Incidental Mutation 'R1711:Cfap54'
ID 190593
Institutional Source Beutler Lab
Gene Symbol Cfap54
Ensembl Gene ENSMUSG00000020014
Gene Name cilia and flagella associated protein 54
Synonyms LOC380653, Gm872, 4930485B16Rik
MMRRC Submission 039744-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.086) question?
Stock # R1711 (G1)
Quality Score 225
Status Not validated
Chromosome 10
Chromosomal Location 92611481-92917480 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 92846882 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Proline at position 1028 (T1028P)
Ref Sequence ENSEMBL: ENSMUSP00000148636 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168110] [ENSMUST00000170065] [ENSMUST00000212902]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000168110
AA Change: T1028P

PolyPhen 2 Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000129517
Gene: ENSMUSG00000020014
AA Change: T1028P

DomainStartEndE-ValueType
low complexity region 3 37 N/A INTRINSIC
low complexity region 39 48 N/A INTRINSIC
Pfam:DUF4486 104 642 1.1e-269 PFAM
low complexity region 842 851 N/A INTRINSIC
low complexity region 902 915 N/A INTRINSIC
Blast:FN3 916 1002 4e-48 BLAST
low complexity region 1409 1426 N/A INTRINSIC
low complexity region 1974 1984 N/A INTRINSIC
low complexity region 2354 2370 N/A INTRINSIC
low complexity region 2500 2513 N/A INTRINSIC
low complexity region 2605 2616 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000170065
Predicted Effect probably damaging
Transcript: ENSMUST00000212902
AA Change: T1028P

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.6%
  • 20x: 93.6%
Validation Efficiency
MGI Phenotype PHENOTYPE: Homozygous inactivation of this gene causes background-dependent lethality and hydroencephaly, male sterility associated with defects in spermiogenesis, and impaired mucociliary clearance. Airway epithelial cilia show structural defects and a decrease in ciliary beat frequency and cilia-driven flow. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 111 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2210408I21Rik C T 13: 77,418,039 (GRCm39) T741I possibly damaging Het
Aadacl4fm2 A T 4: 144,281,976 (GRCm39) I272K probably damaging Het
Acot3 A T 12: 84,100,347 (GRCm39) Q41L probably damaging Het
Actl7b G A 4: 56,740,165 (GRCm39) Q398* probably null Het
Adgrb2 C A 4: 129,886,417 (GRCm39) Q186K probably damaging Het
Akr1a1 A G 4: 116,495,171 (GRCm39) probably null Het
Ap3s2 A T 7: 79,530,238 (GRCm39) F192L probably damaging Het
Apobr T G 7: 126,184,151 (GRCm39) probably null Het
Arhgap5 A G 12: 52,566,128 (GRCm39) N1033S probably damaging Het
Arid3c G T 4: 41,725,947 (GRCm39) R219S probably damaging Het
Bves C T 10: 45,223,961 (GRCm39) T207M probably damaging Het
