Incidental Mutation 'R8219:Fam161b'
ID636573
Institutional Source Beutler Lab
Gene Symbol Fam161b
Ensembl Gene ENSMUSG00000021234
Gene Namefamily with sequence similarity 161, member B
Synonyms
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.059) question?
Stock #R8219 (G1)
Quality Score225.009
Status Validated
Chromosome12
Chromosomal Location84345309-84361833 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 84346874 bp
ZygosityHeterozygous
Amino Acid Change Glutamic Acid to Glycine at position 575 (E575G)
Ref Sequence ENSEMBL: ENSMUSP00000021659 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021659] [ENSMUST00000045931] [ENSMUST00000065536]
Predicted Effect probably benign
Transcript: ENSMUST00000021659
AA Change: E575G

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000021659
Gene: ENSMUSG00000021234
AA Change: E575G

DomainStartEndE-ValueType
low complexity region 57 65 N/A INTRINSIC
low complexity region 93 107 N/A INTRINSIC
Pfam:UPF0564 168 535 5.3e-100 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000045931
SMART Domains Protein: ENSMUSP00000045550
Gene: ENSMUSG00000042472

DomainStartEndE-ValueType
ZnF_C2H2 219 243 1.04e-3 SMART
ZnF_C2H2 249 273 6.88e-4 SMART
ZnF_C2H2 279 303 1.13e-4 SMART
ZnF_C2H2 309 333 1.45e-2 SMART
ZnF_C2H2 339 361 5.59e-4 SMART
low complexity region 400 417 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000065536
AA Change: E575G

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000070407
Gene: ENSMUSG00000021234
AA Change: E575G

