Incidental Mutation 'IGL02177:Fam184b'
ID 283165
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fam184b
Ensembl Gene ENSMUSG00000015879
Gene Name family with sequence similarity 184, member B
Synonyms 9630031F12Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02177
Quality Score
Status
Chromosome 5
Chromosomal Location 45687047-45796843 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to T at 45690157 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 817 (Y817*)
Ref Sequence ENSEMBL: ENSMUSP00000016023 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000016023] [ENSMUST00000156481]
AlphaFold Q0KK56
Predicted Effect probably null
Transcript: ENSMUST00000016023
AA Change: Y817*
SMART Domains Protein: ENSMUSP00000016023
Gene: ENSMUSG00000015879
AA Change: Y817*

DomainStartEndE-ValueType
Pfam:FAM184 50 248 7.7e-28 PFAM
coiled coil region 284 337 N/A INTRINSIC
coiled coil region 387 495 N/A INTRINSIC
low complexity region 515 525 N/A INTRINSIC
coiled coil region 575 620 N/A INTRINSIC
coiled coil region 686 775 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000156481
SMART Domains Protein: ENSMUSP00000115882
Gene: ENSMUSG00000015804

DomainStartEndE-ValueType
low complexity region 11 26 N/A INTRINSIC
Pfam:Med28 72 136 4.5e-21 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000198680
Predicted Effect noncoding transcript
Transcript: ENSMUST00000199190
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele are viable and exhibit no overt phenotypic abnormalities. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Add3 T G 19: 53,205,323 (GRCm39) Y24* probably null Het
Catsperb A G 12: 101,507,721 (GRCm39) Y496C probably damaging Het
Ccdc183 C T 2: 25,502,095 (GRCm39) E260K probably benign Het
Ccdc81 A C 7: 89,524,988 (GRCm39) M531R possibly damaging Het
Cyp3a16 T A 5: 145,386,964 (GRCm39) N342I probably benign Het
Defb43 T C 14: 63,249,266 (GRCm39) V3A probably benign Het
Dpyd T A 3: 118,858,559 (GRCm39) I591N possibly damaging Het
Dpysl5 T G 5: 30,902,622 (GRCm39) V18G probably damaging Het
Erc2 A T 14: 27,620,580 (GRCm39) M69L probably benign Het
Fyb1 G T 15: 6,688,047 (GRCm39) probably null Het
Gpr33 G T 12: 52,070,863 (GRCm39) Q59K probably benign Het
Heatr3 T G 8: 88,883,351 (GRCm39) F278V probably benign Het
Hectd1 A T 12: 51,819,103 (GRCm39) D1292E probably damaging Het
Herc1 A T 9: 66,341,793 (GRCm39) M1861L probably benign Het
Hspg2 T A 4: 137,242,627 (GRCm39) L614Q probably damaging Het
Itpr3 A G 17: 27,318,588 (GRCm39) R915G possibly damaging Het
Jhy T C 9: 40,809,553 (GRCm39) D646G probably damaging Het
Lrig1 T A 6: 94,640,977 (GRCm39) N76I possibly damaging Het
Macc1 A G 12: 119,429,292 (GRCm39) D814G probably damaging Het
Mapk8ip1 T C 2: 92,217,092 (GRCm39) D401G probably damaging Het
Nedd4 T A 9: 72,654,439 (GRCm39) S865T probably damaging Het
Or9s27 G A 1: 92,516,479 (GRCm39) M142I possibly damaging Het
Pi4ka A T 16: 17,136,146 (GRCm39) D937E probably benign Het
Prkcd T A 14: 30,327,844 (GRCm39) I81F probably damaging Het
Ranbp9 A T 13: 43,573,193 (GRCm39) C280S probably damaging Het
Ror2 C T 13: 53,264,764 (GRCm39) S764N probably damaging Het
Scn1b T C 7: 30,816,655 (GRCm39) *219W probably null Het
Slain2 T C 5: 73,072,008 (GRCm39) V14A probably benign Het
Soat1 A T 1: 156,268,073 (GRCm39) probably benign Het
Tbc1d4 T A 14: 101,692,375 (GRCm39) M1030L possibly damaging Het
Tenm4 T C 7: 96,544,869 (GRCm39) V2295A probably benign Het
Tmem135 A G 7: 88,987,661 (GRCm39) Y46H probably damaging Het
Tnfsf18 A T 1: 161,331,354 (GRCm39) D168V probably damaging Het
