Mutagenetix > Incidental Mutations

Incidental Mutation 'R0068:Mroh1'

16365

Institutional Source

Beutler Lab

Gene Symbol

Mroh1

Ensembl Gene

ENSMUSG00000022558

Gene Name

maestro heat-like repeat family member 1

Synonyms

Heatr7a, D330001F17Rik

MMRRC Submission

038359-MU

Accession Numbers

Is this an essential gene?

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

Stock #

R0068 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

76380261-76453038 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

A to G at 76446692 bp

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000094115 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000096385] [ENSMUST00000159218]

Predicted Effect

probably benign
Transcript: ENSMUST00000096385

SMART Domains

Protein: ENSMUSP00000094115
Gene: ENSMUSG00000022558

Domain	Start	End	E-Value	Type
low complexity region	442	455	N/A	INTRINSIC
low complexity region	594	607	N/A	INTRINSIC
low complexity region	799	810	N/A	INTRINSIC
low complexity region	935	946	N/A	INTRINSIC
low complexity region	1191	1202	N/A	INTRINSIC
low complexity region	1355	1367	N/A	INTRINSIC
low complexity region	1488	1502	N/A	INTRINSIC
Pfam:HEAT	1610	1640	2.2e-5	PFAM

Predicted Effect

SMART Domains

Protein: ENSMUSP00000124811
Gene: ENSMUSG00000022558

Domain	Start	End	E-Value	Type
low complexity region	442	455	N/A	INTRINSIC
low complexity region	594	607	N/A	INTRINSIC
low complexity region	790	801	N/A	INTRINSIC
low complexity region	926	937	N/A	INTRINSIC
low complexity region	1182	1193	N/A	INTRINSIC
low complexity region	1346	1358	N/A	INTRINSIC
low complexity region	1479	1493	N/A	INTRINSIC
Pfam:HEAT	1601	1631	1.3e-5	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000160525

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000160806

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000160986

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000161683

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000161962

Coding Region Coverage

1x: 89.9%
3x: 97.6%
10x: 82.1%
20x: 74.0%

Validation Efficiency

94% (83/88)

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4932438A13Rik	A	G	3: 36,952,221	T1675A	probably benign	Het
Abca9	T	C	11: 110,145,579	N568S	probably damaging	Het
AC104834.1	A	T	15: 101,054,248	I51N	probably damaging	Het
Aldoart2	G	T	12: 55,565,448	E53*	probably null	Het
Ankra2	C	T	13: 98,273,383	Q137*	probably null	Het
Arpc1a	C	T	5: 145,091,244	T21I	possibly damaging	Het
Arvcf	T	C	16: 18,396,954		probably benign	Het
Ash1l	C	A	3: 89,007,317	S1751R	probably benign	Het
Bsn	C	A	9: 108,112,137	G2139C	probably damaging	Het
Cbl	A	T	9: 44,154,194	S22T	probably damaging	Het
Ccdc148	T	C	2: 58,827,617	E530G	probably benign	Het
Cct3	A	G	3: 88,318,465	D365G	probably benign	Het
Cep85	A	T	4: 134,154,295	H332Q	probably benign	Het
Cwf19l1	A	T	19: 44,131,499	Y68N	probably damaging	Het
Dlc1	T	A	8: 36,937,721	M305L	probably benign	Het
Dnm1l	C	A	16: 16,324,019	G288C	probably damaging	Het
Exoc7	T	C	11: 116,304,906	Y83C	probably damaging	Het
Flnb	A	G	14: 7,915,290	N1474D	possibly damaging	Het
Ghrhr	C	T	6: 55,380,864		probably benign	Het
Gucy1b1	T	C	3: 82,034,878	T525A	probably benign	Het
Hhip	T	G	8: 79,989,256	D557A	probably damaging	Het
Hps5	A	G	7: 46,777,042		probably benign	Het
Igsf10	A	T	3: 59,330,624	V712D	probably damaging	Het
Irf6	G	T	1: 193,165,759		probably benign	Het
Itpr3	T	C	17: 27,104,060		probably benign	Het
Jag2	A	G	12: 112,915,193		probably benign	Het
Kansl1l	A	G	1: 66,720,888	V911A	probably benign	Het
Kdm3b	C	T	18: 34,824,774	T1064I	probably benign	Het
Lrriq1	T	A	10: 103,063,418	Q1654L	probably benign	Het
Ltbp1	A	G	17: 75,359,409	T1366A	probably damaging	Het
Napb	G	A	2: 148,698,923		probably benign	Het
Nebl	T	A	2: 17,434,971	R164*	probably null	Het
Npc1	G	C	18: 12,208,367	P532A	probably benign	Het
Nrp2	G	T	1: 62,745,377	K228N	possibly damaging	Het
Olfr275	T	A	4: 52,825,503	Y35*	probably null	Het
Plekhg1	A	T	10: 3,940,502	Y386F	probably damaging	Het
Pmfbp1	G	C	8: 109,542,379		probably benign	Het
Poln	T	C	5: 34,077,088		probably benign	Het
Polr1c	A	G	17: 46,244,903	V200A	probably benign	Het
Ppil1	A	T	17: 29,252,256	F92I	probably damaging	Het
Ptchd3	T	G	11: 121,842,972	L896R	probably damaging	Het
Rev3l	A	G	10: 39,824,831	N1775D	possibly damaging	Het
Robo4	G	A	9: 37,404,477	R342Q	probably benign	Het
Rusc2	T	C	4: 43,424,100		probably benign	Het
S100pbp	T	C	4: 129,144,456		probably benign	Het
Slc25a48	T	C	13: 56,451,211	V118A	probably damaging	Het
Slc38a10	T	C	11: 120,134,853	D219G	probably damaging	Het
Slc38a2	C	T	15: 96,691,292		probably null	Het
Slc39a12	A	G	2: 14,435,678	E480G	probably benign	Het
Tab2	C	A	10: 7,919,677	R347L	probably damaging	Het
Tas2r123	T	C	6: 132,847,992	I284T	possibly damaging	Het
Tex9	A	G	9: 72,486,769		probably benign	Het
Tifab	A	G	13: 56,176,405	L75P	probably damaging	Het
Tmc5	T	A	7: 118,634,237	D91E	probably benign	Het
Tnks1bp1	T	A	2: 85,062,352	D212E	probably benign	Het
Ugcg	A	G	4: 59,217,130	D218G	probably benign	Het
Zfp451	A	T	1: 33,777,625	L198I	probably damaging	Het

