Mutagenetix > Incidental Mutation

Incidental Mutation 'R4979:Ccdc80'

384706

Institutional Source

Beutler Lab

Gene Symbol

Ccdc80

Ensembl Gene

ENSMUSG00000022665

Gene Name

coiled-coil domain containing 80

Synonyms

DRO1, Urb, Ssg1, 2610001E17Rik

MMRRC Submission

042574-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.082) question?

Stock #

R4979 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

44913770-44948287 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 44936650 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Methionine at position 692 (V692M)

Ref Sequence

ENSEMBL: ENSMUSP00000097097 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000061050] [ENSMUST00000099498]

AlphaFold

Q8R2G6

Predicted Effect

possibly damaging
Transcript: ENSMUST00000061050
AA Change: V692M

PolyPhen 2 Score 0.896 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000058752
Gene: ENSMUSG00000022665
AA Change: V692M

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
Pfam:DUF4174	141	270	2.2e-31	PFAM
low complexity region	294	308	N/A	INTRINSIC
low complexity region	335	380	N/A	INTRINSIC
low complexity region	482	497	N/A	INTRINSIC
coiled coil region	554	587	N/A	INTRINSIC
Pfam:DUF4174	614	748	3.1e-36	PFAM
Pfam:DUF4174	770	901	2.1e-36	PFAM
low complexity region	917	940	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000099498
AA Change: V692M

PolyPhen 2 Score 0.896 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000097097
Gene: ENSMUSG00000022665
AA Change: V692M

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
Pfam:DUF4174	140	271	8.9e-34	PFAM
low complexity region	294	308	N/A	INTRINSIC
low complexity region	335	380	N/A	INTRINSIC
low complexity region	482	497	N/A	INTRINSIC
coiled coil region	554	587	N/A	INTRINSIC
Pfam:DUF4174	613	749	1.4e-21	PFAM
Pfam:DUF4174	769	902	3.5e-39	PFAM
low complexity region	917	940	N/A	INTRINSIC

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.2%
3x: 98.4%
10x: 96.7%
20x: 93.4%

Validation Efficiency

99% (79/80)

