Mutagenetix > Incidental Mutation

Incidental Mutation 'R6419:Zfp493'

518026

Institutional Source

Beutler Lab

Gene Symbol

Zfp493

Ensembl Gene

ENSMUSG00000090659

Gene Name

zinc finger protein 493

Synonyms

2900054J07Rik

MMRRC Submission

044561-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.082) question?

Stock #

R6419 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

67927812-67937201 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 67934526 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 160 (T160A)

Ref Sequence

ENSEMBL: ENSMUSP00000132282 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000164936] [ENSMUST00000181319] [ENSMUST00000220570]

AlphaFold

E9Q1L8

Predicted Effect

probably benign
Transcript: ENSMUST00000164936
AA Change: T160A

PolyPhen 2 Score 0.161 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000132282
Gene: ENSMUSG00000090659
AA Change: T160A

Domain	Start	End	E-Value	Type
KRAB	5	65	3.47e-32	SMART
ZnF_C2H2	81	103	2.27e-4	SMART
ZnF_C2H2	109	131	3.95e-4	SMART
ZnF_C2H2	137	159	7.37e-4	SMART
ZnF_C2H2	165	187	6.32e-3	SMART
ZnF_C2H2	193	215	2.99e-4	SMART
ZnF_C2H2	221	243	9.73e-4	SMART
ZnF_C2H2	249	271	2.57e-3	SMART
ZnF_C2H2	277	299	1.53e-1	SMART
ZnF_C2H2	305	327	1.1e-2	SMART
ZnF_C2H2	333	355	5.42e-2	SMART
ZnF_C2H2	361	383	1.26e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000180507

Predicted Effect

probably benign
Transcript: ENSMUST00000181319

SMART Domains

Protein: ENSMUSP00000137936
Gene: ENSMUSG00000090659

Domain	Start	End	E-Value	Type
KRAB	5	65	3.47e-32	SMART
low complexity region	80	88	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000220570

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000223540

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 97.6%
20x: 92.3%

Validation Efficiency

96% (67/70)

