Mutagenetix > Incidental Mutation

Incidental Mutation 'R8025:Mcrs1'

617668

Institutional Source

Beutler Lab

Gene Symbol

Mcrs1

Ensembl Gene

ENSMUSG00000037570

Gene Name

microspherule protein 1

Synonyms

MSP58, P78, C78274, ICP22BP

MMRRC Submission

067464-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R8025 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

99140698-99149838 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

G to A at 99144814 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Stop codon at position 267 (Q267*)

Ref Sequence

ENSEMBL: ENSMUSP00000043901 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000041190] [ENSMUST00000041415] [ENSMUST00000163506] [ENSMUST00000229359] [ENSMUST00000229671] [ENSMUST00000229926]

AlphaFold

Q99L90

Predicted Effect

probably null
Transcript: ENSMUST00000041190
AA Change: Q267*

SMART Domains

Protein: ENSMUSP00000043901
Gene: ENSMUSG00000037570
AA Change: Q267*

Domain	Start	End	E-Value	Type
low complexity region	44	57	N/A	INTRINSIC
low complexity region	81	113	N/A	INTRINSIC
Pfam:MCRS_N	134	331	5.7e-98	PFAM
FHA	362	419	2.04e-6	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000041415

SMART Domains

Protein: ENSMUSP00000040548
Gene: ENSMUSG00000037579

Domain	Start	End	E-Value	Type
PAS	20	88	3.94e0	SMART
PAC	94	136	9.92e-6	SMART
low complexity region	148	159	N/A	INTRINSIC
Pfam:Ion_trans	224	523	3.8e-34	PFAM
Pfam:Ion_trans_2	453	517	1e-12	PFAM
cNMP	593	708	2.04e-16	SMART
low complexity region	781	800	N/A	INTRINSIC
low complexity region	857	872	N/A	INTRINSIC
coiled coil region	886	918	N/A	INTRINSIC
low complexity region	977	993	N/A	INTRINSIC
low complexity region	1022	1035	N/A	INTRINSIC
low complexity region	1054	1062	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000163506
AA Change: Q254*

SMART Domains

Protein: ENSMUSP00000131407
Gene: ENSMUSG00000037570
AA Change: Q254*

Domain	Start	End	E-Value	Type
low complexity region	31	44	N/A	INTRINSIC
low complexity region	68	100	N/A	INTRINSIC
Pfam:MCRS_N	121	318	2.4e-97	PFAM
FHA	349	406	2.04e-6	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000229359

Predicted Effect

probably benign
Transcript: ENSMUST00000229671

Predicted Effect

probably benign
Transcript: ENSMUST00000229926

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

100% (61/61)

