Incidental Mutation 'R3618:Cfap161'
ID 268518
Institutional Source Beutler Lab
Gene Symbol Cfap161
Ensembl Gene ENSMUSG00000011154
Gene Name cilia and flagella associated protein 161
Synonyms 1700026D08Rik
MMRRC Submission 040675-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # R3618 (G1)
Quality Score 181
Status Not validated
Chromosome 7
Chromosomal Location 83423309-83444088 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to C at 83429390 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 209 (Y209*)
Ref Sequence ENSEMBL: ENSMUSP00000114051 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000011298] [ENSMUST00000119134] [ENSMUST00000149671]
AlphaFold Q6P8Y0
Predicted Effect probably null
Transcript: ENSMUST00000011298
AA Change: Y209*
Predicted Effect probably null
Transcript: ENSMUST00000119134
AA Change: Y209*
Predicted Effect probably benign
Transcript: ENSMUST00000149671
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208785
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110002E22Rik A G 3: 137,774,168 (GRCm39) E1119G probably damaging Het
Ahnak2 A G 12: 112,749,842 (GRCm39) I132T probably damaging Het
Arhgap29 G A 3: 121,782,176 (GRCm39) D63N possibly damaging Het
Bsn T A 9: 107,994,760 (GRCm39) probably null Het
Drp2 A C X: 133,340,717 (GRCm39) D458A probably benign Het
Efcab6 T C 15: 83,834,270 (GRCm39) H446R probably benign Het
Enpep G C 3: 129,077,807 (GRCm39) S603R possibly damaging Het
F13a1 G A 13: 37,127,967 (GRCm39) T337I probably damaging Het
Fhod3 TGAGGAGGAGGAGGAGGA TGAGGAGGAGGAGGA 18: 25,153,722 (GRCm39) probably benign Het
Hcfc1 A T X: 72,993,694 (GRCm39) V1157D probably benign Het
Inava A C 1: 136,142,110 (GRCm39) V663G probably benign Het
Ino80 T C 2: 119,277,353 (GRCm39) D374G probably null Het
Kif1a T C 1: 93,004,765 (GRCm39) E143G probably null Het
Larp1 A T 11: 57,948,172 (GRCm39) E990D probably benign Het
Larp7 C A 3: 127,330,614 (GRCm39) E568* probably null Het
Ltn1 A T 16: 87,217,787 (GRCm39) S298R probably damaging Het
Mcm10 A G 2: 5,001,913 (GRCm39) probably null Het
Mef2a G A 7: 66,918,075 (GRCm39) S111L probably benign Het
Mroh1 A G 15: 76,336,546 (GRCm39) T1590A possibly damaging Het
Ncoa6 A T 2: 155,249,709 (GRCm39) H1198Q possibly damaging Het
Ogg1 A G 6: 113,305,334 (GRCm39) E49G probably damaging Het
Palm3 T A 8: 84,755,973 (GRCm39) V495E probably benign Het
Pam A G 1: 97,762,157 (GRCm39) F809L probably damaging Het
Parp3 T C 9: 106,352,262 (GRCm39) E88G possibly damaging Het
Ptprs A G 17: 56,735,965 (GRCm39) I156T probably benign Het
Pus7l T A 15: 94,425,788 (GRCm39) I538F probably damaging Het
Rgs8 A G 1: 153,566,742 (GRCm39) T98A probably null Het
Ryr2 C T 13: 11,787,466 (GRCm39) probably null Het
Slc8a2 A G 7: 15,886,824 (GRCm39) N656D possibly damaging Het
Stard9 C T 2: 120,529,500 (GRCm39) T1919I possibly damaging Het
Tbcel T C 9: 42,372,591 (GRCm39) probably benign Het
Trpv3 A T 11: 73,186,281 (GRCm39) I691F probably damaging Het
Uba2 A G 7: 33,853,907 (GRCm39) probably null Het
Usp53 A C 3: 122,728,061 (GRCm39) S840R probably benign Het
Vmn2r100 A T 17: 19,743,692 (GRCm39) I452F probably benign Het
Zbtb48 A T 4: 152,110,484 (GRCm39) probably null Het
Zfp385b G A 2: 77,246,233 (GRCm39) P177S probably benign Het
Zfp42 T C 8: 43,748,938 (GRCm39) R188G possibly damaging Het
Other mutations in Cfap161
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01827:Cfap161 APN 7 83,442,648 (GRCm39) missense possibly damaging 0.86
IGL01999:Cfap161 APN 7 83,440,899 (GRCm39) missense probably damaging 1.00
IGL02291:Cfap161 APN 7 83,440,847 (GRCm39) missense probably benign 0.01
IGL02444:Cfap161 APN 7 83,425,353 (GRCm39) missense probably damaging 1.00
R0492:Cfap161 UTSW 7 83,443,245 (GRCm39) missense possibly damaging 0.90
R0652:Cfap161 UTSW 7 83,442,484 (GRCm39) missense probably null 0.01
R1599:Cfap161 UTSW 7 83,425,287 (GRCm39) missense possibly damaging 0.84
R1828:Cfap161 UTSW 7 83,440,932 (GRCm39) critical splice acceptor site probably null
R2117:Cfap161 UTSW 7 83,425,184 (GRCm39) missense possibly damaging 0.63
R2262:Cfap161 UTSW 7 83,442,580 (GRCm39) missense probably benign 0.37
R4015:Cfap161 UTSW 7 83,429,479 (GRCm39) missense probably benign 0.01
R5821:Cfap161 UTSW 7 83,425,188 (GRCm39) missense probably benign 0.38
R6477:Cfap161 UTSW 7 83,443,230 (GRCm39) nonsense probably null
R6478:Cfap161 UTSW 7 83,442,484 (GRCm39) missense probably benign 0.00
R7108:Cfap161 UTSW 7 83,442,518 (GRCm39) missense possibly damaging 0.60
R7203:Cfap161 UTSW 7 83,425,258 (GRCm39) missense probably damaging 0.97
R7582:Cfap161 UTSW 7 83,426,290 (GRCm39) missense possibly damaging 0.69
R8714:Cfap161 UTSW 7 83,442,482 (GRCm39) missense probably benign 0.11
R8762:Cfap161 UTSW 7 83,443,282 (GRCm39) missense possibly damaging 0.92
R9587:Cfap161 UTSW 7 83,440,878 (GRCm39) missense probably damaging 1.00
R9665:Cfap161 UTSW 7 83,442,579 (GRCm39) missense probably benign 0.00
R9702:Cfap161 UTSW 7 83,442,652 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- AGACTGGTGCTATCCACATTTG -3'
(R):5'- TTGCAGTGCAGTCCCTTTGG -3'

Sequencing Primer
(F):5'- TACAGTGAGCCTCTGCTT -3'
(R):5'- AACTTCCTGGGTAGCTGTGACTC -3'
Posted On 2015-02-19