Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01936:Serpinb3b'

180652

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Serpinb3b

Ensembl Gene

ENSMUSG00000073602

Gene Name

serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 3B

Synonyms

Scca2-rs

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.054) question?

Stock #

IGL01936

Quality Score

Status

Chromosome

Chromosomal Location

107081691-107088844 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 107082368 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Leucine at position 299 (M299L)

Ref Sequence

ENSEMBL: ENSMUSP00000132370 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000086694] [ENSMUST00000166100]

AlphaFold

Q9D1Q5

Predicted Effect

probably benign
Transcript: ENSMUST00000086694
AA Change: M299L

PolyPhen 2 Score 0.130 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000083901
Gene: ENSMUSG00000073602
AA Change: M299L

Domain	Start	End	E-Value	Type
SERPIN	13	387	4.75e-181	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000166100
AA Change: M299L

PolyPhen 2 Score 0.130 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000132370
Gene: ENSMUSG00000073602
AA Change: M299L

Domain	Start	End	E-Value	Type
SERPIN	13	387	4.75e-181	SMART

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts3	T	A	5: 90,009,282 (GRCm39)	H127L	probably benign	Het
Adamtsl3	T	C	7: 82,244,579 (GRCm39)	V419A	possibly damaging	Het
Arhgap31	T	A	16: 38,423,287 (GRCm39)	L926F	probably damaging	Het
Asgr2	A	T	11: 69,988,877 (GRCm39)		probably null	Het
C3ar1	T	A	6: 122,828,194 (GRCm39)	T8S	probably benign	Het
Caskin2	T	C	11: 115,695,543 (GRCm39)	I273V	probably damaging	Het
Ccnl2	T	A	4: 155,904,856 (GRCm39)	C242S	probably damaging	Het
Cdkn2a	A	T	4: 89,212,569 (GRCm39)		probably null	Het
Cfap45	T	G	1: 172,361,616 (GRCm39)	M231R	probably damaging	Het
Clcn7	A	C	17: 25,374,350 (GRCm39)	N464H	probably benign	Het
Col20a1	T	A	2: 180,651,161 (GRCm39)		probably benign	Het
Col7a1	T	A	9: 108,797,067 (GRCm39)		probably benign	Het
Cops7a	T	C	6: 124,939,379 (GRCm39)	D90G	probably benign	Het
Ctcf	T	C	8: 106,396,864 (GRCm39)	V363A	probably benign	Het
Cyp2j12	A	G	4: 96,021,306 (GRCm39)	V100A	probably benign	Het
Dcaf1	T	A	9: 106,736,800 (GRCm39)	F1085Y	possibly damaging	Het
Drc7	T	A	8: 95,800,760 (GRCm39)	F594Y	possibly damaging	Het
Ehbp1l1	C	A	19: 5,768,277 (GRCm39)	E1009*	probably null	Het
Epg5	C	A	18: 78,028,316 (GRCm39)	R1286S	probably damaging	Het
Etv1	T	C	12: 38,885,060 (GRCm39)		probably benign	Het
Exosc7	T	C	9: 122,964,956 (GRCm39)		probably benign	Het
Fam227a	T	C	15: 79,496,747 (GRCm39)	D610G	possibly damaging	Het
Fat4	T	A	3: 39,033,923 (GRCm39)	M2525K	probably benign	Het
Gimap5	G	T	6: 48,729,999 (GRCm39)	A190S	probably damaging	Het
