Mutagenetix > Incidental Mutation

Incidental Mutation 'R8895:Adamts10'

677989

Institutional Source

Beutler Lab

Gene Symbol

Adamts10

Ensembl Gene

ENSMUSG00000024299

Gene Name

ADAM metallopeptidase with thrombospondin type 1 motif 10

Synonyms

ZnMP

MMRRC Submission

068754-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.325) question?

Stock #

R8895 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

33743178-33772756 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 33768270 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Histidine at position 814 (R814H)

Ref Sequence

ENSEMBL: ENSMUSP00000084905 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000087623] [ENSMUST00000172922] [ENSMUST00000173013] [ENSMUST00000173030] [ENSMUST00000173241] [ENSMUST00000173931]

AlphaFold

P58459

Predicted Effect

probably damaging
Transcript: ENSMUST00000087623
AA Change: R814H

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000084905
Gene: ENSMUSG00000024299
AA Change: R814H

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:Pep_M12B_propep	40	180	1.3e-33	PFAM
Pfam:Reprolysin_5	237	432	5e-15	PFAM
Pfam:Reprolysin_4	237	448	5e-11	PFAM
Pfam:Reprolysin	239	457	1.6e-25	PFAM
Pfam:Reprolysin_2	257	447	1.2e-13	PFAM
Pfam:Reprolysin_3	261	403	5.7e-13	PFAM
TSP1	550	602	7.21e-11	SMART
Pfam:ADAM_spacer1	706	818	1.3e-27	PFAM
TSP1	828	885	4.73e-6	SMART
TSP1	887	940	4.35e-2	SMART
TSP1	948	1003	2.66e-2	SMART
TSP1	1006	1058	9.98e-5	SMART
Pfam:PLAC	1070	1102	8.4e-12	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000172922

SMART Domains

Protein: ENSMUSP00000133891
Gene: ENSMUSG00000024299

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:Pep_M12B_propep	39	180	1.1e-30	PFAM
SCOP:d1bkca_	238	271	4e-7	SMART
low complexity region	285	296	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000173013

SMART Domains

Protein: ENSMUSP00000134181
Gene: ENSMUSG00000024299

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:Pep_M12B_propep	39	180	9.6e-31	PFAM
SCOP:d1bkca_	238	271	3e-7	SMART
low complexity region	285	296	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000173030

SMART Domains

Protein: ENSMUSP00000134549
Gene: ENSMUSG00000024299

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:Pep_M12B_propep	39	180	9.6e-31	PFAM
SCOP:d1bkca_	238	271	3e-7	SMART
low complexity region	285	296	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000173241

SMART Domains

Protein: ENSMUSP00000134298
Gene: ENSMUSG00000024299

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:Pep_M12B_propep	39	180	9.6e-31	PFAM
SCOP:d1bkca_	238	271	3e-7	SMART
low complexity region	285	296	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000173931

SMART Domains

Protein: ENSMUSP00000133434
Gene: ENSMUSG00000024299

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:Pep_M12B_propep	39	180	9.6e-31	PFAM
SCOP:d1bkca_	238	271	3e-7	SMART
low complexity region	285	296	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000174348

SMART Domains

Protein: ENSMUSP00000133856
Gene: ENSMUSG00000024299

Domain	Start	End	E-Value	Type
Pfam:Reprolysin_5	23	220	2.6e-16	PFAM
Pfam:Reprolysin_4	23	235	2.6e-12	PFAM
Pfam:Reprolysin	25	243	1e-26	PFAM
Pfam:Reprolysin_2	43	233	7.1e-15	PFAM
Pfam:Reprolysin_3	47	189	4.7e-14	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (74/74)

MGI Phenotype

FUNCTION: This gene encodes a member of "a disintegrin and metalloproteinase with thrombospondin motifs" (ADAMTS) family of multi-domain matrix-associated metalloendopeptidases that have diverse roles in tissue morphogenesis and pathophysiological remodeling, in inflammation and in vascular biology. The encoded preproprotein undergoes proteolytic processing to generate a functional, zinc-dependent metallopeptidase enzyme. [provided by RefSeq, Jul 2016]