Cacna1d T C 14: 29,788,013 (GRCm39) K1619R probably damaging Het
Caps2 A T 10: 112,026,883 (GRCm39) D223V possibly damaging Het
Cd3g A C 9: 44,885,640 (GRCm39) L35R probably damaging Het
Cdh23 A T 10: 60,359,315 (GRCm39) V261E probably benign Het
Ch25h C A 19: 34,451,686 (GRCm39) V281L probably benign Het
Cip2a A C 16: 48,837,849 (GRCm39) I850L probably benign Het
Clu G T 14: 66,218,354 (GRCm39) V405L possibly damaging Het
Col6a3 A T 1: 90,757,935 (GRCm39) H6Q probably damaging Het
Cps1 G A 1: 67,207,533 (GRCm39) probably null Het
Ctr9 T C 7: 110,654,870 (GRCm39) S1134P unknown Het
Cts7 C T 13: 61,500,624 (GRCm39) G308S probably damaging Het
Cyp2c39 C A 19: 39,555,335 (GRCm39) T385K probably damaging Het
Dennd5a A T 7: 109,517,919 (GRCm39) D596E probably benign Het
Disc1 T A 8: 125,851,349 (GRCm39) I413K probably benign Het
Dll3 C T 7: 27,993,922 (GRCm39) G505D probably damaging Het
Dnah3 A G 7: 119,677,794 (GRCm39) W377R probably damaging Het
Dop1b A G 16: 93,596,814 (GRCm39) D1792G probably damaging Het
Dpep3 T A 8: 106,700,325 (GRCm39) R460S probably benign Het
Ebf4 A G 2: 130,200,751 (GRCm39) N302S probably damaging Het
Efcab3 A G 11: 104,611,514 (GRCm39) K452R probably benign Het
Egflam T C 15: 7,319,396 (GRCm39) E194G possibly damaging Het
Ep400 A T 5: 110,841,174 (GRCm39) probably benign Het
Ercc6 T C 14: 32,248,133 (GRCm39) M228T probably damaging Het
Fbxo9 T C 9: 77,994,529 (GRCm39) T264A probably damaging Het
Fcrl5 C A 3: 87,364,721 (GRCm39) P486T possibly damaging Het
Fyb1 T C 15: 6,609,960 (GRCm39) F178L probably damaging Het
Gaa T A 11: 119,171,286 (GRCm39) I646N probably damaging Het
Gm5431 A T 11: 48,785,853 (GRCm39) V174E possibly damaging Het
Gnpat T G 8: 125,613,691 (GRCm39) probably null Het
Gucy1a2 G T 9: 3,759,622 (GRCm39) R476I probably benign Het
Hars1 A G 18: 36,904,156 (GRCm39) L241P probably damaging Het
Haus5 G A 7: 30,357,328 (GRCm39) Q399* probably null Het
Hephl1 T C 9: 14,970,542 (GRCm39) E984G probably damaging Het
Hmces C T 6: 87,898,574 (GRCm39) Q132* probably null Het
Hsp90b1 G T 10: 86,530,389 (GRCm39) T490K probably damaging Het
Idh2 T G 7: 79,748,906 (GRCm39) E125A probably damaging Het
Ipo13 G T 4: 117,761,719 (GRCm39) H465Q probably benign Het
Isca2 C A 12: 84,820,393 (GRCm39) T31K probably damaging Het
Itga9 T C 9: 118,527,529 (GRCm39) V560A probably benign Het
Jhy G A 9: 40,822,453 (GRCm39) Q562* probably null Het
Kcnj5 A G 9: 32,233,865 (GRCm39) I150T probably damaging Het
Kmt2a A G 9: 44,752,918 (GRCm39) I1419T unknown Het
Lix1 T C 17: 17,666,320 (GRCm39) F160L possibly damaging Het
Lonrf2 G A 1: 38,852,357 (GRCm39) P165S probably benign Het
Map4k1 A T 7: 28,688,777 (GRCm39) Q276L possibly damaging Het
Mmp9 G A 2: 164,791,342 (GRCm39) G171S probably damaging Het
Mvp C A 7: 126,594,907 (GRCm39) probably null Het
