Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02951:Prp2'

366008

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Prp2

Ensembl Gene

ENSMUSG00000058295

Gene Name

proline rich protein 2

Synonyms

MP14

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL02951

Quality Score

Status

Chromosome

Chromosomal Location

132572874-132577665 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 132576788 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 25 (N25S)

Ref Sequence

ENSEMBL: ENSMUSP00000135942 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000076061] [ENSMUST00000178961]

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000076061
AA Change: N25S

SMART Domains

Protein: ENSMUSP00000075435
Gene: ENSMUSG00000058295
AA Change: N25S

Domain	Start	End	E-Value	Type
signal peptide	1	16	N/A	INTRINSIC
low complexity region	24	44	N/A	INTRINSIC
low complexity region	49	299	N/A	INTRINSIC
low complexity region	302	316	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000178961
AA Change: N25S

SMART Domains

Protein: ENSMUSP00000135942
Gene: ENSMUSG00000058295
AA Change: N25S

Domain	Start	End	E-Value	Type
signal peptide	1	16	N/A	INTRINSIC
low complexity region	24	44	N/A	INTRINSIC
low complexity region	49	299	N/A	INTRINSIC
low complexity region	302	316	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: This gene encodes a member of the heterogeneous family of proline-rich salivary glycoproteins. The expression of this gene is dramatically induced in the parotid and submandibular glands of mice by beta-adrenergic stimulation. The encoded protein serves an important dental function by protecting mice against toxic dietary polyphenols such as tannins and influence the visco-elastic properties of the mucus. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 6. [provided by RefSeq, Nov 2015]

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610028H24Rik	C	A	10: 76,290,536 (GRCm39)		probably benign	Het
Acot10	G	A	15: 20,665,868 (GRCm39)	T291I	probably benign	Het
Adam34l	T	G	8: 44,080,125 (GRCm39)	H33P	possibly damaging	Het
Atp13a3	A	G	16: 30,157,439 (GRCm39)		probably null	Het
Atp2a1	C	T	7: 126,049,399 (GRCm39)	V548M	possibly damaging	Het
Bsn	G	A	9: 107,992,812 (GRCm39)	S980L	probably damaging	Het
Ccdc158	A	G	5: 92,797,865 (GRCm39)	M425T	probably damaging	Het
Cdh23	A	G	10: 60,147,143 (GRCm39)	L2733S	probably damaging	Het
Chd3	C	T	11: 69,251,874 (GRCm39)		probably null	Het
Cimap1d	T	C	10: 79,475,811 (GRCm39)	N251S	probably benign	Het
Dock2	T	C	11: 34,260,448 (GRCm39)		probably benign	Het
Elfn2	T	C	15: 78,556,082 (GRCm39)	K822E	probably damaging	Het
Eps15l1	G	A	8: 73,112,240 (GRCm39)	S764L	probably benign	Het
Etl4	C	A	2: 20,806,348 (GRCm39)		probably benign	Het
Faap24	C	A	7: 35,092,376 (GRCm39)	K180N	probably damaging	Het
Fhod1	G	A	8: 106,057,862 (GRCm39)	R888W	probably damaging	Het
Fus	T	C	7: 127,581,009 (GRCm39)		probably benign	Het
Gm3453	T	C	14: 5,976,168 (GRCm38)	E201G	possibly damaging	Het
Gnpat	G	T	8: 125,597,644 (GRCm39)	D69Y	probably benign	Het
Gpaa1	T	A	15: 76,217,019 (GRCm39)		probably benign	Het
Gsta1	A	T	9: 78,149,819 (GRCm39)	K211*	probably null	Het
Lct	G	T	1: 128,227,948 (GRCm39)	Q1182K	probably damaging	Het
Mroh1	T	C	15: 76,311,836 (GRCm39)	L523P	probably damaging	Het
Mrpl46	A	G	7: 78,425,200 (GRCm39)		probably benign	Het
Mst1r	G	T	9: 107,785,403 (GRCm39)	V354F	possibly damaging	Het
Myo15b	A	G	11: 115,772,127 (GRCm39)	D299G	probably damaging	Het
Myo6	G	A	9: 80,171,516 (GRCm39)	V506I	possibly damaging	Het
Nadk	A	C	4: 155,671,933 (GRCm39)	K271Q	probably benign	Het
Nbas	A	G	12: 13,412,542 (GRCm39)	R954G	probably benign	Het
Nbr1	T	A	11: 101,462,805 (GRCm39)		probably null	Het
Nup88	T	C	11: 70,835,698 (GRCm39)	D587G	possibly damaging	Het
Oas1a	A	T	5: 121,043,727 (GRCm39)	F135Y	probably damaging	Het
Obscn	A	G	11: 58,885,339 (GRCm39)		probably benign	Het
Or4k42	T	G	2: 111,320,465 (GRCm39)	I13L	probably benign	Het
Parp14	G	A	16: 35,678,903 (GRCm39)	T355I	probably benign	Het
Pdgfd	G	T	9: 6,288,494 (GRCm39)	L43F	probably damaging	Het
Pou5f2	T	C	13: 78,173,237 (GRCm39)	S60P	probably benign	Het
Ptprq	A	T	10: 107,503,321 (GRCm39)	F779Y	probably benign	Het
Rims2	C	T	15: 39,398,334 (GRCm39)	R1078C	probably damaging	Het
Rnf38	G	T	4: 44,129,619 (GRCm39)	S425*	probably null	Het
Rps21	T	A	2: 179,899,840 (GRCm39)	I59N	probably damaging	Het
Scn5a	A	T	9: 119,324,751 (GRCm39)	F1359Y	probably damaging	Het
Slc35b2	A	G	17: 45,875,694 (GRCm39)	E67G	probably damaging	Het
Slc37a2	A	G	9: 37,166,611 (GRCm39)	F15L	probably benign	Het
Snapc4	A	C	2: 26,260,847 (GRCm39)	N465K	probably benign	Het
Spata31f1a	C	T	4: 42,850,696 (GRCm39)	E487K	probably benign	Het
Stxbp2	A	T	8: 3,691,971 (GRCm39)	I538F	probably benign	Het
Taco1	A	G	11: 105,960,353 (GRCm39)	N98S	probably benign	Het
Tcea3	T	C	4: 135,985,299 (GRCm39)		probably null	Het
Thada	T	C	17: 84,751,456 (GRCm39)	S507G	probably benign	Het
Tmem132b	T	A	5: 125,864,611 (GRCm39)	C906S	probably damaging	Het
Trpm2	A	T	10: 77,765,112 (GRCm39)	I963N	possibly damaging	Het
Usp10	A	G	8: 120,673,825 (GRCm39)	T397A	probably benign	Het
Usp3	G	A	9: 66,449,832 (GRCm39)	R160*	probably null	Het
Utp15	T	C	13: 98,394,460 (GRCm39)	Y144C	probably damaging	Het
Xpc	G	A	6: 91,483,831 (GRCm39)	R172W	probably damaging	Het

