Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02335:Mmrn1'

289700

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Mmrn1

Ensembl Gene

ENSMUSG00000054641

Gene Name

multimerin 1

Synonyms

4921530G03Rik, Emilin4

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL02335

Quality Score

Status

Chromosome

Chromosomal Location

60924976-60989378 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 60977147 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Isoleucine at position 804 (N804I)

Ref Sequence

ENSEMBL: ENSMUSP00000145156 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000129603] [ENSMUST00000204333]

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000129603
AA Change: N804I

PolyPhen 2 Score 0.787 (Sensitivity: 0.85; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000119609
Gene: ENSMUSG00000054641
AA Change: N804I

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
low complexity region	80	92	N/A	INTRINSIC
Pfam:EMI	193	262	3.3e-12	PFAM
coiled coil region	303	338	N/A	INTRINSIC
coiled coil region	658	688	N/A	INTRINSIC
coiled coil region	808	846	N/A	INTRINSIC
low complexity region	981	992	N/A	INTRINSIC
EGF	1026	1059	1.62e-5	SMART
C1Q	1076	1210	6.74e-49	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000204333
AA Change: N804I

PolyPhen 2 Score 0.787 (Sensitivity: 0.85; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000145156
Gene: ENSMUSG00000054641
AA Change: N804I

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
low complexity region	80	92	N/A	INTRINSIC
Pfam:EMI	193	262	7.7e-13	PFAM
coiled coil region	303	338	N/A	INTRINSIC
coiled coil region	658	688	N/A	INTRINSIC
coiled coil region	808	846	N/A	INTRINSIC
low complexity region	981	992	N/A	INTRINSIC
EGF	1025	1058	1.62e-5	SMART
C1Q	1075	1209	6.74e-49	SMART

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Multimerin is a massive, soluble protein found in platelets and in the endothelium of blood vessels. It is comprised of subunits linked by interchain disulfide bonds to form large, variably sized homomultimers. Multimerin is a factor V/Va-binding protein and may function as a carrier protein for platelet factor V. It may also have functions as an extracellular matrix or adhesive protein. Recently, patients with an unusual autosomal-dominant bleeding disorder (factor V Quebec) were found to have a deficiency of platelet multimerin. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 45 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5830411N06Rik	A	T	7: 140,296,540	N526Y	probably damaging	Het
A4gnt	C	T	9: 99,620,213	T142I	probably benign	Het
Acaca	A	G	11: 84,214,258	T147A	possibly damaging	Het
Agbl3	A	G	6: 34,799,750	D397G	probably damaging	Het
Ank1	C	T	8: 23,135,638	T1597M	possibly damaging	Het
Arl4d	A	G	11: 101,666,929	T94A	possibly damaging	Het
Cd22	A	G	7: 30,876,134	I161T	probably damaging	Het
Clcn7	C	T	17: 25,146,847	L166F	probably benign	Het
Cnbd1	G	T	4: 19,055,095	N110K	possibly damaging	Het
Col14a1	A	T	15: 55,463,769		probably benign	Het
Col6a6	C	T	9: 105,784,101	V270M	probably damaging	Het
Cox8b	C	A	7: 140,899,077	G42W	probably damaging	Het
Csn1s1	A	T	5: 87,680,845	D275V	probably benign	Het
Cubn	T	A	2: 13,427,834		probably null	Het
Dctn2	T	C	10: 127,275,821		probably benign	Het
Dnm1l	A	G	16: 16,342,740		probably benign	Het
Dpp4	T	C	2: 62,334,644	E687G	probably benign	Het
Fbxw20	T	C	9: 109,223,309	K249E	possibly damaging	Het
Fhl2	C	T	1: 43,128,390	W181*	probably null	Het
G2e3	T	A	12: 51,369,158	M559K	probably benign	Het
Gdap1l1	A	T	2: 163,447,595	Y160F	possibly damaging	Het
Gm1110	T	C	9: 26,881,763	I572M	probably benign	Het
Gm5538	G	A	3: 59,743,605	M49I	probably benign	Het
Gpatch2l	T	A	12: 86,256,937		probably benign	Het
Kcnq4	A	G	4: 120,715,854	L250P	probably damaging	Het
Lamc2	A	T	1: 153,166,216	N57K	probably benign	Het
Lingo1	A	G	9: 56,620,081	L408P	probably damaging	Het
Mroh7	A	G	4: 106,707,782	L545S	probably damaging	Het
Nup188	T	A	2: 30,323,636		probably null	Het
Olfr1442	T	C	19: 12,674,238	I11T	probably damaging	Het
Olfr1494	A	G	19: 13,749,934	D276G	probably benign	Het
Olfr96	A	G	17: 37,225,326	N67S	probably damaging	Het
Pls1	A	T	9: 95,784,183	N138K	probably benign	Het
Prkch	C	A	12: 73,702,512	N345K	probably benign	Het
Reps1	T	C	10: 18,056,117		probably null	Het
Rrp7a	T	C	15: 83,122,691	E15G	probably benign	Het
Scn1a	T	A	2: 66,277,661	T1557S	possibly damaging	Het
Smtn	T	C	11: 3,526,215	E602G	probably damaging	Het
Syvn1	T	C	19: 6,050,093		probably null	Het
Tbxas1	A	G	6: 39,023,080	D267G	probably damaging	Het
Topbp1	A	G	9: 103,328,523	N787D	probably damaging	Het
Vmn2r22	T	G	6: 123,638,092	S180R	probably damaging	Het
Zfp345	T	A	2: 150,474,543	E48D	possibly damaging	Het
Zfp608	G	A	18: 54,897,437	Q1144*	probably null	Het
Zfp936	T	A	7: 43,187,267	L34Q	probably damaging	Het

