Mutagenetix > Incidental Mutation

Incidental Mutation 'R5561:Morc1'

436631

Institutional Source

Beutler Lab

Gene Symbol

Morc1

Ensembl Gene

ENSMUSG00000022652

Gene Name

microrchidia 1

Synonyms

MMRRC Submission

043118-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.217) question?

Stock #

R5561 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

48431237-48630900 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 48449348 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Phenylalanine at position 89 (L89F)

Ref Sequence

ENSEMBL: ENSMUSP00000023330 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000023330]

AlphaFold

Q9WVL5

Predicted Effect

probably benign
Transcript: ENSMUST00000023330
AA Change: L89F

PolyPhen 2 Score 0.430 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000023330
Gene: ENSMUSG00000022652
AA Change: L89F

Domain	Start	End	E-Value	Type
Pfam:HATPase_c_3	24	161	3.8e-21	PFAM
low complexity region	196	206	N/A	INTRINSIC
coiled coil region	281	311	N/A	INTRINSIC
Pfam:zf-CW	481	528	2e-14	PFAM
low complexity region	639	651	N/A	INTRINSIC
coiled coil region	885	916	N/A	INTRINSIC

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 97.9%
20x: 93.4%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the human homolog of mouse morc and like the mouse protein it is testis-specific. Mouse studies support a testis-specific function since only male knockout mice are infertile; infertility is the only apparent defect. These studies further support a role for this protein early in spermatogenesis, possibly by affecting entry into apoptosis because testis from knockout mice show greatly increased numbers of apoptotic cells. [provided by RefSeq, Jan 2009]
PHENOTYPE: Inactivation of this locus results in small testes and male sterility, the latter owing to meiotic arrest. Mutant females exhibited histologically normal ovaries and were fertile. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921530L21Rik	C	A	14: 95,882,371	A188E	probably benign	Het
A630095N17Rik	T	C	1: 75,220,537		probably benign	Het
Acyp2	C	T	11: 30,506,354	E98K	possibly damaging	Het
Adgrv1	A	G	13: 81,476,564	L3762P	probably damaging	Het
Amn1	G	A	6: 149,185,024	R4W	probably damaging	Het
Atxn1	G	T	13: 45,566,871	T516N	possibly damaging	Het
Atxn7	A	T	14: 14,089,260	T259S	probably benign	Het
Bsn	C	G	9: 108,105,511	R3681P	unknown	Het
C8b	T	C	4: 104,784,448	Y194H	possibly damaging	Het
Ccdc110	T	G	8: 45,940,609	S119R	probably benign	Het
Ceacam20	A	T	7: 19,970,393	Q123L	possibly damaging	Het
Clip3	A	G	7: 30,298,849	D240G	possibly damaging	Het
Col24a1	T	C	3: 145,298,827	F22S	probably benign	Het
Dlg5	T	A	14: 24,177,792	M354L	probably benign	Het
Dnajb12	GC	G	10: 59,892,752		probably null	Het
Dnase1l3	A	G	14: 7,967,847	V282A	probably damaging	Het
Dnhd1	G	A	7: 105,714,821	G4127S	probably damaging	Het
Eed	G	A	7: 89,967,793	R165W	probably damaging	Het
Ephb2	C	T	4: 136,661,406	V627M	probably damaging	Het
Fancc	T	C	13: 63,317,387	E502G	possibly damaging	Het
Fbf1	T	C	11: 116,157,820	D105G	probably damaging	Het
Fer	T	A	17: 64,037,585	Y246*	probably null	Het
Fer1l6	A	G	15: 58,660,825	K1792E	probably damaging	Het
Foxi2	A	G	7: 135,411,647	D202G	probably damaging	Het
Gm11595	G	A	11: 99,772,555	R100C	unknown	Het
H2-DMb2	G	T	17: 34,145,471		probably null	Het
Helq	G	T	5: 100,787,050	D491E	probably benign	Het
Hgsnat	A	G	8: 25,946,334	V564A	possibly damaging	Het
Hjurp	GT	GTT	1: 88,266,524		probably null	Het
Hs3st5	T	A	10: 36,833,429	V320D	probably damaging	Het
Ifit1bl1	A	T	19: 34,593,797	L420*	probably null	Het
Ift80	T	G	3: 68,967,863	N178T	probably benign	Het
Ing4	C	T	6: 125,047,060	T89I	possibly damaging	Het
Lcp1	G	A	14: 75,212,508	D386N	probably benign	Het
Mdc1	T	A	17: 35,848,546	I606K	probably benign	Het
Mllt10	T	A	2: 18,109,845	M120K	probably damaging	Het
Mroh2a	GCCC	GC	1: 88,232,257		probably null	Het
Nav3	C	A	10: 109,716,552	D1810Y	probably damaging	Het
Obscn	G	A	11: 59,036,093	T5532M	probably damaging	Het
Olfr527	C	T	7: 140,336,152	Q97*	probably null	Het
Olfr716	A	G	7: 107,148,090	N258S	probably benign	Het
Opn3	C	T	1: 175,665,587	R137H	probably damaging	Het
Palld	G	A	8: 61,516,585	A993V	probably damaging	Het
Ppp1r12c	A	T	7: 4,486,356		probably null	Het
Prdm4	TCTCCTCCT	TCTCCT	10: 85,893,123		probably null	Het
Rapgef2	A	T	3: 79,088,643		probably null	Het
Ring1	T	C	17: 34,021,458	E382G	possibly damaging	Het
Rpl22l1	T	A	3: 28,806,820	N61K	probably benign	Het
Rpp14	A	G	14: 8,090,558		probably null	Het
Rusc2	C	T	4: 43,415,932	Q413*	probably null	Het
Slco3a1	A	G	7: 74,318,499	I491T	possibly damaging	Het
Smtnl1	C	T	2: 84,818,395	V172I	probably benign	Het
Spats2l	T	A	1: 57,900,621		probably null	Het
Spire1	T	A	18: 67,506,646	N266Y	probably damaging	Het
Stox2	T	C	8: 47,193,006	H473R	probably damaging	Het
Syne2	C	T	12: 76,094,458	R121*	probably null	Het
Synrg	G	A	11: 84,002,240		probably null	Het
Tm9sf1	C	T	14: 55,638,097	V397M	probably damaging	Het
Trabd	T	C	15: 89,081,984	M48T	probably benign	Het
Ttn	T	A	2: 76,707,233	I26457F	possibly damaging	Het
Uggt2	C	T	14: 119,041,527	R856Q	probably benign	Het
Ugt1a5	T	A	1: 88,166,317	M89K	probably benign	Het
Vmn2r53	A	T	7: 12,601,420	S104R	probably damaging	Het
Zdhhc12	A	T	2: 30,092,484	L53Q	probably null	Het

