Mutagenetix > Incidental Mutation

Incidental Mutation 'R2111:Adprhl1'

232553

Institutional Source

Beutler Lab

Gene Symbol

Adprhl1

Ensembl Gene

ENSMUSG00000031448

Gene Name

ADP-ribosylhydrolase like 1

Synonyms

D330008N11Rik, Arh2

MMRRC Submission

040115-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2111 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

13271663-13304162 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 13298694 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Histidine at position 79 (Y79H)

Ref Sequence

ENSEMBL: ENSMUSP00000145145 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000033825] [ENSMUST00000168498] [ENSMUST00000171619] [ENSMUST00000204916]

AlphaFold

Q8BGK2

Predicted Effect

probably damaging
Transcript: ENSMUST00000033825
AA Change: Y79H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000033825
Gene: ENSMUSG00000031448
AA Change: Y79H

Domain	Start	End	E-Value	Type
Pfam:ADP_ribosyl_GH	6	327	1.2e-53	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000168498

SMART Domains

Protein: ENSMUSP00000131920
Gene: ENSMUSG00000031448

Domain	Start	End	E-Value	Type
Pfam:ADP_ribosyl_GH	69	196	9e-17	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000171619

SMART Domains

Protein: ENSMUSP00000132014
Gene: ENSMUSG00000031448

Domain	Start	End	E-Value	Type
Pfam:ADP_ribosyl_GH	1	135	4.9e-18	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000204916
AA Change: Y79H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000145145
Gene: ENSMUSG00000031448
AA Change: Y79H

Domain	Start	End	E-Value	Type
Pfam:ADP_ribosyl_GH	6	327	4.2e-49	PFAM
low complexity region	509	527	N/A	INTRINSIC
low complexity region	955	969	N/A	INTRINSIC
internal_repeat_1	1047	1150	1.82e-5	PROSPERO
internal_repeat_1	1157	1274	1.82e-5	PROSPERO
low complexity region	1275	1290	N/A	INTRINSIC

Meta Mutation Damage Score

0.6401

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.4%
20x: 95.6%

Validation Efficiency

100% (86/86)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] ADP-ribosylation is a reversible posttranslational modification used to regulate protein function. ADP-ribosyltransferases (see ART1; MIM 601625) transfer ADP-ribose from NAD+ to the target protein, and ADP-ribosylhydrolases, such as ADPRHL1, reverse the reaction (Glowacki et al., 2002 [PubMed 12070318]).[supplied by OMIM, Mar 2008]

