Mutagenetix > Incidental Mutation

Incidental Mutation 'R4729:Zfp677'

358719

Institutional Source

Beutler Lab

Gene Symbol

Zfp677

Ensembl Gene

ENSMUSG00000062743

Gene Name

zinc finger protein 677

Synonyms

A830058L05Rik

MMRRC Submission

041603-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.078) question?

Stock #

R4729 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

21604010-21619527 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 21617680 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Serine at position 246 (C246S)

Ref Sequence

ENSEMBL: ENSMUSP00000125295 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000056107] [ENSMUST00000162659]

AlphaFold

Q6PEP4

Predicted Effect

possibly damaging
Transcript: ENSMUST00000056107
AA Change: C246S

PolyPhen 2 Score 0.509 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000052667
Gene: ENSMUSG00000062743
AA Change: C246S

Domain	Start	End	E-Value	Type
KRAB	13	75	1.11e-21	SMART
ZnF_C2H2	185	207	2.95e-3	SMART
ZnF_C2H2	213	235	3.95e-4	SMART
ZnF_C2H2	241	263	2.09e-3	SMART
ZnF_C2H2	269	291	6.42e-4	SMART
ZnF_C2H2	297	319	5.5e-3	SMART
ZnF_C2H2	325	347	1.98e-4	SMART
ZnF_C2H2	353	375	1.98e-4	SMART
ZnF_C2H2	381	403	1.47e-3	SMART
ZnF_C2H2	409	431	1.28e-3	SMART
ZnF_C2H2	437	459	3.95e-4	SMART
ZnF_C2H2	465	487	1.04e-3	SMART
ZnF_C2H2	493	515	8.47e-4	SMART
ZnF_C2H2	521	543	7.49e-5	SMART
ZnF_C2H2	549	571	1.18e-2	SMART
ZnF_C2H2	577	599	6.08e-5	SMART
ZnF_C2H2	610	632	4.17e-3	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000162659
AA Change: C246S

PolyPhen 2 Score 0.509 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000125295
Gene: ENSMUSG00000062743
AA Change: C246S

Domain	Start	End	E-Value	Type
KRAB	13	75	1.11e-21	SMART
Pfam:zf-H2C2_2	118	140	2.9e-5	PFAM
ZnF_C2H2	185	207	2.95e-3	SMART
ZnF_C2H2	213	235	3.95e-4	SMART
ZnF_C2H2	241	263	2.09e-3	SMART
ZnF_C2H2	269	291	6.42e-4	SMART
ZnF_C2H2	297	319	5.5e-3	SMART
ZnF_C2H2	325	347	1.98e-4	SMART
ZnF_C2H2	353	375	1.98e-4	SMART
ZnF_C2H2	381	403	1.47e-3	SMART
ZnF_C2H2	409	431	1.28e-3	SMART
ZnF_C2H2	437	459	3.95e-4	SMART
ZnF_C2H2	465	487	1.04e-3	SMART
ZnF_C2H2	493	515	8.47e-4	SMART
ZnF_C2H2	521	543	7.49e-5	SMART
ZnF_C2H2	549	571	1.18e-2	SMART
ZnF_C2H2	577	599	6.08e-5	SMART
ZnF_C2H2	610	632	4.17e-3	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000232365

