Mutagenetix > Incidental Mutation

Incidental Mutation 'R0520:Zfp81'

48489

Institutional Source

Beutler Lab

Gene Symbol

Zfp81

Ensembl Gene

ENSMUSG00000003929

Gene Name

zinc finger protein 81

Synonyms

Hszfp36, D330034E10Rik, KRAB13, C330034P10Rik, Zfp78

MMRRC Submission

038713-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.339) question?

Stock #

R0520 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

33548316-33577852 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 33553351 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 488 (S488P)

Ref Sequence

ENSEMBL: ENSMUSP00000050728 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000054072]

AlphaFold

B8JJZ7

Predicted Effect

probably damaging
Transcript: ENSMUST00000054072
AA Change: S488P

PolyPhen 2 Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000050728
Gene: ENSMUSG00000003929
AA Change: S488P

Domain	Start	End	E-Value	Type
KRAB	4	55	1.15e-14	SMART
ZnF_C2H2	222	244	1.04e-3	SMART
ZnF_C2H2	250	272	1.53e-1	SMART
ZnF_C2H2	278	300	1.33e-1	SMART
ZnF_C2H2	306	328	5.21e-4	SMART
ZnF_C2H2	334	356	2.2e-2	SMART
ZnF_C2H2	362	384	1.58e-3	SMART
ZnF_C2H2	390	412	1.64e-1	SMART
ZnF_C2H2	418	440	7.67e-2	SMART
ZnF_C2H2	446	468	1.89e-1	SMART
ZnF_C2H2	474	496	2.86e-1	SMART
ZnF_C2H2	502	524	1.08e-1	SMART

Meta Mutation Damage Score

0.1564

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 94.2%

Validation Efficiency

100% (72/72)

