Mutagenetix > Incidental Mutation

Incidental Mutation 'R7486:Adam21'

580194

Institutional Source

Beutler Lab

Gene Symbol

Adam21

Ensembl Gene

ENSMUSG00000008438

Gene Name

a disintegrin and metallopeptidase domain 21

Synonyms

ADAM31

MMRRC Submission

045560-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7486 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

81605358-81615248 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 81605657 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 702 (I702V)

Ref Sequence

ENSEMBL: ENSMUSP00000008582 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000008582]

AlphaFold

Q9JI76

Predicted Effect

probably benign
Transcript: ENSMUST00000008582
AA Change: I702V

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000008582
Gene: ENSMUSG00000008438
AA Change: I702V

Domain	Start	End	E-Value	Type
signal peptide	1	33	N/A	INTRINSIC
Pfam:Pep_M12B_propep	39	164	5.1e-21	PFAM
Pfam:Reprolysin_4	212	389	2.5e-11	PFAM
Pfam:Reprolysin	212	402	7.3e-50	PFAM
Pfam:Reprolysin_5	214	400	5.8e-19	PFAM
Pfam:Reprolysin_2	233	393	1.3e-14	PFAM
Pfam:Reprolysin_3	236	356	6.5e-16	PFAM
DISIN	419	494	2.45e-37	SMART
ACR	495	631	6.49e-62	SMART
EGF	637	667	2.03e1	SMART
transmembrane domain	687	709	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

