Mutagenetix > Incidental Mutation

Incidental Mutation 'R7180:Unc45a'

568515

Institutional Source

Beutler Lab

Gene Symbol

Unc45a

Ensembl Gene

ENSMUSG00000030533

Gene Name

unc-45 myosin chaperone A

Synonyms

MMRRC Submission

045233-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7180 (G1)

Quality Score

159.009

Status

Validated

Chromosome

Chromosomal Location

79975040-79990748 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to T at 79979569 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s): [ENSMUST00000032748] [ENSMUST00000107368] [ENSMUST00000133728] [ENSMUST00000154428]

AlphaFold

Q99KD5

Predicted Effect

probably benign
Transcript: ENSMUST00000032748

SMART Domains

Protein: ENSMUSP00000032748
Gene: ENSMUSG00000030533

Domain	Start	End	E-Value	Type
TPR	21	54	9.53e-2	SMART
TPR	58	91	5.48e-2	SMART
TPR	92	125	7.45e-4	SMART
Blast:ARM	183	224	6e-9	BLAST
Blast:ARM	226	266	1e-7	BLAST
Pfam:UNC45-central	287	505	1.2e-43	PFAM
Blast:ARM	679	717	4e-13	BLAST
Blast:ARM	720	762	4e-12	BLAST
Blast:ARM	764	804	8e-16	BLAST
low complexity region	833	845	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000107368

SMART Domains

Protein: ENSMUSP00000102991
Gene: ENSMUSG00000030533

Domain	Start	End	E-Value	Type
TPR	21	54	9.53e-2	SMART
TPR	58	91	5.48e-2	SMART
TPR	92	125	7.45e-4	SMART
Blast:ARM	183	224	6e-9	BLAST
Blast:ARM	226	266	1e-7	BLAST
Pfam:UNC45-central	314	505	2.4e-38	PFAM
Blast:ARM	679	717	4e-13	BLAST
Blast:ARM	720	762	4e-12	BLAST
Blast:ARM	764	804	8e-16	BLAST
low complexity region	833	845	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000133728

SMART Domains

Protein: ENSMUSP00000123399
Gene: ENSMUSG00000030533

Domain	Start	End	E-Value	Type
TPR	6	39	9.53e-2	SMART
TPR	43	76	5.48e-2	SMART
TPR	77	110	7.45e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000154428

SMART Domains

Protein: ENSMUSP00000119665
Gene: ENSMUSG00000030533

Domain	Start	End	E-Value	Type
TPR	21	54	9.53e-2	SMART
TPR	58	91	5.48e-2	SMART
TPR	92	125	7.45e-4	SMART
Blast:ARM	183	224	4e-9	BLAST
Blast:ARM	226	266	6e-8	BLAST
Pfam:UNC45-central	287	505	3.5e-44	PFAM
low complexity region	597	608	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000206363

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

99% (80/81)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] UNC45A plays a role in cell proliferation and myoblast fusion, binds progesterone receptor (PGR; MIM 607311) and HSP90 (HSPCA; MIM 140571), and acts as a regulator of the progesterone receptor chaperoning pathway (Price et al., 2002 [PubMed 12356907]; Chadli et al., 2006 [PubMed 16478993]).[supplied by OMIM, Mar 2008]

