Mutagenetix > Incidental Mutation

Incidental Mutation 'R5312:Cfap210'

405625

Institutional Source

Beutler Lab

Gene Symbol

Cfap210

Ensembl Gene

ENSMUSG00000070883

Gene Name

cilia and flagella associated protein 210

Synonyms

4930578N16Rik, 4930525K21Rik, Ccdc173

MMRRC Submission

042895-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.073) question?

Stock #

R5312 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

69588377-69619919 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 69617602 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 60 (T60A)

Ref Sequence

ENSEMBL: ENSMUSP00000092548 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000028494] [ENSMUST00000094942] [ENSMUST00000112266] [ENSMUST00000151298] [ENSMUST00000180290]

AlphaFold

A0JLY1

Predicted Effect

probably benign
Transcript: ENSMUST00000028494

SMART Domains

Protein: ENSMUSP00000028494
Gene: ENSMUSG00000027088

Domain	Start	End	E-Value	Type
Pfam:Put_Phosphatase	3	239	1.2e-98	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000094942
AA Change: T60A

PolyPhen 2 Score 0.918 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000092548
Gene: ENSMUSG00000070883
AA Change: T60A

Domain	Start	End	E-Value	Type
coiled coil region	47	131	N/A	INTRINSIC
Pfam:TPH	142	475	8.9e-22	PFAM
low complexity region	494	508	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000112266

SMART Domains

Protein: ENSMUSP00000107885
Gene: ENSMUSG00000027088

Domain	Start	End	E-Value	Type
Pfam:Put_Phosphatase	3	239	9.3e-99	PFAM
Pfam:HAD_2	5	128	8.9e-7	PFAM
Pfam:HAD	5	187	3.2e-15	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000128765

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000131100

Predicted Effect

probably benign
Transcript: ENSMUST00000151298

SMART Domains

Protein: ENSMUSP00000118021
Gene: ENSMUSG00000027088

Domain	Start	End	E-Value	Type
Pfam:Put_Phosphatase	3	51	2.9e-20	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000180290

SMART Domains

Protein: ENSMUSP00000136471
Gene: ENSMUSG00000027088

Domain	Start	End	E-Value	Type
Pfam:Put_Phosphatase	3	239	9.3e-99	PFAM
Pfam:HAD_2	5	128	8.9e-7	PFAM
Pfam:HAD	5	187	3.2e-15	PFAM

Meta Mutation Damage Score

0.0719

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 97.0%
20x: 94.2%

Validation Efficiency

100% (60/60)

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca15	T	C	7: 119,944,592 (GRCm39)	V409A	probably damaging	Het
Abtb1	A	G	6: 88,815,240 (GRCm39)	F297L	probably damaging	Het
Adam22	C	A	5: 8,140,182 (GRCm39)	G202W	probably damaging	Het
Adgrg3	G	A	8: 95,766,492 (GRCm39)	V388I	probably benign	Het
Adnp	T	C	2: 168,026,108 (GRCm39)	T396A	probably benign	Het
Ank2	T	C	3: 126,753,417 (GRCm39)	Q288R	probably damaging	Het
Bdp1	T	C	13: 100,234,109 (GRCm39)		probably null	Het
Cdc45	C	T	16: 18,614,647 (GRCm39)	R205H	probably damaging	Het
Ceacam23	T	G	7: 17,643,067 (GRCm39)	H492Q	probably damaging	Het
Cntnap5c	A	T	17: 58,666,249 (GRCm39)	E1093V	probably benign	Het
Cplx3	A	T	9: 57,518,360 (GRCm39)	L343Q	probably damaging	Het
Dmrta1	A	C	4: 89,580,284 (GRCm39)	N415H	probably damaging	Het
Dnaaf5	T	A	5: 139,138,617 (GRCm39)	V266E	probably damaging	Het
Dot1l	A	G	10: 80,620,471 (GRCm39)	Q511R	possibly damaging	Het
Ehmt1	A	G	2: 24,774,207 (GRCm39)	V201A	probably damaging	Het
Fancg	A	G	4: 43,003,019 (GRCm39)	F613L	probably benign	Het
Fbxo10	A	T	4: 45,042,036 (GRCm39)	I731N	possibly damaging	Het
Fchsd1	C	T	18: 38,092,926 (GRCm39)		probably benign	Het
Ighv1-74	A	G	12: 115,766,501 (GRCm39)	S39P	probably damaging	Het
Kbtbd11	A	G	8: 15,078,589 (GRCm39)	D396G	possibly damaging	Het
Klc1	A	G	12: 111,762,055 (GRCm39)	K575R	possibly damaging	Het
Mki67	A	T	7: 135,302,559 (GRCm39)	V825E	probably damaging	Het
Mus81	T	C	19: 5,533,522 (GRCm39)	K489R	possibly damaging	Het
Myog	A	G	1: 134,218,064 (GRCm39)	K91E	probably damaging	Het
Nfil3	A	T	13: 53,121,656 (GRCm39)	V416E	probably damaging	Het
Nup160	G	T	2: 90,563,176 (GRCm39)	E1314*	probably null	Het
Nwd2	C	T	5: 63,963,415 (GRCm39)	Q1000*	probably null	Het
Or4g17	T	C	2: 111,210,179 (GRCm39)	V278A	possibly damaging	Het
Or4k35	T	G	2: 111,100,655 (GRCm39)	D19A	probably benign	Het
Or6c66b	A	C	10: 129,377,134 (GRCm39)	M243L	probably benign	Het
Or6c75	T	A	10: 129,337,383 (GRCm39)	V210E	probably damaging	Het
Ppp4r4	T	A	12: 103,573,147 (GRCm39)		probably null	Het
Pramel16	A	T	4: 143,675,665 (GRCm39)	I387N	possibly damaging	Het
Psg27	C	A	7: 18,290,958 (GRCm39)	R415L	probably benign	Het
Ptprr	T	A	10: 116,024,324 (GRCm39)	S212T	probably benign	Het
Ramp3	T	C	11: 6,624,888 (GRCm39)	F61L	probably damaging	Het
Rap1gds1	A	G	3: 138,664,389 (GRCm39)	L322P	probably damaging	Het
Rnf5	A	G	17: 34,820,562 (GRCm39)	F175S	probably benign	Het
Sema4a	G	A	3: 88,344,343 (GRCm39)	S636F	probably damaging	Het
Sfrp2	A	G	3: 83,676,708 (GRCm39)	D193G	probably damaging	Het
Slc26a5	T	C	5: 22,052,258 (GRCm39)	S24G	probably damaging	Het
Slco1a8	A	T	6: 141,918,058 (GRCm39)	F606Y	probably benign	Het
Spg21	A	G	9: 65,376,084 (GRCm39)	I31V	probably benign	Het
Tmem45a2	T	C	16: 56,859,370 (GRCm39)	D287G	possibly damaging	Het
Utrn	A	T	10: 12,603,513 (GRCm39)	D627E	probably damaging	Het
Vmn2r103	A	T	17: 20,013,296 (GRCm39)	N139I	probably benign	Het
Vps35l	T	C	7: 118,412,799 (GRCm39)	I629T	probably damaging	Het
Washc5	A	T	15: 59,217,377 (GRCm39)		probably null	Het
Zfp667	T	C	7: 6,308,466 (GRCm39)	I378T	probably benign	Het
Zfp949	A	C	9: 88,449,236 (GRCm39)	T14P	possibly damaging	Het