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.1%
20x: 94.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930562C15Rik	T	A	16: 4,667,187 (GRCm39)	L220H	unknown	Het
Amt	T	A	9: 108,177,851 (GRCm39)	L272Q	probably damaging	Het
Ank2	G	C	3: 126,770,545 (GRCm39)	Y894*	probably null	Het
Ankzf1	T	A	1: 75,170,908 (GRCm39)	F105I	probably damaging	Het
Aox4	C	A	1: 58,298,236 (GRCm39)	Y1067*	probably null	Het
BC034090	T	A	1: 155,100,836 (GRCm39)	Q476L	probably damaging	Het
Bhmt	G	T	13: 93,763,871 (GRCm39)	R57S	probably damaging	Het
Cacna1c	A	T	6: 118,633,136 (GRCm39)	F964L	probably damaging	Het
Celsr3	A	C	9: 108,724,851 (GRCm39)	S396R	probably benign	Het
Cpne4	C	A	9: 104,799,755 (GRCm39)	Q191K	probably damaging	Het
Csnk1g2	T	C	10: 80,475,038 (GRCm39)	Y352H	probably benign	Het
D630003M21Rik	A	G	2: 158,058,623 (GRCm39)	S426P	probably damaging	Het
Dennd10	T	A	19: 60,823,309 (GRCm39)	F315I	probably benign	Het
Dido1	G	T	2: 180,329,443 (GRCm39)	N326K	probably benign	Het
E2f2	T	A	4: 135,911,760 (GRCm39)	I257N	probably damaging	Het
Elfn1	T	G	5: 139,959,413 (GRCm39)	F806V	probably damaging	Het
Eml6	T	A	11: 29,783,204 (GRCm39)	Y559F	probably damaging	Het
Erich6	A	G	3: 58,543,480 (GRCm39)		probably null	Het
Fam78a	T	C	2: 31,972,617 (GRCm39)	N101S	probably damaging	Het
Fam83h	A	G	15: 75,874,185 (GRCm39)	S1051P	probably benign	Het
Galns	C	T	8: 123,330,195 (GRCm39)	G112D	probably damaging	Het
Gm9923	A	G	10: 72,145,524 (GRCm39)	K125R	probably damaging	Het
Hectd3	G	A	4: 116,854,415 (GRCm39)	V326M	probably damaging	Het
Iars2	A	G	1: 185,048,248 (GRCm39)	S495P	possibly damaging	Het
Ice1	T	C	13: 70,754,503 (GRCm39)	R528G	probably damaging	Het
Igkv12-38	T	A	6: 69,920,368 (GRCm39)	Y50F	possibly damaging	Het
Inpp5j	T	C	11: 3,445,025 (GRCm39)	S883G	probably damaging	Het
Irf8	T	C	8: 121,480,178 (GRCm39)	S139P	probably damaging	Het
Itpr2	A	G	6: 146,274,671 (GRCm39)	F837S	probably damaging	Het
Kcnq4	G	T	4: 120,570,271 (GRCm39)	D357E	possibly damaging	Het
Klhl1	A	G	14: 96,517,584 (GRCm39)	L364P	probably damaging	Het
Krt7	A	G	15: 101,318,439 (GRCm39)	I309V	probably benign	Het
Krt76	G	T	15: 101,797,516 (GRCm39)	A281D	probably damaging	Het
Lancl2	T	C	6: 57,714,697 (GRCm39)	F430L	probably damaging	Het
Llgl2	T	C	11: 115,739,125 (GRCm39)	V332A	probably damaging	Het
Lrrc26	A	T	2: 25,180,076 (GRCm39)	T26S	probably benign	Het
Lrrk1	T	A	7: 65,912,041 (GRCm39)	M1840L	probably benign	Het
