Mutagenetix > Incidental Mutation

Incidental Mutation 'R7582:Zfp617'

586804

Institutional Source

Beutler Lab

Gene Symbol

Zfp617

Ensembl Gene

ENSMUSG00000066880

Gene Name

zinc finger protein 617

Synonyms

Zfps11-6, Zinc finger protein s11-6

MMRRC Submission

045665-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.242) question?

Stock #

R7582 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

72676669-72688474 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 72685864 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Asparagine at position 65 (Y65N)

Ref Sequence

ENSEMBL: ENSMUSP00000112926 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000119003] [ENSMUST00000131544]

AlphaFold

Q91WM0

Predicted Effect

probably benign
Transcript: ENSMUST00000119003
AA Change: Y65N

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000112926
Gene: ENSMUSG00000066880
AA Change: Y65N

Domain	Start	End	E-Value	Type
KRAB	4	56	1.08e-10	SMART
ZnF_C2H2	167	189	8.47e-4	SMART
ZnF_C2H2	195	217	8.34e-3	SMART
ZnF_C2H2	223	245	1.28e-3	SMART
ZnF_C2H2	251	273	1.28e-3	SMART
ZnF_C2H2	279	301	1.58e-3	SMART
ZnF_C2H2	307	329	1.28e-3	SMART
ZnF_C2H2	335	357	9.73e-4	SMART
ZnF_C2H2	363	385	6.42e-4	SMART
ZnF_C2H2	391	413	4.47e-3	SMART
ZnF_C2H2	419	441	1.38e-3	SMART
ZnF_C2H2	447	469	1.2e-3	SMART
ZnF_C2H2	475	497	1.56e-2	SMART
ZnF_C2H2	503	525	2.36e-2	SMART
ZnF_C2H2	531	553	4.98e-1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000131544
AA Change: Y65N

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000120213
Gene: ENSMUSG00000066880
AA Change: Y65N

Domain	Start	End	E-Value	Type
KRAB	4	56	1.08e-10	SMART
ZnF_C2H2	167	189	8.47e-4	SMART
ZnF_C2H2	195	217	8.34e-3	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgb	A	G	10: 10,266,565 (GRCm39)	V1007A	probably damaging	Het
Adgrl3	T	C	5: 81,841,523 (GRCm39)	V800A	probably damaging	Het
Ankfn1	T	A	11: 89,417,445 (GRCm39)	M56L	probably benign	Het
Arfgap3	A	C	15: 83,187,302 (GRCm39)	V72G	possibly damaging	Het
B3galnt2	C	T	13: 14,165,986 (GRCm39)	R294W	probably damaging	Het
Cadm1	G	T	9: 47,708,740 (GRCm39)	D157Y	probably damaging	Het
Castor1	T	C	11: 4,170,457 (GRCm39)	V151A	probably benign	Het
Ccdc81	A	T	7: 89,525,353 (GRCm39)	Y474N	probably damaging	Het
Cdkl4	T	A	17: 80,841,264 (GRCm39)	K297I	probably benign	Het
Cep128	G	A	12: 91,314,340 (GRCm39)	T146M	probably damaging	Het
Cfap161	T	C	7: 83,426,290 (GRCm39)	N236S	possibly damaging	Het
Chil3	A	T	3: 106,071,572 (GRCm39)	W31R	probably damaging	Het
Cmtm2b	C	T	8: 105,049,353 (GRCm39)	S86F	probably damaging	Het
Cntnap5a	G	A	1: 116,374,362 (GRCm39)	G958D	probably damaging	Het
Col6a5	A	G	9: 105,822,625 (GRCm39)	L244P	unknown	Het
Crat	C	T	2: 30,294,577 (GRCm39)	R497Q	probably benign	Het
Cul9	A	G	17: 46,821,905 (GRCm39)	Y1857H	probably damaging	Het
Dst	A	G	1: 34,208,964 (GRCm39)	Q1154R	probably damaging	Het
Fgg	G	A	3: 82,921,445 (GRCm39)	G376D	probably damaging	Het
Fmn2	T	C	1: 174,526,356 (GRCm39)	S1392P	probably damaging	Het
Focad	T	C	4: 88,147,615 (GRCm39)	V418A	probably benign	Het
Foxf1	A	T	8: 121,811,430 (GRCm39)	H98L	possibly damaging	Het
Frmd4a	C	CA	2: 4,599,408 (GRCm39)		probably null	Het
Fry	C	A	5: 150,419,847 (GRCm39)	T639K		Het
Fryl	A	G	5: 73,179,843 (GRCm39)		probably null	Het
Gdpd4	A	G	7: 97,607,012 (GRCm39)		probably null	Het
Gpt2	A	G	8: 86,246,145 (GRCm39)	K368R	probably damaging	Het
Hc	A	T	2: 34,881,278 (GRCm39)	V1447E	possibly damaging	Het
Kmt5a	A	G	5: 124,597,982 (GRCm39)	T280A	probably benign	Het
Lrrc4b	G	T	7: 44,111,234 (GRCm39)	V369L	probably benign	Het
Ly6g5c	A	G	17: 35,330,783 (GRCm39)	M102V	probably benign	Het
Malrd1	A	G	2: 15,700,081 (GRCm39)	S643G	unknown	Het
Mib2	T	C	4: 155,739,267 (GRCm39)	N904S	probably benign	Het
Mug2	G	A	6: 122,056,603 (GRCm39)	V1183I	probably damaging	Het
Nckap1l	C	T	15: 103,390,587 (GRCm39)	T786I	probably damaging	Het
Neb	T	C	2: 52,224,504 (GRCm39)		probably benign	Het
Neu3	A	G	7: 99,463,174 (GRCm39)	V183A	probably benign	Het
Nod1	A	G	6: 54,921,292 (GRCm39)	L342P	probably damaging	Het
Nop58	T	C	1: 59,740,097 (GRCm39)	V163A	probably damaging	Het
Npr3	C	T	15: 11,895,768 (GRCm39)	G293R	probably null	Het
Obscn	T	A	11: 58,952,253 (GRCm39)	K3939*	probably null	Het
Or4d10c	G	A	19: 12,065,370 (GRCm39)	A262V	probably benign	Het
Or4g16	T	A	2: 111,136,793 (GRCm39)	M81K	probably damaging	Het
Or5k16	A	T	16: 58,736,410 (GRCm39)	M198K	possibly damaging	Het
Or5p76	A	G	7: 108,123,058 (GRCm39)	I33T	probably benign	Het
Or8b12b	T	C	9: 37,684,117 (GRCm39)	L54P	probably damaging	Het
P2ry6	A	G	7: 100,587,784 (GRCm39)	Y192H	probably damaging	Het
Paxbp1	A	G	16: 90,819,555 (GRCm39)		probably null	Het
Pign	G	A	1: 105,577,092 (GRCm39)	T197I	probably benign	Het
Pirb	A	T	7: 3,716,817 (GRCm39)		probably null	Het
Pkdrej	C	A	15: 85,703,122 (GRCm39)	R938L	possibly damaging	Het
Psg21	A	G	7: 18,381,128 (GRCm39)	*472R	probably null	Het
Rabgap1l	A	T	1: 160,509,654 (GRCm39)	S474R	probably benign	Het
Rrn3	C	T	16: 13,628,375 (GRCm39)	Q519*	probably null	Het
Seh1l	A	T	18: 67,908,188 (GRCm39)	K37*	probably null	Het
Shprh	A	G	10: 11,040,449 (GRCm39)	S641G	probably benign	Het
Slc4a1	T	G	11: 102,243,403 (GRCm39)	S743R	probably damaging	Het
Snx13	C	T	12: 35,174,534 (GRCm39)	R688*	probably null	Het
Tlr11	C	T	14: 50,599,186 (GRCm39)	Q391*	probably null	Het
Tmbim4	A	G	10: 120,053,471 (GRCm39)	H90R	probably benign	Het
Trav8d-1	T	C	14: 53,016,326 (GRCm39)	S71P	possibly damaging	Het
Trbv5	G	A	6: 41,039,617 (GRCm39)	R74Q	probably benign	Het
Tril	A	G	6: 53,795,921 (GRCm39)	S434P	probably benign	Het
Uhmk1	A	G	1: 170,027,570 (GRCm39)	Y376H	probably damaging	Het
Uty	A	G	Y: 1,170,914 (GRCm39)	C317R	probably damaging	Het
Vmp1	C	T	11: 86,476,225 (GRCm39)	C377Y	probably benign	Het
Vwa8	A	C	14: 79,219,674 (GRCm39)		probably null	Het
Wdr41	T	C	13: 95,142,275 (GRCm39)	S150P	probably damaging	Het
Zfp800	A	C	6: 28,244,089 (GRCm39)	V292G	probably damaging	Het