Glcci1	T	A	6: 8,579,596 (GRCm39)	S79T	probably damaging	Het
Gpnmb	C	T	6: 49,024,384 (GRCm39)	T233I	probably null	Het
Hdac1-ps	T	C	17: 78,799,558 (GRCm39)	V183A	probably damaging	Het
Hyls1	T	C	9: 35,473,363 (GRCm39)	I18V	probably benign	Het
Ighv1-63	C	T	12: 115,459,274 (GRCm39)	E108K	probably damaging	Het
Ighv5-12	C	A	12: 113,665,927 (GRCm39)	R57L	probably damaging	Het
Igkv5-37	T	C	6: 69,940,323 (GRCm39)	Y107C	probably damaging	Het
Il20ra	T	A	10: 19,631,591 (GRCm39)	V264D	probably damaging	Het
Jph1	A	T	1: 17,167,608 (GRCm39)	V74E	probably damaging	Het
Kcnab1	C	T	3: 65,265,695 (GRCm39)	L280F	probably damaging	Het
Kcnk1	T	C	8: 126,751,826 (GRCm39)	F144S	probably damaging	Het
Kcnq1	G	A	7: 142,738,241 (GRCm39)	E294K	possibly damaging	Het
Kdm4b	T	A	17: 56,704,355 (GRCm39)	V813E	probably damaging	Het
Kntc1	T	A	5: 123,949,439 (GRCm39)	F1937I	probably damaging	Het
Ldb2	G	A	5: 44,637,586 (GRCm39)	R241W	probably damaging	Het
Lgr5	T	C	10: 115,288,319 (GRCm39)	N703S	probably damaging	Het
Map4k1	A	T	7: 28,688,032 (GRCm39)	M227L	possibly damaging	Het
Mbnl1	T	A	3: 60,520,940 (GRCm39)	M268K	possibly damaging	Het
Mcm2	C	A	6: 88,868,708 (GRCm39)	G350C	probably damaging	Het
Myh2	A	T	11: 67,082,599 (GRCm39)	T1390S	possibly damaging	Het
Npat	T	A	9: 53,469,526 (GRCm39)		probably benign	Het
Nr2e1	T	A	10: 42,443,969 (GRCm39)	D251V	possibly damaging	Het
Or1x2	A	G	11: 50,918,162 (GRCm39)	N111S	probably benign	Het
Or4d10	C	T	19: 12,051,421 (GRCm39)	V192I	probably benign	Het
Or5b107	C	A	19: 13,142,767 (GRCm39)	P130T	probably damaging	Het
Plekha5	T	A	6: 140,470,621 (GRCm39)	H87Q	probably damaging	Het
Polr3a	A	G	14: 24,529,256 (GRCm39)	V368A	probably damaging	Het
Psmb8	T	A	17: 34,419,168 (GRCm39)	L154Q	probably damaging	Het
Rab40c	A	C	17: 26,103,644 (GRCm39)	C140G	probably damaging	Het
Ranbp17	G	A	11: 33,437,689 (GRCm39)	T183I	probably benign	Het
Ruvbl2	T	C	7: 45,078,122 (GRCm39)	E117G	probably damaging	Het
Smpdl3a	A	G	10: 57,678,530 (GRCm39)	H111R	probably damaging	Het
Sspo	C	A	6: 48,452,821 (GRCm39)	P2843H	probably damaging	Het
Stk39	T	C	2: 68,144,908 (GRCm39)	T389A	probably benign	Het
Synrg	T	A	11: 83,910,531 (GRCm39)	F1000Y	probably benign	Het
Thbs2	C	T	17: 14,908,076 (GRCm39)	S229N	probably benign	Het
Thsd1	G	A	8: 22,742,247 (GRCm39)	C305Y	probably damaging	Het
Ticrr	C	A	7: 79,344,297 (GRCm39)	D1387E	probably benign	Het
Tmem145	G	T	7: 25,010,816 (GRCm39)	A383S	probably damaging	Het
Tmprss4	A	G	9: 45,090,718 (GRCm39)	V187A	probably damaging	Het
Unc13c	T	A	9: 73,600,524 (GRCm39)	M1407L	probably benign	Het
Vps39	C	T	2: 120,153,609 (GRCm39)	G655D	probably benign	Het
Wwtr1	T	C	3: 57,482,241 (GRCm39)		probably benign	Het
Xrn1	T	C	9: 95,930,397 (GRCm39)	S1535P	probably damaging	Het