Other mutations in Mmrn1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00640:Mmrn1	APN	6	60,977,513 (GRCm38)	missense	probably benign
IGL00742:Mmrn1	APN	6	60,958,120 (GRCm38)	missense	probably damaging	1.00
IGL00917:Mmrn1	APN	6	60,975,910 (GRCm38)	nonsense	probably null
IGL01121:Mmrn1	APN	6	60,975,944 (GRCm38)	missense	possibly damaging	0.46
IGL01393:Mmrn1	APN	6	60,960,708 (GRCm38)	splice site	probably benign
IGL01697:Mmrn1	APN	6	60,976,493 (GRCm38)	missense	possibly damaging	0.46
IGL01737:Mmrn1	APN	6	60,977,161 (GRCm38)	missense	probably benign
IGL01944:Mmrn1	APN	6	60,971,183 (GRCm38)	critical splice donor site	probably null
IGL01987:Mmrn1	APN	6	60,944,573 (GRCm38)	missense	probably benign	0.31
IGL02005:Mmrn1	APN	6	60,960,744 (GRCm38)	missense	probably damaging	1.00
IGL02190:Mmrn1	APN	6	60,987,193 (GRCm38)	missense	probably benign	0.13
IGL02421:Mmrn1	APN	6	60,944,822 (GRCm38)	missense	probably benign	0.00
IGL02530:Mmrn1	APN	6	60,958,176 (GRCm38)	missense	possibly damaging	0.73
IGL02709:Mmrn1	APN	6	60,973,046 (GRCm38)	missense	probably damaging	1.00
IGL03139:Mmrn1	APN	6	60,976,340 (GRCm38)	missense	probably damaging	0.99
IGL03228:Mmrn1	APN	6	60,944,892 (GRCm38)	missense	probably benign	0.02
IGL03272:Mmrn1	APN	6	60,988,435 (GRCm38)	missense	probably damaging	1.00
IGL03410:Mmrn1	APN	6	60,975,835 (GRCm38)	missense	probably benign	0.36
H8562:Mmrn1	UTSW	6	60,958,180 (GRCm38)	missense	probably damaging	0.98
K2124:Mmrn1	UTSW	6	60,976,033 (GRCm38)	missense	possibly damaging	0.87
R0145:Mmrn1	UTSW	6	60,973,010 (GRCm38)	missense	probably damaging	1.00
R0164:Mmrn1	UTSW	6	60,975,815 (GRCm38)	splice site	probably benign
R0352:Mmrn1	UTSW	6	60,944,971 (GRCm38)	missense	probably benign	0.03
R0400:Mmrn1	UTSW	6	60,977,115 (GRCm38)	missense	probably benign	0.00
R0538:Mmrn1	UTSW	6	60,976,469 (GRCm38)	missense	probably benign	0.00
R0907:Mmrn1	UTSW	6	60,973,119 (GRCm38)	missense	probably benign	0.09
R1117:Mmrn1	UTSW	6	60,976,325 (GRCm38)	missense	possibly damaging	0.51
R1383:Mmrn1	UTSW	6	60,976,322 (GRCm38)	missense	probably damaging	1.00
R1542:Mmrn1	UTSW	6	60,945,118 (GRCm38)	missense	probably damaging	0.98
R1591:Mmrn1	UTSW	6	60,944,771 (GRCm38)	nonsense	probably null
R1599:Mmrn1	UTSW	6	60,945,037 (GRCm38)	missense	probably benign
R1733:Mmrn1	UTSW	6	60,977,101 (GRCm38)	missense	probably benign	0.00
R2005:Mmrn1	UTSW	6	60,976,084 (GRCm38)	missense	possibly damaging	0.88
R2056:Mmrn1	UTSW	6	60,944,805 (GRCm38)	missense	probably benign	0.00
R2144:Mmrn1	UTSW	6	60,945,075 (GRCm38)	missense	possibly damaging	0.54
R2299:Mmrn1	UTSW	6	60,976,441 (GRCm38)	missense	probably damaging	0.99
R3836:Mmrn1	UTSW	6	60,944,847 (GRCm38)	missense	probably benign
R3837:Mmrn1	UTSW	6	60,944,847 (GRCm38)	missense	probably benign
R4206:Mmrn1	UTSW	6	60,958,180 (GRCm38)	missense	probably damaging	0.98
R4414:Mmrn1	UTSW	6	60,944,586 (GRCm38)	missense	probably damaging	1.00
