Mutagenetix > Incidental Mutation

Incidental Mutation 'RF005:Ccdc69'

602771

Institutional Source

Beutler Lab

Gene Symbol

Ccdc69

Ensembl Gene

ENSMUSG00000049588

Gene Name

coiled-coil domain containing 69

Synonyms

D11Ertd461e, 2210021E03Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

RF005 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

54940557-54968957 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 54951349 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Proline at position 24 (L24P)

Ref Sequence

ENSEMBL: ENSMUSP00000054840 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000055040] [ENSMUST00000108880]

AlphaFold

Q3TCJ8

Predicted Effect

probably damaging
Transcript: ENSMUST00000055040
AA Change: L24P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000054840
Gene: ENSMUSG00000049588
AA Change: L24P

Domain	Start	End	E-Value	Type
coiled coil region	112	142	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000108880
AA Change: L24P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000104508
Gene: ENSMUSG00000049588
AA Change: L24P

Domain	Start	End	E-Value	Type
coiled coil region	112	142	N/A	INTRINSIC

Meta Mutation Damage Score

0.1962

Coding Region Coverage

1x: 99.8%
3x: 99.7%
10x: 99.4%
20x: 98.6%

Validation Efficiency

94% (65/69)

Allele List at MGI

Other mutations in this stock

Total: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5430401F13Rik	AGAAAGGAAAAGGTGGCCAG	AGAAAGGAAAAGGTGGCCAGCAAAAACAGAAAGGAAAAGGTGGCCAG	6: 131,529,847 (GRCm39)		probably benign	Het
A030005L19Rik	CTGCTG	CTGCTGTGGATGCTG	1: 82,891,306 (GRCm39)		probably benign	Het
Abca1	G	T	4: 53,049,125 (GRCm39)	T1651N	probably damaging	Het
Adamtsl3	A	G	7: 82,261,603 (GRCm39)	T40A		Het
Adgra3	A	T	5: 50,170,729 (GRCm39)		probably null	Het
Apcs	A	T	1: 172,721,809 (GRCm39)	M179K	probably damaging	Het
Baiap2	G	A	11: 119,887,355 (GRCm39)	E217K	possibly damaging	Het
Bltp3a	A	T	17: 28,104,505 (GRCm39)	D517V	probably damaging	Het
Cdh16	T	G	8: 105,343,684 (GRCm39)	N604T	probably damaging	Het
Cfb	C	T	17: 35,077,022 (GRCm39)	V538I	possibly damaging	Het
Col6a3	A	G	1: 90,738,984 (GRCm39)	S1022P	probably benign	Het
Cpeb1	A	G	7: 81,011,554 (GRCm39)	L129S	possibly damaging	Het
Crybg1	A	G	10: 43,880,741 (GRCm39)	V149A	probably benign	Het
Cyp4f16	C	A	17: 32,764,169 (GRCm39)		probably null	Het
Dlg5	G	A	14: 24,208,561 (GRCm39)	Q882*	probably null	Het
Fsip2	T	A	2: 82,822,876 (GRCm39)	I6203K	probably benign	Het
Gabre	CCGGCT	CCGGCTACGGCT	X: 71,313,651 (GRCm39)		probably null	Het
Gprc5d	A	T	6: 135,093,517 (GRCm39)	L130Q	probably damaging	Het
H13	G	A	2: 152,511,589 (GRCm39)	E30K	probably damaging	Het
Hmcn1	T	A	1: 150,510,897 (GRCm39)	K3609*	probably null	Het
Hsdl2	GCTGCAG	GCTGCAGCAGCAGCCACATCTGCAG	4: 59,610,652 (GRCm39)		probably benign	Het
Kl	A	C	5: 150,876,885 (GRCm39)	Y235S	probably benign	Het
Map6d1	G	A	16: 20,059,750 (GRCm39)	T105I	probably benign	Het
Mast4	GGTGGTGGTGG	GGTGGTGGTGGTGGTGG	13: 102,872,815 (GRCm39)		probably benign	Het
Mbd1	TGTCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGC	TATCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGC	18: 74,406,644 (GRCm39)		probably benign	Het
Mms22l	A	G	4: 24,517,207 (GRCm39)	I363V	probably benign	Het
Myo7a	T	C	7: 97,742,824 (GRCm39)	I391V	probably benign	Het
Nab2	A	T	10: 127,500,233 (GRCm39)	D286E	probably benign	Het
Nrxn1	G	A	17: 90,670,304 (GRCm39)	R1144C	probably damaging	Het
Or51q1	A	G	7: 103,628,768 (GRCm39)	D123G	probably damaging	Het
Or52j3	T	C	7: 102,835,898 (GRCm39)	I30T	possibly damaging	Het
Or5al5	T	C	2: 85,961,414 (GRCm39)	M198V	probably benign	Het
Pan2	G	A	10: 128,151,404 (GRCm39)	E842K	probably benign	Het
Pate11	T	C	9: 36,386,970 (GRCm39)	S13P	possibly damaging	Het
Polr1has	CACCACCACCACCACCACCAC	CACCACCACCACCACCACCACAACCACCACCACCACCACCAC	17: 37,275,940 (GRCm39)		probably benign	Het
Prex2	A	C	1: 11,255,390 (GRCm39)	D1145A	possibly damaging	Het
Prop1	A	C	11: 50,841,957 (GRCm39)	Y150D	possibly damaging	Het
Prp2	AGGCCCACAGCAGCGACCCCCTCAAGGCCCACCACCACCAGGTGGCCCACAGCCGAGACCCCCTCAAGGCCCACCACC	AGGCCCACAGCCGAGACCCCCTCAAGGCCCACCACC	6: 132,577,464 (GRCm39)		probably benign	Het
Psip1	T	C	4: 83,378,735 (GRCm39)	I353M	probably damaging	Het
Rapgef1	C	A	2: 29,597,207 (GRCm39)		probably null	Het
Rgl1	G	A	1: 152,397,114 (GRCm39)	S684L	probably benign	Het
Sbf2	T	A	7: 109,916,215 (GRCm39)	D1552V	probably damaging	Het
Scpppq1	A	C	5: 104,222,725 (GRCm39)		probably null	Het
Serpinh1	C	T	7: 98,995,410 (GRCm39)	V391M	probably damaging	Het
Slc35e4	A	T	11: 3,857,960 (GRCm39)	L215Q	possibly damaging	Het
Tbl3	TCTT	TCTTCTT	17: 24,921,515 (GRCm39)		probably benign	Het
Tex15	T	A	8: 34,066,705 (GRCm39)	M2045K	probably benign	Het
Tmprss15	T	C	16: 78,750,689 (GRCm39)	*1070W	probably null	Het
Trav15-2-dv6-2	GAA	GAACAA	14: 53,887,211 (GRCm39)		probably benign	Het
Trav15-2-dv6-2	GGGAG	GGGAGGAG	14: 53,887,207 (GRCm39)		probably benign	Het
Trav15-2-dv6-2	GGAG	GGAGGAG	14: 53,887,208 (GRCm39)		probably benign	Het
Trim33	GCCCCGGCCCCCG	GCCCCG	3: 103,187,528 (GRCm39)		probably null	Het
Triobp	GACAA	GACAACCCCAGGACTCCCTGTGCCCAACGGAACAA	15: 78,851,261 (GRCm39)		probably benign	Het
Tub	C	A	7: 108,621,846 (GRCm39)	Q95K	probably benign	Het
Usp9y	T	A	Y: 1,435,046 (GRCm39)	Q261L	probably benign	Het
Utp20	A	T	10: 88,661,319 (GRCm39)	D29E	probably damaging	Het
Vill	G	A	9: 118,889,507 (GRCm39)	V148M	probably damaging	Het
Vmn2r120	C	T	17: 57,828,991 (GRCm39)	E535K	possibly damaging	Het
Zfp451	A	T	1: 33,815,873 (GRCm39)	Y692*	probably null	Het
Zfp599	A	C	9: 22,165,180 (GRCm39)	V65G	probably benign	Het
Zfp808	T	C	13: 62,319,113 (GRCm39)	V114A	probably benign	Het