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit early embryonic lethality. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930579G24Rik	T	G	3: 79,536,635 (GRCm39)	L51R	probably damaging	Het
Actl7b	T	C	4: 56,741,137 (GRCm39)	T74A	probably damaging	Het
Aip	C	A	19: 4,165,346 (GRCm39)	A207S	probably benign	Het
AL732309.1	A	G	2: 25,136,331 (GRCm39)		probably benign	Het
Apcdd1	G	T	18: 63,069,979 (GRCm39)	C82F	probably damaging	Het
Arhgap42	T	G	9: 9,005,823 (GRCm39)	I736L	probably benign	Het
Baz1a	A	T	12: 54,955,921 (GRCm39)	I1056N	probably benign	Het
Bzw2	T	C	12: 36,157,517 (GRCm39)	E316G	probably damaging	Het
Carns1	A	T	19: 4,216,505 (GRCm39)	I559N	probably damaging	Het
Chrnb2	A	T	3: 89,668,649 (GRCm39)	V222E	probably damaging	Het
Cngb3	A	T	4: 19,280,960 (GRCm39)	N10Y	possibly damaging	Het
Dennd1b	A	G	1: 139,038,158 (GRCm39)	K267E		Het
Dhx32	A	G	7: 133,323,100 (GRCm39)	Y705H	probably damaging	Het
Dnah7c	G	A	1: 46,496,456 (GRCm39)	V114I	probably benign	Het
Dnah8	T	A	17: 30,960,311 (GRCm39)	C2229*	probably null	Het
Dync2i2	T	C	2: 29,938,730 (GRCm39)	Q51R	probably benign	Het
Gm14401	T	C	2: 176,778,249 (GRCm39)	F112L	probably damaging	Het
Gm57858	C	A	3: 36,073,136 (GRCm39)	R382L	probably damaging	Het
Habp4	G	A	13: 64,322,645 (GRCm39)	R238H	probably benign	Het
Herpud1	A	G	8: 95,119,149 (GRCm39)	Y301C	probably damaging	Het
Itih5	G	A	2: 10,245,833 (GRCm39)	A641T	probably benign	Het
Kcns3	A	T	12: 11,141,846 (GRCm39)	N284K	probably damaging	Het
Midn	G	A	10: 79,991,126 (GRCm39)	A379T	probably benign	Het
Muc21	GTGCTGGATTCAGTGGTGGGCAGGGTGGGGGTAGAGCCTGAGCCACTGCTGGATGCAGTGGTGGTCAGGGTGGGTGTAGAGCCTGAGCCA	GTGCTGGATGCAGTGGTGGTCAGGGTGGGTGTAGAGCCTGAGCCA	17: 35,931,879 (GRCm39)		probably benign	Het
Odad2	A	T	18: 7,127,224 (GRCm39)	N996K	probably benign	Het
Or2d36	A	G	7: 106,746,930 (GRCm39)	M136V	possibly damaging	Het
Or4d2b	A	T	11: 87,779,777 (GRCm39)		probably null	Het
Or51f5	T	C	7: 102,424,463 (GRCm39)	V244A	probably benign	Het
Or5m11	A	T	2: 85,781,856 (GRCm39)	I150F	probably benign	Het
Or7e175	T	C	9: 20,048,928 (GRCm39)	V172A	probably benign	Het
Parpbp	T	C	10: 87,928,970 (GRCm39)	D490G	probably benign	Het
Pcbp2	T	A	15: 102,396,711 (GRCm39)	S262R	probably benign	Het
Pcdhgc5	T	C	18: 37,953,992 (GRCm39)	I422T	possibly damaging	Het
Pcsk5	T	A	19: 17,538,415 (GRCm39)		probably benign	Het
Plxna1	G	A	6: 89,308,254 (GRCm39)	R1278W	probably damaging	Het
Polr1c	A	G	17: 46,555,974 (GRCm39)	L162P	probably damaging	Het
Rasl2-9	A	G	7: 5,128,481 (GRCm39)	S150P	probably damaging	Het
Raver2	C	A	4: 100,960,162 (GRCm39)	S214*	probably null	Het
Rbpjl	C	A	2: 164,252,166 (GRCm39)		probably benign	Het
Rec114	T	G	9: 58,567,605 (GRCm39)	E127A	possibly damaging	Het
Recql5	C	A	11: 115,818,938 (GRCm39)	L209F	probably damaging	Het
Rgs11	T	C	17: 26,423,359 (GRCm39)		probably null	Het
Rgs3	C	A	4: 62,608,831 (GRCm39)	H366N	probably damaging	Het
Rnf148	C	T	6: 23,654,196 (GRCm39)	D267N	possibly damaging	Het
Scn1a	T	C	2: 66,148,557 (GRCm39)	N1007S	probably benign	Het
Sdcbp	A	G	4: 6,393,022 (GRCm39)	T220A	probably benign	Het
Sema5a	A	G	15: 32,548,928 (GRCm39)	N134S	probably benign	Het
Smg1	G	A	7: 117,806,212 (GRCm39)	Q210*	probably null	Het
Snx7	A	G	3: 117,626,526 (GRCm39)	V328A	probably benign	Het
Sult1c2	A	T	17: 54,138,837 (GRCm39)	S247T	probably benign	Het
Tceanc2	C	T	4: 106,996,997 (GRCm39)		probably null	Het
Tead3	T	C	17: 28,554,009 (GRCm39)	D141G	probably benign	Het
Tlcd5	T	A	9: 43,022,848 (GRCm39)	T169S	probably benign	Het
Ube3b	T	C	5: 114,546,270 (GRCm39)	M692T	probably damaging	Het
Vmn1r188	T	C	13: 22,272,084 (GRCm39)	F13L	probably benign	Het
Vmn2r3	A	G	3: 64,182,871 (GRCm39)	V276A	possibly damaging	Het
Vmn2r57	A	G	7: 41,076,183 (GRCm39)	I443T	probably benign	Het
Vps33a	T	C	5: 123,696,738 (GRCm39)	N305S	possibly damaging	Het
Vps33b	A	T	7: 79,940,094 (GRCm39)		probably benign	Het
Wdr72	T	A	9: 74,050,781 (GRCm39)	M91K	probably benign	Het
Xylb	T	C	9: 119,210,569 (GRCm39)	F351L	probably damaging	Het
Zan	C	T	5: 137,404,614 (GRCm39)	D3883N	unknown	Het
Zfp82	T	A	7: 29,756,278 (GRCm39)	H268L	probably damaging	Het

