Mutagenetix > Incidental Mutation

Incidental Mutation 'R1440:Adam12'

160929

Institutional Source

Beutler Lab

Gene Symbol

Adam12

Ensembl Gene

ENSMUSG00000054555

Gene Name

ADAM metallopeptidase domain 12

Synonyms

Mltna, ADAM12

MMRRC Submission

039495-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.386) question?

Stock #

R1440 (G1)

Quality Score

215

Status

Validated

Chromosome

Chromosomal Location

133484928-133826826 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 133533543 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Methionine at position 445 (T445M)

Ref Sequence

ENSEMBL: ENSMUSP00000065213 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000067680] [ENSMUST00000138363]

AlphaFold

Q61824

Predicted Effect

probably benign
Transcript: ENSMUST00000067680
AA Change: T445M

PolyPhen 2 Score 0.032 (Sensitivity: 0.95; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000065213
Gene: ENSMUSG00000054555
AA Change: T445M

Domain	Start	End	E-Value	Type
signal peptide	1	31	N/A	INTRINSIC
Pfam:Pep_M12B_propep	35	165	1.1e-27	PFAM
Pfam:Reprolysin_5	210	392	2.1e-24	PFAM
Pfam:Reprolysin_4	210	408	3.8e-16	PFAM
Pfam:Reprolysin	212	414	1.4e-74	PFAM
Pfam:Reprolysin_2	232	404	6e-18	PFAM
Pfam:Reprolysin_3	236	359	1.3e-16	PFAM
DISIN	431	506	4.29e-42	SMART
ACR	507	650	1.75e-67	SMART
transmembrane domain	705	727	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000138363
AA Change: T123M

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000114874
Gene: ENSMUSG00000054555
AA Change: T123M

Domain	Start	End	E-Value	Type
Pfam:Reprolysin	4	92	4.5e-24	PFAM
Pfam:Reprolysin_2	6	82	2.1e-11	PFAM
Pfam:Reprolysin_5	9	70	2.8e-11	PFAM
Pfam:Reprolysin_4	11	87	8.9e-8	PFAM
DISIN	109	184	4.29e-42	SMART
ACR	185	328	1.75e-67	SMART
transmembrane domain	383	405	N/A	INTRINSIC

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 98.8%
3x: 97.7%
10x: 94.0%
20x: 84.7%

Validation Efficiency

95% (94/99)

