Mutagenetix > Incidental Mutation

Incidental Mutation 'R3963:Psg29'

312179

Institutional Source

Beutler Lab

Gene Symbol

Psg29

Ensembl Gene

ENSMUSG00000023159

Gene Name

pregnancy-specific beta-1-glycoprotein 29

Synonyms

cea17

MMRRC Submission

040932-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.052) question?

Stock #

R3963 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

16937402-16949681 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 16942510 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Glutamine at position 170 (H170Q)

Ref Sequence

ENSEMBL: ENSMUSP00000075320 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000075934]

AlphaFold

Q3URN6

Predicted Effect

probably benign
Transcript: ENSMUST00000075934
AA Change: H170Q

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000075320
Gene: ENSMUSG00000023159
AA Change: H170Q

Domain	Start	End	E-Value	Type
IG	40	137	7.77e-1	SMART
IG	156	257	8.72e-4	SMART
IG	276	377	2.44e0	SMART
IGc2	393	457	3.06e-8	SMART

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 94.8%

Validation Efficiency

100% (61/61)

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts18	T	C	8: 114,504,443 (GRCm39)	D59G	probably benign	Het
Ank2	A	T	3: 126,728,245 (GRCm39)	S783T	probably benign	Het
Arfgef3	T	C	10: 18,468,025 (GRCm39)	D1725G	probably damaging	Het
B3gnt5	A	G	16: 19,587,798 (GRCm39)	S6G	probably benign	Het
Btbd8	G	A	5: 107,655,222 (GRCm39)	C1007Y	probably damaging	Het
Ccdc82	C	A	9: 13,252,011 (GRCm39)	T101K	possibly damaging	Het
Ccdc85a	A	C	11: 28,526,396 (GRCm39)	M376R	probably benign	Het
Cd200r1	T	A	16: 44,613,158 (GRCm39)	C255S	probably benign	Het
Cdc23	T	C	18: 34,779,972 (GRCm39)	M119V	probably benign	Het
Cers3	G	T	7: 66,435,823 (GRCm39)	A261S	probably benign	Het
Clptm1	C	T	7: 19,372,121 (GRCm39)	W238*	probably null	Het
Cr2	A	G	1: 194,842,047 (GRCm39)	V302A	probably damaging	Het
Cyp4a31	A	G	4: 115,431,969 (GRCm39)		probably benign	Het
Dennd4a	T	A	9: 64,769,613 (GRCm39)	I440N	probably damaging	Het
Dsc2	C	T	18: 20,184,284 (GRCm39)	V35I	probably damaging	Het
Dyrk1a	T	A	16: 94,464,605 (GRCm39)	M71K	probably benign	Het
Exoc3l2	G	A	7: 19,229,181 (GRCm39)	G200S	probably benign	Het
Fhip2a	T	C	19: 57,361,442 (GRCm39)	L122P	possibly damaging	Het
Fkbp15	A	T	4: 62,258,914 (GRCm39)	I114N	probably damaging	Het
Fpr-rs6	G	A	17: 20,402,479 (GRCm39)	P294L	probably damaging	Het
Frmd6	A	G	12: 70,940,638 (GRCm39)	T428A	probably benign	Het
G6pd2	T	A	5: 61,966,228 (GRCm39)	M1K	probably null	Het
Gdf3	C	T	6: 122,583,717 (GRCm39)	V217I	probably benign	Het
Grm7	G	T	6: 110,623,309 (GRCm39)	V161F	probably damaging	Het
Gtf3c1	T	C	7: 125,292,397 (GRCm39)		probably null	Het
Hrg	G	A	16: 22,774,825 (GRCm39)	V152I	possibly damaging	Het
Itpkc	T	C	7: 26,926,934 (GRCm39)	T327A	probably damaging	Het
Jade1	T	C	3: 41,555,845 (GRCm39)	V304A	probably damaging	Het
Leo1	C	A	9: 75,357,762 (GRCm39)		probably benign	Het
Lrrc7	A	T	3: 157,866,042 (GRCm39)	L1233Q	probably damaging	Het
Ltbp3	G	A	19: 5,804,050 (GRCm39)	R854Q	probably benign	Het
Matn2	C	A	15: 34,388,937 (GRCm39)	Y342*	probably null	Het
Minar1	G	A	9: 89,483,963 (GRCm39)	T478I	probably damaging	Het
Mlh3	T	C	12: 85,315,454 (GRCm39)	H244R	possibly damaging	Het
Mmaa	A	T	8: 79,994,843 (GRCm39)	V321E	probably damaging	Het
Ntng1	T	A	3: 109,842,184 (GRCm39)	L196F	probably damaging	Het
Oas1e	A	G	5: 120,932,205 (GRCm39)	V146A	probably damaging	Het
Or52z1	G	T	7: 103,437,241 (GRCm39)	T81K	probably benign	Het
Plcxd2	T	C	16: 45,800,864 (GRCm39)	K120R	probably damaging	Het
Prex2	G	T	1: 11,180,581 (GRCm39)	C382F	possibly damaging	Het
Ptprk	A	G	10: 28,427,661 (GRCm39)	T747A	probably damaging	Het
Qki	G	A	17: 10,435,394 (GRCm39)		probably benign	Het
Rpusd2	A	G	2: 118,869,085 (GRCm39)	T503A	probably benign	Het
Rtn3	T	C	19: 7,435,510 (GRCm39)	S142G	probably damaging	Het
Slco1a5	C	T	6: 142,194,370 (GRCm39)		probably null	Het
Snap91	A	T	9: 86,657,665 (GRCm39)	W509R	probably damaging	Het
Srsf3	C	T	17: 29,255,430 (GRCm39)		probably benign	Het
Tmem267	A	T	13: 119,629,175 (GRCm39)		probably null	Het
Tmem63a	G	A	1: 180,790,679 (GRCm39)	D446N	possibly damaging	Het
Tnfaip8	C	A	18: 50,223,653 (GRCm39)	H154N	possibly damaging	Het
Trim35	T	C	14: 66,541,503 (GRCm39)	L209P	probably damaging	Het
Ttf1	A	G	2: 28,954,816 (GRCm39)	E60G	possibly damaging	Het
Ttf2	T	C	3: 100,849,136 (GRCm39)		probably benign	Het
Tubg2	T	C	11: 101,051,224 (GRCm39)		probably null	Het
Ubap1l	C	T	9: 65,276,477 (GRCm39)		probably benign	Het
Usp48	A	T	4: 137,360,750 (GRCm39)	R26*	probably null	Het
Vmn1r222	A	G	13: 23,417,102 (GRCm39)	V37A	probably benign	Het
Vmn2r4	T	A	3: 64,322,572 (GRCm39)	N49I	probably damaging	Het
Zfp979	A	T	4: 147,697,588 (GRCm39)	C374S	probably benign	Het

