Mutagenetix > Incidental Mutation

Incidental Mutation 'R6254:Muc6'

505986

Institutional Source

Beutler Lab

Gene Symbol

Muc6

Ensembl Gene

ENSMUSG00000048191

Gene Name

mucin 6, gastric

Synonyms

MMRRC Submission

044371-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.186) question?

Stock #

R6254 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

141633456-141655319 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 141651115 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 252 (N252S)

Ref Sequence

ENSEMBL: ENSMUSP00000140483 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000062451] [ENSMUST00000189314] [ENSMUST00000190907]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000062451
AA Change: N252S

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

SMART Domains

Protein: ENSMUSP00000049941
Gene: ENSMUSG00000048191
AA Change: N252S

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
VWD	29	234	2.49e-14	SMART
C8	267	340	5.46e-3	SMART
Pfam:TIL	344	399	5.6e-14	PFAM
VWC	401	469	2.57e-7	SMART
VWD	428	591	4.81e-30	SMART
C8	627	703	8.84e-21	SMART
SCOP:d1coua_	706	769	7e-9	SMART
Pfam:TIL	806	869	1.9e-9	PFAM
VWC	871	941	8.52e-3	SMART
VWD	898	1060	1.59e-30	SMART
C8	1096	1170	5.52e-31	SMART
Blast:CT	1184	1236	2e-19	BLAST
low complexity region	1240	1269	N/A	INTRINSIC
low complexity region	1275	1293	N/A	INTRINSIC
low complexity region	1313	1337	N/A	INTRINSIC
low complexity region	1345	1374	N/A	INTRINSIC
internal_repeat_3	1375	1560	6.78e-17	PROSPERO
internal_repeat_2	1426	1751	8.94e-34	PROSPERO
low complexity region	1761	1780	N/A	INTRINSIC
low complexity region	1867	1887	N/A	INTRINSIC
low complexity region	1896	1910	N/A	INTRINSIC
low complexity region	1912	1946	N/A	INTRINSIC
low complexity region	1990	2004	N/A	INTRINSIC
low complexity region	2010	2020	N/A	INTRINSIC
internal_repeat_2	2036	2430	8.94e-34	PROSPERO
internal_repeat_3	2329	2516	6.78e-17	PROSPERO
low complexity region	2519	2536	N/A	INTRINSIC
low complexity region	2564	2587	N/A	INTRINSIC
low complexity region	2605	2630	N/A	INTRINSIC
low complexity region	2642	2677	N/A	INTRINSIC
low complexity region	2729	2762	N/A	INTRINSIC
Blast:CT	2765	2852	1e-44	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000189314
AA Change: N211S

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000140388
Gene: ENSMUSG00000048191
AA Change: N211S

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
VWD	29	193	2.64e-27	SMART
C8	226	299	5.46e-3	SMART
Pfam:TIL	303	358	1.4e-13	PFAM
VWC	360	428	2.57e-7	SMART
VWD	387	550	4.81e-30	SMART
C8	586	662	8.84e-21	SMART
internal_repeat_2	665	754	5.76e-7	PROSPERO
Pfam:TIL	765	828	6.4e-9	PFAM
VWC	830	900	8.52e-3	SMART
VWD	857	1019	1.59e-30	SMART
C8	1055	1129	5.52e-31	SMART
low complexity region	1199	1228	N/A	INTRINSIC
low complexity region	1234	1252	N/A	INTRINSIC
low complexity region	1272	1296	N/A	INTRINSIC
low complexity region	1304	1333	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000190907
AA Change: N252S

PolyPhen 2 Score 0.088 (Sensitivity: 0.93; Specificity: 0.85)

