Mutagenetix > Incidental Mutation

Incidental Mutation 'R9610:Plg'

724182

Institutional Source

Beutler Lab

Gene Symbol

Plg

Ensembl Gene

ENSMUSG00000059481

Gene Name

plasminogen

Synonyms

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.226) question?

Stock #

R9610 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

12597496-12638271 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 12609213 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Histidine at position 173 (Y173H)

Ref Sequence

ENSEMBL: ENSMUSP00000014578 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000014578]

AlphaFold

P20918

Predicted Effect

probably benign
Transcript: ENSMUST00000014578
AA Change: Y173H

PolyPhen 2 Score 0.119 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000014578
Gene: ENSMUSG00000059481
AA Change: Y173H

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
PAN_AP	20	97	8.67e-14	SMART
KR	101	183	1.31e-41	SMART
KR	184	264	5.4e-43	SMART
KR	273	354	3.45e-50	SMART
KR	375	456	3.9e-49	SMART
KR	479	562	5.53e-40	SMART
Tryp_SPc	581	805	4.11e-94	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a secreted blood zymogen that is activated by proteolysis and converted to plasmin and angiostatin. Plasmin dissolves fibrin in blood clots and is an important protease in many other cellular processes while angiostatin inhibits angiogenesis. Defects in this gene are likely a cause of thrombophilia and ligneous conjunctivitis. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Dec 2009]
PHENOTYPE: Homozygous null mutants exhibit retarded growth, variable rectal prolapse, impaired fertility and lactation in females, early mortality, and widespread fibrin deposition and thrombotic lesions in liver, lung, stomach and other tissues. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts19	A	T	18: 59,023,399 (GRCm39)	T265S	probably benign	Het
Arhgef5	A	G	6: 43,257,890 (GRCm39)	I1311M	probably damaging	Het
Bcr	T	A	10: 74,990,743 (GRCm39)	Y750N	probably damaging	Het
Bcr	T	A	10: 74,990,745 (GRCm39)	Y750*	probably null	Het
Btbd16	T	A	7: 130,407,595 (GRCm39)	M295K	probably benign	Het
Ccdc88a	T	C	11: 29,427,316 (GRCm39)	L1007P	possibly damaging	Het
Cnep1r1	A	G	8: 88,860,457 (GRCm39)	*126W	probably null	Het
Cstf1	T	A	2: 172,214,984 (GRCm39)	I35N	probably benign	Het
Cstpp1	T	C	2: 91,135,127 (GRCm39)	D111G	probably damaging	Het
Cul9	A	G	17: 46,830,823 (GRCm39)	L1690P	possibly damaging	Het
Dnm2	A	T	9: 21,414,973 (GRCm39)	K677*	probably null	Het
Dscaml1	C	A	9: 45,579,522 (GRCm39)	N356K	possibly damaging	Het
Dvl3	A	G	16: 20,346,008 (GRCm39)	D446G	probably damaging	Het
Ecm2	A	G	13: 49,668,518 (GRCm39)	N74D	probably benign	Het
Ecm2	A	G	13: 49,681,216 (GRCm39)	I450M	probably damaging	Het
Emc1	T	A	4: 139,091,035 (GRCm39)	D460E	probably benign	Het
Fhip2b	T	C	14: 70,824,258 (GRCm39)	Y493C	probably benign	Het
Fuom	T	A	7: 139,679,828 (GRCm39)	E121V	possibly damaging	Het
