Mutagenetix > Incidental Mutation

Incidental Mutation 'R7689:Zfp658'

593268

Institutional Source

Beutler Lab

Gene Symbol

Zfp658

Ensembl Gene

ENSMUSG00000056592

Gene Name

zinc finger protein 658

Synonyms

MMRRC Submission

045753-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7689 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

43211680-43224885 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 43224102 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Glutamine at position 792 (H792Q)

Ref Sequence

ENSEMBL: ENSMUSP00000005597 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000005597] [ENSMUST00000058104] [ENSMUST00000107972] [ENSMUST00000205769]

AlphaFold

Q5PPQ4

Predicted Effect

probably benign
Transcript: ENSMUST00000005597
AA Change: H792Q

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000005597
Gene: ENSMUSG00000056592
AA Change: H792Q

Domain	Start	End	E-Value	Type
KRAB	23	83	3.7e-27	SMART
ZnF_C2H2	276	295	8.84e1	SMART
ZnF_C2H2	301	323	5.81e-2	SMART
ZnF_C2H2	328	350	1.5e-4	SMART
ZnF_C2H2	356	378	1.84e-4	SMART
ZnF_C2H2	384	406	3.16e-3	SMART
ZnF_C2H2	412	434	1.45e-2	SMART
ZnF_C2H2	440	462	4.87e-4	SMART
ZnF_C2H2	468	490	4.87e-4	SMART
ZnF_C2H2	496	518	6.88e-4	SMART
ZnF_C2H2	524	546	1.69e-3	SMART
ZnF_C2H2	552	574	9.73e-4	SMART
ZnF_C2H2	580	602	1.82e-3	SMART
ZnF_C2H2	608	630	3.16e-3	SMART
ZnF_C2H2	636	658	8.94e-3	SMART
ZnF_C2H2	664	686	3.74e-5	SMART
ZnF_C2H2	692	714	2.99e-4	SMART
ZnF_C2H2	720	742	5.21e-4	SMART
ZnF_C2H2	748	770	2.79e-4	SMART
ZnF_C2H2	776	798	1.58e-3	SMART
ZnF_C2H2	804	826	3.44e-4	SMART
ZnF_C2H2	832	854	5.59e-4	SMART
ZnF_C2H2	860	882	5.81e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000058104

SMART Domains

Protein: ENSMUSP00000050968
Gene: ENSMUSG00000030469

Domain	Start	End	E-Value	Type
KRAB	49	109	1.18e-20	SMART
ZnF_C2H2	285	305	4.16e1	SMART
ZnF_C2H2	341	363	1.2e-3	SMART
ZnF_C2H2	369	391	9.08e-4	SMART
ZnF_C2H2	397	419	6.67e-2	SMART
ZnF_C2H2	425	447	7.9e-4	SMART
ZnF_C2H2	453	475	3.34e-2	SMART
ZnF_C2H2	481	503	1.38e-3	SMART
ZnF_C2H2	509	531	5.42e-2	SMART
ZnF_C2H2	537	559	3.78e-1	SMART
ZnF_C2H2	565	587	2.43e-4	SMART
ZnF_C2H2	593	615	4.54e-4	SMART
ZnF_C2H2	621	643	4.24e-4	SMART
ZnF_C2H2	649	671	6.42e-4	SMART
ZnF_C2H2	677	699	1.47e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000107972
AA Change: H792Q

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000103606
Gene: ENSMUSG00000056592
AA Change: H792Q