SMART Domains

Protein: ENSMUSP00000140483
Gene: ENSMUSG00000048191
AA Change: N252S

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
VWD	29	234	1.2e-16	SMART
C8	267	340	4.2e-7	SMART
Pfam:TIL	344	399	7.2e-11	PFAM
VWC_def	401	469	1.2e-9	SMART
VWD	428	591	2.4e-32	SMART
C8	627	703	6.7e-25	SMART
SCOP:d1coua_	706	769	5e-9	SMART
Pfam:TIL	806	869	3.3e-6	PFAM
VWC_def	871	941	4.1e-5	SMART
VWD	898	1060	7.7e-33	SMART
C8	1096	1170	4.2e-35	SMART
Blast:CT	1184	1236	2e-19	BLAST
low complexity region	1240	1269	N/A	INTRINSIC
low complexity region	1275	1293	N/A	INTRINSIC
low complexity region	1313	1337	N/A	INTRINSIC
low complexity region	1345	1374	N/A	INTRINSIC
low complexity region	1406	1419	N/A	INTRINSIC
internal_repeat_1	1426	1822	3.44e-48	PROSPERO
low complexity region	1826	1845	N/A	INTRINSIC
low complexity region	1932	1952	N/A	INTRINSIC
low complexity region	1961	1975	N/A	INTRINSIC
low complexity region	1977	2011	N/A	INTRINSIC
low complexity region	2055	2069	N/A	INTRINSIC
low complexity region	2075	2085	N/A	INTRINSIC
internal_repeat_1	2101	2501	3.44e-48	PROSPERO
low complexity region	2504	2524	N/A	INTRINSIC
low complexity region	2584	2601	N/A	INTRINSIC
low complexity region	2629	2652	N/A	INTRINSIC
low complexity region	2670	2695	N/A	INTRINSIC
low complexity region	2707	2742	N/A	INTRINSIC
low complexity region	2794	2827	N/A	INTRINSIC
Blast:CT	2830	2917	1e-44	BLAST

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.2%
20x: 94.4%

Validation Efficiency

100% (82/82)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the mucin protein family. Mucins are high molecular weight glycoproteins produced by many epithelial tissues. The protein encoded by this gene is secreted and forms an insoluble mucous barrier that protects the gut lumen. [provided by RefSeq, Dec 2016]

