Mutagenetix > Incidental Mutation

Incidental Mutation 'R7198:Zfp677'

560111

Institutional Source

Beutler Lab

Gene Symbol

Zfp677

Ensembl Gene

ENSMUSG00000062743

Gene Name

zinc finger protein 677

Synonyms

A830058L05Rik

MMRRC Submission

045337-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.086) question?

Stock #

R7198 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

21604010-21619527 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 21618679 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Glycine at position 579 (C579G)

Ref Sequence

ENSEMBL: ENSMUSP00000052667 (fasta)

Gene Model

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

AlphaFold

Q6PEP4

Predicted Effect

probably damaging
Transcript: ENSMUST00000056107
AA Change: C579G

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000052667
Gene: ENSMUSG00000062743
AA Change: C579G

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

probably damaging
Transcript: ENSMUST00000162659
AA Change: C579G

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000125295
Gene: ENSMUSG00000062743
AA Change: C579G

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

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.4%

Validation Efficiency

98% (62/63)

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca8a	C	T	11: 109,969,481 (GRCm39)	S365N	probably damaging	Het
Baiap3	G	A	17: 25,462,814 (GRCm39)	R1075C	probably benign	Het
Baz2b	A	G	2: 59,792,550 (GRCm39)	L526P	probably benign	Het
Bbs1	A	T	19: 4,945,043 (GRCm39)	L376Q	probably damaging	Het
Bcl9	T	A	3: 97,112,511 (GRCm39)	M1315L	possibly damaging	Het
Bcl9	T	C	3: 97,116,183 (GRCm39)	Q837R	probably damaging	Het
Cct2	A	G	10: 116,889,029 (GRCm39)	V490A	probably benign	Het
Cdh23	T	C	10: 60,148,378 (GRCm39)	Y2663C	possibly damaging	Het
Chit1	A	G	1: 134,078,229 (GRCm39)	K346E	possibly damaging	Het
Chl1	A	G	6: 103,683,517 (GRCm39)	Y781C	probably damaging	Het
Col12a1	A	C	9: 79,557,314 (GRCm39)	L1938R	possibly damaging	Het
Cpxm2	T	A	7: 131,681,813 (GRCm39)	N239Y	probably damaging	Het
Cyp3a41b	A	G	5: 145,519,330 (GRCm39)	Y54H	probably benign	Het
Dclk1	A	C	3: 55,385,296 (GRCm39)	D369A	possibly damaging	Het
Dnai4	A	G	4: 102,919,610 (GRCm39)	V498A	probably damaging	Het
Dpy19l3	T	C	7: 35,449,190 (GRCm39)	N71S	possibly damaging	Het
Efcab3	T	A	11: 104,642,711 (GRCm39)	N1111K	probably benign	Het
Fer	T	A	17: 64,228,683 (GRCm39)	V186E	possibly damaging	Het
Gm11042	T	A	12: 74,361,888 (GRCm39)	H39L	unknown	Het
Gm14325	A	G	2: 177,473,798 (GRCm39)	I428T	probably benign	Het
Gm47995	A	G	1: 151,074,404 (GRCm39)	E69G	possibly damaging	Het
Gm6176	T	A	7: 21,750,596 (GRCm39)	I112F	probably damaging	Het
Hivep2	T	A	10: 14,005,710 (GRCm39)	D769E	probably benign	Het
Hsdl1	C	T	8: 120,294,607 (GRCm39)	V40I	probably benign	Het
