Mutagenetix > Incidental Mutation

Incidental Mutation 'R2516:Mmrn2'

253841

Institutional Source

Beutler Lab

Gene Symbol

Mmrn2

Ensembl Gene

ENSMUSG00000041445

Gene Name

multimerin 2

Synonyms

ENDOGLYX1, EndoGlyx-1, Emilin3

MMRRC Submission

040420-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.051) question?

Stock #

R2516 (G1)

Quality Score

178

Status

Validated

Chromosome

Chromosomal Location

34097461-34126244 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 34120759 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Lysine at position 543 (M543K)

Ref Sequence

ENSEMBL: ENSMUSP00000107539 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000111908]

AlphaFold

A6H6E2

Predicted Effect

probably benign
Transcript: ENSMUST00000111908
AA Change: M543K

PolyPhen 2 Score 0.123 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000107539
Gene: ENSMUSG00000041445
AA Change: M543K

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
Pfam:EMI	55	127	1.1e-15	PFAM
low complexity region	174	186	N/A	INTRINSIC
low complexity region	356	362	N/A	INTRINSIC
coiled coil region	387	480	N/A	INTRINSIC
coiled coil region	533	583	N/A	INTRINSIC
coiled coil region	688	715	N/A	INTRINSIC
Pfam:C1q	821	940	1.5e-27	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000227130

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.1%

Validation Efficiency

98% (65/66)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein belonging to the member of elastin microfibril interface-located (EMILIN) protein family. This family member is an extracellular matrix glycoprotein that can interfere with tumor angiogenesis and growth. It serves as a transforming growth factor beta antagonist and can interfere with the VEGF-A/VEGFR2 pathway. A related pseudogene has been identified on chromosome 6. [provided by RefSeq, Aug 2012]