Other mutations in Morc1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00763:Morc1	APN	16	48612326	missense	probably damaging	0.98
IGL00815:Morc1	APN	16	48460692	missense	possibly damaging	0.62
IGL00939:Morc1	APN	16	48452589	missense	probably damaging	0.99
IGL01321:Morc1	APN	16	48582462	missense	probably benign	0.00
IGL01410:Morc1	APN	16	48612314	missense	probably benign	0.16
IGL01557:Morc1	APN	16	48498766	missense	probably damaging	1.00
IGL02118:Morc1	APN	16	48587104	missense	probably benign	0.01
IGL02626:Morc1	APN	16	48615760	missense	probably damaging	0.96
IGL02692:Morc1	APN	16	48510233	missense	probably null	0.95
IGL02812:Morc1	APN	16	48558506	splice site	probably benign
IGL03232:Morc1	APN	16	48630802	missense	probably benign	0.06
IGL03331:Morc1	APN	16	48612368	splice site	probably benign
IGL03408:Morc1	APN	16	48442412	missense	probably damaging	1.00
R0545:Morc1	UTSW	16	48565657	missense	probably benign	0.05
R0569:Morc1	UTSW	16	48587122	missense	probably benign	0.02
R0699:Morc1	UTSW	16	48592614	missense	probably benign	0.01
R1717:Morc1	UTSW	16	48452477	missense	probably benign	0.01
R1728:Morc1	UTSW	16	48612297	missense	probably benign	0.10
R1803:Morc1	UTSW	16	48622638	missense	probably benign	0.14
R1864:Morc1	UTSW	16	48592530	missense	probably benign	0.01
R2008:Morc1	UTSW	16	48565646	missense	probably benign	0.41
R2070:Morc1	UTSW	16	48592611	missense	probably benign	0.00
R2071:Morc1	UTSW	16	48592611	missense	probably benign	0.00
R4851:Morc1	UTSW	16	48561617	missense	probably benign	0.02
R5013:Morc1	UTSW	16	48502336	missense	probably benign	0.11
R5081:Morc1	UTSW	16	48502352	missense	probably benign	0.01
R5259:Morc1	UTSW	16	48630769	missense	probably benign	0.12
R5342:Morc1	UTSW	16	48618509	missense	probably damaging	0.99
R5481:Morc1	UTSW	16	48561485	splice site	probably null
R6356:Morc1	UTSW	16	48437289	missense	probably damaging	1.00
R6526:Morc1	UTSW	16	48587124	nonsense	probably null
R6743:Morc1	UTSW	16	48502320	missense	probably damaging	0.98
R6940:Morc1	UTSW	16	48479845	nonsense	probably null
R6994:Morc1	UTSW	16	48565621	missense	probably benign	0.00
R6994:Morc1	UTSW	16	48618546	missense	probably benign	0.39
R7009:Morc1	UTSW	16	48627070	missense	possibly damaging	0.69
R7346:Morc1	UTSW	16	48630900	splice site	probably null
R7357:Morc1	UTSW	16	48622590	missense	probably benign	0.14
R7448:Morc1	UTSW	16	48431345	missense	probably damaging	0.97
R7840:Morc1	UTSW	16	48498784	missense	probably benign	0.03
R8417:Morc1	UTSW	16	48460740	missense	probably damaging	0.99
X0013:Morc1	UTSW	16	48587068	missense	probably benign	0.04
X0027:Morc1	UTSW	16	48498811	missense	probably damaging	1.00
Z1176:Morc1	UTSW	16	48587058	missense	probably benign	0.03
Z1177:Morc1	UTSW	16	48565706	missense	probably benign	0.05

Predicted Primers

PCR Primer
(F):5'- TCCTTGTGGACTGTCCCAAAG -3'
(R):5'- TTTTCATGTTGCAAAGAGCTGCG -3'

Sequencing Primer
(F):5'- TGGACTGTCCCAAAGGCTATG -3'
(R):5'- TGCAAAGAGCTGCGTCAGTTATG -3'

Posted On

2016-10-24