Mylk3 T A 8: 86,091,460 (GRCm39) E115V probably damaging Het
Nebl T A 2: 17,393,565 (GRCm39) T603S probably damaging Het
Nudt15 T C 14: 73,760,776 (GRCm39) D105G probably benign Het
Or12j2 A C 7: 139,915,912 (GRCm39) T46P possibly damaging Het
Or2w1b G A 13: 21,300,476 (GRCm39) V205I probably benign Het
Or51b6 T A 7: 103,555,906 (GRCm39) W87R probably damaging Het
Or52i2 G T 7: 102,319,369 (GRCm39) V81L probably damaging Het
Or52l1 A T 7: 104,829,967 (GRCm39) H199Q probably damaging Het
Or8g2b A G 9: 39,751,581 (GRCm39) M284V probably benign Het
Osbpl9 A T 4: 108,923,415 (GRCm39) C495S probably damaging Het
Pamr1 A G 2: 102,471,197 (GRCm39) T507A probably benign Het
Pcdhb9 T A 18: 37,536,380 (GRCm39) C791* probably null Het
Pcgf6 T C 19: 47,038,957 (GRCm39) E101G probably damaging Het
Pdgfrl A T 8: 41,438,831 (GRCm39) I256F probably benign Het
Pdzd7 T C 19: 45,033,950 (GRCm39) R45G possibly damaging Het
Pecr C T 1: 72,316,568 (GRCm39) V46I possibly damaging Het
Pgr A G 9: 8,922,715 (GRCm39) probably null Het
Pik3c2a A T 7: 116,017,162 (GRCm39) Y198* probably null Het
Pp2d1 T A 17: 53,822,338 (GRCm39) M243L possibly damaging Het
Ppp1r1a T A 15: 103,441,919 (GRCm39) I50L possibly damaging Het
Proc T C 18: 32,260,459 (GRCm39) D222G probably benign Het
Ptprq T A 10: 107,370,560 (GRCm39) R2044* probably null Het
Ranbp2 T C 10: 58,296,341 (GRCm39) V326A probably benign Het
Reep6 T A 10: 80,169,815 (GRCm39) F122I possibly damaging Het
Rubcn C A 16: 32,663,471 (GRCm39) R388S probably damaging Het
Rusc1 A G 3: 88,996,600 (GRCm39) L62P probably damaging Het
Satb2 T C 1: 56,889,448 (GRCm39) N423S probably damaging Het
Scart1 G T 7: 139,800,522 (GRCm39) C101F probably damaging Het
Serpinb9d A G 13: 33,384,731 (GRCm39) K236R probably benign Het
Slc4a7 A G 14: 14,765,709 (GRCm38) R680G probably benign Het
Slitrk1 T A 14: 109,150,528 (GRCm39) Y61F probably benign Het
Son A G 16: 91,457,114 (GRCm39) probably benign Het
Sparc T A 11: 55,286,602 (GRCm39) probably null Het
Spon2 A G 5: 33,373,729 (GRCm39) F194S probably damaging Het
Spta1 A G 1: 174,068,608 (GRCm39) E2136G probably damaging Het
Stat4 T C 1: 52,146,084 (GRCm39) S746P probably damaging Het
Stk31 T A 6: 49,446,238 (GRCm39) S958R probably benign Het
Stom T A 2: 35,205,929 (GRCm39) I267F probably damaging Het
Stx12 A T 4: 132,585,788 (GRCm39) D197E probably damaging Het
Taok3 A T 5: 117,393,991 (GRCm39) N588I possibly damaging Het
Tgs1 A G 4: 3,598,658 (GRCm39) D657G probably damaging Het
Trim6 A G 7: 103,882,044 (GRCm39) T432A probably damaging Het
Trim72 C G 7: 127,603,757 (GRCm39) C34W probably damaging Het
Trpc4ap A T 2: 155,499,664 (GRCm39) I286N probably benign Het
Ttn A G 2: 76,693,905 (GRCm39) V321A possibly damaging Het