R4590:Mmrn1	UTSW	6	60,960,813 (GRCm38)	missense	probably damaging	1.00
R4707:Mmrn1	UTSW	6	60,988,473 (GRCm38)	missense	probably benign	0.12
R4820:Mmrn1	UTSW	6	60,973,043 (GRCm38)	missense	probably benign	0.04
R4880:Mmrn1	UTSW	6	60,976,439 (GRCm38)	missense	probably benign	0.15
R5166:Mmrn1	UTSW	6	60,976,490 (GRCm38)	missense	probably benign	0.04
R5324:Mmrn1	UTSW	6	60,976,586 (GRCm38)	missense	probably damaging	1.00
R5887:Mmrn1	UTSW	6	60,987,074 (GRCm38)	missense	probably benign
R5917:Mmrn1	UTSW	6	60,973,150 (GRCm38)	critical splice donor site	probably null
R6108:Mmrn1	UTSW	6	60,975,976 (GRCm38)	missense	possibly damaging	0.83
R6539:Mmrn1	UTSW	6	60,987,184 (GRCm38)	missense	probably benign	0.01
R6996:Mmrn1	UTSW	6	60,977,383 (GRCm38)	missense	probably benign	0.04
R7064:Mmrn1	UTSW	6	60,988,540 (GRCm38)	nonsense	probably null
R7073:Mmrn1	UTSW	6	60,988,427 (GRCm38)	missense	probably damaging	1.00
R7213:Mmrn1	UTSW	6	60,944,543 (GRCm38)	start gained	probably benign
R7256:Mmrn1	UTSW	6	60,976,114 (GRCm38)	missense	probably damaging	0.98
R7324:Mmrn1	UTSW	6	60,944,933 (GRCm38)	nonsense	probably null
R7350:Mmrn1	UTSW	6	60,976,336 (GRCm38)	nonsense	probably null
R7388:Mmrn1	UTSW	6	60,976,252 (GRCm38)	missense	probably benign	0.43
R7652:Mmrn1	UTSW	6	60,977,506 (GRCm38)	missense	probably benign	0.14
R7664:Mmrn1	UTSW	6	60,976,705 (GRCm38)	missense	probably benign	0.44
R7810:Mmrn1	UTSW	6	60,976,325 (GRCm38)	missense	probably benign	0.18
R7832:Mmrn1	UTSW	6	60,987,060 (GRCm38)	splice site	probably null
R7979:Mmrn1	UTSW	6	60,975,977 (GRCm38)	missense	probably damaging	0.96
R8071:Mmrn1	UTSW	6	60,944,524 (GRCm38)	start gained	probably benign
R8130:Mmrn1	UTSW	6	60,960,723 (GRCm38)	missense	probably damaging	1.00
R8277:Mmrn1	UTSW	6	60,977,236 (GRCm38)	missense	probably benign	0.19
R8353:Mmrn1	UTSW	6	60,988,377 (GRCm38)	missense	probably damaging	1.00
R8453:Mmrn1	UTSW	6	60,988,377 (GRCm38)	missense	probably damaging	1.00
R8472:Mmrn1	UTSW	6	60,988,396 (GRCm38)	missense	probably damaging	1.00
R8758:Mmrn1	UTSW	6	60,987,209 (GRCm38)	missense	possibly damaging	0.54
R8803:Mmrn1	UTSW	6	60,988,287 (GRCm38)	missense	probably damaging	1.00
R8879:Mmrn1	UTSW	6	60,976,529 (GRCm38)	missense	probably damaging	0.99
R8907:Mmrn1	UTSW	6	60,976,093 (GRCm38)	missense	probably damaging	1.00
R8983:Mmrn1	UTSW	6	60,976,058 (GRCm38)	missense	probably benign	0.04
R9200:Mmrn1	UTSW	6	60,976,876 (GRCm38)	missense	probably damaging	1.00
R9287:Mmrn1	UTSW	6	60,975,955 (GRCm38)	missense	probably damaging	1.00
R9387:Mmrn1	UTSW	6	60,958,192 (GRCm38)	nonsense	probably null
R9612:Mmrn1	UTSW	6	60,976,424 (GRCm38)	missense	probably damaging	0.96
R9674:Mmrn1	UTSW	6	60,971,088 (GRCm38)	nonsense	probably null
X0026:Mmrn1	UTSW	6	60,976,013 (GRCm38)	missense	probably benign	0.09
Z1176:Mmrn1	UTSW	6	60,945,034 (GRCm38)	missense	probably benign	0.37
Z1177:Mmrn1	UTSW	6	60,987,098 (GRCm38)	missense	possibly damaging	0.83

Posted On

2015-04-16