Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03288:Stxbp5'

415814

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Stxbp5

Ensembl Gene

ENSMUSG00000019790

Gene Name

syntaxin binding protein 5 (tomosyn)

Synonyms

LGL3, tomosyn 1, 0710001E20Rik, 4930565N16Rik

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

IGL03288

Quality Score

Status

Chromosome

Chromosomal Location

9631291-9776823 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to T at 9742447 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000123253 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000038213] [ENSMUST00000125200] [ENSMUST00000141722]

AlphaFold

Q8K400

Predicted Effect

probably null
Transcript: ENSMUST00000038213

SMART Domains

Protein: ENSMUSP00000044535
Gene: ENSMUSG00000019790

Domain	Start	End	E-Value	Type
low complexity region	17	28	N/A	INTRINSIC
WD40	46	86	2.21e1	SMART
WD40	88	127	5.94e0	SMART
WD40	132	171	1.97e2	SMART
WD40	185	225	1.99e0	SMART
WD40	228	266	5.69e-4	SMART
Pfam:LLGL	276	385	2e-36	PFAM
WD40	386	465	2.88e-1	SMART
WD40	491	530	3.68e1	SMART
low complexity region	572	591	N/A	INTRINSIC
low complexity region	713	724	N/A	INTRINSIC
Pfam:Lgl_C	771	1050	2.7e-8	PFAM
PDB:1URQ\|A	1086	1145	2e-33	PDB

Predicted Effect

probably null
Transcript: ENSMUST00000125200

SMART Domains

Protein: ENSMUSP00000121507
Gene: ENSMUSG00000019790

Domain	Start	End	E-Value	Type
low complexity region	17	28	N/A	INTRINSIC
WD40	46	86	2.21e1	SMART
WD40	88	127	5.94e0	SMART
WD40	132	171	1.97e2	SMART
WD40	185	225	1.99e0	SMART
WD40	228	266	5.69e-4	SMART
Pfam:LLGL	273	385	1.6e-46	PFAM
WD40	386	465	2.88e-1	SMART
WD40	491	530	3.68e1	SMART
low complexity region	572	591	N/A	INTRINSIC
low complexity region	722	730	N/A	INTRINSIC
Pfam:Lgl_C	839	994	1.9e-8	PFAM
PDB:1URQ\|A	1033	1092	2e-33	PDB

Predicted Effect

probably null
Transcript: ENSMUST00000141722

SMART Domains

Protein: ENSMUSP00000123253
Gene: ENSMUSG00000019790

Domain	Start	End	E-Value	Type
low complexity region	17	28	N/A	INTRINSIC
WD40	46	86	2.21e1	SMART
WD40	88	127	5.94e0	SMART
WD40	132	171	1.97e2	SMART
WD40	185	225	1.99e0	SMART
WD40	228	266	5.69e-4	SMART
Pfam:LLGL	273	385	1.7e-46	PFAM
WD40	386	465	2.88e-1	SMART
WD40	491	530	3.68e1	SMART
low complexity region	572	591	N/A	INTRINSIC
low complexity region	739	747	N/A	INTRINSIC
Pfam:Lgl_C	856	1011	2e-8	PFAM
PDB:1URQ\|A	1050	1109	2e-33	PDB