Allele List at MGI

Other mutations in this stock

Total: 89 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9330161L09Rik	T	C	12: 103,373,848 (GRCm39)		probably benign	Het
Abca2	A	T	2: 25,327,517 (GRCm39)	I669F	possibly damaging	Het
Adam9	C	T	8: 25,472,142 (GRCm39)		probably benign	Het
Akp3	A	T	1: 87,054,607 (GRCm39)		probably null	Het
Alpk2	T	C	18: 65,482,845 (GRCm39)	S388G	probably benign	Het
Amph	G	A	13: 19,300,436 (GRCm39)		probably benign	Het
Arr3	T	A	X: 99,658,247 (GRCm39)	F269L	possibly damaging	Het
Atp2a2	A	G	5: 122,597,609 (GRCm39)	F808S	probably damaging	Het
Baz1a	T	A	12: 54,958,170 (GRCm39)	N1027I	probably damaging	Het
C2cd4c	G	T	10: 79,448,255 (GRCm39)	H297Q	probably damaging	Het
Calr3	T	A	8: 73,181,112 (GRCm39)	D160V	probably damaging	Het
Cdc42ep1	C	T	15: 78,731,692 (GRCm39)	R46C	probably damaging	Het
Cdh23	G	T	10: 60,141,362 (GRCm39)	F3127L	probably damaging	Het
Cfhr4	T	A	1: 139,702,417 (GRCm39)		probably benign	Het
Cps1	T	A	1: 67,216,139 (GRCm39)	D821E	probably benign	Het
Cyp2e1	C	A	7: 140,353,547 (GRCm39)	T328K	probably damaging	Het
Dcp1a	T	C	14: 30,241,327 (GRCm39)	V379A	probably benign	Het
Dst	T	C	1: 34,208,259 (GRCm39)	S737P	probably damaging	Het
Dtx2	C	T	5: 136,059,431 (GRCm39)	S493F	probably damaging	Het
Eci2	A	G	13: 35,174,699 (GRCm39)		probably null	Het
Ercc6l2	A	G	13: 63,982,563 (GRCm39)	T126A	probably damaging	Het
Fgf6	T	C	6: 126,992,723 (GRCm39)	S59P	probably damaging	Het
Fmnl2	A	G	2: 52,995,549 (GRCm39)	E424G	probably damaging	Het
Gapvd1	G	T	2: 34,574,329 (GRCm39)	A1256D	probably benign	Het
Gcfc2	C	A	6: 81,900,759 (GRCm39)	D24E	probably benign	Het
Gigyf2	A	G	1: 87,368,452 (GRCm39)	H1044R	probably damaging	Het
Gk2	T	C	5: 97,604,164 (GRCm39)	I225V	probably benign	Het
Gm3944	C	A	12: 18,903,895 (GRCm39)	S8*	probably null	Het
Gnl3l	A	G	X: 149,780,290 (GRCm39)	S217P	probably damaging	Het
Gpr156	A	G	16: 37,799,113 (GRCm39)	D109G	probably benign	Het
Hoxd1	A	T	2: 74,593,710 (GRCm39)	T89S	probably benign	Het
Ift172	G	A	5: 31,443,423 (GRCm39)	T112M	probably benign	Het
Igkv1-115	C	A	6: 68,138,613 (GRCm39)	S72*	probably null	Het
Ildr1	A	G	16: 36,542,341 (GRCm39)	E247G	probably damaging	Het
Insr	A	G	8: 3,219,748 (GRCm39)	S925P	probably benign	Het
Itpr1	T	G	6: 108,355,270 (GRCm39)		probably benign	Het
Khdrbs3	C	T	15: 68,896,673 (GRCm39)	T111I	probably benign	Het
Mageb3	A	G	2: 121,785,306 (GRCm39)		probably null	Het
Mcf2l	A	T	8: 13,051,867 (GRCm39)	K433N	probably damaging	Het
Mdn1	A	G	4: 32,700,409 (GRCm39)	E1456G	probably damaging	Het
Mta1	C	T	12: 113,095,248 (GRCm39)	T467I	probably damaging	Het
Mtr	A	T	13: 12,259,487 (GRCm39)	I196N	possibly damaging	Het
Mtus1	G	T	8: 41,475,608 (GRCm39)	P819T	probably damaging	Het
Myh1	G	A	11: 67,105,446 (GRCm39)	D1079N	possibly damaging	Het