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4932443I19Rik	A	G	8: 13,706,043 (GRCm38)	D26G	possibly damaging	Het
Adam6b	A	T	12: 113,489,570 (GRCm38)	L2F	probably damaging	Het
Ank2	T	A	3: 126,941,804 (GRCm38)		probably benign	Het
Anpep	T	G	7: 79,839,233 (GRCm38)	D369A	probably damaging	Het
App	T	C	16: 84,978,177 (GRCm38)	E599G	probably damaging	Het
Asphd1	C	T	7: 126,948,868 (GRCm38)	V88I	probably benign	Het
Atad5	A	T	11: 80,127,389 (GRCm38)	I1389F	probably damaging	Het
Blm	T	C	7: 80,480,342 (GRCm38)	N950S	probably benign	Het
Bsn	A	T	9: 108,111,866 (GRCm38)	M2229K	probably damaging	Het
Cacna2d2	A	G	9: 107,509,216 (GRCm38)	M181V	probably benign	Het
Cadps2	T	A	6: 23,329,163 (GRCm38)		probably null	Het
Cdh1	T	A	8: 106,663,798 (GRCm38)	V590D	probably damaging	Het
Cdk5rap2	G	A	4: 70,364,032 (GRCm38)	T160M	probably damaging	Het
Chrna5	A	G	9: 55,006,456 (GRCm38)	M325V	probably benign	Het
Clca3a2	A	G	3: 144,802,134 (GRCm38)	I116T	probably benign	Het
Cyp2c23	T	C	19: 44,005,463 (GRCm38)	K488R	probably benign	Het
Edil3	T	A	13: 89,319,729 (GRCm38)	I451N	probably damaging	Het
Exph5	T	G	9: 53,372,710 (GRCm38)	S364A	possibly damaging	Het
Fam84b	A	G	15: 60,823,801 (GRCm38)	I32T	probably damaging	Het
Fam98c	A	G	7: 29,154,517 (GRCm38)	S209P	probably damaging	Het
Fat3	G	A	9: 15,996,145 (GRCm38)	L2854F	probably benign	Het
Fbxo38	T	C	18: 62,505,500 (GRCm38)		probably null	Het
Fermt2	T	C	14: 45,476,059 (GRCm38)	D205G	probably damaging	Het
Fmnl1	G	A	11: 103,196,315 (GRCm38)		probably benign	Het
Fn3k	A	G	11: 121,435,068 (GRCm38)	E27G	probably damaging	Het
Foxj2	A	G	6: 122,838,139 (GRCm38)	H378R	probably damaging	Het
Fubp1	A	G	3: 152,232,408 (GRCm38)	K140E	possibly damaging	Het
Gm4788	A	G	1: 139,754,390 (GRCm38)	I156T	probably damaging	Het
Gm7694	A	T	1: 170,302,534 (GRCm38)	C98*	probably null	Het
Golgb1	T	C	16: 36,913,978 (GRCm38)	S1196P	probably damaging	Het
Gpm6a	G	A	8: 55,047,396 (GRCm38)		probably null	Het
Hltf	T	A	3: 20,063,829 (GRCm38)	N80K	possibly damaging	Het
Il1rap	G	A	16: 26,695,270 (GRCm38)	R251H	probably benign	Het
Ipo7	T	A	7: 110,049,060 (GRCm38)	D688E	probably benign	Het
Itgal	T	A	7: 127,325,203 (GRCm38)	N897K	probably damaging	Het
Itsn2	A	G	12: 4,624,982 (GRCm38)		probably null	Het
Kcnk13	A	G	12: 99,965,372 (GRCm38)		probably benign	Het
Kdm7a	A	G	6: 39,170,269 (GRCm38)	L248P	probably damaging	Het
Kmt2c	T	C	5: 25,349,874 (GRCm38)	E1254G	possibly damaging	Het
Ldah	G	A	12: 8,275,912 (GRCm38)		probably benign	Het
Lingo1	T	A	9: 56,620,087 (GRCm38)	D406V	possibly damaging	Het
