Mutagenetix > Incidental Mutation

Incidental Mutation 'R7011:Adam19'

545034

Institutional Source

Beutler Lab

Gene Symbol

Adam19

Ensembl Gene

ENSMUSG00000011256

Gene Name

a disintegrin and metallopeptidase domain 19 (meltrin beta)

Synonyms

Mltnb

MMRRC Submission

045112-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7011 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

46055992-46147343 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 46143018 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Proline to Serine at position 886 (P886S)

Ref Sequence

ENSEMBL: ENSMUSP00000011400 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000011400]

AlphaFold

O35674

Predicted Effect

probably benign
Transcript: ENSMUST00000011400
AA Change: P886S

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000011400
Gene: ENSMUSG00000011256
AA Change: P886S

Domain	Start	End	E-Value	Type
signal peptide	1	26	N/A	INTRINSIC
Pfam:Pep_M12B_propep	32	163	9.4e-27	PFAM
Pfam:Reprolysin_5	209	388	1.9e-25	PFAM
Pfam:Reprolysin_4	209	399	1.5e-15	PFAM
Pfam:Reprolysin	211	409	1.3e-68	PFAM
Pfam:Reprolysin_2	231	399	6.1e-19	PFAM
Pfam:Reprolysin_3	235	357	1.2e-19	PFAM
DISIN	426	501	9.7e-41	SMART
ACR	502	650	7.46e-62	SMART
transmembrane domain	704	726	N/A	INTRINSIC
low complexity region	788	797	N/A	INTRINSIC
low complexity region	832	846	N/A	INTRINSIC
low complexity region	886	905	N/A	INTRINSIC

Meta Mutation Damage Score

0.0717

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 98.9%

Validation Efficiency

96% (66/69)