Nav1	C	T	1: 135,376,742 (GRCm39)	R1694Q	probably damaging	Het
Neb	A	G	2: 52,174,275 (GRCm39)	I1528T	probably benign	Het
Nek1	T	A	8: 61,577,360 (GRCm39)		probably null	Het
Nes	A	G	3: 87,884,618 (GRCm39)	E915G	probably benign	Het
Nlrp4f	T	C	13: 65,347,167 (GRCm39)	I30M	probably benign	Het
Nup153	A	G	13: 46,837,404 (GRCm39)	S1273P	probably benign	Het
Nup155	A	G	15: 8,150,951 (GRCm39)	I334V	probably benign	Het
Or10j2	A	T	1: 173,097,879 (GRCm39)	M46L	probably benign	Het
Or1e1f	A	G	11: 73,855,740 (GRCm39)	Y102C	probably damaging	Het
Or5b3	G	A	19: 13,388,307 (GRCm39)	A125T	probably damaging	Het
Or5d41	A	G	2: 88,054,818 (GRCm39)	V186A	possibly damaging	Het
Or6d13	T	C	6: 116,517,611 (GRCm39)	Y66H	possibly damaging	Het
Or8b46	T	A	9: 38,450,576 (GRCm39)	N128K	probably benign	Het
Or8k38	G	T	2: 86,488,781 (GRCm39)	T7K	probably damaging	Het
Parn	G	A	16: 13,420,933 (GRCm39)	S473L	probably damaging	Het
Pcnt	T	C	10: 76,256,360 (GRCm39)	K627E	probably damaging	Het
Pja2	T	A	17: 64,597,031 (GRCm39)	D553V	probably damaging	Het
Prune2	T	C	19: 17,185,602 (GRCm39)	F3004L	probably damaging	Het
Rasgrp3	T	C	17: 75,807,753 (GRCm39)		probably null	Het
Rdh13	A	G	7: 4,448,482 (GRCm39)	V10A	probably benign	Het
Rimbp2	T	C	5: 128,850,565 (GRCm39)	Y906C	probably damaging	Het
Ripor1	T	C	8: 106,341,344 (GRCm39)	F59S	probably damaging	Het
Rnf185	T	C	11: 3,382,393 (GRCm39)		probably benign	Het
Runx3	T	C	4: 134,882,627 (GRCm39)	V107A	probably damaging	Het
Scn3b	T	C	9: 40,193,741 (GRCm39)	V156A	probably benign	Het
Serpina3a	G	A	12: 104,082,481 (GRCm39)	A85T	probably damaging	Het
Slc12a7	C	T	13: 73,933,274 (GRCm39)	R111*	probably null	Het
Slc5a5	A	T	8: 71,342,395 (GRCm39)		probably null	Het
Snx13	A	T	12: 35,188,084 (GRCm39)	L787F	probably damaging	Het
Spef2	A	T	15: 9,589,659 (GRCm39)	M1535K	probably damaging	Het
Sphkap	T	G	1: 83,253,602 (GRCm39)	K1382N	probably benign	Het
Tagap1	A	G	17: 7,224,259 (GRCm39)	S146P	probably benign	Het
Tagln3	A	G	16: 45,531,957 (GRCm39)	Y192H	probably damaging	Het
Tbc1d15	A	C	10: 115,076,819 (GRCm39)	S22A	possibly damaging	Het
Tbc1d31	A	G	15: 57,796,040 (GRCm39)	E211G	probably benign	Het
Tmod3	A	G	9: 75,416,645 (GRCm39)	V229A	probably damaging	Het
Ubr2	A	G	17: 47,274,071 (GRCm39)		probably null	Het
Ugt2b36	T	C	5: 87,240,100 (GRCm39)	E95G	probably benign	Het
Unc45b	G	A	11: 82,802,515 (GRCm39)	A4T	probably benign	Het
Usp40	A	G	1: 87,877,936 (GRCm39)	I1117T	probably benign	Het
Vcan	T	A	13: 89,841,422 (GRCm39)	D414V	probably damaging	Het
Xrn1	C	A	9: 95,921,885 (GRCm39)	H1433N	probably benign	Het
Zfp353-ps	T	A	8: 42,536,005 (GRCm39)		noncoding transcript	Het
Zfp74	G	A	7: 29,634,443 (GRCm39)	Q422*	probably null	Het
Zmym3	A	T	X: 100,450,993 (GRCm39)	V1208D	probably damaging	Het

