Mutagenetix > Incidental Mutation

Incidental Mutation 'R9423:Ccdc177'

712450

Institutional Source

Beutler Lab

Gene Symbol

Ccdc177

Ensembl Gene

ENSMUSG00000062961

Gene Name

coiled-coil domain containing 177

Synonyms

Gm1568, LOC380768

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.110) question?

Stock #

R9423 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

80802221-80807489 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 80804162 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Alanine at position 704 (D704A)

Ref Sequence

ENSEMBL: ENSMUSP00000072982 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000073251]

AlphaFold

Q3UHB8

Predicted Effect

unknown
Transcript: ENSMUST00000073251
AA Change: D704A

SMART Domains

Protein: ENSMUSP00000072982
Gene: ENSMUSG00000062961
AA Change: D704A

Domain	Start	End	E-Value	Type
low complexity region	7	20	N/A	INTRINSIC
low complexity region	28	49	N/A	INTRINSIC
internal_repeat_1	116	139	2.91e-5	PROSPERO
low complexity region	146	159	N/A	INTRINSIC
low complexity region	165	227	N/A	INTRINSIC
low complexity region	229	263	N/A	INTRINSIC
Pfam:DUF4659	332	705	1.9e-115	PFAM

Meta Mutation Damage Score

0.0704

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (23/23)

Allele List at MGI

Other mutations in this stock

Total: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aatk	A	G	11: 119,901,520 (GRCm39)	S959P	probably damaging	Het
Abca13	T	C	11: 9,240,395 (GRCm39)	S753P	probably damaging	Het
Abcb10	A	G	8: 124,688,819 (GRCm39)	S486P		Het
Adamts19	G	T	18: 59,023,427 (GRCm39)	R274L	possibly damaging	Het
Ahcyl1	C	T	3: 107,578,476 (GRCm39)	E254K	probably damaging	Het
Cd200r3	T	C	16: 44,771,895 (GRCm39)	V53A	probably benign	Het
Cdc42bpg	T	C	19: 6,363,329 (GRCm39)	L429P	probably damaging	Het
Cdh23	T	C	10: 60,148,387 (GRCm39)	D2660G	probably damaging	Het
Cfap61	G	T	2: 145,985,155 (GRCm39)	A1000S	probably damaging	Het
Col28a1	T	C	6: 7,999,601 (GRCm39)	T1039A	probably benign	Het
Ctsd	A	G	7: 141,939,212 (GRCm39)	L71P	probably damaging	Het
Dab2ip	C	T	2: 35,599,966 (GRCm39)	T251M	probably damaging	Het
Dcaf8	T	A	1: 172,007,524 (GRCm39)	I331N	probably damaging	Het
Dcp2	C	T	18: 44,538,361 (GRCm39)	R173C	probably damaging	Het
Dgka	C	T	10: 128,557,055 (GRCm39)	C640Y	probably damaging	Het
Entrep3	T	A	3: 89,092,007 (GRCm39)	L155Q	probably damaging	Het
Gm10801	AAGT	AAGTAGT	2: 98,494,148 (GRCm39)		probably null	Het
Gpr141	T	C	13: 19,935,995 (GRCm39)	N260S	probably benign	Het
Htr2a	T	A	14: 74,943,516 (GRCm39)	F365L	probably damaging	Het
Kdm5b	T	C	1: 134,515,705 (GRCm39)	Y110H	possibly damaging	Het
Ktn1	A	G	14: 47,912,318 (GRCm39)	T362A	probably benign	Het
Ltbp1	G	A	17: 75,597,112 (GRCm39)	S581N	probably benign	Het
Nr1h4	C	A	10: 89,309,688 (GRCm39)	R347L	possibly damaging	Het
Or4f60	A	T	2: 111,902,808 (GRCm39)	M40K	possibly damaging	Het
Or8g26	G	T	9: 39,095,838 (GRCm39)	M118I	probably damaging	Het
Parg	T	G	14: 31,939,662 (GRCm39)	F563V	probably damaging	Het
Pfkfb3	T	C	2: 11,487,276 (GRCm39)	Y378C	probably damaging	Het
Pierce1	TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC	TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC	2: 28,356,122 (GRCm39)		probably benign	Het
Pitpnm2	A	C	5: 124,271,469 (GRCm39)	L368R	probably benign	Het
Pkd1l3	A	G	8: 110,350,312 (GRCm39)	T386A	possibly damaging	Het
Plch2	C	A	4: 155,071,049 (GRCm39)	C1110F		Het
Poc5	T	C	13: 96,547,114 (GRCm39)	V459A	probably damaging	Het
Pou4f3	T	C	18: 42,528,959 (GRCm39)	S301P	probably damaging	Het
Rpf2	T	C	10: 40,101,336 (GRCm39)	D233G	possibly damaging	Het
Rsf1	G	GACGGCGGCT	7: 97,229,116 (GRCm39)		probably benign	Het
Samd4b	A	G	7: 28,113,633 (GRCm39)	Y111H	probably benign	Het
Serpinb10	C	T	1: 107,466,179 (GRCm39)	T55M	probably benign	Het
Serpinb1a	C	T	13: 33,026,910 (GRCm39)	C344Y	probably benign	Het
Shprh	T	C	10: 11,081,007 (GRCm39)	V1524A	probably damaging	Het
Sirt1	T	C	10: 63,158,025 (GRCm39)	H463R	probably damaging	Het
Skor2	T	A	18: 76,948,300 (GRCm39)	L674Q	probably damaging	Het
Slc3a2	T	A	19: 8,690,189 (GRCm39)	K201M	possibly damaging	Het
Spata31h1	C	A	10: 82,123,459 (GRCm39)	V3184L	possibly damaging	Het
Stam	C	A	2: 14,146,564 (GRCm39)	Q421K	possibly damaging	Het
Steap4	G	A	5: 8,026,720 (GRCm39)	V228M	probably damaging	Het
Tacr3	A	G	3: 134,638,043 (GRCm39)	Y400C	probably benign	Het
Tecpr1	A	G	5: 144,155,396 (GRCm39)	V54A	probably damaging	Het
Tgm3	A	T	2: 129,880,527 (GRCm39)	E444D	probably benign	Het
Trim30a	A	T	7: 104,078,410 (GRCm39)	L222Q	probably damaging	Het
Trmt1l	T	C	1: 151,325,817 (GRCm39)	Y421H	possibly damaging	Het
Usp24	T	C	4: 106,288,867 (GRCm39)	F2500L	probably damaging	Het
Vmn2r54	T	A	7: 12,349,441 (GRCm39)	S714C	probably damaging	Het
Washc5	A	G	15: 59,227,735 (GRCm39)	I409T	probably benign	Het
Zfta	T	C	19: 7,397,624 (GRCm39)	L57P	probably damaging	Het

