Mutagenetix > Incidental Mutation

Incidental Mutation 'R1919:Col6a3'

212795

Institutional Source

Beutler Lab

Gene Symbol

Col6a3

Ensembl Gene

ENSMUSG00000048126

Gene Name

collagen, type VI, alpha 3

Synonyms

Col6a-3

MMRRC Submission

039937-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1919 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

90765923-90843971 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 90822359 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 251 (N251S)

Ref Sequence

ENSEMBL: ENSMUSP00000057131 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000056925] [ENSMUST00000097653] [ENSMUST00000130846] [ENSMUST00000187753] [ENSMUST00000188587]

AlphaFold

no structure available at present

PDB Structure

Crystal structure of the Collagen VI alpha3 N5 domain [X-RAY DIFFRACTION]
Crystal structure of the Collagen VI alpha3 N5 domain R1061Q [X-RAY DIFFRACTION]

Predicted Effect

possibly damaging
Transcript: ENSMUST00000056925
AA Change: N251S

PolyPhen 2 Score 0.658 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000057131
Gene: ENSMUSG00000048126
AA Change: N251S

Domain	Start	End	E-Value	Type
VWA	36	214	3.58e-42	SMART
VWA	239	415	3.34e-42	SMART
VWA	442	617	7.27e-43	SMART
VWA	636	813	7.8e-43	SMART
VWA	834	1010	4.21e-39	SMART
VWA	1024	1203	3.02e-40	SMART
VWA	1228	1406	1.1e-42	SMART
VWA	1431	1604	9.17e-40	SMART
VWA	1634	1807	1.78e-37	SMART
VWA	1833	2022	7.92e-3	SMART
Pfam:Collagen	2033	2094	2e-10	PFAM
Pfam:Collagen	2077	2142	2.8e-10	PFAM
low complexity region	2179	2222	N/A	INTRINSIC
low complexity region	2228	2279	N/A	INTRINSIC
Pfam:Collagen	2311	2373	7.9e-11	PFAM
VWA	2397	2576	3.95e-21	SMART
VWA	2614	2813	2.25e-25	SMART
low complexity region	2864	2880	N/A	INTRINSIC
low complexity region	2886	2900	N/A	INTRINSIC
low complexity region	2903	2941	N/A	INTRINSIC
low complexity region	2945	3024	N/A	INTRINSIC
low complexity region	3039	3076	N/A	INTRINSIC
low complexity region	3091	3103	N/A	INTRINSIC
FN3	3104	3183	4.6e-1	SMART
KU	3226	3279	4.34e-24	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000097653

SMART Domains

Protein: ENSMUSP00000137585
Gene: ENSMUSG00000048126

Domain	Start	End	E-Value	Type
VWA	35	210	7.27e-43	SMART
VWA	227	403	4.21e-39	SMART
VWA	417	596	3.02e-40	SMART
VWA	621	799	1.1e-42	SMART
VWA	824	997	9.17e-40	SMART
VWA	1027	1200	1.78e-37	SMART
VWA	1226	1415	7.92e-3	SMART
Pfam:Collagen	1426	1486	9.2e-10	PFAM
Pfam:Collagen	1473	1539	2.2e-9	PFAM
low complexity region	1572	1615	N/A	INTRINSIC
low complexity region	1621	1672	N/A	INTRINSIC
low complexity region	1690	1704	N/A	INTRINSIC
low complexity region	1713	1734	N/A	INTRINSIC
VWA	1790	1969	3.95e-21	SMART
VWA	2007	2206	2.25e-25	SMART
low complexity region	2257	2273	N/A	INTRINSIC
low complexity region	2279	2293	N/A	INTRINSIC
low complexity region	2296	2334	N/A	INTRINSIC
low complexity region	2338	2417	N/A	INTRINSIC
low complexity region	2432	2469	N/A	INTRINSIC
low complexity region	2484	2496	N/A	INTRINSIC
FN3	2497	2576	4.6e-1	SMART
KU	2619	2672	4.34e-24	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000130846
AA Change: N251S

PolyPhen 2 Score 0.058 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000115210
Gene: ENSMUSG00000048126
AA Change: N251S

Domain	Start	End	E-Value	Type
VWA	36	214	3.58e-42	SMART
VWA	239	415	3.34e-42	SMART
VWA	442	617	7.27e-43	SMART
VWA	636	813	7.8e-43	SMART
VWA	834	1010	4.21e-39	SMART
VWA	1024	1203	3.02e-40	SMART
VWA	1228	1406	1.1e-42	SMART
VWA	1431	1604	9.17e-40	SMART
Pfam:VWA	1636	1703	1.4e-14	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000187753
AA Change: N45S

PolyPhen 2 Score 0.031 (Sensitivity: 0.95; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000140280
Gene: ENSMUSG00000048126
AA Change: N45S