Lyst	G	A	13: 13,812,486 (GRCm39)	C966Y	probably damaging	Het
Mad1l1	T	A	5: 140,247,266 (GRCm39)	S354C	possibly damaging	Het
Mbtps1	C	T	8: 120,252,159 (GRCm39)	G577D	probably damaging	Het
Mycbp2	C	T	14: 103,426,027 (GRCm39)	R2366H	probably damaging	Het
Myo18a	T	G	11: 77,668,511 (GRCm39)		probably null	Het
Naip5	G	A	13: 100,358,639 (GRCm39)	R866C	possibly damaging	Het
Nav2	T	A	7: 49,102,567 (GRCm39)	V455E	probably benign	Het
Neb	A	G	2: 52,153,674 (GRCm39)	I2417T	possibly damaging	Het
Nme5	C	T	18: 34,702,890 (GRCm39)	A133T	probably benign	Het
Nradd	T	C	9: 110,450,979 (GRCm39)	D51G	possibly damaging	Het
Pard3b	A	G	1: 62,250,843 (GRCm39)	R591G	probably damaging	Het
Pcbp4	T	C	9: 106,337,929 (GRCm39)	F73S	probably damaging	Het
Pcdhb11	C	T	18: 37,555,419 (GRCm39)	Q250*	probably null	Het
Pde1c	T	A	6: 56,049,194 (GRCm39)	K766N	probably damaging	Het
Phf21b	G	A	15: 84,738,942 (GRCm39)	Q40*	probably null	Het
Prr14	A	G	7: 127,073,868 (GRCm39)	D244G	probably benign	Het
Rab11fip5	C	T	6: 85,351,249 (GRCm39)	A88T	probably damaging	Het
Rad54l2	A	T	9: 106,593,317 (GRCm39)	S428T	probably benign	Het
Rdh9	A	G	10: 127,612,621 (GRCm39)	I90V	probably benign	Het
Rhag	G	T	17: 41,139,292 (GRCm39)	G76C	probably damaging	Het
Riok3	T	A	18: 12,261,984 (GRCm39)	V6E	possibly damaging	Het
Rnf7l	A	T	10: 63,257,244 (GRCm39)	V92E	probably damaging	Het
Scn10a	A	G	9: 119,500,592 (GRCm39)	I229T	probably damaging	Het
Slco1a1	G	T	6: 141,854,695 (GRCm39)	T652K	probably benign	Het
Slit1	T	A	19: 41,635,459 (GRCm39)	I345F	probably damaging	Het
Snrnp200	A	T	2: 127,074,857 (GRCm39)	I1477F	probably damaging	Het
Snx31	G	A	15: 36,523,698 (GRCm39)	T328I	possibly damaging	Het
Strn	A	G	17: 78,965,390 (GRCm39)	F634S	probably damaging	Het
Tmem101	C	T	11: 102,047,155 (GRCm39)	G6R	probably benign	Het
Tmem199	C	G	11: 78,399,506 (GRCm39)	G131R	probably benign	Het
Trim66	A	G	7: 109,055,267 (GRCm39)		probably null	Het
Ttn	G	T	2: 76,681,929 (GRCm39)		probably benign	Het
Upk3bl	T	C	5: 136,086,247 (GRCm39)	L61P	probably benign	Het
Vmn2r108	A	G	17: 20,692,632 (GRCm39)	Y75H	probably damaging	Het
Vmn2r91	T	A	17: 18,327,906 (GRCm39)	I500K	probably damaging	Het
Vps18	C	T	2: 119,124,272 (GRCm39)	R400C	probably damaging	Het
Zeb1	C	T	18: 5,767,286 (GRCm39)	P599L	probably damaging	Het
Zfhx4	G	T	3: 5,464,557 (GRCm39)	A1572S	probably damaging	Het
Zfp719	T	A	7: 43,239,834 (GRCm39)	I474N	probably damaging	Het