Utp4 T A 8: 107,645,352 (GRCm39) I583N probably damaging Het
Wdfy2 G T 14: 63,181,546 (GRCm39) M225I probably benign Het
Wfdc1 A G 8: 120,407,776 (GRCm39) T134A probably benign Het
Wnt9b A G 11: 103,622,954 (GRCm39) S150P probably damaging Het
Zbtb46 A T 2: 181,053,477 (GRCm39) F412I probably damaging Het
Zc3h15 G A 2: 83,491,492 (GRCm39) R240H probably benign Het
Zfp11 A T 5: 129,733,737 (GRCm39) Y575N probably benign Het
Zfp687 T C 3: 94,919,200 (GRCm39) M191V probably benign Het
Other mutations in Cfap54
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01329:Cfap54 APN 10 92,917,385 (GRCm39) missense unknown
IGL02034:Cfap54 APN 10 92,897,347 (GRCm39) missense probably damaging 0.99
IGL02082:Cfap54 APN 10 92,917,320 (GRCm39) missense unknown
IGL02434:Cfap54 APN 10 92,902,616 (GRCm39) missense probably benign 0.20
R0011:Cfap54 UTSW 10 92,901,087 (GRCm39) missense probably damaging 0.97
R0011:Cfap54 UTSW 10 92,901,087 (GRCm39) missense probably damaging 0.97
R0032:Cfap54 UTSW 10 92,768,559 (GRCm39) missense probably benign 0.04
R0032:Cfap54 UTSW 10 92,768,559 (GRCm39) missense probably benign 0.04
R0040:Cfap54 UTSW 10 92,812,901 (GRCm39) missense probably benign 0.33
R0044:Cfap54 UTSW 10 92,871,295 (GRCm39) missense probably null 0.46
R0086:Cfap54 UTSW 10 92,864,456 (GRCm39) missense possibly damaging 0.86
R0104:Cfap54 UTSW 10 92,864,514 (GRCm39) missense probably damaging 1.00
R0194:Cfap54 UTSW 10 92,870,524 (GRCm39) unclassified probably benign
R0234:Cfap54 UTSW 10 92,735,022 (GRCm39) nonsense probably null
R0308:Cfap54 UTSW 10 92,721,226 (GRCm39) missense unknown
R0332:Cfap54 UTSW 10 92,871,319 (GRCm39) missense probably damaging 1.00
R0409:Cfap54 UTSW 10 92,612,075 (GRCm39) missense probably benign 0.00
R0433:Cfap54 UTSW 10 92,814,942 (GRCm39) splice site probably benign
R0436:Cfap54 UTSW 10 92,874,837 (GRCm39) missense possibly damaging 0.95
R0463:Cfap54 UTSW 10 92,710,805 (GRCm39) critical splice donor site probably null
R0523:Cfap54 UTSW 10 92,744,745 (GRCm39) utr 3 prime probably benign
R0551:Cfap54 UTSW 10 92,860,984 (GRCm39) missense probably benign 0.35
R0595:Cfap54 UTSW 10 92,720,598 (GRCm39) missense unknown
R0617:Cfap54 UTSW 10 92,665,512 (GRCm39) splice site probably benign
R0632:Cfap54 UTSW 10 92,720,958 (GRCm39) missense unknown
R0730:Cfap54 UTSW 10 92,870,599 (GRCm39) missense probably benign 0.05
R0786:Cfap54 UTSW 10 92,803,397 (GRCm39) missense possibly damaging 0.72
R0883:Cfap54 UTSW 10 92,706,531 (GRCm39) missense unknown
R1004:Cfap54 UTSW 10 92,902,558 (GRCm39) splice site probably benign
R1033:Cfap54 UTSW 10 92,675,311 (GRCm39) missense probably benign 0.07
R1168:Cfap54 UTSW 10 92,773,782 (GRCm39) missense probably damaging 0.99
R1186:Cfap54 UTSW 10 92,711,856 (GRCm39) missense unknown