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:VWA	35	74	1.2e-8	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000188587

SMART Domains

Protein: ENSMUSP00000140858
Gene: ENSMUSG00000048126

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
VWA	35	210	4.7e-45	SMART
VWA	227	403	2.7e-41	SMART
VWA	417	596	2e-42	SMART
VWA	621	799	7e-45	SMART
VWA	824	997	5.8e-42	SMART
VWA	1027	1200	1.1e-39	SMART
VWA	1226	1415	4.8e-5	SMART
Pfam:Collagen	1426	1486	3.8e-8	PFAM
Pfam:Collagen	1473	1539	9.1e-8	PFAM
low complexity region	1572	1615	N/A	INTRINSIC
low complexity region	1621	1672	N/A	INTRINSIC
low complexity region	1690	1704	N/A	INTRINSIC
low complexity region	1713	1734	N/A	INTRINSIC
VWA	1790	1969	2.4e-23	SMART
VWA	2007	2206	1.4e-27	SMART
low complexity region	2257	2273	N/A	INTRINSIC
low complexity region	2279	2293	N/A	INTRINSIC
low complexity region	2296	2334	N/A	INTRINSIC
low complexity region	2338	2417	N/A	INTRINSIC
low complexity region	2432	2469	N/A	INTRINSIC
low complexity region	2484	2496	N/A	INTRINSIC
FN3	2497	2576	2.2e-3	SMART
KU	2619	2672	2.1e-26	SMART

