Mutagenetix > Incidental Mutations

Incidental Mutation 'R7074:Muc16'

549105

Institutional Source

Beutler Lab

Gene Symbol

Muc16

Ensembl Gene

ENSMUSG00000109564

Gene Name

mucin 16

Synonyms

1110008I14Rik, LOC385009

MMRRC Submission

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.231) question?

Stock #

R7074 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

18495455-18674530 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 18655650 bp

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 1858 (T1858A)

Ref Sequence

ENSEMBL: ENSMUSP00000147104 (fasta)

Predicted Effect

unknown
Transcript: ENSMUST00000208663
AA Change: T1858A

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Homozygous null mice are viable and fertile with no gross histological abnormalities. Homozygous male mice father larger litters when crossed to wild-type females. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl4	A	T	4: 144,613,863	I53L	probably benign	Het
Acss2	T	C	2: 155,522,041	L80P	possibly damaging	Het
Adam3	A	T	8: 24,694,347	F546I	probably benign	Het
Adtrp	A	T	13: 41,828,141		probably null	Het
Anapc1	G	T	2: 128,678,274	P208T	probably damaging	Het
Ankrd33	A	G	15: 101,119,549	K281R	probably benign	Het
Bcl11b	A	G	12: 107,989,507	S128P	probably benign	Het
Ccdc57	T	C	11: 120,903,374	K265E	possibly damaging	Het
Cep72	A	G	13: 74,051,580	C244R	probably benign	Het
Cope	A	G	8: 70,312,887	Q303R	probably benign	Het
Cpd	T	A	11: 76,813,594	N398I	probably damaging	Het
Cplx1	C	T	5: 108,548,527		probably null	Het
Dixdc1	T	A	9: 50,689,914	E344D	possibly damaging	Het
Dock7	A	T	4: 98,945,208	F1951I	unknown	Het
Ell2	C	A	13: 75,761,887	L119M	probably damaging	Het
Faap24	A	T	7: 35,395,102	I91K	possibly damaging	Het
Fubp3	T	C	2: 31,595,294	S107P	probably damaging	Het
Gas2l2	T	A	11: 83,423,067	Q473L	probably benign	Het
Ghr	A	T	15: 3,333,391	Y200N	probably damaging	Het
Gm4950	G	A	18: 51,865,449	Q145*	probably null	Het
Gm826	C	T	2: 160,311,890	V78I	unknown	Het
Gnas	G	A	2: 174,285,049	E126K	probably damaging	Het
Grip2	A	T	6: 91,784,708	V235E	probably benign	Het
Hmgcl	A	G	4: 135,953,867	H88R	probably benign	Het
Htr7	A	G	19: 36,056,883	V124A	probably damaging	Het
Igf2r	T	A	17: 12,714,116	I840F	possibly damaging	Het
Ints8	T	C	4: 11,204,574	I961V	possibly damaging	Het
Jmy	A	T	13: 93,453,931	S555T	probably benign	Het
Klk1b27	G	A	7: 44,056,553	G227S	probably damaging	Het
Lao1	A	C	4: 118,968,185	T401P	probably damaging	Het
Lrwd1	C	T	5: 136,123,657	V547I	probably benign	Het
Mttp	C	A	3: 138,107,273	R532L	possibly damaging	Het
Myo18a	T	A	11: 77,842,561	D1409E	probably benign	Het
Ncor2	T	A	5: 125,049,366	R554*	probably null	Het
Olfr127	T	A	17: 37,903,827	Y94N	possibly damaging	Het
Olfr168	T	A	16: 19,530,105	I272F	possibly damaging	Het
Olfr222	T	C	11: 59,571,009	T244A	probably damaging	Het
Olfr22-ps1	A	T	11: 73,955,149	H153L	probably benign	Het
Olfr690	A	G	7: 105,329,268	M308T	probably benign	Het
Prkar2b	A	G	12: 31,972,148	Y213H	probably damaging	Het
Prkd3	T	A	17: 78,974,807	K306*	probably null	Het
Psd2	A	G	18: 36,010,684	E681G	probably benign	Het
Sel1l2	T	A	2: 140,263,442	N276I	probably damaging	Het
Smox	C	T	2: 131,522,111	A45V	possibly damaging	Het
Smyd1	A	G	6: 71,237,375	V214A	probably damaging	Het
Spag5	T	C	11: 78,305,042		probably null	Het
Trem3	C	T	17: 48,249,881	R127W	probably damaging	Het
Ttn	G	A	2: 76,918,081	T4208I	probably benign	Het
Tubgcp6	A	G	15: 89,120,636	F260S	probably damaging	Het
Vmn1r51	A	T	6: 90,129,672	D190V	probably benign	Het
Zc3h14	A	G	12: 98,758,600	I174V	possibly damaging	Het
Zfp423	G	A	8: 87,782,432	T428I	probably benign	Het
Zfp608	T	A	18: 54,897,382	N1162I	possibly damaging	Het
Zmym5	T	C	14: 56,804,798	M8V	probably benign	Het

