Mutagenetix > Incidental Mutation

Incidental Mutation 'R4463:Psg27'

330221

Institutional Source

Beutler Lab

Gene Symbol

Psg27

Ensembl Gene

ENSMUSG00000070797

Gene Name

pregnancy-specific beta-1-glycoprotein 27

Synonyms

cea15, EG545925

MMRRC Submission

041721-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4463 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

18290439-18301230 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 18291010 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Lysine at position 398 (Q398K)

Ref Sequence

ENSEMBL: ENSMUSP00000092388 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000094794]

AlphaFold

Q497W2

Predicted Effect

possibly damaging
Transcript: ENSMUST00000094794
AA Change: Q398K

PolyPhen 2 Score 0.461 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000092388
Gene: ENSMUSG00000070797
AA Change: Q398K

Domain	Start	End	E-Value	Type
IG	39	140	4.13e-5	SMART
IG	159	260	5.89e-1	SMART
IG	279	380	1.39e-2	SMART
IGc2	396	460	3.62e-10	SMART

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 97.2%
20x: 95.1%

Validation Efficiency

100% (57/57)

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb1a	T	C	5: 8,769,981 (GRCm39)		probably benign	Het
Abcc8	T	C	7: 45,756,005 (GRCm39)		probably null	Het
Alox12e	A	G	11: 70,209,082 (GRCm39)	L388P	probably damaging	Het
Aspm	T	A	1: 139,382,748 (GRCm39)	S27T	possibly damaging	Het
Capn2	G	A	1: 182,307,329 (GRCm39)		probably benign	Het
Catspere1	G	A	1: 177,765,279 (GRCm39)		noncoding transcript	Het
Ccdc158	T	C	5: 92,782,159 (GRCm39)	D820G	probably null	Het
Cdkn2d	C	G	9: 21,202,185 (GRCm39)	V21L	probably benign	Het
Chd9	T	A	8: 91,705,627 (GRCm39)	D761E	probably benign	Het
Chst8	T	C	7: 34,374,645 (GRCm39)	D398G	probably damaging	Het
Clns1a	T	C	7: 97,370,156 (GRCm39)		probably benign	Het
Cyp3a57	A	T	5: 145,318,084 (GRCm39)	Y355F	probably damaging	Het
Cyp4f37	A	G	17: 32,846,710 (GRCm39)		probably null	Het
Eif1ad11	A	G	12: 87,994,129 (GRCm39)	D119G	probably benign	Het
Eipr1	G	A	12: 28,909,338 (GRCm39)	A202T	probably damaging	Het
Fam83a	T	C	15: 57,858,655 (GRCm39)	S232P	probably damaging	Het
Fastkd2	C	T	1: 63,774,968 (GRCm39)		probably benign	Het
Fcgbpl1	A	G	7: 27,850,144 (GRCm39)	M1197V	probably benign	Het
Fgfr4	G	A	13: 55,304,280 (GRCm39)	V107I	probably benign	Het
Gatad1	G	T	5: 3,697,404 (GRCm39)	S72R	probably benign	Het
Gli2	T	C	1: 118,763,738 (GRCm39)	D1471G	probably damaging	Het
Gm1330	A	T	2: 148,845,064 (GRCm39)	Y36*	probably null	Het
Gm29125	T	C	1: 80,360,903 (GRCm39)		noncoding transcript	Het
Idi1	G	A	13: 8,937,508 (GRCm39)		probably benign	Het
Itgbl1	C	T	14: 124,078,080 (GRCm39)	T190I	probably damaging	Het
Kbtbd3	G	A	9: 4,331,257 (GRCm39)	G544R	probably damaging	Het
Kifc3	T	C	8: 95,828,744 (GRCm39)	T638A	probably damaging	Het
Lama1	G	A	17: 68,068,695 (GRCm39)	C798Y	probably damaging	Het
Larp6	C	A	9: 60,644,279 (GRCm39)	H140N	probably damaging	Het
Mctp1	A	T	13: 76,860,206 (GRCm39)	D108V	probably damaging	Het
Myzap	G	T	9: 71,462,933 (GRCm39)	D204E	probably benign	Het
Neb	GCC	GC	2: 52,169,734 (GRCm39)		probably null	Het
Or13p8	T	C	4: 118,583,855 (GRCm39)	V137A	probably benign	Het
Or1j20	T	C	2: 36,760,205 (GRCm39)	I209T	probably benign	Het
Or4c102	T	C	2: 88,422,976 (GRCm39)	V276A	possibly damaging	Het
Phka1	A	G	X: 101,588,990 (GRCm39)	V818A	probably benign	Het
Plek	T	C	11: 16,931,873 (GRCm39)	Y326C	possibly damaging	Het
Pp2d1	A	G	17: 53,822,886 (GRCm39)	I60T	probably benign	Het
Prmt3	T	C	7: 49,467,837 (GRCm39)	Y348H	probably damaging	Het
Raver1	T	C	9: 21,003,123 (GRCm39)	T51A	probably benign	Het
Ripk2	T	C	4: 16,151,968 (GRCm39)	N197S	possibly damaging	Het
Sectm1a	T	A	11: 120,960,477 (GRCm39)	I113L	probably benign	Het
Slc2a4	G	A	11: 69,834,148 (GRCm39)		probably benign	Het
Snph	A	T	2: 151,436,035 (GRCm39)	S229T	probably damaging	Het
Stpg4	A	G	17: 87,697,101 (GRCm39)	F183L	probably benign	Het
Tango6	A	T	8: 107,415,706 (GRCm39)	T176S	probably benign	Het
Vmn1r196	A	G	13: 22,477,853 (GRCm39)	Q164R	probably benign	Het
Vstm4	T	A	14: 32,639,833 (GRCm39)	L236Q	probably damaging	Het
Xylb	A	G	9: 119,215,433 (GRCm39)	D462G	probably benign	Het
Zc2hc1c	A	G	12: 85,337,071 (GRCm39)	R243G	probably damaging	Het