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 protein that localizes to the cell surface. About a third of the mice lacking the encoded protein die before weaning. Overexpression of the encoded protein in a mouse model of Duchenne muscular dystrophy alleviates the muscle pathology by preventing cell necrosis and inflammation. [provided by RefSeq, May 2016]
PHENOTYPE: Homozygous null mice display partial postnatal lethality, decreased brown fat, and impaired formation of neck and interscapular muscles. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 91 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930447C04Rik	T	G	12: 72,928,195 (GRCm39)	N512T	possibly damaging	Het
Aadacl2	A	T	3: 59,932,313 (GRCm39)	H276L	probably damaging	Het
Ash2l	A	T	8: 26,317,406 (GRCm39)	F290L	probably benign	Het
Asxl3	C	T	18: 22,658,281 (GRCm39)	P2097L	probably benign	Het
Atmin	A	G	8: 117,684,115 (GRCm39)	I592V	probably damaging	Het
Atxn2	T	C	5: 121,941,145 (GRCm39)		probably null	Het
BC004004	T	C	17: 29,515,665 (GRCm39)		probably null	Het
Cacna1e	T	C	1: 154,437,552 (GRCm39)	N328S	possibly damaging	Het
Cacna2d1	A	T	5: 16,560,493 (GRCm39)	K765I	probably damaging	Het
Cc2d1a	A	G	8: 84,860,604 (GRCm39)		probably null	Het
Ccdc28b	A	G	4: 129,514,408 (GRCm39)	V198A	probably benign	Het
Ces1b	G	T	8: 93,794,736 (GRCm39)	R288S	probably damaging	Het
Cfap100	T	G	6: 90,389,166 (GRCm39)	T198P	probably benign	Het
Clint1	T	C	11: 45,781,610 (GRCm39)	S227P	probably damaging	Het
Cntn5	C	A	9: 10,145,344 (GRCm39)	C122F	probably damaging	Het
Col3a1	A	G	1: 45,382,472 (GRCm39)		probably null	Het
Cyp4a10	A	C	4: 115,386,646 (GRCm39)	D431A	probably damaging	Het
Cyp4f16	CTATG	CTATGTATG	17: 32,769,708 (GRCm39)		probably null	Het
Dlc1	A	T	8: 37,060,617 (GRCm39)		probably benign	Het
Dlgap2	T	C	8: 14,777,060 (GRCm39)	S102P	probably benign	Het
Dnah7b	G	A	1: 46,117,753 (GRCm39)		probably benign	Het
Dock10	A	C	1: 80,526,853 (GRCm39)	S1124A	probably benign	Het
Dscam	C	T	16: 96,621,151 (GRCm39)	R519H	probably damaging	Het
Efcab3	A	T	11: 104,999,581 (GRCm39)		probably benign	Het
Evi2a	G	T	11: 79,418,096 (GRCm39)	N171K	probably damaging	Het
Fbxl15	T	C	19: 46,318,684 (GRCm39)	L286P	probably damaging	Het
Fpr1	T	A	17: 18,097,525 (GRCm39)	I155F	probably benign	Het
Gcat	C	T	15: 78,918,194 (GRCm39)	A84V	probably null	Het
Gls	A	G	1: 52,230,293 (GRCm39)	F473L	possibly damaging	Het
Gnat1	T	C	9: 107,554,164 (GRCm39)	D169G	probably damaging	Het
Grm3	A	C	5: 9,639,958 (GRCm39)	M29R	probably benign	Het
Herc1	A	T	9: 66,375,085 (GRCm39)	D3303V	probably damaging	Het
Ibsp	G	A	5: 104,458,405 (GRCm39)	G314D	unknown	Het
Irag2	C	T	6: 145,120,237 (GRCm39)	T484M	possibly damaging	Het
Lgr6	C	A	1: 134,915,210 (GRCm39)	A513S	probably damaging	Het
Lrriq4	T	A	3: 30,704,910 (GRCm39)	C313S	probably damaging	Het
Marchf10	G	T	11: 105,281,409 (GRCm39)	T292K	probably damaging	Het
Mcoln2	C	A	3: 145,896,137 (GRCm39)	Y6*	probably null	Het
Mup4	A	G	4: 59,958,076 (GRCm39)	I164T	probably damaging	Het
Myo1b	T	C	1: 51,817,717 (GRCm39)		probably benign	Het