Coding Region Coverage

1x: 97.5%
3x: 97.0%
10x: 95.7%
20x: 93.3%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the alpha-3 chain, one of the three alpha chains of type VI collagen, a beaded filament collagen found in most connective tissues. The alpha-3 chain of type VI collagen is much larger than the alpha-1 and -2 chains. This difference in size is largely due to an increase in the number of subdomains, similar to von Willebrand Factor type A domains, that are found in the amino terminal globular domain of all the alpha chains. These domains have been shown to bind extracellular matrix proteins, an interaction that explains the importance of this collagen in organizing matrix components. Mutations in the type VI collagen genes are associated with Bethlem myopathy, a rare autosomal dominant proximal myopathy with early childhood onset. Mutations in this gene are also a cause of Ullrich congenital muscular dystrophy, also referred to as Ullrich scleroatonic muscular dystrophy, an autosomal recessive congenital myopathy that is more severe than Bethlem myopathy. Multiple transcript variants have been identified, but the full-length nature of only some of these variants has been described. [provided by RefSeq, Jun 2009]
PHENOTYPE: Mice homozygous for a hypomorphic allele exhibit mild myopathy, decreased skeletal muscle weight, increased collagen deposition in muscles, skeletal muscle interstitial fibrosis and abnormal tendon collagen fibril morphology. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 94 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110002E22Rik	A	G	3: 138,067,270 (GRCm38)	E740G	probably damaging	Het
4930474N05Rik	G	T	14: 36,095,457 (GRCm38)	V105F	possibly damaging	Het
4932438A13Rik	A	G	3: 37,006,983 (GRCm38)		probably null	Het
Actr10	A	G	12: 70,942,330 (GRCm38)	I74M	probably benign	Het
Aen	T	C	7: 78,905,912 (GRCm38)	Y108H	probably damaging	Het
Afm	A	T	5: 90,524,920 (GRCm38)	K205*	probably null	Het
Ankrd27	T	A	7: 35,632,985 (GRCm38)	S846T	probably benign	Het
Ano3	A	G	2: 110,885,007 (GRCm38)	S29P	probably benign	Het
Apaf1	C	T	10: 91,077,614 (GRCm38)	W138*	probably null	Het
Arfgef1	C	T	1: 10,199,878 (GRCm38)	A349T	probably benign	Het
Arhgef4	A	G	1: 34,811,140 (GRCm38)	Q1798R	probably damaging	Het
Astn1	G	A	1: 158,509,971 (GRCm38)	V416I	probably damaging	Het
Atxn2l	G	A	7: 126,493,168 (GRCm38)	T70I	probably damaging	Het
Auh	G	A	13: 52,835,496 (GRCm38)	P308L	probably benign	Het
Bspry	T	A	4: 62,494,797 (GRCm38)	C256S	probably damaging	Het
C3	C	A	17: 57,220,135 (GRCm38)	W771C	probably damaging	Het
Camkv	A	G	9: 107,947,088 (GRCm38)	D233G	possibly damaging	Het
Catsperd	T	A	17: 56,635,548 (GRCm38)	V109E	probably damaging	Het
Cd101	A	G	3: 101,018,917 (GRCm38)	L162P	probably damaging	Het
Cdr2l	A	G	11: 115,392,777 (GRCm38)	T154A	probably damaging	Het
Clca3a2	G	C	3: 144,810,696 (GRCm38)	Q380E	probably benign	Het
Cttnbp2nl	A	G	3: 105,011,278 (GRCm38)	V82A	possibly damaging	Het
Cux1	G	A	5: 136,363,319 (GRCm38)	Q194*	probably null	Het
Daam2	T	C	17: 49,485,457 (GRCm38)	E361G	probably benign	Het
Dcaf17	A	T	2: 71,078,172 (GRCm38)		probably null	Het
Dnaic1	T	C	4: 41,570,020 (GRCm38)		probably null	Het
Eml5	T	C	12: 98,798,839 (GRCm38)	Y1617C	probably damaging	Het
Epb41l4b	T	C	4: 57,040,993 (GRCm38)	E490G	probably damaging	Het
Epha7	T	C	4: 28,963,969 (GRCm38)	M988T	possibly damaging	Het
Fancm	T	C	12: 65,105,520 (GRCm38)	C917R	possibly damaging	Het
Fnip1	C	T	11: 54,480,684 (GRCm38)	T177I	probably damaging	Het
Gm12169	A	G	11: 46,528,531 (GRCm38)	D58G	possibly damaging	Het
Gm3604	G	T	13: 62,369,942 (GRCm38)	H201N	probably benign	Het
Gnpda1	T	C	18: 38,333,190 (GRCm38)		probably null	Het