Other mutations in Zfp677

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00481:Zfp677	APN	17	21,617,930 (GRCm39)	missense	probably benign	0.33
IGL01973:Zfp677	APN	17	21,617,169 (GRCm39)	missense	probably damaging	1.00
IGL02206:Zfp677	APN	17	21,613,499 (GRCm39)	missense	probably damaging	1.00
IGL03240:Zfp677	APN	17	21,617,135 (GRCm39)	missense	probably damaging	0.99
IGL03409:Zfp677	APN	17	21,617,107 (GRCm39)	missense	probably damaging	1.00
R0622:Zfp677	UTSW	17	21,617,962 (GRCm39)	missense	probably benign	0.04
R0972:Zfp677	UTSW	17	21,618,572 (GRCm39)	missense	probably damaging	1.00
R1519:Zfp677	UTSW	17	21,617,499 (GRCm39)	missense	possibly damaging	0.91
R2155:Zfp677	UTSW	17	21,617,970 (GRCm39)	missense	probably benign	0.01
R2316:Zfp677	UTSW	17	21,617,582 (GRCm39)	missense	probably benign	0.38
R2866:Zfp677	UTSW	17	21,617,518 (GRCm39)	nonsense	probably null
R2989:Zfp677	UTSW	17	21,617,114 (GRCm39)	missense	probably benign	0.11
R3955:Zfp677	UTSW	17	21,618,079 (GRCm39)	missense	possibly damaging	0.95
R4075:Zfp677	UTSW	17	21,618,421 (GRCm39)	missense	probably damaging	1.00
R4134:Zfp677	UTSW	17	21,618,043 (GRCm39)	missense	probably benign	0.01
R4229:Zfp677	UTSW	17	21,618,544 (GRCm39)	missense	probably damaging	1.00
R4843:Zfp677	UTSW	17	21,612,788 (GRCm39)	missense	probably benign	0.23
R5023:Zfp677	UTSW	17	21,618,056 (GRCm39)	missense	probably damaging	1.00
R5316:Zfp677	UTSW	17	21,617,410 (GRCm39)	missense	probably damaging	0.99
R5420:Zfp677	UTSW	17	21,618,175 (GRCm39)	missense	probably damaging	1.00
R5694:Zfp677	UTSW	17	21,618,021 (GRCm39)	missense	probably damaging	0.99
R5837:Zfp677	UTSW	17	21,617,648 (GRCm39)	missense	probably damaging	1.00
R5888:Zfp677	UTSW	17	21,618,520 (GRCm39)	missense	probably damaging	1.00
R6007:Zfp677	UTSW	17	21,617,918 (GRCm39)	missense	probably damaging	1.00
R6119:Zfp677	UTSW	17	21,618,070 (GRCm39)	missense	possibly damaging	0.55
R6190:Zfp677	UTSW	17	21,617,530 (GRCm39)	missense	possibly damaging	0.91
R6518:Zfp677	UTSW	17	21,618,392 (GRCm39)	missense	probably damaging	1.00
R7198:Zfp677	UTSW	17	21,618,679 (GRCm39)	missense	probably damaging	1.00
R7391:Zfp677	UTSW	17	21,618,653 (GRCm39)	missense	possibly damaging	0.56
R7801:Zfp677	UTSW	17	21,618,277 (GRCm39)	missense	probably damaging	1.00
R7808:Zfp677	UTSW	17	21,617,647 (GRCm39)	missense	probably damaging	1.00
R8202:Zfp677	UTSW	17	21,613,535 (GRCm39)	missense	probably damaging	1.00
R8206:Zfp677	UTSW	17	21,612,717 (GRCm39)	splice site	probably null
R8885:Zfp677	UTSW	17	21,618,350 (GRCm39)	missense	probably benign
R8965:Zfp677	UTSW	17	21,617,155 (GRCm39)	missense	probably damaging	1.00
R9062:Zfp677	UTSW	17	21,612,815 (GRCm39)	critical splice donor site	probably null
R9167:Zfp677	UTSW	17	21,613,460 (GRCm39)	missense	probably damaging	1.00
R9371:Zfp677	UTSW	17	21,618,053 (GRCm39)	missense	probably damaging	1.00
R9638:Zfp677	UTSW	17	21,618,056 (GRCm39)	missense	probably damaging	1.00
R9752:Zfp677	UTSW	17	21,618,511 (GRCm39)	missense	probably damaging	1.00
RF003:Zfp677	UTSW	17	21,617,704 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTCAGCTCTACACACAGACTG -3'
(R):5'- ACAAACATTGCACGTGTAGGG -3'

Sequencing Primer
(F):5'- TTGGAGAAAAACCACACCAGTG -3'
(R):5'- AAACATTGCACGTGTAGGGTTTCTC -3'

Posted On

2015-11-11