Mutagenetix > Incidental Mutation

Incidental Mutation 'R1667:Cox7c'

187311

Institutional Source

Beutler Lab

Gene Symbol

Cox7c

Ensembl Gene

ENSMUSG00000017778

Gene Name

cytochrome c oxidase subunit 7C

Synonyms

Cox7c1, COXVIIc

MMRRC Submission

039703-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R1667 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

86192917-86194914 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 86194003 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 7 (S7P)

Ref Sequence

ENSEMBL: ENSMUSP00000117385 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078764] [ENSMUST00000131011] [ENSMUST00000132233]

AlphaFold

P17665

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000017922

Predicted Effect

probably benign
Transcript: ENSMUST00000078764

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000082983

Predicted Effect

probably benign
Transcript: ENSMUST00000131011

SMART Domains

Protein: ENSMUSP00000115419
Gene: ENSMUSG00000017778

Domain	Start	End	E-Value	Type
Pfam:COX7C	1	62	1.1e-28	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000132233
AA Change: S7P

PolyPhen 2 Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.5%
20x: 93.0%

Validation Efficiency

99% (76/77)

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgra1	G	A	7: 139,425,564 (GRCm39)	A26T	possibly damaging	Het
Adgrg3	T	A	8: 95,760,001 (GRCm39)	Y73*	probably null	Het
Alk	A	T	17: 72,218,562 (GRCm39)	V761E	probably damaging	Het
Ankrd13a	T	C	5: 114,924,794 (GRCm39)	V93A	possibly damaging	Het
Anks1b	T	C	10: 90,347,046 (GRCm39)		probably null	Het
Arb2a	T	A	13: 77,907,635 (GRCm39)	M1K	probably null	Het
Ascl1	T	C	10: 87,328,655 (GRCm39)	N99S	probably benign	Het
Atm	A	T	9: 53,412,232 (GRCm39)	L972Q	probably damaging	Het
Atp2c1	A	T	9: 105,309,996 (GRCm39)	L566Q	probably null	Het
Bank1	T	A	3: 135,799,057 (GRCm39)	Y629F	probably damaging	Het
Bod1l	G	T	5: 41,974,118 (GRCm39)	L2399I	probably benign	Het
Bub1b	G	A	2: 118,471,670 (GRCm39)	G1010D	probably benign	Het
Ces1b	G	A	8: 93,783,532 (GRCm39)	H563Y	possibly damaging	Het
Cfap70	T	C	14: 20,454,225 (GRCm39)	E853G	probably benign	Het
Cfh	T	C	1: 140,033,261 (GRCm39)	E779G	probably benign	Het
Cyp2c67	A	G	19: 39,632,034 (GRCm39)		probably null	Het
Dhx30	G	T	9: 109,914,513 (GRCm39)	L995I	possibly damaging	Het
Dhx30	G	C	9: 109,914,514 (GRCm39)	N957K	possibly damaging	Het
Dsc3	T	C	18: 20,124,617 (GRCm39)	T36A	possibly damaging	Het
Dstyk	A	G	1: 132,384,657 (GRCm39)	D717G	probably damaging	Het
Dusp10	A	G	1: 183,769,055 (GRCm39)	D7G	probably damaging	Het
E230001N04Rik	T	G	17: 28,742,935 (GRCm39)		noncoding transcript	Het
Ece2	T	C	16: 20,456,588 (GRCm39)	S330P	possibly damaging	Het
Frmd5	ATAGTGGAATTGTTCAAACTC	ATAGTGGAATTGTTCAAACTCTAGTGGAATTGTTCAAACTC	2: 121,379,211 (GRCm39)		probably null	Het
Gata3	T	C	2: 9,882,360 (GRCm39)	H14R	possibly damaging	Het
Ggta1	T	A	2: 35,304,295 (GRCm39)	I75F	possibly damaging	Het
Hcn1	A	T	13: 117,739,609 (GRCm39)	I124F	unknown	Het
Herpud1	A	C	8: 95,115,994 (GRCm39)	D53A	probably damaging	Het
Inhba	T	A	13: 16,201,209 (GRCm39)	L257Q	possibly damaging	Het
Itga10	C	T	3: 96,559,054 (GRCm39)		probably benign	Het