Other mutations in Zfp617

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00671:Zfp617	APN	8	72,686,386 (GRCm39)	nonsense	probably null
R2116:Zfp617	UTSW	8	72,686,009 (GRCm39)	missense	probably benign	0.05
R3840:Zfp617	UTSW	8	72,685,961 (GRCm39)	missense	probably damaging	1.00
R3841:Zfp617	UTSW	8	72,685,961 (GRCm39)	missense	probably damaging	1.00
R4587:Zfp617	UTSW	8	72,683,003 (GRCm39)	missense	probably damaging	0.98
R4691:Zfp617	UTSW	8	72,686,659 (GRCm39)	missense	probably benign	0.13
R5264:Zfp617	UTSW	8	72,686,885 (GRCm39)	missense	probably damaging	0.98
R5783:Zfp617	UTSW	8	72,686,308 (GRCm39)	missense	probably damaging	1.00
R6046:Zfp617	UTSW	8	72,687,257 (GRCm39)	missense	probably damaging	1.00
R6197:Zfp617	UTSW	8	72,687,098 (GRCm39)	missense	probably benign	0.01
R6403:Zfp617	UTSW	8	72,683,015 (GRCm39)	missense	probably benign	0.26
R6890:Zfp617	UTSW	8	72,686,010 (GRCm39)	missense	probably benign	0.35
R7124:Zfp617	UTSW	8	72,686,384 (GRCm39)	missense	probably damaging	1.00
R7747:Zfp617	UTSW	8	72,682,033 (GRCm39)	splice site	probably null
R8907:Zfp617	UTSW	8	72,686,927 (GRCm39)	missense	probably damaging	1.00
R9666:Zfp617	UTSW	8	72,686,539 (GRCm39)	missense	probably benign	0.05

Predicted Primers

PCR Primer
(F):5'- CTTTGGGGAAAATACTGAGAAACC -3'
(R):5'- ATGTGTTTTGCATCTAGTCTGACC -3'

Sequencing Primer
(F):5'- CCACATGATTACCACTGCTTTGAC -3'
(R):5'- CTGACCTCTGAGGGACACATTTAG -3'

Posted On

2019-10-24