Mutagenetix > Incidental Mutation

Incidental Mutation 'R7223:Gp2'

561941

Institutional Source

Beutler Lab

Gene Symbol

Gp2

Ensembl Gene

ENSMUSG00000030954

Gene Name

glycoprotein 2 zymogen granule membrane

Synonyms

2310037I18Rik

MMRRC Submission

045295-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7223 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

119041760-119058495 bp(-) (GRCm39)

Type of Mutation

critical splice donor site (2 bp from exon)

DNA Base Change (assembly)

A to G at 119050721 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000146487 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000033255] [ENSMUST00000207887]

AlphaFold

Q9D733

Predicted Effect

probably null
Transcript: ENSMUST00000033255

SMART Domains

Protein: ENSMUSP00000033255
Gene: ENSMUSG00000030954

Domain	Start	End	E-Value	Type
signal peptide	1	24	N/A	INTRINSIC
Blast:ZP	164	213	1e-11	BLAST
ZP	225	477	5.39e-79	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000207887

Meta Mutation Damage Score

0.9493

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an integral membrane protein that is secreted from intracellular zymogen granules and associates with the plasma membrane via glycosylphosphatidylinositol (GPI) linkage. The encoded protein binds pathogens such as enterobacteria, thereby playing an important role in the innate immune response. The C-terminus of this protein is related to the C-terminus of the protein encoded by the neighboring gene, uromodulin (UMOD). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]
PHENOTYPE: Homozygous null mice display no obvious abnormalities in pancreas morphology and function, development, growth, weight, behavior, life span, or fertility. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb11	A	T	2: 69,104,487 (GRCm39)	V733E	probably benign	Het
Adam34	A	T	8: 44,105,041 (GRCm39)	N201K	probably benign	Het
Aldh3b2	A	C	19: 4,029,592 (GRCm39)	S322R	probably damaging	Het
Anpep	A	T	7: 79,475,058 (GRCm39)	L914Q	probably damaging	Het
Arhgap30	T	C	1: 171,235,139 (GRCm39)	F535S	probably damaging	Het
Baiap3	G	A	17: 25,462,814 (GRCm39)	R1075C	probably benign	Het
Baz2a	G	T	10: 127,948,475 (GRCm39)	G252V	probably damaging	Het
Brinp3	T	A	1: 146,776,812 (GRCm39)	S420T	possibly damaging	Het
