Mutagenetix > Incidental Mutation

Incidental Mutation 'R0220:Zfp1005'

33769

Institutional Source

Beutler Lab

Gene Symbol

Zfp1005

Ensembl Gene

ENSMUSG00000079008

Gene Name

zinc finger protein 1005

Synonyms

Gm10749, EG640962, Gm14124

MMRRC Submission

038469-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.070) question?

Stock #

R0220 (G1)

Quality Score

125

Status

Not validated

Chromosome

Chromosomal Location

150099437-150112220 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 150110595 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Histidine at position 428 (Q428H)

Ref Sequence

ENSEMBL: ENSMUSP00000105548 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000109922]

AlphaFold

A2AU83

Predicted Effect

unknown
Transcript: ENSMUST00000109922
AA Change: Q428H

SMART Domains

Protein: ENSMUSP00000105548
Gene: ENSMUSG00000079008
AA Change: Q428H

Domain	Start	End	E-Value	Type
KRAB	4	66	9.26e-19	SMART
ZnF_C2H2	103	125	7.49e-5	SMART
ZnF_C2H2	131	151	9.46e0	SMART
ZnF_C2H2	159	181	5.9e-3	SMART
ZnF_C2H2	187	209	6.67e-2	SMART
ZnF_C2H2	215	237	4.87e-4	SMART
ZnF_C2H2	243	265	2.82e0	SMART
ZnF_C2H2	271	293	2.2e2	SMART
ZnF_C2H2	299	321	1.4e-4	SMART
ZnF_C2H2	327	349	1.6e-4	SMART
ZnF_C2H2	355	377	1.18e-2	SMART
ZnF_C2H2	383	405	1.38e-3	SMART
ZnF_C2H2	411	433	9.56e1	SMART
ZnF_C2H2	439	461	6.99e-5	SMART
ZnF_C2H2	467	489	2.99e-4	SMART
ZnF_C2H2	495	517	7.78e-3	SMART
ZnF_C2H2	523	545	1.04e-3	SMART
ZnF_C2H2	551	573	1.6e-4	SMART
ZnF_C2H2	579	601	1.18e-2	SMART
ZnF_C2H2	607	629	4.54e-4	SMART
ZnF_C2H2	635	657	4.24e-4	SMART
ZnF_C2H2	663	685	1.2e-3	SMART
ZnF_C2H2	691	713	8.47e-4	SMART

