Mutagenetix > Incidental Mutation

Incidental Mutation 'R7095:Adam32'

550425

Institutional Source

Beutler Lab

Gene Symbol

Adam32

Ensembl Gene

ENSMUSG00000037437

Gene Name

a disintegrin and metallopeptidase domain 32

Synonyms

MMRRC Submission

045243-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7095 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

25326156-25438820 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 25404086 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Valine at position 242 (D242V)

Ref Sequence

ENSEMBL: ENSMUSP00000113627 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000119720] [ENSMUST00000121438]

AlphaFold

Q8K410

Predicted Effect

possibly damaging
Transcript: ENSMUST00000119720
AA Change: D242V

PolyPhen 2 Score 0.754 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000113076
Gene: ENSMUSG00000037437
AA Change: D242V

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
Pfam:Pep_M12B_propep	32	145	4.5e-32	PFAM
Pfam:Reprolysin	187	384	4.1e-66	PFAM
Pfam:Reprolysin_3	211	318	6.2e-7	PFAM
DISIN	400	481	2.69e-16	SMART
ACR	482	622	6.83e-38	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000121438
AA Change: D242V

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

SMART Domains

Protein: ENSMUSP00000113627
Gene: ENSMUSG00000037437
AA Change: D242V

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
Pfam:Pep_M12B_propep	24	145	8.4e-26	PFAM
Pfam:Reprolysin	187	384	1.3e-68	PFAM
DISIN	400	481	2.69e-16	SMART
ACR	482	622	6.83e-38	SMART
EGF	631	660	1.73e0	SMART
transmembrane domain	689	711	N/A	INTRINSIC
low complexity region	719	754	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000174059

SMART Domains

Protein: ENSMUSP00000134680
Gene: ENSMUSG00000037437

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:Pep_M12B_propep	19	141	4.6e-27	PFAM

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.2%

Validation Efficiency

99% (71/72)

MGI Phenotype

FUNCTION: This gene encodes a member of the disintegrin family of membrane-anchored proteins that play a role in diverse biological processes such as brain development, fertilization, tumor development and inflammation. The encoded protein undergoes proteolytic processing to generate a mature polypeptide comprised of an metalloprotease, disintegrin and epidermal growth factor-like domains. This gene was found to be expressed predominantly in the pachytene spermatocytes, where the processed protein is localized to the sperm surface. This gene is located in a cluster of other disintegrin and metallopeptidase family genes on chromosome 8. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar processing to generate mature protein. [provided by RefSeq, Sep 2015]

