) S507G probably benign Het
Tmem132b T A 5: 125,864,611 (GRCm39) C906S probably damaging Het
Trpm2 A T 10: 77,765,112 (GRCm39) I963N possibly damaging Het
Usp10 A G 8: 120,673,825 (GRCm39) T397A probably benign Het
Usp3 G A 9: 66,449,832 (GRCm39) R160* probably null Het
Utp15 T C 13: 98,394,460 (GRCm39) Y144C probably damaging Het
Xpc G A 6: 91,483,831 (GRCm39) R172W probably damaging Het
Other mutations in 2610028H24Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02400:2610028H24Rik APN 10 76,290,644 (GRCm39) missense possibly damaging 0.75
PIT4283001:2610028H24Rik UTSW 10 76,285,093 (GRCm39) start codon destroyed probably benign 0.01
R0013:2610028H24Rik UTSW 10 76,293,346 (GRCm39) missense probably benign 0.32
R0295:2610028H24Rik UTSW 10 76,290,642 (GRCm39) missense probably damaging 0.99
R2018:2610028H24Rik UTSW 10 76,293,899 (GRCm39) missense possibly damaging 0.85
R2019:2610028H24Rik UTSW 10 76,293,899 (GRCm39) missense possibly damaging 0.85
R2128:2610028H24Rik UTSW 10 76,293,349 (GRCm39) missense possibly damaging 0.93
R2129:2610028H24Rik UTSW 10 76,293,349 (GRCm39) missense possibly damaging 0.93
R4776:2610028H24Rik UTSW 10 76,293,346 (GRCm39) missense probably benign 0.16
R5638:2610028H24Rik UTSW 10 76,288,729 (GRCm39) missense probably benign 0.17
R5808:2610028H24Rik UTSW 10 76,286,482 (GRCm39) missense probably damaging 1.00
R5896:2610028H24Rik UTSW 10 76,288,664 (GRCm39) missense probably benign 0.01
R5990:2610028H24Rik UTSW 10 76,285,123 (GRCm39) missense probably benign 0.08
R6238:2610028H24Rik UTSW 10 76,285,096 (GRCm39) missense possibly damaging 0.86
R6505:2610028H24Rik UTSW 10 76,285,115 (GRCm39) missense probably benign 0.02
R7741:2610028H24Rik UTSW 10 76,290,551 (GRCm39) missense probably damaging 0.99
R9210:2610028H24Rik UTSW 10 76,287,165 (GRCm39) missense probably damaging 0.99
R9558:2610028H24Rik UTSW 10 76,290,576 (GRCm39) missense probably damaging 1.00
X0026:2610028H24Rik UTSW 10 76,293,925 (GRCm39) missense possibly damaging 0.91
Z1176:2610028H24Rik UTSW 10 76,288,697 (GRCm39) missense probably damaging 1.00
Posted On 2015-12-18