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 96.9%
20x: 94.6%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2700049A03Rik	T	C	12: 71,195,194 (GRCm39)		probably null	Het
Abcc5	A	G	16: 20,187,852 (GRCm39)	V863A	probably benign	Het
Anxa6	A	C	11: 54,872,588 (GRCm39)		probably null	Het
Armc10	A	G	5: 21,866,582 (GRCm39)	K296R	probably benign	Het
Arpc2	T	A	1: 74,287,293 (GRCm39)	F38I	probably damaging	Het
Ass1	A	T	2: 31,404,831 (GRCm39)	N371Y	probably damaging	Het
Bcl6	T	A	16: 23,784,969 (GRCm39)	H677L	possibly damaging	Het
Bcl7a	G	A	5: 123,489,982 (GRCm39)	V49I	probably damaging	Het
Ccnj	T	C	19: 40,833,254 (GRCm39)	L144P	probably damaging	Het
Cdh8	G	T	8: 99,838,311 (GRCm39)	P510T	probably benign	Het
Cgnl1	C	A	9: 71,632,225 (GRCm39)	K375N	possibly damaging	Het
Cubn	C	A	2: 13,361,520 (GRCm39)	R1695L	probably damaging	Het
Cyp3a59	G	A	5: 146,035,080 (GRCm39)	V253I	probably benign	Het
Cyp4f13	A	G	17: 33,148,476 (GRCm39)	I208T	probably damaging	Het
Dennd4a	A	C	9: 64,759,727 (GRCm39)	E277D	probably damaging	Het
Depdc1a	G	A	3: 159,229,542 (GRCm39)	V625I	probably benign	Het
Dot1l	A	T	10: 80,621,692 (GRCm39)	D448V	probably damaging	Het
Efhc1	A	G	1: 21,037,582 (GRCm39)	D253G	probably damaging	Het
Eme1	T	A	11: 94,541,084 (GRCm39)	E246V	probably null	Het
Foxred1	A	G	9: 35,120,749 (GRCm39)	L128P	probably damaging	Het
Gm4787	G	T	12: 81,425,422 (GRCm39)	S245R	probably damaging	Het
Gm5141	T	A	13: 62,922,271 (GRCm39)	K299N	probably damaging	Het
Greb1	C	A	12: 16,732,287 (GRCm39)	R1558L	probably damaging	Het
Ip6k3	A	T	17: 27,364,203 (GRCm39)	F282I	probably damaging	Het
Kdm2a	T	C	19: 4,374,947 (GRCm39)	D288G	possibly damaging	Het
Kdm4d	A	T	9: 14,374,418 (GRCm39)	V480E	probably benign	Het
Kif26a	A	T	12: 112,123,824 (GRCm39)	Q143L	probably damaging	Het
Klhl41	G	A	2: 69,500,829 (GRCm39)	D97N	probably benign	Het
Krt34	C	T	11: 99,929,519 (GRCm39)		probably benign	Het
Lcn11	A	T	2: 25,667,843 (GRCm39)	H77L	probably benign	Het
Megf6	G	A	4: 154,342,672 (GRCm39)	R529H	probably damaging	Het
Mipol1	A	G	12: 57,503,936 (GRCm39)	E368G	probably damaging	Het
Mtus1	A	T	8: 41,447,609 (GRCm39)	M442K	probably damaging	Het
Naca	T	C	10: 127,879,255 (GRCm39)		probably benign	Het
Nbea	G	A	3: 55,912,724 (GRCm39)	T1021I	probably benign	Het
Nfib	A	T	4: 82,215,013 (GRCm39)	V530E	probably damaging	Het
Nptx1	A	G	11: 119,435,467 (GRCm39)	V283A	probably damaging	Het
Opn5	A	G	17: 42,907,495 (GRCm39)	V127A	probably benign	Het
Or4c126	G	T	2: 89,824,206 (GRCm39)	L156F	probably benign	Het
Or5h22	A	T	16: 58,895,095 (GRCm39)	M116K	probably damaging	Het
Pcgf6	A	G	19: 47,028,529 (GRCm39)	V291A	probably benign	Het
Pilrb2	C	A	5: 137,869,459 (GRCm39)	R47L	probably benign	Het
Prom2	A	C	2: 127,383,027 (GRCm39)	S72A	probably benign	Het
Sema3e	T	C	5: 14,214,167 (GRCm39)	F144S	possibly damaging	Het
Sephs1	A	G	2: 4,904,371 (GRCm39)	T250A	probably benign	Het
Smarcc2	A	T	10: 128,319,505 (GRCm39)	D798V	probably benign	Het
Taf5	T	C	19: 47,068,999 (GRCm39)	S563P	probably damaging	Het
Topaz1	A	G	9: 122,578,368 (GRCm39)	H426R	possibly damaging	Het
Tpgs1	T	A	10: 79,511,271 (GRCm39)	C138S	possibly damaging	Het
Traf1	A	T	2: 34,839,115 (GRCm39)	V70D	probably benign	Het
Ttn	T	C	2: 76,641,737 (GRCm39)	Y13453C	probably damaging	Het
Ubxn4	T	A	1: 128,183,931 (GRCm39)	V97D	possibly damaging	Het
Ugt1a8	A	T	1: 88,016,057 (GRCm39)	I157L	probably benign	Het
Vmn2r13	A	T	5: 109,304,332 (GRCm39)	C700S	probably damaging	Het
Wee1	A	T	7: 109,723,733 (GRCm39)	D216V	probably benign	Het
Zc3h4	T	C	7: 16,163,198 (GRCm39)	Y533H	unknown	Het
Zfp81	A	G	17: 33,555,698 (GRCm39)	I43T	possibly damaging	Het
Zfp963	A	T	8: 70,196,145 (GRCm39)	Y103N	probably benign	Het
Zfp963	A	T	8: 70,196,143 (GRCm39)	Y103*	probably null	Het
Zzef1	G	T	11: 72,756,792 (GRCm39)	D1126Y	probably damaging	Het

