Mutagenetix > Incidental Mutation

Incidental Mutation 'R0103:Ccdc106'

17881

Institutional Source

Beutler Lab

Gene Symbol

Ccdc106

Ensembl Gene

ENSMUSG00000035228

Gene Name

coiled-coil domain containing 106

Synonyms

MMRRC Submission

038389-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.111) question?

Stock #

R0103 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

5056847-5063784 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 5060544 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Lysine at position 35 (Q35K)

Ref Sequence

ENSEMBL: ENSMUSP00000104211 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000005041] [ENSMUST00000045543] [ENSMUST00000069324] [ENSMUST00000108571] [ENSMUST00000207097] [ENSMUST00000208728] [ENSMUST00000207974] [ENSMUST00000208161] [ENSMUST00000209099] [ENSMUST00000208570] [ENSMUST00000208042] [ENSMUST00000207215]

AlphaFold

Q3ULM0

Predicted Effect

probably benign
Transcript: ENSMUST00000005041

SMART Domains

Protein: ENSMUSP00000005041
Gene: ENSMUSG00000030435

Domain	Start	End	E-Value	Type
low complexity region	23	62	N/A	INTRINSIC
PDB:1JMT\|B	85	112	9e-13	PDB
RRM	150	227	1.26e-11	SMART
low complexity region	242	257	N/A	INTRINSIC
RRM	260	333	8.64e-19	SMART
RRM	377	462	3.04e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000045543

SMART Domains

Protein: ENSMUSP00000041033
Gene: ENSMUSG00000035228

Domain	Start	End	E-Value	Type
coiled coil region	62	101	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000069324

SMART Domains

Protein: ENSMUSP00000065861
Gene: ENSMUSG00000055633

Domain	Start	End	E-Value	Type
low complexity region	2	30	N/A	INTRINSIC
ZnF_C2H2	92	114	3.39e-3	SMART
ZnF_C2H2	120	142	1.18e-2	SMART
ZnF_C2H2	150	172	1.04e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000108571
AA Change: Q35K

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000104211
Gene: ENSMUSG00000035228
AA Change: Q35K

Domain	Start	End	E-Value	Type
Pfam:CCDC106	117	337	1.4e-100	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000123644

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000145534

Predicted Effect

probably benign
Transcript: ENSMUST00000207097

Predicted Effect

probably benign
Transcript: ENSMUST00000208728

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000208606

Predicted Effect

probably benign
Transcript: ENSMUST00000207974

Predicted Effect

probably benign
Transcript: ENSMUST00000208161

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000207960

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000208419

Predicted Effect

probably benign
Transcript: ENSMUST00000209099

Predicted Effect

probably benign
Transcript: ENSMUST00000208570

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000207523

Predicted Effect

probably benign
Transcript: ENSMUST00000208042

Predicted Effect

probably benign
Transcript: ENSMUST00000207215

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000207548

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 89.4%
3x: 86.4%
10x: 77.8%
20x: 63.0%

Validation Efficiency

91% (89/98)