Allele List at MGI

Other mutations in this stock

Total: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acod1	T	C	14: 103,288,952 (GRCm39)	I154T	possibly damaging	Het
Acr	G	T	15: 89,457,430 (GRCm39)	C226F	probably damaging	Het
Aff1	C	T	5: 103,995,617 (GRCm39)	R1070*	probably null	Het
Aldh9a1	C	T	1: 167,188,960 (GRCm39)		probably benign	Het
Apaf1	A	T	10: 90,915,851 (GRCm39)	H12Q	probably damaging	Het
Asic1	A	T	15: 99,593,416 (GRCm39)	I291F	probably damaging	Het
Aspm	T	A	1: 139,406,558 (GRCm39)	M1815K	possibly damaging	Het
Asxl3	A	T	18: 22,656,043 (GRCm39)	D1351V	probably damaging	Het
Atg9a	C	T	1: 75,163,178 (GRCm39)	W299*	probably null	Het
B3gntl1	C	A	11: 121,514,314 (GRCm39)	V313F	possibly damaging	Het
B4galnt4	T	A	7: 140,647,286 (GRCm39)	C345*	probably null	Het
Bicc1	A	T	10: 70,793,020 (GRCm39)	F211L	probably damaging	Het
Cachd1	T	G	4: 100,754,900 (GRCm39)	V117G	probably damaging	Het
Cdc16	G	A	8: 13,810,569 (GRCm39)		probably null	Het
Cers6	C	T	2: 68,935,435 (GRCm39)	Q312*	probably null	Het
Csta2	A	G	16: 36,073,461 (GRCm39)	I16V	probably benign	Het
Dclre1c	A	G	2: 3,437,512 (GRCm39)	H115R	probably damaging	Het
Ddx20	T	C	3: 105,594,692 (GRCm39)	T18A	probably benign	Het
Dhx57	A	G	17: 80,565,604 (GRCm39)	V816A	possibly damaging	Het
Dlgap1	C	T	17: 70,823,989 (GRCm39)	Q325*	probably null	Het
Dnaja1	A	T	4: 40,728,072 (GRCm39)	M178L	probably benign	Het
Ecd	A	T	14: 20,378,732 (GRCm39)	S454T	probably benign	Het
Efcab6	G	A	15: 83,834,247 (GRCm39)	H454Y	probably benign	Het
Exo1	T	A	1: 175,727,031 (GRCm39)	D447E	probably benign	Het
F5	T	G	1: 164,037,156 (GRCm39)	I1965S	probably benign	Het
Fbn2	A	G	18: 58,146,821 (GRCm39)	C2692R	probably damaging	Het
Fggy	T	A	4: 95,489,340 (GRCm39)	L152Q	probably damaging	Het
Glb1	ACCC	ACC	9: 114,250,812 (GRCm39)		probably null	Het
Gm9871	A	G	6: 101,778,540 (GRCm39)		noncoding transcript	Het
Gnai2	A	T	9: 107,497,372 (GRCm39)	D7E	probably benign	Het
Gon7	C	T	12: 102,724,047 (GRCm39)		probably benign	Het
H2-K2	A	T	17: 34,216,390 (GRCm39)	V272E	probably damaging	Het
Hectd4	G	T	5: 121,469,770 (GRCm39)	R2555L	possibly damaging	Het
Hexb	T	C	13: 97,317,618 (GRCm39)	R360G	probably benign	Het
Igsf9b	C	A	9: 27,234,546 (GRCm39)	S470R	probably benign	Het
Inpp5d	T	C	1: 87,633,642 (GRCm39)		probably benign	Het
Inpp5k	C	A	11: 75,530,356 (GRCm39)	Y265*	probably null	Het
Klhl33	T	G	14: 51,129,140 (GRCm39)	E436D	probably damaging	Het
Krt80	A	G	15: 101,267,898 (GRCm39)	L13P	probably benign	Het
Krtap19-2	C	T	16: 88,670,749 (GRCm39)		probably benign	Het
Marchf10	T	C	11: 105,280,708 (GRCm39)	T526A	probably benign	Het
Mcrs1	A	G	15: 99,146,336 (GRCm39)		probably null	Het
Msh2	G	T	17: 88,024,972 (GRCm39)	V617F	possibly damaging	Het
Nckap1	A	C	2: 80,371,874 (GRCm39)		probably benign	Het
Nek4	T	A	14: 30,681,263 (GRCm39)		probably benign	Het
Or7h8	G	A	9: 20,123,791 (GRCm39)	V49I	probably benign	Het
Or8b12b	T	C	9: 37,684,849 (GRCm39)	V298A	probably benign	Het
Or8k22	G	T	2: 86,163,475 (GRCm39)	T75K	probably damaging	Het
Or9s14	T	A	1: 92,536,471 (GRCm39)	V304E	probably damaging	Het
Osgin1	A	G	8: 120,169,247 (GRCm39)	H48R	probably damaging	Het
Pam	T	A	1: 97,811,920 (GRCm39)	T369S	probably benign	Het
Pclo	C	T	5: 14,763,844 (GRCm39)	Q821*	probably null	Het
Plekhm1	T	C	11: 103,285,770 (GRCm39)	I222V	probably benign	Het
Ptprg	T	G	14: 12,199,783 (GRCm38)	N65K	possibly damaging	Het
Pum2	T	A	12: 8,771,710 (GRCm39)	V351E	probably damaging	Het
Slc25a54	T	A	3: 109,014,546 (GRCm39)		probably benign	Het
Smchd1	A	T	17: 71,736,538 (GRCm39)	D587E	possibly damaging	Het
Stap1	A	G	5: 86,238,823 (GRCm39)	M164V	probably benign	Het
Stat5a	T	C	11: 100,752,252 (GRCm39)	V30A	probably damaging	Het
Stk36	T	G	1: 74,641,365 (GRCm39)		probably benign	Het
Tiam1	G	T	16: 89,614,839 (GRCm39)		probably benign	Het
Tmc5	T	C	7: 118,265,799 (GRCm39)	M553T	probably damaging	Het
Tmem14a	T	A	1: 21,299,636 (GRCm39)	Y89N	possibly damaging	Het
Tpp2	A	G	1: 44,029,690 (GRCm39)	Y991C	probably damaging	Het
Ttc7	A	G	17: 87,666,579 (GRCm39)	K615E	possibly damaging	Het
Ubac2	C	T	14: 122,231,754 (GRCm39)	P227S	probably damaging	Het
Vit	A	C	17: 78,932,588 (GRCm39)	K565T	probably damaging	Het
Vps13c	T	C	9: 67,853,133 (GRCm39)	F2409L	possibly damaging	Het
Wdr64	A	G	1: 175,553,958 (GRCm39)	T173A	probably damaging	Het
Zfp759	T	C	13: 67,285,419 (GRCm39)	I60T	probably benign	Het
Zic2	CCCACCACCACCATCACCACCACCACC	CCCACCATCACCACCACCACC	14: 122,713,776 (GRCm39)		probably benign	Het

