Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00956:Zfp609'

28221

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Zfp609

Ensembl Gene

ENSMUSG00000040524

Gene Name

zinc finger protein 609

Synonyms

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.620) question?

Stock #

IGL00956

Quality Score

Status

Chromosome

Chromosomal Location

65599673-65734846 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 65610045 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Histidine at position 973 (Y973H)

Ref Sequence

ENSEMBL: ENSMUSP00000124089 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000159109]

AlphaFold

Q8BZ47

Predicted Effect

probably benign
Transcript: ENSMUST00000159109
AA Change: Y973H

PolyPhen 2 Score 0.178 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000124089
Gene: ENSMUSG00000040524
AA Change: Y973H

Domain	Start	End	E-Value	Type
low complexity region	83	101	N/A	INTRINSIC
low complexity region	125	139	N/A	INTRINSIC
low complexity region	155	176	N/A	INTRINSIC
low complexity region	259	269	N/A	INTRINSIC
low complexity region	365	376	N/A	INTRINSIC
low complexity region	386	405	N/A	INTRINSIC
ZnF_C2H2	495	520	2.14e0	SMART
low complexity region	629	638	N/A	INTRINSIC
low complexity region	657	667	N/A	INTRINSIC
low complexity region	724	738	N/A	INTRINSIC
low complexity region	1000	1020	N/A	INTRINSIC
low complexity region	1210	1219	N/A	INTRINSIC
low complexity region	1257	1273	N/A	INTRINSIC
low complexity region	1329	1348	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159878

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 20 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Cdhr2	G	T	13: 54,866,156 (GRCm39)	V319F	probably damaging	Het
Chac2	A	G	11: 30,936,225 (GRCm39)	S8P	probably damaging	Het
Clec4b2	T	A	6: 123,179,110 (GRCm39)	Y137*	probably null	Het
Dbt	G	A	3: 116,339,763 (GRCm39)	G384S	probably benign	Het
Duox1	G	T	2: 122,153,787 (GRCm39)	R370L	probably benign	Het
Hnrnpm	C	A	17: 33,868,876 (GRCm39)	R517L	probably damaging	Het
Iigp1c	A	C	18: 60,379,262 (GRCm39)	T266P	probably damaging	Het
Iqschfp	C	A	3: 68,533,184 (GRCm39)	A255E	probably damaging	Het
Kcnh7	G	A	2: 62,607,983 (GRCm39)	R533C	probably damaging	Het
Nckap5	A	C	1: 125,952,755 (GRCm39)	L1266V	probably damaging	Het
Opcml	A	G	9: 28,586,624 (GRCm39)	N121S	possibly damaging	Het
Rad54b	T	A	4: 11,597,833 (GRCm39)	N239K	probably damaging	Het
Rp1	T	C	1: 4,422,435 (GRCm39)	D215G	probably damaging	Het
Scaf8	T	C	17: 3,221,422 (GRCm39)	I303T	unknown	Het
Slc35f3	G	A	8: 127,108,963 (GRCm39)	A171T	probably damaging	Het
Tlk2	T	A	11: 105,138,418 (GRCm39)	I322N	probably benign	Het
Tubb4a	A	G	17: 57,393,072 (GRCm39)	V66A	probably benign	Het
Ubxn2a	C	T	12: 4,933,956 (GRCm39)	A152T	probably benign	Het
Ush2a	A	T	1: 188,485,719 (GRCm39)	D2943V	probably damaging	Het
Wdr62	A	G	7: 29,960,764 (GRCm39)	V55A	probably damaging	Het

