Mutagenetix > Incidental Mutation

Incidental Mutation 'R7311:Zfp780b'

567583

Institutional Source

Beutler Lab

Gene Symbol

Zfp780b

Ensembl Gene

ENSMUSG00000063047

Gene Name

zinc finger protein 780B

Synonyms

B230208L21Rik

MMRRC Submission

045367-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.063) question?

Stock #

R7311 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

27658560-27678596 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 27662588 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 656 (F656L)

Ref Sequence

ENSEMBL: ENSMUSP00000146224 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000081618] [ENSMUST00000205874] [ENSMUST00000206685]

AlphaFold

E9Q2S6

Predicted Effect

possibly damaging
Transcript: ENSMUST00000081618
AA Change: F656L

PolyPhen 2 Score 0.922 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000080324
Gene: ENSMUSG00000063047
AA Change: F656L

Domain	Start	End	E-Value	Type
KRAB	14	75	8.48e-36	SMART
ZnF_C2H2	171	193	2.91e-2	SMART
ZnF_C2H2	199	221	3.44e-4	SMART
ZnF_C2H2	227	249	3.11e-2	SMART
ZnF_C2H2	255	277	2.4e-3	SMART
ZnF_C2H2	283	305	2.15e-5	SMART
ZnF_C2H2	311	333	1.18e-2	SMART
ZnF_C2H2	339	361	1.47e-3	SMART
ZnF_C2H2	367	389	1.79e-2	SMART
ZnF_C2H2	395	417	2.24e-3	SMART
ZnF_C2H2	423	445	7.9e-4	SMART
ZnF_C2H2	451	473	8.34e-3	SMART
ZnF_C2H2	479	501	7.9e-4	SMART
ZnF_C2H2	507	529	3.16e-3	SMART
ZnF_C2H2	535	557	1.58e-3	SMART
ZnF_C2H2	563	585	9.08e-4	SMART
ZnF_C2H2	591	613	1.36e-2	SMART
ZnF_C2H2	619	641	1.04e-3	SMART
ZnF_C2H2	647	669	1.2e-3	SMART
ZnF_C2H2	675	697	2.24e-3	SMART
ZnF_C2H2	703	725	1.03e-2	SMART
ZnF_C2H2	731	753	4.17e-3	SMART
ZnF_C2H2	759	781	1.78e2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000205874

