Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02486:Myom1'

295452

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Myom1

Ensembl Gene

ENSMUSG00000024049

Gene Name

myomesin 1

Synonyms

skelemin, D430047A17Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL02486

Quality Score

Status

Chromosome

Chromosomal Location

71019521-71126856 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

G to T at 71099944 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000136266 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000024847] [ENSMUST00000073211] [ENSMUST00000179759]

AlphaFold

Q62234

Predicted Effect

probably benign
Transcript: ENSMUST00000024847

SMART Domains

Protein: ENSMUSP00000024847
Gene: ENSMUSG00000024049

Domain	Start	End	E-Value	Type
low complexity region	62	94	N/A	INTRINSIC
low complexity region	188	210	N/A	INTRINSIC
low complexity region	228	244	N/A	INTRINSIC
IG	264	351	1.16e-8	SMART
IG	397	480	5.84e-5	SMART
FN3	490	573	4.48e-13	SMART
FN3	618	701	1.61e-14	SMART
FN3	719	800	1.43e-11	SMART
FN3	818	904	4.99e-11	SMART
FN3	923	1008	2.04e-16	SMART
IG	1025	1110	3.1e0	SMART
IG_like	1133	1219	1.34e1	SMART
IG_like	1253	1319	4.79e0	SMART
IG_like	1356	1433	1.54e2	SMART
IGc2	1469	1537	2.05e-9	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000073211

SMART Domains

Protein: ENSMUSP00000072945
Gene: ENSMUSG00000024049

Domain	Start	End	E-Value	Type
low complexity region	62	94	N/A	INTRINSIC
low complexity region	188	210	N/A	INTRINSIC
low complexity region	228	244	N/A	INTRINSIC
IG	264	351	1.16e-8	SMART
IG	397	480	5.84e-5	SMART
FN3	490	573	4.48e-13	SMART
FN3	618	701	1.61e-14	SMART
FN3	719	800	1.43e-11	SMART
low complexity region	857	870	N/A	INTRINSIC
FN3	916	1002	4.99e-11	SMART
FN3	1021	1106	2.04e-16	SMART
IG	1123	1208	3.1e0	SMART
IG_like	1231	1317	1.34e1	SMART
IG_like	1351	1417	4.79e0	SMART
IG_like	1454	1531	1.54e2	SMART
IGc2	1567	1635	2.05e-9	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000179759

SMART Domains

Protein: ENSMUSP00000136266
Gene: ENSMUSG00000024049

Domain	Start	End	E-Value	Type
low complexity region	62	94	N/A	INTRINSIC
low complexity region	188	210	N/A	INTRINSIC
low complexity region	228	244	N/A	INTRINSIC
IG	264	351	1.16e-8	SMART
IG	397	480	5.84e-5	SMART
FN3	490	573	4.48e-13	SMART
FN3	618	701	1.61e-14	SMART
FN3	719	800	1.43e-11	SMART
FN3	818	904	4.99e-11	SMART
FN3	923	1008	2.04e-16	SMART
IG	1025	1110	3.1e0	SMART
IG_like	1133	1219	1.34e1	SMART
IG_like	1253	1319	4.79e0	SMART
IG_like	1356	1433	1.54e2	SMART
IGc2	1469	1537	2.05e-9	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000180743