MGI Phenotype

PHENOTYPE: Mice homozygous for a null allele exhibit increased adiposity, hyperglycemia, glucose intolerance, impaired insulin secretion, and altered energy intake and expenditure when fed a high-fat diet. Mice homozygous for a different null allele develop thyroid adenomas and ovarian carcinomas. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700010I14Rik	G	A	17: 9,220,643 (GRCm39)	E381K	probably damaging	Het
Abca1	T	C	4: 53,085,092 (GRCm39)		probably null	Het
Abca7	C	T	10: 79,840,617 (GRCm39)	Q870*	probably null	Het
Ambp	C	T	4: 63,070,888 (GRCm39)	V64M	probably benign	Het
Ank1	T	C	8: 23,622,212 (GRCm39)	V1542A	probably damaging	Het
Anln	T	C	9: 22,287,797 (GRCm39)	Y168C	probably benign	Het
Apoa4	T	A	9: 46,152,803 (GRCm39)	N29K	probably benign	Het
Arfgef1	T	C	1: 10,283,334 (GRCm39)	T192A	probably damaging	Het
Atad2b	G	T	12: 5,084,513 (GRCm39)	D1420Y	probably damaging	Het
Baiap3	A	G	17: 25,465,336 (GRCm39)	W648R	possibly damaging	Het
Bank1	A	G	3: 135,960,662 (GRCm39)	L198P	probably damaging	Het
Bicd2	A	G	13: 49,532,940 (GRCm39)	K509E	possibly damaging	Het
Cacna1e	T	C	1: 154,289,739 (GRCm39)	D1821G	probably damaging	Het
Ccdc88a	C	T	11: 29,432,133 (GRCm39)	Q308*	probably null	Het
Ccl8	T	C	11: 82,006,973 (GRCm39)	V62A	probably damaging	Het
Clspn	C	A	4: 126,472,179 (GRCm39)	P951Q	probably damaging	Het
Cngb1	T	A	8: 95,985,785 (GRCm39)	I858F	probably damaging	Het
Cspp1	T	A	1: 10,196,688 (GRCm39)	N900K	probably damaging	Het
Ctc1	C	T	11: 68,924,328 (GRCm39)	A960V	probably damaging	Het
Ctnnd2	A	G	15: 31,009,221 (GRCm39)	E1106G	probably damaging	Het
Dido1	C	T	2: 180,302,606 (GRCm39)	R1766H	probably damaging	Het
Dipk1a	A	T	5: 108,057,400 (GRCm39)	L386*	probably null	Het
Dnajc13	G	T	9: 104,063,922 (GRCm39)	N1341K	probably damaging	Het
Dnase1l1	C	T	X: 73,320,644 (GRCm39)		probably null	Homo
E2f8	G	A	7: 48,524,918 (GRCm39)		probably benign	Het
Entpd8	A	G	2: 24,972,967 (GRCm39)	D91G	possibly damaging	Het
Fars2	A	G	13: 36,388,564 (GRCm39)	R18G	possibly damaging	Het
Fcgbp	A	G	7: 27,816,995 (GRCm39)	S2486G	probably benign	Het
Fibin	C	T	2: 110,192,963 (GRCm39)	D60N	possibly damaging	Het
Fpgs	A	G	2: 32,577,379 (GRCm39)		probably benign	Het
Galnt15	A	G	14: 31,765,247 (GRCm39)	D303G	probably damaging	Het
Gli3	C	A	13: 15,899,049 (GRCm39)	T812K	possibly damaging	Het
Gpbar1	G	C	1: 74,318,404 (GRCm39)	A216P	probably benign	Het
Grin2d	A	G	7: 45,507,357 (GRCm39)	I448T	probably benign	Het