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca13	A	C	11: 9,223,951 (GRCm39)	R443S	probably damaging	Het
Adgrl3	A	G	5: 81,940,194 (GRCm39)		probably benign	Het
Anapc1	T	C	2: 128,522,372 (GRCm39)		probably benign	Het
Aqr	T	A	2: 113,979,497 (GRCm39)	I313F	probably damaging	Het
Arfgap3	A	T	15: 83,206,922 (GRCm39)		probably benign	Het
Asah2	G	T	19: 31,996,377 (GRCm39)	H374N	probably benign	Het
Catspere2	A	G	1: 177,943,771 (GRCm39)	N703D	unknown	Het
Ccm2l	G	T	2: 152,909,839 (GRCm39)	E64*	probably null	Het
Cep85l	A	T	10: 53,154,270 (GRCm39)	D776E	possibly damaging	Het
Cfap52	T	A	11: 67,815,951 (GRCm39)	I611F	possibly damaging	Het
Cldn22	C	T	8: 48,277,589 (GRCm39)	T9M	probably benign	Het
Coa7	T	C	4: 108,195,338 (GRCm39)	L89P	possibly damaging	Het
Cox7a2l	A	T	17: 83,821,701 (GRCm39)	Y2N	probably damaging	Het
Cyp27a1	A	C	1: 74,775,074 (GRCm39)	E301A	probably benign	Het
Dennd4c	A	G	4: 86,730,683 (GRCm39)	Y860C	probably benign	Het
Dhx58	T	C	11: 100,586,096 (GRCm39)	T642A	probably damaging	Het
Dlg4	A	G	11: 69,922,019 (GRCm39)	Y87C	probably damaging	Het
Dnah6	C	T	6: 73,069,155 (GRCm39)	E2511K	probably damaging	Het
Entpd5	C	A	12: 84,443,717 (GRCm39)	E9*	probably null	Het
Fbln2	A	C	6: 91,248,532 (GRCm39)	I1066L	probably benign	Het
Fhl2	C	T	1: 43,192,381 (GRCm39)	R4H	probably benign	Het
Frmpd1	T	A	4: 45,229,884 (GRCm39)	I17K	probably damaging	Het
Gbp7	T	A	3: 142,252,299 (GRCm39)	N627K	probably benign	Het
Gnptab	A	G	10: 88,265,381 (GRCm39)	Y331C	probably damaging	Het
Hibadh	T	A	6: 52,534,862 (GRCm39)	M173L	probably benign	Het
Itga1	T	C	13: 115,152,790 (GRCm39)	I211V	probably benign	Het
Keg1	A	T	19: 12,696,280 (GRCm39)	I155F	possibly damaging	Het
Ltb	A	G	17: 35,414,016 (GRCm39)		probably benign	Het
Manea	A	T	4: 26,329,080 (GRCm39)		probably null	Het
Ms4a4a	T	A	19: 11,370,048 (GRCm39)	M202K	possibly damaging	Het
Myo3a	T	G	2: 22,436,360 (GRCm39)		probably benign	Het
Myo9b	C	T	8: 71,776,493 (GRCm39)		probably benign	Het
Nanos3	C	T	8: 84,902,763 (GRCm39)	R133Q	probably damaging	Het
Ncor1	G	T	11: 62,233,871 (GRCm39)	Q444K	possibly damaging	Het
Nek7	A	T	1: 138,471,980 (GRCm39)	C53*	probably null	Het
Obscn	G	T	11: 58,953,522 (GRCm39)	Y4044*	probably null	Het
Pcsk6	T	C	7: 65,578,845 (GRCm39)		probably benign	Het
Phax	T	A	18: 56,695,785 (GRCm39)	V7D	probably benign	Het
Phxr4	T	C	9: 13,343,087 (GRCm39)		probably benign	Het
Pkhd1	T	A	1: 20,593,583 (GRCm39)	D1510V	probably benign	Het
Pkhd1l1	T	C	15: 44,460,537 (GRCm39)	C4249R	probably benign	Het
Prpf39	T	C	12: 65,102,057 (GRCm39)	V378A	possibly damaging	Het
Psd2	A	G	18: 36,137,770 (GRCm39)	N455S	probably damaging	Het
Ptpro	T	A	6: 137,420,592 (GRCm39)	V1007D	probably damaging	Het
Rab4b	A	G	7: 26,873,927 (GRCm39)	I117T	probably benign	Het
Rad9b	A	T	5: 122,469,590 (GRCm39)	V348E	probably damaging	Het
Rcor1	T	C	12: 111,076,212 (GRCm39)		probably benign	Het
Rhoc	A	T	3: 104,699,307 (GRCm39)	E32V	possibly damaging	Het
Rnf40	T	G	7: 127,199,743 (GRCm39)	V925G	probably damaging	Het
Slc25a32	A	T	15: 38,963,292 (GRCm39)	Y176*	probably null	Het
Slc7a1	T	A	5: 148,289,236 (GRCm39)	K4*	probably null	Het
Taar2	G	A	10: 23,817,393 (GRCm39)	R311H	probably benign	Het
Taar4	A	T	10: 23,837,304 (GRCm39)	N305Y	probably damaging	Het
Tcaf1	G	T	6: 42,663,324 (GRCm39)	D185E	probably benign	Het
Tmem138	T	C	19: 10,552,316 (GRCm39)	N62S	possibly damaging	Het
Tnfrsf25	C	T	4: 152,201,405 (GRCm39)	P65S	possibly damaging	Het
Trp53bp1	A	T	2: 121,067,240 (GRCm39)	S495R	possibly damaging	Het
Trpv3	T	C	11: 73,184,805 (GRCm39)	F597S	probably damaging	Het
Ugt2a3	A	G	5: 87,484,577 (GRCm39)	V149A	possibly damaging	Het
Ush2a	T	G	1: 188,051,267 (GRCm39)	I251R	possibly damaging	Het
Vamp4	T	C	1: 162,417,108 (GRCm39)	C114R	possibly damaging	Het
Zc3h13	T	A	14: 75,567,908 (GRCm39)	V1067E	probably damaging	Het
Zcwpw1	G	A	5: 137,808,375 (GRCm39)	W274*	probably null	Het