Allele List at MGI

Other mutations in this stock

Total: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930578G10Rik	T	C	4: 42,812,473 (GRCm39)		probably benign	Het
Abcc2	T	A	19: 43,825,947 (GRCm39)		probably null	Het
Adamts12	C	T	15: 11,215,759 (GRCm39)	T260M	possibly damaging	Het
Adamts20	C	T	15: 94,231,556 (GRCm39)	V878I	possibly damaging	Het
Adgrl4	A	G	3: 151,144,953 (GRCm39)	E34G	probably damaging	Het
Asah1	A	T	8: 41,796,803 (GRCm39)	I293N	probably damaging	Het
Atosa	G	A	9: 74,916,619 (GRCm39)	S413N	probably benign	Het
B3galt2	A	T	1: 143,522,839 (GRCm39)	E325V	possibly damaging	Het
Baz1b	T	A	5: 135,271,348 (GRCm39)	H1310Q	probably benign	Het
Ccdc125	T	A	13: 100,826,834 (GRCm39)	N204K	probably damaging	Het
Cd36	C	T	5: 18,002,150 (GRCm39)	D284N	probably benign	Het
Cdh12	T	C	15: 21,520,483 (GRCm39)	L316S	probably damaging	Het
Cenpv	T	C	11: 62,416,008 (GRCm39)	K247R	probably benign	Het
Cldn18	T	C	9: 99,574,801 (GRCm39)	H257R	possibly damaging	Het
Cnot8	T	A	11: 58,004,891 (GRCm39)	Y197N	probably damaging	Het
Cog3	A	T	14: 75,962,178 (GRCm39)	C554*	probably null	Het
Col4a4	A	G	1: 82,444,207 (GRCm39)		probably null	Het
Cops5	G	A	1: 10,103,532 (GRCm39)	T158I	probably damaging	Het
Dhh	A	G	15: 98,792,282 (GRCm39)	F242S	probably damaging	Het
Dot1l	T	C	10: 80,627,315 (GRCm39)	V1512A	possibly damaging	Het
Dstn	T	G	2: 143,781,907 (GRCm39)	I116S	possibly damaging	Het
Egfem1	G	A	3: 29,711,398 (GRCm39)	D326N	probably damaging	Het
Enpp3	A	T	10: 24,684,089 (GRCm39)	Y52N	probably damaging	Het
Gabra2	A	G	5: 71,119,426 (GRCm39)	S359P	probably benign	Het
Gbp7	G	A	3: 142,252,214 (GRCm39)	G599E	probably benign	Het
Gcat	T	G	15: 78,920,264 (GRCm39)	I198S	probably damaging	Het
Gm8439	A	G	4: 120,466,755 (GRCm39)	K82R	unknown	Het
Grin2b	A	G	6: 135,717,965 (GRCm39)	F709S	probably damaging	Het
Grm3	T	C	5: 9,620,201 (GRCm39)	N348D	probably damaging	Het
Hdgfl1	G	A	13: 26,954,075 (GRCm39)		probably benign	Het
Hmgxb3	G	T	18: 61,285,296 (GRCm39)	D564E	possibly damaging	Het
Igkv4-61	C	A	6: 69,394,138 (GRCm39)	A31S	possibly damaging	Het
Impg1	A	G	9: 80,287,300 (GRCm39)	V305A	probably benign	Het
Ints7	T	A	1: 191,334,414 (GRCm39)	S313T	possibly damaging	Het
Knl1	T	A	2: 118,899,484 (GRCm39)	I395K	probably benign	Het
Lactb2	A	T	1: 13,708,459 (GRCm39)	Y196*	probably null	Het
Lad1	T	C	1: 135,759,630 (GRCm39)	S509P	possibly damaging	Het
Ltf	T	C	9: 110,860,090 (GRCm39)	F504L	possibly damaging	Het
Med4	A	T	14: 73,751,363 (GRCm39)	D104V	probably damaging	Het
Mrpl58	A	T	11: 115,301,073 (GRCm39)	N128Y	probably damaging	Het
Ndufs2	T	C	1: 171,068,668 (GRCm39)	T54A	probably benign	Het
Notch2	G	T	3: 98,007,705 (GRCm39)		probably null	Het
Ntng1	A	T	3: 109,690,169 (GRCm39)	N424K	possibly damaging	Het
Ntrk2	G	A	13: 59,009,113 (GRCm39)	W301*	probably null	Het
Or5b116	T	A	19: 13,423,131 (GRCm39)	S252T	probably benign	Het
Otud6b	A	G	4: 14,822,766 (GRCm39)	S113P	possibly damaging	Het
Pcdhb20	A	G	18: 37,638,608 (GRCm39)	N378S	probably damaging	Het
Polr3b	T	C	10: 84,473,975 (GRCm39)	S185P	possibly damaging	Het
Ptprn	G	A	1: 75,240,681 (GRCm39)	R31C	probably benign	Het
Rgsl1	C	T	1: 153,698,117 (GRCm39)	V478M	probably damaging	Het
Sema6b	A	T	17: 56,439,784 (GRCm39)	L19*	probably null	Het
Slfn8	A	G	11: 82,894,881 (GRCm39)		probably null	Het
Spen	A	T	4: 141,203,621 (GRCm39)	S1669T	unknown	Het
Syne2	T	C	12: 76,143,740 (GRCm39)	F1522L	probably damaging	Het
Tarbp1	C	T	8: 127,185,783 (GRCm39)	A470T	possibly damaging	Het
Tent4a	A	C	13: 69,658,785 (GRCm39)	M350R	possibly damaging	Het
Tiam1	C	A	16: 89,694,912 (GRCm39)	E182*	probably null	Het
Tmem231	G	A	8: 112,653,524 (GRCm39)		probably benign	Het
Trip12	C	T	1: 84,771,591 (GRCm39)	A186T	probably damaging	Het
Ufc1	C	T	1: 171,116,529 (GRCm39)	A147T	probably damaging	Het
Vmn1r199	A	G	13: 22,567,777 (GRCm39)	K314R	possibly damaging	Het
Vmn2r13	A	T	5: 109,323,085 (GRCm39)	I68K	possibly damaging	Het
Vmn2r77	A	T	7: 86,460,767 (GRCm39)	I698F	probably damaging	Het
Vmn2r86	T	C	10: 130,282,795 (GRCm39)	K607R	probably damaging	Het
Vwa3b	T	C	1: 37,196,457 (GRCm39)	V28A	probably benign	Het
Wdr19	A	G	5: 65,373,236 (GRCm39)	N166S	possibly damaging	Het
Wfdc17	G	A	11: 83,595,634 (GRCm39)	G33R	probably damaging	Het
Zfp330	T	G	8: 83,491,545 (GRCm39)	K209N	probably benign	Het
Zfp974	A	T	7: 27,610,940 (GRCm39)	C262S	possibly damaging	Het