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acnat2	A	C	4: 49,381,803 (GRCm39)	Y196*	probably null	Het
Agrn	C	T	4: 156,256,296 (GRCm39)	R1405H	probably benign	Het
Agtpbp1	G	A	13: 59,613,852 (GRCm39)	H1030Y	probably benign	Het
Ankrd37	C	T	8: 46,452,891 (GRCm39)		probably benign	Het
Ap1g2	G	C	14: 55,341,908 (GRCm39)	P218R	probably damaging	Het
Ap2a1	C	T	7: 44,573,228 (GRCm39)		probably null	Het
Apc2	T	A	10: 80,146,990 (GRCm39)	D681E	possibly damaging	Het
Arhgef5	T	A	6: 43,252,142 (GRCm39)	N964K	possibly damaging	Het
BC028528	CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT	CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT	3: 95,795,448 (GRCm39)		probably benign	Het
Ccnf	T	A	17: 24,442,889 (GRCm39)	M773L	probably benign	Het
Ces1e	A	C	8: 93,941,772 (GRCm39)	S234A	probably damaging	Het
Ces1g	T	A	8: 94,029,576 (GRCm39)	E552V	probably benign	Het
Ctcfl	A	T	2: 172,947,770 (GRCm39)		probably null	Het
Dkk2	T	A	3: 131,791,953 (GRCm39)	S54T	probably damaging	Het
Dll1	A	G	17: 15,595,131 (GRCm39)	S49P	probably benign	Het
Dscam	C	A	16: 96,626,764 (GRCm39)	A382S	probably damaging	Het
Eif4a3l1	T	A	6: 136,306,535 (GRCm39)	I332N	probably damaging	Het
Eif5b	A	T	1: 38,088,155 (GRCm39)	M1020L	probably damaging	Het
Elp1	A	T	4: 56,796,535 (GRCm39)	S118R	probably damaging	Het
Enpp4	T	C	17: 44,412,928 (GRCm39)	D202G	probably benign	Het
Eps8	A	T	6: 137,456,072 (GRCm39)	I803N	possibly damaging	Het
Etv2	C	A	7: 30,335,074 (GRCm39)	G28V	probably damaging	Het
Fadd	A	T	7: 144,134,522 (GRCm39)	V121E	probably damaging	Het
Fam149b	T	C	14: 20,431,853 (GRCm39)	Y545H	probably benign	Het
Fbxl21	A	T	13: 56,671,340 (GRCm39)	M1L	probably benign	Het
Flg2	T	C	3: 93,110,140 (GRCm39)	S723P	unknown	Het
Gm4884	C	T	7: 40,693,633 (GRCm39)	T534I	possibly damaging	Het
Gpbar1	A	T	1: 74,317,792 (GRCm39)	I12F	possibly damaging	Het
Gpr151	A	T	18: 42,712,021 (GRCm39)	L219*	probably null	Het
Hdgfl2	T	A	17: 56,404,532 (GRCm39)		probably null	Het
Hectd4	A	G	5: 121,446,405 (GRCm39)	M200V	probably benign	Het
Idua	A	G	5: 108,828,761 (GRCm39)	N335S	probably benign	Het
Ifit1bl1	A	T	19: 34,571,302 (GRCm39)	F385Y	probably damaging	Het
Ift172	T	C	5: 31,411,606 (GRCm39)	D1624G	probably damaging	Het
Igsf9b	A	T	9: 27,233,964 (GRCm39)	T388S	possibly damaging	Het
Insyn2b	A	G	11: 34,369,873 (GRCm39)	K526E	probably damaging	Het
Jak2	A	G	19: 29,259,811 (GRCm39)	I237V	probably benign	Het
Kat5	C	A	19: 5,653,989 (GRCm39)	K398N	probably damaging	Het