Gpatch8	A	G	11: 102,508,142 (GRCm38)		probably null	Het
H2-M3	T	C	17: 37,271,189 (GRCm38)	Y179H	possibly damaging	Het
H2-Q10	C	A	17: 35,470,488 (GRCm38)	S62R	probably damaging	Het
Hipk2	G	A	6: 38,818,984 (GRCm38)	R117*	probably null	Het
Hrg	A	T	16: 22,954,457 (GRCm38)	Q113H	probably damaging	Het
Kcnj16	T	C	11: 111,024,953 (GRCm38)	V147A	possibly damaging	Het
Kif1a	T	C	1: 93,019,031 (GRCm38)	I1650V	possibly damaging	Het
Kmt2a	C	T	9: 44,820,345 (GRCm38)		probably benign	Het
Krt90	A	T	15: 101,557,230 (GRCm38)	Y319N	probably damaging	Het
Lipo4	T	C	19: 33,499,271 (GRCm38)	N359S	possibly damaging	Het
Lrp1b	G	T	2: 41,728,729 (GRCm38)	T225K	probably benign	Het
Map1a	C	T	2: 121,307,012 (GRCm38)	P2532S	probably damaging	Het
Mmrn2	A	G	14: 34,397,643 (GRCm38)	D193G	probably benign	Het
Mpped2	T	A	2: 106,867,032 (GRCm38)	I284N	probably damaging	Het
Msh6	A	G	17: 87,985,125 (GRCm38)	H436R	probably benign	Het
Mterf3	A	T	13: 66,930,062 (GRCm38)	S48T	probably damaging	Het
Muc5b	T	C	7: 141,846,031 (GRCm38)	F414L	unknown	Het
Mylk4	A	T	13: 32,724,853 (GRCm38)	D90E	probably benign	Het
Nploc4	A	G	11: 120,404,229 (GRCm38)	Y420H	probably damaging	Het
Npr2	T	A	4: 43,640,578 (GRCm38)	Y344N	probably damaging	Het
Nsun5	A	G	5: 135,375,598 (GRCm38)	T397A	probably benign	Het
Ntsr2	A	T	12: 16,654,110 (GRCm38)	Q204L	probably damaging	Het
Nwd2	T	A	5: 63,806,180 (GRCm38)	Y1036N	probably damaging	Het
Oacyl	T	C	18: 65,710,547 (GRCm38)	V105A	possibly damaging	Het
Olfr791	T	A	10: 129,527,049 (GRCm38)	V274D	probably damaging	Het
Parp3	T	A	9: 106,475,117 (GRCm38)	Q70L	possibly damaging	Het
Parp4	T	C	14: 56,624,017 (GRCm38)	S936P	probably damaging	Het
Pdzd3	T	C	9: 44,250,303 (GRCm38)	D93G	possibly damaging	Het
Phkb	A	G	8: 85,922,161 (GRCm38)	E202G	probably benign	Het
Pink1	T	C	4: 138,314,020 (GRCm38)	N530S	probably benign	Het
Pou3f2	T	C	4: 22,487,119 (GRCm38)	D338G	probably damaging	Het
Prss8	G	T	7: 127,929,858 (GRCm38)	L9I	probably benign	Het
Ptpn22	G	A	3: 103,876,738 (GRCm38)		probably null	Het
Rad54b	A	C	4: 11,601,693 (GRCm38)	N416T	probably damaging	Het
Rasef	A	G	4: 73,744,114 (GRCm38)	S200P	possibly damaging	Het
Rb1	T	A	14: 73,212,990 (GRCm38)	K645*	probably null	Het
Robo2	C	T	16: 73,899,154 (GRCm38)	G1367D	probably benign	Het
Rp1	A	G	1: 4,352,671 (GRCm38)	V52A	probably damaging	Het
Samd13	T	C	3: 146,662,712 (GRCm38)	T23A	probably benign	Het
Scn7a	T	C	2: 66,699,973 (GRCm38)	H676R	probably damaging	Het
Serpinb6b	A	G	13: 32,978,240 (GRCm38)	I222V	probably benign	Het
Slc2a8	T	C	2: 32,980,079 (GRCm38)	Y150C	probably damaging	Het
Slc7a6os	C	A	8: 106,210,564 (GRCm38)	R88L	probably damaging	Het
Slc8a2	A	G	7: 16,152,920 (GRCm38)	I657V	probably benign	Het
Slit2	C	A	5: 48,191,016 (GRCm38)		probably benign	Het
Spire2	A	G	8: 123,363,071 (GRCm38)	D447G	probably benign	Het
Sptlc3	A	G	2: 139,566,675 (GRCm38)	N237D	possibly damaging	Het
Stk3	G	A	15: 35,073,217 (GRCm38)	T119I	probably damaging	Het
Suv39h2	G	A	2: 3,464,316 (GRCm38)	T334I	probably damaging	Het
Syt5	G	T	7: 4,540,279 (GRCm38)	T327N	probably damaging	Het
Tcof1	T	C	18: 60,816,084 (GRCm38)	D1253G	possibly damaging	Het
Tnks	A	T	8: 34,875,232 (GRCm38)	V388D	probably damaging	Het
Ugt2b1	T	C	5: 86,926,000 (GRCm38)	T167A	probably benign	Het
Usp40	G	A	1: 87,995,842 (GRCm38)	R236C	possibly damaging	Het
Utrn	T	C	10: 12,455,480 (GRCm38)	D2904G	probably benign	Het
Vmn1r226	T	C	17: 20,687,580 (GRCm38)	S25P	probably damaging	Het
Vmn2r23	T	C	6: 123,713,010 (GRCm38)	S282P	possibly damaging	Het
Vps45	T	C	3: 96,046,440 (GRCm38)	E200G	probably benign	Het
Wnt7b	T	A	15: 85,559,080 (GRCm38)	I41F	probably damaging	Het
Zmym6	T	A	4: 127,103,414 (GRCm38)	N275K	probably damaging	Het