MGI Phenotype

FUNCTION: This gene encodes a member of a disintegrin and metalloprotease (ADAM) family of endoproteases that play important roles in various biological processes including cell signaling, adhesion and migration. The encoded preproprotein undergoes proteolytic processing to generate a mature, functional metalloprotease enzyme. The encoded protein functions in the regulation of spermatogenesis in the testes and neurogenesis in the central nervous system. [provided by RefSeq, May 2016]
PHENOTYPE: Mice homozygous for disruptions in this gene display a normal phenotype. [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
Adgre5	T	C	8: 84,450,515 (GRCm39)	E815G	probably damaging	Het
Adgrl2	A	G	3: 148,523,330 (GRCm39)	V298A		Het
Akp3	A	G	1: 87,053,201 (GRCm39)	D91G	probably damaging	Het
Ano8	A	G	8: 71,937,642 (GRCm39)		probably null	Het
Blvra	T	C	2: 126,929,243 (GRCm39)	S136P	unknown	Het
Cacul1	T	A	19: 60,568,868 (GRCm39)	M97L	probably benign	Het
Ccdc80	T	C	16: 44,946,542 (GRCm39)	V827A	probably damaging	Het
Cep68	T	C	11: 20,192,166 (GRCm39)	E11G	probably benign	Het
Cfap221	A	T	1: 119,851,322 (GRCm39)	V813E	possibly damaging	Het
Chd6	A	G	2: 160,791,923 (GRCm39)	V2478A	probably damaging	Het
Chmp6	T	C	11: 119,807,783 (GRCm39)	F148S	probably benign	Het
Clca3a2	T	A	3: 144,503,362 (GRCm39)	I863F	probably damaging	Het
Cnnm2	T	C	19: 46,750,513 (GRCm39)	V101A	possibly damaging	Het
Cpne8	A	T	15: 90,400,109 (GRCm39)		probably null	Het
Dmbt1	T	G	7: 130,668,192 (GRCm39)	C483G	unknown	Het
Dnah7b	G	A	1: 46,329,894 (GRCm39)	G3246D	probably damaging	Het
Dnajc3	C	A	14: 119,209,816 (GRCm39)	T297K	probably benign	Het
Dpm3	A	G	3: 89,174,034 (GRCm39)		probably null	Het
Eef2k	A	G	7: 120,457,793 (GRCm39)	N51D	probably benign	Het
Erc1	G	A	6: 119,571,907 (GRCm39)	Q1022*	probably null	Het
Ercc5	T	A	1: 44,187,224 (GRCm39)	M1K	probably null	Het
Fam114a2	C	T	11: 57,404,515 (GRCm39)	G83D	probably damaging	Het
Fat4	C	A	3: 39,011,576 (GRCm39)	Y2225*	probably null	Het
Frk	G	A	10: 34,423,292 (GRCm39)	W123*	probably null	Het
Gm11568	T	A	11: 99,749,292 (GRCm39)	C166S	unknown	Het
Gpr153	A	G	4: 152,366,858 (GRCm39)	D337G	probably benign	Het
Gpt2	T	C	8: 86,252,235 (GRCm39)	F517L	probably damaging	Het
Gsg1	C	T	6: 135,214,427 (GRCm39)	E361K	probably benign	Het
Hsfy2	G	A	1: 56,676,130 (GRCm39)	R136*	probably null	Het
Insm1	G	A	2: 146,065,738 (GRCm39)	R518H	probably damaging	Het
Kank1	G	A	19: 25,388,193 (GRCm39)	C622Y	probably damaging	Het
Katnb1	T	A	8: 95,825,357 (GRCm39)	S640R	probably damaging	Het
Kcnmb4	A	G	10: 116,254,180 (GRCm39)	V199A	probably benign	Het
Lamb1	T	G	12: 31,337,441 (GRCm39)	S391A	probably benign	Het
Larp7-ps	A	T	4: 92,079,506 (GRCm39)	V105E	probably benign	Het
Macf1	T	G	4: 123,303,374 (GRCm39)	D376A	probably benign	Het
Map7d1	C	A	4: 126,128,179 (GRCm39)	R614L	unknown	Het
Mcm8	C	T	2: 132,681,440 (GRCm39)	R667W	probably damaging	Het
Med13l	C	T	5: 118,866,539 (GRCm39)	T531I	probably benign	Het
Mstn	G	T	1: 53,103,128 (GRCm39)	A155S	probably damaging	Het
Mycbp2	C	T	14: 103,434,690 (GRCm39)	R2251K	probably damaging	Het
Myo19	T	C	11: 84,796,463 (GRCm39)	S692P	probably benign	Het
Nipbl	A	T	15: 8,325,120 (GRCm39)	N2514K	probably benign	Het
Nkd2	T	A	13: 73,995,561 (GRCm39)		probably benign	Het
Nox3	T	A	17: 3,720,219 (GRCm39)	Y322F	probably damaging	Het
Nt5dc1	A	G	10: 34,275,805 (GRCm39)	Y135H	probably benign	Het
Oog3	T	A	4: 143,884,742 (GRCm39)	H398L	probably benign	Het
Or10g9	T	A	9: 39,912,181 (GRCm39)	Y114F	probably benign	Het
Or12j4	C	T	7: 140,045,947 (GRCm39)		probably benign	Het
Or1e29	T	C	11: 73,667,847 (GRCm39)	Y102C	probably damaging	Het
Otogl	A	G	10: 107,657,849 (GRCm39)	L1027P	probably damaging	Het
Pcdh20	T	A	14: 88,706,050 (GRCm39)	I417F	possibly damaging	Het
Pcdha12	T	A	18: 37,154,610 (GRCm39)	V443E	probably damaging	Het
Pcdhga2	A	G	18: 37,803,461 (GRCm39)	D435G	probably benign	Het
Pcnt	G	T	10: 76,254,270 (GRCm39)	T853K	probably benign	Het
Pcnt	T	C	10: 76,254,271 (GRCm39)	T853A	probably benign	Het
Pgghg	T	A	7: 140,522,393 (GRCm39)	S57R	probably benign	Het
Ppm1m	T	C	9: 106,073,810 (GRCm39)	D301G	probably damaging	Het
Ppp6r1	A	G	7: 4,642,899 (GRCm39)	V519A	probably benign	Het
Prss41	ACAGCAGCAGCAGCAGCAGCA	ACAGCAGCAGCAGCAGCA	17: 24,063,072 (GRCm39)		probably benign	Het
Rasa3	C	T	8: 13,640,201 (GRCm39)		probably null	Het
Robo4	T	C	9: 37,316,870 (GRCm39)	V395A	probably damaging	Het
Scrib	A	G	15: 75,929,499 (GRCm39)	S1123P	probably damaging	Het
Setd1b	A	G	5: 123,301,655 (GRCm39)	K45E	probably benign	Het
Slc14a1	T	C	18: 78,154,739 (GRCm39)	S216G	probably benign	Het
Slc25a45	A	G	19: 5,934,997 (GRCm39)	Y282C	probably damaging	Het
Slc6a5	T	C	7: 49,567,078 (GRCm39)	S255P	possibly damaging	Het
Smc2	A	T	4: 52,462,861 (GRCm39)	Q617L	possibly damaging	Het
Spo11	G	A	2: 172,825,870 (GRCm39)	D103N	probably benign	Het
Tcf20	A	T	15: 82,737,935 (GRCm39)	M1172K	possibly damaging	Het
Tesc	T	A	5: 118,184,382 (GRCm39)	S21T	probably benign	Het
Tie1	C	A	4: 118,337,101 (GRCm39)		probably null	Het
Trim24	T	G	6: 37,934,774 (GRCm39)		probably null	Het
Trpm7	A	G	2: 126,673,115 (GRCm39)		probably null	Het
Unc13d	T	C	11: 115,965,259 (GRCm39)	D193G	possibly damaging	Het
Upk3a	A	T	15: 84,902,225 (GRCm39)		probably null	Het
Vmn2r25	T	C	6: 123,800,101 (GRCm39)	N747S	probably damaging	Het
Wipf1	GCCTCCTCCTCCTCCTCCTCCTCC	GCCTCCTCCTCCTCCTCCTCC	2: 73,270,418 (GRCm39)		probably benign	Het
Zbtb2	G	A	10: 4,319,025 (GRCm39)	Q334*	probably null	Het
Zfp653	T	C	9: 21,967,824 (GRCm39)	N494D	probably damaging	Het
Zfp865	A	G	7: 5,034,259 (GRCm39)	D748G	possibly damaging	Het
Zzef1	T	C	11: 72,755,612 (GRCm39)	S1014P	possibly damaging	Het