Lmbrd2	T	A	15: 9,175,283 (GRCm39)	V398E	possibly damaging	Het
Lrp1	T	C	10: 127,392,834 (GRCm39)	N2744D	probably damaging	Het
Lrrd1	T	C	5: 3,901,459 (GRCm39)	I588T	probably damaging	Het
Ltn1	A	G	16: 87,215,382 (GRCm39)	F418L	probably damaging	Het
Magi1	T	A	6: 93,792,731 (GRCm39)	D169V	probably benign	Het
Mpdz	T	C	4: 81,253,988 (GRCm39)	E1048G	probably damaging	Het
Myh9	T	C	15: 77,692,110 (GRCm39)	I150V	probably benign	Het
Nckap1	A	T	2: 80,337,236 (GRCm39)	M1006K	probably benign	Het
Nkain1	C	T	4: 130,533,925 (GRCm38)	V132I	probably benign	Het
Npy6r	A	T	18: 44,409,223 (GRCm39)	M215L	probably benign	Het
Nr3c2	A	T	8: 77,635,592 (GRCm39)	Q231L	probably damaging	Het
Obox5	C	T	7: 15,491,849 (GRCm39)	P88L	probably benign	Het
Or10a48	A	G	7: 108,425,186 (GRCm39)	S7P	probably damaging	Het
Or9k7	T	C	10: 130,046,811 (GRCm39)	T63A	probably benign	Het
P2rx7	A	G	5: 122,818,883 (GRCm39)	D435G	possibly damaging	Het
Pdzd2	T	A	15: 12,376,209 (GRCm39)	S1309C	probably damaging	Het
Pex5l	C	T	3: 33,078,840 (GRCm39)		probably null	Het
Pip	T	A	6: 41,824,565 (GRCm39)	C18S	probably damaging	Het
Pla2g7	C	T	17: 43,909,967 (GRCm39)	T157M	probably damaging	Het
Plce1	A	G	19: 38,768,229 (GRCm39)	Y2168C	probably damaging	Het
Rgs2	T	C	1: 143,877,886 (GRCm39)	T137A	probably benign	Het
Rpl32	T	A	6: 115,784,768 (GRCm39)	I31F	possibly damaging	Het
Ryr2	T	C	13: 11,701,864 (GRCm39)	Y2931C	probably damaging	Het
Slc4a4	G	A	5: 89,194,095 (GRCm39)	E192K	probably damaging	Het
Slc4a7	G	A	14: 14,765,580 (GRCm38)	A521T	probably damaging	Het
Smchd1	T	C	17: 71,701,818 (GRCm39)	E1058G	probably damaging	Het
Sorbs1	G	C	19: 40,365,244 (GRCm39)	R180G	probably benign	Het
Ssc5d	A	G	7: 4,939,600 (GRCm39)	T679A	probably benign	Het
Tas2r130	A	C	6: 131,607,211 (GRCm39)	S195A	probably benign	Het
Tas2r135	C	T	6: 42,382,685 (GRCm39)	R75*	probably null	Het
Terf2ip	G	T	8: 112,738,052 (GRCm39)		probably benign	Het
Tm6sf2	G	A	8: 70,528,656 (GRCm39)	R136K	probably benign	Het
Tmprss15	A	G	16: 78,764,886 (GRCm39)	L858P	probably damaging	Het
Topaz1	A	G	9: 122,626,770 (GRCm39)	D1466G	possibly damaging	Het
Trip4	A	T	9: 65,764,627 (GRCm39)	L446Q	probably damaging	Het
Trpv3	G	T	11: 73,168,818 (GRCm39)	V93L	probably benign	Het
Ubl4b	A	T	3: 107,461,962 (GRCm39)	H99Q	probably damaging	Het
Vmn1r47	G	T	6: 89,999,335 (GRCm39)	A156S	probably damaging	Het
Vmn2r33	T	A	7: 7,566,896 (GRCm39)	H72L	probably benign	Het
Zeb1	G	A	18: 5,767,867 (GRCm39)	V793M	possibly damaging	Het
Zfp628	C	A	7: 4,924,063 (GRCm39)	Q762K	probably benign	Het