Carmil3	T	C	14: 55,733,695 (GRCm39)	F359S	possibly damaging	Het
Ccdc124	A	T	8: 71,321,170 (GRCm39)	L190Q	probably damaging	Het
Ccr6	T	C	17: 8,474,972 (GRCm39)	V59A	probably damaging	Het
Ccr8	T	A	9: 119,923,683 (GRCm39)	I266N	probably damaging	Het
Cdh23	T	A	10: 60,167,596 (GRCm39)	E1798V	probably damaging	Het
Cdk5rap2	T	C	4: 70,153,684 (GRCm39)	N1713S	probably benign	Het
Cep19	T	A	16: 31,922,833 (GRCm39)	I33N	probably damaging	Het
Cers3	A	T	7: 66,433,163 (GRCm39)	Y196F	probably damaging	Het
Cidea	T	C	18: 67,499,491 (GRCm39)	I126T	probably damaging	Het
Copg2	A	T	6: 30,789,689 (GRCm39)	Y546*	probably null	Het
Cul3	A	T	1: 80,264,717 (GRCm39)	V261E	probably benign	Het
Cyp2g1	A	T	7: 26,514,057 (GRCm39)	D221V	probably damaging	Het
Cyp8b1	G	A	9: 121,744,163 (GRCm39)	H390Y	probably damaging	Het
Daam1	T	C	12: 72,035,717 (GRCm39)	F971L	probably damaging	Het
Dnajc24	G	A	2: 105,832,311 (GRCm39)	S24L	possibly damaging	Het
Dpysl3	T	C	18: 43,571,107 (GRCm39)	S56G	probably benign	Het
Esp1	A	G	17: 41,041,972 (GRCm39)	D88G	probably benign	Het
Fam171b	A	G	2: 83,708,574 (GRCm39)	T359A	probably damaging	Het
Fam186b	T	C	15: 99,177,718 (GRCm39)	E536G	possibly damaging	Het
Fbxo3	T	C	2: 103,873,357 (GRCm39)	V156A	possibly damaging	Het
Gls2	C	A	10: 128,035,063 (GRCm39)	H65Q	probably benign	Het
Gpcpd1	T	A	2: 132,375,976 (GRCm39)	K435I	probably benign	Het
Gpx6	T	A	13: 21,501,840 (GRCm39)		probably null	Het
Hps3	A	T	3: 20,084,583 (GRCm39)	S202T	probably benign	Het
Htr1d	T	A	4: 136,170,812 (GRCm39)	L347H	probably damaging	Het
Igfals	T	C	17: 25,100,208 (GRCm39)	L433P	probably damaging	Het
Ilvbl	C	T	10: 78,419,530 (GRCm39)	H537Y	probably benign	Het
Iqgap2	A	T	13: 95,765,480 (GRCm39)	M1530K	probably damaging	Het
Jarid2	A	G	13: 45,049,798 (GRCm39)	T247A	possibly damaging	Het
L3hypdh	C	T	12: 72,120,783 (GRCm39)	V323I	possibly damaging	Het
Lama3	C	T	18: 12,715,665 (GRCm39)	T1707I	possibly damaging	Het
Map6	G	T	7: 98,917,232 (GRCm39)	A2S	probably damaging	Het
Mfap3	T	A	11: 57,421,066 (GRCm39)	I349K	probably benign	Het
Mybl2	A	G	2: 162,914,625 (GRCm39)	T248A	probably benign	Het
N6amt1	A	G	16: 87,159,548 (GRCm39)	*151W	probably null	Het
Nhlrc1	A	G	13: 47,167,684 (GRCm39)	V191A	probably benign	Het
Nkx2-5	T	C	17: 27,058,594 (GRCm39)	E120G	possibly damaging	Het
