Mutagenetix > Incidental Mutation

Incidental Mutation 'R7541:Rmdn2'

583915

Institutional Source

Beutler Lab

Gene Symbol

Rmdn2

Ensembl Gene

ENSMUSG00000036368

Gene Name

regulator of microtubule dynamics 2

Synonyms

Fam82a1

MMRRC Submission

045613-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.104) question?

Stock #

R7541 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

79919292-80000621 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 79935297 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Cysteine at position 137 (S137C)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000040368] [ENSMUST00000224618] [ENSMUST00000225357]

AlphaFold

Q8BSE0

Predicted Effect

probably benign
Transcript: ENSMUST00000040368

SMART Domains

Protein: ENSMUSP00000044543
Gene: ENSMUSG00000036368

Domain	Start	End	E-Value	Type
transmembrane domain	9	28	N/A	INTRINSIC
low complexity region	41	54	N/A	INTRINSIC
Blast:PAS	70	133	4e-16	BLAST
low complexity region	137	149	N/A	INTRINSIC
SCOP:d1hxia_	290	386	4e-5	SMART

Predicted Effect

SMART Domains

Protein: ENSMUSP00000083761
Gene: ENSMUSG00000036368
AA Change: S137C

Domain	Start	End	E-Value	Type
low complexity region	195	210	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000224618

Predicted Effect

probably benign
Transcript: ENSMUST00000225357

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.2%

Validation Efficiency

96% (51/53)

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acss2	G	A	2: 155,416,610 (GRCm39)		probably null	Het
Adamts10	G	A	17: 33,750,590 (GRCm39)	R210H	probably benign	Het
Als2	T	C	1: 59,206,775 (GRCm39)		probably null	Het
Aplp2	A	T	9: 31,063,652 (GRCm39)	M652K	possibly damaging	Het
Atrn	A	G	2: 130,803,491 (GRCm39)	I560M	possibly damaging	Het
Bicc1	T	C	10: 70,782,434 (GRCm39)	D602G	possibly damaging	Het
Bnip5	G	A	17: 29,124,298 (GRCm39)	R335W	probably damaging	Het
Cd200l2	T	A	16: 45,348,855 (GRCm39)	T106S	possibly damaging	Het
Cdh4	A	G	2: 179,086,603 (GRCm39)		probably null	Het
Clasp1	T	A	1: 118,470,727 (GRCm39)		probably null	Het
Col6a6	A	G	9: 105,644,523 (GRCm39)	I1255T	probably damaging	Het
Comp	G	T	8: 70,834,000 (GRCm39)	V672L	probably damaging	Het
Dbnl	T	G	11: 5,745,486 (GRCm39)	D122E	probably damaging	Het
Dgkz	G	A	2: 91,773,020 (GRCm39)	R346C	probably damaging	Het
Dnhd1	C	T	7: 105,327,516 (GRCm39)	R54C	probably damaging	Het
Elmo3	T	C	8: 106,033,346 (GRCm39)	I121T	probably damaging	Het
Fam184b	A	G	5: 45,699,574 (GRCm39)	L614P	probably damaging	Het
Fbh1	T	C	2: 11,754,348 (GRCm39)	R797G	probably benign	Het
Fcgbpl1	T	A	7: 27,843,681 (GRCm39)	C856*	probably null	Het
Gata6	A	G	18: 11,059,108 (GRCm39)	T392A	probably damaging	Het
Gm29609	A	G	5: 31,311,576 (GRCm39)	F855S	probably benign	Het
Gm3424	T	C	14: 17,337,195 (GRCm39)	N88D	possibly damaging	Het
Gnas	T	A	2: 174,139,892 (GRCm39)	S80T	unknown	Het
Hsd17b14	C	A	7: 45,215,570 (GRCm39)	P190Q	probably damaging	Het
Iqch	C	T	9: 63,352,803 (GRCm39)	V955I	possibly damaging	Het
Kcnt2	T	C	1: 140,304,122 (GRCm39)	V164A	probably benign	Het
Krt87	A	G	15: 101,336,515 (GRCm39)	L46P	probably damaging	Het
Lef1	A	G	3: 130,984,748 (GRCm39)	M237V	probably benign	Het
Lmbr1l	A	T	15: 98,807,267 (GRCm39)		probably null	Het
Lrrc49	T	C	9: 60,517,686 (GRCm39)	I408V	probably damaging	Het
Luc7l3	T	C	11: 94,186,791 (GRCm39)	S365G	unknown	Het
Marchf2	A	T	17: 33,922,032 (GRCm39)	C109*	probably null	Het
Metrnl	T	A	11: 121,606,796 (GRCm39)	C284S	probably damaging	Het
Mmachc	G	A	4: 116,563,082 (GRCm39)	T91I	probably benign	Het
Mrps7	T	G	11: 115,497,696 (GRCm39)	M187R	probably damaging	Het
Ncapd3	A	G	9: 26,978,336 (GRCm39)	E845G	probably damaging	Het
Nscme3l	G	A	19: 5,553,439 (GRCm39)	P114L	probably benign	Het
Ooep	T	A	9: 78,285,347 (GRCm39)	T90S	possibly damaging	Het
Or13c25	A	T	4: 52,911,376 (GRCm39)	D139E	probably benign	Het
Or2y1g	T	A	11: 49,171,160 (GRCm39)	F62I	probably damaging	Het
Pcdhb18	A	T	18: 37,624,662 (GRCm39)	D664V	probably damaging	Het
Pigz	T	C	16: 31,763,949 (GRCm39)	S336P	probably benign	Het
Pou2f2	A	T	7: 24,815,553 (GRCm39)	D71E	probably benign	Het
Reep6	G	T	10: 80,171,033 (GRCm39)	R303L	possibly damaging	Het
Rnf220	A	T	4: 117,347,127 (GRCm39)	L95H	probably damaging	Het
Rsf1	CGGCGGCGG	CGGCGGCGGGGGCGGCGG	7: 97,229,118 (GRCm39)		probably benign	Het
Stxbp1	A	T	2: 32,708,517 (GRCm39)	S83T	probably damaging	Het
Tcstv7b	A	T	13: 120,702,515 (GRCm39)	M104L	probably benign	Het
Trappc11	T	C	8: 47,958,617 (GRCm39)		probably null	Het
Ttn	G	T	2: 76,621,645 (GRCm39)	D15598E	probably damaging	Het
Vav2	T	A	2: 27,165,014 (GRCm39)	R645W	probably damaging	Het
Vmn1r169	T	A	7: 23,277,412 (GRCm39)	V268D	probably benign	Het
Zp2	A	T	7: 119,735,279 (GRCm39)	C365S	probably damaging	Het