Other mutations in Adam21

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02186:Adam21	APN	12	81,605,983 (GRCm39)	missense	possibly damaging	0.61
IGL02311:Adam21	APN	12	81,607,666 (GRCm39)	missense	probably benign	0.01
IGL03132:Adam21	APN	12	81,607,148 (GRCm39)	nonsense	probably null
IGL03225:Adam21	APN	12	81,606,043 (GRCm39)	missense	probably benign	0.00
BB009:Adam21	UTSW	12	81,606,938 (GRCm39)	missense	probably damaging	0.98
BB019:Adam21	UTSW	12	81,606,938 (GRCm39)	missense	probably damaging	0.98
R0305:Adam21	UTSW	12	81,607,059 (GRCm39)	missense	possibly damaging	0.96
R0634:Adam21	UTSW	12	81,607,126 (GRCm39)	missense	probably benign	0.01
R1415:Adam21	UTSW	12	81,606,321 (GRCm39)	nonsense	probably null
R1961:Adam21	UTSW	12	81,606,282 (GRCm39)	nonsense	probably null
R1996:Adam21	UTSW	12	81,606,376 (GRCm39)	missense	possibly damaging	0.79
R2159:Adam21	UTSW	12	81,607,241 (GRCm39)	missense	probably benign	0.17
R2215:Adam21	UTSW	12	81,607,064 (GRCm39)	missense	probably damaging	1.00
R3780:Adam21	UTSW	12	81,606,047 (GRCm39)	missense	probably damaging	1.00
R3964:Adam21	UTSW	12	81,607,583 (GRCm39)	missense	possibly damaging	0.46
R4356:Adam21	UTSW	12	81,605,594 (GRCm39)	missense	probably damaging	0.99
R4503:Adam21	UTSW	12	81,607,672 (GRCm39)	missense	probably benign
R4795:Adam21	UTSW	12	81,607,748 (GRCm39)	missense	probably benign	0.06
R4925:Adam21	UTSW	12	81,607,163 (GRCm39)	missense	probably benign
R4932:Adam21	UTSW	12	81,605,692 (GRCm39)	missense	probably benign	0.14
R5110:Adam21	UTSW	12	81,606,989 (GRCm39)	missense	probably benign	0.40
R5831:Adam21	UTSW	12	81,605,875 (GRCm39)	missense	probably benign	0.06
R6289:Adam21	UTSW	12	81,607,480 (GRCm39)	missense	probably damaging	1.00
R6500:Adam21	UTSW	12	81,606,380 (GRCm39)	missense	probably benign	0.01
R7077:Adam21	UTSW	12	81,605,893 (GRCm39)	missense	probably damaging	1.00
R7083:Adam21	UTSW	12	81,607,015 (GRCm39)	missense	possibly damaging	0.81
R7173:Adam21	UTSW	12	81,606,008 (GRCm39)	missense	probably benign	0.24
R7176:Adam21	UTSW	12	81,607,022 (GRCm39)	missense	possibly damaging	0.94
R7232:Adam21	UTSW	12	81,607,330 (GRCm39)	missense	probably damaging	0.99
R7371:Adam21	UTSW	12	81,607,064 (GRCm39)	missense	probably damaging	1.00
R7522:Adam21	UTSW	12	81,605,722 (GRCm39)	missense	possibly damaging	0.78
R7918:Adam21	UTSW	12	81,607,378 (GRCm39)	missense	possibly damaging	0.64
R7932:Adam21	UTSW	12	81,606,938 (GRCm39)	missense	probably damaging	0.98
R8040:Adam21	UTSW	12	81,607,211 (GRCm39)	missense	probably benign	0.04
R8486:Adam21	UTSW	12	81,607,550 (GRCm39)	missense	probably benign	0.08
R8750:Adam21	UTSW	12	81,607,247 (GRCm39)	nonsense	probably null
R8881:Adam21	UTSW	12	81,606,650 (GRCm39)	missense	probably benign	0.02
R9084:Adam21	UTSW	12	81,606,160 (GRCm39)	missense	probably damaging	1.00
R9541:Adam21	UTSW	12	81,607,724 (GRCm39)	missense	probably benign
R9564:Adam21	UTSW	12	81,605,833 (GRCm39)	missense	probably damaging	1.00
Z1088:Adam21	UTSW	12	81,607,460 (GRCm39)	missense	probably damaging	1.00
Z1176:Adam21	UTSW	12	81,606,517 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCCTGGTGACAATATTTCTGATAC -3'
(R):5'- GCTTGCCTTCCTGAGACTTG -3'

Sequencing Primer
(F):5'- TCCTGTAAACTCTCAGAAATATGCC -3'
(R):5'- CCTTCCTGAGACTTGTAATAGGAAGG -3'

Posted On

2019-10-07