Incidental Mutation 'R6828:Fam170b'
ID 534276
Institutional Source Beutler Lab
Gene Symbol Fam170b
Ensembl Gene ENSMUSG00000078127
Gene Name family with sequence similarity 170, member B
Synonyms 4922501K12Rik
MMRRC Submission 045020-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # R6828 (G1)
Quality Score 225.009
Status Not validated
Chromosome 14
Chromosomal Location 32555938-32558746 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 32557915 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 250 (D250G)
Ref Sequence ENSEMBL: ENSMUSP00000100529 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000104926]
AlphaFold E9PXT9
Predicted Effect probably damaging
Transcript: ENSMUST00000104926
AA Change: D250G

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000100529
Gene: ENSMUSG00000078127
AA Change: D250G

DomainStartEndE-ValueType
low complexity region 71 96 N/A INTRINSIC
ZnF_C2H2 202 223 1.81e1 SMART
low complexity region 241 252 N/A INTRINSIC
SCOP:d1lsha3 280 312 6e-3 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.4%
  • 20x: 98.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca17 A T 17: 24,545,389 (GRCm39) M349K possibly damaging Het
Akap12 A G 10: 4,304,606 (GRCm39) E472G probably damaging Het
Ap2s1 T C 7: 16,482,626 (GRCm39) Y94H probably damaging Het
Apeh A G 9: 107,964,237 (GRCm39) F530L probably damaging Het
Aplnr G A 2: 84,970,103 (GRCm39) probably benign Het
Arid3b A G 9: 57,717,446 (GRCm39) probably null Het
Ash1l A C 3: 88,983,420 (GRCm39) D2874A probably benign Het
Aurka T A 2: 172,199,172 (GRCm39) R277S probably damaging Het
Calhm4 A G 10: 33,919,953 (GRCm39) F105L possibly damaging Het
Ccar1 C A 10: 62,600,209 (GRCm39) W574L probably damaging Het
Cd8b1 T C 6: 71,311,100 (GRCm39) F207L probably benign Het
Clec14a T C 12: 58,315,290 (GRCm39) R111G probably damaging Het
Clk3 G A 9: 57,668,132 (GRCm39) T263I possibly damaging Het
Col11a2 A G 17: 34,272,607 (GRCm39) probably null Het
Col5a3 C T 9: 20,709,748 (GRCm39) G604D unknown Het
Cracdl T C 1: 37,663,898 (GRCm39) T667A possibly damaging Het
Crb2 ACTGCTGCTGCTGCTGCTGCTGC ACTGCTGCTGCTGCTGCTGC 2: 37,666,421 (GRCm39) probably benign Het
Ctps1 A T 4: 120,405,335 (GRCm39) V369D probably damaging Het
Dennd5b A G 6: 148,895,244 (GRCm39) I1262T probably damaging Het
Dmxl1 C T 18: 50,054,091 (GRCm39) P2566S probably damaging Het
Foxs1 G A 2: 152,775,048 (GRCm39) Q2* probably null Het
Frmpd1 T C 4: 45,275,383 (GRCm39) V512A probably damaging Het
Fry G A 5: 150,389,911 (GRCm39) probably null Het
Gria1 A G 11: 57,180,288 (GRCm39) Y677C probably damaging Het
Igdcc4 T C 9: 65,029,979 (GRCm39) I343T probably benign Het
Igkv1-132 T C 6: 67,736,697 (GRCm39) V5A probably benign Het
Ikzf5 A T 7: 130,993,401 (GRCm39) C256S probably damaging Het
Itk G A 11: 46,232,045 (GRCm39) H297Y probably damaging Het
Lamb3 A G 1: 193,017,756 (GRCm39) E879G probably benign Het
Lpin2 T C 17: 71,529,123 (GRCm39) V127A probably damaging Het
Man2b1 C A 8: 85,813,548 (GRCm39) P247T possibly damaging Het
Meak7 G A 8: 120,499,306 (GRCm39) T62I possibly damaging Het
Mxd3 T C 13: 55,473,967 (GRCm39) K122E probably benign Het
Npr1 C A 3: 90,372,120 (GRCm39) V231L probably benign Het
Nsd2 C T 5: 34,050,912 (GRCm39) A1263V probably damaging Het
Olfm4 A G 14: 80,258,973 (GRCm39) D374G probably damaging Het
Optc A T 1: 133,825,605 (GRCm39) I307N probably damaging Het
Or5p80 A C 7: 108,229,500 (GRCm39) Q100H possibly damaging Het
Or6c3b A T 10: 129,527,863 (GRCm39) S16T probably damaging Het
Pecr C A 1: 72,306,616 (GRCm39) E222* probably null Het
Pibf1 A G 14: 99,423,987 (GRCm39) N520S probably benign Het
Rhoj A G 12: 75,355,653 (GRCm39) N19S probably benign Het
Rock2 G A 12: 16,992,960 (GRCm39) probably null Het
Rpa1 G A 11: 75,205,697 (GRCm39) T220I probably damaging Het
Sdf2l1 C G 16: 16,950,158 (GRCm39) R6P probably benign Het
Sipa1l3 G A 7: 29,038,457 (GRCm39) H397Y probably benign Het
Snrk T C 9: 121,966,632 (GRCm39) I185T probably damaging Het
Srrt A T 5: 137,295,230 (GRCm39) V300E probably damaging Het
Taok2 A T 7: 126,471,047 (GRCm39) probably null Het
Tmem131 T C 1: 36,843,724 (GRCm39) K1379R possibly damaging Het
Usp15 T C 10: 122,963,894 (GRCm39) I543V probably damaging Het
Zfp553 A G 7: 126,835,447 (GRCm39) E334G probably damaging Het
Zim1 T C 7: 6,680,688 (GRCm39) Y325C probably damaging Het
Other mutations in Fam170b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03093:Fam170b APN 14 32,557,482 (GRCm39) missense probably damaging 1.00
R0279:Fam170b UTSW 14 32,556,025 (GRCm39) start gained probably benign
R0594:Fam170b UTSW 14 32,558,271 (GRCm39) missense unknown
R1496:Fam170b UTSW 14 32,557,588 (GRCm39) missense probably damaging 1.00
R1675:Fam170b UTSW 14 32,557,359 (GRCm39) nonsense probably null
R1766:Fam170b UTSW 14 32,557,843 (GRCm39) missense possibly damaging 0.94
R2240:Fam170b UTSW 14 32,557,825 (GRCm39) missense probably damaging 1.00
R6361:Fam170b UTSW 14 32,558,028 (GRCm39) missense unknown
R7487:Fam170b UTSW 14 32,557,776 (GRCm39) missense probably damaging 1.00
R7575:Fam170b UTSW 14 32,558,155 (GRCm39) missense unknown
R8962:Fam170b UTSW 14 32,557,336 (GRCm39) missense probably benign 0.14
R9102:Fam170b UTSW 14 32,557,404 (GRCm39) missense probably damaging 1.00
R9631:Fam170b UTSW 14 32,557,641 (GRCm39) missense probably damaging 1.00
Z1176:Fam170b UTSW 14 32,557,761 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AGACTGCAAGCACTACTGC -3'
(R):5'- GCAGCAATTCAAAATGCTGGAG -3'

Sequencing Primer
(F):5'- AGACTGAGGACCCTGTGGAC -3'
(R):5'- AACGGCTGCTGCTTCAGTG -3'
Posted On 2018-09-12