Il21	C	A	3: 37,286,653 (GRCm39)	S21I	probably damaging	Het
Iqce	G	T	5: 140,677,376 (GRCm39)	D148E	probably damaging	Het
Iqcg	T	A	16: 32,839,884 (GRCm39)	E354V	probably damaging	Het
Iws1	T	C	18: 32,226,320 (GRCm39)		probably benign	Het
Ly75	C	T	2: 60,206,238 (GRCm39)	G144S	probably damaging	Het
Marco	C	A	1: 120,421,954 (GRCm39)	M83I	probably benign	Het
Mettl6	A	T	14: 31,201,752 (GRCm39)	L185H	probably damaging	Het
Mppe1	C	T	18: 67,362,773 (GRCm39)	G154D	probably damaging	Het
Mrpl42	T	C	10: 95,326,237 (GRCm39)	E85G	probably benign	Het
Neb	A	G	2: 52,079,921 (GRCm39)	V5518A	probably damaging	Het
Or12d13	A	T	17: 37,647,759 (GRCm39)	F121L	probably benign	Het
Or52p1	T	A	7: 104,267,812 (GRCm39)	F317I	probably null	Het
Or5b105	A	T	19: 13,080,053 (GRCm39)	I199N	probably damaging	Het
Or7a42	T	A	10: 78,791,766 (GRCm39)	C242*	probably null	Het
Or7d10	G	T	9: 19,831,655 (GRCm39)	S50I	probably benign	Het
Perm1	A	G	4: 156,302,034 (GRCm39)	T193A	probably benign	Het
Prkd2	T	A	7: 16,582,652 (GRCm39)	C172S	probably damaging	Het
Prr23a3	T	A	9: 98,747,431 (GRCm39)	D128E	possibly damaging	Het
Prss28	A	G	17: 25,528,711 (GRCm39)	Y51C	probably damaging	Het
Psmb1	A	T	17: 15,696,451 (GRCm39)	M85K	probably benign	Het
Rae1	T	A	2: 172,854,401 (GRCm39)		probably benign	Het
Rasal1	A	G	5: 120,816,741 (GRCm39)	D759G	probably benign	Het
Rcvrn	G	A	11: 67,586,246 (GRCm39)	G2R	probably damaging	Het
Robo3	C	T	9: 37,334,640 (GRCm39)	A597T	probably damaging	Het
Rsf1	GCG	GCGACGGCGCCG	7: 97,229,114 (GRCm39)		probably benign	Homo
Sdcbp	T	A	4: 6,378,980 (GRCm39)	Y22*	probably null	Het
Sin3a	T	C	9: 57,025,360 (GRCm39)	F1069L	probably damaging	Het
Slitrk3	C	T	3: 72,957,129 (GRCm39)	V548I	possibly damaging	Het
Tbc1d22a	A	G	15: 86,275,287 (GRCm39)	H403R	probably damaging	Het
Tbr1	G	T	2: 61,635,593 (GRCm39)		probably null	Het
Tiam2	T	A	17: 3,555,985 (GRCm39)	D65E	probably damaging	Het
Tpcn2	A	G	7: 144,813,833 (GRCm39)	S488P	probably benign	Het
Trav9-2	T	C	14: 53,828,695 (GRCm39)	S22P	probably damaging	Het
Trim34a	T	A	7: 103,897,069 (GRCm39)	N44K	probably benign	Het
Unc79	C	G	12: 103,078,691 (GRCm39)	P1619A	probably benign	Het
Usp22	A	T	11: 61,048,042 (GRCm39)	V426E	probably damaging	Het
Vhl	A	T	6: 113,601,159 (GRCm39)	M20L	unknown	Het
Vmn1r215	G	A	13: 23,260,064 (GRCm39)	A35T	probably benign	Het
Vmn1r222	G	A	13: 23,416,602 (GRCm39)	L204F	possibly damaging	Het
Zfp871	A	T	17: 32,994,829 (GRCm39)	H115Q	probably damaging	Het
Zpr1	T	A	9: 46,189,640 (GRCm39)	F340L	probably benign	Het

