Incidental Mutation 'IGL02170:Fam98a'
ID 282902
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fam98a
Ensembl Gene ENSMUSG00000002017
Gene Name family with sequence similarity 98, member A
Synonyms 2810405J04Rik
Accession Numbers
Essential gene? Possibly essential (E-score: 0.642) question?
Stock # IGL02170
Quality Score
Status
Chromosome 17
Chromosomal Location 75844081-75858941 bp(-) (GRCm39)
Type of Mutation critical splice acceptor site
DNA Base Change (assembly) C to T at 75847187 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000108126 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000112507] [ENSMUST00000112507]
AlphaFold Q3TJZ6
Predicted Effect probably null
Transcript: ENSMUST00000112507
SMART Domains Protein: ENSMUSP00000108126
Gene: ENSMUSG00000002017

DomainStartEndE-ValueType
Pfam:DUF2465 11 328 1.1e-137 PFAM
low complexity region 334 396 N/A INTRINSIC
low complexity region 401 441 N/A INTRINSIC
low complexity region 448 481 N/A INTRINSIC
low complexity region 485 501 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000112507
SMART Domains Protein: ENSMUSP00000108126
Gene: ENSMUSG00000002017

DomainStartEndE-ValueType
Pfam:DUF2465 11 328 1.1e-137 PFAM
low complexity region 334 396 N/A INTRINSIC
low complexity region 401 441 N/A INTRINSIC
low complexity region 448 481 N/A INTRINSIC
low complexity region 485 501 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000140729
Predicted Effect noncoding transcript
Transcript: ENSMUST00000141969
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2610318N02Rik G A 16: 16,936,196 (GRCm39) P176L probably damaging Het
4932414N04Rik A G 2: 68,561,467 (GRCm39) M265V probably benign Het
A2ml1 T C 6: 128,524,173 (GRCm39) E1153G possibly damaging Het
Adam22 T C 5: 8,184,845 (GRCm39) T452A probably benign Het
Ambra1 A G 2: 91,597,432 (GRCm39) T56A possibly damaging Het
Atp1a4 A G 1: 172,062,103 (GRCm39) V674A possibly damaging Het
Ccnb1 A T 13: 100,919,994 (GRCm39) Y172* probably null Het
Chrdl2 A T 7: 99,683,821 (GRCm39) T416S possibly damaging Het
Col6a5 A G 9: 105,805,621 (GRCm39) L1095P unknown Het
Dhx16 T C 17: 36,200,361 (GRCm39) C901R probably damaging Het
Dip2c A G 13: 9,656,371 (GRCm39) T732A probably benign Het
Dnah12 A C 14: 26,495,069 (GRCm39) I1376L probably damaging Het
Dock2 A T 11: 34,217,949 (GRCm39) L1207Q probably damaging Het
Eif2ak1 A T 5: 143,816,278 (GRCm39) H192L probably benign Het
Evi5 T A 5: 107,969,750 (GRCm39) T54S probably benign Het
Fam151a T C 4: 106,592,795 (GRCm39) probably null Het
Frmd4a G A 2: 4,570,988 (GRCm39) R306K probably damaging Het
Fxyd7 C A 7: 30,744,432 (GRCm39) V28L possibly damaging Het
Gabrb1 T A 5: 72,294,073 (GRCm39) I449K probably damaging Het
Gkn3 G T 6: 87,360,493 (GRCm39) D167E possibly damaging Het
Gm14496 A T 2: 181,638,144 (GRCm39) Y406F probably damaging Het
Gm8603 T A 17: 13,737,073 (GRCm39) noncoding transcript Het
Hecw1 T C 13: 14,438,743 (GRCm39) N880S possibly damaging Het
Hivep2 C A 10: 14,003,548 (GRCm39) Q49K possibly damaging Het
Hscb T A 5: 110,987,492 (GRCm39) S35C probably damaging Het
Hspa12a T G 19: 58,793,113 (GRCm39) K357N probably benign Het
Kcnu1 A T 8: 26,427,588 (GRCm39) I302F probably damaging Het
Krtap5-3 T A 7: 141,756,215 (GRCm39) C351S unknown Het
Mvd A G 8: 123,164,747 (GRCm39) V142A probably benign Het
Myo1f A T 17: 33,797,246 (GRCm39) I143L probably benign Het
Ncoa7 T A 10: 30,565,849 (GRCm39) E599D possibly damaging Het
Nfasc A T 1: 132,538,104 (GRCm39) C495* probably null Het
Nfx1 G A 4: 41,018,019 (GRCm39) G920E probably damaging Het
Nlrp4g T G 9: 124,348,980 (GRCm38) noncoding transcript Het
Nup85 T A 11: 115,468,757 (GRCm39) V200E probably damaging Het
Or2z2 T A 11: 58,345,906 (GRCm39) I290F probably damaging Het
