Mutagenetix > Incidental Mutation

Incidental Mutation 'R8824:Zfp780b'

673326

Institutional Source

Beutler Lab

Gene Symbol

Zfp780b

Ensembl Gene

ENSMUSG00000063047

Gene Name

zinc finger protein 780B

Synonyms

B230208L21Rik

MMRRC Submission

068657-MU

Accession Numbers

Essential gene?

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

Stock #

R8824 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

27658560-27678596 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 27662893 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 554 (Y554C)

Ref Sequence

ENSEMBL: ENSMUSP00000146224 (fasta)

Gene Model

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

AlphaFold

E9Q2S6

Predicted Effect

probably benign
Transcript: ENSMUST00000081618
AA Change: Y554C

PolyPhen 2 Score 0.447 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000080324
Gene: ENSMUSG00000063047
AA Change: Y554C

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

probably benign
Transcript: ENSMUST00000206685
AA Change: Y554C

PolyPhen 2 Score 0.447 (Sensitivity: 0.89; Specificity: 0.90)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.5%
20x: 98.5%

Validation Efficiency

100% (63/63)

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Accsl	A	T	2: 93,693,195 (GRCm39)	V260D	probably damaging	Het
Adora2a	G	A	10: 75,162,013 (GRCm39)	A51T	probably damaging	Het
Afg1l	G	A	10: 42,314,383 (GRCm39)	P128S	possibly damaging	Het
Ago4	C	A	4: 126,400,977 (GRCm39)	V623L	probably benign	Het
Akap11	A	T	14: 78,753,787 (GRCm39)	N112K		Het
C1ra	A	T	6: 124,494,654 (GRCm39)	I306F	probably damaging	Het
Ccdc73	A	G	2: 104,822,222 (GRCm39)	N724D	possibly damaging	Het
Cd248	A	G	19: 5,119,645 (GRCm39)	I498V	probably benign	Het
Clrn1	A	T	3: 58,792,314 (GRCm39)	S50T	probably benign	Het
Col7a1	A	G	9: 108,796,093 (GRCm39)	K1553R	unknown	Het
Cxcr6	A	C	9: 123,640,006 (GRCm39)	T343P	probably benign	Het
Cyp11b2	T	A	15: 74,727,914 (GRCm39)	Q56L	probably damaging	Het
Dip2a	A	G	10: 76,114,320 (GRCm39)		probably null	Het
Dnmbp	A	G	19: 43,838,276 (GRCm39)	V742A	probably benign	Het
Dusp16	A	T	6: 134,716,732 (GRCm39)	S192T	probably benign	Het
Ehbp1	A	T	11: 22,182,053 (GRCm39)	D87E	probably damaging	Het
Fgl1	A	G	8: 41,652,748 (GRCm39)	V150A	probably benign	Het
Flt3	T	C	5: 147,271,673 (GRCm39)	D873G	probably damaging	Het
Gart	T	C	16: 91,427,591 (GRCm39)	D469G	possibly damaging	Het
Gm28168	T	G	1: 117,875,625 (GRCm39)	S85A	probably benign	Het
Golgb1	A	G	16: 36,736,051 (GRCm39)	D1807G	probably benign	Het
Grm8	A	G	6: 27,761,351 (GRCm39)	L291S	probably damaging	Het
Gucy2d	C	T	7: 98,092,676 (GRCm39)	P18S	possibly damaging	Het
Ifna15	C	T	4: 88,475,998 (GRCm39)	C162Y	probably damaging	Het
Iqub	C	A	6: 24,479,307 (GRCm39)	E412*	probably null	Het