Other mutations in Muc16

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01330:Muc16	APN	9	18508507	missense	possibly damaging	0.89
IGL01878:Muc16	APN	9	18495543	missense	possibly damaging	0.90
IGL02394:Muc16	APN	9	18498700	missense	probably damaging	0.99
IGL02553:Muc16	APN	9	18498553	critical splice donor site	probably null
R0400:Muc16	UTSW	9	18510534	missense	possibly damaging	0.74
R1620:Muc16	UTSW	9	18510477	missense	possibly damaging	0.89
R1695:Muc16	UTSW	9	18497433	missense	probably damaging	1.00
R3196:Muc16	UTSW	9	18497830	missense	probably damaging	1.00
R5982:Muc16	UTSW	9	18647146	missense	unknown
R5990:Muc16	UTSW	9	18659243	missense	unknown
R6024:Muc16	UTSW	9	18646671	missense	unknown
R6026:Muc16	UTSW	9	18659858	missense	unknown
R6028:Muc16	UTSW	9	18657176	missense	unknown
R6083:Muc16	UTSW	9	18657212	missense	unknown
R6089:Muc16	UTSW	9	18643252	missense	unknown
R6109:Muc16	UTSW	9	18655359	missense	unknown
R6127:Muc16	UTSW	9	18657878	missense	unknown
R6130:Muc16	UTSW	9	18590698	missense	probably damaging	1.00
R6146:Muc16	UTSW	9	18497797	missense	probably damaging	0.98
R6161:Muc16	UTSW	9	18647818	missense	unknown
R6164:Muc16	UTSW	9	18558379	missense	probably damaging	1.00
R6185:Muc16	UTSW	9	18654473	missense	unknown
R6192:Muc16	UTSW	9	18658689	missense	unknown
R6217:Muc16	UTSW	9	18655446	missense	unknown
R6232:Muc16	UTSW	9	18656998	missense	unknown
R6246:Muc16	UTSW	9	18577067	intron	probably null
R6255:Muc16	UTSW	9	18655599	missense	unknown
R6280:Muc16	UTSW	9	18579317	critical splice donor site	probably null
R6286:Muc16	UTSW	9	18644389	missense	unknown
R6287:Muc16	UTSW	9	18659034	missense	unknown
R6307:Muc16	UTSW	9	18647588	missense	unknown
R6310:Muc16	UTSW	9	18641950	missense	probably benign	0.00
R6316:Muc16	UTSW	9	18641819	missense	probably benign	0.01
R6335:Muc16	UTSW	9	18660708	missense	unknown
R6345:Muc16	UTSW	9	18654926	missense	unknown
R6349:Muc16	UTSW	9	18657329	missense	unknown
R6366:Muc16	UTSW	9	18646044	missense	unknown
R6393:Muc16	UTSW	9	18647399	nonsense	probably null
R6440:Muc16	UTSW	9	18641359	missense	probably benign	0.01
R6458:Muc16	UTSW	9	18641721	missense	probably benign	0.01
R6460:Muc16	UTSW	9	18640516	missense	probably benign	0.01
R6481:Muc16	UTSW	9	18550677	critical splice donor site	probably null
R6539:Muc16	UTSW	9	18637325	missense	probably benign	0.25
R6551:Muc16	UTSW	9	18562562	missense	possibly damaging	0.95
R6596:Muc16	UTSW	9	18566715	missense	probably benign	0.18
R6601:Muc16	UTSW	9	18637570	missense	probably benign	0.10
R6602:Muc16	UTSW	9	18609476	intron	probably null
R6615:Muc16	UTSW	9	18647188	missense	unknown
R6625:Muc16	UTSW	9	18660278	missense	unknown
R6668:Muc16	UTSW	9	18640385	missense	probably benign	0.03
R6697:Muc16	UTSW	9	18641291	missense	probably benign	0.01
R6710:Muc16	UTSW	9	18642070	missense	possibly damaging	0.95
R6727:Muc16	UTSW	9	18566690	critical splice donor site	probably null
R6789:Muc16	UTSW	9	18559986	missense	probably benign	0.40
R6806:Muc16	UTSW	9	18537910	critical splice donor site	probably null
R6874:Muc16	UTSW	9	18658769	nonsense	probably null
R6894:Muc16	UTSW	9	18495576	missense	possibly damaging	0.92
R6913:Muc16	UTSW	9	18642663	missense	unknown
R6919:Muc16	UTSW	9	18660299	missense	unknown
R6939:Muc16	UTSW	9	18638537	missense	probably benign	0.04