Other mutations in Col6a3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00391:Col6a3	APN	1	90,828,255 (GRCm38)	missense	probably damaging	1.00
IGL00425:Col6a3	APN	1	90,782,026 (GRCm38)	missense	unknown
IGL00541:Col6a3	APN	1	90,802,142 (GRCm38)	missense	possibly damaging	0.83
IGL01063:Col6a3	APN	1	90,802,332 (GRCm38)	missense	probably damaging	1.00
IGL01094:Col6a3	APN	1	90,803,933 (GRCm38)	missense	possibly damaging	0.93
IGL01138:Col6a3	APN	1	90,807,510 (GRCm38)	missense	probably damaging	1.00
IGL01291:Col6a3	APN	1	90,802,292 (GRCm38)	missense	probably damaging	1.00
IGL01674:Col6a3	APN	1	90,802,514 (GRCm38)	missense	probably damaging	1.00
IGL01756:Col6a3	APN	1	90,779,162 (GRCm38)	missense	unknown
IGL01827:Col6a3	APN	1	90,802,319 (GRCm38)	missense	probably damaging	1.00
IGL01845:Col6a3	APN	1	90,796,571 (GRCm38)	missense	probably damaging	1.00
IGL01869:Col6a3	APN	1	90,773,048 (GRCm38)	missense	unknown
IGL01900:Col6a3	APN	1	90,795,010 (GRCm38)	critical splice donor site	probably null
IGL01925:Col6a3	APN	1	90,802,236 (GRCm38)	missense	possibly damaging	0.95
IGL02002:Col6a3	APN	1	90,782,136 (GRCm38)	splice site	probably benign
IGL02115:Col6a3	APN	1	90,807,651 (GRCm38)	missense	probably damaging	0.99
IGL02302:Col6a3	APN	1	90,781,760 (GRCm38)	missense	unknown
IGL02313:Col6a3	APN	1	90,811,606 (GRCm38)	missense	probably damaging	1.00
IGL02458:Col6a3	APN	1	90,779,197 (GRCm38)	missense	unknown
IGL02821:Col6a3	APN	1	90,803,878 (GRCm38)	missense	probably damaging	1.00
IGL02828:Col6a3	APN	1	90,796,559 (GRCm38)	missense	probably damaging	1.00
IGL03112:Col6a3	APN	1	90,811,520 (GRCm38)	nonsense	probably null
IGL03129:Col6a3	APN	1	90,821,862 (GRCm38)	missense	probably damaging	1.00
IGL03132:Col6a3	APN	1	90,803,893 (GRCm38)	missense	probably damaging	1.00
IGL03148:Col6a3	APN	1	90,827,866 (GRCm38)	missense	probably benign	0.33
IGL03251:Col6a3	APN	1	90,810,176 (GRCm38)	missense	probably damaging	1.00
bailey	UTSW	1	90,767,606 (GRCm38)	critical splice acceptor site	probably benign
barnum	UTSW	1	90,779,152 (GRCm38)	missense	unknown
Boneless	UTSW	1	90,779,059 (GRCm38)	missense	unknown
Noodloid	UTSW	1	90,779,289 (GRCm38)	missense	unknown
randolf	UTSW	1	90,787,951 (GRCm38)	missense	unknown
stringy	UTSW	1	90,803,678 (GRCm38)	nonsense	probably null
wonder	UTSW	1	90,791,923 (GRCm38)	critical splice donor site	probably null
ANU05:Col6a3	UTSW	1	90,802,292 (GRCm38)	missense	probably damaging	1.00
IGL03048:Col6a3	UTSW	1	90,810,248 (GRCm38)	missense	possibly damaging	0.58
PIT4810001:Col6a3	UTSW	1	90,778,794 (GRCm38)	missense	unknown
R0020:Col6a3	UTSW	1	90,811,550 (GRCm38)	missense	probably damaging	0.99
R0020:Col6a3	UTSW	1	90,811,550 (GRCm38)	missense	probably damaging	0.99
R0033:Col6a3	UTSW	1	90,802,245 (GRCm38)	missense	probably damaging	1.00
R0033:Col6a3	UTSW	1	90,802,245 (GRCm38)	missense	probably damaging	1.00
R0105:Col6a3	UTSW	1	90,798,161 (GRCm38)	missense	possibly damaging	0.65
R0116:Col6a3	UTSW	1	90,813,551 (GRCm38)	missense	probably damaging	1.00
R0167:Col6a3	UTSW	1	90,798,173 (GRCm38)	missense	probably damaging	1.00
R0319:Col6a3	UTSW	1	90,807,704 (GRCm38)	missense	possibly damaging	0.95
R0348:Col6a3	UTSW	1	90,828,049 (GRCm38)	missense	probably damaging	1.00
R0365:Col6a3	UTSW	1	90,788,216 (GRCm38)	missense	unknown
R0512:Col6a3	UTSW	1	90,821,798 (GRCm38)	intron	probably benign
R0564:Col6a3	UTSW	1	90,807,734 (GRCm38)	missense	probably damaging	1.00
R0635:Col6a3	UTSW	1	90,808,086 (GRCm38)	splice site	probably null
R0667:Col6a3	UTSW	1	90,828,101 (GRCm38)	missense	probably damaging	0.98