Other mutations in Psg29

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01020:Psg29	APN	7	16,942,657 (GRCm39)	missense	probably benign	0.42
IGL01107:Psg29	APN	7	16,938,850 (GRCm39)	missense	probably benign	0.01
IGL01348:Psg29	APN	7	16,944,598 (GRCm39)	missense	probably benign	0.09
IGL01353:Psg29	APN	7	16,938,938 (GRCm39)	missense	possibly damaging	0.54
IGL02546:Psg29	APN	7	16,942,707 (GRCm39)	missense	probably damaging	1.00
IGL02611:Psg29	APN	7	16,942,716 (GRCm39)	missense	probably benign	0.15
IGL02982:Psg29	APN	7	16,945,632 (GRCm39)	missense	probably damaging	0.98
IGL03072:Psg29	APN	7	16,942,719 (GRCm39)	missense	probably benign	0.06
macular	UTSW	7	16,944,460 (GRCm39)	missense	probably benign	0.23
papular	UTSW	7	16,945,837 (GRCm39)	makesense	probably null
R1744:Psg29	UTSW	7	16,944,278 (GRCm39)	missense	probably damaging	1.00
R2272:Psg29	UTSW	7	16,944,621 (GRCm39)	missense	probably benign	0.19
R3054:Psg29	UTSW	7	16,942,727 (GRCm39)	missense	probably benign	0.29
R3790:Psg29	UTSW	7	16,938,950 (GRCm39)	missense	possibly damaging	0.71
R4464:Psg29	UTSW	7	16,944,575 (GRCm39)	missense	possibly damaging	0.61
R4740:Psg29	UTSW	7	16,942,458 (GRCm39)	missense	probably benign	0.00
R4774:Psg29	UTSW	7	16,944,460 (GRCm39)	missense	probably benign	0.23
R4902:Psg29	UTSW	7	16,945,837 (GRCm39)	makesense	probably null
R4977:Psg29	UTSW	7	16,942,556 (GRCm39)	missense	probably damaging	1.00
R5071:Psg29	UTSW	7	16,945,763 (GRCm39)	missense	probably damaging	1.00
R5072:Psg29	UTSW	7	16,945,763 (GRCm39)	missense	probably damaging	1.00
R5074:Psg29	UTSW	7	16,945,763 (GRCm39)	missense	probably damaging	1.00
R5169:Psg29	UTSW	7	16,945,578 (GRCm39)	missense	probably damaging	1.00
R5415:Psg29	UTSW	7	16,945,561 (GRCm39)	splice site	probably null
R5729:Psg29	UTSW	7	16,944,459 (GRCm39)	missense	probably damaging	0.98
R6023:Psg29	UTSW	7	16,944,437 (GRCm39)	missense	possibly damaging	0.82
R6127:Psg29	UTSW	7	16,945,671 (GRCm39)	missense	probably benign	0.00
R6900:Psg29	UTSW	7	16,938,857 (GRCm39)	nonsense	probably null
R7142:Psg29	UTSW	7	16,944,546 (GRCm39)	missense	probably damaging	1.00
R7297:Psg29	UTSW	7	16,944,616 (GRCm39)	nonsense	probably null
R7448:Psg29	UTSW	7	16,945,648 (GRCm39)	missense	possibly damaging	0.90
R7973:Psg29	UTSW	7	16,944,462 (GRCm39)	missense	probably benign	0.03
R8027:Psg29	UTSW	7	16,942,565 (GRCm39)	missense	possibly damaging	0.69
R8979:Psg29	UTSW	7	16,937,544 (GRCm39)	start gained	probably benign
R9744:Psg29	UTSW	7	16,944,495 (GRCm39)	missense	probably benign	0.01
X0017:Psg29	UTSW	7	16,944,586 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- TACCCGCTCAGAACTGTGTC -3'
(R):5'- ATCTGTACCCAGTACTCGTAGG -3'

Sequencing Primer
(F):5'- CGCTCAGAACTGTGTCTCATC -3'
(R):5'- CGTAGGGTGTATAATCCAGCATCC -3'

Posted On

2015-04-29