Mutagenetix > Incidental Mutation

Incidental Mutation 'R7165:Ccdc77'

557869

Institutional Source

Beutler Lab

Gene Symbol

Ccdc77

Ensembl Gene

ENSMUSG00000030177

Gene Name

coiled-coil domain containing 77

Synonyms

2700091N06Rik, 2400002C23Rik

MMRRC Submission

045262-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7165 (G1)

Quality Score

182.009

Status

Validated

Chromosome

Chromosomal Location

120301283-120341330 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 120327193 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Proline at position 84 (L84P)

Ref Sequence

ENSEMBL: ENSMUSP00000032283 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000032283] [ENSMUST00000112703] [ENSMUST00000127146] [ENSMUST00000136829] [ENSMUST00000144131] [ENSMUST00000146667] [ENSMUST00000163827]

AlphaFold

Q9CZH8

Predicted Effect

probably damaging
Transcript: ENSMUST00000032283
AA Change: L84P

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000032283
Gene: ENSMUSG00000030177
AA Change: L84P

Domain	Start	End	E-Value	Type
coiled coil region	57	120	N/A	INTRINSIC
low complexity region	221	235	N/A	INTRINSIC
coiled coil region	346	380	N/A	INTRINSIC
coiled coil region	414	445	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000112703
AA Change: L66P

PolyPhen 2 Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000108323
Gene: ENSMUSG00000030177
AA Change: L66P

Domain	Start	End	E-Value	Type
coiled coil region	39	102	N/A	INTRINSIC
low complexity region	203	217	N/A	INTRINSIC
internal_repeat_1	258	283	9.62e-5	PROSPERO
internal_repeat_1	321	348	9.62e-5	PROSPERO
low complexity region	352	369	N/A	INTRINSIC
coiled coil region	396	427	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000127146
AA Change: L66P

PolyPhen 2 Score 0.499 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000120896
Gene: ENSMUSG00000030177
AA Change: L66P

Domain	Start	End	E-Value	Type
coiled coil region	39	102	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000136829
AA Change: L84P

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000126554
Gene: ENSMUSG00000030177
AA Change: L84P

Domain	Start	End	E-Value	Type
coiled coil region	57	120	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000144131
AA Change: L66P

PolyPhen 2 Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000127096
Gene: ENSMUSG00000030177
AA Change: L66P

Domain	Start	End	E-Value	Type
coiled coil region	39	102	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000146667
AA Change: L84P

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000114664
Gene: ENSMUSG00000030177
AA Change: L84P

Domain	Start	End	E-Value	Type
coiled coil region	57	91	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000163827
AA Change: L66P

PolyPhen 2 Score 0.516 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000131970
Gene: ENSMUSG00000030177
AA Change: L66P

Domain	Start	End	E-Value	Type
coiled coil region	39	102	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.8%

Validation Efficiency

98% (79/81)

