Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02572:Morn4'

299067

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Morn4

Ensembl Gene

ENSMUSG00000049670

Gene Name

MORN repeat containing 4

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.196) question?

Stock #

IGL02572

Quality Score

Status

Chromosome

Chromosomal Location

42063378-42074796 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to G at 42064886 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000062887 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000051772]

AlphaFold

Q6PGF2

Predicted Effect

probably benign
Transcript: ENSMUST00000051772

SMART Domains

Protein: ENSMUSP00000062887
Gene: ENSMUSG00000049670

Domain	Start	End	E-Value	Type
MORN	14	35	1.64e-5	SMART
MORN	37	58	4.15e-2	SMART
MORN	60	81	1.86e-4	SMART
MORN	83	104	1.84e0	SMART

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A630001G21Rik	T	C	1: 85,652,892 (GRCm39)	N92S	probably damaging	Het
Abca2	T	C	2: 25,323,329 (GRCm39)	L99P	possibly damaging	Het
Adam19	T	A	11: 46,022,548 (GRCm39)	Y500*	probably null	Het
Amy1	A	T	3: 113,358,722 (GRCm39)		probably benign	Het
Aox3	T	C	1: 58,197,526 (GRCm39)	I624T	probably damaging	Het
Atad3a	C	T	4: 155,838,041 (GRCm39)	D244N	possibly damaging	Het
Atp5mf	C	A	5: 145,124,047 (GRCm39)		probably benign	Het
Bbof1	G	A	12: 84,475,139 (GRCm39)	D443N	probably damaging	Het
Bod1l	G	A	5: 41,978,573 (GRCm39)	Q914*	probably null	Het
C330011M18Rik	A	G	8: 84,793,208 (GRCm39)		probably benign	Het
Cgref1	A	G	5: 31,090,911 (GRCm39)	V301A	probably benign	Het
Coa6	T	C	8: 127,149,480 (GRCm39)	Y19H	probably damaging	Het
Cop1	T	A	1: 159,136,448 (GRCm39)		probably benign	Het
Dmrta1	T	C	4: 89,579,795 (GRCm39)	S252P	probably benign	Het
Dnaaf5	T	G	5: 139,170,384 (GRCm39)	S484A	probably benign	Het
Dspp	A	T	5: 104,324,935 (GRCm39)	S433C	probably damaging	Het
Efcab5	G	A	11: 77,028,714 (GRCm39)	R206*	probably null	Het
Epop	A	T	11: 97,519,027 (GRCm39)	S361T	probably benign	Het
Fat3	T	A	9: 15,871,802 (GRCm39)	T3530S	probably benign	Het
Flvcr1	A	G	1: 190,757,843 (GRCm39)	Y108H	probably damaging	Het
Fsip2	T	G	2: 82,822,347 (GRCm39)	S6027A	probably benign	Het
Galnt14	A	G	17: 73,842,262 (GRCm39)	L209P	probably damaging	Het
Hif3a	C	A	7: 16,784,513 (GRCm39)	R25L	probably null	Het
Hsf5	A	G	11: 87,522,521 (GRCm39)		probably benign	Het
Il22ra2	A	T	10: 19,502,492 (GRCm39)	T104S	probably benign	Het
Klrk1	A	G	6: 129,592,316 (GRCm39)	S138P	probably damaging	Het
Lrp5	G	T	19: 3,664,283 (GRCm39)	Q815K	probably benign	Het
Nlrp14	T	A	7: 106,781,929 (GRCm39)	Y375*	probably null	Het
Nsd1	T	A	13: 55,443,943 (GRCm39)	M1714K	probably damaging	Het
Or2aj6	T	A	16: 19,443,848 (GRCm39)	M1L	probably benign	Het
Or5aq7	G	A	2: 86,938,710 (GRCm39)	T7I	possibly damaging	Het
Or6c213	T	A	10: 129,574,735 (GRCm39)	D17V	possibly damaging	Het
Pappa2	C	T	1: 158,678,786 (GRCm39)	A877T	probably benign	Het
Pcsk2	G	A	2: 143,532,262 (GRCm39)	A137T	probably damaging	Het
Piezo1	A	G	8: 123,212,044 (GRCm39)	V2054A	probably benign	Het
Rad52	A	G	6: 119,892,188 (GRCm39)		probably benign	Het
Rnf123	G	A	9: 107,945,501 (GRCm39)	R390*	probably null	Het
Rusf1	A	T	7: 127,889,752 (GRCm39)		probably benign	Het
Sbno1	A	G	5: 124,519,740 (GRCm39)		probably benign	Het
Scrn1	C	T	6: 54,489,186 (GRCm39)	D312N	probably benign	Het
Sin3b	A	G	8: 73,471,109 (GRCm39)	Q352R	probably benign	Het
Slc25a28	A	G	19: 43,652,885 (GRCm39)	Y259H	probably damaging	Het
Sppl2a	T	C	2: 126,768,216 (GRCm39)	M151V	probably benign	Het
Srrm1	G	A	4: 135,052,415 (GRCm39)	P658L	unknown	Het
Stra8	G	A	6: 34,916,094 (GRCm39)	D280N	probably damaging	Het
Thbs2	A	T	17: 14,897,275 (GRCm39)	D744E	possibly damaging	Het
Tiparp	A	G	3: 65,439,310 (GRCm39)	T27A	probably benign	Het
Tmem38a	T	C	8: 73,333,818 (GRCm39)	F99S	probably damaging	Het
Tmod3	T	C	9: 75,416,667 (GRCm39)	T222A	probably benign	Het
Tnn	A	G	1: 159,913,677 (GRCm39)	I1272T	probably damaging	Het
Tnpo1	A	T	13: 98,985,667 (GRCm39)	I829N	probably damaging	Het
Trpm5	A	T	7: 142,641,613 (GRCm39)		probably benign	Het
Ttn	A	G	2: 76,598,215 (GRCm39)	V19566A	probably damaging	Het
V1ra8	A	G	6: 90,180,040 (GRCm39)	D81G	probably damaging	Het
Zdhhc20	A	G	14: 58,127,564 (GRCm39)	V25A	probably benign	Het