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The giant protein titin, together with its associated proteins, interconnects the major structure of sarcomeres, the M bands and Z discs. The C-terminal end of the titin string extends into the M line, where it binds tightly to M-band constituents of apparent molecular masses of 190 kD (myomesin 1) and 165 kD (myomesin 2). This protein, myomesin 1, like myomesin 2, titin, and other myofibrillar proteins contains structural modules with strong homology to either fibronectin type III (motif I) or immunoglobulin C2 (motif II) domains. Myomesin 1 and myomesin 2 each have a unique N-terminal region followed by 12 modules of motif I or motif II, in the arrangement II-II-I-I-I-I-I-II-II-II-II-II. The two proteins share 50% sequence identity in this repeat-containing region. The head structure formed by these 2 proteins on one end of the titin string extends into the center of the M band. The integrating structure of the sarcomere arises from muscle-specific members of the superfamily of immunoglobulin-like proteins. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 43 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2010106E10Rik	T	A	X: 112,515,258 (GRCm38)	N147K	probably benign	Het
9330182L06Rik	T	A	5: 9,422,323 (GRCm38)	V340E	probably benign	Het
BC052040	T	C	2: 115,777,006 (GRCm38)	V280A	possibly damaging	Het
Bcas1	T	C	2: 170,406,398 (GRCm38)	D201G	probably damaging	Het
Bmp1	T	A	14: 70,504,776 (GRCm38)	D333V	possibly damaging	Het
Btbd11	C	A	10: 85,640,555 (GRCm38)	P900H	probably damaging	Het
Capn6	T	C	X: 143,804,677 (GRCm38)	E535G	probably benign	Het
Chac2	T	C	11: 30,977,625 (GRCm38)	D86G	probably damaging	Het
Col14a1	T	A	15: 55,388,696 (GRCm38)		probably benign	Het
Daam1	T	C	12: 71,947,145 (GRCm38)		probably benign	Het
Eno4	A	G	19: 58,945,665 (GRCm38)		probably null	Het
Fat1	T	C	8: 45,025,072 (GRCm38)	V2385A	probably benign	Het
Ffar4	T	C	19: 38,113,760 (GRCm38)	I281T	possibly damaging	Het
Flcn	C	T	11: 59,801,043 (GRCm38)	W260*	probably null	Het
Fry	T	G	5: 150,491,177 (GRCm38)	S496A	probably damaging	Het
Gk	T	A	X: 85,715,668 (GRCm38)	I373F	possibly damaging	Het
Gpr108	T	C	17: 57,235,977 (GRCm38)	N528S	probably damaging	Het
Hey1	T	A	3: 8,666,519 (GRCm38)	R50W	probably damaging	Het
Hgf	A	G	5: 16,602,289 (GRCm38)	Y393C	probably damaging	Het
Hmcn2	A	T	2: 31,420,095 (GRCm38)	E3260D	probably damaging	Het
Ift172	A	G	5: 31,257,583 (GRCm38)	I1365T	probably damaging	Het
Letmd1	A	G	15: 100,475,111 (GRCm38)	R31G	probably damaging	Het
Mak16	T	C	8: 31,160,586 (GRCm38)		probably benign	Het
Mapkapk3	C	T	9: 107,289,268 (GRCm38)	G26D	probably damaging	Het
Mphosph8	T	C	14: 56,688,387 (GRCm38)	V603A	possibly damaging	Het
Neb	T	A	2: 52,282,603 (GRCm38)	N1564I	possibly damaging	Het
Nox1	C	T	X: 134,092,811 (GRCm38)	G433D	probably damaging	Het
Olfr133	T	A	17: 38,149,221 (GRCm38)	L211Q	probably damaging	Het
Olfr554	A	T	7: 102,640,420 (GRCm38)	H58L	probably damaging	Het
Olfr641	T	C	7: 104,040,410 (GRCm38)	S205P	probably damaging	Het
Olfr745	T	C	14: 50,642,632 (GRCm38)	F111S	probably damaging	Het
Rcc2	T	C	4: 140,710,362 (GRCm38)	W135R	probably damaging	Het
Rgl2	A	G	17: 33,935,980 (GRCm38)	I205V	probably damaging	Het
Robo4	G	A	9: 37,408,374 (GRCm38)	G640E	probably damaging	Het
Slc26a5	A	G	5: 21,846,325 (GRCm38)	F64L	probably damaging	Het
Slc27a2	A	G	2: 126,553,350 (GRCm38)	T66A	probably benign	Het
St18	T	C	1: 6,820,083 (GRCm38)	S580P	probably damaging	Het
Syt15	G	A	14: 34,222,976 (GRCm38)	R160K	probably damaging	Het
Tmem63b	A	G	17: 45,673,983 (GRCm38)	S200P	probably damaging	Het
Tnks	T	A	8: 34,851,198 (GRCm38)	N841I	probably damaging	Het
Tnr	G	A	1: 159,852,094 (GRCm38)		probably null	Het
Unc13d	A	G	11: 116,069,806 (GRCm38)		probably benign	Het
Usp4	T	C	9: 108,351,029 (GRCm38)	L74P	probably damaging	Het

