Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02609:Vpreb1b'

300430

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Vpreb1b

Ensembl Gene

ENSMUSG00000059280

Gene Name

V-set pre-B cell surrogate light chain 1B

Synonyms

Vpreb-2, Vpreb2

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.120) question?

Stock #

IGL02609

Quality Score

Status

Chromosome

Chromosomal Location

17798292-17799137 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to C at 17798558 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000074835 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000075371]

AlphaFold

P13373

Predicted Effect

probably benign
Transcript: ENSMUST00000075371

SMART Domains

Protein: ENSMUSP00000074835
Gene: ENSMUSG00000059280

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
IGv	36	117	1.31e-25	SMART

Coding Region Coverage

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for null mutations at both Vpreb1 and Vpreb2 show impaired B-cell development. Fewer small pre-BII and immature B- cells are in bone marrow and numbers of B-cells in spleen and peritoneum are reduced. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 43 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A930011G23Rik	A	G	5: 99,381,854 (GRCm39)		probably benign	Het
Aadacl4fm5	T	A	4: 144,506,307 (GRCm39)	D128V	probably damaging	Het
Adcy10	T	G	1: 165,366,044 (GRCm39)	Y520*	probably null	Het
Agrn	A	T	4: 156,259,680 (GRCm39)		probably benign	Het
AI661453	A	T	17: 47,779,297 (GRCm39)		probably benign	Het
Arhgap6	A	G	X: 167,961,062 (GRCm39)		probably benign	Het
Asxl2	T	C	12: 3,550,018 (GRCm39)	S587P	probably damaging	Het
B3gntl1	A	G	11: 121,535,427 (GRCm39)		probably benign	Het
Bahcc1	T	C	11: 120,180,224 (GRCm39)	F2527L	possibly damaging	Het
Baz2b	T	A	2: 59,747,713 (GRCm39)	M1317L	possibly damaging	Het
Bcas3	A	T	11: 85,348,720 (GRCm39)	K204I	probably damaging	Het
Bpnt2	T	A	4: 4,767,763 (GRCm39)	R338*	probably null	Het
C1qtnf1	T	C	11: 118,338,830 (GRCm39)	F167L	probably damaging	Het
Cfap58	C	T	19: 47,963,941 (GRCm39)	T523M	possibly damaging	Het
Ddb1	T	A	19: 10,599,830 (GRCm39)	C680S	possibly damaging	Het
Eef1d	T	C	15: 75,768,162 (GRCm39)	Q200R	probably null	Het
Gm10717	A	T	9: 3,026,287 (GRCm39)	Y195F	probably damaging	Het
Gm28557	T	A	13: 67,219,083 (GRCm39)	K214*	probably null	Het
Gm8229	A	C	14: 44,604,082 (GRCm39)	E90D	probably benign	Het
Hhla1	T	C	15: 65,802,463 (GRCm39)		probably benign	Het
Hivep1	C	T	13: 42,309,130 (GRCm39)	H457Y	probably damaging	Het
Htr2c	T	C	X: 145,976,756 (GRCm39)		probably benign	Het
Ifi44	A	T	3: 151,438,134 (GRCm39)	S384R	probably damaging	Het
Kirrel2	T	C	7: 30,147,765 (GRCm39)	T628A	probably benign	Het
Kmt2d	T	C	15: 98,749,674 (GRCm39)		probably benign	Het
Larp4b	T	A	13: 9,220,716 (GRCm39)	I655N	probably damaging	Het
Lrrd1	G	A	5: 3,908,803 (GRCm39)	V692I	probably benign	Het
Lypd8l	A	T	11: 58,503,442 (GRCm39)	C29S	probably damaging	Het
Nes	T	C	3: 87,884,528 (GRCm39)	I929T	probably benign	Het
Ogfr	T	C	2: 180,234,308 (GRCm39)		probably benign	Het
Pwwp3a	A	T	10: 80,065,917 (GRCm39)	E57V	probably damaging	Het
Rfx2	G	T	17: 57,112,404 (GRCm39)	P43Q	probably benign	Het
Rnf123	G	A	9: 107,945,501 (GRCm39)	R390*	probably null	Het
Sh3tc1	T	C	5: 35,864,516 (GRCm39)	K495R	probably damaging	Het
Slit1	A	T	19: 41,590,743 (GRCm39)	C1310S	probably damaging	Het
Srrm1	G	A	4: 135,052,415 (GRCm39)	P658L	unknown	Het
Stk35	T	C	2: 129,643,721 (GRCm39)	V235A	probably damaging	Het
Syde2	T	G	3: 145,704,275 (GRCm39)	V142G	probably benign	Het
Tgfb3	A	G	12: 86,124,613 (GRCm39)	F32L	probably benign	Het
Tmem35a	T	C	X: 133,205,446 (GRCm39)	F121L	probably damaging	Het
Trp53bp2	T	A	1: 182,281,289 (GRCm39)	D963E	probably benign	Het
Vmn1r26	A	G	6: 57,985,860 (GRCm39)	S110P	probably damaging	Het
Xrn2	A	T	2: 146,891,945 (GRCm39)	T721S	probably benign	Het

Other mutations in Vpreb1b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0045:Vpreb1b	UTSW	16	17,798,631 (GRCm39)	missense	probably damaging	1.00
R2157:Vpreb1b	UTSW	16	17,798,934 (GRCm39)	nonsense	probably null
R6395:Vpreb1b	UTSW	16	17,798,771 (GRCm39)	missense	probably damaging	0.99
R6890:Vpreb1b	UTSW	16	17,798,820 (GRCm39)	missense	probably damaging	1.00
R6996:Vpreb1b	UTSW	16	17,798,441 (GRCm39)	missense	probably benign
R8437:Vpreb1b	UTSW	16	17,798,753 (GRCm39)	missense	probably damaging	1.00
R9227:Vpreb1b	UTSW	16	17,798,801 (GRCm39)	missense	probably damaging	0.99
R9473:Vpreb1b	UTSW	16	17,798,565 (GRCm39)	missense	probably benign	0.01

Posted On

2015-04-16