Mutagenetix > Incidental Mutation

Incidental Mutation 'R1819:Zer1'

204678

Institutional Source

Beutler Lab

Gene Symbol

Zer1

Ensembl Gene

ENSMUSG00000039686

Gene Name

zyg-11 related, cell cycle regulator

Synonyms

Zyg11bl, C230075L19Rik

MMRRC Submission

039847-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.134) question?

Stock #

R1819 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

29987295-30014597 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 30000230 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Threonine at position 317 (A317T)

Ref Sequence

ENSEMBL: ENSMUSP00000046441 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000044751] [ENSMUST00000113677]

AlphaFold

Q80ZJ6

Predicted Effect

probably benign
Transcript: ENSMUST00000044751
AA Change: A317T

PolyPhen 2 Score 0.184 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000046441
Gene: ENSMUSG00000039686
AA Change: A317T

Domain	Start	End	E-Value	Type
SCOP:d1jdha_	405	774	3e-15	SMART
Blast:ARM	440	480	2e-18	BLAST
Blast:ARM	524	569	4e-24	BLAST
Blast:ARM	571	613	6e-22	BLAST
Blast:ARM	617	656	7e-8	BLAST
Blast:ARM	686	724	6e-18	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000113677
AA Change: A304T

PolyPhen 2 Score 0.035 (Sensitivity: 0.94; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000109307
Gene: ENSMUSG00000039686
AA Change: A304T

Domain	Start	End	E-Value	Type
SCOP:d1jdha_	392	761	3e-15	SMART
Blast:ARM	427	467	2e-18	BLAST
Blast:ARM	511	556	4e-24	BLAST
Blast:ARM	558	600	2e-21	BLAST
Blast:ARM	604	643	7e-8	BLAST
Blast:ARM	673	711	6e-18	BLAST

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000131858

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133354

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000139128

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000149818

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000154231

Meta Mutation Damage Score

0.0607

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 95.1%
20x: 91.9%

Validation Efficiency

100% (91/91)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a subunit of an E3 ubiquitin ligase complex that may be involved in meiosis. The encoded protein contains three leucine-rich repeat motifs. [provided by RefSeq, Nov 2012]