Other mutations in Adprhl1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL03268:Adprhl1	APN	8	13,296,170 (GRCm39)	splice site	probably benign
BB003:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
BB004:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
BB005:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
BB006:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
BB013:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
BB014:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
BB015:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
BB016:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
R0244:Adprhl1	UTSW	8	13,292,391 (GRCm39)	splice site	probably benign
R0636:Adprhl1	UTSW	8	13,298,702 (GRCm39)	missense	probably damaging	1.00
R1295:Adprhl1	UTSW	8	13,298,624 (GRCm39)	missense	probably damaging	1.00
R2112:Adprhl1	UTSW	8	13,298,694 (GRCm39)	missense	probably damaging	1.00
R2184:Adprhl1	UTSW	8	13,292,559 (GRCm39)	missense	probably benign	0.00
R4411:Adprhl1	UTSW	8	13,296,114 (GRCm39)	missense	probably benign	0.16
R4412:Adprhl1	UTSW	8	13,296,114 (GRCm39)	missense	probably benign	0.16
R4413:Adprhl1	UTSW	8	13,296,114 (GRCm39)	missense	probably benign	0.16
R4615:Adprhl1	UTSW	8	13,292,250 (GRCm39)	critical splice donor site	probably null
R4618:Adprhl1	UTSW	8	13,292,250 (GRCm39)	critical splice donor site	probably null
R5016:Adprhl1	UTSW	8	13,274,889 (GRCm39)	missense	possibly damaging	0.88
R5058:Adprhl1	UTSW	8	13,292,625 (GRCm39)	missense	probably damaging	1.00
R5060:Adprhl1	UTSW	8	13,298,621 (GRCm39)	missense	possibly damaging	0.63
R5209:Adprhl1	UTSW	8	13,292,563 (GRCm39)	nonsense	probably null
R6103:Adprhl1	UTSW	8	13,272,055 (GRCm39)	missense	possibly damaging	0.91
R6158:Adprhl1	UTSW	8	13,274,977 (GRCm39)	missense	possibly damaging	0.93
R6221:Adprhl1	UTSW	8	13,275,634 (GRCm39)	missense	probably benign	0.01
R6971:Adprhl1	UTSW	8	13,273,476 (GRCm39)	missense	probably benign
R7087:Adprhl1	UTSW	8	13,271,856 (GRCm39)	missense	probably damaging	0.99
R7362:Adprhl1	UTSW	8	13,295,534 (GRCm39)	missense	probably damaging	1.00
R7404:Adprhl1	UTSW	8	13,275,118 (GRCm39)	missense	probably damaging	0.99
R7422:Adprhl1	UTSW	8	13,272,873 (GRCm39)	missense	probably benign	0.28
R7439:Adprhl1	UTSW	8	13,273,069 (GRCm39)	missense	probably benign	0.01
R7441:Adprhl1	UTSW	8	13,273,069 (GRCm39)	missense	probably benign	0.01
R7772:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
R7773:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
R7774:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
R7776:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
R7876:Adprhl1	UTSW	8	13,273,509 (GRCm39)	missense	probably benign	0.00
R7877:Adprhl1	UTSW	8	13,275,316 (GRCm39)	nonsense	probably null
R7926:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
R7927:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
R7928:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
R7929:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
R7944:Adprhl1	UTSW	8	13,271,929 (GRCm39)	missense	probably damaging	0.99
R7945:Adprhl1	UTSW	8	13,271,929 (GRCm39)	missense	probably damaging	0.99
R7946:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
R7947:Adprhl1	UTSW	8	13,298,682 (GRCm39)	missense	probably damaging	1.00
R7949:Adprhl1	UTSW	8	13,274,225 (GRCm39)	missense	possibly damaging	0.93
R8155:Adprhl1	UTSW	8	13,271,764 (GRCm39)	missense	probably damaging	0.99
R8182:Adprhl1	UTSW	8	13,272,774 (GRCm39)	missense	probably benign	0.07
R8753:Adprhl1	UTSW	8	13,272,118 (GRCm39)	missense	possibly damaging	0.91
R8799:Adprhl1	UTSW	8	13,272,474 (GRCm39)	missense	probably benign	0.00
R8893:Adprhl1	UTSW	8	13,274,511 (GRCm39)	missense	probably benign	0.11
R9022:Adprhl1	UTSW	8	13,274,352 (GRCm39)	missense	probably benign	0.00
R9161:Adprhl1	UTSW	8	13,272,270 (GRCm39)	missense	probably damaging	0.99
R9227:Adprhl1	UTSW	8	13,271,974 (GRCm39)	missense	probably benign	0.27
R9228:Adprhl1	UTSW	8	13,275,279 (GRCm39)	missense	probably benign
R9283:Adprhl1	UTSW	8	13,273,540 (GRCm39)	missense	probably benign
R9426:Adprhl1	UTSW	8	13,274,034 (GRCm39)	missense	possibly damaging	0.93
R9648:Adprhl1	UTSW	8	13,273,245 (GRCm39)	missense	probably benign	0.40
Z1176:Adprhl1	UTSW	8	13,275,613 (GRCm39)	missense	probably benign	0.01
Z1177:Adprhl1	UTSW	8	13,295,476 (GRCm39)	missense	possibly damaging	0.68

Predicted Primers

PCR Primer
(F):5'- ATACCACACCAAGTGTCGG -3'
(R):5'- TGGATGTTCCCTAGACCCTC -3'

Sequencing Primer
(F):5'- ACAGGGTCCCTAACTGCAG -3'
(R):5'- ATGTTCCCTAGACCCTCGGGAC -3'

Posted On

2014-09-18