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb11	A	T	2: 69,159,673 (GRCm39)	I6N	possibly damaging	Het
Aen	T	C	7: 78,555,616 (GRCm39)	V188A	probably damaging	Het
Afg3l1	A	G	8: 124,228,693 (GRCm39)	E753G	probably damaging	Het
Alas1	G	A	9: 106,115,859 (GRCm39)	T385I	probably damaging	Het
Alms1	C	A	6: 85,644,945 (GRCm39)		probably benign	Het
Ankrd65	A	G	4: 155,875,868 (GRCm39)	T30A	possibly damaging	Het
App	T	C	16: 84,775,117 (GRCm39)	S582G	probably damaging	Het
Arfgef1	A	T	1: 10,223,879 (GRCm39)	V1473E	possibly damaging	Het
Arhgap21	G	A	2: 20,859,809 (GRCm39)	P1196S	probably damaging	Het
Arhgap24	A	G	5: 103,039,776 (GRCm39)	T238A	probably benign	Het
Atf7	T	C	15: 102,437,439 (GRCm39)		probably benign	Het
Best1	G	T	19: 9,970,675 (GRCm39)	S55*	probably null	Het
Capn11	A	G	17: 45,944,725 (GRCm39)	V514A	probably damaging	Het
Cep104	T	A	4: 154,073,603 (GRCm39)	M52K	probably damaging	Het
Clca3a1	C	T	3: 144,443,619 (GRCm39)		probably null	Het
Cyp3a25	T	C	5: 145,939,837 (GRCm39)		probably null	Het
Dmxl2	G	A	9: 54,307,378 (GRCm39)	P2197S	probably damaging	Het
Drosha	T	C	15: 12,859,551 (GRCm39)		probably null	Het
Exosc9	A	G	3: 36,617,311 (GRCm39)	K355R	probably benign	Het
Fut1	A	C	7: 45,268,622 (GRCm39)	H192P	probably benign	Het
Gm572	T	A	4: 148,748,841 (GRCm39)	V166D	possibly damaging	Het
Gm9966	C	T	7: 95,607,735 (GRCm39)	P19S	unknown	Het
Gmds	C	T	13: 32,284,456 (GRCm39)	V219I	probably damaging	Het
Gsn	G	A	2: 35,173,965 (GRCm39)	E25K	probably benign	Het
Il4i1	T	C	7: 44,489,315 (GRCm39)	F368S	probably damaging	Het
Irak1bp1	T	C	9: 82,712,373 (GRCm39)	L98P	probably damaging	Het
Khdrbs3	T	C	15: 68,896,544 (GRCm39)		probably benign	Het
Kndc1	T	C	7: 139,501,738 (GRCm39)	I925T	probably damaging	Het
Laptm4a	T	C	12: 8,988,151 (GRCm39)	I296T	probably benign	Het
Lpl	A	T	8: 69,340,170 (GRCm39)	H55L	probably benign	Het
Lrrk2	C	A	15: 91,640,130 (GRCm39)	N1558K	probably benign	Het
Mfsd2a	A	G	4: 122,844,280 (GRCm39)	L289P	probably damaging	Het
Mnat1	T	C	12: 73,228,550 (GRCm39)		probably benign	Het
Msto1	A	T	3: 88,819,200 (GRCm39)		probably null	Het
Mtus1	A	G	8: 41,535,776 (GRCm39)	Y647H	probably damaging	Het
Nars1	A	T	18: 64,638,087 (GRCm39)	V289E	probably damaging	Het
Oit3	T	A	10: 59,264,167 (GRCm39)	K322N	probably damaging	Het
Oit3	G	A	10: 59,277,507 (GRCm39)		probably benign	Het
Or4k1	T	C	14: 50,377,440 (GRCm39)	I219V	probably benign	Het
Or5b113	T	A	19: 13,342,557 (GRCm39)	C188*	probably null	Het
Or5m12	A	G	2: 85,734,900 (GRCm39)	I166T	probably benign	Het
Or6c211	G	A	10: 129,506,155 (GRCm39)	R78W	probably damaging	Het
Pecr	A	T	1: 72,316,469 (GRCm39)	C79S	probably damaging	Het
Plekhn1	T	C	4: 156,307,116 (GRCm39)	D478G	probably damaging	Het
Pls1	A	T	9: 95,658,616 (GRCm39)	M264K	probably benign	Het
Ptprj	C	A	2: 90,305,340 (GRCm39)		probably benign	Het
Pygm	A	G	19: 6,447,631 (GRCm39)	D646G	probably benign	Het
Rif1	GCCACCA	GCCA	2: 52,000,336 (GRCm39)		probably benign	Het
Scn8a	T	C	15: 100,867,043 (GRCm39)	V283A	probably benign	Het
Shisa5	T	C	9: 108,885,575 (GRCm39)		probably null	Het
Slc10a4	A	G	5: 73,165,848 (GRCm39)	I246V	possibly damaging	Het
Slc1a1	A	T	19: 28,870,312 (GRCm39)	I104F	probably benign	Het
Slc22a8	A	G	19: 8,587,559 (GRCm39)	Y511C	probably benign	Het
Slc6a5	A	G	7: 49,606,210 (GRCm39)	N706S	probably benign	Het
Sos2	T	C	12: 69,697,433 (GRCm39)	K96E	probably damaging	Het
Stom	G	A	2: 35,205,977 (GRCm39)	R251*	probably null	Het
Sycp1	T	C	3: 102,752,382 (GRCm39)	E800G	probably benign	Het
Tab2	G	A	10: 7,783,245 (GRCm39)	P679L	probably damaging	Het
Tiam2	G	A	17: 3,503,657 (GRCm39)	V945I	probably damaging	Het
Trpm5	G	T	7: 142,628,254 (GRCm39)	P1007Q	probably damaging	Het
Uchl1	T	G	5: 66,839,956 (GRCm39)	I139S	probably damaging	Het
Vmn1r232	A	G	17: 21,134,288 (GRCm39)	I104T	possibly damaging	Het
Vmn2r97	G	A	17: 19,167,814 (GRCm39)	M689I	probably benign	Het
Zc3h18	A	T	8: 123,129,904 (GRCm39)		probably benign	Het
Zfhx4	C	T	3: 5,468,418 (GRCm39)	P2859S	probably benign	Het
Zfp456	T	C	13: 67,510,491 (GRCm39)	K99R	probably benign	Het

