Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01410:Memo1'

79943

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Memo1

Ensembl Gene

ENSMUSG00000058704

Gene Name

mediator of cell motility 1

Synonyms

D930048L02Rik, 0610016J10Rik

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

IGL01410

Quality Score

Status

Chromosome

Chromosomal Location

74506031-74602516 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

G to A at 74548976 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Stop codon at position 121 (R121*)

Ref Sequence

ENSEMBL: ENSMUSP00000077553 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078459]

AlphaFold

Q91VH6

Predicted Effect

probably null
Transcript: ENSMUST00000078459
AA Change: R121*

SMART Domains

Protein: ENSMUSP00000077553
Gene: ENSMUSG00000058704
AA Change: R121*

Domain	Start	End	E-Value	Type
Pfam:Memo	9	293	3.7e-84	PFAM

Coding Region Coverage

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a floxed allele activated postnatally exhibit a reduced life span, increased insulin sensitivity, small stature, graying hair, alopecia, kyphosis, loss of subcutaneous fat, loss of spermatozoa in the epididymis and increased active vitamin D. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aox1	T	A	1: 58,145,184 (GRCm39)		probably null	Het
Aspm	C	T	1: 139,410,182 (GRCm39)	T1359I	probably benign	Het
Atp13a2	A	G	4: 140,719,509 (GRCm39)	D26G	probably benign	Het
Atrnl1	G	A	19: 58,119,536 (GRCm39)	A1343T	probably damaging	Het
Ccsap	A	C	8: 124,585,969 (GRCm39)	S61A	probably damaging	Het
Cdh1	A	T	8: 107,384,485 (GRCm39)	M318L	probably benign	Het
Cfap69	G	A	5: 5,696,979 (GRCm39)	P106S	probably damaging	Het
Cfp	G	A	X: 20,795,963 (GRCm39)	T88I	probably damaging	Het
Chst1	A	T	2: 92,444,475 (GRCm39)	I316F	probably damaging	Het
Col7a1	A	T	9: 108,793,686 (GRCm39)	D1382V	unknown	Het
Cr2	T	A	1: 194,845,542 (GRCm39)	M514L	possibly damaging	Het
Cubn	G	A	2: 13,470,719 (GRCm39)	H558Y	probably benign	Het
Cul9	A	T	17: 46,839,572 (GRCm39)	M802K	probably damaging	Het
Dennd2d	A	T	3: 106,398,542 (GRCm39)	I169L	probably damaging	Het
Dnah11	T	A	12: 118,010,991 (GRCm39)	K162*	probably null	Het
Dnah3	T	A	7: 119,566,943 (GRCm39)	T2428S	possibly damaging	Het
Dock11	T	A	X: 35,301,296 (GRCm39)	H1284Q	probably damaging	Het
Flrt2	T	A	12: 95,745,966 (GRCm39)	D101E	probably damaging	Het
Gabrr2	G	A	4: 33,085,626 (GRCm39)	V349M	probably damaging	Het
Gli2	C	A	1: 118,764,621 (GRCm39)	V1177L	probably benign	Het
Gm16506	A	G	14: 43,961,630 (GRCm39)	Y206H	probably benign	Het
Gm5612	C	T	9: 18,338,869 (GRCm39)		probably benign	Het
Gvin3	C	T	7: 106,202,258 (GRCm39)		noncoding transcript	Het
Heg1	C	T	16: 33,545,936 (GRCm39)	T460I	possibly damaging	Het
Lgals9	T	G	11: 78,863,977 (GRCm39)	D56A	probably damaging	Het
Lpgat1	A	T	1: 191,508,544 (GRCm39)		probably null	Het
Megf6	T	A	4: 154,337,020 (GRCm39)		probably null	Het
Megf8	G	A	7: 25,059,296 (GRCm39)	M2265I	probably benign	Het
Morc1	T	C	16: 48,432,677 (GRCm39)	V715A	probably benign	Het
Mycbp2	A	T	14: 103,466,928 (GRCm39)		probably null	Het
Ncapg2	T	A	12: 116,388,270 (GRCm39)	V318D	possibly damaging	Het
Ndst1	T	C	18: 60,833,517 (GRCm39)	Y498C	probably damaging	Het
Nod1	C	T	6: 54,921,341 (GRCm39)	A326T	probably damaging	Het
Or2ag15	A	G	7: 106,340,706 (GRCm39)	V145A	probably benign	Het
Or4c11	T	A	2: 88,695,864 (GRCm39)	M305K	probably benign	Het
Peg3	T	C	7: 6,710,624 (GRCm39)	S1533G	probably benign	Het
Pgc	G	T	17: 48,045,165 (GRCm39)	G361V	probably damaging	Het
Phka1	C	T	X: 101,629,712 (GRCm39)	R477H	probably damaging	Het
Plagl2	C	T	2: 153,074,574 (GRCm39)	R109Q	probably damaging	Het
Prr36	T	A	8: 4,266,230 (GRCm39)	I107F	probably benign	Het
Ptpdc1	T	A	13: 48,740,080 (GRCm39)	R450S	probably damaging	Het
Ptprb	A	T	10: 116,138,179 (GRCm39)	D361V	possibly damaging	Het
Rbm44	A	G	1: 91,096,551 (GRCm39)	D970G	probably benign	Het
Scrn2	T	G	11: 96,921,396 (GRCm39)	V52G	probably benign	Het
Sdk1	C	T	5: 142,197,875 (GRCm39)	T2176I	probably benign	Het
Serpina1d	T	A	12: 103,729,993 (GRCm39)	E396D	probably benign	Het
Slc38a5	A	C	X: 8,146,070 (GRCm39)	Q465P	probably benign	Het
Slc38a5	G	T	X: 8,146,071 (GRCm39)	Q465H	probably benign	Het
Smarca1	T	C	X: 46,981,255 (GRCm39)	T48A	possibly damaging	Het
Trak2	A	T	1: 58,962,766 (GRCm39)	I132N	probably damaging	Het
Trank1	A	G	9: 111,194,117 (GRCm39)	T714A	probably benign	Het
Trank1	T	C	9: 111,194,327 (GRCm39)	S784P	probably benign	Het
Trp53i13	G	A	11: 77,399,083 (GRCm39)		probably benign	Het
Trrap	A	C	5: 144,767,831 (GRCm39)	D2596A	probably benign	Het
Ttyh1	A	T	7: 4,127,656 (GRCm39)	T19S	probably damaging	Het
Tyk2	C	T	9: 21,020,660 (GRCm39)	V947M	probably damaging	Het
Ugt2b34	G	A	5: 87,040,689 (GRCm39)	A411V	possibly damaging	Het
Virma	T	A	4: 11,518,929 (GRCm39)	Y725*	probably null	Het
Vmn1r192	A	G	13: 22,372,079 (GRCm39)	L47P	probably damaging	Het
Vmn2r74	T	C	7: 85,610,500 (GRCm39)	D64G	possibly damaging	Het