Lrriq1	A	T	10: 103,215,451 (GRCm38)	V480E	probably benign	Het
Mtcl1	C	T	17: 66,358,134 (GRCm38)	R1142H	probably benign	Het
Mtmr3	G	A	11: 4,497,381 (GRCm38)	Q360*	probably null	Het
Naa20	T	C	2: 145,903,320 (GRCm38)	L4P	probably damaging	Het
Neb	T	A	2: 52,222,961 (GRCm38)	I4274L	probably benign	Het
Noa1	A	T	5: 77,309,669 (GRCm38)	F130I	probably benign	Het
Nrg4	G	T	9: 55,236,512 (GRCm38)	H87N	possibly damaging	Het
Olfr1024	T	A	2: 85,904,505 (GRCm38)	Y183F	probably damaging	Het
Olfr632	T	A	7: 103,937,534 (GRCm38)	H51Q	probably benign	Het
P3h3	C	T	6: 124,845,601 (GRCm38)	E536K	probably damaging	Het
Pcdhb11	T	C	18: 37,421,718 (GRCm38)	S34P	probably damaging	Het
Pik3r1	T	C	13: 101,689,406 (GRCm38)	T71A	possibly damaging	Het
Plaur	T	A	7: 24,466,800 (GRCm38)	C99S	possibly damaging	Het
Plekha5	G	A	6: 140,586,436 (GRCm38)	G501E	probably damaging	Het
Plxnd1	C	T	6: 115,977,960 (GRCm38)	V614M	probably benign	Het
Ppp2r3a	T	C	9: 101,148,587 (GRCm38)	D307G	possibly damaging	Het
Prl3d3	C	T	13: 27,157,470 (GRCm38)	S28F	possibly damaging	Het
Prpf40a	T	C	2: 53,157,915 (GRCm38)	M197V	probably benign	Het
Ptk7	C	A	17: 46,572,642 (GRCm38)	Q832H	probably damaging	Het
Qser1	T	C	2: 104,790,090 (GRCm38)	S126G	probably benign	Het
Rab3ip	A	T	10: 116,915,867 (GRCm38)	C332S	probably damaging	Het
Raly	C	A	2: 154,857,366 (GRCm38)	T30K	probably damaging	Het
Rbp2	G	T	9: 98,490,647 (GRCm38)	S13I	probably benign	Het
Rps6ka1	C	T	4: 133,867,224 (GRCm38)	M159I	possibly damaging	Het
Rufy3	C	T	5: 88,584,309 (GRCm38)	T57I	probably benign	Het
Samd4	A	G	14: 47,016,631 (GRCm38)	D184G	probably damaging	Het
Slc35f3	T	C	8: 126,321,094 (GRCm38)	C58R	possibly damaging	Het
Smarca4	T	C	9: 21,699,877 (GRCm38)	I1467T	probably damaging	Het
Spag17	T	G	3: 100,065,585 (GRCm38)	I1371S	probably benign	Het
Sptan1	T	C	2: 30,007,549 (GRCm38)	L1228P	possibly damaging	Het
Stk31	C	T	6: 49,421,697 (GRCm38)	A344V	probably benign	Het
Supt16	A	G	14: 52,170,834 (GRCm38)	W885R	probably damaging	Het
Tdrd9	T	A	12: 112,025,900 (GRCm38)		probably null	Het
Tmod1	A	G	4: 46,078,469 (GRCm38)		probably null	Het
Tnfsf13	A	C	11: 69,684,483 (GRCm38)		probably null	Het
Trim75	C	A	8: 64,983,442 (GRCm38)	E119*	probably null	Het
Wdr6	T	C	9: 108,574,911 (GRCm38)	Y591C	probably damaging	Het
Wdr86	C	T	5: 24,718,283 (GRCm38)	R137H	probably benign	Het
Ythdf1	T	A	2: 180,911,150 (GRCm38)	Y424F	probably damaging	Het
Zfp984	G	T	4: 147,756,186 (GRCm38)	S69R	possibly damaging	Het
Zyg11a	A	G	4: 108,181,794 (GRCm38)	F743L	probably damaging	Het