Other mutations in Mmrn2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01523:Mmrn2	APN	14	34,125,174 (GRCm39)	missense	probably damaging	1.00
IGL02529:Mmrn2	APN	14	34,120,570 (GRCm39)	missense	possibly damaging	0.74
IGL02590:Mmrn2	APN	14	34,121,224 (GRCm39)	nonsense	probably null
P0037:Mmrn2	UTSW	14	34,125,022 (GRCm39)	missense	probably damaging	1.00
R0323:Mmrn2	UTSW	14	34,119,991 (GRCm39)	missense	probably damaging	0.97
R0499:Mmrn2	UTSW	14	34,119,913 (GRCm39)	missense	probably damaging	1.00
R1073:Mmrn2	UTSW	14	34,118,251 (GRCm39)	critical splice donor site	probably null
R1422:Mmrn2	UTSW	14	34,118,196 (GRCm39)	missense	probably damaging	1.00
R1455:Mmrn2	UTSW	14	34,121,089 (GRCm39)	missense	probably benign	0.00
R1584:Mmrn2	UTSW	14	34,097,642 (GRCm39)	missense	probably benign	0.19
R1702:Mmrn2	UTSW	14	34,119,871 (GRCm39)	missense	probably benign	0.34
R1919:Mmrn2	UTSW	14	34,119,600 (GRCm39)	missense	probably benign	0.10
R1961:Mmrn2	UTSW	14	34,120,432 (GRCm39)	splice site	probably null
R2267:Mmrn2	UTSW	14	34,121,449 (GRCm39)	missense	probably benign	0.41
R2268:Mmrn2	UTSW	14	34,121,449 (GRCm39)	missense	probably benign	0.41
R2571:Mmrn2	UTSW	14	34,124,896 (GRCm39)	missense	probably damaging	0.99
R2696:Mmrn2	UTSW	14	34,120,372 (GRCm39)	missense	probably damaging	1.00
R2892:Mmrn2	UTSW	14	34,118,587 (GRCm39)	missense	probably benign	0.01
R2919:Mmrn2	UTSW	14	34,124,879 (GRCm39)	missense	possibly damaging	0.72
R3611:Mmrn2	UTSW	14	34,120,632 (GRCm39)	missense	probably benign	0.00
R3898:Mmrn2	UTSW	14	34,121,517 (GRCm39)	splice site	probably null
R3899:Mmrn2	UTSW	14	34,121,517 (GRCm39)	splice site	probably null
R3900:Mmrn2	UTSW	14	34,121,517 (GRCm39)	splice site	probably null
R4363:Mmrn2	UTSW	14	34,119,934 (GRCm39)	missense	probably damaging	0.99
R4392:Mmrn2	UTSW	14	34,119,573 (GRCm39)	missense	probably damaging	1.00
R4510:Mmrn2	UTSW	14	34,125,016 (GRCm39)	missense	possibly damaging	0.67
R4511:Mmrn2	UTSW	14	34,125,016 (GRCm39)	missense	possibly damaging	0.67
R4993:Mmrn2	UTSW	14	34,118,355 (GRCm39)	missense	probably damaging	1.00
R5026:Mmrn2	UTSW	14	34,121,158 (GRCm39)	missense	probably benign	0.07
R5263:Mmrn2	UTSW	14	34,121,541 (GRCm39)	missense	probably benign
R5478:Mmrn2	UTSW	14	34,118,539 (GRCm39)	missense	probably benign	0.11
R5606:Mmrn2	UTSW	14	34,119,581 (GRCm39)	missense	probably damaging	1.00
R6059:Mmrn2	UTSW	14	34,119,548 (GRCm39)	nonsense	probably null
R6279:Mmrn2	UTSW	14	34,119,614 (GRCm39)	missense	probably benign
R6300:Mmrn2	UTSW	14	34,119,614 (GRCm39)	missense	probably benign
R6938:Mmrn2	UTSW	14	34,120,671 (GRCm39)	missense	probably benign	0.22
R7491:Mmrn2	UTSW	14	34,121,374 (GRCm39)	missense	probably damaging	1.00
R7607:Mmrn2	UTSW	14	34,120,897 (GRCm39)	missense	possibly damaging	0.58
R7979:Mmrn2	UTSW	14	34,118,138 (GRCm39)	nonsense	probably null
R7999:Mmrn2	UTSW	14	34,119,879 (GRCm39)	missense	probably benign	0.30
R8113:Mmrn2	UTSW	14	34,119,593 (GRCm39)	missense	probably benign	0.39
R9063:Mmrn2	UTSW	14	34,120,567 (GRCm39)	missense	probably benign	0.04
R9092:Mmrn2	UTSW	14	34,118,587 (GRCm39)	missense	probably benign	0.00
R9180:Mmrn2	UTSW	14	34,121,158 (GRCm39)	missense	probably benign	0.07
R9327:Mmrn2	UTSW	14	34,097,473 (GRCm39)	unclassified	probably benign
R9476:Mmrn2	UTSW	14	34,120,407 (GRCm39)	missense	possibly damaging	0.94
R9510:Mmrn2	UTSW	14	34,120,407 (GRCm39)	missense	possibly damaging	0.94
R9606:Mmrn2	UTSW	14	34,119,654 (GRCm39)	missense	possibly damaging	0.58
X0064:Mmrn2	UTSW	14	34,121,109 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- ACCTTACCCTGCAGCATCTG -3'
(R):5'- TATCATCTCCTCCCCGAAGAGTG -3'

Sequencing Primer
(F):5'- GCAGACCTCATTAAGTATGTCAAGG -3'
(R):5'- TCCCCGAAGAGTGCAGCTAG -3'

Posted On

2014-12-04