Other mutations in Ccdc177

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01598:Ccdc177	APN	12	80,805,519 (GRCm39)	missense	unknown
IGL02433:Ccdc177	APN	12	80,804,372 (GRCm39)	missense	unknown
R0829:Ccdc177	UTSW	12	80,806,253 (GRCm39)	missense	probably damaging	0.96
R1739:Ccdc177	UTSW	12	80,806,013 (GRCm39)	missense	probably damaging	1.00
R1970:Ccdc177	UTSW	12	80,805,486 (GRCm39)	missense	unknown
R2337:Ccdc177	UTSW	12	80,805,465 (GRCm39)	missense	unknown
R5001:Ccdc177	UTSW	12	80,804,160 (GRCm39)	missense	unknown
R5164:Ccdc177	UTSW	12	80,805,336 (GRCm39)	missense	unknown
R5249:Ccdc177	UTSW	12	80,805,282 (GRCm39)	missense	unknown
R5461:Ccdc177	UTSW	12	80,804,816 (GRCm39)	missense	unknown
R6802:Ccdc177	UTSW	12	80,806,057 (GRCm39)	missense	probably damaging	1.00
R7051:Ccdc177	UTSW	12	80,805,927 (GRCm39)	missense	probably damaging	0.98
R7412:Ccdc177	UTSW	12	80,805,792 (GRCm39)	missense	possibly damaging	0.85
R7510:Ccdc177	UTSW	12	80,804,457 (GRCm39)	missense	unknown
R7511:Ccdc177	UTSW	12	80,804,457 (GRCm39)	missense	unknown
R7712:Ccdc177	UTSW	12	80,804,712 (GRCm39)	nonsense	probably null
R8036:Ccdc177	UTSW	12	80,804,897 (GRCm39)	missense	unknown
R8693:Ccdc177	UTSW	12	80,804,582 (GRCm39)	missense	unknown
R8708:Ccdc177	UTSW	12	80,805,891 (GRCm39)	missense	probably benign	0.08
R8862:Ccdc177	UTSW	12	80,804,208 (GRCm39)	missense	unknown
R8894:Ccdc177	UTSW	12	80,806,077 (GRCm39)	missense	probably damaging	1.00
R9727:Ccdc177	UTSW	12	80,806,044 (GRCm39)	missense	probably benign	0.04
Z1177:Ccdc177	UTSW	12	80,804,510 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- AATACCATGTCTGCCTTCTCAG -3'
(R):5'- TTCAGACCCGCCTGGAAAAG -3'

Sequencing Primer
(F):5'- CAGTGCCTCATTAATGGTTCATTAG -3'
(R):5'- AGCTGCTGCAGGCCATTG -3'

Posted On

2022-05-16