R1429:Cfap54 UTSW 10 92,656,900 (GRCm39) missense probably benign 0.01
R1443:Cfap54 UTSW 10 92,768,583 (GRCm39) missense probably damaging 1.00
R1467:Cfap54 UTSW 10 92,805,625 (GRCm39) missense probably benign 0.01
R1467:Cfap54 UTSW 10 92,805,625 (GRCm39) missense probably benign 0.01
R1557:Cfap54 UTSW 10 92,820,089 (GRCm39) missense possibly damaging 0.68
R1687:Cfap54 UTSW 10 92,768,502 (GRCm39) missense probably damaging 1.00
R1690:Cfap54 UTSW 10 92,871,304 (GRCm39) missense possibly damaging 0.95
R1756:Cfap54 UTSW 10 92,883,923 (GRCm39) missense probably damaging 1.00
R1769:Cfap54 UTSW 10 92,740,125 (GRCm39) critical splice donor site probably null
R1835:Cfap54 UTSW 10 92,798,237 (GRCm39) missense probably benign 0.35
R1889:Cfap54 UTSW 10 92,870,572 (GRCm39) missense possibly damaging 0.94
R1915:Cfap54 UTSW 10 92,720,564 (GRCm39) missense unknown
R1958:Cfap54 UTSW 10 92,833,204 (GRCm39) missense probably benign 0.18
R2005:Cfap54 UTSW 10 92,720,630 (GRCm39) missense unknown
R2018:Cfap54 UTSW 10 92,852,466 (GRCm39) missense probably benign 0.00
R2045:Cfap54 UTSW 10 92,874,671 (GRCm39) splice site probably null
R2059:Cfap54 UTSW 10 92,778,841 (GRCm39) unclassified probably benign
R2100:Cfap54 UTSW 10 92,837,799 (GRCm39) missense possibly damaging 0.84
R2110:Cfap54 UTSW 10 92,722,229 (GRCm39) missense unknown
R2392:Cfap54 UTSW 10 92,860,873 (GRCm39) critical splice donor site probably null
R2508:Cfap54 UTSW 10 92,833,236 (GRCm39) missense possibly damaging 0.72
R2852:Cfap54 UTSW 10 92,776,017 (GRCm39) missense probably damaging 1.00
R2857:Cfap54 UTSW 10 92,881,144 (GRCm39) missense probably damaging 0.99
R2871:Cfap54 UTSW 10 92,757,281 (GRCm39) missense possibly damaging 0.86
R2871:Cfap54 UTSW 10 92,757,281 (GRCm39) missense possibly damaging 0.86
R3107:Cfap54 UTSW 10 92,830,545 (GRCm39) missense probably benign 0.04
R3108:Cfap54 UTSW 10 92,830,545 (GRCm39) missense probably benign 0.04
R3157:Cfap54 UTSW 10 92,834,918 (GRCm39) missense probably benign 0.03
R3158:Cfap54 UTSW 10 92,834,918 (GRCm39) missense probably benign 0.03
R3159:Cfap54 UTSW 10 92,834,918 (GRCm39) missense probably benign 0.03
R3161:Cfap54 UTSW 10 92,881,140 (GRCm39) missense probably damaging 1.00
R3162:Cfap54 UTSW 10 92,881,140 (GRCm39) missense probably damaging 1.00
R3162:Cfap54 UTSW 10 92,881,140 (GRCm39) missense probably damaging 1.00
R3508:Cfap54 UTSW 10 92,721,286 (GRCm39) missense unknown
R3730:Cfap54 UTSW 10 92,847,335 (GRCm39) nonsense probably null
R3770:Cfap54 UTSW 10 92,714,398 (GRCm39) missense unknown
R3776:Cfap54 UTSW 10 92,880,962 (GRCm39) missense probably damaging 1.00
R3778:Cfap54 UTSW 10 92,740,206 (GRCm39) utr 3 prime probably benign
R3795:Cfap54 UTSW 10 92,778,735 (GRCm39) unclassified probably benign
R3834:Cfap54 UTSW 10 92,636,985 (GRCm39) splice site probably benign
