Mutagenetix > Incidental Mutation

Incidental Mutation 'R5729:Psg29'

452656

Institutional Source

Beutler Lab

Gene Symbol

Psg29

Ensembl Gene

ENSMUSG00000023159

Gene Name

pregnancy-specific beta-1-glycoprotein 29

Synonyms

cea17

MMRRC Submission

043346-MU

Accession Numbers

Essential gene?

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

Stock #

R5729 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

16937402-16949681 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 16944459 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Isoleucine at position 323 (N323I)

Ref Sequence

ENSEMBL: ENSMUSP00000075320 (fasta)

Gene Model

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

AlphaFold

Q3URN6

Predicted Effect

probably damaging
Transcript: ENSMUST00000075934
AA Change: N323I

PolyPhen 2 Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000075320
Gene: ENSMUSG00000023159
AA Change: N323I

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

0.6467

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 97.2%
20x: 95.2%

Validation Efficiency

97% (62/64)

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adss2	A	T	1: 177,623,824 (GRCm39)	V46E	possibly damaging	Het
Aldoart2	T	C	12: 55,612,690 (GRCm39)	V205A	probably benign	Het
Atp1a2	A	G	1: 172,120,938 (GRCm39)	S45P	probably damaging	Het
Atp4a	A	G	7: 30,411,851 (GRCm39)	K29E	possibly damaging	Het
AU040320	T	A	4: 126,724,208 (GRCm39)	D428E	probably damaging	Het
Bend7	T	C	2: 4,768,085 (GRCm39)	L347P	probably damaging	Het
Cacna2d1	T	A	5: 16,140,037 (GRCm39)	L9*	probably null	Het
Ccdc103	A	T	11: 102,773,904 (GRCm39)	I50F	probably damaging	Het
Cdc5l	T	C	17: 45,737,495 (GRCm39)	I88V	probably benign	Het
Cracr2a	T	C	6: 127,584,199 (GRCm39)	V86A	possibly damaging	Het
Cybb	C	G	X: 9,316,989 (GRCm39)	D246H	probably benign	Het
Dgkd	C	T	1: 87,864,054 (GRCm39)	Q90*	probably null	Het
Dnajc21	A	T	15: 10,449,682 (GRCm39)	D446E	probably benign	Het
Fam13a	T	G	6: 58,916,292 (GRCm39)	R648S	probably damaging	Het
Gabrg2	A	G	11: 41,858,450 (GRCm39)	V226A	probably damaging	Het
Gm5499	A	T	17: 87,385,944 (GRCm39)		noncoding transcript	Het
Gprc5c	G	T	11: 114,755,093 (GRCm39)	V257L	possibly damaging	Het
Irf2bp1	G	T	7: 18,739,172 (GRCm39)	E271*	probably null	Het
Krt86	T	G	15: 101,374,429 (GRCm39)	V274G	probably benign	Het
Lats2	A	T	14: 57,960,192 (GRCm39)	C151S	probably benign	Het
Mapk3	A	T	7: 126,363,979 (GRCm39)	T254S	probably benign	Het
Mat2b	A	T	11: 40,573,373 (GRCm39)	M202K	probably damaging	Het
Mos	A	G	4: 3,870,971 (GRCm39)	Y282H	probably benign	Het
Myo3b	A	G	2: 69,936,083 (GRCm39)	K108R	probably damaging	Het
Naa16	A	G	14: 79,593,220 (GRCm39)	Y417H	probably damaging	Het
Oat	A	T	7: 132,159,984 (GRCm39)	I412N	probably damaging	Het
Or4d11	A	T	19: 12,013,272 (GRCm39)	I278N	probably damaging	Het
Pcdh1	A	T	18: 38,335,999 (GRCm39)	V73D	probably damaging	Het
Pigv	A	T	4: 133,392,134 (GRCm39)	Y345*	probably null	Het
Pitpnc1	G	T	11: 107,228,264 (GRCm39)	F34L	probably benign	Het
Plxnd1	A	G	6: 115,942,838 (GRCm39)	L1282P	probably damaging	Het
Ppp1r3a	T	C	6: 14,719,762 (GRCm39)	D384G	probably benign	Het
Ppp2ca	G	A	11: 52,008,856 (GRCm39)	E119K	probably damaging	Het
Rasa4	T	C	5: 136,122,016 (GRCm39)	V108A	probably benign	Het
Rbm14	A	G	19: 4,852,577 (GRCm39)		probably benign	Het
Rfc1	A	T	5: 65,434,795 (GRCm39)	V657E	probably damaging	Het
Rhcg	A	T	7: 79,250,371 (GRCm39)	N237K	probably damaging	Het
Rpgrip1	A	G	14: 52,397,617 (GRCm39)	Q1302R	probably benign	Het
Rragc	A	G	4: 123,818,645 (GRCm39)	M287V	possibly damaging	Het
Scn7a	A	G	2: 66,572,301 (GRCm39)		probably null	Het
Sema6a	C	T	18: 47,414,410 (GRCm39)	C506Y	probably damaging	Het
Senp1	G	T	15: 97,964,412 (GRCm39)	H267Q	possibly damaging	Het
Skor2	A	G	18: 76,946,578 (GRCm39)	E100G	unknown	Het
Slc38a11	A	T	2: 65,147,365 (GRCm39)	C371S	probably benign	Het
Snai3	G	A	8: 123,181,629 (GRCm39)	A276V	probably benign	Het
Sp110	C	G	1: 85,516,839 (GRCm39)	E219D	probably damaging	Het
Spag6	C	T	2: 18,720,525 (GRCm39)	T99I	probably benign	Het
Spop	A	G	11: 95,376,675 (GRCm39)	I243V	possibly damaging	Het
Sra1	A	T	18: 36,800,496 (GRCm39)		probably benign	Het
Stag3	T	A	5: 138,288,485 (GRCm39)	S140T	possibly damaging	Het
Stx16	G	A	2: 173,935,292 (GRCm39)	G156R	probably damaging	Het
Tbc1d2b	G	C	9: 90,089,925 (GRCm39)	A868G	probably benign	Het
Tead2	A	G	7: 44,870,166 (GRCm39)		probably benign	Het
Tmem53	C	A	4: 117,125,669 (GRCm39)	H261N	probably damaging	Het
Ube4a	A	T	9: 44,844,627 (GRCm39)	S932T	probably damaging	Het
Usp9y	A	T	Y: 1,381,339 (GRCm39)	D827E	probably damaging	Het
Vmn2r53	T	C	7: 12,334,733 (GRCm39)	E309G	probably damaging	Het
Wrn	T	C	8: 33,758,806 (GRCm39)	S1026G	probably benign	Het
Zfp646	G	A	7: 127,484,626 (GRCm39)	A1760T	probably damaging	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
R3963:Psg29	UTSW	7	16,942,510 (GRCm39)	missense	probably benign	0.01
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
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'- GCACCTCTTCCAAACTCATGG -3'
(R):5'- ACCCAGTCCTGACAGTCTAGTG -3'

Sequencing Primer
(F):5'- ACTCATGGTTGAAGCAGTGCC -3'
(R):5'- CAGAGTCCATTGAGAGTCACTTAAC -3'

Posted On

2017-01-03