Or2y10	T	A	11: 49,454,925 (GRCm39)	M59K	probably damaging	Het
Or52r1b	C	A	7: 102,690,839 (GRCm39)	T46N	possibly damaging	Het
Or8b41	T	C	9: 38,055,049 (GRCm39)	V201A	probably benign	Het
Or8k28	T	A	2: 86,286,211 (GRCm39)	I135F	possibly damaging	Het
Pcdha8	T	G	18: 37,126,201 (GRCm39)	L228V	probably benign	Het
Pcsk2	A	G	2: 143,532,253 (GRCm39)	T134A	possibly damaging	Het
Phldb3	G	A	7: 24,324,078 (GRCm39)	R484Q	probably benign	Het
Pipox	A	G	11: 77,772,012 (GRCm39)	S371P	probably damaging	Het
Plekhg1	T	C	10: 3,823,343 (GRCm39)	S159P		Het
Psme4	C	T	11: 30,824,226 (GRCm39)	P1737S	probably benign	Het
Pygm	G	A	19: 6,438,893 (GRCm39)	D328N	probably benign	Het
Rabgef1	A	T	5: 130,219,801 (GRCm39)	E88V	probably benign	Het
Rims2	G	T	15: 39,300,428 (GRCm39)	R245L	probably benign	Het
Slc38a4	T	C	15: 96,908,226 (GRCm39)	I172V	probably damaging	Het
Slc4a10	T	A	2: 62,099,009 (GRCm39)	Y586N	probably damaging	Het
Snap91	C	T	9: 86,761,610 (GRCm39)		probably benign	Het
Sorcs1	C	T	19: 50,178,480 (GRCm39)	V881I	probably benign	Het
Spef2	A	T	15: 9,601,726 (GRCm39)	V1512E	unknown	Het
Sufu	T	C	19: 46,441,716 (GRCm39)	I292T	possibly damaging	Het
Tet1	T	C	10: 62,649,450 (GRCm39)	N87D	possibly damaging	Het
Tmem108	T	C	9: 103,376,733 (GRCm39)	T239A	not run	Het
Tmem121	A	T	12: 113,152,114 (GRCm39)	K111*	probably null	Het
Tpp2	T	A	1: 44,008,048 (GRCm39)	D417E	probably damaging	Het
Tpr	G	A	1: 150,315,007 (GRCm39)	E2025K	possibly damaging	Het
Trappc3	C	T	4: 126,168,945 (GRCm39)	A145V	possibly damaging	Het
Ttn	T	C	2: 76,721,325 (GRCm39)	D6754G	probably null	Het
Unc13c	T	A	9: 73,536,473 (GRCm39)	M1627L	probably benign	Het
Ush2a	A	G	1: 188,542,414 (GRCm39)	I3327V	probably benign	Het
Vmn1r74	C	T	7: 11,580,894 (GRCm39)	Q65*	probably null	Het
Wdr18	G	A	10: 79,796,202 (GRCm39)	R69H	probably damaging	Het
Zbed5	G	T	5: 129,929,279 (GRCm39)	D132Y	probably damaging	Het
Zfp644	A	T	5: 106,785,448 (GRCm39)	Y366*	probably null	Het
Zfyve26	T	C	12: 79,292,945 (GRCm39)	N2068S	probably damaging	Het
Zic2	T	C	14: 122,713,503 (GRCm39)	F139S	probably damaging	Het
Zmynd11	T	C	13: 9,760,198 (GRCm39)	Q141R	probably benign	Het
Zrsr2-ps1	A	G	11: 22,923,388 (GRCm39)	E54G	probably benign	Het
Zscan10	G	A	17: 23,828,456 (GRCm39)	D333N	probably benign	Het

