Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03184:Pcgf5'

412411

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Pcgf5

Ensembl Gene

ENSMUSG00000024805

Gene Name

polycomb group ring finger 5

Synonyms

0610009F02Rik, 9530023M17Rik, 5830406C17Rik, 5830443C21Rik, 1110054A01Rik

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.572) question?

Stock #

IGL03184

Quality Score

Status

Chromosome

Chromosomal Location

36325729-36438370 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to G at 36412076 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000153206 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000062389] [ENSMUST00000071267] [ENSMUST00000224679] [ENSMUST00000224772] [ENSMUST00000224971] [ENSMUST00000225411] [ENSMUST00000225920]

AlphaFold

Q3UK78

Predicted Effect

probably benign
Transcript: ENSMUST00000062389

SMART Domains

Protein: ENSMUSP00000058730
Gene: ENSMUSG00000024805

Domain	Start	End	E-Value	Type
RING	18	56	4.05e-5	SMART
low complexity region	86	96	N/A	INTRINSIC
Pfam:RAWUL	146	230	2.4e-19	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000071267

SMART Domains

Protein: ENSMUSP00000071245
Gene: ENSMUSG00000024805

Domain	Start	End	E-Value	Type
RING	18	56	4.05e-5	SMART
low complexity region	86	96	N/A	INTRINSIC
Pfam:RAWUL	146	230	2.4e-19	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000224679

Predicted Effect

probably benign
Transcript: ENSMUST00000224772

Predicted Effect

probably benign
Transcript: ENSMUST00000224859

Predicted Effect

probably benign
Transcript: ENSMUST00000224971

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000225050

Predicted Effect

probably benign
Transcript: ENSMUST00000225411

Predicted Effect

probably benign
Transcript: ENSMUST00000225920

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000225185

Coding Region Coverage

Validation Efficiency

MGI Phenotype

PHENOTYPE: Bone marrow cells from mice homozygous for a conditional allele exhibit normal hematopoietic and progenitor cell function. [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
2210408I21Rik	T	C	13: 77,471,570 (GRCm39)	Y992H	possibly damaging	Het
Actmap	A	G	7: 26,896,432 (GRCm39)		probably benign	Het
Adcy7	T	A	8: 89,035,271 (GRCm39)	D58E	probably benign	Het
Aff2	G	A	X: 68,810,840 (GRCm39)	V404M	possibly damaging	Het
Ankhd1	T	A	18: 36,780,830 (GRCm39)	L1961M	probably damaging	Het
Brms1l	T	C	12: 55,915,062 (GRCm39)	*324Q	probably null	Het
Bub1b	T	C	2: 118,440,258 (GRCm39)		probably benign	Het
Cacna1b	A	G	2: 24,548,501 (GRCm39)		probably null	Het
Clrn1	T	A	3: 58,753,645 (GRCm39)	T239S	probably benign	Het
Clta	T	C	4: 44,025,514 (GRCm39)	Y145H	probably benign	Het
Coro6	T	C	11: 77,354,779 (GRCm39)	V14A	probably damaging	Het
Cyp4a30b	A	G	4: 115,316,216 (GRCm39)	D314G	probably damaging	Het
Fn1	T	C	1: 71,648,656 (GRCm39)	N1418D	probably benign	Het
Fshr	A	C	17: 89,354,068 (GRCm39)	L97V	possibly damaging	Het
Gcm2	T	C	13: 41,258,888 (GRCm39)	Q152R	probably damaging	Het
Gcnt2	A	G	13: 41,041,660 (GRCm39)	N273S	probably benign	Het
Gm11437	A	T	11: 84,047,090 (GRCm39)		probably benign	Het
Gm4559	A	G	7: 141,828,046 (GRCm39)	S19P	unknown	Het
Igsf8	T	G	1: 172,146,199 (GRCm39)	I462R	probably damaging	Het
Kirrel3	T	C	9: 34,919,052 (GRCm39)	F243S	probably damaging	Het
Krt80	C	T	15: 101,250,135 (GRCm39)	V37M	probably damaging	Het
Lama4	T	C	10: 38,954,839 (GRCm39)	Y1131H	probably damaging	Het
Mrpl21	T	C	19: 3,342,529 (GRCm39)		probably benign	Het
Mtcl1	T	C	17: 66,661,209 (GRCm39)	N923S	probably benign	Het
Nectin2	G	A	7: 19,472,231 (GRCm39)	P53S	possibly damaging	Het
Nup98	G	A	7: 101,832,752 (GRCm39)	T335I	probably damaging	Het
Or2y1e	C	A	11: 49,218,568 (GRCm39)	T110K	probably damaging	Het
Or4a74	T	C	2: 89,439,912 (GRCm39)	D178G	probably damaging	Het
Or4e5	A	G	14: 52,728,380 (GRCm39)	S14P	probably benign	Het
Or51a42	T	A	7: 103,708,054 (GRCm39)	I252F	probably damaging	Het
Or6c69c	T	C	10: 129,910,627 (GRCm39)	M116T	possibly damaging	Het
Pcdhb14	A	G	18: 37,582,085 (GRCm39)	E397G	probably benign	Het
Pclo	C	T	5: 14,764,457 (GRCm39)	P1025L	probably damaging	Het
Pdcd1lg2	C	A	19: 29,431,911 (GRCm39)	F226L	probably benign	Het
Pik3ca	T	A	3: 32,494,035 (GRCm39)	S332R	probably benign	Het
Plek	A	T	11: 16,931,887 (GRCm39)	D321E	probably benign	Het
Pm20d2	A	G	4: 33,179,241 (GRCm39)	F333L	probably damaging	Het
Polk	T	C	13: 96,620,491 (GRCm39)	T570A	probably benign	Het
Rpgrip1l	G	A	8: 92,027,437 (GRCm39)	L201F	probably damaging	Het
Serpinb2	T	A	1: 107,452,607 (GRCm39)	L395H	probably damaging	Het
Slc9c1	T	G	16: 45,368,003 (GRCm39)	S197R	probably damaging	Het
Smg1	T	A	7: 117,779,603 (GRCm39)	E1264V	possibly damaging	Het
Sned1	A	G	1: 93,202,390 (GRCm39)	D678G	probably benign	Het
Sorcs2	A	G	5: 36,188,556 (GRCm39)	S851P	probably benign	Het
Srcap	A	G	7: 127,129,674 (GRCm39)		probably benign	Het
Tbck	T	C	3: 132,441,864 (GRCm39)	Y557H	probably damaging	Het
Tfap2d	T	C	1: 19,189,110 (GRCm39)	S219P	probably damaging	Het
Trim9	T	C	12: 70,297,995 (GRCm39)	D570G	probably damaging	Het
Usp25	A	G	16: 76,878,541 (GRCm39)	Y655C	probably damaging	Het
Utrn	T	A	10: 12,585,910 (GRCm39)	T956S	probably benign	Het
Vmn1r68	T	A	7: 10,261,799 (GRCm39)	I100F	probably benign	Het
Vps13a	A	T	19: 16,631,734 (GRCm39)	S2634T	probably benign	Het
Zfp472	T	A	17: 33,196,390 (GRCm39)	L155*	probably null	Het
Zfp808	A	G	13: 62,317,381 (GRCm39)	I43M	possibly damaging	Het

