Mutagenetix > Incidental Mutation

Incidental Mutation 'R2159:Parm1'

235036

Institutional Source

Beutler Lab

Gene Symbol

Parm1

Ensembl Gene

ENSMUSG00000034981

Gene Name

prostate androgen-regulated mucin-like protein 1

Synonyms

2210012L08Rik, 9130213B05Rik

MMRRC Submission

040162-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.107) question?

Stock #

R2159 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

91665559-91771870 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 91760923 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 265 (Y265C)

Ref Sequence

ENSEMBL: ENSMUSP00000042844 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000040576]

AlphaFold

Q923D3

Predicted Effect

probably damaging
Transcript: ENSMUST00000040576
AA Change: Y265C

PolyPhen 2 Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000042844
Gene: ENSMUSG00000034981
AA Change: Y265C

Domain	Start	End	E-Value	Type
Pfam:PARM	15	296	5.3e-120	PFAM

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.3%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam21	G	A	12: 81,607,241 (GRCm39)	P174S	probably benign	Het
Aida	C	T	1: 183,103,234 (GRCm39)	P185S	probably benign	Het
Alg11	T	G	8: 22,555,861 (GRCm39)	I374R	probably benign	Het
Ano9	T	C	7: 140,688,030 (GRCm39)	I229V	probably benign	Het
Apob	A	T	12: 8,060,081 (GRCm39)	L2821F	probably benign	Het
Atp10b	C	T	11: 43,042,680 (GRCm39)	T80I	possibly damaging	Het
BC024139	T	C	15: 76,005,688 (GRCm39)	H478R	probably damaging	Het
Btbd1	A	T	7: 81,450,804 (GRCm39)	D325E	possibly damaging	Het
Camk2a	G	A	18: 61,090,257 (GRCm39)	C199Y	probably damaging	Het
Casp3	A	G	8: 47,087,323 (GRCm39)	D90G	probably damaging	Het
Ccnt2	A	G	1: 127,702,891 (GRCm39)	H71R	probably benign	Het
Cdk2ap1	G	A	5: 124,486,667 (GRCm39)	R65*	probably null	Het
Cebpb	G	T	2: 167,531,173 (GRCm39)	A78S	probably benign	Het
Col5a3	A	G	9: 20,682,606 (GRCm39)	F1613L	unknown	Het
Cpd	T	C	11: 76,688,467 (GRCm39)	D935G	probably damaging	Het
Csmd3	CCTTTGCGCTT	CCTT	15: 47,604,632 (GRCm39)		probably null	Het
Cwc27	A	G	13: 104,940,837 (GRCm39)	I174T	probably damaging	Het
Cyp21a1	C	A	17: 35,021,378 (GRCm39)	R331L	probably benign	Het
Dnah5	A	G	15: 28,252,691 (GRCm39)	T795A	probably benign	Het
Eif2ak2	A	G	17: 79,181,447 (GRCm39)	V100A	possibly damaging	Het
Foxa3	A	G	7: 18,748,109 (GRCm39)	V339A	probably benign	Het
Gp2	T	C	7: 119,051,507 (GRCm39)	D236G	probably benign	Het
Gprc6a	CAAA	CA	10: 51,491,776 (GRCm39)		probably null	Het
Gzmd	T	A	14: 56,368,153 (GRCm39)	H102L	probably damaging	Het
Klk1b1	A	T	7: 43,619,857 (GRCm39)	I139F	probably damaging	Het
Lcmt2	G	A	2: 120,969,766 (GRCm39)	P439L	probably damaging	Het
Loxl4	C	T	19: 42,588,446 (GRCm39)	A570T	probably damaging	Het
Mga	T	A	2: 119,750,124 (GRCm39)	H674Q	probably damaging	Het
Mybpc3	A	T	2: 90,955,715 (GRCm39)	K583M	probably damaging	Het
Ncoa6	G	T	2: 155,249,633 (GRCm39)	P1224T	probably damaging	Het
Nostrin	A	G	2: 69,011,266 (GRCm39)		probably null	Het
Or13e8	T	C	4: 43,697,110 (GRCm39)	H21R	probably benign	Het
Or4c3	A	T	2: 89,851,882 (GRCm39)	V176E	probably damaging	Het
Oxsr1	A	C	9: 119,133,880 (GRCm39)	D58E	possibly damaging	Het
Phf10	C	T	17: 15,172,926 (GRCm39)	E304K	probably damaging	Het
Prmt5	T	C	14: 54,752,795 (GRCm39)	T139A	probably benign	Het
Ptgir	A	G	7: 16,640,794 (GRCm39)	M29V	possibly damaging	Het
Ptp4a3	A	G	15: 73,623,865 (GRCm39)	T32A	probably benign	Het
Pwwp2b	A	T	7: 138,834,844 (GRCm39)	D95V	possibly damaging	Het
Rad51ap2	T	C	12: 11,507,752 (GRCm39)	L558S	possibly damaging	Het
Rapgef4	A	G	2: 72,005,225 (GRCm39)	D80G	probably damaging	Het
Sec24a	T	G	11: 51,603,177 (GRCm39)	H757P	probably damaging	Het
Sema4d	T	C	13: 51,874,571 (GRCm39)	N129D	probably damaging	Het
Serpini1	A	G	3: 75,531,251 (GRCm39)	T323A	probably benign	Het
Setd1a	G	A	7: 127,384,661 (GRCm39)	R504H	possibly damaging	Het
Sftpb	T	C	6: 72,286,770 (GRCm39)	C226R	probably damaging	Het
Sp8	T	C	12: 118,812,441 (GRCm39)	S99P	possibly damaging	Het
Srgap3	A	G	6: 112,748,339 (GRCm39)	F438L	probably damaging	Het
Stim2	T	C	5: 54,267,156 (GRCm39)	Y365H	probably damaging	Het
Stk36	A	G	1: 74,673,896 (GRCm39)	Q1263R	probably benign	Het
Tectb	C	G	19: 55,169,431 (GRCm39)		probably benign	Het
Troap	G	T	15: 98,975,467 (GRCm39)	A184S	probably damaging	Het
Ttn	G	A	2: 76,729,671 (GRCm39)		probably benign	Het
Vmn2r108	C	A	17: 20,689,363 (GRCm39)	A531S	probably benign	Het
Vmn2r12	T	A	5: 109,239,340 (GRCm39)	I408F	probably benign	Het
Vmn2r8	T	A	5: 108,950,169 (GRCm39)	E226V	probably benign	Het
Vmo1	A	G	11: 70,404,608 (GRCm39)	F131S	probably benign	Het
Vwf	T	C	6: 125,603,304 (GRCm39)	F885L	probably damaging	Het
Wdpcp	A	T	11: 21,807,476 (GRCm39)	M618L	probably benign	Het
Wdr90	T	C	17: 26,070,715 (GRCm39)	E1072G	probably benign	Het