Other mutations in Gp2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00338:Gp2	APN	7	119,053,613 (GRCm39)	missense	probably damaging	0.96
IGL00818:Gp2	APN	7	119,049,350 (GRCm39)	missense	possibly damaging	0.82
IGL01830:Gp2	APN	7	119,050,765 (GRCm39)	missense	probably damaging	1.00
IGL02088:Gp2	APN	7	119,053,692 (GRCm39)	missense	probably damaging	1.00
IGL02284:Gp2	APN	7	119,049,406 (GRCm39)	missense	probably damaging	1.00
IGL02812:Gp2	APN	7	119,051,452 (GRCm39)	missense	probably benign	0.01
IGL03049:Gp2	APN	7	119,049,517 (GRCm39)	missense	possibly damaging	0.82
IGL03368:Gp2	APN	7	119,052,097 (GRCm39)	missense	probably damaging	1.00
IGL03369:Gp2	APN	7	119,050,783 (GRCm39)	missense	probably damaging	0.98
PIT4687001:Gp2	UTSW	7	119,050,801 (GRCm39)	missense	possibly damaging	0.48
R0179:Gp2	UTSW	7	119,051,540 (GRCm39)	missense	possibly damaging	0.81
R0367:Gp2	UTSW	7	119,053,791 (GRCm39)	missense	probably damaging	1.00
R0544:Gp2	UTSW	7	119,053,719 (GRCm39)	missense	probably benign	0.00
R0973:Gp2	UTSW	7	119,053,766 (GRCm39)	missense	probably damaging	1.00
R0973:Gp2	UTSW	7	119,053,766 (GRCm39)	missense	probably damaging	1.00
R0974:Gp2	UTSW	7	119,053,766 (GRCm39)	missense	probably damaging	1.00
R1413:Gp2	UTSW	7	119,050,853 (GRCm39)	missense	probably benign	0.15
R1557:Gp2	UTSW	7	119,049,302 (GRCm39)	missense	probably damaging	1.00
R1638:Gp2	UTSW	7	119,050,721 (GRCm39)	critical splice donor site	probably null
R1709:Gp2	UTSW	7	119,050,808 (GRCm39)	missense	probably null	1.00
R1932:Gp2	UTSW	7	119,053,455 (GRCm39)	missense	possibly damaging	0.81
R2109:Gp2	UTSW	7	119,052,155 (GRCm39)	missense	probably benign
R2159:Gp2	UTSW	7	119,051,507 (GRCm39)	missense	probably benign	0.06
R2285:Gp2	UTSW	7	119,049,308 (GRCm39)	missense	possibly damaging	0.82
R4657:Gp2	UTSW	7	119,056,391 (GRCm39)	missense	probably benign	0.38
R4829:Gp2	UTSW	7	119,056,407 (GRCm39)	missense	possibly damaging	0.56
R4854:Gp2	UTSW	7	119,051,422 (GRCm39)	missense	possibly damaging	0.72
R4927:Gp2	UTSW	7	119,052,118 (GRCm39)	missense	probably benign	0.00
R5022:Gp2	UTSW	7	119,048,337 (GRCm39)	missense	probably damaging	1.00
R5033:Gp2	UTSW	7	119,053,514 (GRCm39)	missense	probably damaging	0.99
R5443:Gp2	UTSW	7	119,053,821 (GRCm39)	missense	possibly damaging	0.60
R5444:Gp2	UTSW	7	119,053,821 (GRCm39)	missense	possibly damaging	0.60
R5681:Gp2	UTSW	7	119,051,517 (GRCm39)	missense	possibly damaging	0.92
R5732:Gp2	UTSW	7	119,048,331 (GRCm39)	missense	probably damaging	1.00
R5964:Gp2	UTSW	7	119,048,352 (GRCm39)	missense	probably benign	0.02
R6963:Gp2	UTSW	7	119,052,120 (GRCm39)	missense	probably benign	0.03
R7014:Gp2	UTSW	7	119,050,868 (GRCm39)	missense	probably damaging	1.00
R7087:Gp2	UTSW	7	119,049,455 (GRCm39)	missense	probably damaging	0.99
R7497:Gp2	UTSW	7	119,053,829 (GRCm39)	missense	probably damaging	1.00
R8165:Gp2	UTSW	7	119,049,375 (GRCm39)	missense	probably damaging	1.00
R8343:Gp2	UTSW	7	119,042,010 (GRCm39)	missense	probably benign	0.01
R8344:Gp2	UTSW	7	119,042,010 (GRCm39)	missense	probably benign	0.01
R8345:Gp2	UTSW	7	119,042,010 (GRCm39)	missense	probably benign	0.01
R8431:Gp2	UTSW	7	119,042,010 (GRCm39)	missense	probably benign	0.01
R8432:Gp2	UTSW	7	119,042,010 (GRCm39)	missense	probably benign	0.01
R8463:Gp2	UTSW	7	119,053,554 (GRCm39)	missense	probably damaging	1.00
R9169:Gp2	UTSW	7	119,041,929 (GRCm39)	missense	probably benign
R9439:Gp2	UTSW	7	119,053,433 (GRCm39)	missense	probably damaging	1.00
X0026:Gp2	UTSW	7	119,042,042 (GRCm39)	missense	probably benign	0.01

Predicted Primers

PCR Primer
(F):5'- TCACCAGTGCCTTGATCATAC -3'
(R):5'- TGGGAACACTGACCATAGAAC -3'

Sequencing Primer
(F):5'- CACCAGTGCCTTGATCATACTGAATG -3'
(R):5'- TCTGAGTTCAAGATATACCTACACAC -3'

Posted On

2019-06-26