MGI Phenotype

FUNCTION: This gene encodes a cell surface glycoprotein and member of the ADAM (a disintegrin and metalloproteinase) family of endopeptidases. The encoded protein may play a role in the ectodomain shedding of neuregulin proteins. Homozygous knockout mice for this gene exhibit heart development defects and perinatal lethality. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that undergoes proteolytic processing to generate a mature protein product. [provided by RefSeq, Aug 2015]
PHENOTYPE: Homozygous null mice exhibit cardiac developmental defects and die perinatally. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Anapc1	C	T	2: 128,648,681 (GRCm38)		probably null	Het
Ankrd34c	C	A	9: 89,728,948 (GRCm38)	G447*	probably null	Het
Apbb1ip	A	T	2: 22,835,931 (GRCm38)	E238D	probably damaging	Het
Arfgap1	T	C	2: 180,972,142 (GRCm38)	L110P	probably damaging	Het
Arhgap21	G	A	2: 20,848,878 (GRCm38)	T1901I	possibly damaging	Het
Brpf1	C	A	6: 113,318,466 (GRCm38)	Q679K	probably benign	Het
Btnl2	A	G	17: 34,363,513 (GRCm38)	E351G	probably damaging	Het
Cd209f	T	A	8: 4,104,859 (GRCm38)	T80S	probably benign	Het
Cdc16	A	G	8: 13,769,451 (GRCm38)	E349G	probably damaging	Het
Cfap53	A	T	18: 74,329,493 (GRCm38)	D436V	probably benign	Het
Crhr2	A	T	6: 55,099,210 (GRCm38)		probably null	Het
Cux1	T	C	5: 136,360,033 (GRCm38)	K226E	probably damaging	Het
Ddr2	A	T	1: 169,982,103 (GRCm38)	D768E	probably damaging	Het
Dhx8	T	C	11: 101,741,520 (GRCm38)	L435P	probably damaging	Het
Dnah11	AGGCC	AGGCCGGCC	12: 117,922,018 (GRCm38)		probably null	Het
Eif4ebp1	G	A	8: 27,273,344 (GRCm38)	R55Q	probably damaging	Het
Fbxo18	T	A	2: 11,762,963 (GRCm38)	D358V	probably damaging	Het
Fra10ac1	T	A	19: 38,188,794 (GRCm38)	E304D	probably benign	Het
Gabrb2	T	C	11: 42,626,661 (GRCm38)	S399P	possibly damaging	Het
Gpatch2l	G	A	12: 86,244,184 (GRCm38)	R47H	probably damaging	Het
Gprin2	G	T	14: 34,195,436 (GRCm38)	H126N	probably null	Het
Gucy1a1	A	G	3: 82,109,115 (GRCm38)	S189P	probably damaging	Het
Htr1d	T	C	4: 136,443,006 (GRCm38)	M182T	probably benign	Het
Lipc	A	G	9: 70,818,954 (GRCm38)	F73L	probably benign	Het
Liph	A	G	16: 21,984,097 (GRCm38)	I74T	probably damaging	Het
Lrif1	T	G	3: 106,732,285 (GRCm38)	Y229D	probably damaging	Het
Magel2	C	T	7: 62,378,533 (GRCm38)	T395I	possibly damaging	Het
Magi3	T	C	3: 104,105,754 (GRCm38)	N139S	probably damaging	Het
Man2c1	T	A	9: 57,137,833 (GRCm38)	V336E	probably damaging	Het
Mapk12	A	T	15: 89,135,600 (GRCm38)	Y135N	probably damaging	Het
Mapkapk3	C	T	9: 107,289,396 (GRCm38)		probably benign	Het
Mast1	A	T	8: 84,911,945 (GRCm38)	Y653*	probably null	Het
Muc16	T	A	9: 18,637,543 (GRCm38)	H5818L	probably benign	Het
Muc16	T	A	9: 18,637,451 (GRCm38)	I5849F	probably benign	Het
Ndufa10	A	G	1: 92,470,859 (GRCm38)	S68P	probably damaging	Het
Nedd1	C	A	10: 92,690,773 (GRCm38)	L503F	probably benign	Het
Nr1i3	A	G	1: 171,214,358 (GRCm38)	M4V	probably benign	Het
Olfr1121	G	A	2: 87,372,260 (GRCm38)	A243T	possibly damaging	Het
Olfr1307	A	T	2: 111,944,686 (GRCm38)	F257I	probably benign	Het
Olfr1501	T	C	19: 13,839,039 (GRCm38)	I45V	probably benign	Het
Olfr332	T	A	11: 58,490,144 (GRCm38)	I204F	possibly damaging	Het
Papd7	C	T	13: 69,500,080 (GRCm38)	G489S	probably damaging	Het
Pcdh18	A	T	3: 49,754,782 (GRCm38)	S695T	probably benign	Het
Pcdha1	T	C	18: 36,930,535 (GRCm38)	I84T	probably damaging	Het
Plek	T	A	11: 16,994,760 (GRCm38)	D90V	possibly damaging	Het
Ppp6r1	A	G	7: 4,646,826 (GRCm38)	C47R	probably damaging	Het
Psg27	G	C	7: 18,556,873 (GRCm38)	N468K	probably benign	Het
Ptchd4	G	A	17: 42,503,868 (GRCm38)	E887K	probably benign	Het
Rabgap1	C	T	2: 37,540,480 (GRCm38)	L678F	probably damaging	Het
Rmdn3	T	C	2: 119,138,423 (GRCm38)	Y429C	probably damaging	Het
Ros1	A	T	10: 52,180,176 (GRCm38)	C73S	probably damaging	Het
Rtkn2	G	A	10: 67,979,665 (GRCm38)		probably benign	Het
Slc25a42	A	G	8: 70,186,702 (GRCm38)	S242P	probably damaging	Het
Smtnl1	T	A	2: 84,818,409 (GRCm38)	D167V	probably benign	Het
Smurf2	A	G	11: 106,833,784 (GRCm38)	L511P	probably benign	Het
Stbd1	A	T	5: 92,605,118 (GRCm38)	K156*	probably null	Het
Tenm4	G	T	7: 96,896,135 (GRCm38)	G2453*	probably null	Het
Tpr	A	G	1: 150,433,772 (GRCm38)	K1760E	probably damaging	Het
Triobp	T	A	15: 78,978,723 (GRCm38)	L1427Q	probably damaging	Het
Uaca	A	G	9: 60,870,368 (GRCm38)	E679G	probably damaging	Het
Ucn3	T	G	13: 3,941,421 (GRCm38)	H77P	possibly damaging	Het
Wnk2	T	A	13: 49,071,091 (GRCm38)	D998V	probably damaging	Het
Xrcc3	A	G	12: 111,804,535 (GRCm38)	V320A	probably damaging	Het
Zdbf2	A	G	1: 63,306,766 (GRCm38)	T1435A	possibly damaging	Het
Zfp36l2	G	T	17: 84,186,433 (GRCm38)	H259N	possibly damaging	Het
Zfp619	A	T	7: 39,537,762 (GRCm38)	H1072L	probably damaging	Het
Zfy2	T	A	Y: 2,107,127 (GRCm38)	E502D	possibly damaging	Het
Zfyve16	G	A	13: 92,521,987 (GRCm38)	P472L	probably benign	Het

