Mutagenetix > Incidental Mutation

Incidental Mutation 'R6631:Serpina3i'

525156

Institutional Source

Beutler Lab

Gene Symbol

Serpina3i

Ensembl Gene

ENSMUSG00000079014

Gene Name

serine (or cysteine) peptidase inhibitor, clade A, member 3I

Synonyms

alpha-1 antiproteinase, antitrypsin, 2B2, Gm6930

MMRRC Submission

044753-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.059) question?

Stock #

R6631 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

104229381-104235631 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 104232725 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 210 (D210G)

Ref Sequence

ENSEMBL: ENSMUSP00000105584 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000109958]

AlphaFold

D3Z450

Predicted Effect

probably damaging
Transcript: ENSMUST00000109958
AA Change: D210G

PolyPhen 2 Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000105584
Gene: ENSMUSG00000079014
AA Change: D210G

Domain	Start	End	E-Value	Type
SERPIN	46	407	8.45e-187	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000109960

Meta Mutation Damage Score

0.2775

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.0%
20x: 93.9%

Validation Efficiency

96% (50/52)

Allele List at MGI

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4931406C07Rik	A	T	9: 15,203,326 (GRCm39)	N159K	probably damaging	Het
Arhgef10l	T	C	4: 140,245,058 (GRCm39)		probably benign	Het
Atosa	A	G	9: 74,861,107 (GRCm39)	D4G	possibly damaging	Het
Avil	A	G	10: 126,843,618 (GRCm39)	S153G	possibly damaging	Het
C2cd3	G	A	7: 100,067,747 (GRCm39)	D877N	probably damaging	Het
Clca3a2	G	A	3: 144,519,405 (GRCm39)	A257V	probably benign	Het
Cramp1	T	A	17: 25,202,931 (GRCm39)	H366L	probably benign	Het
Cyp2c37	C	T	19: 39,998,287 (GRCm39)	S393L	probably damaging	Het
Defb8	T	A	8: 19,495,950 (GRCm39)	I37L	probably benign	Het
Dennd4b	C	A	3: 90,185,039 (GRCm39)		probably null	Het
Eps8l2	G	A	7: 140,936,115 (GRCm39)	R223H	probably damaging	Het
Erbin	A	G	13: 103,961,400 (GRCm39)	L1302P	probably benign	Het
Exoc3l	A	G	8: 106,021,993 (GRCm39)	W37R	probably damaging	Het
Fap	T	C	2: 62,333,725 (GRCm39)	N668S	probably damaging	Het
Gas7	A	G	11: 67,565,107 (GRCm39)	N250S	probably damaging	Het
H2bc12	T	A	13: 22,220,391 (GRCm39)	V112E	probably damaging	Het
Hivep1	C	A	13: 42,309,956 (GRCm39)	P732Q	probably damaging	Het
Irx4	G	T	13: 73,416,545 (GRCm39)	A314S	probably benign	Het
Itgb8	A	T	12: 119,144,712 (GRCm39)	L332*	probably null	Het
Kctd19	A	G	8: 106,111,960 (GRCm39)		probably null	Het
Kif14	G	A	1: 136,443,697 (GRCm39)	S1290N	probably benign	Het
Klk1b3	C	T	7: 43,850,888 (GRCm39)	T140I	probably benign	Het
Lama1	A	G	17: 68,081,477 (GRCm39)	N1305D	probably benign	Het
Lrp1	A	T	10: 127,410,201 (GRCm39)	V1515E	probably damaging	Het
Man2b1	A	G	8: 85,813,440 (GRCm39)		probably null	Het
Mocos	A	G	18: 24,832,988 (GRCm39)	T818A	probably benign	Het
Mpc2	G	T	1: 165,307,081 (GRCm39)	W94L	probably benign	Het
Mrc1	G	A	2: 14,243,296 (GRCm39)	V141I	probably benign	Het
Nalcn	T	C	14: 123,697,663 (GRCm39)	T538A	probably benign	Het
Ndufs3	G	A	2: 90,732,744 (GRCm39)	T114M	probably damaging	Het
Noct	T	C	3: 51,157,621 (GRCm39)	C320R	probably damaging	Het
Or5b117	T	A	19: 13,431,185 (GRCm39)	Q232L	probably benign	Het
Pcdha11	G	T	18: 37,138,844 (GRCm39)	A158S	probably damaging	Het
Pcdhga8	T	A	18: 37,860,109 (GRCm39)	D388E	probably benign	Het
Peg3	T	C	7: 6,712,069 (GRCm39)	E1051G	possibly damaging	Het
Phlda2	T	A	7: 143,055,918 (GRCm39)	I104F	probably damaging	Het
Polr2a	A	G	11: 69,626,339 (GRCm39)	S1604P	possibly damaging	Het
Pomt2	C	T	12: 87,186,417 (GRCm39)		probably null	Het
Ppp6r2	G	A	15: 89,137,458 (GRCm39)		probably null	Het
Prdm2	T	G	4: 142,861,454 (GRCm39)	Q612P	probably benign	Het
Prr5	C	A	15: 84,586,978 (GRCm39)	R243S	probably damaging	Het
Ptgdr2	T	C	19: 10,918,233 (GRCm39)	I250T	probably benign	Het
Rad54l2	A	T	9: 106,590,739 (GRCm39)	C462*	probably null	Het
Sec16a	T	A	2: 26,329,969 (GRCm39)	E682V	probably damaging	Het
Slain2	T	A	5: 73,114,748 (GRCm39)	D326E	probably benign	Het
Sned1	A	G	1: 93,209,374 (GRCm39)	E829G	probably damaging	Het
Steap4	G	A	5: 8,026,995 (GRCm39)	W319*	probably null	Het
Taar8c	A	G	10: 23,977,701 (GRCm39)	V37A	probably benign	Het
Tdrd12	T	A	7: 35,184,654 (GRCm39)	Y753F	probably damaging	Het
Tnxb	A	G	17: 34,937,222 (GRCm39)	S3770G	probably damaging	Het
Trrap	A	G	5: 144,708,460 (GRCm39)	N48S	possibly damaging	Het
Zfp558	C	A	9: 18,368,219 (GRCm39)	G190*	probably null	Het