Other mutations in Serpinb3b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00504:Serpinb3b	APN	1	107,085,411 (GRCm39)	missense	probably benign	0.20
IGL00543:Serpinb3b	APN	1	107,085,396 (GRCm39)	critical splice donor site	probably null
IGL00846:Serpinb3b	APN	1	107,083,579 (GRCm39)	missense	probably damaging	1.00
IGL00851:Serpinb3b	APN	1	107,087,435 (GRCm39)	missense	probably damaging	1.00
IGL01017:Serpinb3b	APN	1	107,082,187 (GRCm39)	missense	probably benign	0.31
IGL01083:Serpinb3b	APN	1	107,085,473 (GRCm39)	missense	possibly damaging	0.57
IGL01300:Serpinb3b	APN	1	107,083,573 (GRCm39)	critical splice donor site	probably benign
IGL01306:Serpinb3b	APN	1	107,082,395 (GRCm39)	missense	probably damaging	1.00
IGL01604:Serpinb3b	APN	1	107,082,454 (GRCm39)	missense	probably benign	0.00
IGL02125:Serpinb3b	APN	1	107,082,474 (GRCm39)	missense	probably damaging	1.00
IGL03185:Serpinb3b	APN	1	107,084,662 (GRCm39)	missense	probably benign	0.01
ANU23:Serpinb3b	UTSW	1	107,082,395 (GRCm39)	missense	probably damaging	1.00
R0329:Serpinb3b	UTSW	1	107,087,433 (GRCm39)	missense	probably damaging	1.00
R0330:Serpinb3b	UTSW	1	107,087,433 (GRCm39)	missense	probably damaging	1.00
R1465:Serpinb3b	UTSW	1	107,083,573 (GRCm39)	critical splice donor site	probably null
R1465:Serpinb3b	UTSW	1	107,083,573 (GRCm39)	critical splice donor site	probably null
R1635:Serpinb3b	UTSW	1	107,082,403 (GRCm39)	missense	probably benign	0.16
R1713:Serpinb3b	UTSW	1	107,083,164 (GRCm39)	missense	probably benign	0.00
R1898:Serpinb3b	UTSW	1	107,082,317 (GRCm39)	missense	possibly damaging	0.85
R2252:Serpinb3b	UTSW	1	107,083,208 (GRCm39)	missense	possibly damaging	0.71
R3430:Serpinb3b	UTSW	1	107,082,425 (GRCm39)	missense	probably benign	0.21
R4382:Serpinb3b	UTSW	1	107,083,273 (GRCm39)	missense	probably damaging	0.97
R4741:Serpinb3b	UTSW	1	107,082,200 (GRCm39)	missense	probably benign	0.01
R4855:Serpinb3b	UTSW	1	107,082,270 (GRCm39)	missense	possibly damaging	0.59
R4974:Serpinb3b	UTSW	1	107,082,445 (GRCm39)	missense	probably benign	0.01
R4982:Serpinb3b	UTSW	1	107,085,484 (GRCm39)	missense	probably benign	0.03
R5519:Serpinb3b	UTSW	1	107,087,506 (GRCm39)	start codon destroyed	probably null	1.00
R6846:Serpinb3b	UTSW	1	107,082,403 (GRCm39)	missense	probably benign	0.16
R7815:Serpinb3b	UTSW	1	107,084,625 (GRCm39)	missense	probably damaging	1.00
R7860:Serpinb3b	UTSW	1	107,085,467 (GRCm39)	missense	probably damaging	1.00
R9720:Serpinb3b	UTSW	1	107,083,669 (GRCm39)	missense	probably benign
R9746:Serpinb3b	UTSW	1	107,082,403 (GRCm39)	missense	possibly damaging	0.88
R9773:Serpinb3b	UTSW	1	107,085,416 (GRCm39)	missense	possibly damaging	0.54
Z1088:Serpinb3b	UTSW	1	107,085,481 (GRCm39)	missense	probably damaging	1.00

Posted On

2014-05-07