Allele List at MGI

Other mutations in this stock

Total: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcf1	A	G	17: 36,268,403 (GRCm39)	V809A	possibly damaging	Het
Adamts9	T	A	6: 92,864,672 (GRCm39)	H763L	probably benign	Het
Aff1	A	G	5: 103,990,951 (GRCm39)	D967G	probably damaging	Het
Anpep	A	T	7: 79,491,950 (GRCm39)	L17Q	possibly damaging	Het
Appbp2	G	T	11: 85,125,553 (GRCm39)	S28*	probably null	Het
Bach1	G	A	16: 87,516,179 (GRCm39)	R240Q	probably benign	Het
Bod1l	A	G	5: 41,952,411 (GRCm39)		probably null	Het
Capn5	G	A	7: 97,775,038 (GRCm39)	T534I	probably benign	Het
Cbx2	T	C	11: 118,918,885 (GRCm39)	I150T	probably damaging	Het
Cdh11	A	G	8: 103,384,899 (GRCm39)	V392A	probably damaging	Het
Cenpf	A	T	1: 189,391,373 (GRCm39)	C803S	probably benign	Het
Cep135	A	G	5: 76,741,905 (GRCm39)	T114A	probably benign	Het
Chd2	A	T	7: 73,121,629 (GRCm39)	D994E	probably damaging	Het
Chtf18	C	A	17: 25,941,652 (GRCm39)	W584C	probably damaging	Het
Dclk2	C	T	3: 86,700,566 (GRCm39)	R638H	probably damaging	Het
Dgkh	C	A	14: 78,865,224 (GRCm39)	M172I	probably benign	Het
Dpy19l2	T	G	9: 24,607,110 (GRCm39)	H117P	probably benign	Het
Dzip3	A	T	16: 48,748,153 (GRCm39)	N908K	probably benign	Het
Erc2	A	T	14: 27,620,550 (GRCm39)	N393Y	probably damaging	Het
Fam118b	T	C	9: 35,132,786 (GRCm39)	E291G	possibly damaging	Het
Fam193a	C	T	5: 34,615,378 (GRCm39)	L816F	probably damaging	Het
Fat2	A	G	11: 55,202,157 (GRCm39)	Y306H	probably damaging	Het
Fndc10	C	T	4: 155,779,574 (GRCm39)	T206I	probably damaging	Het
Fzd1	GGGACTCCTCCACCTCCCTGGA	GGGA	5: 4,805,824 (GRCm39)		probably benign	Het
Gsk3a	A	T	7: 24,933,279 (GRCm39)	Y177N	probably damaging	Het
Haus5	T	C	7: 30,358,997 (GRCm39)	T222A	probably benign	Het
Igfbp7	G	T	5: 77,549,337 (GRCm39)	Q189K	probably benign	Het
Inppl1	A	T	7: 101,476,663 (GRCm39)	Y771*	probably null	Het
Iqck	A	T	7: 118,514,814 (GRCm39)	Y234F	probably damaging	Het
Irs1	G	T	1: 82,267,819 (GRCm39)	C132*	probably null	Het
Jmjd1c	T	G	10: 67,055,411 (GRCm39)	V277G	probably benign	Het
Klhl22	G	A	16: 17,610,614 (GRCm39)	V622M	probably damaging	Het
Kri1	C	T	9: 21,190,728 (GRCm39)	E378K		Het
Lilra6	C	T	7: 3,916,196 (GRCm39)	G221D	probably damaging	Het
Mecom	T	C	3: 30,035,103 (GRCm39)	E191G	probably damaging	Het
Mgrn1	T	A	16: 4,745,528 (GRCm39)		probably null	Het
Mical1	C	T	10: 41,355,206 (GRCm39)		probably null	Het
Mlxipl	T	C	5: 135,162,884 (GRCm39)	Y711H	possibly damaging	Het
Mpl	T	A	4: 118,301,260 (GRCm39)	H535L		Het
Mtarc1	A	G	1: 184,527,437 (GRCm39)	L297P	probably damaging	Het
Mtfr2	C	A	10: 20,228,666 (GRCm39)	H71N	probably benign	Het
Mtrf1	GCCTTC	GC	14: 79,660,931 (GRCm39)		probably null	Het
Myh15	A	G	16: 48,992,272 (GRCm39)	Q1582R	possibly damaging	Het
Neb	C	T	2: 52,067,635 (GRCm39)	E6062K	possibly damaging	Het
Nlrp4c	G	A	7: 6,063,792 (GRCm39)	A67T	probably damaging	Het
Noc3l	T	A	19: 38,800,789 (GRCm39)	H231L	probably benign	Het
Odf1	T	C	15: 38,219,803 (GRCm39)	Y44H	possibly damaging	Het
Or52e2	G	A	7: 102,804,537 (GRCm39)	T139I	probably damaging	Het
Or52s1b	C	T	7: 102,822,253 (GRCm39)	R197H	probably benign	Het
Or5j3	C	T	2: 86,129,021 (GRCm39)	P287L	probably benign	Het
Otol1	G	T	3: 69,926,027 (GRCm39)	E67D	probably benign	Het
Otud7b	A	G	3: 96,062,554 (GRCm39)	S598G	probably benign	Het
Ppwd1	T	A	13: 104,342,134 (GRCm39)	T607S	probably benign	Het
Prag1	A	G	8: 36,569,714 (GRCm39)	N99S	probably benign	Het
Ralgds	C	A	2: 28,439,320 (GRCm39)	Q737K	possibly damaging	Het
Scyl2	T	C	10: 89,505,549 (GRCm39)	H98R	probably damaging	Het
Secisbp2	A	C	13: 51,831,290 (GRCm39)	Q575H	probably benign	Het
Slc9a5	A	T	8: 106,084,268 (GRCm39)	H497L	probably benign	Het
Sufu	T	A	19: 46,464,027 (GRCm39)	V414E	probably damaging	Het
Tbc1d22b	A	T	17: 29,818,843 (GRCm39)	E399V	probably damaging	Het
Tcp10c	G	A	17: 13,576,196 (GRCm39)	V59I	probably benign	Het
Tdpoz3	T	C	3: 93,734,368 (GRCm39)	S348P	probably benign	Het
Tmem219	A	T	7: 126,490,928 (GRCm39)	F176L	probably damaging	Het
Trav6-2	A	G	14: 52,905,291 (GRCm39)	D104G	probably damaging	Het
Uba7	A	G	9: 107,860,538 (GRCm39)	K927R	probably benign	Het
Vps54	T	G	11: 21,221,720 (GRCm39)	D158E	probably benign	Het
Xpnpep1	C	T	19: 53,000,196 (GRCm39)		probably null	Het
Xpo7	G	A	14: 70,942,146 (GRCm39)	R73W	probably damaging	Het
Zfp532	A	T	18: 65,815,969 (GRCm39)	M781L	probably benign	Het
Zfp930	T	A	8: 69,681,193 (GRCm39)	I295K	probably benign	Het