Other mutations in Adam19

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01433:Adam19	APN	11	46,112,783 (GRCm38)	missense	probably damaging	1.00
IGL01727:Adam19	APN	11	46,121,553 (GRCm38)	missense	probably benign
IGL01758:Adam19	APN	11	46,112,924 (GRCm38)	missense	probably benign	0.01
IGL02160:Adam19	APN	11	46,139,695 (GRCm38)	missense	probably damaging	0.99
IGL02421:Adam19	APN	11	46,137,553 (GRCm38)	missense	probably damaging	0.96
IGL02572:Adam19	APN	11	46,131,721 (GRCm38)	nonsense	probably null
IGL02995:Adam19	APN	11	46,136,349 (GRCm38)	missense	probably benign	0.00
IGL03171:Adam19	APN	11	46,138,854 (GRCm38)	missense	probably damaging	0.98
IGL03237:Adam19	APN	11	46,137,556 (GRCm38)	missense	probably benign
R0003:Adam19	UTSW	11	46,128,789 (GRCm38)	missense	probably damaging	1.00
R0026:Adam19	UTSW	11	46,136,259 (GRCm38)	missense	probably damaging	1.00
R0158:Adam19	UTSW	11	46,143,034 (GRCm38)	missense	probably damaging	1.00
R0304:Adam19	UTSW	11	46,127,392 (GRCm38)	missense	possibly damaging	0.91
R0488:Adam19	UTSW	11	46,138,930 (GRCm38)	missense	probably damaging	0.98
R0501:Adam19	UTSW	11	46,123,130 (GRCm38)	missense	probably damaging	1.00
R0591:Adam19	UTSW	11	46,121,411 (GRCm38)	splice site	probably benign
R0734:Adam19	UTSW	11	46,127,403 (GRCm38)	missense	probably damaging	0.99
R0747:Adam19	UTSW	11	46,118,495 (GRCm38)	splice site	probably null
R0771:Adam19	UTSW	11	46,121,453 (GRCm38)	missense	possibly damaging	0.92
R1052:Adam19	UTSW	11	46,127,265 (GRCm38)	missense	probably damaging	0.99
R1573:Adam19	UTSW	11	46,113,618 (GRCm38)	splice site	probably benign
R1735:Adam19	UTSW	11	46,138,917 (GRCm38)	missense	probably benign	0.26
R1830:Adam19	UTSW	11	46,127,278 (GRCm38)	missense	probably damaging	0.98
R1911:Adam19	UTSW	11	46,121,454 (GRCm38)	missense	probably damaging	1.00
R2092:Adam19	UTSW	11	46,060,904 (GRCm38)	splice site	probably null
R3749:Adam19	UTSW	11	46,137,610 (GRCm38)	missense	probably benign	0.00
R3893:Adam19	UTSW	11	46,128,838 (GRCm38)	missense	probably damaging	1.00
R3916:Adam19	UTSW	11	46,060,935 (GRCm38)	missense	probably benign	0.25
R3917:Adam19	UTSW	11	46,060,935 (GRCm38)	missense	probably benign	0.25
R4506:Adam19	UTSW	11	46,118,444 (GRCm38)	missense	possibly damaging	0.67
R4767:Adam19	UTSW	11	46,138,977 (GRCm38)	critical splice donor site	probably null
R5055:Adam19	UTSW	11	46,123,169 (GRCm38)	missense	probably damaging	1.00
R5313:Adam19	UTSW	11	46,131,776 (GRCm38)	missense	probably damaging	1.00
R5329:Adam19	UTSW	11	46,125,026 (GRCm38)	missense	probably damaging	0.99
R5567:Adam19	UTSW	11	46,136,250 (GRCm38)	missense	probably damaging	1.00
R5602:Adam19	UTSW	11	46,136,315 (GRCm38)	missense	probably benign
R6198:Adam19	UTSW	11	46,121,502 (GRCm38)	missense	probably damaging	1.00
R6875:Adam19	UTSW	11	46,112,875 (GRCm38)	missense	probably benign
R7163:Adam19	UTSW	11	46,131,717 (GRCm38)	missense	probably benign
R7213:Adam19	UTSW	11	46,121,471 (GRCm38)	missense	probably benign	0.20
R7267:Adam19	UTSW	11	46,121,576 (GRCm38)	nonsense	probably null
R7896:Adam19	UTSW	11	46,137,543 (GRCm38)	missense	probably damaging	1.00
R8012:Adam19	UTSW	11	46,065,046 (GRCm38)	missense	possibly damaging	0.74
R8059:Adam19	UTSW	11	46,136,466 (GRCm38)	splice site	probably benign
R8243:Adam19	UTSW	11	46,125,082 (GRCm38)	missense	probably damaging	1.00
R8357:Adam19	UTSW	11	46,140,112 (GRCm38)	missense	probably damaging	0.96
R8419:Adam19	UTSW	11	46,125,023 (GRCm38)	missense	possibly damaging	0.77
R8457:Adam19	UTSW	11	46,140,112 (GRCm38)	missense	probably damaging	0.96
R9163:Adam19	UTSW	11	46,127,349 (GRCm38)	missense	probably benign	0.02
R9349:Adam19	UTSW	11	46,131,743 (GRCm38)	nonsense	probably null
R9489:Adam19	UTSW	11	46,137,622 (GRCm38)	missense	probably benign	0.10
R9579:Adam19	UTSW	11	46,118,435 (GRCm38)	missense	probably benign	0.00
R9641:Adam19	UTSW	11	46,136,322 (GRCm38)	missense	probably damaging	1.00
X0067:Adam19	UTSW	11	46,056,115 (GRCm38)	start codon destroyed	probably null	0.06

Predicted Primers

PCR Primer
(F):5'- TTTGGCTGTGACCCAGAAGATAC -3'
(R):5'- AGGAAATTCAAACCTCCCTTTGC -3'

Sequencing Primer
(F):5'- CTGTGACCCAGAAGATACTAGGC -3'
(R):5'- TGCTCATGTAAGGTACAGCC -3'

Posted On

2019-05-13