Other mutations in Zfp493

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01419:Zfp493	APN	13	67,934,921 (GRCm39)	missense	probably benign	0.06
IGL02367:Zfp493	APN	13	67,935,089 (GRCm39)	nonsense	probably null
R0647:Zfp493	UTSW	13	67,931,994 (GRCm39)	missense	possibly damaging	0.92
R1478:Zfp493	UTSW	13	67,934,680 (GRCm39)	missense	probably damaging	1.00
R1617:Zfp493	UTSW	13	67,931,999 (GRCm39)	missense	probably damaging	1.00
R1990:Zfp493	UTSW	13	67,934,388 (GRCm39)	missense	probably damaging	1.00
R4007:Zfp493	UTSW	13	67,932,038 (GRCm39)	splice site	probably benign
R4700:Zfp493	UTSW	13	67,934,736 (GRCm39)	missense	probably damaging	1.00
R4782:Zfp493	UTSW	13	67,934,322 (GRCm39)	missense	probably null	0.97
R5376:Zfp493	UTSW	13	67,934,437 (GRCm39)	missense	possibly damaging	0.81
R5395:Zfp493	UTSW	13	67,931,965 (GRCm39)	nonsense	probably null
R5909:Zfp493	UTSW	13	67,934,717 (GRCm39)	nonsense	probably null
R6066:Zfp493	UTSW	13	67,935,069 (GRCm39)	missense	possibly damaging	0.90
R6561:Zfp493	UTSW	13	67,934,338 (GRCm39)	missense	possibly damaging	0.92
R6625:Zfp493	UTSW	13	67,934,514 (GRCm39)	nonsense	probably null
R6714:Zfp493	UTSW	13	67,934,499 (GRCm39)	missense	probably benign	0.06
R7678:Zfp493	UTSW	13	67,927,814 (GRCm39)	start gained	probably benign
R7782:Zfp493	UTSW	13	67,935,123 (GRCm39)	missense	probably benign	0.31
R8262:Zfp493	UTSW	13	67,934,976 (GRCm39)	missense	probably damaging	1.00
R8317:Zfp493	UTSW	13	67,931,958 (GRCm39)	missense	probably benign	0.42
R9469:Zfp493	UTSW	13	67,934,325 (GRCm39)	missense	probably benign	0.05
R9586:Zfp493	UTSW	13	67,932,017 (GRCm39)	missense	possibly damaging	0.86
X0021:Zfp493	UTSW	13	67,934,497 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- AGTGATTCCTCAACCTCTGC -3'
(R):5'- CTCCAGTATGAACTTTTCGGTGAAC -3'

Sequencing Primer
(F):5'- CCCTATCAGTGTAAACAATGTGGG -3'
(R):5'- CTTTTCGGTGAACAGTAAGTCC -3'

Posted On

2018-05-24