Other mutations in Zfp609

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01688:Zfp609	APN	9	65,611,307 (GRCm39)	missense	probably benign
IGL01718:Zfp609	APN	9	65,609,682 (GRCm39)	nonsense	probably null
IGL01860:Zfp609	APN	9	65,610,116 (GRCm39)	missense	possibly damaging	0.82
IGL02441:Zfp609	APN	9	65,610,611 (GRCm39)	missense	possibly damaging	0.92
IGL02490:Zfp609	APN	9	65,611,250 (GRCm39)	missense	possibly damaging	0.92
IGL02614:Zfp609	APN	9	65,610,072 (GRCm39)	missense	probably damaging	0.96
IGL02794:Zfp609	APN	9	65,611,602 (GRCm39)	missense	possibly damaging	0.83
IGL02959:Zfp609	APN	9	65,610,675 (GRCm39)	missense	probably benign
IGL02967:Zfp609	APN	9	65,604,901 (GRCm39)	missense	possibly damaging	0.83
IGL03036:Zfp609	APN	9	65,609,927 (GRCm39)	missense	possibly damaging	0.89
IGL03182:Zfp609	APN	9	65,608,287 (GRCm39)	missense	probably benign	0.02
H8441:Zfp609	UTSW	9	65,702,169 (GRCm39)	missense	possibly damaging	0.82
R0304:Zfp609	UTSW	9	65,608,470 (GRCm39)	missense	possibly damaging	0.89
R0487:Zfp609	UTSW	9	65,609,916 (GRCm39)	missense	unknown
R0505:Zfp609	UTSW	9	65,610,744 (GRCm39)	missense	possibly damaging	0.92
R0684:Zfp609	UTSW	9	65,638,483 (GRCm39)	missense	probably benign	0.01
R1480:Zfp609	UTSW	9	65,610,593 (GRCm39)	missense	possibly damaging	0.82
R1507:Zfp609	UTSW	9	65,702,059 (GRCm39)	missense	possibly damaging	0.92
R1579:Zfp609	UTSW	9	65,611,754 (GRCm39)	missense	possibly damaging	0.90
R1655:Zfp609	UTSW	9	65,610,836 (GRCm39)	missense	possibly damaging	0.46
R1692:Zfp609	UTSW	9	65,702,593 (GRCm39)	missense	probably damaging	0.98
R1701:Zfp609	UTSW	9	65,638,282 (GRCm39)	missense	probably benign	0.05
R1735:Zfp609	UTSW	9	65,610,374 (GRCm39)	nonsense	probably null
R1883:Zfp609	UTSW	9	65,702,040 (GRCm39)	missense	probably benign
R1970:Zfp609	UTSW	9	65,702,559 (GRCm39)	missense	probably damaging	0.96
R2059:Zfp609	UTSW	9	65,611,716 (GRCm39)	missense	possibly damaging	0.83
R2302:Zfp609	UTSW	9	65,702,179 (GRCm39)	missense	possibly damaging	0.66
R3404:Zfp609	UTSW	9	65,608,454 (GRCm39)	missense	possibly damaging	0.68
R3405:Zfp609	UTSW	9	65,608,454 (GRCm39)	missense	possibly damaging	0.68
R4514:Zfp609	UTSW	9	65,610,977 (GRCm39)	missense	possibly damaging	0.46
R4533:Zfp609	UTSW	9	65,610,890 (GRCm39)	missense	probably benign	0.00
R5043:Zfp609	UTSW	9	65,608,109 (GRCm39)	missense	probably damaging	0.97
R5499:Zfp609	UTSW	9	65,610,137 (GRCm39)	missense	probably benign	0.00
R7081:Zfp609	UTSW	9	65,609,723 (GRCm39)	missense	possibly damaging	0.46
R7514:Zfp609	UTSW	9	65,613,418 (GRCm39)	missense	probably benign	0.05
R7677:Zfp609	UTSW	9	65,604,456 (GRCm39)	missense	possibly damaging	0.61
R7684:Zfp609	UTSW	9	65,638,362 (GRCm39)	missense	possibly damaging	0.66
R8229:Zfp609	UTSW	9	65,610,782 (GRCm39)	missense	possibly damaging	0.66
R8266:Zfp609	UTSW	9	65,610,996 (GRCm39)	missense	possibly damaging	0.66
R8278:Zfp609	UTSW	9	65,604,804 (GRCm39)	missense	possibly damaging	0.90
R8934:Zfp609	UTSW	9	65,610,561 (GRCm39)	missense	possibly damaging	0.90
R8938:Zfp609	UTSW	9	65,610,561 (GRCm39)	missense	possibly damaging	0.90
R8940:Zfp609	UTSW	9	65,610,561 (GRCm39)	missense	possibly damaging	0.90
R8986:Zfp609	UTSW	9	65,610,561 (GRCm39)	missense	possibly damaging	0.90
R9267:Zfp609	UTSW	9	65,608,328 (GRCm39)	missense	possibly damaging	0.90
R9456:Zfp609	UTSW	9	65,611,125 (GRCm39)	missense
R9561:Zfp609	UTSW	9	65,604,512 (GRCm39)	nonsense	probably null
X0028:Zfp609	UTSW	9	65,604,362 (GRCm39)	small deletion	probably benign

Posted On

2013-04-17