Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00899:Bpifb9a'

26823

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Bpifb9a

Ensembl Gene

ENSMUSG00000067998

Gene Name

BPI fold containing family B, member 9A

Synonyms

4833413D08Rik, vomeromodulin

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL00899

Quality Score

Status

Chromosome

Chromosomal Location

154257854-154271245 bp(+) (GRCm38)

Type of Mutation

splice site (6 bp from exon)

DNA Base Change (assembly)

T to C at 154264727 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000086314 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000088924]

AlphaFold

Q80XI7

Predicted Effect

probably null
Transcript: ENSMUST00000088924

SMART Domains

Protein: ENSMUSP00000086314
Gene: ENSMUSG00000067998

Domain	Start	End	E-Value	Type
low complexity region	60	77	N/A	INTRINSIC
low complexity region	122	157	N/A	INTRINSIC
low complexity region	167	181	N/A	INTRINSIC
low complexity region	184	203	N/A	INTRINSIC
Pfam:LBP_BPI_CETP	216	377	1.1e-11	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000126084

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000147299

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 36 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
AU018091	A	G	7: 3,158,763	I442T	probably benign	Het
Ccp110	T	A	7: 118,722,684	C521S	probably benign	Het
Chd6	A	G	2: 161,029,298		probably benign	Het
Cndp2	A	T	18: 84,677,376	D133E	probably damaging	Het
Crygs	T	C	16: 22,806,562	E43G	possibly damaging	Het
Ednra	C	T	8: 77,675,071	G197R	probably damaging	Het
Esyt1	A	G	10: 128,517,063	L656P	probably damaging	Het
Ets1	C	T	9: 32,752,808	P118L	probably damaging	Het
Fam98c	A	G	7: 29,152,853		probably benign	Het
Foxi1	G	A	11: 34,205,772	T286I	probably benign	Het
Gimap5	G	A	6: 48,753,173	A226T	possibly damaging	Het
Heatr1	C	T	13: 12,435,176	A2017V	probably benign	Het
Ikbkb	T	C	8: 22,660,447	S740G	possibly damaging	Het
Inppl1	A	T	7: 101,829,158	I617N	probably damaging	Het
Itpkb	T	C	1: 180,332,993	L228P	probably benign	Het
Kcnc4	T	A	3: 107,458,463	D143V	possibly damaging	Het
Krtdap	T	A	7: 30,789,962		probably null	Het
Lilra6	T	A	7: 3,913,057	T268S	probably damaging	Het
M6pr	A	G	6: 122,315,395	E183G	possibly damaging	Het
Muc5ac	T	A	7: 141,812,703	V2168D	possibly damaging	Het
Nbea	A	G	3: 55,642,845	S2721P	probably benign	Het
Olfr352	A	T	2: 36,870,210	I215L	probably benign	Het
Pqbp1	T	C	X: 7,896,004	N94S	probably benign	Het
Prl3d2	T	C	13: 27,122,349	S20P	probably damaging	Het
Psmb2	T	C	4: 126,707,557	I151T	probably benign	Het
Rapgef6	G	T	11: 54,620,018	E107*	probably null	Het
Slc2a13	T	C	15: 91,497,399	T296A	probably benign	Het
Tcl1b4	A	G	12: 105,204,657	T55A	probably damaging	Het
Tg	T	C	15: 66,674,073		probably null	Het
Trim80	T	G	11: 115,447,665	N440K	probably benign	Het
Ttc13	C	T	8: 124,688,847		probably benign	Het
Ttc38	T	A	15: 85,844,462	I205N	possibly damaging	Het
Ufl1	T	C	4: 25,262,238	D336G	probably damaging	Het
Vmn2r74	A	T	7: 85,957,130	I336K	probably benign	Het
Zbtb26	G	T	2: 37,436,258	Y255*	probably null	Het
Zfp462	T	A	4: 55,007,732	V57E	probably damaging	Het

Other mutations in Bpifb9a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00833:Bpifb9a	APN	2	154264275	nonsense	probably null
IGL01998:Bpifb9a	APN	2	154268200	critical splice donor site	probably null
IGL02158:Bpifb9a	APN	2	154266813	splice site	probably benign
IGL02331:Bpifb9a	APN	2	154262387	missense	possibly damaging	0.45
R0066:Bpifb9a	UTSW	2	154266841	missense	possibly damaging	0.95
R0480:Bpifb9a	UTSW	2	154264688	missense	probably benign	0.33
R0545:Bpifb9a	UTSW	2	154261950	nonsense	probably null
R0904:Bpifb9a	UTSW	2	154264225	splice site	probably benign
R1028:Bpifb9a	UTSW	2	154262407	missense	possibly damaging	0.45
R1158:Bpifb9a	UTSW	2	154262264	missense	probably benign	0.08
R1465:Bpifb9a	UTSW	2	154271021	missense	possibly damaging	0.85
R1465:Bpifb9a	UTSW	2	154271021	missense	possibly damaging	0.85
R1902:Bpifb9a	UTSW	2	154261991	missense	probably benign	0.00
R2015:Bpifb9a	UTSW	2	154268200	critical splice donor site	probably null
R2152:Bpifb9a	UTSW	2	154260135	missense	probably benign	0.28
R2206:Bpifb9a	UTSW	2	154264241	splice site	probably null
R5410:Bpifb9a	UTSW	2	154270235	missense	probably benign	0.05
R5731:Bpifb9a	UTSW	2	154262243	missense	possibly damaging	0.87
R5818:Bpifb9a	UTSW	2	154262295	missense	probably damaging	0.98
R5865:Bpifb9a	UTSW	2	154266836	missense	probably benign	0.26
R6564:Bpifb9a	UTSW	2	154260178	missense	probably benign	0.00
R7291:Bpifb9a	UTSW	2	154267696	missense	probably damaging	1.00
R7294:Bpifb9a	UTSW	2	154267696	missense	probably damaging	1.00
R7295:Bpifb9a	UTSW	2	154267696	missense	probably damaging	1.00
R7453:Bpifb9a	UTSW	2	154264695	missense	probably damaging	0.99
R7570:Bpifb9a	UTSW	2	154262263	missense	possibly damaging	0.46
R8187:Bpifb9a	UTSW	2	154269457	missense	probably benign	0.00
R8245:Bpifb9a	UTSW	2	154262726	missense	probably benign	0.00
R8459:Bpifb9a	UTSW	2	154260233	missense	probably damaging	0.98
R8481:Bpifb9a	UTSW	2	154269479	missense	probably benign

Posted On

2013-04-17