Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03149:Serpina9'

411017

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Serpina9

Ensembl Gene

ENSMUSG00000058260

Gene Name

serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 9

Synonyms

Centerin, 2310014L03Rik

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.048) question?

Stock #

IGL03149

Quality Score

Status

Chromosome

Chromosomal Location

103962877-103979911 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

G to A at 103974869 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Stop codon at position 95 (Q95*)

Ref Sequence

ENSEMBL: ENSMUSP00000130064 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000058464] [ENSMUST00000164023]

AlphaFold

Q9D7D2

Predicted Effect

probably null
Transcript: ENSMUST00000058464
AA Change: Q95*

SMART Domains

Protein: ENSMUSP00000058535
Gene: ENSMUSG00000058260
AA Change: Q95*

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
SERPIN	55	415	1.27e-158	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000164023
AA Change: Q95*

SMART Domains

Protein: ENSMUSP00000130064
Gene: ENSMUSG00000058260
AA Change: Q95*

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
SERPIN	55	205	8.9e-4	SMART

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Arhgap10	A	G	8: 78,136,167 (GRCm39)		probably benign	Het
Arhgap42	A	G	9: 9,008,085 (GRCm39)	I546T	possibly damaging	Het
Arsj	A	T	3: 126,233,053 (GRCm39)		probably benign	Het
Ash2l	A	G	8: 26,308,650 (GRCm39)	V543A	probably benign	Het
B4galnt3	A	G	6: 120,208,555 (GRCm39)		probably benign	Het
Blvra	T	A	2: 126,924,871 (GRCm39)	V11E	probably damaging	Het
Calcb	T	C	7: 114,319,371 (GRCm39)	L51P	probably damaging	Het
Cd36	T	A	5: 18,025,563 (GRCm39)	K52N	probably benign	Het
Cebpz	T	C	17: 79,229,982 (GRCm39)	N857S	probably benign	Het
Ces1b	A	G	8: 93,791,502 (GRCm39)		probably benign	Het
Clspn	T	C	4: 126,470,295 (GRCm39)		probably benign	Het
Cr2	A	T	1: 194,848,674 (GRCm39)	L283H	probably damaging	Het
Ctc1	T	C	11: 68,921,987 (GRCm39)	V811A	possibly damaging	Het
Ctsk	T	C	3: 95,408,730 (GRCm39)	S65P	possibly damaging	Het
Ddx51	A	G	5: 110,801,600 (GRCm39)	N83D	probably benign	Het
Eci2	T	C	13: 35,172,296 (GRCm39)	T146A	probably benign	Het
Erbin	T	C	13: 103,977,671 (GRCm39)	N629D	possibly damaging	Het
Etfbkmt	A	G	6: 149,045,781 (GRCm39)	E45G	probably damaging	Het
Fat4	A	G	3: 39,045,834 (GRCm39)	N3951S	probably damaging	Het
Fktn	T	C	4: 53,744,653 (GRCm39)	V311A	probably benign	Het
Garem1	G	T	18: 21,264,523 (GRCm39)	P534T	probably damaging	Het
Gm8237	A	G	14: 5,864,451 (GRCm38)	I37T	probably benign	Het
Ikzf5	T	C	7: 130,998,494 (GRCm39)	K13E	probably damaging	Het
Kl	T	A	5: 150,906,200 (GRCm39)	C523*	probably null	Het
Klhl7	G	A	5: 24,364,687 (GRCm39)	V574I	probably benign	Het
Lyst	T	C	13: 13,856,029 (GRCm39)	V2450A	probably benign	Het
Map3k6	A	T	4: 132,976,999 (GRCm39)	I819F	probably damaging	Het
Mphosph9	T	C	5: 124,401,074 (GRCm39)	E891G	probably damaging	Het
Myo7b	A	G	18: 32,147,355 (GRCm39)	S63P	probably damaging	Het
Ndufaf7	C	T	17: 79,252,439 (GRCm39)	R283C	possibly damaging	Het
Nepro	G	T	16: 44,547,462 (GRCm39)	A60S	probably damaging	Het
Nop56	T	C	2: 130,119,445 (GRCm39)	S354P	probably damaging	Het
Nwd2	T	A	5: 63,963,338 (GRCm39)	L974H	probably damaging	Het
Or4a80	T	C	2: 89,583,172 (GRCm39)		probably null	Het
Or52ad1	A	T	7: 102,996,056 (GRCm39)	H26Q	probably benign	Het
Pacsin3	T	A	2: 91,091,852 (GRCm39)		probably benign	Het
Parp12	C	T	6: 39,091,165 (GRCm39)	D142N	probably benign	Het
Pcdh15	G	A	10: 74,466,527 (GRCm39)	D1449N	probably damaging	Het
Pcsk7	C	T	9: 45,820,778 (GRCm39)	T70M	probably benign	Het
Pld4	T	C	12: 112,733,263 (GRCm39)	F280L	probably benign	Het
Ppm1k	C	A	6: 57,501,759 (GRCm39)	A135S	probably damaging	Het
Prkcq	A	T	2: 11,237,356 (GRCm39)	Y45F	probably benign	Het
Prom1	T	A	5: 44,187,076 (GRCm39)	I385F	probably damaging	Het
Prss12	A	G	3: 123,299,036 (GRCm39)	N603D	probably benign	Het
Ptbp2	G	T	3: 119,514,074 (GRCm39)	T501K	possibly damaging	Het
Ranbp17	C	A	11: 33,193,183 (GRCm39)	R957L	possibly damaging	Het
Rasl10a	T	C	11: 5,008,429 (GRCm39)	Y42H	possibly damaging	Het
Serpinb1b	C	A	13: 33,269,275 (GRCm39)	Q3K	possibly damaging	Het
Sgo2b	T	A	8: 64,379,617 (GRCm39)	M1072L	probably benign	Het
Slc1a5	T	C	7: 16,523,745 (GRCm39)	V250A	probably damaging	Het
Slc30a6	T	C	17: 74,730,018 (GRCm39)	S303P	probably damaging	Het
Tbc1d2	A	T	4: 46,637,619 (GRCm39)	I209N	probably benign	Het
Tmc4	T	A	7: 3,670,177 (GRCm39)	I484L	probably benign	Het
Ttll5	G	A	12: 85,965,758 (GRCm39)	E36K	probably damaging	Het
Unc93b1	A	G	19: 3,994,041 (GRCm39)	M391V	probably benign	Het
Xpo5	T	A	17: 46,526,740 (GRCm39)		probably null	Het