Jmy	T	A	13: 93,634,878 (GRCm39)	S313C	probably damaging	Het
Lpo	G	A	11: 87,698,067 (GRCm39)		probably benign	Het
Lsg1	T	C	16: 30,390,170 (GRCm39)	E315G	probably damaging	Het
Lsm14a	T	A	7: 34,065,079 (GRCm39)	T167S	possibly damaging	Het
Lsmem1	GTACATACATACATACATACATACATACA	GTACATACATACATACATACATACATACATACA	12: 40,235,260 (GRCm39)		probably null	Het
Map3k2	T	C	18: 32,336,845 (GRCm39)		probably benign	Het
Mapk12	A	T	15: 89,024,344 (GRCm39)	M81K	probably damaging	Het
Matn2	T	A	15: 34,378,878 (GRCm39)	C305S	probably damaging	Het
Mgam	T	C	6: 40,653,978 (GRCm39)	Y844H	possibly damaging	Het
Mgat5b	A	G	11: 116,838,203 (GRCm39)	R281G	probably benign	Het
Mon1b	T	G	8: 114,368,589 (GRCm39)	C497G	probably damaging	Het
Mybbp1a	A	T	11: 72,336,043 (GRCm39)	H452L	probably benign	Het
Mybl2	A	G	2: 162,917,616 (GRCm39)	T41A	probably damaging	Het
Ncoa5	A	G	2: 164,843,623 (GRCm39)	V540A	probably damaging	Het
Nup93	T	A	8: 95,019,315 (GRCm39)	V47E	possibly damaging	Het
Or10a4	A	T	7: 106,696,977 (GRCm39)	M102L	probably benign	Het
Or5j3	A	G	2: 86,129,080 (GRCm39)	M307V	probably null	Het
Orc6	T	A	8: 86,031,914 (GRCm39)	C100S	possibly damaging	Het
Otogl	G	T	10: 107,649,826 (GRCm39)	Y1176*	probably null	Het
Patj	A	T	4: 98,301,264 (GRCm39)	D183V	probably damaging	Het
Pik3r3	A	G	4: 116,079,514 (GRCm39)	T4A	probably damaging	Het
Pla2g4d	G	A	2: 120,100,631 (GRCm39)		probably benign	Het
Pla2r1	A	G	2: 60,250,601 (GRCm39)	I1407T	probably benign	Het
Pramel13	A	T	4: 144,119,606 (GRCm39)	C320*	probably null	Het
Prex2	A	T	1: 11,256,981 (GRCm39)	H1231L	probably benign	Het
Prkca	A	G	11: 107,874,772 (GRCm39)	V390A	probably damaging	Het
Psmd13	T	A	7: 140,470,522 (GRCm39)	W255R	probably damaging	Het
Rec8	T	A	14: 55,856,253 (GRCm39)	N37K	probably damaging	Het
Rnf207	C	T	4: 152,397,672 (GRCm39)	E361K	probably benign	Het
Serpina3f	T	A	12: 104,183,699 (GRCm39)	L187Q	probably damaging	Het
Skint11	A	T	4: 114,051,978 (GRCm39)	T109S	probably damaging	Het
Slc7a8	A	G	14: 54,962,306 (GRCm39)	S443P	probably damaging	Het
Slc8b1	T	A	5: 120,659,147 (GRCm39)	F197Y	probably benign	Het
Sox2	T	C	3: 34,704,568 (GRCm39)	Y2H	probably damaging	Het
Speg	T	A	1: 75,387,193 (GRCm39)		probably benign	Het
Tlr3	T	C	8: 45,853,874 (GRCm39)	N149D	probably benign	Het
Trim60	A	C	8: 65,454,116 (GRCm39)	D44E	probably benign	Het
Ugt1a7c	A	G	1: 88,023,657 (GRCm39)	Y272C	probably damaging	Het
Vmn1r4	T	A	6: 56,933,738 (GRCm39)	Y81N	probably damaging	Het
Vmn2r73	A	T	7: 85,506,889 (GRCm39)	C808S	probably benign	Het
Ythdf3	T	C	3: 16,259,056 (GRCm39)	I412T	possibly damaging	Het
Zfp672	T	C	11: 58,206,921 (GRCm39)	T467A	possibly damaging	Het
Zfp985	A	T	4: 147,668,407 (GRCm39)	Q425L	possibly damaging	Het

Other mutations in Cox7c

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R1614:Cox7c	UTSW	13	86,193,904 (GRCm39)	missense	probably benign	0.01
R5374:Cox7c	UTSW	13	86,194,739 (GRCm39)	missense	probably benign	0.00
R5981:Cox7c	UTSW	13	86,194,780 (GRCm39)	missense	possibly damaging	0.80
R8848:Cox7c	UTSW	13	86,193,900 (GRCm39)	missense	possibly damaging	0.49
R9112:Cox7c	UTSW	13	86,194,837 (GRCm39)	unclassified	probably benign

Predicted Primers

Posted On

2014-05-09