Other mutations in Parm1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01363:Parm1	APN	5	91,760,877 (GRCm39)	missense	probably damaging	0.98
R0243:Parm1	UTSW	5	91,742,153 (GRCm39)	missense	possibly damaging	0.94
R0601:Parm1	UTSW	5	91,742,123 (GRCm39)	missense	probably benign	0.10
R1538:Parm1	UTSW	5	91,742,306 (GRCm39)	missense	possibly damaging	0.71
R2256:Parm1	UTSW	5	91,741,980 (GRCm39)	missense	possibly damaging	0.93
R2853:Parm1	UTSW	5	91,742,124 (GRCm39)	missense	probably benign	0.01
R2859:Parm1	UTSW	5	91,742,165 (GRCm39)	missense	possibly damaging	0.71
R2938:Parm1	UTSW	5	91,742,328 (GRCm39)	missense	possibly damaging	0.52
R4095:Parm1	UTSW	5	91,742,039 (GRCm39)	missense	probably benign
R4222:Parm1	UTSW	5	91,741,726 (GRCm39)	missense	probably benign	0.00
R4883:Parm1	UTSW	5	91,741,775 (GRCm39)	missense	possibly damaging	0.71
R6599:Parm1	UTSW	5	91,741,718 (GRCm39)	missense	possibly damaging	0.86
R6723:Parm1	UTSW	5	91,770,856 (GRCm39)	missense	probably damaging	0.97
R6799:Parm1	UTSW	5	91,742,070 (GRCm39)	missense	possibly damaging	0.93
R6885:Parm1	UTSW	5	91,742,069 (GRCm39)	missense	possibly damaging	0.71
R7714:Parm1	UTSW	5	91,741,791 (GRCm39)	missense	possibly damaging	0.93
R7783:Parm1	UTSW	5	91,741,724 (GRCm39)	missense	probably benign
R8004:Parm1	UTSW	5	91,742,132 (GRCm39)	missense	probably benign	0.00
R9623:Parm1	UTSW	5	91,760,923 (GRCm39)	missense	probably damaging	0.98
R9678:Parm1	UTSW	5	91,742,144 (GRCm39)	missense	possibly damaging	0.71
Z1177:Parm1	UTSW	5	91,742,088 (GRCm39)	missense	probably benign	0.41

Predicted Primers

PCR Primer
(F):5'- GGTGCATCGCATCCTTCAAG -3'
(R):5'- CTAGGTAAGCCTTATCCCATGATGTC -3'

Sequencing Primer
(F):5'- TCGCATCCTTCAAGGGAGACATG -3'
(R):5'- AAACTGTCTGCCCCTGACTG -3'

Posted On

2014-10-01