Ncam1	A	G	9: 49,456,100 (GRCm39)	I506T	probably damaging	Het
Notch1	A	T	2: 26,370,976 (GRCm39)		probably benign	Het
Nr4a3	A	T	4: 48,051,777 (GRCm39)	Q177L	probably benign	Het
Nsun4	A	G	4: 115,910,147 (GRCm39)	S138P	possibly damaging	Het
Or1a1	A	G	11: 74,086,505 (GRCm39)	M59V	probably damaging	Het
Or2b6	G	T	13: 21,823,560 (GRCm39)	N44K	probably benign	Het
Or2d36	A	T	7: 106,747,405 (GRCm39)	N294I	probably damaging	Het
Or4k5	T	C	14: 50,385,815 (GRCm39)	N172S	probably damaging	Het
Pagr1a	A	T	7: 126,615,469 (GRCm39)		probably benign	Het
Pcdhb2	A	T	18: 37,429,343 (GRCm39)	I82L	probably benign	Het
Pds5b	A	T	5: 150,677,882 (GRCm39)	N500I	probably damaging	Het
Pik3r6	A	T	11: 68,422,271 (GRCm39)	E223D	possibly damaging	Het
Pkhd1l1	A	T	15: 44,404,384 (GRCm39)		probably benign	Het
Prex1	T	C	2: 166,422,383 (GRCm39)	D1204G	probably damaging	Het
Prickle1	C	T	15: 93,402,955 (GRCm39)	E244K	possibly damaging	Het
Ptprd	A	T	4: 76,002,789 (GRCm39)	V211E	probably damaging	Het
Rad51d	G	A	11: 82,781,179 (GRCm39)	R23*	probably null	Het
Rapgef6	G	A	11: 54,517,534 (GRCm39)	G262R	probably damaging	Het
Reln	A	G	5: 22,333,600 (GRCm39)		probably benign	Het
Rev1	T	C	1: 38,127,286 (GRCm39)	T325A	probably damaging	Het
Rnd3	T	A	2: 51,022,518 (GRCm39)	I175L	probably benign	Het
Rp1	C	A	1: 4,417,619 (GRCm39)	L1164F	probably damaging	Het
S100a7a	T	C	3: 90,562,942 (GRCm39)	V43A	probably benign	Het
Scaper	A	C	9: 55,510,202 (GRCm39)	Y1104*	probably null	Het
Scn2a	T	A	2: 65,594,938 (GRCm39)	V1929D	probably benign	Het
Scn3a	T	C	2: 65,359,785 (GRCm39)	N141S	possibly damaging	Het
Slc12a7	T	G	13: 73,949,127 (GRCm39)	L718R	probably damaging	Het
Slc15a2	T	C	16: 36,605,005 (GRCm39)		probably benign	Het
Slc35b3	G	A	13: 39,138,110 (GRCm39)	Q100*	probably null	Het
Slc9a5	T	A	8: 106,081,785 (GRCm39)	V170E	possibly damaging	Het
Snx5	T	G	2: 144,096,731 (GRCm39)	K278T	possibly damaging	Het
Sorbs2	T	C	8: 46,243,000 (GRCm39)		probably benign	Het
Stab1	C	T	14: 30,873,647 (GRCm39)	W1008*	probably null	Het
Stab2	C	T	10: 86,697,231 (GRCm39)		probably null	Het
Tacc3	A	G	5: 33,825,321 (GRCm39)	E377G	probably benign	Het
Tango6	T	C	8: 107,415,671 (GRCm39)	L164P	probably damaging	Het
Tbc1d12	T	A	19: 38,902,796 (GRCm39)	S570T	possibly damaging	Het
Thbs1	T	C	2: 117,944,836 (GRCm39)	F217L	probably damaging	Het
Tmbim6	T	A	15: 99,300,004 (GRCm39)	V40E	probably damaging	Het
Tmigd1	A	T	11: 76,800,986 (GRCm39)	N158Y	probably damaging	Het
Top3b	C	T	16: 16,710,641 (GRCm39)	R824*	probably null	Het
Tram1l1	A	T	3: 124,115,580 (GRCm39)	K247*	probably null	Het
Tsc2	T	C	17: 24,833,366 (GRCm39)	Y686C	probably damaging	Het
Tsga10	T	C	1: 37,858,680 (GRCm39)	Q218R	probably damaging	Het
Uba6	G	T	5: 86,288,282 (GRCm39)	A439D	probably damaging	Het
Ubn1	C	A	16: 4,895,158 (GRCm39)	P735T	probably damaging	Het
Usp40	A	G	1: 87,909,808 (GRCm39)	S549P	probably benign	Het
Utp20	T	C	10: 88,655,201 (GRCm39)	T176A	probably benign	Het
Utp4	T	G	8: 107,624,685 (GRCm39)		probably benign	Het
Xpo5	C	T	17: 46,518,853 (GRCm39)		probably benign	Het
Zfp979	A	T	4: 147,698,493 (GRCm39)	I72K	possibly damaging	Het