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Syntaxin 1 is a component of the 7S and 20S SNARE complexes which are involved in docking and fusion of synaptic vesicles with the presynaptic plasma membrane. This gene encodes a syntaxin 1 binding protein. In rat, a similar protein dissociates syntaxin 1 from the Munc18/n-Sec1/rbSec1 complex to form a 10S complex, an intermediate which can be converted to the 7S SNARE complex. Thus this protein is thought to be involved in neurotransmitter release by stimulating SNARE complex formation. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a null allele exhibit some background sensitive prenatal lethality and increased synaptic transmission. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 42 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Arap2	T	C	5: 62,761,959 (GRCm39)	K1589R	probably benign	Het
Armc3	T	C	2: 19,240,293 (GRCm39)	F17L	probably damaging	Het
Ccdc17	T	A	4: 116,456,626 (GRCm39)	L465H	probably damaging	Het
Cdh9	A	T	15: 16,856,135 (GRCm39)	D725V	probably damaging	Het
Cert1	T	A	13: 96,770,700 (GRCm39)	D536E	probably benign	Het
Chl1	C	T	6: 103,652,058 (GRCm39)	R309C	probably damaging	Het
Dbt	T	A	3: 116,341,847 (GRCm39)	*483K	probably null	Het
Ddx46	A	G	13: 55,785,907 (GRCm39)	D29G	unknown	Het
Des	T	C	1: 75,338,985 (GRCm39)	I222T	possibly damaging	Het
Dnah8	A	G	17: 30,891,323 (GRCm39)	N776S	probably benign	Het
Fbn1	A	T	2: 125,145,103 (GRCm39)	L2712Q	probably benign	Het
Glb1l3	A	C	9: 26,729,601 (GRCm39)	V622G	probably damaging	Het
Grin2a	T	C	16: 9,487,704 (GRCm39)	D398G	possibly damaging	Het
Itgb3	T	C	11: 104,524,293 (GRCm39)	M143T	probably damaging	Het
Lama2	G	A	10: 27,245,047 (GRCm39)	R245C	probably damaging	Het
Lgals9	G	A	11: 78,875,626 (GRCm39)	A6V	probably benign	Het
Lman2l	A	T	1: 36,482,628 (GRCm39)	Y83N	probably damaging	Het
Lrp2	T	A	2: 69,256,383 (GRCm39)	T4586S	probably benign	Het
Med10	T	C	13: 69,963,816 (GRCm39)		probably benign	Het
Myo18b	A	C	5: 112,937,863 (GRCm39)	L1754R	probably damaging	Het
Myom2	T	C	8: 15,172,679 (GRCm39)	L1202S	probably damaging	Het
Nav3	T	C	10: 109,594,878 (GRCm39)	E1441G	probably damaging	Het
Nme8	T	C	13: 19,880,776 (GRCm39)	E60G	possibly damaging	Het
Npffr2	G	T	5: 89,731,020 (GRCm39)	A317S	probably damaging	Het
Nrxn2	A	G	19: 6,540,726 (GRCm39)	D893G	probably damaging	Het
Nup153	T	C	13: 46,858,681 (GRCm39)	E410G	possibly damaging	Het
Or11h7	T	C	14: 50,890,832 (GRCm39)	I46T	possibly damaging	Het
Or7e178	A	G	9: 20,247,207 (GRCm39)		probably null	Het
Pcdhb10	A	G	18: 37,546,358 (GRCm39)	D478G	probably damaging	Het
Phf13	T	C	4: 152,076,826 (GRCm39)	D122G	possibly damaging	Het
Pkhd1	A	T	1: 20,271,243 (GRCm39)	H3103Q	probably benign	Het
Prr11	A	C	11: 86,987,787 (GRCm39)		probably null	Het
Rac3	C	T	11: 120,614,092 (GRCm39)	T118M	possibly damaging	Het
Rad54b	T	C	4: 11,569,833 (GRCm39)	S50P	possibly damaging	Het
Rp1	T	C	1: 4,419,747 (GRCm39)	Q455R	possibly damaging	Het
Semp2l1	T	A	1: 32,584,841 (GRCm39)	E356D	probably benign	Het
Sorl1	T	C	9: 41,944,858 (GRCm39)		probably benign	Het
Spink5	A	T	18: 44,147,827 (GRCm39)	I858F	possibly damaging	Het
Svep1	A	C	4: 58,116,532 (GRCm39)	V906G	probably benign	Het
Tlr4	A	G	4: 66,757,990 (GRCm39)	E261G	probably damaging	Het
Zfp704	C	T	3: 9,504,951 (GRCm39)		probably benign	Het
Zfyve9	A	T	4: 108,580,996 (GRCm39)		probably benign	Het