Other mutations in Rmdn2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01628:Rmdn2	APN	17	79,979,817 (GRCm39)	nonsense	probably null
R0052:Rmdn2	UTSW	17	79,957,760 (GRCm39)	missense	probably damaging	0.99
R0052:Rmdn2	UTSW	17	79,957,760 (GRCm39)	missense	probably damaging	0.99
R0127:Rmdn2	UTSW	17	79,977,998 (GRCm39)	missense	probably damaging	1.00
R0206:Rmdn2	UTSW	17	79,957,716 (GRCm39)	splice site	probably benign
R0440:Rmdn2	UTSW	17	79,975,384 (GRCm39)	missense	probably damaging	1.00
R0720:Rmdn2	UTSW	17	79,975,458 (GRCm39)	critical splice donor site	probably null
R1163:Rmdn2	UTSW	17	79,966,880 (GRCm39)	missense	probably benign	0.00
R3746:Rmdn2	UTSW	17	79,977,981 (GRCm39)	splice site	probably null
R4966:Rmdn2	UTSW	17	79,974,304 (GRCm39)	missense	probably damaging	1.00
R5137:Rmdn2	UTSW	17	79,975,418 (GRCm39)	missense	probably benign	0.02
R5259:Rmdn2	UTSW	17	79,975,446 (GRCm39)	missense	probably damaging	1.00
R6439:Rmdn2	UTSW	17	79,934,971 (GRCm39)	intron	probably benign
R6991:Rmdn2	UTSW	17	79,928,739 (GRCm39)	start gained	probably benign
R7046:Rmdn2	UTSW	17	79,928,808 (GRCm39)	missense	probably damaging	1.00
R7322:Rmdn2	UTSW	17	79,929,040 (GRCm39)	missense	probably damaging	1.00
R8246:Rmdn2	UTSW	17	79,979,966 (GRCm39)	nonsense	probably null
R8359:Rmdn2	UTSW	17	79,935,580 (GRCm39)	missense
R8393:Rmdn2	UTSW	17	79,975,459 (GRCm39)	critical splice donor site	probably null
R8462:Rmdn2	UTSW	17	79,978,053 (GRCm39)	missense	probably damaging	1.00
R9472:Rmdn2	UTSW	17	79,989,096 (GRCm39)	missense	possibly damaging	0.74
R9496:Rmdn2	UTSW	17	79,975,425 (GRCm39)	missense	possibly damaging	0.80
R9549:Rmdn2	UTSW	17	79,935,339 (GRCm39)	missense
R9602:Rmdn2	UTSW	17	79,975,440 (GRCm39)	missense	probably damaging	1.00
R9617:Rmdn2	UTSW	17	79,928,790 (GRCm39)	missense	probably benign	0.27
R9698:Rmdn2	UTSW	17	79,957,729 (GRCm39)	critical splice acceptor site	probably null

Predicted Primers

PCR Primer
(F):5'- CAACTACACACTTATGTCCGTG -3'
(R):5'- GGGTAAGGCGTTCTCTCAAAAC -3'

Sequencing Primer
(F):5'- GACATAGTTTACTGCGGAGATTCC -3'
(R):5'- GTAAGGCGTTCTCTCAAAACTCCAG -3'

Posted On

2019-10-17