Other mutations in Zfp81

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
feuer	UTSW	17	33,553,307 (GRCm39)	nonsense	probably null
R0143:Zfp81	UTSW	17	33,554,095 (GRCm39)	missense	possibly damaging	0.85
R0220:Zfp81	UTSW	17	33,555,698 (GRCm39)	missense	possibly damaging	0.93
R0611:Zfp81	UTSW	17	33,553,593 (GRCm39)	missense	probably benign	0.02
R1171:Zfp81	UTSW	17	33,554,254 (GRCm39)	missense	probably benign
R1613:Zfp81	UTSW	17	33,553,757 (GRCm39)	missense	probably damaging	0.98
R1779:Zfp81	UTSW	17	33,554,080 (GRCm39)	missense	probably benign	0.06
R1970:Zfp81	UTSW	17	33,554,475 (GRCm39)	missense	probably benign
R2063:Zfp81	UTSW	17	33,554,278 (GRCm39)	missense	probably benign	0.03
R2314:Zfp81	UTSW	17	33,553,597 (GRCm39)	missense	probably damaging	0.99
R2898:Zfp81	UTSW	17	33,553,274 (GRCm39)	nonsense	probably null
R3115:Zfp81	UTSW	17	33,553,537 (GRCm39)	missense	possibly damaging	0.80
R4207:Zfp81	UTSW	17	33,553,890 (GRCm39)	missense	probably damaging	1.00
R4497:Zfp81	UTSW	17	33,553,677 (GRCm39)	missense	possibly damaging	0.47
R4498:Zfp81	UTSW	17	33,553,677 (GRCm39)	missense	possibly damaging	0.47
R5756:Zfp81	UTSW	17	33,553,307 (GRCm39)	nonsense	probably null
R5964:Zfp81	UTSW	17	33,555,819 (GRCm39)	missense	probably damaging	0.99
R6671:Zfp81	UTSW	17	33,554,413 (GRCm39)	missense	probably benign	0.17
R7728:Zfp81	UTSW	17	33,555,791 (GRCm39)	missense	possibly damaging	0.95
R9047:Zfp81	UTSW	17	33,553,387 (GRCm39)	missense	probably damaging	1.00
R9561:Zfp81	UTSW	17	33,553,774 (GRCm39)	missense	probably benign	0.15
R9800:Zfp81	UTSW	17	33,554,411 (GRCm39)	nonsense	probably null
Z1176:Zfp81	UTSW	17	33,553,803 (GRCm39)	missense	possibly damaging	0.95

Predicted Primers

PCR Primer
(F):5'- CAGCAAGCTGGATACAAAGACTCTCAA -3'
(R):5'- GCTTTCATTCATCCAAGGGCCTGTTA -3'

Sequencing Primer
(F):5'- ACATGTGaaggctttcccac -3'
(R):5'- tcacactggagagaaaccttac -3'

Posted On

2013-06-12