Allele List at MGI

Other mutations in this stock

Total: 81 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acoxl	C	A	2: 127,965,028 (GRCm39)	A624E	probably benign	Het
Adnp	A	G	2: 168,024,287 (GRCm39)	S1003P	probably benign	Het
Akap8l	T	C	17: 32,557,386 (GRCm39)	D75G	probably damaging	Het
Ap4e1	A	T	2: 126,905,238 (GRCm39)	T970S	possibly damaging	Het
Asb3	T	A	11: 30,979,029 (GRCm39)	N106K	probably damaging	Het
Atp1a3	T	C	7: 24,678,390 (GRCm39)	I988V	probably benign	Het
Camta1	A	G	4: 151,169,157 (GRCm39)	L198S	possibly damaging	Het
Ccne1	C	T	7: 37,798,726 (GRCm39)	A298T	probably damaging	Het
Cdc42bpb	T	A	12: 111,287,951 (GRCm39)	E532V	probably damaging	Het
Clasp2	G	A	9: 113,615,467 (GRCm39)		probably null	Het
Cntnap5b	C	A	1: 100,003,887 (GRCm39)	T289N	possibly damaging	Het
Dcun1d4	A	G	5: 73,648,538 (GRCm39)		probably null	Het
Dnah14	A	G	1: 181,532,100 (GRCm39)	T2296A	probably benign	Het
Dnaja4	A	T	9: 54,616,516 (GRCm39)	Q173L	probably damaging	Het
Dync2h1	G	A	9: 7,050,479 (GRCm39)	A3190V	probably benign	Het
Frrs1	T	A	3: 116,671,920 (GRCm39)	I6N	probably benign	Het
Fscn1	T	C	5: 142,957,801 (GRCm39)	V477A	probably benign	Het
Fsip2	G	A	2: 82,811,541 (GRCm39)	G2620E	possibly damaging	Het
Glp1r	C	T	17: 31,128,297 (GRCm39)	A92V	probably benign	Het
Gpr137b	A	T	13: 13,542,205 (GRCm39)	M204K	probably damaging	Het
Gstm1	A	G	3: 107,923,693 (GRCm39)	V104A	probably benign	Het
Gtf2e1	A	T	16: 37,356,228 (GRCm39)	N101K	probably damaging	Het
Igsf9b	T	C	9: 27,245,536 (GRCm39)	F1168L	probably benign	Het
Itpr2	A	T	6: 146,195,589 (GRCm39)	V1629E	probably damaging	Het
Kat14	A	G	2: 144,235,918 (GRCm39)	T428A	probably benign	Het
Kif21b	T	C	1: 136,077,186 (GRCm39)	Y403H	probably damaging	Het
Lpcat1	G	C	13: 73,662,649 (GRCm39)	A533P	probably benign	Het
Lrp2	A	T	2: 69,336,917 (GRCm39)	I1285N	probably damaging	Het
Mboat1	A	T	13: 30,408,398 (GRCm39)	Y187F	probably damaging	Het
Mkx	T	C	18: 7,002,525 (GRCm39)	N7S	probably damaging	Het
Mrps27	A	T	13: 99,551,307 (GRCm39)	T357S	possibly damaging	Het
Muc21	A	G	17: 35,932,870 (GRCm39)	S439P	unknown	Het
Naa35	A	G	13: 59,733,997 (GRCm39)	D9G	probably benign	Het
Ncoa4	T	A	14: 31,897,940 (GRCm39)	N253K	probably damaging	Het
Neb	A	G	2: 52,160,318 (GRCm39)	Y2232H	probably damaging	Het
Nlk	G	A	11: 78,481,793 (GRCm39)	Q223*	probably null	Het
Npas2	T	A	1: 39,331,798 (GRCm39)	I71N	possibly damaging	Het
Nup107	T	A	10: 117,609,267 (GRCm39)	Q364L	probably damaging	Het
Or8g17	T	A	9: 38,934,566 (GRCm39)		probably benign	Het
Otof	C	T	5: 30,532,964 (GRCm39)	G1593S	probably damaging	Het
Panx3	G	T	9: 37,575,381 (GRCm39)	H160Q	probably damaging	Het
Pappa	T	A	4: 65,180,110 (GRCm39)	H990Q	probably damaging	Het
Pax4	G	A	6: 28,446,136 (GRCm39)	P119L	probably damaging	Het
Pcdhb20	T	A	18: 37,638,123 (GRCm39)	D216E	probably damaging	Het
Pcdhgb8	T	A	18: 37,896,231 (GRCm39)	S434T	possibly damaging	Het
Pf4	T	C	5: 90,920,448 (GRCm39)	V3A	probably benign	Het
Phf24	T	C	4: 42,938,325 (GRCm39)	S229P	probably benign	Het
Plcd3	A	G	11: 102,970,439 (GRCm39)	F200S	probably damaging	Het
Ppp1r16a	A	G	15: 76,575,104 (GRCm39)	H4R	probably damaging	Het
Pramel15	A	G	4: 144,099,389 (GRCm39)	C459R	probably damaging	Het
Prdm10	A	G	9: 31,227,738 (GRCm39)		probably null	Het
Prim2	A	G	1: 33,667,474 (GRCm39)		probably null	Het
Prkg1	T	A	19: 30,562,599 (GRCm39)	H550L	probably damaging	Het
Prrc2c	G	T	1: 162,501,086 (GRCm39)	T2809N	possibly damaging	Het
Ptx3	A	G	3: 66,132,391 (GRCm39)	E304G	probably benign	Het
Ralgps2	A	G	1: 156,655,818 (GRCm39)	F369L	probably benign	Het
Rasgrp1	G	A	2: 117,168,885 (GRCm39)	T31I	probably benign	Het
Rbsn	A	T	6: 92,168,315 (GRCm39)	M373K	probably benign	Het
Rnf168	C	G	16: 32,101,179 (GRCm39)	R120G	probably benign	Het
Rp1	A	G	1: 4,420,140 (GRCm39)	I324T	probably damaging	Het
Samd11	T	C	4: 156,336,747 (GRCm39)	S31G	probably benign	Het
Sart3	A	T	5: 113,884,056 (GRCm39)	L652Q	probably benign	Het
Scrn2	A	G	11: 96,924,634 (GRCm39)	E421G	probably benign	Het
Sik2	A	T	9: 50,828,397 (GRCm39)	L215Q	probably damaging	Het
Speer4a3	AACT	A	5: 26,155,849 (GRCm39)		probably benign	Het
Stard9	A	T	2: 120,534,639 (GRCm39)	K3632M	probably damaging	Het
Swt1	A	T	1: 151,264,428 (GRCm39)	D695E	probably damaging	Het
Tead3	T	A	17: 28,552,228 (GRCm39)	M357L	probably benign	Het
Tgfbi	A	T	13: 56,775,829 (GRCm39)	T292S	probably damaging	Het
Tmc7	T	C	7: 118,155,157 (GRCm39)	H247R	probably benign	Het
Trmt10b	T	A	4: 45,308,549 (GRCm39)	D236E	probably damaging	Het
Tshz1	C	A	18: 84,034,052 (GRCm39)	V119L	probably damaging	Het
Ttn	A	C	2: 76,658,258 (GRCm39)	V12374G	unknown	Het
Tubgcp2	A	G	7: 139,585,274 (GRCm39)	Y484H	probably damaging	Het
Ubr4	G	C	4: 139,177,824 (GRCm39)	A1947P		Het
Uggt1	A	C	1: 36,194,188 (GRCm39)	V1350G	probably benign	Het
Vmn1r173	A	T	7: 23,402,076 (GRCm39)	M104L	probably benign	Het
Xirp1	A	T	9: 119,848,113 (GRCm39)	C257S	probably damaging	Het
Zfyve26	A	G	12: 79,327,179 (GRCm39)	S724P	probably damaging	Het
Zmpste24	A	T	4: 120,940,091 (GRCm39)	L185Q	probably null	Het
Zpld1	G	A	16: 55,052,594 (GRCm39)	A340V	probably benign	Het