R3891:Cfap54 UTSW 10 92,874,708 (GRCm39) missense possibly damaging 0.87
R3932:Cfap54 UTSW 10 92,665,619 (GRCm39) missense probably benign 0.03
R3973:Cfap54 UTSW 10 92,675,333 (GRCm39) missense possibly damaging 0.95
R3974:Cfap54 UTSW 10 92,675,333 (GRCm39) missense possibly damaging 0.95
R3976:Cfap54 UTSW 10 92,675,333 (GRCm39) missense possibly damaging 0.95
R3978:Cfap54 UTSW 10 92,798,274 (GRCm39) missense probably benign 0.01
R4190:Cfap54 UTSW 10 92,720,885 (GRCm39) missense unknown
R4389:Cfap54 UTSW 10 92,803,362 (GRCm39) missense probably benign 0.37
R4542:Cfap54 UTSW 10 92,860,991 (GRCm39) missense probably benign 0.12
R4564:Cfap54 UTSW 10 92,675,402 (GRCm39) unclassified probably benign
R4576:Cfap54 UTSW 10 92,879,090 (GRCm39) critical splice donor site probably null
R4620:Cfap54 UTSW 10 92,805,619 (GRCm39) missense probably benign 0.01
R4714:Cfap54 UTSW 10 92,651,780 (GRCm39) missense probably benign 0.01
R4762:Cfap54 UTSW 10 92,897,315 (GRCm39) splice site probably null
R4776:Cfap54 UTSW 10 92,808,556 (GRCm39) missense possibly damaging 0.96
R4819:Cfap54 UTSW 10 92,672,339 (GRCm39) nonsense probably null
R4827:Cfap54 UTSW 10 92,737,937 (GRCm39) utr 3 prime probably benign
R4832:Cfap54 UTSW 10 92,803,390 (GRCm39) missense probably benign 0.01
R4965:Cfap54 UTSW 10 92,902,661 (GRCm39) missense probably benign 0.23
R5001:Cfap54 UTSW 10 92,800,396 (GRCm39) missense probably benign 0.01
R5060:Cfap54 UTSW 10 92,875,013 (GRCm39) missense probably damaging 1.00
R5067:Cfap54 UTSW 10 92,902,628 (GRCm39) missense probably benign 0.17
R5069:Cfap54 UTSW 10 92,773,636 (GRCm39) missense probably benign
R5094:Cfap54 UTSW 10 92,734,861 (GRCm39) utr 3 prime probably benign
R5109:Cfap54 UTSW 10 92,773,753 (GRCm39) missense probably benign 0.03
R5127:Cfap54 UTSW 10 92,722,249 (GRCm39) splice site probably null
R5143:Cfap54 UTSW 10 92,865,020 (GRCm39) missense possibly damaging 0.73
R5147:Cfap54 UTSW 10 92,773,700 (GRCm39) missense probably benign 0.00
R5158:Cfap54 UTSW 10 92,901,059 (GRCm39) missense probably damaging 1.00
R5256:Cfap54 UTSW 10 92,880,885 (GRCm39) splice site probably null
R5256:Cfap54 UTSW 10 92,770,953 (GRCm39) nonsense probably null
R5266:Cfap54 UTSW 10 92,651,764 (GRCm39) missense probably benign 0.16
R5304:Cfap54 UTSW 10 92,656,968 (GRCm39) missense probably damaging 0.97
R5369:Cfap54 UTSW 10 92,897,119 (GRCm39) intron probably benign
R5406:Cfap54 UTSW 10 92,837,720 (GRCm39) missense probably benign 0.33
R5471:Cfap54 UTSW 10 92,864,522 (GRCm39) missense probably damaging 1.00
R5485:Cfap54 UTSW 10 92,864,979 (GRCm39) missense probably damaging 1.00
R5540:Cfap54 UTSW 10 92,808,470 (GRCm39) missense possibly damaging 0.85
R5586:Cfap54 UTSW 10 92,808,473 (GRCm39) nonsense probably null