Other mutations in Ccdc69

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02656:Ccdc69	APN	11	54,943,263 (GRCm39)	missense	possibly damaging	0.85
R0140:Ccdc69	UTSW	11	54,941,325 (GRCm39)	missense	possibly damaging	0.83
R0433:Ccdc69	UTSW	11	54,943,716 (GRCm39)	splice site	probably null
R1334:Ccdc69	UTSW	11	54,943,805 (GRCm39)	missense	probably damaging	0.96
R1749:Ccdc69	UTSW	11	54,941,979 (GRCm39)	missense	probably null	1.00
R2013:Ccdc69	UTSW	11	54,941,983 (GRCm39)	missense	probably benign	0.03
R2082:Ccdc69	UTSW	11	54,943,215 (GRCm39)	missense	probably damaging	1.00
R5176:Ccdc69	UTSW	11	54,951,296 (GRCm39)	missense	probably benign	0.00
R5191:Ccdc69	UTSW	11	54,943,719 (GRCm39)	critical splice donor site	probably null
R5768:Ccdc69	UTSW	11	54,945,856 (GRCm39)	missense	possibly damaging	0.81
R5896:Ccdc69	UTSW	11	54,943,716 (GRCm39)	splice site	probably null
R7476:Ccdc69	UTSW	11	54,942,024 (GRCm39)	missense	possibly damaging	0.89
R9489:Ccdc69	UTSW	11	54,945,856 (GRCm39)	missense	possibly damaging	0.81
RF024:Ccdc69	UTSW	11	54,951,349 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GGTAGACTTCCAGGAGATGC -3'
(R):5'- ACTTGCTATGGCTCAGAGGG -3'

Sequencing Primer
(F):5'- CTTCCAGGAGATGCTTTCAAAAGG -3'
(R):5'- GGGTTTCTGCCCTGGCTC -3'

Posted On

2019-12-04