Other mutations in Serpina3i

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00658:Serpina3i	APN	12	104,231,429 (GRCm39)	missense	possibly damaging	0.47
IGL01311:Serpina3i	APN	12	104,233,946 (GRCm39)	missense	probably damaging	1.00
IGL02661:Serpina3i	APN	12	104,231,515 (GRCm39)	nonsense	probably null
IGL02819:Serpina3i	APN	12	104,234,761 (GRCm39)	missense	probably damaging	1.00
FR4340:Serpina3i	UTSW	12	104,231,423 (GRCm39)	small insertion	probably benign
PIT4431001:Serpina3i	UTSW	12	104,231,432 (GRCm39)	missense	probably benign	0.03
R0091:Serpina3i	UTSW	12	104,231,423 (GRCm39)	missense	probably damaging	0.97
R0678:Serpina3i	UTSW	12	104,232,978 (GRCm39)	critical splice donor site	probably null
R1624:Serpina3i	UTSW	12	104,234,897 (GRCm39)	makesense	probably null
R4604:Serpina3i	UTSW	12	104,234,036 (GRCm39)	missense	possibly damaging	0.91
R4814:Serpina3i	UTSW	12	104,231,470 (GRCm39)	missense	probably benign	0.00
R5213:Serpina3i	UTSW	12	104,231,914 (GRCm39)	missense	probably benign
R5464:Serpina3i	UTSW	12	104,234,751 (GRCm39)	missense	possibly damaging	0.62
R5504:Serpina3i	UTSW	12	104,232,862 (GRCm39)	missense	probably damaging	1.00
R5723:Serpina3i	UTSW	12	104,231,759 (GRCm39)	missense	probably benign	0.09
R5828:Serpina3i	UTSW	12	104,231,474 (GRCm39)	missense	probably benign	0.35
R5922:Serpina3i	UTSW	12	104,232,766 (GRCm39)	missense	probably benign	0.15
R6194:Serpina3i	UTSW	12	104,232,762 (GRCm39)	missense	probably benign	0.21
R6235:Serpina3i	UTSW	12	104,232,791 (GRCm39)	missense	probably damaging	1.00
R6469:Serpina3i	UTSW	12	104,232,776 (GRCm39)	missense	probably damaging	1.00
R7993:Serpina3i	UTSW	12	104,231,407 (GRCm39)	missense	possibly damaging	0.80
R8437:Serpina3i	UTSW	12	104,231,963 (GRCm39)	missense	probably damaging	1.00
R8680:Serpina3i	UTSW	12	104,231,387 (GRCm39)	missense	possibly damaging	0.61
R9157:Serpina3i	UTSW	12	104,231,672 (GRCm39)	missense	probably damaging	1.00
R9249:Serpina3i	UTSW	12	104,231,728 (GRCm39)	nonsense	probably null
R9303:Serpina3i	UTSW	12	104,234,881 (GRCm39)	missense	probably damaging	0.98
R9305:Serpina3i	UTSW	12	104,234,881 (GRCm39)	missense	probably damaging	0.98
R9313:Serpina3i	UTSW	12	104,231,672 (GRCm39)	missense	probably damaging	1.00
R9424:Serpina3i	UTSW	12	104,234,730 (GRCm39)	missense	probably benign
R9572:Serpina3i	UTSW	12	104,234,743 (GRCm39)	missense	probably damaging	1.00
R9576:Serpina3i	UTSW	12	104,234,730 (GRCm39)	missense	probably benign
Z1176:Serpina3i	UTSW	12	104,233,989 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CAGAGTTCTGTGTCTTCCAAGGG -3'
(R):5'- TGCAAGCTGGTTTCCACCTG -3'

Sequencing Primer
(F):5'- TGTCTTCCAAGGGGTTTCTAATC -3'
(R):5'- GCATCTTGCCCTGGTCAG -3'

Posted On

2018-06-22