Fyco1	T	C	9: 123,657,585 (GRCm39)	T864A	possibly damaging	Het
Galk2	T	C	2: 125,817,218 (GRCm39)	Y336H	probably damaging	Het
Gcsh	T	A	8: 117,720,125 (GRCm39)	Y14F	probably benign	Het
Grip1	G	A	10: 119,874,569 (GRCm39)	E778K	possibly damaging	Het
Gucy2g	T	C	19: 55,194,605 (GRCm39)	I937M	probably damaging	Het
Hsp90ab1	T	C	17: 45,880,600 (GRCm39)	I370M	possibly damaging	Het
Hypk	T	C	2: 121,288,154 (GRCm39)	S72P	probably damaging	Het
Izumo1r	T	G	9: 14,811,840 (GRCm39)	I183L	possibly damaging	Het
Kctd13	G	T	7: 126,544,180 (GRCm39)	G293C	probably damaging	Het
Kmt2d	CTGTTG	CTG	15: 98,743,057 (GRCm39)		probably benign	Het
Krt13	T	C	11: 100,012,318 (GRCm39)	S2G	probably benign	Het
Mark4	C	A	7: 19,167,338 (GRCm39)	R467L	possibly damaging	Het
Mrps33	T	A	6: 39,779,422 (GRCm39)	K91M	probably damaging	Het
Muc5ac	T	A	7: 141,350,078 (GRCm39)	V608D	possibly damaging	Het
Myb	G	A	10: 21,030,627 (GRCm39)	Q57*	probably null	Het
Or51f1	T	G	7: 102,506,147 (GRCm39)	H114P	probably damaging	Het
Peg10	GCAC	GCACCAC	6: 4,756,452 (GRCm39)		probably benign	Het
Phldb3	G	A	7: 24,328,372 (GRCm39)	V639M	probably damaging	Het
Pip4k2c	A	C	10: 127,036,069 (GRCm39)	L266R	probably damaging	Het
Pmp22	G	T	11: 63,024,065 (GRCm39)	V25F	probably benign	Het
Ppp1r16b	T	A	2: 158,537,998 (GRCm39)	Y40N	probably damaging	Het
Prl5a1	A	G	13: 28,329,492 (GRCm39)	E57G	possibly damaging	Het
Psmb10	A	G	8: 106,664,144 (GRCm39)	F75S	probably benign	Het
Ptprm	C	A	17: 67,000,483 (GRCm39)	R1167M	probably damaging	Het
Rbm46	T	C	3: 82,771,541 (GRCm39)	H358R	probably benign	Het
Rgl1	A	G	1: 152,397,115 (GRCm39)	S684P	probably benign	Het
Rmnd5b	T	C	11: 51,517,869 (GRCm39)	I162V	probably damaging	Het
Sh3d19	T	C	3: 86,014,529 (GRCm39)	V440A	possibly damaging	Het
Sik1	T	A	17: 32,073,246 (GRCm39)	K70M	probably damaging	Het
Slc44a4	C	T	17: 35,147,793 (GRCm39)	S611F	probably benign	Het
Stk32a	A	G	18: 43,430,620 (GRCm39)	I177V	probably benign	Het
Syt7	G	A	19: 10,421,459 (GRCm39)	D548N	probably benign	Het
Tcf7l2	A	G	19: 55,899,038 (GRCm39)	D215G	probably null	Het
Tex14	T	A	11: 87,377,084 (GRCm39)	F143I	probably damaging	Het
Tjp3	A	G	10: 81,119,411 (GRCm39)	V26A	possibly damaging	Het
Tpx2	T	A	2: 152,715,124 (GRCm39)	V115D	probably benign	Het
Tubb2b	C	A	13: 34,311,742 (GRCm39)	K350N	probably damaging	Het
Usf3	T	C	16: 44,036,936 (GRCm39)	V472A	probably benign	Het
Vps13b	G	T	15: 35,642,555 (GRCm39)	G1389V	possibly damaging	Het
Vps39	T	C	2: 120,172,485 (GRCm39)	R183G	probably damaging	Het
Wnk4	G	T	11: 101,159,250 (GRCm39)	E556*	probably null	Het
Xpo7	T	A	14: 70,925,617 (GRCm39)	E474V	probably benign	Het
Zbtb18	A	G	1: 177,275,341 (GRCm39)	R234G	probably null	Het
Zc3h14	T	A	12: 98,737,663 (GRCm39)	I50N	possibly damaging	Het
Zfat	A	G	15: 68,051,655 (GRCm39)	V713A	possibly damaging	Het
Zfp462	T	C	4: 55,009,545 (GRCm39)	S504P	possibly damaging	Het
Zmiz1	T	C	14: 25,651,022 (GRCm39)	V502A	probably benign	Het