R5614:Cfap54 UTSW 10 92,880,911 (GRCm39) missense probably damaging 1.00
R5634:Cfap54 UTSW 10 92,740,125 (GRCm39) critical splice donor site probably benign
R5680:Cfap54 UTSW 10 92,814,879 (GRCm39) nonsense probably null
R5797:Cfap54 UTSW 10 92,803,438 (GRCm39) missense probably benign 0.11
R5859:Cfap54 UTSW 10 92,852,386 (GRCm39) nonsense probably null
R5878:Cfap54 UTSW 10 92,800,423 (GRCm39) missense probably benign 0.01
R5910:Cfap54 UTSW 10 92,901,043 (GRCm39) missense probably damaging 0.99
R5936:Cfap54 UTSW 10 92,798,274 (GRCm39) missense probably benign 0.01
R5994:Cfap54 UTSW 10 92,874,943 (GRCm39) missense probably damaging 0.99
R6080:Cfap54 UTSW 10 92,881,197 (GRCm39) missense possibly damaging 0.64
R6268:Cfap54 UTSW 10 92,874,771 (GRCm39) missense probably damaging 1.00
R6296:Cfap54 UTSW 10 92,902,708 (GRCm39) missense probably damaging 1.00
R6409:Cfap54 UTSW 10 92,803,354 (GRCm39) missense probably benign 0.04
R6545:Cfap54 UTSW 10 92,672,319 (GRCm39) missense probably benign 0.31
R6570:Cfap54 UTSW 10 92,651,820 (GRCm39) missense unknown
R6597:Cfap54 UTSW 10 92,834,902 (GRCm39) missense possibly damaging 0.85
R6702:Cfap54 UTSW 10 92,704,596 (GRCm39) missense unknown
R6703:Cfap54 UTSW 10 92,704,596 (GRCm39) missense unknown
R6720:Cfap54 UTSW 10 92,656,981 (GRCm39) missense probably benign 0.07
R6841:Cfap54 UTSW 10 92,710,877 (GRCm39) missense unknown
R6910:Cfap54 UTSW 10 92,672,374 (GRCm39) missense probably benign 0.29
R6953:Cfap54 UTSW 10 92,830,540 (GRCm39) missense probably benign 0.19
R7009:Cfap54 UTSW 10 92,710,881 (GRCm39) missense unknown
R7129:Cfap54 UTSW 10 92,852,433 (GRCm39) missense probably benign 0.06
R7131:Cfap54 UTSW 10 92,656,966 (GRCm39) missense probably benign 0.03
R7171:Cfap54 UTSW 10 92,612,072 (GRCm39) missense probably damaging 0.99
R7189:Cfap54 UTSW 10 92,773,590 (GRCm39) missense unknown
R7225:Cfap54 UTSW 10 92,740,236 (GRCm39) missense unknown
R7270:Cfap54 UTSW 10 92,675,320 (GRCm39) missense probably benign 0.03
R7323:Cfap54 UTSW 10 92,637,000 (GRCm39) missense probably benign 0.00
R7380:Cfap54 UTSW 10 92,883,840 (GRCm39) missense probably damaging 1.00
R7395:Cfap54 UTSW 10 92,720,565 (GRCm39) missense unknown
R7411:Cfap54 UTSW 10 92,704,617 (GRCm39) missense unknown
R7503:Cfap54 UTSW 10 92,723,298 (GRCm39) splice site probably null
R7622:Cfap54 UTSW 10 92,792,806 (GRCm39) missense unknown
R7679:Cfap54 UTSW 10 92,803,374 (GRCm39) missense probably benign 0.01
R7776:Cfap54 UTSW 10 92,704,603 (GRCm39) missense unknown
R7844:Cfap54 UTSW 10 92,737,920 (GRCm39) missense unknown
R7980:Cfap54 UTSW 10 92,817,922 (GRCm39) missense possibly damaging 0.95
R7988:Cfap54 UTSW 10 92,737,941 (GRCm39) missense unknown
R8101:Cfap54 UTSW 10 92,720,658 (GRCm39) missense unknown