Other mutations in Prp2

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01383:Prp2	APN	6	132,576,841 (GRCm39)	missense	unknown
PIT4458001:Prp2	UTSW	6	132,577,510 (GRCm39)	missense	unknown
R2034:Prp2	UTSW	6	132,572,947 (GRCm39)	splice site	probably null
R2432:Prp2	UTSW	6	132,576,874 (GRCm39)	missense	unknown
R5283:Prp2	UTSW	6	132,577,606 (GRCm39)	missense	unknown
R7761:Prp2	UTSW	6	132,577,306 (GRCm39)	nonsense	probably null
R7877:Prp2	UTSW	6	132,572,928 (GRCm39)	missense	unknown
R8033:Prp2	UTSW	6	132,577,391 (GRCm39)	missense	unknown
R8062:Prp2	UTSW	6	132,577,651 (GRCm39)	missense	unknown
R8695:Prp2	UTSW	6	132,576,932 (GRCm39)	missense	unknown
R8696:Prp2	UTSW	6	132,577,322 (GRCm39)	missense	unknown
R8938:Prp2	UTSW	6	132,577,581 (GRCm39)	missense	unknown
RF005:Prp2	UTSW	6	132,577,464 (GRCm39)	small deletion	probably benign
RF016:Prp2	UTSW	6	132,577,475 (GRCm39)	small deletion	probably benign
RF039:Prp2	UTSW	6	132,577,464 (GRCm39)	small deletion	probably benign
RF052:Prp2	UTSW	6	132,577,475 (GRCm39)	small deletion	probably benign
RF054:Prp2	UTSW	6	132,577,484 (GRCm39)	frame shift	probably null
RF057:Prp2	UTSW	6	132,577,493 (GRCm39)	frame shift	probably null
X0053:Prp2	UTSW	6	132,577,559 (GRCm39)	missense	unknown
Z1176:Prp2	UTSW	6	132,577,200 (GRCm39)	missense	unknown
Z1177:Prp2	UTSW	6	132,572,933 (GRCm39)	missense	unknown

Posted On

2015-12-18