Other mutations in Adam12

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00474:Adam12	APN	7	133,511,610 (GRCm39)	missense	possibly damaging	0.51
IGL01403:Adam12	APN	7	133,521,339 (GRCm39)	missense	probably benign	0.00
IGL01482:Adam12	APN	7	133,569,577 (GRCm39)	missense	probably damaging	1.00
IGL01922:Adam12	APN	7	133,539,201 (GRCm39)	nonsense	probably null
IGL02397:Adam12	APN	7	133,511,548 (GRCm39)	splice site	probably benign
IGL03401:Adam12	APN	7	133,518,192 (GRCm39)	missense	probably damaging	1.00
R0122:Adam12	UTSW	7	133,614,077 (GRCm39)	missense	probably benign	0.45
R0200:Adam12	UTSW	7	133,576,145 (GRCm39)	splice site	probably null
R0463:Adam12	UTSW	7	133,576,145 (GRCm39)	splice site	probably null
R0927:Adam12	UTSW	7	133,599,959 (GRCm39)	missense	probably damaging	1.00
R1258:Adam12	UTSW	7	133,539,176 (GRCm39)	missense	probably damaging	1.00
R1483:Adam12	UTSW	7	133,531,754 (GRCm39)	missense	probably benign	0.41
R1692:Adam12	UTSW	7	133,489,673 (GRCm39)	makesense	probably null
R1797:Adam12	UTSW	7	133,569,590 (GRCm39)	missense	probably benign	0.03
R2134:Adam12	UTSW	7	133,614,017 (GRCm39)	nonsense	probably null
R2230:Adam12	UTSW	7	133,521,347 (GRCm39)	missense	probably damaging	1.00
R2350:Adam12	UTSW	7	133,521,253 (GRCm39)	missense	probably damaging	1.00
R2944:Adam12	UTSW	7	133,577,236 (GRCm39)	missense	probably null	0.02
R3688:Adam12	UTSW	7	133,566,525 (GRCm39)	nonsense	probably null
R3747:Adam12	UTSW	7	133,774,594 (GRCm39)	missense	probably damaging	0.96
R3749:Adam12	UTSW	7	133,774,594 (GRCm39)	missense	probably damaging	0.96
R3750:Adam12	UTSW	7	133,774,594 (GRCm39)	missense	probably damaging	0.96
R4028:Adam12	UTSW	7	133,531,725 (GRCm39)	missense	probably damaging	1.00
R4130:Adam12	UTSW	7	133,514,653 (GRCm39)	missense	probably damaging	1.00
R4131:Adam12	UTSW	7	133,514,653 (GRCm39)	missense	probably damaging	1.00
R4346:Adam12	UTSW	7	133,583,264 (GRCm39)	missense	possibly damaging	0.82
R4701:Adam12	UTSW	7	133,518,191 (GRCm39)	missense	possibly damaging	0.64
R4887:Adam12	UTSW	7	133,774,550 (GRCm39)	missense	possibly damaging	0.74
R5355:Adam12	UTSW	7	133,489,671 (GRCm39)	makesense	probably null
R5468:Adam12	UTSW	7	133,577,202 (GRCm39)	missense	probably damaging	1.00
R5486:Adam12	UTSW	7	133,509,401 (GRCm39)	missense	possibly damaging	0.75
R5990:Adam12	UTSW	7	133,533,465 (GRCm39)	missense	probably damaging	1.00
R6504:Adam12	UTSW	7	133,531,713 (GRCm39)	missense	probably damaging	1.00
R6783:Adam12	UTSW	7	133,576,126 (GRCm39)	missense	probably damaging	1.00
R7117:Adam12	UTSW	7	133,518,191 (GRCm39)	missense	probably benign	0.00
R7263:Adam12	UTSW	7	133,521,240 (GRCm39)	missense	possibly damaging	0.68
R7749:Adam12	UTSW	7	133,826,542 (GRCm39)	missense	unknown
R7820:Adam12	UTSW	7	133,599,917 (GRCm39)	missense	probably benign	0.00
R7880:Adam12	UTSW	7	133,511,691 (GRCm39)	missense	possibly damaging	0.94
R7891:Adam12	UTSW	7	133,599,961 (GRCm39)	missense	probably benign	0.00
R8114:Adam12	UTSW	7	133,569,617 (GRCm39)	missense	probably damaging	1.00
R8160:Adam12	UTSW	7	133,569,770 (GRCm39)	splice site	probably null
R8683:Adam12	UTSW	7	133,491,929 (GRCm39)	missense	possibly damaging	0.49
R9236:Adam12	UTSW	7	133,614,022 (GRCm39)	missense	probably benign	0.03
R9277:Adam12	UTSW	7	133,521,561 (GRCm39)	missense	probably benign	0.00
R9480:Adam12	UTSW	7	133,736,470 (GRCm39)	missense	probably damaging	0.98
R9515:Adam12	UTSW	7	133,509,373 (GRCm39)	missense	probably benign	0.03
R9599:Adam12	UTSW	7	133,566,454 (GRCm39)	missense	probably damaging	0.99
X0057:Adam12	UTSW	7	133,614,044 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- AGGTAAACCTGGCATGACGCTGAG -3'
(R):5'- TGATCTGAGATGCTCCCAACTTCCC -3'

Sequencing Primer
(F):5'- ATGGAGCTAAGACCCTTATTCGC -3'
(R):5'- TCCTCCTGAGAAGGCTACATGAG -3'

Posted On

2014-03-14