Incidental Mutation 'IGL02702:Prelid3a'
ID 304185
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Prelid3a
Ensembl Gene ENSMUSG00000024530
Gene Name PRELI domain containing 3A
Synonyms A230074A19Rik, Slmo1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.202) question?
Stock # IGL02702
Quality Score
Status
Chromosome 18
Chromosomal Location 67597936-67612905 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 67606864 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glutamic Acid at position 85 (D85E)
Ref Sequence ENSEMBL: ENSMUSP00000025411 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025411]
AlphaFold Q8VE85
Predicted Effect probably damaging
Transcript: ENSMUST00000025411
AA Change: D85E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000025411
Gene: ENSMUSG00000024530
AA Change: D85E

DomainStartEndE-ValueType
Pfam:PRELI 15 170 1.7e-52 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abtb1 C T 6: 88,815,120 (GRCm39) V337I probably benign Het
Adam11 G A 11: 102,667,864 (GRCm39) V750I probably benign Het
Alms1 T C 6: 85,576,831 (GRCm39) V129A probably benign Het
Cacna1d T A 14: 29,845,490 (GRCm39) K560* probably null Het
Cntn1 A G 15: 92,189,482 (GRCm39) probably benign Het
Cpne2 T C 8: 95,296,651 (GRCm39) V530A probably benign Het
Fbxo21 T C 5: 118,138,575 (GRCm39) L507P probably damaging Het
Fndc4 T C 5: 31,451,079 (GRCm39) K204R probably damaging Het
Gnrhr G T 5: 86,330,128 (GRCm39) N297K possibly damaging Het
Grin2b A G 6: 135,716,130 (GRCm39) F729S probably damaging Het
Hdac3 C A 18: 38,074,147 (GRCm39) R359L probably benign Het
Met T C 6: 17,534,142 (GRCm39) S662P possibly damaging Het
Mphosph9 T A 5: 124,398,052 (GRCm39) E1081D probably damaging Het
Mycbp2 T G 14: 103,457,560 (GRCm39) T1546P probably benign Het
Nlrp9a T A 7: 26,264,381 (GRCm39) M767K possibly damaging Het
Olfm5 A G 7: 103,803,564 (GRCm39) Y300H probably damaging Het
Or8b47 T A 9: 38,435,856 (GRCm39) V276D probably damaging Het
Pcf11 A T 7: 92,310,826 (GRCm39) N178K possibly damaging Het
Polr3a T C 14: 24,520,945 (GRCm39) I571M probably benign Het
Ppef2 T A 5: 92,379,678 (GRCm39) R557W probably benign Het
Rb1cc1 A G 1: 6,310,247 (GRCm39) E215G probably damaging Het
Rbm12 C T 2: 155,937,480 (GRCm39) probably benign Het
Recql4 C T 15: 76,591,485 (GRCm39) G501R probably damaging Het
Sema3e T C 5: 14,283,740 (GRCm39) probably benign Het
Shisa6 A C 11: 66,110,788 (GRCm39) L318V probably damaging Het
Slu7 T C 11: 43,329,719 (GRCm39) probably benign Het
Spink12 T C 18: 44,237,836 (GRCm39) V38A probably benign Het
Syne2 A G 12: 76,144,698 (GRCm39) D1549G probably damaging Het
Tet1 A G 10: 62,715,531 (GRCm39) V88A possibly damaging Het
Tmem200a C T 10: 25,869,501 (GRCm39) G256D probably damaging Het
Ttn G T 2: 76,714,835 (GRCm39) probably benign Het
Ugt2b34 T C 5: 87,040,750 (GRCm39) I391V probably benign Het
Zfp292 A T 4: 34,809,415 (GRCm39) L1215I probably benign Het
Zfp410 C A 12: 84,372,550 (GRCm39) N125K probably damaging Het
Other mutations in Prelid3a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03059:Prelid3a APN 18 67,609,909 (GRCm39) nonsense probably null
R2294:Prelid3a UTSW 18 67,605,941 (GRCm39) missense probably damaging 1.00
R4112:Prelid3a UTSW 18 67,605,967 (GRCm39) missense probably damaging 1.00
R4113:Prelid3a UTSW 18 67,605,967 (GRCm39) missense probably damaging 1.00
R5553:Prelid3a UTSW 18 67,610,093 (GRCm39) missense probably damaging 1.00
R5951:Prelid3a UTSW 18 67,598,011 (GRCm39) missense probably benign
R8207:Prelid3a UTSW 18 67,606,018 (GRCm39) missense probably benign 0.00
R8445:Prelid3a UTSW 18 67,606,848 (GRCm39) missense probably damaging 1.00
R8698:Prelid3a UTSW 18 67,610,122 (GRCm39) missense probably damaging 0.99
Posted On 2015-04-16