Allele List at MGI

Other mutations in this stock

Total: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930567H17Rik	G	A	X: 69,437,994 (GRCm39)	R100W	possibly damaging	Het
Akr1a1	A	G	4: 116,498,260 (GRCm39)	L95P	probably damaging	Het
Amigo2	G	T	15: 97,143,389 (GRCm39)	N344K	probably damaging	Het
Ankrd11	T	C	8: 123,621,014 (GRCm39)	D946G	possibly damaging	Het
Arb2a	T	A	13: 78,147,773 (GRCm39)	N280K	probably damaging	Het
Btnl6	T	G	17: 34,734,391 (GRCm39)	I124L	probably benign	Het
Bzw2	A	T	12: 36,173,982 (GRCm39)	C97*	probably null	Het
Celsr2	G	A	3: 108,320,880 (GRCm39)	T644I	possibly damaging	Het
Cep85l	A	T	10: 53,224,911 (GRCm39)	L226Q	possibly damaging	Het
Ces1g	T	C	8: 94,046,512 (GRCm39)	K338E	possibly damaging	Het
Cldn10	G	A	14: 119,092,507 (GRCm39)	D36N	probably damaging	Het
Cntnap4	T	A	8: 113,479,598 (GRCm39)	I261N	probably benign	Het
Csnk1g1	T	C	9: 65,915,109 (GRCm39)		probably null	Het
Cyp2c69	T	C	19: 39,869,910 (GRCm39)	D104G	possibly damaging	Het
Cyp3a11	T	C	5: 145,797,330 (GRCm39)	T350A	probably benign	Het
Daw1	T	A	1: 83,187,011 (GRCm39)	C274S	probably damaging	Het
Dmtn	T	C	14: 70,850,144 (GRCm39)	T267A	probably benign	Het
Dock5	A	G	14: 68,055,112 (GRCm39)	Y585H	possibly damaging	Het
Dsg2	T	G	18: 20,723,126 (GRCm39)	V384G	probably damaging	Het
Elmo1	C	T	13: 20,748,630 (GRCm39)	L492F	probably damaging	Het
Fmo1	T	C	1: 162,657,827 (GRCm39)	D438G	probably benign	Het
Folr2	C	T	7: 101,489,408 (GRCm39)	V244M	unknown	Het
Galnt18	T	C	7: 111,378,709 (GRCm39)	I16V	possibly damaging	Het
Gm10036	C	A	18: 15,966,207 (GRCm39)	Y119*	probably null	Het
Gria4	A	G	9: 4,664,951 (GRCm39)	S102P	probably damaging	Het
Hc	A	T	2: 34,890,861 (GRCm39)	N1318K	probably benign	Het
Ifitm1	T	C	7: 140,549,499 (GRCm39)	L94P	probably damaging	Het
Iqca1l	T	C	5: 24,755,628 (GRCm39)	D298G	probably benign	Het
Itga9	G	A	9: 118,510,835 (GRCm39)	V455M	probably damaging	Het
Kank4	C	T	4: 98,653,747 (GRCm39)	V894I	possibly damaging	Het
Kcnip2	T	A	19: 45,785,100 (GRCm39)		probably benign	Het
Lamb1	A	G	12: 31,352,953 (GRCm39)	T885A	possibly damaging	Het
Lamp5	A	G	2: 135,902,874 (GRCm39)	T198A	probably benign	Het
Ldc1	T	C	4: 130,105,223 (GRCm39)	K316E	probably benign	Het
Lipi	A	T	16: 75,352,710 (GRCm39)	L376I	probably benign	Het
Lrrc37	T	A	11: 103,509,656 (GRCm39)	T771S	unknown	Het