Domain	Start	End	E-Value	Type
KRAB	23	83	3.7e-27	SMART
ZnF_C2H2	276	295	8.84e1	SMART
ZnF_C2H2	301	323	5.81e-2	SMART
ZnF_C2H2	328	350	1.5e-4	SMART
ZnF_C2H2	356	378	1.84e-4	SMART
ZnF_C2H2	384	406	3.16e-3	SMART
ZnF_C2H2	412	434	1.45e-2	SMART
ZnF_C2H2	440	462	4.87e-4	SMART
ZnF_C2H2	468	490	4.87e-4	SMART
ZnF_C2H2	496	518	6.88e-4	SMART
ZnF_C2H2	524	546	1.69e-3	SMART
ZnF_C2H2	552	574	9.73e-4	SMART
ZnF_C2H2	580	602	1.82e-3	SMART
ZnF_C2H2	608	630	3.16e-3	SMART
ZnF_C2H2	636	658	8.94e-3	SMART
ZnF_C2H2	664	686	3.74e-5	SMART
ZnF_C2H2	692	714	2.99e-4	SMART
ZnF_C2H2	720	742	5.21e-4	SMART
ZnF_C2H2	748	770	2.79e-4	SMART
ZnF_C2H2	776	798	1.58e-3	SMART
ZnF_C2H2	804	826	3.44e-4	SMART
ZnF_C2H2	832	854	5.59e-4	SMART
ZnF_C2H2	860	882	5.81e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000205769