Predicted Effect

possibly damaging
Transcript: ENSMUST00000206685
AA Change: F656L

PolyPhen 2 Score 0.922 (Sensitivity: 0.81; Specificity: 0.94)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 83 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700001K19Rik	A	G	12: 110,635,184 (GRCm39)	V118A	probably benign	Het
Accsl	C	T	2: 93,696,160 (GRCm39)	G146D	possibly damaging	Het
Acsm1	A	T	7: 119,237,305 (GRCm39)	H206L	probably damaging	Het
Acta2	A	G	19: 34,219,186 (GRCm39)	Y339H	probably damaging	Het
Adcy2	T	C	13: 68,779,073 (GRCm39)	D989G	probably damaging	Het
Ahnak	G	A	19: 8,979,507 (GRCm39)	A264T	probably benign	Het
Ahnak	A	G	19: 8,987,191 (GRCm39)	D2825G	possibly damaging	Het
Akt1	G	T	12: 112,623,587 (GRCm39)	T291K	probably damaging	Het
Arhgap24	A	G	5: 103,040,551 (GRCm39)	D589G	probably damaging	Het
B4galnt3	G	A	6: 120,192,396 (GRCm39)	Q447*	probably null	Het
BC024063	C	T	10: 81,945,993 (GRCm39)	R538C	possibly damaging	Het
Bod1l	A	G	5: 41,951,676 (GRCm39)	S2912P	possibly damaging	Het
Bysl	A	G	17: 47,912,710 (GRCm39)	V360A	possibly damaging	Het
C1qb	A	G	4: 136,607,877 (GRCm39)	V162A	possibly damaging	Het
Ccdc57	G	A	11: 120,764,567 (GRCm39)	P736L	probably benign	Het
Cep290	T	A	10: 100,373,580 (GRCm39)	F1287I	probably damaging	Het
Cntn1	T	C	15: 92,130,156 (GRCm39)		probably null	Het
Col6a3	C	T	1: 90,750,013 (GRCm39)	G274R	probably damaging	Het
Cplane1	G	T	15: 8,210,399 (GRCm39)	V291F	probably damaging	Het
Cyb5r4	T	C	9: 86,937,835 (GRCm39)	C285R	probably damaging	Het
Cyp4f39	G	A	17: 32,708,629 (GRCm39)	C392Y	probably damaging	Het
Dcun1d3	A	T	7: 119,458,734 (GRCm39)	D100E	probably damaging	Het
Dhx58	A	T	11: 100,588,997 (GRCm39)	D516E	probably benign	Het
Dock5	T	A	14: 68,065,951 (GRCm39)	I351F	probably benign	Het
Elmod2	A	C	8: 84,046,041 (GRCm39)		probably null	Het
Endov	G	A	11: 119,398,077 (GRCm39)	A281T	probably benign	Het
Epyc	A	G	10: 97,485,562 (GRCm39)	M1V	probably null	Het
Espnl	T	A	1: 91,251,290 (GRCm39)	H128Q	probably damaging	Het
Fam20a	A	T	11: 109,565,454 (GRCm39)	C452*	probably null	Het
Fam241b	A	G	10: 61,944,733 (GRCm39)	V88A	probably damaging	Het
Fbxl9	A	G	8: 106,042,299 (GRCm39)		probably benign	Het
Fgd3	A	T	13: 49,450,166 (GRCm39)	S28T	possibly damaging	Het
Fmn1	C	A	2: 113,356,025 (GRCm39)	P920Q	unknown	Het
Gpr139	G	C	7: 118,744,089 (GRCm39)	D165E	probably benign	Het
Hoxb1	A	G	11: 96,257,927 (GRCm39)	T286A	possibly damaging	Het
Ifi204	T	A	1: 173,587,134 (GRCm39)	E174D	probably benign	Het
Igf2bp2	A	G	16: 21,880,632 (GRCm39)	I555T	possibly damaging	Het
Ighv1-85	A	G	12: 115,963,799 (GRCm39)	I67T	probably damaging	Het
Ihh	G	C	1: 74,990,306 (GRCm39)	P23R	unknown	Het
Irx2	T	C	13: 72,779,396 (GRCm39)	S227P	probably damaging	Het
Itga4	A	G	2: 79,086,526 (GRCm39)	I68V	probably benign	Het
Jsrp1	T	A	10: 80,647,906 (GRCm39)	T51S	probably benign	Het
Khdc4	T	C	3: 88,619,002 (GRCm39)	S569P	probably damaging	Het
Kifc2	G	T	15: 76,547,010 (GRCm39)	G306V	probably damaging	Het
L3mbtl2	T	A	15: 81,551,588 (GRCm39)	S85T	possibly damaging	Het
Lama1	T	C	17: 68,074,380 (GRCm39)	S944P		Het
Lama4	T	A	10: 38,902,631 (GRCm39)	C202S	probably damaging	Het
Morc3	G	A	16: 93,646,061 (GRCm39)	D218N	probably damaging	Het
Mrtfb	T	A	16: 13,223,718 (GRCm39)	Y866*	probably null	Het
Myorg	A	G	4: 41,498,577 (GRCm39)	I351T	probably damaging	Het
N4bp2l1	G	A	5: 150,496,389 (GRCm39)	T179I	probably damaging	Het
Narf	A	G	11: 121,139,976 (GRCm39)	E270G	probably benign	Het
Nsd2	A	G	5: 34,049,380 (GRCm39)	D1205G	probably damaging	Het
Or10x1	T	C	1: 174,196,759 (GRCm39)	V92A	probably benign	Het
Or5an11	T	C	19: 12,246,068 (GRCm39)	V158A	probably benign	Het
Parl	T	C	16: 20,106,625 (GRCm39)	T195A	probably benign	Het
Phrf1	A	G	7: 140,820,846 (GRCm39)	I158V	unknown	Het
Phtf1	T	C	3: 103,904,980 (GRCm39)	F543L	possibly damaging	Het
Plod2	T	A	9: 92,466,611 (GRCm39)	D190E	probably damaging	Het
Polr1a	G	T	6: 71,927,863 (GRCm39)	K871N	possibly damaging	Het
Ppp2r5a	A	T	1: 191,089,998 (GRCm39)	I252K	probably damaging	Het
Ptgir	T	A	7: 16,640,973 (GRCm39)	D88E	probably damaging	Het
Raly	T	C	2: 154,699,340 (GRCm39)	V48A	probably damaging	Het
Ripor1	T	A	8: 106,344,447 (GRCm39)	L527*	probably null	Het
Rnf213	T	C	11: 119,307,373 (GRCm39)	S678P		Het
Rpf1	T	A	3: 146,212,918 (GRCm39)	Q306L	probably benign	Het
Rpl14	T	C	9: 120,403,171 (GRCm39)	I122T	probably damaging	Het
Scn9a	C	A	2: 66,314,748 (GRCm39)	A1657S	possibly damaging	Het
Serpinb10	A	G	1: 107,474,477 (GRCm39)	Y213C	probably damaging	Het
Slc25a23	A	G	17: 57,359,827 (GRCm39)	L308P	probably damaging	Het
Smg9	T	A	7: 24,120,058 (GRCm39)	M387K	probably benign	Het
Socs3	G	A	11: 117,858,614 (GRCm39)	P148L	probably benign	Het
Susd3	A	G	13: 49,401,906 (GRCm39)	L14P	probably benign	Het
Syt14	T	A	1: 192,662,858 (GRCm39)	M80L	probably benign	Het
Tmprss2	T	A	16: 97,369,616 (GRCm39)	Y386F	possibly damaging	Het
Tmx3	T	A	18: 90,558,195 (GRCm39)	S416T	probably benign	Het
Treh	A	G	9: 44,597,245 (GRCm39)	T555A	probably benign	Het
Ttc5	T	G	14: 51,003,400 (GRCm39)	Q428P	probably damaging	Het
Vmn2r73	A	G	7: 85,521,192 (GRCm39)	S259P	possibly damaging	Het
Vps4b	A	T	1: 106,719,434 (GRCm39)	V38E	probably damaging	Het
Wdr83	C	A	8: 85,802,890 (GRCm39)	R177L	probably benign	Het
Zfp995	A	T	17: 22,099,641 (GRCm39)	F198I	probably benign	Het
Zswim8	A	T	14: 20,771,552 (GRCm39)	Y1495F	probably damaging	Het