Krt4	T	A	15: 101,829,077 (GRCm39)	D312V		Het
Krtap26-1	T	C	16: 88,444,324 (GRCm39)	Y99C	probably damaging	Het
Krtap26-1	A	T	16: 88,444,303 (GRCm39)	I106N	probably damaging	Het
Lipn	T	C	19: 34,062,116 (GRCm39)	I357T	probably benign	Het
Lrrc14b	A	G	13: 74,512,068 (GRCm39)	L4P	probably damaging	Het
Mrgpra9	A	T	7: 46,885,041 (GRCm39)	C209S	probably benign	Het
Myh7b	A	G	2: 155,472,301 (GRCm39)	N1291D	probably benign	Het
Myo5a	A	G	9: 75,074,328 (GRCm39)	T746A	probably damaging	Het
Myom2	A	C	8: 15,164,169 (GRCm39)	E1021D	possibly damaging	Het
Ncoa2	C	T	1: 13,247,409 (GRCm39)	R338H	probably benign	Het
Ncor2	A	G	5: 125,195,821 (GRCm39)	F91L		Het
Neb	C	G	2: 52,106,923 (GRCm39)	A4407P	probably damaging	Het
Or10u4	C	T	10: 129,801,661 (GRCm39)	V297M	probably damaging	Het
Or1j18	A	T	2: 36,625,203 (GRCm39)	Y290F	probably damaging	Het
Or4b1b	A	G	2: 90,126,356 (GRCm39)	I283T	probably damaging	Het
Or5d47	A	G	2: 87,804,347 (GRCm39)	F221L	probably benign	Het
Or5p76	T	G	7: 108,122,350 (GRCm39)	Y269S	probably benign	Het
Or5w12	T	C	2: 87,502,304 (GRCm39)	M136V	possibly damaging	Het
Peg10	T	TCCC	6: 4,756,451 (GRCm39)		probably benign	Het
Piwil4	C	A	9: 14,638,771 (GRCm39)	K298N	probably benign	Het
Prkcz	G	A	4: 155,429,285 (GRCm39)		probably benign	Het
Prkg2	G	A	5: 99,090,067 (GRCm39)	P691L	possibly damaging	Het
Ptprc	T	A	1: 138,041,446 (GRCm39)	K89*	probably null	Het
Rapgef3	C	T	15: 97,664,789 (GRCm39)	A25T	probably benign	Het
Rreb1	C	T	13: 38,114,492 (GRCm39)	T617I	probably damaging	Het
Rsph1	A	C	17: 31,492,350 (GRCm39)	V72G	possibly damaging	Het
Shc2	A	G	10: 79,473,536 (GRCm39)	V50A	probably benign	Het
Slc38a9	G	A	13: 112,838,021 (GRCm39)	R262H	probably benign	Het
Slco6c1	T	A	1: 97,055,884 (GRCm39)	N6Y	possibly damaging	Het
Smarca5	A	G	8: 81,431,961 (GRCm39)	F886L	probably benign	Het
Tas1r2	A	G	4: 139,381,074 (GRCm39)		probably benign	Het
Tnrc6c	T	A	11: 117,630,680 (GRCm39)		probably benign	Het
Trim30b	T	A	7: 104,007,113 (GRCm39)		probably benign	Het
Trim55	T	C	3: 19,727,126 (GRCm39)	S398P	probably benign	Het
Ttc39c	T	A	18: 12,820,003 (GRCm39)		probably benign	Het
Ubxn10	A	G	4: 138,463,178 (GRCm39)		probably null	Het
Usf3	A	G	16: 44,035,976 (GRCm39)	N152S	probably benign	Het
Vps13b	T	A	15: 35,533,445 (GRCm39)	V839E	probably damaging	Het
Zeb1	T	A	18: 5,748,680 (GRCm39)		probably benign	Het
Zhx2	C	T	15: 57,684,676 (GRCm39)	T15I	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
R7311:Zfp780b	UTSW	7	27,662,588 (GRCm39)	missense	possibly damaging	0.92
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
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'- CCTTGCACTCAAAGGGTCTG -3'
(R):5'- CCACACAAGTGTAATGAGTGTGG -3'

Sequencing Primer
(F):5'- CACTACTGTGAGATTTCTGATGACG -3'
(R):5'- ATCCATTCTGGTGAGAGACCC -3'

Posted On

2021-07-15