Other mutations in Memo1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01570:Memo1	APN	17	74,524,103 (GRCm39)	splice site	probably benign
IGL02709:Memo1	APN	17	74,552,027 (GRCm39)	missense	probably damaging	1.00
IGL03172:Memo1	APN	17	74,551,996 (GRCm39)	missense	probably damaging	1.00
Tummy	UTSW	17	74,508,273 (GRCm39)	missense	probably damaging	1.00
R0067:Memo1	UTSW	17	74,532,453 (GRCm39)	missense	probably damaging	1.00
R1068:Memo1	UTSW	17	74,532,550 (GRCm39)	missense	probably damaging	1.00
R1962:Memo1	UTSW	17	74,552,003 (GRCm39)	missense	possibly damaging	0.54
R1964:Memo1	UTSW	17	74,552,003 (GRCm39)	missense	possibly damaging	0.54
R2029:Memo1	UTSW	17	74,552,049 (GRCm39)	missense	probably null	0.99
R3236:Memo1	UTSW	17	74,509,347 (GRCm39)	missense	probably damaging	1.00
R4284:Memo1	UTSW	17	74,562,293 (GRCm39)	critical splice acceptor site	probably null
R4285:Memo1	UTSW	17	74,562,293 (GRCm39)	critical splice acceptor site	probably null
R4287:Memo1	UTSW	17	74,562,293 (GRCm39)	critical splice acceptor site	probably null
R4427:Memo1	UTSW	17	74,509,302 (GRCm39)	missense	probably benign	0.01
R4583:Memo1	UTSW	17	74,565,456 (GRCm39)	nonsense	probably null
R4607:Memo1	UTSW	17	74,565,456 (GRCm39)	nonsense	probably null
R4608:Memo1	UTSW	17	74,565,456 (GRCm39)	nonsense	probably null
R6118:Memo1	UTSW	17	74,509,302 (GRCm39)	missense	possibly damaging	0.52
R6769:Memo1	UTSW	17	74,508,273 (GRCm39)	missense	probably damaging	1.00
R6771:Memo1	UTSW	17	74,508,273 (GRCm39)	missense	probably damaging	1.00
R7226:Memo1	UTSW	17	74,509,338 (GRCm39)	missense	probably damaging	1.00
R7996:Memo1	UTSW	17	74,565,491 (GRCm39)	missense	probably damaging	1.00
R9696:Memo1	UTSW	17	74,524,041 (GRCm39)	missense	probably damaging	1.00

Posted On

2013-11-05