Other mutations in Adam32

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00775:Adam32	APN	8	25,411,370 (GRCm39)	missense	probably damaging	1.00
IGL00793:Adam32	APN	8	25,327,846 (GRCm39)	splice site	probably benign
IGL01317:Adam32	APN	8	25,362,597 (GRCm39)	missense	probably damaging	1.00
IGL01475:Adam32	APN	8	25,362,664 (GRCm39)	missense	probably damaging	1.00
IGL01501:Adam32	APN	8	25,404,369 (GRCm39)	missense	probably damaging	1.00
IGL01659:Adam32	APN	8	25,360,790 (GRCm39)	splice site	probably benign
IGL01994:Adam32	APN	8	25,392,812 (GRCm39)	splice site	probably benign
IGL02137:Adam32	APN	8	25,362,610 (GRCm39)	missense	probably damaging	1.00
IGL02393:Adam32	APN	8	25,410,069 (GRCm39)	missense	probably damaging	1.00
IGL02516:Adam32	APN	8	25,388,612 (GRCm39)	missense	probably damaging	1.00
IGL02892:Adam32	APN	8	25,368,727 (GRCm39)	intron	probably benign
IGL02929:Adam32	APN	8	25,362,659 (GRCm39)	missense	possibly damaging	0.81
IGL03273:Adam32	APN	8	25,411,356 (GRCm39)	missense	probably damaging	1.00
PIT4515001:Adam32	UTSW	8	25,404,342 (GRCm39)	missense	possibly damaging	0.88
R0088:Adam32	UTSW	8	25,404,083 (GRCm39)	missense	probably damaging	1.00
R0098:Adam32	UTSW	8	25,404,405 (GRCm39)	missense	possibly damaging	0.79
R0098:Adam32	UTSW	8	25,404,405 (GRCm39)	missense	possibly damaging	0.79
R0189:Adam32	UTSW	8	25,412,353 (GRCm39)	critical splice acceptor site	probably null
R1740:Adam32	UTSW	8	25,411,314 (GRCm39)	missense	probably damaging	1.00
R1853:Adam32	UTSW	8	25,388,642 (GRCm39)	missense	probably benign	0.02
R2090:Adam32	UTSW	8	25,391,456 (GRCm39)	critical splice donor site	probably null
R2906:Adam32	UTSW	8	25,353,520 (GRCm39)	missense	probably damaging	1.00
R2907:Adam32	UTSW	8	25,353,520 (GRCm39)	missense	probably damaging	1.00
R4304:Adam32	UTSW	8	25,391,545 (GRCm39)	missense	probably damaging	1.00
R4612:Adam32	UTSW	8	25,362,752 (GRCm39)	missense	probably damaging	1.00
R4673:Adam32	UTSW	8	25,374,471 (GRCm39)	missense	probably damaging	1.00
R4786:Adam32	UTSW	8	25,353,509 (GRCm39)	missense	probably damaging	1.00
R5292:Adam32	UTSW	8	25,354,467 (GRCm39)	missense	possibly damaging	0.85
R5398:Adam32	UTSW	8	25,362,595 (GRCm39)	missense	possibly damaging	0.95
R5524:Adam32	UTSW	8	25,412,328 (GRCm39)	missense	probably damaging	0.99
R5939:Adam32	UTSW	8	25,404,138 (GRCm39)	missense	probably damaging	1.00
R6350:Adam32	UTSW	8	25,353,445 (GRCm39)	missense	possibly damaging	0.86
R6766:Adam32	UTSW	8	25,362,646 (GRCm39)	missense	probably damaging	0.96
R6893:Adam32	UTSW	8	25,368,770 (GRCm39)	missense	probably damaging	1.00
R7241:Adam32	UTSW	8	25,388,510 (GRCm39)	missense	probably benign	0.00
R7457:Adam32	UTSW	8	25,374,635 (GRCm39)	missense	probably damaging	0.98
R7864:Adam32	UTSW	8	25,412,292 (GRCm39)	missense	probably benign	0.11
R8083:Adam32	UTSW	8	25,362,752 (GRCm39)	missense	probably damaging	1.00
R8248:Adam32	UTSW	8	25,391,486 (GRCm39)	missense	possibly damaging	0.93
R8376:Adam32	UTSW	8	25,409,936 (GRCm39)	missense	possibly damaging	0.81
R8681:Adam32	UTSW	8	25,327,811 (GRCm39)	missense	unknown
R9154:Adam32	UTSW	8	25,438,769 (GRCm39)	small deletion	probably benign
R9391:Adam32	UTSW	8	25,374,472 (GRCm39)	missense	probably damaging	0.99
Z1176:Adam32	UTSW	8	25,438,766 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- CTGGATTAAGCTATAGCATGTGTC -3'
(R):5'- TATGATTACTTGGGCTCTGACAG -3'

Sequencing Primer
(F):5'- AGCTATAGCATGTGTCTTATGTTTTC -3'
(R):5'- GCTCTGACAGCAATATTGTAA -3'

Posted On

2019-05-15