Trdn T C 10: 33,015,169 (GRCm39) V41A probably damaging Het
Trpc5 G T X: 143,264,234 (GRCm39) L208I probably damaging Het
Vmn1r50 T C 6: 90,085,139 (GRCm39) Y295H probably benign Het
Vmn2r18 T G 5: 151,510,274 (GRCm39) H33P possibly damaging Het
Vmn2r84 T C 10: 130,227,881 (GRCm39) I118M probably benign Het
Other mutations in Fam184b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00163:Fam184b APN 5 45,697,091 (GRCm39) missense probably benign 0.17
IGL00781:Fam184b APN 5 45,712,534 (GRCm39) splice site probably null
IGL01636:Fam184b APN 5 45,741,637 (GRCm39) missense probably benign 0.00
IGL02008:Fam184b APN 5 45,690,165 (GRCm39) missense possibly damaging 0.75
IGL02123:Fam184b APN 5 45,796,493 (GRCm39) missense possibly damaging 0.92
IGL02192:Fam184b APN 5 45,695,062 (GRCm39) missense probably benign 0.00
IGL02478:Fam184b APN 5 45,695,039 (GRCm39) missense probably damaging 0.99
IGL03368:Fam184b APN 5 45,689,166 (GRCm39) missense possibly damaging 0.91
R0003:Fam184b UTSW 5 45,712,536 (GRCm39) splice site probably benign
R0129:Fam184b UTSW 5 45,690,120 (GRCm39) missense probably damaging 1.00
R0420:Fam184b UTSW 5 45,741,854 (GRCm39) missense probably damaging 1.00
R0647:Fam184b UTSW 5 45,741,932 (GRCm39) missense probably benign
R1215:Fam184b UTSW 5 45,741,520 (GRCm39) missense probably damaging 1.00
R1374:Fam184b UTSW 5 45,712,485 (GRCm39) missense probably benign
R1466:Fam184b UTSW 5 45,737,851 (GRCm39) splice site probably benign
R1773:Fam184b UTSW 5 45,741,676 (GRCm39) missense possibly damaging 0.60
R1865:Fam184b UTSW 5 45,689,231 (GRCm39) missense possibly damaging 0.91
R3615:Fam184b UTSW 5 45,740,157 (GRCm39) missense possibly damaging 0.56
R3616:Fam184b UTSW 5 45,740,157 (GRCm39) missense possibly damaging 0.56
R4180:Fam184b UTSW 5 45,697,106 (GRCm39) missense probably benign 0.00
R4375:Fam184b UTSW 5 45,699,685 (GRCm39) missense probably benign
R4674:Fam184b UTSW 5 45,740,230 (GRCm39) nonsense probably null
R4942:Fam184b UTSW 5 45,730,649 (GRCm39) missense probably damaging 0.97
R5021:Fam184b UTSW 5 45,730,604 (GRCm39) missense probably benign 0.01
R5450:Fam184b UTSW 5 45,697,143 (GRCm39) missense probably benign
R5731:Fam184b UTSW 5 45,710,471 (GRCm39) missense probably benign 0.00
R5858:Fam184b UTSW 5 45,796,461 (GRCm39) missense probably damaging 0.99
R6032:Fam184b UTSW 5 45,740,238 (GRCm39) missense probably benign 0.01
R6032:Fam184b UTSW 5 45,740,238 (GRCm39) missense probably benign 0.01
R6060:Fam184b UTSW 5 45,710,489 (GRCm39) missense probably damaging 0.99
R6088:Fam184b UTSW 5 45,741,354 (GRCm39) missense probably damaging 1.00
R6416:Fam184b UTSW 5 45,694,995 (GRCm39) missense probably benign 0.04
R6932:Fam184b UTSW 5 45,690,243 (GRCm39) splice site probably null
R6956:Fam184b UTSW 5 45,688,099 (GRCm39) missense probably damaging 0.97
R6965:Fam184b UTSW 5 45,712,477 (GRCm39) missense probably benign
R7229:Fam184b UTSW 5 45,741,517 (GRCm39) missense probably damaging 1.00
R7303:Fam184b UTSW 5 45,699,568 (GRCm39) critical splice donor site probably null
R7429:Fam184b UTSW 5 45,698,230 (GRCm39) missense probably benign
R7522:Fam184b UTSW 5 45,688,093 (GRCm39) missense probably damaging 1.00
R7541:Fam184b UTSW 5 45,699,574 (GRCm39) missense probably damaging 0.99
R7942:Fam184b UTSW 5 45,741,595 (GRCm39) missense probably benign 0.16
R8172:Fam184b UTSW 5 45,741,709 (GRCm39) missense possibly damaging 0.86
R9470:Fam184b UTSW 5 45,741,854 (GRCm39) missense probably damaging 1.00
R9649:Fam184b UTSW 5 45,796,484 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16