Incidental Mutation 'R4609:Fem1c'
ID344555
Institutional Source Beutler Lab
Gene Symbol Fem1c
Ensembl Gene ENSMUSG00000033319
Gene Namefem-1 homolog c (C.elegans)
Synonyms
MMRRC Submission 041820-MU
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R4609 (G1)
Quality Score225
Status Validated
Chromosome18
Chromosomal Location46501746-46525971 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 46505948 bp
ZygosityHeterozygous
Amino Acid Change Isoleucine to Asparagine at position 329 (I329N)
Ref Sequence ENSEMBL: ENSMUSP00000038816 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000036226]
Predicted Effect probably damaging
Transcript: ENSMUST00000036226
AA Change: I329N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000038816
Gene: ENSMUSG00000033319
AA Change: I329N

DomainStartEndE-ValueType
ANK 2 31 1.12e3 SMART
ANK 40 70 1.51e-4 SMART
ANK 82 111 2.77e-3 SMART
ANK 115 144 1.12e-3 SMART
ANK 148 177 7.24e-7 SMART
ANK 181 210 9.13e-4 SMART
ANK 213 243 5.67e0 SMART
low complexity region 381 394 N/A INTRINSIC
ANK 481 523 5.67e0 SMART
ANK 527 556 1.88e-5 SMART
Meta Mutation Damage Score 0.2712 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.9%
Validation Efficiency 99% (78/79)
MGI Phenotype PHENOTYPE: Homozygous mutant mice are fertile and show no overt abnormalities. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 77 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
7530416G11Rik T C 15: 85,494,169 D91G unknown Het
Adam10 T C 9: 70,740,143 Y42H probably damaging Het
Baiap3 A T 17: 25,250,261 C183S probably damaging Het
Bbs10 A G 10: 111,301,134 K703E probably benign Het
Bmp1 C T 14: 70,477,966 V910M probably benign Het
Brdt G A 5: 107,359,936 A677T probably benign Het
Cadps2 A T 6: 23,587,579 M304K probably damaging Het
Car9 A T 4: 43,507,267 D71V possibly damaging Het
Chml A T 1: 175,687,157 Y399* probably null Het
Clasp1 A G 1: 118,503,035 probably benign Het
Cntnap5b G A 1: 99,772,847 probably null Het
Cpvl A T 6: 53,974,620 probably null Het
Crocc2 G A 1: 93,168,794 V24M possibly damaging Het
Cxcl16 T C 11: 70,455,429 Y226C probably damaging Het
Dio3 G T 12: 110,280,010 R260L probably damaging Het
Dmxl2 A G 9: 54,446,512 L724P probably damaging Het
Dnah7a A C 1: 53,456,657 F3214V possibly damaging Het
Dpy19l4 A T 4: 11,295,999 Y223* probably null Het
Dpysl4 T C 7: 139,098,621 V499A probably damaging Het
Ets2 A T 16: 95,711,774 K101N probably benign Het
Fam160a2 A G 7: 105,388,224 I384T probably damaging Het
Fbn2 A T 18: 58,190,269 Y200* probably null Het
Gm8919 T C 3: 11,659,470 noncoding transcript Het
H2-Q5 A T 17: 35,397,080 H206L probably benign Het
Hexa T C 9: 59,557,319 F164S probably benign Het
Hk1 G T 10: 62,358,415 probably benign Het
Ick T A 9: 78,167,789 probably benign Het
Itih4 G A 14: 30,901,669 G915R probably damaging Het
Kcnq5 A T 1: 21,405,068 probably null Het
Krtap10-4 A T 10: 77,826,796 probably benign Het
Maml3 G T 3: 51,855,592 H650Q probably damaging Het
Mief1 C A 15: 80,248,253 P112Q probably benign Het
Morc3 A G 16: 93,864,968 E472G probably benign Het
Nap1l1 T A 10: 111,492,880 Y223* probably null Het
Nfix A T 8: 84,726,490 W312R probably damaging Het
Nfkbie A T 17: 45,558,584 N155I probably damaging Het
Nlgn2 A T 11: 69,834,086 M118K probably damaging Het