Other mutations in Muc6

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00091:Muc6	APN	7	141,638,584 (GRCm38)	missense	probably benign	0.06
IGL00466:Muc6	APN	7	141,645,902 (GRCm38)	missense	possibly damaging	0.94
IGL00990:Muc6	APN	7	141,638,890 (GRCm38)	missense	possibly damaging	0.85
IGL01013:Muc6	APN	7	141,648,066 (GRCm38)	nonsense	probably null
IGL01021:Muc6	APN	7	141,637,162 (GRCm38)	missense	possibly damaging	0.53
IGL01061:Muc6	APN	7	141,648,454 (GRCm38)	missense	probably damaging	1.00
IGL01294:Muc6	APN	7	141,646,659 (GRCm38)	missense	probably damaging	1.00
IGL01449:Muc6	APN	7	141,638,614 (GRCm38)	missense	possibly damaging	0.92
IGL01474:Muc6	APN	7	141,651,307 (GRCm38)	missense	probably damaging	1.00
IGL01539:Muc6	APN	7	141,650,041 (GRCm38)	missense	probably benign	0.07
IGL01541:Muc6	APN	7	141,649,804 (GRCm38)	nonsense	probably null
IGL01810:Muc6	APN	7	141,651,062 (GRCm38)	missense	probably damaging	0.97
IGL01941:Muc6	APN	7	141,638,584 (GRCm38)	missense	probably benign	0.06
IGL01954:Muc6	APN	7	141,638,584 (GRCm38)	missense	probably benign	0.06
IGL02096:Muc6	APN	7	141,639,850 (GRCm38)	intron	probably benign
IGL02192:Muc6	APN	7	141,637,804 (GRCm38)	missense	possibly damaging	0.91
IGL02217:Muc6	APN	7	141,649,624 (GRCm38)	missense	probably damaging	1.00
IGL02234:Muc6	APN	7	141,640,575 (GRCm38)	missense	probably benign	0.09
IGL02302:Muc6	APN	7	141,641,496 (GRCm38)	missense	possibly damaging	0.53
IGL02331:Muc6	APN	7	141,640,459 (GRCm38)	missense	possibly damaging	0.53
IGL02531:Muc6	APN	7	141,636,940 (GRCm38)	missense	possibly damaging	0.53
IGL02639:Muc6	APN	7	141,649,578 (GRCm38)	splice site	probably benign
IGL02851:Muc6	APN	7	141,648,361 (GRCm38)	missense	probably damaging	1.00
IGL03026:Muc6	APN	7	141,640,147 (GRCm38)	intron	probably benign
IGL03070:Muc6	APN	7	141,644,567 (GRCm38)	splice site	probably benign
IGL03108:Muc6	APN	7	141,637,489 (GRCm38)	missense	possibly damaging	0.93
IGL03350:Muc6	APN	7	141,652,059 (GRCm38)	missense	probably damaging	1.00
IGL03366:Muc6	APN	7	141,648,082 (GRCm38)	missense	probably damaging	1.00
anticipation	UTSW	7	141,634,450 (GRCm38)	frame shift	probably null
F5770:Muc6	UTSW	7	141,647,613 (GRCm38)	missense	probably benign	0.11
IGL03147:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
R0001:Muc6	UTSW	7	141,641,574 (GRCm38)	missense	possibly damaging	0.53
R0005:Muc6	UTSW	7	141,638,772 (GRCm38)	missense	possibly damaging	0.72
R0147:Muc6	UTSW	7	141,651,990 (GRCm38)	missense	probably damaging	1.00
R0153:Muc6	UTSW	7	141,634,116 (GRCm38)	missense	possibly damaging	0.68
R0227:Muc6	UTSW	7	141,639,559 (GRCm38)	intron	probably benign
R0234:Muc6	UTSW	7	141,649,674 (GRCm38)	missense	possibly damaging	0.95
R0234:Muc6	UTSW	7	141,649,674 (GRCm38)	missense	possibly damaging	0.95
R0304:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
R0379:Muc6	UTSW	7	141,636,955 (GRCm38)	missense	possibly damaging	0.53
R0385:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
R0423:Muc6	UTSW	7	141,652,283 (GRCm38)	missense	probably benign	0.01
R0499:Muc6	UTSW	7	141,640,468 (GRCm38)	missense	probably benign
R0503:Muc6	UTSW	7	141,638,772 (GRCm38)	missense	possibly damaging	0.72
R0757:Muc6	UTSW	7	141,638,584 (GRCm38)	missense	probably benign	0.06
R0792:Muc6	UTSW	7	141,639,559 (GRCm38)	intron	probably benign
R0880:Muc6	UTSW	7	141,637,357 (GRCm38)	missense	possibly damaging	0.91