Other mutations in Zfp1005

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01550:Zfp1005	APN	2	150,108,363 (GRCm39)	splice site	probably benign
R0396:Zfp1005	UTSW	2	150,109,973 (GRCm39)	missense	probably damaging	1.00
R0402:Zfp1005	UTSW	2	150,111,136 (GRCm39)	missense	possibly damaging	0.93
R0446:Zfp1005	UTSW	2	150,109,993 (GRCm39)	missense	possibly damaging	0.71
R0462:Zfp1005	UTSW	2	150,111,122 (GRCm39)	missense	possibly damaging	0.80
R0507:Zfp1005	UTSW	2	150,110,044 (GRCm39)	missense	possibly damaging	0.69
R0605:Zfp1005	UTSW	2	150,110,523 (GRCm39)	missense	unknown
R0838:Zfp1005	UTSW	2	150,111,220 (GRCm39)	missense	possibly damaging	0.74
R1327:Zfp1005	UTSW	2	150,108,070 (GRCm39)	missense	possibly damaging	0.71
R1405:Zfp1005	UTSW	2	150,109,620 (GRCm39)	nonsense	probably null
R1405:Zfp1005	UTSW	2	150,109,620 (GRCm39)	nonsense	probably null
R2114:Zfp1005	UTSW	2	150,109,819 (GRCm39)	missense	unknown
R2140:Zfp1005	UTSW	2	150,111,281 (GRCm39)	missense	probably benign	0.33
R3683:Zfp1005	UTSW	2	150,109,976 (GRCm39)	missense	probably benign	0.41
R3917:Zfp1005	UTSW	2	150,108,039 (GRCm39)	splice site	probably benign
R4084:Zfp1005	UTSW	2	150,108,122 (GRCm39)	missense	possibly damaging	0.85
R4499:Zfp1005	UTSW	2	150,111,362 (GRCm39)	missense	possibly damaging	0.93
R4683:Zfp1005	UTSW	2	150,108,390 (GRCm39)	missense	possibly damaging	0.53
R4762:Zfp1005	UTSW	2	150,109,549 (GRCm39)	missense	possibly damaging	0.53
R4937:Zfp1005	UTSW	2	150,110,680 (GRCm39)	missense	unknown
R5678:Zfp1005	UTSW	2	150,110,425 (GRCm39)	nonsense	probably null
R5696:Zfp1005	UTSW	2	150,111,394 (GRCm39)	missense	possibly damaging	0.52
R5697:Zfp1005	UTSW	2	150,111,394 (GRCm39)	missense	possibly damaging	0.52
R5698:Zfp1005	UTSW	2	150,111,394 (GRCm39)	missense	possibly damaging	0.52
R5769:Zfp1005	UTSW	2	150,110,198 (GRCm39)	missense	possibly damaging	0.87
R5780:Zfp1005	UTSW	2	150,108,139 (GRCm39)	missense	probably benign	0.05
R5973:Zfp1005	UTSW	2	150,109,855 (GRCm39)	missense	unknown
R6662:Zfp1005	UTSW	2	150,108,172 (GRCm39)	critical splice donor site	probably null
R6878:Zfp1005	UTSW	2	150,108,406 (GRCm39)	missense	possibly damaging	0.86
R7037:Zfp1005	UTSW	2	150,108,376 (GRCm39)	missense	possibly damaging	0.86
R7081:Zfp1005	UTSW	2	150,110,189 (GRCm39)	missense	possibly damaging	0.66
R7413:Zfp1005	UTSW	2	150,108,081 (GRCm39)	missense	possibly damaging	0.93
R7725:Zfp1005	UTSW	2	150,110,468 (GRCm39)	missense	unknown
R7781:Zfp1005	UTSW	2	150,109,577 (GRCm39)	missense	possibly damaging	0.53
R8197:Zfp1005	UTSW	2	150,109,577 (GRCm39)	missense	possibly damaging	0.53
R8355:Zfp1005	UTSW	2	150,109,876 (GRCm39)	missense	unknown
R8517:Zfp1005	UTSW	2	150,110,043 (GRCm39)	missense	probably benign	0.33
R8812:Zfp1005	UTSW	2	150,109,624 (GRCm39)	missense	possibly damaging	0.83
R9108:Zfp1005	UTSW	2	150,109,969 (GRCm39)	missense	possibly damaging	0.61
R9488:Zfp1005	UTSW	2	150,110,477 (GRCm39)	missense	unknown
R9499:Zfp1005	UTSW	2	150,109,856 (GRCm39)	missense	unknown
R9551:Zfp1005	UTSW	2	150,109,856 (GRCm39)	missense	unknown
R9567:Zfp1005	UTSW	2	150,109,517 (GRCm39)	missense	possibly damaging	0.53
R9646:Zfp1005	UTSW	2	150,110,104 (GRCm39)	missense	probably benign	0.43
R9709:Zfp1005	UTSW	2	150,110,305 (GRCm39)	missense	possibly damaging	0.47
R9719:Zfp1005	UTSW	2	150,111,304 (GRCm39)	missense	possibly damaging	0.74
R9779:Zfp1005	UTSW	2	150,108,064 (GRCm39)	missense	possibly damaging	0.92
X0022:Zfp1005	UTSW	2	150,109,578 (GRCm39)	missense	possibly damaging	0.53
Z1177:Zfp1005	UTSW	2	150,110,244 (GRCm39)	missense	possibly damaging	0.94
Z1177:Zfp1005	UTSW	2	150,110,237 (GRCm39)	missense	possibly damaging	0.84

Predicted Primers

Posted On

2013-05-09