Nlrp5 A T 7: 23,417,748 Y299F probably benign Het
Nnt T C 13: 119,357,536 I556V possibly damaging Het
Oasl2 A T 5: 114,899,796 I85F possibly damaging Het
Ogg1 A C 6: 113,328,432 T69P probably damaging Het
Olfml2a G T 2: 38,957,721 V431L probably damaging Het
Olfr507 A T 7: 108,622,504 M231L probably benign Het
Olfr984 T C 9: 40,100,806 H228R possibly damaging Het
Palb2 G T 7: 122,124,723 A601E probably benign Het
Pcdhb20 G A 18: 37,505,796 M458I probably benign Het
Pde11a T C 2: 76,291,241 D332G possibly damaging Het
Pkd1l1 C T 11: 8,958,964 E347K unknown Het
Pou2af1 G A 9: 51,238,225 V206I possibly damaging Het
Prr16 A G 18: 51,118,067 D46G possibly damaging Het
Pus1 A G 5: 110,780,318 M1T probably null Het
Pygm T A 19: 6,391,409 V566D possibly damaging Het
Rb1 T A 14: 73,262,514 probably benign Het
Rhoj A T 12: 75,400,206 K200* probably null Het
Rnf213 A G 11: 119,437,695 I1985V possibly damaging Het
Sept11 G T 5: 93,162,254 M305I possibly damaging Het
Setdb2 T C 14: 59,415,704 Y383C probably damaging Het
Sfpq G C 4: 127,021,611 Q65H unknown Het
Stard3nl G T 13: 19,370,264 A180E probably damaging Het
Tanc2 A G 11: 105,910,240 N1094S probably benign Het
Trf C T 9: 103,211,985 A554T possibly damaging Het
Trmt13 T C 3: 116,594,827 probably benign Het
Tubb3 A G 8: 123,420,919 D197G probably damaging Het
Ube2e3 A G 2: 78,918,712 H135R probably damaging Het
Ugt1a10 A T 1: 88,055,482 M1L possibly damaging Het
Vmn1r233 A T 17: 20,994,415 I91N possibly damaging Het
Vmn2r88 A T 14: 51,418,074 D580V probably damaging Het
Vps33b A G 7: 80,291,118 Y593C probably benign Het
Wdr19 A G 5: 65,228,542 T622A possibly damaging Het
Wdr3 C T 3: 100,140,200 R853Q probably damaging Het
Wdr61 A G 9: 54,728,179 V46A probably benign Het
Xirp1 T C 9: 120,016,506 T1104A probably benign Het
Yipf1 G A 4: 107,344,683 probably null Het
Zbtb17 A G 4: 141,466,498 D651G probably damaging Het
Zbtb42 C T 12: 112,680,542 R384W probably damaging Het
Zbtb43 A T 2: 33,454,043 M390K probably benign Het
Zfp462 C T 4: 55,011,889 T1285M probably damaging Het
Other mutations in Fem1c
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01594:Fem1c APN 18 46506276 missense probably benign 0.00
IGL01895:Fem1c APN 18 46505562 missense probably benign 0.00
IGL02612:Fem1c APN 18 46505714 missense probably benign 0.05
IGL02628:Fem1c APN 18 46505952 missense probably damaging 1.00
R0605:Fem1c UTSW 18 46505160 missense probably benign 0.18
R0655:Fem1c UTSW 18 46505160 missense probably benign 0.18
R0735:Fem1c UTSW 18 46505160 missense probably benign 0.18
R1476:Fem1c UTSW 18 46524485 missense probably damaging 1.00
R1509:Fem1c UTSW 18 46524213 missense probably benign
R1704:Fem1c UTSW 18 46506196 missense probably benign 0.05
R1834:Fem1c UTSW 18 46505282 missense probably damaging 1.00
R2297:Fem1c UTSW 18 46506161 missense possibly damaging 0.84
R5119:Fem1c UTSW 18 46506369 missense probably damaging 1.00
R6505:Fem1c UTSW 18 46505875 missense possibly damaging 0.68
R7501:Fem1c UTSW 18 46505801 missense probably damaging 1.00
R7749:Fem1c UTSW 18 46524118 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TAGCCCTGTCCTGTAGCATG -3'
(R):5'- ACTTGGGGCTTTGAAATACTGG -3'

Sequencing Primer
(F):5'- CCTGTCCTGTAGCATGAAGGAG -3'
(R):5'- GCTTTGAAATACTGGAAAAAGGC -3'
Posted On2015-09-25