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2510039O18Rik	T	A	4: 148,029,440 (GRCm39)	F470Y	probably damaging	Het
Adra1a	T	C	14: 66,875,250 (GRCm39)	L75P	probably damaging	Het
Agap1	T	C	1: 89,762,188 (GRCm39)	S560P	probably damaging	Het
Ahcyl	T	C	16: 45,974,970 (GRCm39)	T136A	probably benign	Het
Arrdc4	T	A	7: 68,391,623 (GRCm39)	I215L	probably damaging	Het
Atad3a	C	T	4: 155,840,610 (GRCm39)	A97T	probably damaging	Het
Bcas3	A	T	11: 85,386,713 (GRCm39)	T383S	probably benign	Het
C2cd5	G	A	6: 142,995,951 (GRCm39)	R379*	probably null	Het
Cacna1e	G	T	1: 154,274,549 (GRCm39)	H2138N	probably benign	Het
Card14	A	T	11: 119,216,328 (GRCm39)	D303V	possibly damaging	Het
Ccdc202	T	C	14: 96,119,252 (GRCm39)	V3A	probably benign	Het
Cfhr1	T	C	1: 139,475,478 (GRCm39)	Y331C	unknown	Het
Chp1	G	A	2: 119,415,146 (GRCm39)	D183N	probably benign	Het
Cntn2	T	C	1: 132,443,882 (GRCm39)	T966A	probably benign	Het
Cpne9	T	G	6: 113,266,965 (GRCm39)	C133G	probably damaging	Het
Cspg4b	A	G	13: 113,515,948 (GRCm39)	T121A		Het
Cul7	C	T	17: 46,963,747 (GRCm39)	Q275*	probably null	Het
Cyp11b1	T	C	15: 74,710,897 (GRCm39)	D221G	probably benign	Het
Dmxl1	T	A	18: 49,979,685 (GRCm39)	F107I	probably benign	Het
Dnhd1	A	G	7: 105,363,170 (GRCm39)	I3911V	probably benign	Het
Eif1ad16	A	G	12: 87,985,259 (GRCm39)	Y95H	probably damaging	Het
Eloa	T	C	4: 135,736,595 (GRCm39)	H551R	probably benign	Het
Fam171b	T	A	2: 83,709,732 (GRCm39)	V468D	probably benign	Het
Fat2	A	G	11: 55,200,666 (GRCm39)	W803R	probably damaging	Het
Fbxo43	T	C	15: 36,163,201 (GRCm39)	D2G	probably benign	Het
Fbxo8	A	G	8: 57,041,120 (GRCm39)	T179A	probably benign	Het
Gdap1	A	G	1: 17,231,623 (GRCm39)	T323A	probably damaging	Het
Gm136	T	C	4: 34,743,875 (GRCm39)	N323S	probably null	Het
Gm6899	A	T	11: 26,543,819 (GRCm39)	T129S	unknown	Het
Gnb3	A	T	6: 124,814,183 (GRCm39)	C166S	possibly damaging	Het
Gpr61	A	G	3: 108,057,966 (GRCm39)	F232L	probably damaging	Het
Gpx8	T	C	13: 113,179,711 (GRCm39)	M197V	probably benign	Het
Gse1	G	T	8: 121,295,217 (GRCm39)	R446L	unknown	Het
Itch	A	T	2: 155,054,987 (GRCm39)	T764S	probably benign	Het
Itch	A	G	2: 155,051,922 (GRCm39)	K614E	probably damaging	Het
Itpkb	T	G	1: 180,241,544 (GRCm39)	M738R	probably damaging	Het
Jph1	T	A	1: 17,074,192 (GRCm39)	K609*	probably null	Het
Kcns1	G	A	2: 164,010,241 (GRCm39)	R173C	probably damaging	Het
Larp4b	C	T	13: 9,186,834 (GRCm39)	S54L	probably damaging	Het
Lonrf1	G	T	8: 36,715,918 (GRCm39)	S239*	probably null	Het
Lyst	T	G	13: 13,857,808 (GRCm39)		probably null	Het
Mccc1	T	A	3: 36,015,132 (GRCm39)	R663*	probably null	Het
Mcm3	A	G	1: 20,876,997 (GRCm39)	V646A	probably benign	Het
Mdn1	T	C	4: 32,739,912 (GRCm39)	L3722P	probably damaging	Het
Mmp27	T	G	9: 7,579,002 (GRCm39)	D392E	probably damaging	Het
Ms4a14	A	G	19: 11,279,906 (GRCm39)	I884T	probably benign	Het
Muc4	C	T	16: 32,574,439 (GRCm39)	T963I	probably benign	Het
Muc6	G	C	7: 141,217,659 (GRCm39)	P2338R	probably damaging	Het
Mucl3	C	A	17: 35,948,969 (GRCm39)	S210I	possibly damaging	Het
Nbeal1	G	C	1: 60,276,310 (GRCm39)	V684L	probably benign	Het
Ndrg2	C	T	14: 52,147,812 (GRCm39)	A102T	possibly damaging	Het
Nhsl3	T	C	4: 129,117,566 (GRCm39)	N411S	probably benign	Het
Nos1	A	G	5: 118,035,792 (GRCm39)	D431G	probably damaging	Het
Oog4	CAA	CA	4: 143,164,022 (GRCm39)		probably null	Het
Otog	T	C	7: 45,901,480 (GRCm39)	L393P	probably damaging	Het
Plcl1	A	G	1: 55,736,627 (GRCm39)	N656S	probably damaging	Het
Pole3	C	A	4: 62,443,060 (GRCm39)	V27F	probably damaging	Het
Prrt4	T	A	6: 29,177,140 (GRCm39)	I210F	probably damaging	Het
Ptpn18	G	A	1: 34,512,445 (GRCm39)	D417N	possibly damaging	Het
Rbpms	A	T	8: 34,354,387 (GRCm39)	S53T	possibly damaging	Het
Rgs7	C	A	1: 174,949,296 (GRCm39)	V203L	probably benign	Het
Riok1	A	T	13: 38,229,263 (GRCm39)	D150V	probably damaging	Het
Rrp1b	T	C	17: 32,274,900 (GRCm39)	L335P	probably benign	Het
Rsph6a	T	G	7: 18,801,962 (GRCm39)	I592S	possibly damaging	Het
Skor1	C	T	9: 63,052,661 (GRCm39)	G436D	probably damaging	Het
Slc17a8	T	C	10: 89,433,319 (GRCm39)	T51A	possibly damaging	Het
Slc22a8	T	C	19: 8,585,248 (GRCm39)	S266P	probably damaging	Het
Socs2	A	G	10: 95,250,845 (GRCm39)		probably benign	Het
Tas2r106	A	G	6: 131,655,668 (GRCm39)	I61T	possibly damaging	Het
Tfap2a	T	C	13: 40,882,051 (GRCm39)	N77D	probably damaging	Het
Tmem236	T	A	2: 14,197,076 (GRCm39)	L88Q	probably damaging	Het
Ttc41	A	G	10: 86,595,088 (GRCm39)	E954G	probably damaging	Het
Vmn1r34	G	T	6: 66,613,994 (GRCm39)	S248*	probably null	Het
Wipf1	T	C	2: 73,262,789 (GRCm39)	R483G	probably damaging	Het
Zfhx4	A	G	3: 5,476,946 (GRCm39)	N3187S	probably benign	Het
Zfp202	C	A	9: 40,121,829 (GRCm39)	P309T	probably benign	Het
Zfp39	T	C	11: 58,781,469 (GRCm39)	H431R	probably damaging	Het

