Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03201:Ccdc181'

412983

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Ccdc181

Ensembl Gene

ENSMUSG00000026578

Gene Name

coiled-coil domain containing 181

Synonyms

4930455F23Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL03201

Quality Score

Status

Chromosome

Chromosomal Location

164103154-164115416 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 164108213 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Aspartic acid at position 299 (N299D)

Ref Sequence

ENSEMBL: ENSMUSP00000027867 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000027867]

AlphaFold

Q80ZU5

Predicted Effect

probably benign
Transcript: ENSMUST00000027867
AA Change: N299D

PolyPhen 2 Score 0.128 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000027867
Gene: ENSMUSG00000026578
AA Change: N299D

Domain	Start	End	E-Value	Type
low complexity region	116	122	N/A	INTRINSIC
coiled coil region	334	378	N/A	INTRINSIC
low complexity region	474	485	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A4galt	T	C	15: 83,112,468 (GRCm39)	E105G	probably damaging	Het
Apc	A	G	18: 34,445,429 (GRCm39)	D757G	probably damaging	Het
Arpc3	A	T	5: 122,539,781 (GRCm39)	I45F	probably damaging	Het
C3	C	A	17: 57,529,249 (GRCm39)	V597L	probably damaging	Het
Cdr1	T	A	X: 60,229,154 (GRCm39)	Q4L	unknown	Het
Cep170	G	A	1: 176,564,454 (GRCm39)	S1464F	probably damaging	Het
Cfh	A	G	1: 140,030,557 (GRCm39)	Y826H	probably damaging	Het
Chic2	A	G	5: 75,171,954 (GRCm39)		probably benign	Het
Chrne	T	C	11: 70,509,338 (GRCm39)	H81R	probably benign	Het
Clec4e	A	G	6: 123,260,599 (GRCm39)	I153T	probably benign	Het
Col14a1	A	T	15: 55,272,300 (GRCm39)	D699V	unknown	Het
Cul3	T	G	1: 80,259,144 (GRCm39)	S379R	probably damaging	Het
Cyp3a11	T	A	5: 145,797,189 (GRCm39)	I397F	possibly damaging	Het
Dnah1	T	C	14: 31,022,906 (GRCm39)	K1077R	probably benign	Het
Dnajc18	A	G	18: 35,813,972 (GRCm39)	S266P	probably benign	Het
Dydc1	T	G	14: 40,800,647 (GRCm39)	L74R	probably damaging	Het
Echdc2	G	T	4: 108,027,067 (GRCm39)	A71S	possibly damaging	Het
Fer1l4	T	A	2: 155,886,650 (GRCm39)	D693V	probably benign	Het
Fscn3	T	C	6: 28,430,604 (GRCm39)	V258A	probably benign	Het
Herc2	T	A	7: 55,869,516 (GRCm39)	I4255N	probably damaging	Het
Il1rl2	A	G	1: 40,382,200 (GRCm39)	I171V	possibly damaging	Het
Ino80d	G	T	1: 63,097,467 (GRCm39)	T809K	probably damaging	Het
Lama2	A	T	10: 27,220,566 (GRCm39)	L433*	probably null	Het
Nlrp9c	A	T	7: 26,084,533 (GRCm39)	S349T	probably benign	Het
Parp11	T	C	6: 127,466,981 (GRCm39)	I124T	possibly damaging	Het
Parp8	A	T	13: 116,999,605 (GRCm39)		probably benign	Het
Pgm1	T	C	4: 99,827,236 (GRCm39)	F379L	probably damaging	Het
Phf21b	T	C	15: 84,671,448 (GRCm39)	H482R	probably benign	Het
Phka1	A	C	X: 101,584,716 (GRCm39)		probably null	Het
Plekhh1	T	C	12: 79,100,430 (GRCm39)	W133R	probably damaging	Het
Polr2a	A	C	11: 69,636,516 (GRCm39)	L405*	probably null	Het
Prrg3	T	A	X: 71,010,108 (GRCm39)	V3E	probably damaging	Het
Pth1r	T	C	9: 110,551,648 (GRCm39)	K484E	probably damaging	Het
Rcbtb1	T	C	14: 59,460,727 (GRCm39)	L230P	probably damaging	Het
Slc51a	G	A	16: 32,297,568 (GRCm39)	R110C	probably damaging	Het
Ssbp2	T	C	13: 91,672,720 (GRCm39)	Y27H	probably damaging	Het
Sult2a4	A	G	7: 13,665,692 (GRCm39)	V157A	probably damaging	Het
Tbx15	G	A	3: 99,259,296 (GRCm39)	S389N	probably benign	Het
Ttn	T	G	2: 76,671,424 (GRCm39)		probably benign	Het
Ube2n	T	C	10: 95,378,127 (GRCm39)		probably benign	Het
Wdr95	G	A	5: 149,505,352 (GRCm39)		probably null	Het
Wsb2	T	C	5: 117,514,620 (GRCm39)	S298P	possibly damaging	Het
Zc3h7a	T	C	16: 10,974,166 (GRCm39)		probably null	Het
Zfat	A	G	15: 68,037,758 (GRCm39)	C906R	probably damaging	Het
Zfp747	G	A	7: 126,973,180 (GRCm39)	T330I	probably damaging	Het
Zfp949	A	G	9: 88,450,717 (GRCm39)	R96G	probably benign	Het

Other mutations in Ccdc181

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01631:Ccdc181	APN	1	164,107,713 (GRCm39)	missense	possibly damaging	0.75
IGL02634:Ccdc181	APN	1	164,107,514 (GRCm39)	missense	probably benign	0.00
IGL02902:Ccdc181	APN	1	164,107,470 (GRCm39)	missense	probably benign
R1228:Ccdc181	UTSW	1	164,113,960 (GRCm39)	nonsense	probably null
R1371:Ccdc181	UTSW	1	164,108,172 (GRCm39)	missense	probably benign	0.34
R1819:Ccdc181	UTSW	1	164,110,047 (GRCm39)	nonsense	probably null
R2240:Ccdc181	UTSW	1	164,107,596 (GRCm39)	missense	probably damaging	1.00
R3160:Ccdc181	UTSW	1	164,107,865 (GRCm39)	missense	probably damaging	0.97
R3162:Ccdc181	UTSW	1	164,107,865 (GRCm39)	missense	probably damaging	0.97
R4678:Ccdc181	UTSW	1	164,105,846 (GRCm39)	missense	probably damaging	1.00
R5286:Ccdc181	UTSW	1	164,105,810 (GRCm39)	missense	probably damaging	1.00
R6179:Ccdc181	UTSW	1	164,107,487 (GRCm39)	missense	probably benign	0.21
R6886:Ccdc181	UTSW	1	164,107,665 (GRCm39)	missense	probably damaging	0.96
R7517:Ccdc181	UTSW	1	164,107,989 (GRCm39)	missense	probably damaging	1.00
R7528:Ccdc181	UTSW	1	164,107,527 (GRCm39)	missense	probably benign
R9012:Ccdc181	UTSW	1	164,110,062 (GRCm39)	missense	probably damaging	1.00

Posted On

2016-08-02