Other mutations in Stxbp5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00466:Stxbp5	APN	10	9,675,694 (GRCm39)	missense	probably damaging	1.00
IGL00950:Stxbp5	APN	10	9,684,346 (GRCm39)	splice site	probably benign
IGL01725:Stxbp5	APN	10	9,693,155 (GRCm39)	missense	probably damaging	1.00
IGL02150:Stxbp5	APN	10	9,638,565 (GRCm39)	missense	probably damaging	1.00
IGL02339:Stxbp5	APN	10	9,692,041 (GRCm39)	missense	possibly damaging	0.89
IGL02697:Stxbp5	APN	10	9,638,700 (GRCm39)	nonsense	probably null
IGL02720:Stxbp5	APN	10	9,665,105 (GRCm39)	critical splice donor site	probably null
IGL03155:Stxbp5	APN	10	9,692,034 (GRCm39)	missense	probably null	1.00
Fatty_fish	UTSW	10	9,646,295 (GRCm39)	missense	probably damaging	1.00
reindeer	UTSW	10	9,713,836 (GRCm39)	missense	probably damaging	1.00
H8562:Stxbp5	UTSW	10	9,645,187 (GRCm39)	missense	probably benign	0.36
PIT4544001:Stxbp5	UTSW	10	9,693,048 (GRCm39)	critical splice donor site	probably null
R0025:Stxbp5	UTSW	10	9,638,492 (GRCm39)	missense	probably damaging	1.00
R0025:Stxbp5	UTSW	10	9,638,492 (GRCm39)	missense	probably damaging	1.00
R0219:Stxbp5	UTSW	10	9,646,272 (GRCm39)	missense	probably benign	0.36
R0226:Stxbp5	UTSW	10	9,742,442 (GRCm39)	splice site	probably benign
R0631:Stxbp5	UTSW	10	9,660,102 (GRCm39)	missense	probably benign
R0723:Stxbp5	UTSW	10	9,644,617 (GRCm39)	missense	probably damaging	1.00
R0833:Stxbp5	UTSW	10	9,740,843 (GRCm39)	missense	probably damaging	1.00
R0836:Stxbp5	UTSW	10	9,740,843 (GRCm39)	missense	probably damaging	1.00
R0863:Stxbp5	UTSW	10	9,684,784 (GRCm39)	missense	possibly damaging	0.86
R1225:Stxbp5	UTSW	10	9,688,135 (GRCm39)	missense	possibly damaging	0.94
R1271:Stxbp5	UTSW	10	9,692,013 (GRCm39)	missense	probably damaging	1.00
R1536:Stxbp5	UTSW	10	9,713,836 (GRCm39)	missense	probably damaging	1.00
R1852:Stxbp5	UTSW	10	9,688,042 (GRCm39)	missense	possibly damaging	0.94
R1884:Stxbp5	UTSW	10	9,688,042 (GRCm39)	missense	possibly damaging	0.94
R1902:Stxbp5	UTSW	10	9,688,042 (GRCm39)	missense	possibly damaging	0.94
R1917:Stxbp5	UTSW	10	9,688,042 (GRCm39)	missense	possibly damaging	0.94
R1918:Stxbp5	UTSW	10	9,688,042 (GRCm39)	missense	possibly damaging	0.94
R2174:Stxbp5	UTSW	10	9,711,590 (GRCm39)	missense	possibly damaging	0.69
R3773:Stxbp5	UTSW	10	9,644,671 (GRCm39)	missense	probably damaging	1.00
R3901:Stxbp5	UTSW	10	9,645,163 (GRCm39)	missense	probably damaging	1.00
R3981:Stxbp5	UTSW	10	9,665,060 (GRCm39)	intron	probably benign
R4572:Stxbp5	UTSW	10	9,713,888 (GRCm39)	missense	probably damaging	0.99
R4764:Stxbp5	UTSW	10	9,646,367 (GRCm39)	missense	probably damaging	1.00
R4841:Stxbp5	UTSW	10	9,638,635 (GRCm39)	missense	probably benign	0.06
R4842:Stxbp5	UTSW	10	9,638,635 (GRCm39)	missense	probably benign	0.06
R4884:Stxbp5	UTSW	10	9,688,085 (GRCm39)	nonsense	probably null
