Mutagenetix > Incidental Mutation

Incidental Mutation 'R0545:Cfap58'

44800

Institutional Source

Beutler Lab

Gene Symbol

Cfap58

Ensembl Gene

ENSMUSG00000046585

Gene Name

cilia and flagella associated protein 58

Synonyms

LOC381229, Ccdc147

MMRRC Submission

038737-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.094) question?

Stock #

R0545 (G1)

Quality Score

146

Status

Validated

Chromosome

Chromosomal Location

47937712-48035379 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

G to A at 47941097 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000070533 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000066308]

AlphaFold

B2RW38

Predicted Effect

probably benign
Transcript: ENSMUST00000066308

SMART Domains

Protein: ENSMUSP00000070533
Gene: ENSMUSG00000046585

Domain	Start	End	E-Value	Type
coiled coil region	106	579	N/A	INTRINSIC
coiled coil region	642	706	N/A	INTRINSIC
low complexity region	740	762	N/A	INTRINSIC
coiled coil region	772	832	N/A	INTRINSIC

Coding Region Coverage

1x: 99.6%
3x: 98.8%
10x: 96.9%
20x: 94.0%

Validation Efficiency

99% (66/67)

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921504E06Rik	C	T	2: 19,542,376	R76H	probably damaging	Het
4932438A13Rik	G	A	3: 36,987,690		probably benign	Het
Adnp2	T	C	18: 80,129,401	I598V	probably benign	Het
Ago3	T	C	4: 126,417,232	N63D	probably damaging	Het
Alkbh7	C	T	17: 56,999,012	R138*	probably null	Het
Atp6ap1l	T	C	13: 90,883,663	H300R	probably benign	Het
BC051076	C	T	5: 87,963,490		noncoding transcript	Het
Bpifb9a	T	A	2: 154,261,950	C104*	probably null	Het
Cacna2d2	T	C	9: 107,525,223	L826P	probably damaging	Het
Car5b	G	A	X: 163,979,301	R282C	probably damaging	Het
Ccdc88c	T	C	12: 100,947,188	D526G	probably damaging	Het
Cdh23	T	A	10: 60,331,291	T1861S	probably benign	Het
Ces2f	A	C	8: 104,950,036	M121L	possibly damaging	Het
Chpf2	T	C	5: 24,590,324	S282P	possibly damaging	Het
Cluap1	C	T	16: 3,933,772	R332W	probably damaging	Het
Cma2	A	T	14: 55,973,113	M86L	probably benign	Het
Cog6	A	T	3: 52,996,075	M134K	probably damaging	Het
Col1a1	A	G	11: 94,951,594	D1446G	unknown	Het
Cpne8	T	A	15: 90,497,075	D512V	probably damaging	Het
Ctnna2	T	A	6: 77,605,182	N352I	probably damaging	Het
Cyp2c69	A	C	19: 39,886,661	L16R	probably damaging	Het
Dysf	T	C	6: 84,099,461	S603P	probably damaging	Het
Epha5	A	G	5: 84,067,358		probably null	Het
Ercc3	T	C	18: 32,245,902	S270P	probably damaging	Het
F10	T	A	8: 13,048,249	C151S	probably damaging	Het
Gpr180	T	G	14: 118,160,046	H317Q	possibly damaging	Het
Gstp2	T	C	19: 4,041,633	E32G	possibly damaging	Het
Ikzf5	T	C	7: 131,392,500	T133A	possibly damaging	Het
Itch	G	T	2: 155,182,298	G274*	probably null	Het
Jarid2	T	A	13: 44,902,831	N365K	probably benign	Het
Lama3	T	A	18: 12,561,701	S1295T	possibly damaging	Het
Lipc	A	G	9: 70,812,705	L255P	probably damaging	Het
Lrrc38	A	G	4: 143,350,758	D197G	probably benign	Het
Mfap2	A	G	4: 141,014,185		probably benign	Het
Mfhas1	A	G	8: 35,589,048	K226E	probably damaging	Het
Morc1	A	G	16: 48,565,657	R548G	probably benign	Het
Mrgprb5	T	C	7: 48,168,885	N34S	probably benign	Het
Mroh4	T	C	15: 74,625,427	T182A	probably benign	Het
Mylk	G	C	16: 34,879,475	E403Q	possibly damaging	Het
Myo5a	T	C	9: 75,167,037	F743L	possibly damaging	Het
Notch4	A	C	17: 34,583,433	D1276A	probably damaging	Het
Olfr139	A	G	11: 74,045,047	C76R	possibly damaging	Het
Olfr215	T	A	6: 116,582,656	I97L	probably benign	Het
Olfr394	A	T	11: 73,888,017	Y118*	probably null	Het
Olfr799	T	A	10: 129,647,349	C74S	probably damaging	Het
Plin4	T	A	17: 56,106,567	T353S	probably damaging	Het
Ppp1r9a	A	G	6: 5,115,357	T827A	probably benign	Het
Prlr	C	T	15: 10,317,566	T40I	probably damaging	Het
Psme3	T	C	11: 101,319,904		probably benign	Het
Pygb	A	T	2: 150,815,706	D363V	probably benign	Het
Rsph6a	C	T	7: 19,054,946	Q68*	probably null	Het
Serpini2	A	G	3: 75,258,138	V178A	probably benign	Het
Sh2d2a	T	C	3: 87,851,888		probably benign	Het
Skint7	A	C	4: 111,980,198	M58L	probably benign	Het
Slco3a1	G	T	7: 74,320,553	Y435*	probably null	Het
Stk17b	T	C	1: 53,762,583		probably benign	Het
Tinag	T	A	9: 77,031,710	H162L	possibly damaging	Het
Ttc21a	T	A	9: 119,958,799	L811Q	probably damaging	Het
Ttc41	A	T	10: 86,759,097	M912L	probably benign	Het
Vmn2r98	G	T	17: 19,053,613	V41F	probably benign	Het
Washc5	C	T	15: 59,342,093	C838Y	possibly damaging	Het
Wrnip1	A	G	13: 32,806,813	T352A	probably damaging	Het
Zan	A	C	5: 137,396,177	C4467G	unknown	Het
Zc3h7a	T	C	16: 11,152,333		probably benign	Het
Zfp729a	C	A	13: 67,620,226	C628F	probably benign	Het