Other mutations in Serpina9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01020:Serpina9	APN	12	103,974,845 (GRCm39)	missense	probably damaging	1.00
IGL02228:Serpina9	APN	12	103,974,859 (GRCm39)	missense	probably benign	0.02
IGL02692:Serpina9	APN	12	103,974,665 (GRCm39)	missense	probably damaging	1.00
IGL03134:Serpina9	UTSW	12	103,967,696 (GRCm39)	missense	probably null	0.18
R0119:Serpina9	UTSW	12	103,967,729 (GRCm39)	missense	probably benign	0.18
R0299:Serpina9	UTSW	12	103,967,729 (GRCm39)	missense	probably benign	0.18
R0499:Serpina9	UTSW	12	103,967,729 (GRCm39)	missense	probably benign	0.18
R1477:Serpina9	UTSW	12	103,963,362 (GRCm39)	missense	possibly damaging	0.90
R1912:Serpina9	UTSW	12	103,967,508 (GRCm39)	missense	probably damaging	1.00
R2142:Serpina9	UTSW	12	103,974,568 (GRCm39)	missense	probably benign	0.04
R2221:Serpina9	UTSW	12	103,964,523 (GRCm39)	missense	probably damaging	0.98
R2413:Serpina9	UTSW	12	103,967,485 (GRCm39)	critical splice donor site	probably null
R3939:Serpina9	UTSW	12	103,975,151 (GRCm39)	start codon destroyed	probably benign	0.01
R4515:Serpina9	UTSW	12	103,967,553 (GRCm39)	missense	probably benign	0.14
R5242:Serpina9	UTSW	12	103,974,644 (GRCm39)	missense	probably benign	0.09
R5589:Serpina9	UTSW	12	103,967,728 (GRCm39)	missense	probably benign	0.00
R5900:Serpina9	UTSW	12	103,975,130 (GRCm39)	nonsense	probably null
R6171:Serpina9	UTSW	12	103,974,678 (GRCm39)	nonsense	probably null
R6195:Serpina9	UTSW	12	103,967,666 (GRCm39)	missense	probably damaging	0.96
R6566:Serpina9	UTSW	12	103,963,296 (GRCm39)	missense	possibly damaging	0.61
R6995:Serpina9	UTSW	12	103,967,495 (GRCm39)	missense	probably damaging	1.00
R7762:Serpina9	UTSW	12	103,967,575 (GRCm39)	missense	probably damaging	0.98
R7808:Serpina9	UTSW	12	103,967,484 (GRCm39)	critical splice donor site	probably null
R7860:Serpina9	UTSW	12	103,967,680 (GRCm39)	missense	probably benign	0.01
R7935:Serpina9	UTSW	12	103,964,421 (GRCm39)	missense	probably damaging	1.00
R9041:Serpina9	UTSW	12	103,967,737 (GRCm39)	missense
Z1176:Serpina9	UTSW	12	103,967,543 (GRCm39)	missense	probably damaging	1.00

Posted On

2016-08-02