R0680:Col6a3	UTSW	1	90,778,981 (GRCm38)	missense	unknown
R0736:Col6a3	UTSW	1	90,804,089 (GRCm38)	missense	possibly damaging	0.95
R0737:Col6a3	UTSW	1	90,828,298 (GRCm38)	missense	probably damaging	1.00
R0747:Col6a3	UTSW	1	90,802,653 (GRCm38)	missense	probably damaging	1.00
R1155:Col6a3	UTSW	1	90,794,325 (GRCm38)	missense	probably null	1.00
R1169:Col6a3	UTSW	1	90,822,014 (GRCm38)	missense	possibly damaging	0.67
R1180:Col6a3	UTSW	1	90,781,855 (GRCm38)	missense	unknown
R1225:Col6a3	UTSW	1	90,811,516 (GRCm38)	missense	probably damaging	1.00
R1343:Col6a3	UTSW	1	90,768,347 (GRCm38)	missense	unknown
R1387:Col6a3	UTSW	1	90,822,416 (GRCm38)	intron	probably benign
R1437:Col6a3	UTSW	1	90,801,376 (GRCm38)	missense	probably damaging	1.00
R1448:Col6a3	UTSW	1	90,781,855 (GRCm38)	missense	unknown
R1677:Col6a3	UTSW	1	90,821,861 (GRCm38)	missense	probably benign	0.14
R1681:Col6a3	UTSW	1	90,773,502 (GRCm38)	missense	unknown
R1711:Col6a3	UTSW	1	90,830,213 (GRCm38)	missense	probably damaging	1.00
R1727:Col6a3	UTSW	1	90,796,574 (GRCm38)	critical splice acceptor site	probably null
R1736:Col6a3	UTSW	1	90,779,059 (GRCm38)	missense	unknown
R1738:Col6a3	UTSW	1	90,816,361 (GRCm38)	missense	probably damaging	1.00
R1742:Col6a3	UTSW	1	90,813,794 (GRCm38)	missense	probably damaging	1.00
R1809:Col6a3	UTSW	1	90,827,949 (GRCm38)	missense	probably damaging	1.00
R1851:Col6a3	UTSW	1	90,807,534 (GRCm38)	missense	possibly damaging	0.69
R1852:Col6a3	UTSW	1	90,807,534 (GRCm38)	missense	possibly damaging	0.69
R1872:Col6a3	UTSW	1	90,830,214 (GRCm38)	missense	probably damaging	0.96
R1889:Col6a3	UTSW	1	90,803,711 (GRCm38)	missense	probably benign	0.00
R1895:Col6a3	UTSW	1	90,803,711 (GRCm38)	missense	probably benign	0.00
R1908:Col6a3	UTSW	1	90,811,699 (GRCm38)	missense	probably damaging	1.00
R1973:Col6a3	UTSW	1	90,804,175 (GRCm38)	missense	probably damaging	1.00
R2083:Col6a3	UTSW	1	90,782,011 (GRCm38)	missense	unknown
R2121:Col6a3	UTSW	1	90,810,365 (GRCm38)	missense	probably damaging	1.00
R2197:Col6a3	UTSW	1	90,803,745 (GRCm38)	missense	probably benign	0.09
R2448:Col6a3	UTSW	1	90,813,358 (GRCm38)	missense	probably damaging	1.00
R2831:Col6a3	UTSW	1	90,803,713 (GRCm38)	missense	possibly damaging	0.89
R2877:Col6a3	UTSW	1	90,775,599 (GRCm38)	missense	unknown
R3052:Col6a3	UTSW	1	90,802,130 (GRCm38)	missense	possibly damaging	0.71
R3104:Col6a3	UTSW	1	90,816,302 (GRCm38)	missense	probably damaging	0.99
R3105:Col6a3	UTSW	1	90,816,302 (GRCm38)	missense	probably damaging	0.99
R3106:Col6a3	UTSW	1	90,816,302 (GRCm38)	missense	probably damaging	0.99
R3418:Col6a3	UTSW	1	90,804,091 (GRCm38)	missense	probably benign	0.42
R3419:Col6a3	UTSW	1	90,804,091 (GRCm38)	missense	probably benign	0.42
R3837:Col6a3	UTSW	1	90,780,081 (GRCm38)	missense	unknown
R4007:Col6a3	UTSW	1	90,802,569 (GRCm38)	missense	probably damaging	1.00
R4082:Col6a3	UTSW	1	90,821,883 (GRCm38)	missense	probably damaging	1.00
R4181:Col6a3	UTSW	1	90,807,614 (GRCm38)	missense	probably damaging	1.00
R4200:Col6a3	UTSW	1	90,801,383 (GRCm38)	missense	probably benign	0.28
R4244:Col6a3	UTSW	1	90,786,639 (GRCm38)	missense	unknown
R4297:Col6a3	UTSW	1	90,811,378 (GRCm38)	missense	probably damaging	1.00
R4302:Col6a3	UTSW	1	90,807,614 (GRCm38)	missense	probably damaging	1.00
R4472:Col6a3	UTSW	1	90,822,014 (GRCm38)	missense	probably benign	0.23
R4600:Col6a3	UTSW	1	90,781,904 (GRCm38)	missense	unknown
R4683:Col6a3	UTSW	1	90,773,457 (GRCm38)	missense	unknown
R4788:Col6a3	UTSW	1	90,772,950 (GRCm38)	critical splice donor site	probably null