R4887:Stxbp5	UTSW	10	9,684,844 (GRCm39)	missense	probably benign
R4930:Stxbp5	UTSW	10	9,636,610 (GRCm39)	utr 3 prime	probably benign
R5065:Stxbp5	UTSW	10	9,646,295 (GRCm39)	missense	probably damaging	1.00
R5285:Stxbp5	UTSW	10	9,674,019 (GRCm39)	critical splice acceptor site	probably null
R5306:Stxbp5	UTSW	10	9,675,735 (GRCm39)	missense	probably damaging	1.00
R5455:Stxbp5	UTSW	10	9,684,252 (GRCm39)	missense	probably benign
R5531:Stxbp5	UTSW	10	9,638,668 (GRCm39)	nonsense	probably null
R5605:Stxbp5	UTSW	10	9,645,490 (GRCm39)	intron	probably benign
R5614:Stxbp5	UTSW	10	9,636,638 (GRCm39)	utr 3 prime	probably benign
R5805:Stxbp5	UTSW	10	9,776,330 (GRCm39)	missense	probably benign
R5990:Stxbp5	UTSW	10	9,711,677 (GRCm39)	missense	probably damaging	1.00
R6025:Stxbp5	UTSW	10	9,675,772 (GRCm39)	missense	probably benign	0.00
R6056:Stxbp5	UTSW	10	9,646,430 (GRCm39)	missense	probably benign	0.00
R6147:Stxbp5	UTSW	10	9,684,216 (GRCm39)	missense	possibly damaging	0.93
R6194:Stxbp5	UTSW	10	9,693,083 (GRCm39)	missense	probably damaging	0.99
R6284:Stxbp5	UTSW	10	9,642,931 (GRCm39)	missense	probably damaging	1.00
R6284:Stxbp5	UTSW	10	9,642,923 (GRCm39)	missense	probably benign	0.32
R6394:Stxbp5	UTSW	10	9,774,975 (GRCm39)	nonsense	probably null
R6427:Stxbp5	UTSW	10	9,774,998 (GRCm39)	missense	probably damaging	1.00
R6894:Stxbp5	UTSW	10	9,660,105 (GRCm39)	missense	probably benign	0.00
R7229:Stxbp5	UTSW	10	9,673,931 (GRCm39)	missense	probably damaging	1.00
R7337:Stxbp5	UTSW	10	9,684,874 (GRCm39)	missense	possibly damaging	0.93
R7686:Stxbp5	UTSW	10	9,645,154 (GRCm39)	missense	probably damaging	0.99
R7811:Stxbp5	UTSW	10	9,684,248 (GRCm39)	missense	probably benign
R7974:Stxbp5	UTSW	10	9,646,439 (GRCm39)	splice site	probably null
R8009:Stxbp5	UTSW	10	9,692,046 (GRCm39)	missense	probably damaging	1.00
R8287:Stxbp5	UTSW	10	9,660,129 (GRCm39)	missense	probably benign
R8353:Stxbp5	UTSW	10	9,684,792 (GRCm39)	missense	probably benign	0.30
R8360:Stxbp5	UTSW	10	9,688,003 (GRCm39)	critical splice donor site	probably null
R8453:Stxbp5	UTSW	10	9,684,792 (GRCm39)	missense	probably benign	0.30
R8487:Stxbp5	UTSW	10	9,688,033 (GRCm39)	missense	possibly damaging	0.80
R8548:Stxbp5	UTSW	10	9,693,050 (GRCm39)	missense	probably null	0.98
R8805:Stxbp5	UTSW	10	9,713,859 (GRCm39)	nonsense	probably null
R9172:Stxbp5	UTSW	10	9,645,152 (GRCm39)	missense	possibly damaging	0.94
R9472:Stxbp5	UTSW	10	9,719,101 (GRCm39)	missense	probably damaging	1.00
R9513:Stxbp5	UTSW	10	9,687,754 (GRCm39)	missense	probably benign	0.17
R9649:Stxbp5	UTSW	10	9,774,938 (GRCm39)	missense	probably damaging	0.96
X0020:Stxbp5	UTSW	10	9,638,634 (GRCm39)	missense	possibly damaging	0.47
Z1176:Stxbp5	UTSW	10	9,776,289 (GRCm39)	missense	possibly damaging	0.88

Posted On

2016-08-02