Other mutations in Psg27

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00337:Psg27	APN	7	18,295,729 (GRCm39)	missense	probably damaging	1.00
IGL00417:Psg27	APN	7	18,295,842 (GRCm39)	missense	probably benign	0.22
IGL01344:Psg27	APN	7	18,294,342 (GRCm39)	missense	probably damaging	1.00
IGL01781:Psg27	APN	7	18,298,989 (GRCm39)	missense	probably damaging	1.00
IGL02547:Psg27	APN	7	18,294,553 (GRCm39)	missense	probably benign
IGL02926:Psg27	APN	7	18,291,054 (GRCm39)	missense	probably damaging	0.99
IGL03074:Psg27	APN	7	18,294,454 (GRCm39)	missense	probably benign	0.02
IGL03237:Psg27	APN	7	18,294,417 (GRCm39)	missense	probably benign	0.00
IGL02796:Psg27	UTSW	7	18,295,875 (GRCm39)	missense	probably benign	0.08
R0437:Psg27	UTSW	7	18,294,636 (GRCm39)	splice site	probably benign
R0604:Psg27	UTSW	7	18,290,997 (GRCm39)	missense	probably damaging	0.98
R1163:Psg27	UTSW	7	18,299,234 (GRCm39)	missense	probably damaging	0.99
R2072:Psg27	UTSW	7	18,298,934 (GRCm39)	missense	probably benign	0.16
R2072:Psg27	UTSW	7	18,294,342 (GRCm39)	missense	probably damaging	1.00
R2073:Psg27	UTSW	7	18,294,342 (GRCm39)	missense	probably damaging	1.00
R2074:Psg27	UTSW	7	18,294,342 (GRCm39)	missense	probably damaging	1.00
R2081:Psg27	UTSW	7	18,290,883 (GRCm39)	missense	probably damaging	1.00
R2206:Psg27	UTSW	7	18,301,036 (GRCm39)	nonsense	probably null
R2866:Psg27	UTSW	7	18,295,818 (GRCm39)	missense	probably benign
R3783:Psg27	UTSW	7	18,294,279 (GRCm39)	missense	probably damaging	1.00
R3784:Psg27	UTSW	7	18,294,279 (GRCm39)	missense	probably damaging	1.00
R5312:Psg27	UTSW	7	18,290,958 (GRCm39)	missense	probably benign	0.43
R5885:Psg27	UTSW	7	18,295,711 (GRCm39)	missense	probably damaging	0.96
R6087:Psg27	UTSW	7	18,290,869 (GRCm39)	missense	probably benign	0.05
R7011:Psg27	UTSW	7	18,290,798 (GRCm39)	missense	probably benign	0.00
R7198:Psg27	UTSW	7	18,295,726 (GRCm39)	missense	probably damaging	1.00
R7381:Psg27	UTSW	7	18,301,008 (GRCm39)	missense	probably benign	0.20
R7964:Psg27	UTSW	7	18,299,124 (GRCm39)	missense	probably damaging	1.00
R8398:Psg27	UTSW	7	18,295,837 (GRCm39)	missense	probably benign	0.29
R8472:Psg27	UTSW	7	18,296,015 (GRCm39)	missense	probably benign	0.18
R8818:Psg27	UTSW	7	18,294,337 (GRCm39)	missense	probably damaging	1.00
R9345:Psg27	UTSW	7	18,299,081 (GRCm39)	missense	probably benign	0.02
X0064:Psg27	UTSW	7	18,295,720 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- AAGGCCTCACATTGGTACTCTC -3'
(R):5'- GGCTGAGTCAGGATCATACAG -3'

Sequencing Primer
(F):5'- ACATTGGTACTCTCCAGCATC -3'
(R):5'- CTGAGTCAGGATCATACAGTTTGTAG -3'

Posted On

2015-07-21