Allele List at MGI

Other mutations in this stock

Total: 89 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca8b	T	C	11: 109,871,882 (GRCm39)		probably null	Het
Abhd17a	T	C	10: 80,422,470 (GRCm39)	T71A	probably benign	Het
Acad11	G	A	9: 103,991,738 (GRCm39)		probably null	Het
Adgrf1	C	A	17: 43,620,924 (GRCm39)	T387K	probably benign	Het
Afdn	A	G	17: 14,071,110 (GRCm39)	T783A	probably damaging	Het
Akap13	T	A	7: 75,258,453 (GRCm39)	M359K	probably benign	Het
Asxl3	A	T	18: 22,655,433 (GRCm39)	N1148Y	probably damaging	Het
Atl1	T	C	12: 70,010,074 (GRCm39)	S547P	probably benign	Het
Bace1	A	T	9: 45,768,460 (GRCm39)	T252S	possibly damaging	Het
BC034090	A	G	1: 155,101,575 (GRCm39)	S230P	possibly damaging	Het
Bnc2	A	G	4: 84,210,111 (GRCm39)	F778L	possibly damaging	Het
Capn2	T	A	1: 182,300,162 (GRCm39)	K609N	probably benign	Het
Capn8	T	A	1: 182,426,391 (GRCm39)	I242N	probably damaging	Het
Car9	G	T	4: 43,512,439 (GRCm39)		probably null	Het
Ccdc180	A	G	4: 45,926,195 (GRCm39)	E1135G	possibly damaging	Het
Ccdc181	C	T	1: 164,110,047 (GRCm39)	Q385*	probably null	Het
Cdh10	G	T	15: 18,992,051 (GRCm39)	G437*	probably null	Het
Ceacam1	T	A	7: 25,163,285 (GRCm39)	Q316L	possibly damaging	Het
Cecr2	A	G	6: 120,708,228 (GRCm39)	T77A	probably damaging	Het
Cers4	T	A	8: 4,571,232 (GRCm39)	M267K	probably benign	Het
Csmd3	T	C	15: 47,617,131 (GRCm39)	D1930G	possibly damaging	Het
Cyp2j11	A	T	4: 96,185,976 (GRCm39)	V403D	probably damaging	Het
Cyp4v3	G	A	8: 45,768,673 (GRCm39)	R296C	possibly damaging	Het
Ddx59	A	G	1: 136,360,245 (GRCm39)	I420V	probably damaging	Het
Dnah5	T	A	15: 28,246,546 (GRCm39)	L628*	probably null	Het
Dnah7a	A	C	1: 53,598,307 (GRCm39)	D1409E	probably benign	Het
Dus2	T	A	8: 106,778,480 (GRCm39)	W377R	probably damaging	Het
E330034G19Rik	A	G	14: 24,348,081 (GRCm39)	D111G	probably damaging	Het
Erich4	C	T	7: 25,314,715 (GRCm39)	R66Q	possibly damaging	Het
Fcgbp	G	T	7: 27,784,708 (GRCm39)	R256L	probably benign	Het
Fdxr	A	T	11: 115,166,930 (GRCm39)	F53Y	probably damaging	Het
Fkbp10	G	T	11: 100,306,715 (GRCm39)	A36S	probably benign	Het
Foxo3	A	T	10: 42,073,607 (GRCm39)	D84E	probably benign	Het
Gin1	A	G	1: 97,712,951 (GRCm39)		probably null	Het
Gli3	C	T	13: 15,900,377 (GRCm39)	Q1255*	probably null	Het
Gm4847	T	A	1: 166,465,788 (GRCm39)	H267L	probably damaging	Het
Gpr171	T	C	3: 59,005,341 (GRCm39)	I145V	probably benign	Het
Gpr68	T	A	12: 100,844,662 (GRCm39)	H294L	possibly damaging	Het
Gys2	T	C	6: 142,406,912 (GRCm39)	E148G	probably damaging	Het
Heatr5b	T	C	17: 79,098,940 (GRCm39)	D1320G	probably damaging	Het
Ifnlr1	G	T	4: 135,413,834 (GRCm39)		probably benign	Het
Ift88	G	A	14: 57,692,976 (GRCm39)	E392K	probably damaging	Het
Igsf9b	T	A	9: 27,222,889 (GRCm39)	S97T	probably damaging	Het
