Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01649:Gml2'

102778

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gml2

Ensembl Gene

ENSMUSG00000068600

Gene Name

glycosylphosphatidylinositol anchored molecule like 2

Synonyms

hematopoietic cell-specific transcript, HemT, Hemt1, 1700057K19Rik

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.051) question?

Stock #

IGL01649

Quality Score

Status

Chromosome

Chromosomal Location

74690920-74706720 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

G to T at 74696070 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Stop codon at position 155 (E155*)

Ref Sequence

ENSEMBL: ENSMUSP00000094130 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000096399] [ENSMUST00000188180]

AlphaFold

G5E8L7

Predicted Effect

probably null
Transcript: ENSMUST00000096399
AA Change: E155*

SMART Domains

Protein: ENSMUSP00000094130
Gene: ENSMUSG00000068600
AA Change: E155*

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
LU	47	141	2.06e-7	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000186752

Predicted Effect

probably benign
Transcript: ENSMUST00000188180

SMART Domains

Protein: ENSMUSP00000141185
Gene: ENSMUSG00000068600

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Blast:LU	47	80	2e-15	BLAST

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000188458

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 32 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4931429L15Rik	A	G	9: 46,217,116 (GRCm39)	S220P	probably benign	Het
Adam18	T	C	8: 25,104,912 (GRCm39)	N634S	possibly damaging	Het
Arhgef18	T	A	8: 3,491,211 (GRCm39)		probably benign	Het
Birc6	A	G	17: 74,911,541 (GRCm39)	S1518G	probably benign	Het
Cltc	A	G	11: 86,617,226 (GRCm39)	V341A	probably benign	Het
Dlg5	A	G	14: 24,188,759 (GRCm39)	V1721A	probably damaging	Het
Dnah10	A	T	5: 124,809,553 (GRCm39)	I274F	probably damaging	Het
Dock1	T	A	7: 134,379,139 (GRCm39)	L622Q	probably damaging	Het
Dysf	A	G	6: 84,176,821 (GRCm39)	D1960G	probably damaging	Het
Fat3	T	C	9: 16,288,015 (GRCm39)	T503A	possibly damaging	Het
Glb1	A	G	9: 114,253,016 (GRCm39)	Y73C	probably damaging	Het
Gm9396	G	T	3: 129,862,268 (GRCm39)		noncoding transcript	Het
Ikzf4	G	A	10: 128,471,689 (GRCm39)	R323C	probably damaging	Het
Kiz	A	G	2: 146,731,229 (GRCm39)	T240A	probably benign	Het
Lzts3	T	C	2: 130,477,351 (GRCm39)	K480E	probably damaging	Het
Mcm7	T	C	5: 138,167,698 (GRCm39)	H105R	probably damaging	Het
Mpdz	A	G	4: 81,221,870 (GRCm39)	L1464P	probably damaging	Het
Mrgpra9	A	C	7: 46,884,900 (GRCm39)	L256V	probably benign	Het
Mrpl40	T	C	16: 18,691,329 (GRCm39)	Q127R	probably benign	Het
Myom2	G	T	8: 15,163,755 (GRCm39)	R1003L	probably benign	Het
Nav2	A	G	7: 49,225,477 (GRCm39)	T1806A	probably damaging	Het
Or10x4	T	C	1: 174,218,974 (GRCm39)	L113P	probably damaging	Het
Pibf1	A	T	14: 99,425,199 (GRCm39)	Y562F	possibly damaging	Het
Potefam1	A	T	2: 111,044,921 (GRCm39)		probably benign	Het
Ppm1n	A	T	7: 19,012,122 (GRCm39)		probably benign	Het
Psg17	A	G	7: 18,550,727 (GRCm39)	V376A	possibly damaging	Het
Septin8	T	A	11: 53,425,855 (GRCm39)	F143I	possibly damaging	Het
Sestd1	A	G	2: 77,029,389 (GRCm39)	Y330H	probably damaging	Het
Sntg1	C	T	1: 8,752,193 (GRCm39)		probably benign	Het
Stpg2	C	A	3: 139,125,623 (GRCm39)	P472Q	probably damaging	Het
Thbs1	A	G	2: 117,945,463 (GRCm39)	K314R	probably benign	Het
Vav3	T	C	3: 109,470,078 (GRCm39)	Y508H	probably benign	Het

Other mutations in Gml2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0031:Gml2	UTSW	15	74,696,125 (GRCm39)	missense	probably benign	0.12
R0608:Gml2	UTSW	15	74,693,235 (GRCm39)	critical splice donor site	probably null
R1087:Gml2	UTSW	15	74,695,946 (GRCm39)	missense	possibly damaging	0.73
R1130:Gml2	UTSW	15	74,693,195 (GRCm39)	missense	probably damaging	0.99
R1503:Gml2	UTSW	15	74,693,201 (GRCm39)	nonsense	probably null
R4408:Gml2	UTSW	15	74,696,188 (GRCm39)	intron	probably benign
R6802:Gml2	UTSW	15	74,696,095 (GRCm39)	missense	probably damaging	1.00
R7351:Gml2	UTSW	15	74,693,225 (GRCm39)	missense	possibly damaging	0.57
R7833:Gml2	UTSW	15	74,693,217 (GRCm39)	nonsense	probably null
R7910:Gml2	UTSW	15	74,692,379 (GRCm39)	critical splice acceptor site	probably null
R8513:Gml2	UTSW	15	74,696,004 (GRCm39)	missense	probably damaging	1.00
R8695:Gml2	UTSW	15	74,696,089 (GRCm39)	missense	probably benign	0.05
R9377:Gml2	UTSW	15	74,695,957 (GRCm39)	missense	probably benign	0.02
X0066:Gml2	UTSW	15	74,695,899 (GRCm39)	missense	probably benign	0.01

Posted On

2014-01-21