R1136:Muc6	UTSW	7	141,638,772 (GRCm38)	missense	possibly damaging	0.72
R1170:Muc6	UTSW	7	141,644,233 (GRCm38)	missense	probably damaging	0.99
R1174:Muc6	UTSW	7	141,648,101 (GRCm38)	missense	probably damaging	1.00
R1175:Muc6	UTSW	7	141,648,101 (GRCm38)	missense	probably damaging	1.00
R1189:Muc6	UTSW	7	141,645,855 (GRCm38)	missense	probably damaging	1.00
R1259:Muc6	UTSW	7	141,640,197 (GRCm38)	intron	probably benign
R1293:Muc6	UTSW	7	141,651,990 (GRCm38)	missense	probably damaging	1.00
R1295:Muc6	UTSW	7	141,651,879 (GRCm38)	missense	probably benign	0.04
R1296:Muc6	UTSW	7	141,651,879 (GRCm38)	missense	probably benign	0.04
R1471:Muc6	UTSW	7	141,647,909 (GRCm38)	missense	possibly damaging	0.61
R1472:Muc6	UTSW	7	141,651,879 (GRCm38)	missense	probably benign	0.04
R1548:Muc6	UTSW	7	141,638,772 (GRCm38)	missense	possibly damaging	0.72
R1548:Muc6	UTSW	7	141,652,103 (GRCm38)	splice site	probably benign
R1576:Muc6	UTSW	7	141,634,524 (GRCm38)	missense	possibly damaging	0.92
R1689:Muc6	UTSW	7	141,647,998 (GRCm38)	missense	probably damaging	1.00
R1702:Muc6	UTSW	7	141,650,487 (GRCm38)	missense	probably damaging	1.00
R1792:Muc6	UTSW	7	141,634,458 (GRCm38)	missense	probably benign	0.41
R1924:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
R1938:Muc6	UTSW	7	141,637,098 (GRCm38)	missense	probably damaging	0.99
R1964:Muc6	UTSW	7	141,640,063 (GRCm38)	intron	probably benign
R1964:Muc6	UTSW	7	141,640,062 (GRCm38)	nonsense	probably null
R1975:Muc6	UTSW	7	141,648,101 (GRCm38)	missense	probably damaging	1.00
R2031:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
R2104:Muc6	UTSW	7	141,634,078 (GRCm38)	missense	probably benign	0.23
R2201:Muc6	UTSW	7	141,649,810 (GRCm38)	missense	probably damaging	1.00
R2218:Muc6	UTSW	7	141,646,960 (GRCm38)	missense	probably benign	0.41
R2245:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
R2261:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
R2271:Muc6	UTSW	7	141,637,510 (GRCm38)	missense	possibly damaging	0.53
R2272:Muc6	UTSW	7	141,637,510 (GRCm38)	missense	possibly damaging	0.53
R2284:Muc6	UTSW	7	141,637,924 (GRCm38)	missense	possibly damaging	0.53
R2310:Muc6	UTSW	7	141,637,531 (GRCm38)	missense	possibly damaging	0.53
R2566:Muc6	UTSW	7	141,640,384 (GRCm38)	missense	possibly damaging	0.73
R2975:Muc6	UTSW	7	141,637,038 (GRCm38)	missense	possibly damaging	0.86
R3406:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
R3423:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
R3548:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
R3693:Muc6	UTSW	7	141,648,681 (GRCm38)	splice site	probably benign
R3872:Muc6	UTSW	7	141,640,600 (GRCm38)	missense	probably benign
R4029:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
R4084:Muc6	UTSW	7	141,648,655 (GRCm38)	missense	probably damaging	1.00
R4126:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
R4410:Muc6	UTSW	7	141,637,663 (GRCm38)	missense	possibly damaging	0.91
R4508:Muc6	UTSW	7	141,640,089 (GRCm38)	intron	probably benign
R4509:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
R4518:Muc6	UTSW	7	141,644,222 (GRCm38)	missense	probably benign	0.03
R4594:Muc6	UTSW	7	141,638,772 (GRCm38)	missense	possibly damaging	0.72
R4677:Muc6	UTSW	7	141,639,790 (GRCm38)	intron	probably benign
R4678:Muc6	UTSW	7	141,644,287 (GRCm38)	missense	probably benign	0.09
R4737:Muc6	UTSW	7	141,638,772 (GRCm38)	missense	possibly damaging	0.72
R4737:Muc6	UTSW	7	141,640,159 (GRCm38)	intron	probably benign