Other mutations in Zfp780b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00782:Zfp780b	APN	7	27,664,186 (GRCm39)	missense	probably benign
IGL03088:Zfp780b	APN	7	27,662,417 (GRCm39)	missense	possibly damaging	0.84
IGL03211:Zfp780b	APN	7	27,662,600 (GRCm39)	missense	possibly damaging	0.93
R0403:Zfp780b	UTSW	7	27,671,114 (GRCm39)	missense	possibly damaging	0.47
R1458:Zfp780b	UTSW	7	27,664,252 (GRCm39)	missense	probably damaging	0.99
R1550:Zfp780b	UTSW	7	27,664,282 (GRCm39)	missense	probably benign
R1694:Zfp780b	UTSW	7	27,663,808 (GRCm39)	missense	possibly damaging	0.86
R1823:Zfp780b	UTSW	7	27,662,525 (GRCm39)	missense	possibly damaging	0.93
R2113:Zfp780b	UTSW	7	27,663,298 (GRCm39)	missense	possibly damaging	0.85
R3086:Zfp780b	UTSW	7	27,663,055 (GRCm39)	missense	probably damaging	0.96
R4620:Zfp780b	UTSW	7	27,662,178 (GRCm39)	nonsense	probably null
R5023:Zfp780b	UTSW	7	27,662,873 (GRCm39)	missense	possibly damaging	0.88
R5521:Zfp780b	UTSW	7	27,674,173 (GRCm39)	splice site	probably null
R5582:Zfp780b	UTSW	7	27,664,252 (GRCm39)	missense	probably damaging	0.99
R5677:Zfp780b	UTSW	7	27,662,224 (GRCm39)	missense	probably benign	0.33
R5762:Zfp780b	UTSW	7	27,664,243 (GRCm39)	missense	probably benign
R5998:Zfp780b	UTSW	7	27,664,047 (GRCm39)	missense	probably benign	0.07
R6036:Zfp780b	UTSW	7	27,662,993 (GRCm39)	missense	probably damaging	0.99
R6036:Zfp780b	UTSW	7	27,662,993 (GRCm39)	missense	probably damaging	0.99
R6050:Zfp780b	UTSW	7	27,663,727 (GRCm39)	missense	probably damaging	0.98
R6702:Zfp780b	UTSW	7	27,671,066 (GRCm39)	missense	possibly damaging	0.91
R6703:Zfp780b	UTSW	7	27,671,066 (GRCm39)	missense	possibly damaging	0.91
R7112:Zfp780b	UTSW	7	27,662,566 (GRCm39)	missense	probably damaging	0.98
R7469:Zfp780b	UTSW	7	27,663,382 (GRCm39)	missense	probably benign	0.02
R7561:Zfp780b	UTSW	7	27,664,037 (GRCm39)	missense	possibly damaging	0.92
R7847:Zfp780b	UTSW	7	27,663,843 (GRCm39)	missense	probably benign	0.00
R8412:Zfp780b	UTSW	7	27,662,551 (GRCm39)	missense	possibly damaging	0.64
R8824:Zfp780b	UTSW	7	27,662,893 (GRCm39)	missense	probably benign	0.45
R9219:Zfp780b	UTSW	7	27,663,806 (GRCm39)	missense	probably benign	0.24
R9248:Zfp780b	UTSW	7	27,673,143 (GRCm39)	critical splice donor site	probably null
R9642:Zfp780b	UTSW	7	27,664,135 (GRCm39)	missense	probably benign	0.37
X0024:Zfp780b	UTSW	7	27,662,675 (GRCm39)	missense	probably damaging	0.99
Z1186:Zfp780b	UTSW	7	27,664,082 (GRCm39)	missense	probably benign
Z1186:Zfp780b	UTSW	7	27,663,968 (GRCm39)	missense	possibly damaging	0.73
Z1186:Zfp780b	UTSW	7	27,663,250 (GRCm39)	missense	probably benign
Z1186:Zfp780b	UTSW	7	27,674,203 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- AAGGCCTTTCCACACTCCTG -3'
(R):5'- CAAGTGTAAGCTCTGTGGGTCAG -3'

Sequencing Primer
(F):5'- CTGACACTTAAACGGTTTCTCATCAG -3'
(R):5'- GGGTCAGCCTTCAGACGTAAGTAC -3'

Posted On

2019-06-26