Il18rap	A	G	1: 40,570,687 (GRCm39)	I210V	probably benign	Het
Kcnj11	C	T	7: 45,748,580 (GRCm39)	G248S	probably benign	Het
Kif28	T	C	1: 179,533,319 (GRCm39)	K541E	possibly damaging	Het
Lilrb4a	A	G	10: 51,372,124 (GRCm39)	Y205C	probably damaging	Het
Lima1	T	A	15: 99,717,817 (GRCm39)	H63L	probably benign	Het
Lonrf3	A	G	X: 35,622,361 (GRCm39)	I687V	probably damaging	Het
Lrba	A	G	3: 86,449,941 (GRCm39)	T2099A	possibly damaging	Het
Morn5	C	T	2: 35,942,987 (GRCm39)	T29M	probably damaging	Het
Neurl1b	G	A	17: 26,657,674 (GRCm39)	R22H	probably benign	Het
Nr2e3	T	C	9: 59,850,720 (GRCm39)	I380V	probably damaging	Het
Oas1c	G	A	5: 120,946,800 (GRCm39)	A10V	possibly damaging	Het
Or1e35	T	C	11: 73,797,505 (GRCm39)	E271G	probably benign	Het
Or52e8	C	T	7: 104,624,605 (GRCm39)	V196I	probably benign	Het
P3h3	T	C	6: 124,831,895 (GRCm39)	T297A	probably benign	Het
Pdpk1	T	C	17: 24,329,878 (GRCm39)	K53E	probably damaging	Het
Plec	C	T	15: 76,064,106 (GRCm39)	R2056Q	probably damaging	Het
Plxna2	T	A	1: 194,472,494 (GRCm39)	N1079K	probably benign	Het
Prr12	G	C	7: 44,698,121 (GRCm39)		probably benign	Het
Psip1	A	G	4: 83,376,400 (GRCm39)	S480P	probably benign	Het
Ptpre	A	G	7: 135,270,722 (GRCm39)		probably benign	Het
Pvalb	A	C	15: 78,086,784 (GRCm39)	V44G	probably damaging	Het
Rab3c	T	G	13: 110,220,669 (GRCm39)	Q164P	possibly damaging	Het
Rubcn	T	C	16: 32,647,284 (GRCm39)	K703R	possibly damaging	Het
Setd7	T	G	3: 51,450,060 (GRCm39)	H122P	probably benign	Het
Slc26a8	A	T	17: 28,903,808 (GRCm39)	F19I	probably benign	Het
Slc6a14	A	G	X: 21,607,286 (GRCm39)	D625G	probably benign	Het
Snx6	C	T	12: 54,830,259 (GRCm39)	V67I	possibly damaging	Het
Syngr3	A	G	17: 24,906,696 (GRCm39)	F40L	possibly damaging	Het
Syt8	G	A	7: 141,991,971 (GRCm39)	G21R	possibly damaging	Het
Tagln	A	G	9: 45,842,138 (GRCm39)	F152L	probably benign	Het
Tcf12	G	A	9: 72,016,999 (GRCm39)	T36M	probably damaging	Het
Tdrd6	C	T	17: 43,937,442 (GRCm39)	S1202N	probably benign	Het
Tekt2	T	C	4: 126,217,529 (GRCm39)	K179E	probably damaging	Het
Tekt4	G	T	17: 25,692,785 (GRCm39)		probably null	Het
Tmprss5	G	T	9: 49,018,464 (GRCm39)	R98L	probably benign	Het
Tns1	G	T	1: 73,955,635 (GRCm39)		probably benign	Het
Tpcn1	A	C	5: 120,674,292 (GRCm39)		probably null	Het
Ttc6	T	C	12: 57,741,286 (GRCm39)		probably null	Het
Ttf1	A	G	2: 28,964,796 (GRCm39)	N706S	possibly damaging	Het
Washc4	C	T	10: 83,386,748 (GRCm39)	T124I	probably benign	Het
Wdr17	A	T	8: 55,143,159 (GRCm39)	S140T	probably benign	Het
Wdr19	A	T	5: 65,370,234 (GRCm39)	I123F	possibly damaging	Het
Zfp474	A	G	18: 52,771,872 (GRCm39)	D175G	probably damaging	Het
Zfp598	T	C	17: 24,900,104 (GRCm39)		probably benign	Het
Zfp646	G	A	7: 127,482,292 (GRCm39)	G1490S	probably benign	Het
Zranb3	A	T	1: 127,945,293 (GRCm39)		probably null	Het