Other mutations in Pcgf5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01012:Pcgf5	APN	19	36,420,268 (GRCm39)	missense	probably damaging	1.00
IGL03259:Pcgf5	APN	19	36,433,059 (GRCm39)	missense	probably benign	0.28
Baleen	UTSW	19	36,420,311 (GRCm39)	missense	probably damaging	0.99
whalebone	UTSW	19	36,420,339 (GRCm39)	nonsense	probably null
R0318:Pcgf5	UTSW	19	36,389,590 (GRCm39)	missense	possibly damaging	0.81
R0570:Pcgf5	UTSW	19	36,389,580 (GRCm39)	missense	probably benign	0.00
R0890:Pcgf5	UTSW	19	36,389,544 (GRCm39)	missense	probably benign	0.05
R2238:Pcgf5	UTSW	19	36,414,754 (GRCm39)	missense	probably damaging	0.97
R2239:Pcgf5	UTSW	19	36,414,754 (GRCm39)	missense	probably damaging	0.97
R3904:Pcgf5	UTSW	19	36,417,495 (GRCm39)	missense	probably damaging	1.00
R4050:Pcgf5	UTSW	19	36,420,311 (GRCm39)	missense	probably damaging	0.99
R4209:Pcgf5	UTSW	19	36,414,740 (GRCm39)	missense	possibly damaging	0.81
R4210:Pcgf5	UTSW	19	36,414,740 (GRCm39)	missense	possibly damaging	0.81
R4211:Pcgf5	UTSW	19	36,414,740 (GRCm39)	missense	possibly damaging	0.81
R5202:Pcgf5	UTSW	19	36,414,583 (GRCm39)	missense	probably damaging	1.00
R5997:Pcgf5	UTSW	19	36,412,003 (GRCm39)	missense	probably benign	0.35
R6039:Pcgf5	UTSW	19	36,420,306 (GRCm39)	missense	probably damaging	1.00
R6039:Pcgf5	UTSW	19	36,420,306 (GRCm39)	missense	probably damaging	1.00
R7060:Pcgf5	UTSW	19	36,420,339 (GRCm39)	nonsense	probably null
R8076:Pcgf5	UTSW	19	36,417,483 (GRCm39)	missense	probably damaging	1.00
R8773:Pcgf5	UTSW	19	36,389,348 (GRCm39)	splice site	probably benign

Posted On

2016-08-02