Other mutations in Unc45a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02252:Unc45a	APN	7	79,982,717 (GRCm39)	intron	probably benign
IGL02266:Unc45a	APN	7	79,978,234 (GRCm39)	missense	probably damaging	0.96
IGL02383:Unc45a	APN	7	79,989,410 (GRCm39)	nonsense	probably null
IGL02959:Unc45a	APN	7	79,982,721 (GRCm39)	intron	probably benign
IGL03168:Unc45a	APN	7	79,982,881 (GRCm39)	missense	probably damaging	1.00
PIT4131001:Unc45a	UTSW	7	79,976,109 (GRCm39)	missense	possibly damaging	0.74
R0095:Unc45a	UTSW	7	79,979,291 (GRCm39)	missense	probably damaging	1.00
R0095:Unc45a	UTSW	7	79,979,291 (GRCm39)	missense	probably damaging	1.00
R0276:Unc45a	UTSW	7	79,976,045 (GRCm39)	intron	probably benign
R0373:Unc45a	UTSW	7	79,976,092 (GRCm39)	missense	probably damaging	0.97
R1827:Unc45a	UTSW	7	79,981,488 (GRCm39)	missense	possibly damaging	0.77
R2120:Unc45a	UTSW	7	79,989,846 (GRCm39)	missense	probably benign	0.29
R2440:Unc45a	UTSW	7	79,978,805 (GRCm39)	missense	probably damaging	1.00
R2442:Unc45a	UTSW	7	79,989,417 (GRCm39)	missense	probably damaging	1.00
R2508:Unc45a	UTSW	7	79,988,623 (GRCm39)	missense	probably benign
R3077:Unc45a	UTSW	7	79,988,680 (GRCm39)	missense	probably damaging	0.97
R3108:Unc45a	UTSW	7	79,981,294 (GRCm39)	intron	probably benign
R3109:Unc45a	UTSW	7	79,981,294 (GRCm39)	intron	probably benign
R3620:Unc45a	UTSW	7	79,983,799 (GRCm39)	missense	possibly damaging	0.84
R4471:Unc45a	UTSW	7	79,982,728 (GRCm39)	missense	possibly damaging	0.94
R4644:Unc45a	UTSW	7	79,978,257 (GRCm39)	missense	probably damaging	1.00
R4651:Unc45a	UTSW	7	79,982,777 (GRCm39)	missense	possibly damaging	0.93
R4838:Unc45a	UTSW	7	79,982,783 (GRCm39)	missense	probably damaging	1.00
R5234:Unc45a	UTSW	7	79,978,547 (GRCm39)	missense	probably benign	0.17
R5452:Unc45a	UTSW	7	79,978,787 (GRCm39)	missense	probably damaging	1.00
R5574:Unc45a	UTSW	7	79,984,604 (GRCm39)	missense	probably damaging	0.98
R5750:Unc45a	UTSW	7	79,984,571 (GRCm39)	missense	probably benign	0.17
R6169:Unc45a	UTSW	7	79,978,511 (GRCm39)	missense	possibly damaging	0.92
R6417:Unc45a	UTSW	7	79,989,400 (GRCm39)	missense	probably benign	0.04
R6420:Unc45a	UTSW	7	79,989,400 (GRCm39)	missense	probably benign	0.04
R6486:Unc45a	UTSW	7	79,989,400 (GRCm39)	missense	probably benign	0.04
R6533:Unc45a	UTSW	7	79,983,817 (GRCm39)	missense	probably damaging	1.00
R6734:Unc45a	UTSW	7	79,986,746 (GRCm39)	missense	probably damaging	1.00
R6993:Unc45a	UTSW	7	79,975,403 (GRCm39)	missense	probably damaging	1.00
R7085:Unc45a	UTSW	7	79,976,082 (GRCm39)	missense	possibly damaging	0.87
R7561:Unc45a	UTSW	7	79,981,334 (GRCm39)	missense	possibly damaging	0.63
R8079:Unc45a	UTSW	7	79,981,310 (GRCm39)	missense	probably damaging	1.00
R8395:Unc45a	UTSW	7	79,976,080 (GRCm39)	missense	probably benign	0.08
R8547:Unc45a	UTSW	7	79,975,840 (GRCm39)	missense	possibly damaging	0.76
R9620:Unc45a	UTSW	7	79,975,403 (GRCm39)	missense	probably damaging	1.00
R9621:Unc45a	UTSW	7	79,983,785 (GRCm39)	missense	probably damaging	1.00
R9694:Unc45a	UTSW	7	79,975,403 (GRCm39)	missense	probably damaging	1.00
R9728:Unc45a	UTSW	7	79,978,448 (GRCm39)	missense	probably benign	0.02

Predicted Primers

PCR Primer
(F):5'- AGTACCTGCATCAATCTGGTC -3'
(R):5'- CGCGGTATTTAAAGGGGCATG -3'

Sequencing Primer
(F):5'- TGGTCATTGCATAGCCACCTAGG -3'
(R):5'- CATGGATGGAAGGTAAAGCTCCTTTG -3'

Posted On

2019-08-15