DomainStartEndE-ValueType
low complexity region 57 65 N/A INTRINSIC
low complexity region 93 107 N/A INTRINSIC
Pfam:UPF0564 168 535 8.3e-112 PFAM
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.8%
  • 10x: 99.5%
  • 20x: 98.7%
Validation Efficiency 100% (62/62)
Allele List at MGI
Other mutations in this stock
Total: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933414I15Rik A T 11: 50,942,536 S80T unknown Het
Acnat1 T A 4: 49,447,748 I278F probably benign Het
Adgrf5 A T 17: 43,449,859 Q815L probably benign Het
Aff1 T A 5: 103,846,333 Y1022N probably damaging Het
Ahi1 A G 10: 21,074,436 K1034E probably benign Het
Ano8 A T 8: 71,480,713 L645Q unknown Het
Atg9b A G 5: 24,386,332 L756P probably damaging Het
Atp2b2 A T 6: 113,793,850 I411N probably damaging Het
BC080695 T G 4: 143,571,960 Y158D probably benign Het
Bmp6 T A 13: 38,345,987 C19S unknown Het
Borcs5 A G 6: 134,644,350 H27R probably benign Het
C77080 T A 4: 129,248,153 D65V possibly damaging Het
Cachd1 C A 4: 100,990,962 D1091E probably benign Het
Ccdc186 T A 19: 56,793,345 M801L probably benign Het
Clcn3 A T 8: 60,922,966 M658K probably damaging Het
Col1a1 C T 11: 94,943,358 R500C probably damaging Het
Cul4a T A 8: 13,146,540 D731E possibly damaging Het
Dnajb8 C T 6: 88,222,958 R159C possibly damaging Het
E2f7 T A 10: 110,759,843 V133E probably damaging Het
Fubp1 T A 3: 152,220,466 V275D probably damaging Het
Gabrg1 T A 5: 70,774,300 R367* probably null Het
Gm6902 G A 7: 23,273,718 A128V probably benign Het
Gnptab A G 10: 88,433,792 T786A probably benign Het
Golga2 A G 2: 32,306,480 N981D probably damaging Het
Gsap A T 5: 21,251,115 I437L probably benign Het
Gulp1 A G 1: 44,754,341 probably null Het
Kcnn1 T C 8: 70,852,855 Y237C probably damaging Het
Klhl28 A T 12: 64,951,657 N354K probably benign Het
Lama3 T C 18: 12,439,360 Y541H probably benign Het
Lamc1 A G 1: 153,247,327 Y706H probably damaging Het
Lima1 G T 15: 99,780,790 T590K probably damaging Het
Lrrc38 G A 4: 143,350,733 G189R probably damaging Het
Mrgprb8 G A 7: 48,388,901 V107M possibly damaging Het
Mrpl3 T A 9: 105,057,072 N139K possibly damaging Het
Nudt16 T A 9: 105,130,437 N161I probably damaging Het
Obscn G A 11: 59,122,748 S1091L probably benign Het
Olfr1458 A C 19: 13,102,920 L122R probably damaging Het
Olfr894 A C 9: 38,219,372 D183A probably damaging Het
Oog4 T C 4: 143,439,938 M99V probably benign Het
Osbpl6 A T 2: 76,555,903 D303V probably damaging Het
Pcdhb21 T C 18: 37,514,655 F279S probably damaging Het
Peg3 G A 7: 6,708,365 T1286I probably benign Het
Phax A G 18: 56,575,682 N106S probably damaging Het
Pkdrej A G 15: 85,821,292 Y148H probably damaging Het
Ptprn2 C A 12: 117,184,737 Q706K probably benign Het
Rdh11 T G 12: 79,189,106 K23Q probably benign Het
Rit2 T A 18: 30,975,494 E146V probably damaging Het
Rnf141 T C 7: 110,837,265 probably benign Het
Sars T A 3: 108,445,062 E24V probably benign Het
Sh3tc2 A G 18: 62,011,861 I1129V probably benign Het
Slc10a5 G T 3: 10,335,324 P92Q probably benign Het
Slc24a5 A T 2: 125,085,655 probably null Het
Slc5a8 A G 10: 88,921,699 Y517C probably damaging Het
Slc6a5 A G 7: 49,912,163 M148V probably benign Het
Sorl1 T C 9: 42,041,561 probably null Het
Tgm4 A T 9: 123,045,052 Y119F probably benign Het
Tgm6 A G 2: 130,151,280 K562R probably benign Het
Tlr3 T C 8: 45,397,979 E627G possibly damaging Het
Tmprss11f A G 5: 86,530,019 L297P probably damaging Het
Tpbgl T C 7: 99,625,771 H293R probably benign Het
Trank1 A C 9: 111,364,909 K667T probably damaging Het
Trpm1 A T 7: 64,201,951 Q139L probably benign Het
Ttf2 T G 3: 100,962,563 K398T possibly damaging Het
Xpa A T 4: 46,183,150 M213K probably benign Het
Zmym2 T A 14: 56,925,859 S623T probably benign Het
Other mutations in Fam161b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00540:Fam161b APN 12 84361751 unclassified probably benign
IGL00900:Fam161b APN 12 84355969 missense probably benign 0.05
IGL00905:Fam161b APN 12 84357685 missense probably benign 0.00
IGL01123:Fam161b APN 12 84357664 missense probably benign 0.00
IGL02156:Fam161b APN 12 84354753 missense probably benign 0.00
IGL02630:Fam161b APN 12 84353914 missense probably benign 0.03
IGL02670:Fam161b APN 12 84357594 missense probably benign 0.00
IGL03160:Fam161b APN 12 84353825 missense probably benign 0.05
R0560:Fam161b UTSW 12 84357718 missense probably damaging 0.96
R0569:Fam161b UTSW 12 84348639 missense probably damaging 1.00
R1834:Fam161b UTSW 12 84348778 splice site probably benign
R2070:Fam161b UTSW 12 84356428 missense probably benign 0.00
R3784:Fam161b UTSW 12 84361690 critical splice donor site probably null
R3786:Fam161b UTSW 12 84361690 critical splice donor site probably null
R4697:Fam161b UTSW 12 84348558 unclassified probably benign
R5247:Fam161b UTSW 12 84357750 missense probably damaging 1.00
R5390:Fam161b UTSW 12 84348634 missense probably damaging 0.99
R5668:Fam161b UTSW 12 84356350 missense probably damaging 0.96
R6891:Fam161b UTSW 12 84354780 missense probably damaging 1.00
R7189:Fam161b UTSW 12 84348646 missense probably damaging 1.00
R7410:Fam161b UTSW 12 84357801 missense probably benign 0.04
R7514:Fam161b UTSW 12 84357738 missense possibly damaging 0.76
R8035:Fam161b UTSW 12 84348656 missense probably damaging 1.00
R8428:Fam161b UTSW 12 84357595 missense probably benign 0.00
R8921:Fam161b UTSW 12 84348282 missense probably benign 0.02
X0019:Fam161b UTSW 12 84354973 missense probably benign 0.30
Z1176:Fam161b UTSW 12 84356053 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- GCCTCACATAGACAGTGTTGC -3'
(R):5'- GGCTCTAAGTCATTCCTGTGCC -3'

Sequencing Primer
(F):5'- CTCACATAGACAGTGTTGCTCAGG -3'
(R):5'- CAGCTTTGTCCAGCACTAAAGG -3'
Posted On2020-07-13