R4851:Col6a3	UTSW	1	90,779,289 (GRCm38)	missense	unknown
R4899:Col6a3	UTSW	1	90,802,427 (GRCm38)	missense	probably damaging	0.99
R4904:Col6a3	UTSW	1	90,801,442 (GRCm38)	missense	probably damaging	1.00
R4908:Col6a3	UTSW	1	90,807,524 (GRCm38)	missense	probably damaging	1.00
R4960:Col6a3	UTSW	1	90,804,218 (GRCm38)	missense	probably damaging	1.00
R4981:Col6a3	UTSW	1	90,778,843 (GRCm38)	missense	unknown
R5057:Col6a3	UTSW	1	90,816,130 (GRCm38)	missense	possibly damaging	0.91
R5062:Col6a3	UTSW	1	90,779,352 (GRCm38)	missense	unknown
R5105:Col6a3	UTSW	1	90,798,140 (GRCm38)	missense	possibly damaging	0.81
R5127:Col6a3	UTSW	1	90,768,345 (GRCm38)	missense	unknown
R5166:Col6a3	UTSW	1	90,810,608 (GRCm38)	missense	probably damaging	1.00
R5168:Col6a3	UTSW	1	90,773,639 (GRCm38)	nonsense	probably null
R5196:Col6a3	UTSW	1	90,816,538 (GRCm38)	splice site	probably null
R5230:Col6a3	UTSW	1	90,789,054 (GRCm38)	missense	unknown
R5268:Col6a3	UTSW	1	90,785,243 (GRCm38)	missense	unknown
R5381:Col6a3	UTSW	1	90,775,612 (GRCm38)	missense	unknown
R5392:Col6a3	UTSW	1	90,801,295 (GRCm38)	missense	probably benign	0.41
R5445:Col6a3	UTSW	1	90,782,039 (GRCm38)	nonsense	probably null
R5571:Col6a3	UTSW	1	90,788,216 (GRCm38)	missense	unknown
R5665:Col6a3	UTSW	1	90,827,880 (GRCm38)	missense	probably benign	0.00
R5902:Col6a3	UTSW	1	90,802,199 (GRCm38)	splice site	probably null
R5914:Col6a3	UTSW	1	90,776,200 (GRCm38)	missense	unknown
R5955:Col6a3	UTSW	1	90,811,441 (GRCm38)	missense	probably damaging	1.00
R5977:Col6a3	UTSW	1	90,821,849 (GRCm38)	missense	possibly damaging	0.82
R6006:Col6a3	UTSW	1	90,768,383 (GRCm38)	missense	unknown
R6010:Col6a3	UTSW	1	90,773,497 (GRCm38)	missense	unknown
R6025:Col6a3	UTSW	1	90,828,102 (GRCm38)	missense	probably damaging	1.00
R6151:Col6a3	UTSW	1	90,813,753 (GRCm38)	missense	possibly damaging	0.53
R6154:Col6a3	UTSW	1	90,773,665 (GRCm38)	missense	unknown
R6181:Col6a3	UTSW	1	90,816,374 (GRCm38)	missense	possibly damaging	0.95
R6197:Col6a3	UTSW	1	90,822,341 (GRCm38)	missense	probably damaging	1.00
R6332:Col6a3	UTSW	1	90,822,233 (GRCm38)	missense	probably damaging	1.00
R6362:Col6a3	UTSW	1	90,810,563 (GRCm38)	missense	probably damaging	0.99
R6476:Col6a3	UTSW	1	90,781,812 (GRCm38)	missense	unknown
R6484:Col6a3	UTSW	1	90,791,923 (GRCm38)	critical splice donor site	probably null
R6701:Col6a3	UTSW	1	90,792,462 (GRCm38)	missense	probably benign	0.14
R6702:Col6a3	UTSW	1	90,779,439 (GRCm38)	missense	unknown
R6703:Col6a3	UTSW	1	90,792,462 (GRCm38)	missense	probably benign	0.14
R6703:Col6a3	UTSW	1	90,779,439 (GRCm38)	missense	unknown
R6724:Col6a3	UTSW	1	90,779,152 (GRCm38)	missense	unknown
R6746:Col6a3	UTSW	1	90,779,045 (GRCm38)	missense	unknown
R6797:Col6a3	UTSW	1	90,804,088 (GRCm38)	missense	probably damaging	0.99
R6798:Col6a3	UTSW	1	90,795,009 (GRCm38)	splice site	probably null
R6903:Col6a3	UTSW	1	90,794,207 (GRCm38)	missense	probably damaging	1.00
R6925:Col6a3	UTSW	1	90,816,002 (GRCm38)	missense	probably benign	0.00
R6978:Col6a3	UTSW	1	90,807,470 (GRCm38)	critical splice donor site	probably null
R7058:Col6a3	UTSW	1	90,828,037 (GRCm38)	nonsense	probably null
R7182:Col6a3	UTSW	1	90,803,678 (GRCm38)	nonsense	probably null
R7294:Col6a3	UTSW	1	90,828,283 (GRCm38)	missense	probably damaging	1.00
R7296:Col6a3	UTSW	1	90,827,986 (GRCm38)	missense	probably benign	0.00
R7311:Col6a3	UTSW	1	90,822,291 (GRCm38)	missense	probably damaging	1.00
R7412:Col6a3	UTSW	1	90,828,133 (GRCm38)	missense	probably damaging	0.98
R7561:Col6a3	UTSW	1	90,775,741 (GRCm38)	missense	unknown