Other mutations in Cfap58

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01688:Cfap58	APN	19	47974567	missense	probably benign	0.30
IGL02068:Cfap58	APN	19	47986512	missense	probably damaging	1.00
IGL02609:Cfap58	APN	19	47975502	missense	possibly damaging	0.80
IGL03376:Cfap58	APN	19	48034725	missense	possibly damaging	0.60
PIT4515001:Cfap58	UTSW	19	48034683	missense	probably benign
PIT4618001:Cfap58	UTSW	19	47975514	missense	probably damaging	1.00
R0015:Cfap58	UTSW	19	48029100	missense	probably benign	0.45
R0015:Cfap58	UTSW	19	48029100	missense	probably benign	0.45
R0454:Cfap58	UTSW	19	47974680	critical splice donor site	probably null
R0789:Cfap58	UTSW	19	47955309	missense	probably benign	0.09
R0926:Cfap58	UTSW	19	47962562	missense	probably damaging	0.96
R1148:Cfap58	UTSW	19	47988504	missense	probably damaging	0.96
R1148:Cfap58	UTSW	19	47988504	missense	probably damaging	0.96
R1462:Cfap58	UTSW	19	47962430	missense	probably damaging	1.00
R1462:Cfap58	UTSW	19	47962430	missense	probably damaging	1.00
R1493:Cfap58	UTSW	19	47988504	missense	probably damaging	0.96
R1541:Cfap58	UTSW	19	47983530	missense	probably damaging	1.00
R1629:Cfap58	UTSW	19	47941339	missense	probably benign	0.02
R1648:Cfap58	UTSW	19	47955405	missense	probably benign	0.13
R1837:Cfap58	UTSW	19	48029139	missense	probably damaging	0.98
R2307:Cfap58	UTSW	19	47962486	nonsense	probably null
R2513:Cfap58	UTSW	19	47962542	missense	probably benign	0.03
R3802:Cfap58	UTSW	19	47953059	missense	possibly damaging	0.81
R4233:Cfap58	UTSW	19	47975555	missense	possibly damaging	0.60
R4258:Cfap58	UTSW	19	47949484	splice site	probably null
R4414:Cfap58	UTSW	19	47953041	missense	possibly damaging	0.87
R4763:Cfap58	UTSW	19	47983506	missense	probably damaging	1.00
R5300:Cfap58	UTSW	19	47941156	missense	probably benign	0.09
R5406:Cfap58	UTSW	19	48029102	missense	possibly damaging	0.81
R5497:Cfap58	UTSW	19	48029109	missense	probably benign	0.08
R5635:Cfap58	UTSW	19	47983542	missense	possibly damaging	0.47
R6315:Cfap58	UTSW	19	47941277	missense	probably benign	0.40
R6483:Cfap58	UTSW	19	47983452	missense	probably benign	0.00
R6727:Cfap58	UTSW	19	47955417	missense	probably benign	0.30
R6896:Cfap58	UTSW	19	47944187	missense	probably damaging	0.98
R7461:Cfap58	UTSW	19	47982122	missense	possibly damaging	0.70
R7473:Cfap58	UTSW	19	47974625	nonsense	probably null
R7613:Cfap58	UTSW	19	47982122	missense	possibly damaging	0.70
R7650:Cfap58	UTSW	19	47986528	missense	possibly damaging	0.84
R7982:Cfap58	UTSW	19	47974567	missense	probably benign	0.30
R8083:Cfap58	UTSW	19	47983518	missense	probably damaging	1.00
R8121:Cfap58	UTSW	19	48029104	missense	probably benign	0.40
R8321:Cfap58	UTSW	19	47958147	missense	probably damaging	0.99
R8396:Cfap58	UTSW	19	48029101	missense	probably damaging	1.00
R8462:Cfap58	UTSW	19	47983650	missense	possibly damaging	0.94
R8745:Cfap58	UTSW	19	47941114	nonsense	probably null
R8805:Cfap58	UTSW	19	47953096	missense	probably damaging	0.99
R9049:Cfap58	UTSW	19	48026718	critical splice acceptor site	probably null
R9142:Cfap58	UTSW	19	47986554	critical splice donor site	probably null
R9358:Cfap58	UTSW	19	47974548	nonsense	probably null
R9709:Cfap58	UTSW	19	47975553	missense	probably damaging	1.00
X0067:Cfap58	UTSW	19	47955308	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TGAGGTCGAGGGAACCTTTCCAAC -3'
(R):5'- AGTTCACCACAATCTCTGCGTTCAG -3'

Sequencing Primer
(F):5'- AGGGAACCTTTCCAACATGTAG -3'
(R):5'- ATGAGACGCTTCTCATTCTCGTAAG -3'

Posted On

2013-06-11