Luc7l	T	C	17: 26,472,978 (GRCm39)	I31T	possibly damaging	Het
Malrd1	A	T	2: 15,850,038 (GRCm39)	N1219I	unknown	Het
Mcf2l	C	T	8: 13,034,330 (GRCm39)		probably benign	Het
Mrc1	A	C	2: 14,312,760 (GRCm39)	N894T	probably damaging	Het
Mrpl35	C	T	6: 71,793,271 (GRCm39)	A127T	possibly damaging	Het
Myom2	T	A	8: 15,152,589 (GRCm39)	Y645*	probably null	Het
Naip2	T	C	13: 100,325,644 (GRCm39)	H88R	probably benign	Het
Noc3l	T	A	19: 38,798,751 (GRCm39)	K282N	probably damaging	Het
Nwd2	T	C	5: 63,963,241 (GRCm39)	Y942H	probably damaging	Het
Or10ag2	T	C	2: 87,248,659 (GRCm39)	V87A	probably benign	Het
Or52d1	T	A	7: 103,756,302 (GRCm39)	I272N	probably damaging	Het
Osbpl9	C	A	4: 108,930,333 (GRCm39)	A221S	probably benign	Het
Paip1	T	C	13: 119,566,801 (GRCm39)	L45S	probably benign	Het
Peak1	T	C	9: 56,113,938 (GRCm39)	T1668A	probably benign	Het
Pgap3	A	G	11: 98,281,602 (GRCm39)	F199L	possibly damaging	Het
Ppip5k2	T	C	1: 97,639,544 (GRCm39)	M1061V	probably benign	Het
Ppp6r3	A	T	19: 3,544,017 (GRCm39)	W333R	probably damaging	Het
Ptk2b	T	A	14: 66,412,242 (GRCm39)	N383I	probably benign	Het
Rab21	G	C	10: 115,151,080 (GRCm39)	R58G	probably benign	Het
Rabif	C	T	1: 134,433,935 (GRCm39)	T83I	probably damaging	Het
Rdh7	A	T	10: 127,724,430 (GRCm39)	F18Y	probably benign	Het
Scart2	C	T	7: 139,841,532 (GRCm39)	P279S	possibly damaging	Het
Septin5	A	G	16: 18,441,861 (GRCm39)	M315T	possibly damaging	Het
Slc27a6	A	G	18: 58,715,306 (GRCm39)	Y303C	probably damaging	Het
Slc7a7	T	A	14: 54,607,293 (GRCm39)	M495L	probably benign	Het
Sntg1	T	A	1: 8,748,074 (GRCm39)		probably null	Het
Spred2	T	A	11: 19,951,019 (GRCm39)	I72N	probably benign	Het
St3gal1	A	T	15: 66,980,086 (GRCm39)	I271N	possibly damaging	Het
Stox1	A	T	10: 62,495,386 (GRCm39)	H962Q	probably benign	Het
Supt6	A	T	11: 78,103,664 (GRCm39)	M1347K	probably damaging	Het
Susd2	G	T	10: 75,475,452 (GRCm39)	A484D	possibly damaging	Het
Tmem260	A	G	14: 48,737,845 (GRCm39)		probably benign	Het
Tpbg	C	A	9: 85,726,520 (GRCm39)	A163E	possibly damaging	Het
Tpx2	T	C	2: 152,724,255 (GRCm39)	Y344H	probably damaging	Het
Ttf2	A	T	3: 100,870,028 (GRCm39)	F348L	probably benign	Het
Ttn	A	T	2: 76,663,650 (GRCm39)	V11675E	unknown	Het
Txnl4b	T	A	8: 110,299,467 (GRCm39)	Y142*	probably null	Het
Vmn2r18	G	A	5: 151,485,140 (GRCm39)	R785C	possibly damaging	Het
Zbtb18	T	A	1: 177,276,044 (GRCm39)	V459E	probably damaging	Het