R6953:Muc16	UTSW	9	18640529	missense	probably benign	0.01
R6956:Muc16	UTSW	9	18645026	missense	unknown
R6977:Muc16	UTSW	9	18645337	missense	unknown
R6996:Muc16	UTSW	9	18645897	missense	unknown
R7011:Muc16	UTSW	9	18637451	missense	probably benign	0.26
R7011:Muc16	UTSW	9	18637543	missense	probably benign	0.10
R7012:Muc16	UTSW	9	18495618	critical splice acceptor site	probably null
R7014:Muc16	UTSW	9	18658236	missense	unknown
R7021:Muc16	UTSW	9	18554919	missense	unknown
R7021:Muc16	UTSW	9	18550831	splice site	probably null
R7038:Muc16	UTSW	9	18620468	missense	probably damaging	0.99
R7057:Muc16	UTSW	9	18646079	missense	unknown
R7058:Muc16	UTSW	9	18639755	missense	probably benign	0.10
R7066:Muc16	UTSW	9	18658021	missense	unknown
R7067:Muc16	UTSW	9	18658251	missense	unknown
R7070:Muc16	UTSW	9	18645923	nonsense	probably null
R7085:Muc16	UTSW	9	18644849	missense	unknown
R7088:Muc16	UTSW	9	18592680	missense	probably damaging	0.99
R7107:Muc16	UTSW	9	18637298	missense	probably benign	0.10
R7108:Muc16	UTSW	9	18655233	missense	unknown
R7126:Muc16	UTSW	9	18641216	missense	probably benign	0.01
R7128:Muc16	UTSW	9	18643004	missense	unknown
R7145:Muc16	UTSW	9	18655580	missense	unknown
R7179:Muc16	UTSW	9	18642008	missense	probably benign	0.00
R7194:Muc16	UTSW	9	18674454	missense	unknown
R7211:Muc16	UTSW	9	18498570	missense	probably damaging	1.00
R7213:Muc16	UTSW	9	18641416	missense	probably benign	0.01
R7217:Muc16	UTSW	9	18644076	nonsense	probably null
R7221:Muc16	UTSW	9	18642199	missense	probably benign	0.04
R7265:Muc16	UTSW	9	18656472	missense	unknown
R7326:Muc16	UTSW	9	18585013	missense	probably benign	0.03
R7359:Muc16	UTSW	9	18643020	missense	unknown
R7387:Muc16	UTSW	9	18641720	missense	probably benign	0.01
R7391:Muc16	UTSW	9	18639536	missense	probably benign	0.04
R7398:Muc16	UTSW	9	18637742	missense	possibly damaging	0.46
R7419:Muc16	UTSW	9	18641962	missense	probably benign	0.01
R7431:Muc16	UTSW	9	18607993	missense
R7484:Muc16	UTSW	9	18646768	missense	unknown
R7487:Muc16	UTSW	9	18584799	missense	possibly damaging	0.93
R7497:Muc16	UTSW	9	18645089	missense	unknown
R7515:Muc16	UTSW	9	18639662	missense	probably benign	0.00
R7537:Muc16	UTSW	9	18638135	missense	probably benign	0.06
R7538:Muc16	UTSW	9	18642131	missense	probably benign	0.10
R7538:Muc16	UTSW	9	18655451	missense	unknown
R7543:Muc16	UTSW	9	18644732	missense	unknown
R7566:Muc16	UTSW	9	18638629	missense	probably benign	0.00
R7581:Muc16	UTSW	9	18645614	missense	unknown
R7594:Muc16	UTSW	9	18645062	missense	unknown
R7629:Muc16	UTSW	9	18566785	missense	possibly damaging	0.86
R7664:Muc16	UTSW	9	18607722	missense	probably benign	0.08
R7666:Muc16	UTSW	9	18558427	missense	probably damaging	1.00
R7703:Muc16	UTSW	9	18605282	missense
R7727:Muc16	UTSW	9	18660242	missense	unknown
R7743:Muc16	UTSW	9	18657477	missense	unknown
R7744:Muc16	UTSW	9	18585096	critical splice acceptor site	probably null
R7761:Muc16	UTSW	9	18580574	missense	probably damaging	1.00
R7769:Muc16	UTSW	9	18660507	missense	unknown
R7805:Muc16	UTSW	9	18638493	missense	possibly damaging	0.94
R7827:Muc16	UTSW	9	18595223	missense	possibly damaging	0.83

Predicted Primers

PCR Primer
(F):5'- TACAGTGTATTGGGCCGGAG -3'
(R):5'- CAGATCCTATAACTTATTCTGGGGC -3'

Sequencing Primer
(F):5'- ATGTTTACAGGGCTCACTTCAG -3'
(R):5'- GGGCTCTCTCTACTGTAACTCAGAC -3'

Posted On

2019-05-15