R4981:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
R5008:Muc6	UTSW	7	141,639,559 (GRCm38)	intron	probably benign
R5012:Muc6	UTSW	7	141,636,657 (GRCm38)	missense	possibly damaging	0.96
R5017:Muc6	UTSW	7	141,640,528 (GRCm38)	missense	probably benign
R5027:Muc6	UTSW	7	141,636,436 (GRCm38)	missense	probably benign	0.01
R5058:Muc6	UTSW	7	141,644,224 (GRCm38)	missense	probably benign	0.01
R5069:Muc6	UTSW	7	141,651,299 (GRCm38)	missense	probably damaging	1.00
R5126:Muc6	UTSW	7	141,651,299 (GRCm38)	missense	probably damaging	1.00
R5168:Muc6	UTSW	7	141,639,559 (GRCm38)	intron	probably benign
R5179:Muc6	UTSW	7	141,638,772 (GRCm38)	missense	possibly damaging	0.72
R5198:Muc6	UTSW	7	141,638,772 (GRCm38)	missense	possibly damaging	0.72
R5262:Muc6	UTSW	7	141,651,110 (GRCm38)	missense	possibly damaging	0.78
R5381:Muc6	UTSW	7	141,637,923 (GRCm38)	missense	possibly damaging	0.86
R5454:Muc6	UTSW	7	141,648,813 (GRCm38)	missense	possibly damaging	0.61
R5467:Muc6	UTSW	7	141,636,535 (GRCm38)	missense	possibly damaging	0.53
R5540:Muc6	UTSW	7	141,649,585 (GRCm38)	critical splice donor site	probably null
R5800:Muc6	UTSW	7	141,640,423 (GRCm38)	splice site	probably benign
R5808:Muc6	UTSW	7	141,640,093 (GRCm38)	intron	probably benign
R5865:Muc6	UTSW	7	141,650,504 (GRCm38)	missense	probably damaging	0.97
R5919:Muc6	UTSW	7	141,641,570 (GRCm38)	missense	possibly damaging	0.56
R6024:Muc6	UTSW	7	141,641,574 (GRCm38)	missense	possibly damaging	0.53
R6064:Muc6	UTSW	7	141,648,374 (GRCm38)	missense	probably damaging	1.00
R6126:Muc6	UTSW	7	141,638,772 (GRCm38)	missense	possibly damaging	0.72
R6229:Muc6	UTSW	7	141,640,525 (GRCm38)	missense	probably benign
R6236:Muc6	UTSW	7	141,638,772 (GRCm38)	missense	possibly damaging	0.72
R6245:Muc6	UTSW	7	141,648,821 (GRCm38)	missense	probably damaging	1.00
R6418:Muc6	UTSW	7	141,639,610 (GRCm38)	intron	probably benign
R6609:Muc6	UTSW	7	141,640,433 (GRCm38)	splice site	probably benign
R6610:Muc6	UTSW	7	141,640,433 (GRCm38)	splice site	probably benign
R6611:Muc6	UTSW	7	141,640,433 (GRCm38)	splice site	probably benign
R6623:Muc6	UTSW	7	141,639,559 (GRCm38)	intron	probably benign
R6626:Muc6	UTSW	7	141,639,559 (GRCm38)	intron	probably benign
R6817:Muc6	UTSW	7	141,651,061 (GRCm38)	missense	probably damaging	0.99
R6923:Muc6	UTSW	7	141,637,540 (GRCm38)	missense	possibly damaging	0.91
R6989:Muc6	UTSW	7	141,639,979 (GRCm38)	intron	probably benign
R7001:Muc6	UTSW	7	141,637,407 (GRCm38)	missense	probably damaging	0.99
R7046:Muc6	UTSW	7	141,640,189 (GRCm38)	intron	probably benign
R7097:Muc6	UTSW	7	141,634,450 (GRCm38)	frame shift	probably null
R7099:Muc6	UTSW	7	141,634,450 (GRCm38)	frame shift	probably null
R7101:Muc6	UTSW	7	141,634,450 (GRCm38)	frame shift	probably null
R7107:Muc6	UTSW	7	141,634,450 (GRCm38)	frame shift	probably null
R7108:Muc6	UTSW	7	141,634,450 (GRCm38)	frame shift	probably null
R7112:Muc6	UTSW	7	141,649,277 (GRCm38)	missense	probably damaging	1.00
R7202:Muc6	UTSW	7	141,634,450 (GRCm38)	frame shift	probably null
R7204:Muc6	UTSW	7	141,634,450 (GRCm38)	frame shift	probably null
R7205:Muc6	UTSW	7	141,634,450 (GRCm38)	frame shift	probably null
R7222:Muc6	UTSW	7	141,634,515 (GRCm38)	missense	unknown
R7230:Muc6	UTSW	7	141,649,214 (GRCm38)	missense	probably damaging	1.00
R7278:Muc6	UTSW	7	141,640,575 (GRCm38)	missense	probably benign	0.09
R7483:Muc6	UTSW	7	141,639,823 (GRCm38)	missense	unknown