Other mutations in Myom1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00422:Myom1	APN	17	71,126,098 (GRCm38)	missense	probably damaging	1.00
IGL00845:Myom1	APN	17	71,084,429 (GRCm38)	missense	probably damaging	1.00
IGL00904:Myom1	APN	17	71,099,949 (GRCm38)	splice site	probably benign
IGL00928:Myom1	APN	17	71,089,913 (GRCm38)	missense	probably damaging	1.00
IGL01025:Myom1	APN	17	71,077,917 (GRCm38)	missense	probably damaging	1.00
IGL01548:Myom1	APN	17	71,101,220 (GRCm38)	splice site	probably benign
IGL01588:Myom1	APN	17	71,117,437 (GRCm38)	missense	possibly damaging	0.94
IGL01614:Myom1	APN	17	71,126,178 (GRCm38)	missense	possibly damaging	0.46
IGL01618:Myom1	APN	17	71,099,993 (GRCm38)	missense	possibly damaging	0.87
IGL01619:Myom1	APN	17	71,044,476 (GRCm38)	splice site	probably benign
IGL01766:Myom1	APN	17	71,077,288 (GRCm38)	missense	probably damaging	1.00
IGL02105:Myom1	APN	17	71,047,716 (GRCm38)	splice site	probably benign
IGL02122:Myom1	APN	17	71,092,137 (GRCm38)	missense	probably damaging	1.00
IGL02184:Myom1	APN	17	71,072,137 (GRCm38)	missense	possibly damaging	0.93
IGL02260:Myom1	APN	17	71,108,315 (GRCm38)	nonsense	probably null
IGL02501:Myom1	APN	17	71,072,081 (GRCm38)	critical splice acceptor site	probably null
IGL02642:Myom1	APN	17	71,101,098 (GRCm38)	missense	possibly damaging	0.90
IGL02677:Myom1	APN	17	71,084,349 (GRCm38)	missense	probably damaging	1.00
IGL02719:Myom1	APN	17	71,106,354 (GRCm38)	splice site	probably benign
IGL02945:Myom1	APN	17	71,092,093 (GRCm38)	splice site	probably benign
IGL03086:Myom1	APN	17	71,108,671 (GRCm38)	missense	probably damaging	1.00
IGL03218:Myom1	APN	17	71,084,316 (GRCm38)	missense	possibly damaging	0.46
R0107:Myom1	UTSW	17	71,077,365 (GRCm38)	missense	probably damaging	1.00
R0130:Myom1	UTSW	17	71,045,755 (GRCm38)	missense	probably damaging	0.98
R0133:Myom1	UTSW	17	71,047,787 (GRCm38)	missense	probably damaging	1.00
R0206:Myom1	UTSW	17	71,037,297 (GRCm38)	missense	probably damaging	1.00
R0206:Myom1	UTSW	17	71,037,297 (GRCm38)	missense	probably damaging	1.00
R0352:Myom1	UTSW	17	71,045,749 (GRCm38)	missense	possibly damaging	0.72
R0396:Myom1	UTSW	17	71,034,693 (GRCm38)	missense	probably damaging	1.00
R0496:Myom1	UTSW	17	71,084,306 (GRCm38)	missense	probably damaging	1.00
R0506:Myom1	UTSW	17	71,092,220 (GRCm38)	splice site	probably benign
R0511:Myom1	UTSW	17	71,084,317 (GRCm38)	missense	probably benign	0.22
R0600:Myom1	UTSW	17	71,120,648 (GRCm38)	missense	possibly damaging	0.48
R0699:Myom1	UTSW	17	71,067,313 (GRCm38)	missense	probably damaging	0.98
R0791:Myom1	UTSW	17	71,121,136 (GRCm38)	missense	probably damaging	1.00
R0792:Myom1	UTSW	17	71,121,136 (GRCm38)	missense	probably damaging	1.00
R0963:Myom1	UTSW	17	71,077,767 (GRCm38)	missense	possibly damaging	0.74
R1324:Myom1	UTSW	17	71,052,719 (GRCm38)	missense	probably damaging	0.98
R2102:Myom1	UTSW	17	71,101,029 (GRCm38)	missense	probably damaging	1.00
R2158:Myom1	UTSW	17	71,064,597 (GRCm38)	missense	possibly damaging	0.83
R2336:Myom1	UTSW	17	71,023,194 (GRCm38)	missense	possibly damaging	0.53
R2351:Myom1	UTSW	17	71,034,579 (GRCm38)	missense	probably damaging	0.98
R2442:Myom1	UTSW	17	71,110,735 (GRCm38)	missense	probably damaging	1.00
R2483:Myom1	UTSW	17	71,077,812 (GRCm38)	missense	probably damaging	1.00
R2892:Myom1	UTSW	17	71,034,653 (GRCm38)	missense	probably damaging	1.00