Other mutations in Mcrs1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01322:Mcrs1	APN	15	99,141,266 (GRCm39)	missense	probably damaging	0.97
IGL01338:Mcrs1	APN	15	99,147,382 (GRCm39)	missense	probably damaging	1.00
IGL01975:Mcrs1	APN	15	99,141,559 (GRCm39)	critical splice donor site	probably null
PIT4651001:Mcrs1	UTSW	15	99,144,832 (GRCm39)	missense	probably damaging	1.00
R0125:Mcrs1	UTSW	15	99,142,608 (GRCm39)	unclassified	probably benign
R0520:Mcrs1	UTSW	15	99,146,336 (GRCm39)	splice site	probably null
R0744:Mcrs1	UTSW	15	99,141,330 (GRCm39)	unclassified	probably benign
R0833:Mcrs1	UTSW	15	99,141,330 (GRCm39)	unclassified	probably benign
R0836:Mcrs1	UTSW	15	99,141,330 (GRCm39)	unclassified	probably benign
R2099:Mcrs1	UTSW	15	99,147,827 (GRCm39)	missense	probably benign	0.00
R2133:Mcrs1	UTSW	15	99,141,256 (GRCm39)	missense	probably damaging	1.00
R4557:Mcrs1	UTSW	15	99,141,028 (GRCm39)	missense	probably benign	0.01
R5425:Mcrs1	UTSW	15	99,141,569 (GRCm39)	missense	probably damaging	1.00
R5517:Mcrs1	UTSW	15	99,144,876 (GRCm39)	missense	possibly damaging	0.88
R7129:Mcrs1	UTSW	15	99,146,609 (GRCm39)	missense	probably damaging	1.00
R8012:Mcrs1	UTSW	15	99,147,766 (GRCm39)	missense	probably damaging	1.00
R8015:Mcrs1	UTSW	15	99,146,735 (GRCm39)	nonsense	probably null
R8171:Mcrs1	UTSW	15	99,146,613 (GRCm39)	missense	probably damaging	1.00
R8191:Mcrs1	UTSW	15	99,141,206 (GRCm39)	missense	probably damaging	1.00
R8420:Mcrs1	UTSW	15	99,141,575 (GRCm39)	missense	probably damaging	1.00
R8486:Mcrs1	UTSW	15	99,146,349 (GRCm39)	nonsense	probably null
R8777:Mcrs1	UTSW	15	99,141,237 (GRCm39)	missense	probably damaging	1.00
R8777-TAIL:Mcrs1	UTSW	15	99,141,237 (GRCm39)	missense	probably damaging	1.00
R9626:Mcrs1	UTSW	15	99,146,353 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CAAGGCAGCAGGTTCTGTTG -3'
(R):5'- CTTGATGGAAACCATGCCTG -3'

Sequencing Primer
(F):5'- GCAGGTTCTGTTGCTGCTG -3'
(R):5'- TCCAGTTCCTTGGCCTGGG -3'

Posted On

2020-01-23