Other mutations in Adamts10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01541:Adamts10	APN	17	33,762,205 (GRCm39)	missense	probably benign	0.24
IGL01865:Adamts10	APN	17	33,772,140 (GRCm39)	missense	probably damaging	0.99
IGL02391:Adamts10	APN	17	33,747,785 (GRCm39)	missense	probably benign	0.00
IGL02711:Adamts10	APN	17	33,757,246 (GRCm39)	missense	probably damaging	0.99
R0122:Adamts10	UTSW	17	33,747,454 (GRCm39)	unclassified	probably benign
R0207:Adamts10	UTSW	17	33,764,364 (GRCm39)	missense	possibly damaging	0.64
R0481:Adamts10	UTSW	17	33,768,347 (GRCm39)	nonsense	probably null
R0508:Adamts10	UTSW	17	33,762,692 (GRCm39)	missense	probably damaging	1.00
R0558:Adamts10	UTSW	17	33,769,583 (GRCm39)	missense	probably benign	0.04
R0746:Adamts10	UTSW	17	33,768,521 (GRCm39)	nonsense	probably null
R1027:Adamts10	UTSW	17	33,762,737 (GRCm39)	missense	probably benign	0.44
R1449:Adamts10	UTSW	17	33,764,613 (GRCm39)	missense	probably damaging	0.96
R1471:Adamts10	UTSW	17	33,772,112 (GRCm39)	missense	probably damaging	1.00
R1522:Adamts10	UTSW	17	33,756,293 (GRCm39)	missense	probably benign	0.40
R1631:Adamts10	UTSW	17	33,756,316 (GRCm39)	missense	probably benign	0.25
R1863:Adamts10	UTSW	17	33,770,406 (GRCm39)	critical splice donor site	probably null
R1913:Adamts10	UTSW	17	33,768,529 (GRCm39)	missense	probably benign	0.00
R2091:Adamts10	UTSW	17	33,770,166 (GRCm39)	critical splice donor site	probably null
R2377:Adamts10	UTSW	17	33,747,866 (GRCm39)	missense	probably damaging	1.00
R3743:Adamts10	UTSW	17	33,747,686 (GRCm39)	missense	probably damaging	1.00
R4042:Adamts10	UTSW	17	33,768,514 (GRCm39)	missense	possibly damaging	0.69
R4646:Adamts10	UTSW	17	33,764,529 (GRCm39)	missense	probably damaging	1.00
R4654:Adamts10	UTSW	17	33,756,304 (GRCm39)	missense	possibly damaging	0.89
R4695:Adamts10	UTSW	17	33,750,713 (GRCm39)	missense	possibly damaging	0.95
R4721:Adamts10	UTSW	17	33,764,511 (GRCm39)	splice site	probably null
R4798:Adamts10	UTSW	17	33,747,726 (GRCm39)	missense	probably damaging	1.00
R4896:Adamts10	UTSW	17	33,747,870 (GRCm39)	missense	possibly damaging	0.90
R7454:Adamts10	UTSW	17	33,763,979 (GRCm39)	missense	possibly damaging	0.89
R7494:Adamts10	UTSW	17	33,768,352 (GRCm39)	nonsense	probably null
R7541:Adamts10	UTSW	17	33,750,590 (GRCm39)	missense	probably benign	0.00
R7704:Adamts10	UTSW	17	33,770,126 (GRCm39)	missense	probably damaging	1.00
R7955:Adamts10	UTSW	17	33,764,613 (GRCm39)	missense	probably damaging	0.96
R8154:Adamts10	UTSW	17	33,756,902 (GRCm39)	missense	probably damaging	1.00
R8986:Adamts10	UTSW	17	33,762,668 (GRCm39)	missense	probably benign	0.09
R9116:Adamts10	UTSW	17	33,756,330 (GRCm39)	missense	probably benign	0.31
Z1176:Adamts10	UTSW	17	33,747,762 (GRCm39)	missense	probably damaging	1.00
Z1176:Adamts10	UTSW	17	33,747,761 (GRCm39)	missense	probably damaging	1.00
Z1177:Adamts10	UTSW	17	33,764,568 (GRCm39)	missense	probably damaging	0.99
Z1177:Adamts10	UTSW	17	33,764,403 (GRCm39)	missense	possibly damaging	0.76

Predicted Primers

PCR Primer
(F):5'- ATTTCATCTACGGCAGGGGC -3'
(R):5'- GATTTCGGCACTCCACTACTTG -3'

Sequencing Primer
(F):5'- ACAGAGCCTGGAAGCCCTG -3'
(R):5'- ACTACTTGGACCTGGCTGC -3'

Posted On

2021-08-02