R2897:Myom1	UTSW	17	71,101,220 (GRCm38)	splice site	probably benign
R3440:Myom1	UTSW	17	71,045,663 (GRCm38)	splice site	probably null
R3842:Myom1	UTSW	17	71,045,624 (GRCm38)	missense	probably damaging	1.00
R4249:Myom1	UTSW	17	71,092,140 (GRCm38)	missense	probably damaging	1.00
R4329:Myom1	UTSW	17	71,036,353 (GRCm38)	missense	probably damaging	1.00
R4594:Myom1	UTSW	17	71,100,074 (GRCm38)	missense	possibly damaging	0.73
R4873:Myom1	UTSW	17	71,072,119 (GRCm38)	missense	probably damaging	1.00
R4875:Myom1	UTSW	17	71,072,119 (GRCm38)	missense	probably damaging	1.00
R4876:Myom1	UTSW	17	71,077,410 (GRCm38)	missense	probably damaging	1.00
R5171:Myom1	UTSW	17	71,099,972 (GRCm38)	missense	possibly damaging	0.94
R5540:Myom1	UTSW	17	71,109,787 (GRCm38)	missense	probably damaging	1.00
R5882:Myom1	UTSW	17	71,110,722 (GRCm38)	missense	probably damaging	1.00
R5978:Myom1	UTSW	17	71,117,443 (GRCm38)	missense	probably damaging	1.00
R6039:Myom1	UTSW	17	71,110,751 (GRCm38)	missense	probably damaging	1.00
R6039:Myom1	UTSW	17	71,110,751 (GRCm38)	missense	probably damaging	1.00
R6155:Myom1	UTSW	17	71,108,695 (GRCm38)	critical splice donor site	probably null
R6261:Myom1	UTSW	17	71,126,137 (GRCm38)	missense	probably damaging	1.00
R6284:Myom1	UTSW	17	71,022,892 (GRCm38)	nonsense	probably null
R6313:Myom1	UTSW	17	71,082,488 (GRCm38)	missense	probably benign
R6369:Myom1	UTSW	17	71,101,076 (GRCm38)	missense	probably damaging	1.00
R6545:Myom1	UTSW	17	71,082,305 (GRCm38)	missense	probably benign	0.00
R6738:Myom1	UTSW	17	71,100,398 (GRCm38)	splice site	probably null
R6933:Myom1	UTSW	17	71,052,671 (GRCm38)	missense	probably damaging	1.00
R7168:Myom1	UTSW	17	71,089,947 (GRCm38)	missense	probably benign	0.00
R7286:Myom1	UTSW	17	71,045,549 (GRCm38)	missense	possibly damaging	0.90
R7315:Myom1	UTSW	17	71,080,897 (GRCm38)	critical splice donor site	probably null
R7672:Myom1	UTSW	17	71,084,240 (GRCm38)	missense	possibly damaging	0.92
R7789:Myom1	UTSW	17	71,117,436 (GRCm38)	missense	probably benign	0.03
R7898:Myom1	UTSW	17	71,045,752 (GRCm38)	missense	probably benign	0.25
R8008:Myom1	UTSW	17	71,100,062 (GRCm38)	missense	probably benign	0.30
R8152:Myom1	UTSW	17	71,084,295 (GRCm38)	missense	probably damaging	0.96
R8554:Myom1	UTSW	17	71,036,453 (GRCm38)	missense	possibly damaging	0.94
R8874:Myom1	UTSW	17	71,106,204 (GRCm38)	missense	probably damaging	1.00
R8981:Myom1	UTSW	17	71,084,321 (GRCm38)	missense	probably benign	0.09
R9012:Myom1	UTSW	17	71,100,108 (GRCm38)	missense	probably benign	0.06
R9090:Myom1	UTSW	17	71,067,330 (GRCm38)	missense	probably damaging	1.00
R9193:Myom1	UTSW	17	71,036,300 (GRCm38)	missense	probably damaging	1.00
R9237:Myom1	UTSW	17	71,101,056 (GRCm38)	missense	probably damaging	1.00
R9271:Myom1	UTSW	17	71,067,330 (GRCm38)	missense	probably damaging	1.00
R9355:Myom1	UTSW	17	71,077,893 (GRCm38)	missense	probably damaging	1.00
R9362:Myom1	UTSW	17	71,036,293 (GRCm38)	missense	probably benign	0.00
R9440:Myom1	UTSW	17	71,126,334 (GRCm38)	missense	probably benign	0.00
R9469:Myom1	UTSW	17	71,061,127 (GRCm38)	missense	possibly damaging	0.79
R9568:Myom1	UTSW	17	71,087,481 (GRCm38)	missense	probably damaging	1.00
R9612:Myom1	UTSW	17	71,105,480 (GRCm38)	nonsense	probably null
R9645:Myom1	UTSW	17	71,092,209 (GRCm38)	missense	probably benign	0.01
X0019:Myom1	UTSW	17	71,100,071 (GRCm38)	missense	possibly damaging	0.55

Posted On

2015-04-16