Other mutations in Zfp658

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00465:Zfp658	APN	7	43,216,780 (GRCm39)	missense	probably benign	0.03
IGL00475:Zfp658	APN	7	43,223,500 (GRCm39)	missense	possibly damaging	0.68
IGL01972:Zfp658	APN	7	43,222,134 (GRCm39)	nonsense	probably null
IGL03223:Zfp658	APN	7	43,216,735 (GRCm39)	missense	possibly damaging	0.85
R0135:Zfp658	UTSW	7	43,223,019 (GRCm39)	nonsense	probably null
R1863:Zfp658	UTSW	7	43,223,323 (GRCm39)	missense	possibly damaging	0.78
R1962:Zfp658	UTSW	7	43,223,245 (GRCm39)	missense	possibly damaging	0.93
R2698:Zfp658	UTSW	7	43,222,969 (GRCm39)	missense	possibly damaging	0.53
R3781:Zfp658	UTSW	7	43,223,270 (GRCm39)	missense	probably benign
R4791:Zfp658	UTSW	7	43,223,890 (GRCm39)	missense	possibly damaging	0.93
R5392:Zfp658	UTSW	7	43,222,355 (GRCm39)	missense	probably benign	0.07
R6092:Zfp658	UTSW	7	43,223,951 (GRCm39)	missense	possibly damaging	0.73
R6594:Zfp658	UTSW	7	43,216,701 (GRCm39)	missense	possibly damaging	0.86
R7003:Zfp658	UTSW	7	43,224,172 (GRCm39)	missense	possibly damaging	0.85
R7008:Zfp658	UTSW	7	43,223,336 (GRCm39)	missense	possibly damaging	0.95
R7077:Zfp658	UTSW	7	43,223,413 (GRCm39)	missense	probably benign	0.32
R7793:Zfp658	UTSW	7	43,224,108 (GRCm39)	missense	possibly damaging	0.74
R7939:Zfp658	UTSW	7	43,224,301 (GRCm39)	missense	possibly damaging	0.73
R8672:Zfp658	UTSW	7	43,222,919 (GRCm39)	missense	possibly damaging	0.52
R8828:Zfp658	UTSW	7	43,222,240 (GRCm39)	missense	probably benign
R8995:Zfp658	UTSW	7	43,222,798 (GRCm39)	missense	possibly damaging	0.93
R9021:Zfp658	UTSW	7	43,223,381 (GRCm39)	missense	possibly damaging	0.71
R9259:Zfp658	UTSW	7	43,224,280 (GRCm39)	missense	probably benign	0.02
R9551:Zfp658	UTSW	7	43,222,567 (GRCm39)	missense	probably benign	0.00
R9552:Zfp658	UTSW	7	43,222,567 (GRCm39)	missense	probably benign	0.00
R9571:Zfp658	UTSW	7	43,222,139 (GRCm39)	missense	possibly damaging	0.85
Z1176:Zfp658	UTSW	7	43,222,641 (GRCm39)	missense	possibly damaging	0.72

Predicted Primers

PCR Primer
(F):5'- AGTCCTTTACGTACTCATTCACG -3'
(R):5'- GATGCCTAGGTAAAGATGACTTATTG -3'

Sequencing Primer
(F):5'- TGCCATTACTGCGGGAAATC -3'
(R):5'- GATGACTTATTGTAGAAGCCCTTCC -3'

Posted On

2019-11-12