Or5an1c T C 19: 12,218,120 (GRCm39) M302V probably benign Het
Pask T C 1: 93,238,606 (GRCm39) Q1293R possibly damaging Het
Ppfia2 T A 10: 106,636,646 (GRCm39) S232T probably benign Het
Prr12 G A 7: 44,695,612 (GRCm39) R1285W unknown Het
Rimoc1 C T 15: 4,015,848 (GRCm39) V239I probably benign Het
Rxylt1 A T 10: 121,930,548 (GRCm39) D126E probably damaging Het
Slc1a1 T A 19: 28,880,153 (GRCm39) F278I possibly damaging Het
Sos1 G T 17: 80,705,719 (GRCm39) T1284N probably damaging Het
Sp2 T A 11: 96,847,036 (GRCm39) Q475L probably damaging Het
Spmip2 C A 3: 79,356,741 (GRCm39) probably benign Het
Spmip2 C A 3: 79,356,742 (GRCm39) probably benign Het
Sspo A T 6: 48,444,917 (GRCm39) T2134S possibly damaging Het
Tbx1 C A 16: 18,401,552 (GRCm39) A300S probably benign Het
Uap1 A C 1: 169,994,281 (GRCm39) V65G probably benign Het
Ubr2 G A 17: 47,278,123 (GRCm39) T738I probably benign Het
Uvrag A T 7: 98,758,297 (GRCm39) Y81* probably null Het
Vmn2r116 T G 17: 23,603,907 (GRCm39) I44S probably benign Het
Xkr8 A T 4: 132,455,688 (GRCm39) Y228* probably null Het
Zbtb20 A G 16: 43,430,025 (GRCm39) I106V possibly damaging Het
Zc3h7a C T 16: 10,964,259 (GRCm39) S683N probably benign Het
Zfp146 A T 7: 29,861,905 (GRCm39) C46S possibly damaging Het
Zfp871 T C 17: 32,994,662 (GRCm39) E152G possibly damaging Het
Zfp90 T C 8: 107,146,156 (GRCm39) V57A probably damaging Het
Zhx3 A T 2: 160,621,718 (GRCm39) N816K probably damaging Het
Other mutations in Fam98a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00337:Fam98a APN 17 75,858,742 (GRCm39) missense probably damaging 1.00
IGL00548:Fam98a APN 17 75,845,813 (GRCm39) missense probably damaging 1.00
IGL02399:Fam98a APN 17 75,845,936 (GRCm39) splice site probably benign
IGL03062:Fam98a APN 17 75,847,100 (GRCm39) splice site probably benign
IGL03246:Fam98a APN 17 75,845,848 (GRCm39) missense probably damaging 0.99
R0584:Fam98a UTSW 17 75,851,772 (GRCm39) missense probably damaging 1.00
R0594:Fam98a UTSW 17 75,845,482 (GRCm39) nonsense probably null
R1121:Fam98a UTSW 17 75,845,529 (GRCm39) missense unknown
R1366:Fam98a UTSW 17 75,846,381 (GRCm39) splice site probably benign
R1387:Fam98a UTSW 17 75,845,264 (GRCm39) missense unknown
R1424:Fam98a UTSW 17 75,847,173 (GRCm39) missense probably damaging 1.00
R1533:Fam98a UTSW 17 75,848,276 (GRCm39) missense probably damaging 1.00
R1651:Fam98a UTSW 17 75,854,710 (GRCm39) missense probably benign 0.16
R2211:Fam98a UTSW 17 75,845,940 (GRCm39) critical splice donor site probably null
R4295:Fam98a UTSW 17 75,848,342 (GRCm39) missense probably damaging 1.00
R4350:Fam98a UTSW 17 75,848,220 (GRCm39) missense probably damaging 1.00
R4963:Fam98a UTSW 17 75,845,977 (GRCm39) missense probably damaging 0.99
R5320:Fam98a UTSW 17 75,845,810 (GRCm39) missense probably damaging 1.00
R5383:Fam98a UTSW 17 75,845,576 (GRCm39) missense unknown
R6031:Fam98a UTSW 17 75,846,427 (GRCm39) missense probably damaging 0.98
R6031:Fam98a UTSW 17 75,846,427 (GRCm39) missense probably damaging 0.98
R7058:Fam98a UTSW 17 75,845,384 (GRCm39) missense unknown
R7182:Fam98a UTSW 17 75,846,013 (GRCm39) nonsense probably null
R7505:Fam98a UTSW 17 75,845,233 (GRCm39) missense unknown
R7554:Fam98a UTSW 17 75,854,670 (GRCm39) nonsense probably null
R7566:Fam98a UTSW 17 75,854,657 (GRCm39) missense probably damaging 1.00
R8095:Fam98a UTSW 17 75,845,766 (GRCm39) missense probably damaging 1.00
R8467:Fam98a UTSW 17 75,851,830 (GRCm39) missense probably damaging 1.00
R8790:Fam98a UTSW 17 75,854,684 (GRCm39) missense possibly damaging 0.93
R8827:Fam98a UTSW 17 75,851,824 (GRCm39) missense possibly damaging 0.74
R9375:Fam98a UTSW 17 75,848,330 (GRCm39) missense possibly damaging 0.55
R9625:Fam98a UTSW 17 75,845,474 (GRCm39) missense unknown
Posted On 2015-04-16