Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02163:Gm38392'

282554

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm38392

Ensembl Gene

ENSMUSG00000103766

Gene Name

predicted gene, 38392

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL02163

Quality Score

Status

Chromosome

Chromosomal Location

88150687-88194517 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

G to A at 88152887 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000130767 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000171887]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000163277

Predicted Effect

probably benign
Transcript: ENSMUST00000165196

SMART Domains

Protein: ENSMUSP00000132187
Gene: ENSMUSG00000103766

Domain	Start	End	E-Value	Type
Pfam:Ammonium_transp	1	353	9.7e-70	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000171887

SMART Domains

Protein: ENSMUSP00000130767
Gene: ENSMUSG00000104445

Domain	Start	End	E-Value	Type
low complexity region	3	18	N/A	INTRINSIC
Pfam:Ammonium_transp	22	419	5.9e-74	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 24 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930447A16Rik	T	C	15: 37,439,852 (GRCm39)		probably benign	Het
Armh4	A	G	14: 50,011,614 (GRCm39)	V31A	possibly damaging	Het
Brd8	C	T	18: 34,735,780 (GRCm39)	S899N	probably damaging	Het
Cap1	C	T	4: 122,756,209 (GRCm39)	V396I	probably benign	Het
Ccdc80	T	C	16: 44,916,477 (GRCm39)	V411A	probably benign	Het
Cyp2w1	T	A	5: 139,341,920 (GRCm39)	M111K	probably damaging	Het
Dop1b	T	C	16: 93,559,315 (GRCm39)	V687A	possibly damaging	Het
Fam184a	T	C	10: 53,523,230 (GRCm39)		probably null	Het
Fhip1a	A	G	3: 85,595,859 (GRCm39)	F342S	possibly damaging	Het
Foxred1	A	T	9: 35,117,192 (GRCm39)	L313H	probably damaging	Het
Kmt2d	A	T	15: 98,733,109 (GRCm39)		probably benign	Het
Lrpprc	A	T	17: 85,060,900 (GRCm39)	M591K	probably damaging	Het
Ncr1	A	T	7: 4,344,262 (GRCm39)	S217C	possibly damaging	Het
Or10al7	T	C	17: 38,365,641 (GRCm39)	H281R	probably benign	Het
Or1e1	T	A	11: 73,245,320 (GRCm39)	V247E	probably damaging	Het
Pds5b	T	C	5: 150,679,871 (GRCm39)	F526L	probably benign	Het
Plekhh2	A	T	17: 84,898,223 (GRCm39)	S955C	probably benign	Het
Prpf19	T	A	19: 10,879,800 (GRCm39)	S307R	probably benign	Het
Pwp2	G	A	10: 78,014,119 (GRCm39)	P456S	possibly damaging	Het
Rgs8	C	A	1: 153,547,511 (GRCm39)	T47K	possibly damaging	Het
Samd9l	T	A	6: 3,374,246 (GRCm39)	N1005I	possibly damaging	Het
Tmc4	A	G	7: 3,669,824 (GRCm39)	L20P	probably damaging	Het
Ttc21a	C	T	9: 119,779,901 (GRCm39)	Q403*	probably null	Het
Zbtb43	T	C	2: 33,343,795 (GRCm39)	R477G	possibly damaging	Het

Other mutations in Gm38392

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R4357:Gm38392	UTSW	3	88,154,741 (GRCm39)	missense	probably damaging	1.00

Posted On

2015-04-16