Other mutations in Morn4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00971:Morn4	APN	19	42,064,559 (GRCm39)	missense	possibly damaging	0.53
IGL02933:Morn4	APN	19	42,064,661 (GRCm39)	missense	probably benign	0.01
FR4449:Morn4	UTSW	19	42,064,548 (GRCm39)	small insertion	probably benign
FR4548:Morn4	UTSW	19	42,064,548 (GRCm39)	small insertion	probably benign
R1997:Morn4	UTSW	19	42,064,977 (GRCm39)	missense	possibly damaging	0.71
R2239:Morn4	UTSW	19	42,066,471 (GRCm39)	missense	possibly damaging	0.93
R4409:Morn4	UTSW	19	42,066,986 (GRCm39)	missense	possibly damaging	0.53
R5544:Morn4	UTSW	19	42,064,686 (GRCm39)	missense	possibly damaging	0.71
R5695:Morn4	UTSW	19	42,064,556 (GRCm39)	missense	possibly damaging	0.96
R6986:Morn4	UTSW	19	42,066,453 (GRCm39)	missense	possibly damaging	0.71
R7024:Morn4	UTSW	19	42,066,483 (GRCm39)	missense	possibly damaging	0.92
R8721:Morn4	UTSW	19	42,066,439 (GRCm39)	missense	possibly damaging	0.85
RF025:Morn4	UTSW	19	42,064,550 (GRCm39)	nonsense	probably null
RF030:Morn4	UTSW	19	42,064,550 (GRCm39)	nonsense	probably null
RF036:Morn4	UTSW	19	42,064,553 (GRCm39)	nonsense	probably null
RF040:Morn4	UTSW	19	42,064,550 (GRCm39)	nonsense	probably null
RF042:Morn4	UTSW	19	42,064,550 (GRCm39)	nonsense	probably null
RF044:Morn4	UTSW	19	42,064,553 (GRCm39)	nonsense	probably null
RF057:Morn4	UTSW	19	42,064,545 (GRCm39)	nonsense	probably null
X0063:Morn4	UTSW	19	42,066,407 (GRCm39)	missense	possibly damaging	0.71

Posted On

2015-04-16