R7575:Col6a3	UTSW	1	90,810,599 (GRCm38)	missense	possibly damaging	0.92
R7659:Col6a3	UTSW	1	90,781,745 (GRCm38)	missense	unknown
R7679:Col6a3	UTSW	1	90,811,751 (GRCm38)	missense	possibly damaging	0.49
R7831:Col6a3	UTSW	1	90,796,546 (GRCm38)	nonsense	probably null
R7855:Col6a3	UTSW	1	90,810,621 (GRCm38)	missense	possibly damaging	0.57
R7990:Col6a3	UTSW	1	90,781,855 (GRCm38)	missense	unknown
R8003:Col6a3	UTSW	1	90,775,733 (GRCm38)	missense	unknown
R8007:Col6a3	UTSW	1	90,777,457 (GRCm38)	missense	unknown
R8098:Col6a3	UTSW	1	90,803,661 (GRCm38)	missense	probably benign
R8312:Col6a3	UTSW	1	90,813,690 (GRCm38)	missense	possibly damaging	0.55
R8419:Col6a3	UTSW	1	90,802,213 (GRCm38)	missense	probably damaging	1.00
R8723:Col6a3	UTSW	1	90,767,606 (GRCm38)	critical splice acceptor site	probably benign
R8725:Col6a3	UTSW	1	90,767,606 (GRCm38)	critical splice acceptor site	probably benign
R8737:Col6a3	UTSW	1	90,800,025 (GRCm38)	missense	probably benign	0.10
R8742:Col6a3	UTSW	1	90,767,606 (GRCm38)	critical splice acceptor site	probably benign
R8743:Col6a3	UTSW	1	90,767,606 (GRCm38)	critical splice acceptor site	probably benign
R8744:Col6a3	UTSW	1	90,767,606 (GRCm38)	critical splice acceptor site	probably benign
R8753:Col6a3	UTSW	1	90,767,606 (GRCm38)	critical splice acceptor site	probably benign
R8754:Col6a3	UTSW	1	90,767,606 (GRCm38)	critical splice acceptor site	probably benign
R8773:Col6a3	UTSW	1	90,768,449 (GRCm38)	missense	unknown
R8857:Col6a3	UTSW	1	90,775,763 (GRCm38)	missense	unknown
R8867:Col6a3	UTSW	1	90,787,951 (GRCm38)	missense	unknown
R8887:Col6a3	UTSW	1	90,828,226 (GRCm38)	missense	probably benign
R9011:Col6a3	UTSW	1	90,782,335 (GRCm38)	splice site	probably benign
R9049:Col6a3	UTSW	1	90,779,344 (GRCm38)	missense	unknown
R9142:Col6a3	UTSW	1	90,778,844 (GRCm38)	missense	unknown
R9155:Col6a3	UTSW	1	90,810,579 (GRCm38)	missense	probably benign	0.27
R9249:Col6a3	UTSW	1	90,779,298 (GRCm38)	missense	unknown
R9258:Col6a3	UTSW	1	90,772,981 (GRCm38)	missense	unknown
R9274:Col6a3	UTSW	1	90,779,298 (GRCm38)	missense	unknown
R9276:Col6a3	UTSW	1	90,807,681 (GRCm38)	missense	possibly damaging	0.94
R9315:Col6a3	UTSW	1	90,811,257 (GRCm38)	critical splice donor site	probably null
R9376:Col6a3	UTSW	1	90,781,801 (GRCm38)	missense	unknown
R9377:Col6a3	UTSW	1	90,816,239 (GRCm38)	missense	probably damaging	1.00
R9429:Col6a3	UTSW	1	90,803,863 (GRCm38)	missense	probably benign	0.01
R9439:Col6a3	UTSW	1	90,816,433 (GRCm38)	missense	probably damaging	1.00
R9440:Col6a3	UTSW	1	90,779,346 (GRCm38)	missense	unknown
R9441:Col6a3	UTSW	1	90,777,527 (GRCm38)	nonsense	probably null
R9477:Col6a3	UTSW	1	90,778,899 (GRCm38)	missense	unknown
R9498:Col6a3	UTSW	1	90,785,928 (GRCm38)	nonsense	probably null
R9528:Col6a3	UTSW	1	90,804,067 (GRCm38)	missense	probably damaging	1.00
R9602:Col6a3	UTSW	1	90,803,775 (GRCm38)	missense	probably benign	0.07
RF005:Col6a3	UTSW	1	90,811,262 (GRCm38)	missense	probably benign	0.00
RF012:Col6a3	UTSW	1	90,810,560 (GRCm38)	missense	probably damaging	1.00
X0024:Col6a3	UTSW	1	90,803,637 (GRCm38)	critical splice donor site	probably null
X0063:Col6a3	UTSW	1	90,803,905 (GRCm38)	missense	probably damaging	1.00
X0067:Col6a3	UTSW	1	90,811,529 (GRCm38)	missense	probably damaging	1.00
Z1177:Col6a3	UTSW	1	90,811,728 (GRCm38)	missense	possibly damaging	0.82

Predicted Primers

PCR Primer
(F):5'- CAACCAAGCTGAGCCCTTTC -3'
(R):5'- AGAGACTTCACATTCCTTCATTGAC -3'

Sequencing Primer
(F):5'- TTTCACGGCATCCAGAACTG -3'
(R):5'- GGATGATGCATGTTGGTCA -3'

Posted On

2014-07-14