Incidental Mutation 'IGL01375:1700024P04Rik'
ID78708
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700024P04Rik
Ensembl Gene ENSMUSG00000045022
Gene NameRIKEN cDNA 1700024P04 gene
SynonymsH2BL1
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #IGL01375
Quality Score
Status
Chromosome13
Chromosomal Location98984085-98984565 bp(-) (GRCm38)
Type of Mutationutr 3 prime
DNA Base Change (assembly) A to G at 98984142 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000053046 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000054425]
Predicted Effect probably benign
Transcript: ENSMUST00000054425
SMART Domains Protein: ENSMUSP00000053046
Gene: ENSMUSG00000045022

DomainStartEndE-ValueType
H2B 21 122 1.43e-22 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Anxa2 C T 9: 69,483,019 R68* probably null Het
Apc C T 18: 34,313,654 S1167L probably damaging Het
Aqp2 A G 15: 99,582,102 T149A possibly damaging Het
Asb8 T C 15: 98,141,309 E70G probably damaging Het
Carmil1 T C 13: 24,094,471 I172V possibly damaging Het
Cd38 A G 5: 43,903,597 M172V probably benign Het
Dyrk2 A G 10: 118,860,687 V222A probably damaging Het
Ephb6 T A 6: 41,615,911 probably benign Het
Fam208a A G 14: 27,440,163 R159G probably damaging Het
Fbxo15 T C 18: 84,958,279 S48P possibly damaging Het
Gsdma3 T C 11: 98,629,941 probably null Het
Htr1d A G 4: 136,443,173 T238A probably benign Het
Kcnh3 G A 15: 99,226,993 W108* probably null Het
Kdsr A T 1: 106,727,694 Y272N probably benign Het
Lrp2 A G 2: 69,478,566 probably benign Het
Nup210l G A 3: 90,159,893 V747M probably damaging Het
Olfr1200 A G 2: 88,767,466 V283A probably benign Het
Olfr1512 A G 14: 52,372,408 I215T probably damaging Het
Pfn3 T A 13: 55,414,828 R113S possibly damaging Het
Pik3r4 T C 9: 105,644,604 I123T possibly damaging Het
Plec A T 15: 76,176,440 I3121N probably damaging Het
Prepl C T 17: 85,071,991 G336D possibly damaging Het
Prpf8 C A 11: 75,494,295 A794D possibly damaging Het
Prps1l1 A G 12: 34,985,632 T249A possibly damaging Het
Rptor T A 11: 119,896,436 F1276I possibly damaging Het
Serpina3f G A 12: 104,220,476 V434I unknown Het
Slc25a12 T C 2: 71,308,050 probably benign Het
Slc4a4 T C 5: 89,179,734 C642R probably damaging Het
Slit2 C T 5: 48,281,714 probably benign Het
Tgfbr3 A G 5: 107,136,971 V604A probably benign Het
Tnfrsf1b T C 4: 145,225,416 Y126C probably damaging Het
Traf4 T C 11: 78,160,082 N416S probably benign Het
Trappc10 A G 10: 78,188,899 I1132T possibly damaging Het
Vps8 T A 16: 21,559,372 Y642* probably null Het
Wdr60 G T 12: 116,229,676 A552E possibly damaging Het
Other mutations in 1700024P04Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02148:1700024P04Rik APN 13 98984183 missense probably damaging 1.00
IGL02164:1700024P04Rik APN 13 98984207 missense probably damaging 0.97
R0727:1700024P04Rik UTSW 13 98984227 missense probably benign 0.38
R1257:1700024P04Rik UTSW 13 98984515 start codon destroyed probably null 1.00
R5340:1700024P04Rik UTSW 13 98984443 missense possibly damaging 0.95
R6298:1700024P04Rik UTSW 13 98984466 missense probably benign 0.00
R7695:1700024P04Rik UTSW 13 98984258 missense probably damaging 1.00
Posted On2013-11-05