Other mutations in Ccdc80

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00977:Ccdc80	APN	16	44,916,627 (GRCm39)	missense	probably benign	0.07
IGL01781:Ccdc80	APN	16	44,946,493 (GRCm39)	missense	probably damaging	1.00
IGL01945:Ccdc80	APN	16	44,938,608 (GRCm39)	missense	probably damaging	0.99
IGL02163:Ccdc80	APN	16	44,916,477 (GRCm39)	missense	probably benign
IGL02223:Ccdc80	APN	16	44,915,966 (GRCm39)	missense	probably damaging	1.00
IGL02573:Ccdc80	APN	16	44,915,952 (GRCm39)	missense	probably damaging	1.00
IGL02675:Ccdc80	APN	16	44,936,695 (GRCm39)	missense	probably damaging	1.00
IGL02689:Ccdc80	APN	16	44,916,772 (GRCm39)	nonsense	probably null
R0219:Ccdc80	UTSW	16	44,916,846 (GRCm39)	missense	probably damaging	1.00
R0383:Ccdc80	UTSW	16	44,915,732 (GRCm39)	missense	probably damaging	1.00
R1537:Ccdc80	UTSW	16	44,916,299 (GRCm39)	missense	probably benign	0.21
R1726:Ccdc80	UTSW	16	44,916,368 (GRCm39)	missense	probably benign	0.04
R1885:Ccdc80	UTSW	16	44,917,083 (GRCm39)	missense	probably benign	0.09
R2021:Ccdc80	UTSW	16	44,943,275 (GRCm39)	missense	probably damaging	1.00
R2140:Ccdc80	UTSW	16	44,947,809 (GRCm39)	missense	probably damaging	1.00
R2186:Ccdc80	UTSW	16	44,938,468 (GRCm39)	missense	probably damaging	1.00
R3896:Ccdc80	UTSW	16	44,916,984 (GRCm39)	missense	probably benign	0.11
R3941:Ccdc80	UTSW	16	44,916,455 (GRCm39)	missense	probably benign
R3971:Ccdc80	UTSW	16	44,916,183 (GRCm39)	missense	probably benign	0.22
R4082:Ccdc80	UTSW	16	44,943,290 (GRCm39)	missense	probably damaging	1.00
R4322:Ccdc80	UTSW	16	44,915,951 (GRCm39)	missense	probably damaging	1.00
R4578:Ccdc80	UTSW	16	44,915,849 (GRCm39)	missense	probably damaging	1.00
R4604:Ccdc80	UTSW	16	44,915,928 (GRCm39)	missense	probably damaging	1.00
R4868:Ccdc80	UTSW	16	44,924,776 (GRCm39)	missense	probably damaging	1.00
R4896:Ccdc80	UTSW	16	44,916,261 (GRCm39)	missense	probably benign
R4921:Ccdc80	UTSW	16	44,938,530 (GRCm39)	missense	probably damaging	1.00
R5452:Ccdc80	UTSW	16	44,938,528 (GRCm39)	missense	probably damaging	1.00
R5454:Ccdc80	UTSW	16	44,947,588 (GRCm39)	nonsense	probably null
R5594:Ccdc80	UTSW	16	44,936,626 (GRCm39)	missense	probably benign	0.00
R5661:Ccdc80	UTSW	16	44,947,808 (GRCm39)	missense	probably damaging	1.00
R5701:Ccdc80	UTSW	16	44,936,741 (GRCm39)	missense	possibly damaging	0.51
R6106:Ccdc80	UTSW	16	44,917,073 (GRCm39)	missense	probably benign	0.00
R6393:Ccdc80	UTSW	16	44,916,828 (GRCm39)	missense	possibly damaging	0.88
R6633:Ccdc80	UTSW	16	44,915,271 (GRCm39)	missense	possibly damaging	0.95
R6943:Ccdc80	UTSW	16	44,915,445 (GRCm39)	missense	probably benign	0.00
R7021:Ccdc80	UTSW	16	44,924,804 (GRCm39)	missense	probably damaging	1.00
R7030:Ccdc80	UTSW	16	44,943,252 (GRCm39)	missense	possibly damaging	0.60
R7208:Ccdc80	UTSW	16	44,917,073 (GRCm39)	missense	probably benign	0.12
R7486:Ccdc80	UTSW	16	44,946,542 (GRCm39)	missense	probably damaging	1.00
R7490:Ccdc80	UTSW	16	44,916,763 (GRCm39)	missense	probably damaging	1.00
R7539:Ccdc80	UTSW	16	44,915,445 (GRCm39)	missense	probably benign	0.01
R7562:Ccdc80	UTSW	16	44,943,266 (GRCm39)	missense	probably damaging	1.00
R7723:Ccdc80	UTSW	16	44,946,798 (GRCm39)	splice site	probably null
R7739:Ccdc80	UTSW	16	44,916,186 (GRCm39)	missense	probably benign	0.06
R7740:Ccdc80	UTSW	16	44,924,888 (GRCm39)	missense	possibly damaging	0.67
R8034:Ccdc80	UTSW	16	44,943,238 (GRCm39)	missense	probably damaging	0.96
R8150:Ccdc80	UTSW	16	44,947,792 (GRCm39)	missense	probably damaging	1.00
R8420:Ccdc80	UTSW	16	44,915,612 (GRCm39)	missense	possibly damaging	0.70
R8843:Ccdc80	UTSW	16	44,947,470 (GRCm39)	intron	probably benign
R8983:Ccdc80	UTSW	16	44,924,780 (GRCm39)	missense	possibly damaging	0.92
R9263:Ccdc80	UTSW	16	44,915,949 (GRCm39)	missense	probably damaging	0.99
R9570:Ccdc80	UTSW	16	44,915,449 (GRCm39)	missense	probably benign	0.13
R9584:Ccdc80	UTSW	16	44,915,675 (GRCm39)	missense	probably damaging	0.99
X0012:Ccdc80	UTSW	16	44,916,788 (GRCm39)	missense	probably benign	0.26
Z1176:Ccdc80	UTSW	16	44,936,707 (GRCm39)	missense	probably damaging	1.00
Z1176:Ccdc80	UTSW	16	44,916,570 (GRCm39)	missense	probably benign	0.43
Z1176:Ccdc80	UTSW	16	44,916,149 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- CTGTAAAACTGTTCCCACACATTG -3'
(R):5'- TTACAAACCTTGCCAGTAGGG -3'

Sequencing Primer
(F):5'- GAATGGTCTGCTTTGAGCT -3'
(R):5'- GCACCGTTTGTGGACTTATTGACC -3'

Posted On

2016-05-10