Other mutations in Mroh1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01574:Mroh1	APN	15	76432288	missense	probably benign	0.01
IGL02141:Mroh1	APN	15	76446599	missense	possibly damaging	0.47
IGL02146:Mroh1	APN	15	76434679	splice site	probably benign
IGL02205:Mroh1	APN	15	76437239	missense	possibly damaging	0.81
IGL02261:Mroh1	APN	15	76429160	missense	probably benign	0.03
IGL02818:Mroh1	APN	15	76432401	splice site	probably null
IGL02949:Mroh1	APN	15	76408968	missense	probably damaging	0.97
IGL02951:Mroh1	APN	15	76427636	missense	probably damaging	1.00
IGL03154:Mroh1	APN	15	76452838	missense	probably damaging	1.00
IGL02799:Mroh1	UTSW	15	76392461	critical splice donor site	probably null
R0068:Mroh1	UTSW	15	76446692	splice site	probably benign
R0076:Mroh1	UTSW	15	76451140	missense	probably benign	0.00
R0180:Mroh1	UTSW	15	76428250	missense	probably damaging	0.99
R0315:Mroh1	UTSW	15	76427600	missense	possibly damaging	0.94
R0350:Mroh1	UTSW	15	76432249	missense	probably damaging	0.98
R0399:Mroh1	UTSW	15	76452099	missense	probably benign	0.44
R0835:Mroh1	UTSW	15	76451883	missense	probably damaging	0.96
R0893:Mroh1	UTSW	15	76408938	missense	possibly damaging	0.62
R1109:Mroh1	UTSW	15	76446509	splice site	probably benign
R1527:Mroh1	UTSW	15	76452263	missense	probably benign	0.03
R1595:Mroh1	UTSW	15	76433530	splice site	probably benign
R1900:Mroh1	UTSW	15	76433385	missense	probably benign	0.00
R1901:Mroh1	UTSW	15	76436049	missense	probably benign
R2223:Mroh1	UTSW	15	76408045	critical splice donor site	probably null
R2415:Mroh1	UTSW	15	76421211	missense	probably damaging	0.99
R3113:Mroh1	UTSW	15	76408536	splice site	probably benign
R3437:Mroh1	UTSW	15	76433608	missense	possibly damaging	0.92
R3618:Mroh1	UTSW	15	76452346	missense	possibly damaging	0.55
R3833:Mroh1	UTSW	15	76401619	missense	probably benign	0.08
R4073:Mroh1	UTSW	15	76407985	missense	probably benign	0.13
R4156:Mroh1	UTSW	15	76402126	splice site	probably null
R4276:Mroh1	UTSW	15	76393851	missense	probably damaging	1.00
R4745:Mroh1	UTSW	15	76408530	critical splice donor site	probably null
R5450:Mroh1	UTSW	15	76432347	intron	probably benign
R5574:Mroh1	UTSW	15	76433931	missense	probably benign
R5673:Mroh1	UTSW	15	76430181	missense	probably damaging	1.00
R5970:Mroh1	UTSW	15	76451491	missense	probably benign	0.24
R5993:Mroh1	UTSW	15	76446680	missense	probably damaging	0.99
R6008:Mroh1	UTSW	15	76451357	missense	possibly damaging	0.50
R6082:Mroh1	UTSW	15	76430223	missense	probably benign	0.06
R6302:Mroh1	UTSW	15	76436119	critical splice donor site	probably null
R7030:Mroh1	UTSW	15	76437317	missense	probably benign	0.01
R7098:Mroh1	UTSW	15	76408457	nonsense	probably null
R7334:Mroh1	UTSW	15	76427638	missense	probably benign	0.00
R7337:Mroh1	UTSW	15	76451476	missense	probably benign	0.00
R7352:Mroh1	UTSW	15	76451474	missense	probably benign	0.06
R7446:Mroh1	UTSW	15	76452272	missense	possibly damaging	0.93
R7453:Mroh1	UTSW	15	76433545	missense	probably damaging	1.00
R7669:Mroh1	UTSW	15	76451848	missense	possibly damaging	0.88
R7753:Mroh1	UTSW	15	76433275	missense	possibly damaging	0.62
R7860:Mroh1	UTSW	15	76447332	missense	probably benign	0.00
R7990:Mroh1	UTSW	15	76452275	missense	probably damaging	1.00
R8140:Mroh1	UTSW	15	76433873	missense	probably benign	0.00
R8325:Mroh1	UTSW	15	76432215	frame shift	probably null
R8334:Mroh1	UTSW	15	76446556	missense	probably benign
Z1177:Mroh1	UTSW	15	76423761	missense	probably damaging	1.00

Posted On

2013-01-20