Other mutations in Ccdc106

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02028:Ccdc106	APN	7	5,062,645 (GRCm39)	missense	probably damaging	1.00
R0089:Ccdc106	UTSW	7	5,059,220 (GRCm39)	splice site	probably null
R0103:Ccdc106	UTSW	7	5,060,544 (GRCm39)	missense	probably benign
R0440:Ccdc106	UTSW	7	5,063,244 (GRCm39)	missense	probably damaging	1.00
R0705:Ccdc106	UTSW	7	5,062,539 (GRCm39)	missense	possibly damaging	0.92
R0753:Ccdc106	UTSW	7	5,062,539 (GRCm39)	missense	possibly damaging	0.92
R0767:Ccdc106	UTSW	7	5,062,539 (GRCm39)	missense	possibly damaging	0.92
R0769:Ccdc106	UTSW	7	5,062,539 (GRCm39)	missense	possibly damaging	0.92
R0775:Ccdc106	UTSW	7	5,062,539 (GRCm39)	missense	possibly damaging	0.92
R0788:Ccdc106	UTSW	7	5,060,533 (GRCm39)	unclassified	probably benign
R0817:Ccdc106	UTSW	7	5,062,539 (GRCm39)	missense	possibly damaging	0.92
R0818:Ccdc106	UTSW	7	5,062,539 (GRCm39)	missense	possibly damaging	0.92
R0819:Ccdc106	UTSW	7	5,062,539 (GRCm39)	missense	possibly damaging	0.92
R1161:Ccdc106	UTSW	7	5,062,539 (GRCm39)	missense	possibly damaging	0.92
R1451:Ccdc106	UTSW	7	5,062,527 (GRCm39)	missense	probably damaging	1.00
R1962:Ccdc106	UTSW	7	5,062,539 (GRCm39)	missense	possibly damaging	0.92
R4771:Ccdc106	UTSW	7	5,060,521 (GRCm39)	splice site	probably null
R5306:Ccdc106	UTSW	7	5,061,096 (GRCm39)	missense	probably damaging	1.00
R5327:Ccdc106	UTSW	7	5,063,159 (GRCm39)	unclassified	probably benign
R7256:Ccdc106	UTSW	7	5,063,325 (GRCm39)	missense	probably damaging	0.99
R7467:Ccdc106	UTSW	7	5,063,325 (GRCm39)	missense	probably damaging	0.99
R8852:Ccdc106	UTSW	7	5,062,570 (GRCm39)	missense	probably benign	0.03
R8860:Ccdc106	UTSW	7	5,062,570 (GRCm39)	missense	probably benign	0.03
R8959:Ccdc106	UTSW	7	5,060,500 (GRCm39)	missense	probably benign
R9393:Ccdc106	UTSW	7	5,059,200 (GRCm39)	missense	possibly damaging	0.73

Posted On

2013-03-25