Other mutations in Zer1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01098:Zer1	APN	2	29,998,232 (GRCm39)	critical splice donor site	probably null
IGL01630:Zer1	APN	2	29,991,843 (GRCm39)	missense	probably damaging	1.00
IGL02126:Zer1	APN	2	29,994,928 (GRCm39)	missense	probably benign	0.10
IGL02338:Zer1	APN	2	30,003,405 (GRCm39)	missense	probably damaging	1.00
IGL02817:Zer1	APN	2	29,993,406 (GRCm39)	missense	probably damaging	0.99
PIT4402001:Zer1	UTSW	2	29,991,132 (GRCm39)	missense	probably damaging	0.96
PIT4495001:Zer1	UTSW	2	29,993,555 (GRCm39)	missense	probably benign	0.01
R0390:Zer1	UTSW	2	29,998,225 (GRCm39)	splice site	probably benign
R0506:Zer1	UTSW	2	29,991,819 (GRCm39)	missense	probably damaging	1.00
R0606:Zer1	UTSW	2	29,994,809 (GRCm39)	splice site	probably benign
R0928:Zer1	UTSW	2	29,991,775 (GRCm39)	critical splice donor site	probably null
R1167:Zer1	UTSW	2	29,998,258 (GRCm39)	missense	probably benign	0.00
R2040:Zer1	UTSW	2	29,998,286 (GRCm39)	missense	probably damaging	1.00
R2041:Zer1	UTSW	2	29,998,286 (GRCm39)	missense	probably damaging	1.00
R2042:Zer1	UTSW	2	29,998,286 (GRCm39)	missense	probably damaging	1.00
R2092:Zer1	UTSW	2	29,998,286 (GRCm39)	missense	probably damaging	1.00
R2168:Zer1	UTSW	2	29,994,887 (GRCm39)	missense	probably damaging	1.00
R2243:Zer1	UTSW	2	29,991,139 (GRCm39)	missense	probably damaging	0.99
R2254:Zer1	UTSW	2	29,998,286 (GRCm39)	missense	probably damaging	1.00
R2255:Zer1	UTSW	2	29,998,286 (GRCm39)	missense	probably damaging	1.00
R2311:Zer1	UTSW	2	29,991,834 (GRCm39)	missense	probably damaging	0.99
R2993:Zer1	UTSW	2	29,991,909 (GRCm39)	missense	probably damaging	1.00
R3010:Zer1	UTSW	2	30,003,297 (GRCm39)	missense	probably benign	0.13
R3731:Zer1	UTSW	2	30,000,923 (GRCm39)	missense	probably benign	0.44
R4038:Zer1	UTSW	2	29,997,535 (GRCm39)	missense	probably damaging	1.00
R5241:Zer1	UTSW	2	29,994,982 (GRCm39)	missense	probably damaging	1.00
R5433:Zer1	UTSW	2	29,990,998 (GRCm39)	intron	probably benign
R5443:Zer1	UTSW	2	30,001,008 (GRCm39)	missense	probably damaging	1.00
R5524:Zer1	UTSW	2	29,994,866 (GRCm39)	missense	probably damaging	1.00
R5936:Zer1	UTSW	2	29,997,679 (GRCm39)	missense	probably damaging	0.97
R5999:Zer1	UTSW	2	29,995,009 (GRCm39)	missense	probably damaging	1.00
R6598:Zer1	UTSW	2	30,003,286 (GRCm39)	missense	probably damaging	1.00
R6965:Zer1	UTSW	2	29,991,059 (GRCm39)	missense	possibly damaging	0.87
R7030:Zer1	UTSW	2	30,001,033 (GRCm39)	missense	probably benign	0.00
R7190:Zer1	UTSW	2	29,993,444 (GRCm39)	missense	probably damaging	1.00
R7218:Zer1	UTSW	2	29,995,024 (GRCm39)	missense	probably damaging	1.00
R7252:Zer1	UTSW	2	29,991,904 (GRCm39)	missense	probably damaging	0.99
R7383:Zer1	UTSW	2	30,001,253 (GRCm39)	missense	probably damaging	1.00
R7417:Zer1	UTSW	2	29,992,834 (GRCm39)	missense	probably damaging	1.00
R7459:Zer1	UTSW	2	30,003,337 (GRCm39)	missense	probably damaging	1.00
R7463:Zer1	UTSW	2	30,003,449 (GRCm39)	start gained	probably benign
R7466:Zer1	UTSW	2	29,991,496 (GRCm39)	splice site	probably null
R7477:Zer1	UTSW	2	29,997,988 (GRCm39)	missense	probably null	0.34
R7719:Zer1	UTSW	2	30,001,243 (GRCm39)	missense	probably damaging	1.00
R7813:Zer1	UTSW	2	30,000,385 (GRCm39)	missense	probably damaging	1.00
R7976:Zer1	UTSW	2	29,997,520 (GRCm39)	missense	probably damaging	0.99
R8239:Zer1	UTSW	2	29,991,147 (GRCm39)	critical splice acceptor site	probably null
R8350:Zer1	UTSW	2	29,991,862 (GRCm39)	missense	probably damaging	1.00
R8404:Zer1	UTSW	2	29,995,035 (GRCm39)	critical splice acceptor site	probably null
R8842:Zer1	UTSW	2	30,001,062 (GRCm39)	missense	possibly damaging	0.65
R8896:Zer1	UTSW	2	29,993,430 (GRCm39)	missense	probably damaging	0.99
R8906:Zer1	UTSW	2	30,001,035 (GRCm39)	missense	probably benign	0.31
R8929:Zer1	UTSW	2	30,000,881 (GRCm39)	missense	probably damaging	1.00
R9050:Zer1	UTSW	2	30,001,294 (GRCm39)	missense	probably damaging	1.00
R9066:Zer1	UTSW	2	30,000,686 (GRCm39)	missense	probably damaging	1.00
R9277:Zer1	UTSW	2	30,001,297 (GRCm39)	missense	probably benign	0.00
R9322:Zer1	UTSW	2	30,000,923 (GRCm39)	missense	probably benign	0.00
R9577:Zer1	UTSW	2	29,991,050 (GRCm39)	missense	probably damaging	1.00
R9733:Zer1	UTSW	2	29,997,643 (GRCm39)	missense	probably benign	0.00
X0026:Zer1	UTSW	2	29,994,907 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- GCTGAGGCATCTCACTGGC -3'
(R):5'- GTCCCCACCTGATCTCCAG -3'

Sequencing Primer
(F):5'- AGAGTTCTAAACTGCTGAGCC -3'
(R):5'- ACCTGATCTCCAGCCACCTG -3'

Posted On

2014-06-23