Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00920:Msantd5f1'

27238

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Msantd5f1

Ensembl Gene

ENSMUSG00000095341

Gene Name

Myb/SANT DNA binding domain containing 5 family member 1

Synonyms

Gm428, LOC242502

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL00920

Quality Score

Status

Chromosome

Chromosomal Location

73601753-73605795 bp(+) (GRCm39)

Type of Mutation

utr 3 prime

DNA Base Change (assembly)

T to A at 73605679 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000081515 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000084475]

AlphaFold

Q3UTE2

Predicted Effect

probably benign
Transcript: ENSMUST00000084475

SMART Domains

Protein: ENSMUSP00000081515
Gene: ENSMUSG00000095341

Domain	Start	End	E-Value	Type
low complexity region	69	84	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: This gene belongs to a family of related genes tandemly arranged in two clusters on chromosome 4. This family, which appears to be mouse-specific and composed of multiple highly similar members, is supported by limited transcript data. Members of the family maintain an intact open reading frame although the encoded protein has no known function. This gene is supported by alignment of transcripts. [provided by RefSeq, Apr 2013]

Allele List at MGI

Other mutations in this stock

Total: 25 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Cd209e	T	C	8: 3,899,187 (GRCm39)	D175G	probably damaging	Het
Cep78	T	C	19: 15,958,850 (GRCm39)	I165V	probably benign	Het
Coa7	G	T	4: 108,195,505 (GRCm39)	G145C	possibly damaging	Het
Dpp9	T	C	17: 56,507,599 (GRCm39)	T357A	probably benign	Het
Gm42416	T	A	18: 37,085,820 (GRCm39)	M1K	probably null	Het
Hnrnpm	C	A	17: 33,868,876 (GRCm39)	R517L	probably damaging	Het
Kcnh5	A	T	12: 75,023,267 (GRCm39)	D600E	probably damaging	Het
Ndst4	A	G	3: 125,231,860 (GRCm39)	D143G	probably damaging	Het
Nrros	A	G	16: 31,966,438 (GRCm39)	F14S	probably benign	Het
Or5g9	A	T	2: 85,552,583 (GRCm39)	Y278F	probably damaging	Het
Or8g2b	T	C	9: 39,751,230 (GRCm39)	F167L	probably benign	Het
Pcdh7	A	T	5: 57,877,473 (GRCm39)	I343F	probably damaging	Het
Piwil4	C	T	9: 14,638,733 (GRCm39)	R264H	probably damaging	Het
Pnpt1	A	G	11: 29,107,087 (GRCm39)		probably benign	Het
Pycr2	T	A	1: 180,733,958 (GRCm39)		probably benign	Het
Rfx7	T	A	9: 72,500,638 (GRCm39)	Y133N	probably damaging	Het
Slc17a3	A	G	13: 24,040,464 (GRCm39)	I263V	probably benign	Het
Spink5	A	T	18: 44,136,276 (GRCm39)	E562D	probably damaging	Het
Spty2d1	T	C	7: 46,648,735 (GRCm39)	R65G	probably damaging	Het
Thbs1	C	T	2: 117,943,682 (GRCm39)	T100I	probably damaging	Het
Triml1	T	C	8: 43,591,719 (GRCm39)	N213S	probably damaging	Het
Trp53bp2	T	C	1: 182,272,219 (GRCm39)		probably benign	Het
Vmn2r9	T	C	5: 108,995,890 (GRCm39)	I253V	possibly damaging	Het
Zan	C	T	5: 137,462,786 (GRCm39)	V798I	unknown	Het
Zfp608	C	T	18: 55,022,903 (GRCm39)	M1504I	probably benign	Het

Other mutations in Msantd5f1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00492:Msantd5f1	APN	4	73,605,570 (GRCm39)	missense	probably damaging	0.99
IGL02931:Msantd5f1	APN	4	73,605,602 (GRCm39)	missense	probably damaging	0.99
R1651:Msantd5f1	UTSW	4	73,605,621 (GRCm39)	missense	possibly damaging	0.75
R6862:Msantd5f1	UTSW	4	73,605,621 (GRCm39)	missense	probably benign	0.21
R8205:Msantd5f1	UTSW	4	73,605,542 (GRCm39)	missense	possibly damaging	0.79
R8338:Msantd5f1	UTSW	4	73,605,435 (GRCm39)	missense	possibly damaging	0.86

Posted On

2013-04-17