Other mutations in Cfap210

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00392:Cfap210	APN	2	69,602,328 (GRCm39)	missense	probably benign
IGL01768:Cfap210	APN	2	69,612,471 (GRCm39)	splice site	probably benign
IGL01801:Cfap210	APN	2	69,606,623 (GRCm39)	splice site	probably benign
R0553:Cfap210	UTSW	2	69,619,785 (GRCm39)	missense	probably damaging	1.00
R1226:Cfap210	UTSW	2	69,617,553 (GRCm39)	missense	possibly damaging	0.63
R1867:Cfap210	UTSW	2	69,612,181 (GRCm39)	splice site	probably null
R4821:Cfap210	UTSW	2	69,612,452 (GRCm39)	missense	possibly damaging	0.76
R5309:Cfap210	UTSW	2	69,617,602 (GRCm39)	missense	possibly damaging	0.92
R5916:Cfap210	UTSW	2	69,619,806 (GRCm39)	start codon destroyed	probably null	0.95
R6072:Cfap210	UTSW	2	69,602,402 (GRCm39)	missense	probably benign	0.31
R6232:Cfap210	UTSW	2	69,602,398 (GRCm39)	missense	possibly damaging	0.64
R6236:Cfap210	UTSW	2	69,588,385 (GRCm39)	splice site	probably null
R6909:Cfap210	UTSW	2	69,612,192 (GRCm39)	splice site	probably null
R7497:Cfap210	UTSW	2	69,588,792 (GRCm39)	missense	probably benign	0.04
R7502:Cfap210	UTSW	2	69,606,488 (GRCm39)	missense	probably benign
R7786:Cfap210	UTSW	2	69,612,092 (GRCm39)	missense	probably damaging	1.00
R7934:Cfap210	UTSW	2	69,612,450 (GRCm39)	nonsense	probably null
R8316:Cfap210	UTSW	2	69,612,287 (GRCm39)	critical splice donor site	probably null
R8905:Cfap210	UTSW	2	69,612,104 (GRCm39)	missense	probably benign	0.01
R8977:Cfap210	UTSW	2	69,617,643 (GRCm39)	missense	possibly damaging	0.55
R9117:Cfap210	UTSW	2	69,612,103 (GRCm39)	nonsense	probably null
R9163:Cfap210	UTSW	2	69,606,510 (GRCm39)	missense	probably benign	0.13

Predicted Primers

PCR Primer
(F):5'- TACCAGGTATAAGGCACTACTCAG -3'
(R):5'- GCCAATCTTAAGTTACACATTTGAGGC -3'

Sequencing Primer
(F):5'- GCACTACTCAGAAGCAGCAGTTATTG -3'
(R):5'- AAGTCAGGTGAACTCTTCCTG -3'

Posted On

2016-07-22