Other mutations in Ccdc77

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00163:Ccdc77	APN	6	120,306,045 (GRCm39)	unclassified	probably benign
IGL01323:Ccdc77	APN	6	120,311,757 (GRCm39)	missense	probably benign	0.25
IGL02086:Ccdc77	APN	6	120,316,119 (GRCm39)	missense	possibly damaging	0.89
IGL02388:Ccdc77	APN	6	120,308,858 (GRCm39)	missense	probably benign
R0576:Ccdc77	UTSW	6	120,308,809 (GRCm39)	missense	probably benign	0.00
R1485:Ccdc77	UTSW	6	120,315,101 (GRCm39)	nonsense	probably null
R2422:Ccdc77	UTSW	6	120,316,120 (GRCm39)	missense	probably benign	0.01
R2497:Ccdc77	UTSW	6	120,302,433 (GRCm39)	missense	possibly damaging	0.62
R4906:Ccdc77	UTSW	6	120,311,796 (GRCm39)	missense	probably damaging	0.98
R5104:Ccdc77	UTSW	6	120,325,346 (GRCm39)	splice site	probably null
R6467:Ccdc77	UTSW	6	120,327,242 (GRCm39)	missense	probably damaging	0.99
R7783:Ccdc77	UTSW	6	120,327,334 (GRCm39)	missense	probably damaging	0.97
R8296:Ccdc77	UTSW	6	120,308,870 (GRCm39)	missense	possibly damaging	0.53
R8695:Ccdc77	UTSW	6	120,318,962 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- ATCGAGAATGCCACATGCCG -3'
(R):5'- TCTAAACGTGGTGCTGGCTC -3'

Sequencing Primer
(F):5'- ACAGGTGCATGTGTGACC -3'
(R):5'- GCTCTGGCTTTGGTGATACC -3'

Posted On

2019-06-26