Other mutations in Plg

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00834:Plg	APN	17	12,630,380 (GRCm39)	missense	probably damaging	1.00
IGL01128:Plg	APN	17	12,615,586 (GRCm39)	splice site	probably benign
IGL01522:Plg	APN	17	12,622,956 (GRCm39)	missense	probably damaging	1.00
IGL01981:Plg	APN	17	12,621,934 (GRCm39)	splice site	probably benign
IGL03338:Plg	APN	17	12,637,959 (GRCm39)	missense	probably damaging	1.00
elder	UTSW	17	12,609,107 (GRCm39)	nonsense	probably null
oldster	UTSW	17	12,614,641 (GRCm39)	missense	probably damaging	1.00
R0391:Plg	UTSW	17	12,637,968 (GRCm39)	missense	probably damaging	1.00
R0531:Plg	UTSW	17	12,630,334 (GRCm39)	splice site	probably benign
R0646:Plg	UTSW	17	12,637,623 (GRCm39)	missense	probably damaging	1.00
R0759:Plg	UTSW	17	12,629,838 (GRCm39)	missense	probably damaging	1.00
R1013:Plg	UTSW	17	12,597,608 (GRCm39)	splice site	probably benign
R2116:Plg	UTSW	17	12,603,364 (GRCm39)	missense	probably damaging	0.99
R2442:Plg	UTSW	17	12,629,847 (GRCm39)	missense	probably benign	0.15
R2512:Plg	UTSW	17	12,622,116 (GRCm39)	missense	probably benign
R2879:Plg	UTSW	17	12,622,987 (GRCm39)	missense	possibly damaging	0.92
R3107:Plg	UTSW	17	12,603,316 (GRCm39)	missense	probably benign	0.00
R3405:Plg	UTSW	17	12,622,096 (GRCm39)	missense	possibly damaging	0.65
R4409:Plg	UTSW	17	12,609,150 (GRCm39)	missense	probably damaging	1.00
R4861:Plg	UTSW	17	12,614,622 (GRCm39)	missense	probably benign	0.00
R4861:Plg	UTSW	17	12,614,622 (GRCm39)	missense	probably benign	0.00
R4977:Plg	UTSW	17	12,621,976 (GRCm39)	missense	probably damaging	1.00
R4990:Plg	UTSW	17	12,630,397 (GRCm39)	missense	probably benign
R5319:Plg	UTSW	17	12,622,114 (GRCm39)	missense	possibly damaging	0.49
R5443:Plg	UTSW	17	12,601,070 (GRCm39)	missense	probably benign	0.03
R5635:Plg	UTSW	17	12,614,641 (GRCm39)	missense	probably damaging	1.00
R5981:Plg	UTSW	17	12,597,605 (GRCm39)	critical splice donor site	probably null
R6166:Plg	UTSW	17	12,617,001 (GRCm39)	missense	probably damaging	0.99
R6688:Plg	UTSW	17	12,610,732 (GRCm39)	missense	probably damaging	1.00
R6726:Plg	UTSW	17	12,597,595 (GRCm39)	missense	probably damaging	1.00
R6995:Plg	UTSW	17	12,637,938 (GRCm39)	missense	probably benign	0.00
R7028:Plg	UTSW	17	12,610,723 (GRCm39)	missense	probably damaging	1.00
R7168:Plg	UTSW	17	12,607,446 (GRCm39)	missense	probably damaging	1.00
R7356:Plg	UTSW	17	12,629,798 (GRCm39)	missense	probably damaging	1.00
R8902:Plg	UTSW	17	12,629,790 (GRCm39)	missense	probably benign	0.32
R9035:Plg	UTSW	17	12,609,107 (GRCm39)	nonsense	probably null
R9474:Plg	UTSW	17	12,622,024 (GRCm39)	missense	probably damaging	1.00
R9611:Plg	UTSW	17	12,609,213 (GRCm39)	missense	probably benign	0.12
Z1176:Plg	UTSW	17	12,633,072 (GRCm39)	missense	probably benign	0.02
Z1177:Plg	UTSW	17	12,622,120 (GRCm39)	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- AAGACAGATCTGAACCCTGGAG -3'
(R):5'- TCAGGTCAGAACTGGGACTC -3'

Sequencing Primer
(F):5'- CGTAGCATCTCCTACCTTGTTAATG -3'
(R):5'- CAGACAGAAGGGGGTTTT -3'

Posted On

2022-09-12