Ipmk	A	G	10: 71,183,882 (GRCm39)	H34R	probably damaging	Het
Kcnd3	T	C	3: 105,366,856 (GRCm39)	L242P	probably damaging	Het
Kdm4d	T	C	9: 14,375,316 (GRCm39)	M181V	probably damaging	Het
Lats2	A	T	14: 57,934,582 (GRCm39)	I716N	probably damaging	Het
Liph	T	C	16: 21,784,772 (GRCm39)	Y305C	probably damaging	Het
Ltbp1	T	C	17: 75,533,962 (GRCm39)	V150A	possibly damaging	Het
Ly6d	A	T	15: 74,634,384 (GRCm39)	S69T	probably benign	Het
Meltf	A	G	16: 31,702,617 (GRCm39)	R115G	possibly damaging	Het
Msgn1	G	T	12: 11,258,902 (GRCm39)	D16E	probably benign	Het
Mthfd2l	T	A	5: 91,094,705 (GRCm39)	I58K	probably damaging	Het
Mup18	G	C	4: 61,591,573 (GRCm39)		probably null	Het
Nek10	T	A	14: 14,850,947 (GRCm38)	W331R	probably damaging	Het
Nphp3	A	G	9: 103,881,974 (GRCm39)	Y148C	probably damaging	Het
Or4a47	T	C	2: 89,666,076 (GRCm39)	Y71C	probably damaging	Het
Or5h19	C	T	16: 58,856,456 (GRCm39)	V215I	probably benign	Het
Or6c33	T	A	10: 129,853,760 (GRCm39)	C177S	probably damaging	Het
Oscp1	A	G	4: 125,980,459 (GRCm39)	T325A	possibly damaging	Het
Pcdha4	T	A	18: 37,086,613 (GRCm39)	N265K	probably damaging	Het
Pigq	C	T	17: 26,153,199 (GRCm39)	V331I	probably benign	Het
Plekhg4	A	G	8: 106,105,329 (GRCm39)	E598G	probably damaging	Het
Pou6f2	G	A	13: 18,303,748 (GRCm39)	T120M	probably damaging	Het
Psg27	T	A	7: 18,295,726 (GRCm39)	T240S	probably damaging	Het
Samd12	T	A	15: 53,723,649 (GRCm39)	I15F	probably damaging	Het
Scaf4	A	T	16: 90,049,318 (GRCm39)	D256E	unknown	Het
Scaf8	T	A	17: 3,213,373 (GRCm39)	M154K	unknown	Het
Slc27a1	T	C	8: 72,032,071 (GRCm39)	V64A	possibly damaging	Het
Smc5	G	A	19: 23,237,064 (GRCm39)	R256*	probably null	Het
Snx31	A	G	15: 36,555,455 (GRCm39)	F31L	probably benign	Het
Spag17	T	C	3: 100,002,888 (GRCm39)	S1871P	probably benign	Het
Tdpoz4	T	G	3: 93,704,662 (GRCm39)	S320A	probably benign	Het
Tmprss11c	A	T	5: 86,379,691 (GRCm39)	C406S	probably damaging	Het
Tnip1	G	A	11: 54,808,630 (GRCm39)	A519V	probably benign	Het
Tssc4	T	A	7: 142,624,724 (GRCm39)		probably null	Het
Uba3	A	T	6: 97,182,512 (GRCm39)	M1K	probably null	Het
Usp32	GAACAAGTCCACAACAA	GAACAA	11: 84,913,681 (GRCm39)		probably null	Het
Wnt11	T	C	7: 98,496,588 (GRCm39)	M176T	possibly damaging	Het
Wrn	C	T	8: 33,814,346 (GRCm39)	G366D	probably benign	Het
Xylt1	T	A	7: 117,255,807 (GRCm39)	I793N	probably damaging	Het
Zscan4-ps1	T	A	7: 10,799,626 (GRCm39)	K421M	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
R4729:Zfp677	UTSW	17	21,617,680 (GRCm39)	missense	possibly damaging	0.51
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
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'- ATTTGCATAGTGGAGAGAAGCCTT -3'
(R):5'- GATGCCTTCTAAATGACGAATGG -3'

Sequencing Primer
(F):5'- CATAGTGGAGAGAAGCCTTATAAATG -3'
(R):5'- AGGACCTGTCACAGTCATTG -3'

Posted On

2019-06-26