R8119:Cfap54 UTSW 10 92,704,672 (GRCm39) missense unknown
R8134:Cfap54 UTSW 10 92,714,378 (GRCm39) missense unknown
R8168:Cfap54 UTSW 10 92,744,739 (GRCm39) missense unknown
R8179:Cfap54 UTSW 10 92,833,178 (GRCm39) missense possibly damaging 0.68
R8392:Cfap54 UTSW 10 92,798,279 (GRCm39) missense unknown
R8436:Cfap54 UTSW 10 92,800,398 (GRCm39) missense unknown
R8505:Cfap54 UTSW 10 92,814,855 (GRCm39) missense probably benign 0.03
R8671:Cfap54 UTSW 10 92,790,934 (GRCm39) missense unknown
R8716:Cfap54 UTSW 10 92,800,494 (GRCm39) missense probably benign 0.00
R8816:Cfap54 UTSW 10 92,714,454 (GRCm39) missense unknown
R8822:Cfap54 UTSW 10 92,875,003 (GRCm39) missense probably benign 0.09
R8827:Cfap54 UTSW 10 92,774,110 (GRCm39) missense unknown
R8920:Cfap54 UTSW 10 92,776,199 (GRCm39) critical splice acceptor site probably null
R8924:Cfap54 UTSW 10 92,837,685 (GRCm39) missense probably damaging 0.99
R8954:Cfap54 UTSW 10 92,879,255 (GRCm39) missense probably damaging 1.00
R8963:Cfap54 UTSW 10 92,864,562 (GRCm39) nonsense probably null
R9010:Cfap54 UTSW 10 92,734,921 (GRCm39) missense unknown
R9017:Cfap54 UTSW 10 92,651,883 (GRCm39) missense probably benign 0.07
R9093:Cfap54 UTSW 10 92,651,770 (GRCm39) missense probably benign 0.03
R9095:Cfap54 UTSW 10 92,846,882 (GRCm39) missense probably damaging 1.00
R9142:Cfap54 UTSW 10 92,820,097 (GRCm39) missense possibly damaging 0.87
R9178:Cfap54 UTSW 10 92,830,579 (GRCm39) missense probably benign 0.10
R9196:Cfap54 UTSW 10 92,873,753 (GRCm39) missense probably benign 0.22
R9203:Cfap54 UTSW 10 92,880,990 (GRCm39) missense probably benign 0.30
R9258:Cfap54 UTSW 10 92,770,960 (GRCm39) missense unknown
R9275:Cfap54 UTSW 10 92,875,048 (GRCm39) missense possibly damaging 0.86
R9287:Cfap54 UTSW 10 92,805,565 (GRCm39) missense possibly damaging 0.50
R9289:Cfap54 UTSW 10 92,656,936 (GRCm39) missense possibly damaging 0.83
R9310:Cfap54 UTSW 10 92,798,177 (GRCm39) missense unknown
R9397:Cfap54 UTSW 10 92,833,147 (GRCm39) missense probably damaging 0.96
R9462:Cfap54 UTSW 10 92,737,920 (GRCm39) missense unknown
R9697:Cfap54 UTSW 10 92,792,851 (GRCm39) missense unknown
R9746:Cfap54 UTSW 10 92,637,081 (GRCm39) missense probably benign 0.03
R9755:Cfap54 UTSW 10 92,757,230 (GRCm39) missense unknown
X0022:Cfap54 UTSW 10 92,768,476 (GRCm39) missense probably damaging 1.00
X0022:Cfap54 UTSW 10 92,714,465 (GRCm39) missense unknown
X0027:Cfap54 UTSW 10 92,837,750 (GRCm39) missense possibly damaging 0.86
X0027:Cfap54 UTSW 10 92,714,400 (GRCm39) missense unknown
Z1177:Cfap54 UTSW 10 92,814,888 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GCATTGCCATAGTTCCCAAAACGTC -3'
(R):5'- TTTCCGTTCACAGATACCAGCCG -3'

Sequencing Primer
(F):5'- CTATAGAAGGCAAATTCACTAACGG -3'
(R):5'- CAGATACCAGCCGATGGCAG -3'
Posted On 2014-05-14