R7501:Muc6	UTSW	7	141,637,746 (GRCm38)	missense	probably damaging	0.98
R7601:Muc6	UTSW	7	141,636,541 (GRCm38)	missense	unknown
R7641:Muc6	UTSW	7	141,639,825 (GRCm38)	missense	unknown
R7644:Muc6	UTSW	7	141,637,746 (GRCm38)	missense	probably damaging	0.98
R7645:Muc6	UTSW	7	141,648,658 (GRCm38)	missense	probably benign	0.40
R7659:Muc6	UTSW	7	141,637,060 (GRCm38)	missense	possibly damaging	0.53
R7674:Muc6	UTSW	7	141,639,825 (GRCm38)	missense	unknown
R7679:Muc6	UTSW	7	141,637,746 (GRCm38)	missense	probably damaging	0.98
R7680:Muc6	UTSW	7	141,637,746 (GRCm38)	missense	probably damaging	0.98
R7689:Muc6	UTSW	7	141,637,746 (GRCm38)	missense	probably damaging	0.98
R7690:Muc6	UTSW	7	141,637,746 (GRCm38)	missense	probably damaging	0.98
R7760:Muc6	UTSW	7	141,651,057 (GRCm38)	splice site	probably null
R7806:Muc6	UTSW	7	141,637,474 (GRCm38)	missense	possibly damaging	0.53
R7809:Muc6	UTSW	7	141,640,371 (GRCm38)	missense	probably benign	0.02
R7848:Muc6	UTSW	7	141,645,921 (GRCm38)	missense	possibly damaging	0.53
R7859:Muc6	UTSW	7	141,645,420 (GRCm38)	missense	probably damaging	0.96
R8054:Muc6	UTSW	7	141,645,481 (GRCm38)	missense	probably damaging	1.00
R8085:Muc6	UTSW	7	141,640,462 (GRCm38)	missense	unknown
R8130:Muc6	UTSW	7	141,647,087 (GRCm38)	missense	probably damaging	0.97
R8210:Muc6	UTSW	7	141,649,408 (GRCm38)	critical splice donor site	probably null
R8273:Muc6	UTSW	7	141,640,528 (GRCm38)	missense	unknown
R8294:Muc6	UTSW	7	141,637,350 (GRCm38)	missense	possibly damaging	0.96
R8329:Muc6	UTSW	7	141,640,258 (GRCm38)	missense	unknown
R8379:Muc6	UTSW	7	141,644,312 (GRCm38)	nonsense	probably null
R8537:Muc6	UTSW	7	141,647,917 (GRCm38)	missense	probably benign	0.03
R8736:Muc6	UTSW	7	141,642,172 (GRCm38)	missense	possibly damaging	0.53
R8767:Muc6	UTSW	7	141,643,282 (GRCm38)	missense	probably damaging	1.00
R8902:Muc6	UTSW	7	141,647,524 (GRCm38)	missense	possibly damaging	0.93
R9009:Muc6	UTSW	7	141,637,105 (GRCm38)	missense	possibly damaging	0.73
R9010:Muc6	UTSW	7	141,640,084 (GRCm38)	missense	unknown
R9023:Muc6	UTSW	7	141,651,167 (GRCm38)	nonsense	probably null
R9058:Muc6	UTSW	7	141,638,241 (GRCm38)	missense	possibly damaging	0.61
R9257:Muc6	UTSW	7	141,640,471 (GRCm38)	missense	unknown
R9495:Muc6	UTSW	7	141,651,133 (GRCm38)	missense	probably damaging	0.98
R9563:Muc6	UTSW	7	141,637,870 (GRCm38)	missense	possibly damaging	0.53
R9645:Muc6	UTSW	7	141,637,870 (GRCm38)	missense	possibly damaging	0.53
R9659:Muc6	UTSW	7	141,645,833 (GRCm38)	missense	probably damaging	1.00
R9733:Muc6	UTSW	7	141,636,397 (GRCm38)	missense	unknown
R9787:Muc6	UTSW	7	141,641,481 (GRCm38)	nonsense	probably null
R9788:Muc6	UTSW	7	141,645,833 (GRCm38)	missense	probably damaging	1.00
V7581:Muc6	UTSW	7	141,647,613 (GRCm38)	missense	probably benign	0.11
V7583:Muc6	UTSW	7	141,647,613 (GRCm38)	missense	probably benign	0.11
X0026:Muc6	UTSW	7	141,651,699 (GRCm38)	missense	possibly damaging	0.94
X0058:Muc6	UTSW	7	141,638,400 (GRCm38)	missense	possibly damaging	0.95
Z1177:Muc6	UTSW	7	141,651,391 (GRCm38)	missense	probably benign	0.20
Z1177:Muc6	UTSW	7	141,650,436 (GRCm38)	missense	probably benign	0.29
Z1177:Muc6	UTSW	7	141,637,914 (GRCm38)	missense	possibly damaging	0.72

Predicted Primers

PCR Primer
(F):5'- CTCAAGGTCATATGGGCGAG -3'
(R):5'- TGGGCAAGCTATGTGGACTG -3'

Sequencing Primer
(F):5'- GAGGTCACGTCTTGTATCATACCCAG -3'
(R):5'- CTGTGTGGGAACTTCGATGGAAAG -3'

Posted On

2018-02-28