Mutagenetix > Incidental Mutations

Incidental Mutation 'IGL00157:Serpinb9b'

1035

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Serpinb9b

Ensembl Gene

ENSMUSG00000021403

Gene Name

serine (or cysteine) peptidase inhibitor, clade B, member 9b

Synonyms

1600019A21Rik, Spi10, ovalbumin, SPI-CI, R86

Accession Numbers

Is this an essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL00157

Quality Score

Status

Chromosome

Chromosomal Location

33027416-33041884 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 33035625 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Aspartic acid at position 178 (E178D)

Ref Sequence

ENSEMBL: ENSMUSP00000006392 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000006392]

AlphaFold

Q9DAV6

Predicted Effect

probably benign
Transcript: ENSMUST00000006392
AA Change: E178D

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000006392
Gene: ENSMUSG00000021403
AA Change: E178D

Domain	Start	End	E-Value	Type
SERPIN	13	377	7.86e-164	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000220566

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000221946

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 32 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acp4	A	G	7: 44,253,451	V331A	possibly damaging	Het
Casr	C	A	16: 36,495,810	V633F	probably damaging	Het
Cblb	T	G	16: 52,183,307	V716G	probably benign	Het
Cbln2	C	T	18: 86,716,384	Q156*	probably null	Het
Cnn1	G	T	9: 22,099,397	L14F	possibly damaging	Het
D830013O20Rik	T	C	12: 73,364,247		noncoding transcript	Het
Drd1	A	G	13: 54,053,878	S99P	probably damaging	Het
Fam35a	A	G	14: 34,268,625	V108A	probably benign	Het
Fat1	T	C	8: 44,951,670	V486A	possibly damaging	Het
Galnt7	T	C	8: 57,540,039	N416S	probably damaging	Het
Gm10735	T	C	13: 113,041,484		probably benign	Het
Gm8909	A	T	17: 36,165,354		probably null	Het
Jag2	T	C	12: 112,912,718	T790A	probably benign	Het
Klhdc1	T	A	12: 69,242,008	Y31N	possibly damaging	Het
Lama1	A	T	17: 67,815,928	M2769L	probably benign	Het
Mms19	A	G	19: 41,945,457		probably null	Het
Msrb2	C	A	2: 19,394,341	P172T	probably damaging	Het
Olfr228	T	C	2: 86,483,218	S175G	probably benign	Het
Olfr955	A	G	9: 39,470,243	V161A	probably benign	Het
Pcdhb9	T	A	18: 37,403,279	D775E	possibly damaging	Het
Pkhd1	T	C	1: 20,566,874		probably null	Het
Preb	A	T	5: 30,955,964	D375E	probably damaging	Het
Prkdc	T	C	16: 15,697,226	I1010T	probably damaging	Het
Rbp2	A	G	9: 98,498,897		probably null	Het
Sept9	A	G	11: 117,352,184	T66A	probably damaging	Het
Tg	A	G	15: 66,847,166	Y258C	probably damaging	Het
Tmprss7	T	C	16: 45,663,368	R548G	probably benign	Het
Uba7	G	A	9: 107,979,111	A536T	probably benign	Het
Vmn2r114	G	A	17: 23,291,665	P614S	probably damaging	Het
Xpc	A	G	6: 91,492,264		probably benign	Het
Yrdc	T	C	4: 124,853,961	S86P	probably damaging	Het
Zbed6	G	T	1: 133,657,376	A741D	probably damaging	Het

Other mutations in Serpinb9b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00518:Serpinb9b	APN	13	33039570	missense	probably benign	0.17
IGL01939:Serpinb9b	APN	13	33039665	missense	probably damaging	0.99
IGL02472:Serpinb9b	APN	13	33039970	utr 3 prime	probably benign
IGL02632:Serpinb9b	APN	13	33039823	missense	probably benign	0.01
R0255:Serpinb9b	UTSW	13	33038020	missense	probably benign
R0667:Serpinb9b	UTSW	13	33032926	nonsense	probably null
R0699:Serpinb9b	UTSW	13	33033566	missense	probably benign	0.00
R0703:Serpinb9b	UTSW	13	33032981	missense	probably benign	0.29
R1605:Serpinb9b	UTSW	13	33038129	critical splice donor site	probably null
R1623:Serpinb9b	UTSW	13	33029565	missense	possibly damaging	0.61
R1815:Serpinb9b	UTSW	13	33039904	missense	probably damaging	1.00
R1920:Serpinb9b	UTSW	13	33039548	critical splice acceptor site	probably null
R1987:Serpinb9b	UTSW	13	33029559	missense	probably benign	0.07
R1988:Serpinb9b	UTSW	13	33029559	missense	probably benign	0.07
R3035:Serpinb9b	UTSW	13	33029546	missense	possibly damaging	0.81
R3683:Serpinb9b	UTSW	13	33029598	missense	probably damaging	0.98
R3758:Serpinb9b	UTSW	13	33035588	missense	probably damaging	1.00
R4677:Serpinb9b	UTSW	13	33039823	missense	probably damaging	0.97
R5412:Serpinb9b	UTSW	13	33029513	missense	probably benign	0.00
R5481:Serpinb9b	UTSW	13	33038093	missense	possibly damaging	0.93
R5672:Serpinb9b	UTSW	13	33039599	missense	probably benign	0.01
R5957:Serpinb9b	UTSW	13	33039848	missense	possibly damaging	0.81
R6797:Serpinb9b	UTSW	13	33029484	missense	possibly damaging	0.60
R7586:Serpinb9b	UTSW	13	33039760	missense	probably damaging	1.00
R8115:Serpinb9b	UTSW	13	33035548	missense	probably null	0.94
R8309:Serpinb9b	UTSW	13	33039571	missense	probably damaging	1.00
R8529:Serpinb9b	UTSW	13	33039560	missense	probably benign	0.04
R8802:Serpinb9b	UTSW	13	33029604	missense	probably benign
R8810:Serpinb9b	UTSW	13	33029469	missense	possibly damaging	0.83
R9020:Serpinb9b	UTSW	13	33039904	missense	probably damaging	1.00
R9310:Serpinb9b	UTSW	13	33035540	missense	probably benign
R9424:Serpinb9b	UTSW	13	33029561	missense	probably damaging	0.99
X0019:Serpinb9b	UTSW	13	33035531	nonsense	probably null

Posted On

2011-07-12