Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01372:S100a7l2'

76204

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

S100a7l2

Ensembl Gene

ENSMUSG00000091175

Gene Name

S100 calcium binding protein A7 like 2

Synonyms

9130204L05Rik, LOC229550

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.092) question?

Stock #

IGL01372

Quality Score

Status

Chromosome

Chromosomal Location

90995444-90998110 bp(-) (GRCm39)

Type of Mutation

utr 3 prime

DNA Base Change (assembly)

A to G at 90995616 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000130512 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000166173]

AlphaFold

G3UWB8

Predicted Effect

probably benign
Transcript: ENSMUST00000166173

SMART Domains

Protein: ENSMUSP00000130512
Gene: ENSMUSG00000091175

Domain	Start	End	E-Value	Type
Pfam:S_100	9	48	4.4e-10	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 42 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca7	G	A	10: 79,842,089 (GRCm39)	D1049N	probably benign	Het
Ankdd1a	A	T	9: 65,411,421 (GRCm39)	L362Q	probably damaging	Het
Ankib1	A	T	5: 3,822,594 (GRCm39)	N37K	probably damaging	Het
Ankrd55	T	A	13: 112,459,677 (GRCm39)	D90E	probably damaging	Het
Atp1a2	T	C	1: 172,106,510 (GRCm39)	R831G	probably damaging	Het
Bcar3	A	G	3: 122,316,943 (GRCm39)	D638G	probably damaging	Het
Cabp4	T	A	19: 4,189,322 (GRCm39)	E78D	probably benign	Het
Cmtm8	A	G	9: 114,619,755 (GRCm39)	V130A	possibly damaging	Het
Cyth3	A	G	5: 143,678,393 (GRCm39)	T66A	possibly damaging	Het
Dmbt1	A	T	7: 130,705,409 (GRCm39)	I1171F	possibly damaging	Het
Dnah10	G	A	5: 124,856,218 (GRCm39)	G2060D	probably damaging	Het
Dnah11	T	C	12: 118,156,134 (GRCm39)	H172R	probably damaging	Het
Dnah5	C	T	15: 28,230,636 (GRCm39)	A178V	probably benign	Het
Efcab6	T	G	15: 83,928,505 (GRCm39)	M30L	possibly damaging	Het
Ehbp1l1	T	C	19: 5,765,817 (GRCm39)		probably benign	Het
Eps15	G	A	4: 109,179,303 (GRCm39)	E230K	probably damaging	Het
Fam91a1	A	G	15: 58,301,911 (GRCm39)	I258M	probably damaging	Het
Gm5581	G	A	6: 131,145,366 (GRCm39)		noncoding transcript	Het
Hrh1	G	A	6: 114,456,958 (GRCm39)	V80I	probably damaging	Het
Ldhd	G	A	8: 112,355,032 (GRCm39)	H290Y	probably benign	Het
Lepr	G	A	4: 101,592,774 (GRCm39)	E130K	possibly damaging	Het
Mycbpap	T	C	11: 94,397,282 (GRCm39)	I40V	possibly damaging	Het
Nrap	T	A	19: 56,317,534 (GRCm39)		probably null	Het
Opn5	T	A	17: 42,891,435 (GRCm39)		probably null	Het
Or1j14	T	A	2: 36,417,463 (GRCm39)	I13N	probably benign	Het
Or5ac24	A	G	16: 59,165,524 (GRCm39)	I180T	probably damaging	Het
Otop3	A	T	11: 115,235,930 (GRCm39)	T521S	possibly damaging	Het
Pcsk5	T	G	19: 17,595,108 (GRCm39)	T409P	probably damaging	Het
Pde9a	T	A	17: 31,680,685 (GRCm39)	F322Y	probably benign	Het
Pgm5	T	A	19: 24,710,985 (GRCm39)	I406F	probably damaging	Het
Prrc2b	T	C	2: 32,113,942 (GRCm39)	S1998P	probably damaging	Het
Prune2	T	C	19: 17,102,433 (GRCm39)	Y2531H	probably damaging	Het
Ptprk	T	C	10: 28,445,923 (GRCm39)	V932A	probably benign	Het
Rapgef6	T	A	11: 54,559,437 (GRCm39)		probably benign	Het
Rgsl1	T	A	1: 153,701,887 (GRCm39)	Y224F	probably damaging	Het
Rps6kl1	A	T	12: 85,193,663 (GRCm39)	C143S	probably damaging	Het
Slc5a5	G	A	8: 71,343,020 (GRCm39)		probably benign	Het
Tfb2m	A	G	1: 179,369,878 (GRCm39)	S182P	probably damaging	Het
Tmc3	A	G	7: 83,261,746 (GRCm39)	H608R	probably damaging	Het
Trim37	T	A	11: 87,075,772 (GRCm39)	H459Q	probably benign	Het
Vmn2r71	A	T	7: 85,270,022 (GRCm39)		probably benign	Het
Xirp2	T	C	2: 67,344,334 (GRCm39)	S2192P	possibly damaging	Het

Other mutations in S100a7l2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00231:S100a7l2	APN	3	90,995,665 (GRCm39)	missense	probably benign	0.01
IGL01526:S100a7l2	APN	3	90,995,612 (GRCm39)	utr 3 prime	probably benign
IGL02894:S100a7l2	APN	3	90,995,700 (GRCm39)	missense	probably benign	0.18
IGL03110:S100a7l2	APN	3	90,995,626 (GRCm39)	missense	unknown
IGL03250:S100a7l2	APN	3	90,997,715 (GRCm39)	utr 5 prime	probably benign
R2357:S100a7l2	UTSW	3	90,995,733 (GRCm39)	missense	probably benign	0.35
R3795:S100a7l2	UTSW	3	90,995,730 (GRCm39)	missense	possibly damaging	0.73
R5315:S100a7l2	UTSW	3	90,997,637 (GRCm39)	missense	possibly damaging	0.56
R5495:S100a7l2	UTSW	3	90,997,602 (GRCm39)	missense	possibly damaging	0.93
R6314:S100a7l2	UTSW	3	90,995,683 (GRCm39)	missense	possibly damaging	0.56
R8351:S100a7l2	UTSW	3	90,995,671 (GRCm39)	missense	probably benign	0.01
R8451:S100a7l2	UTSW	3	90,995,671 (GRCm39)	missense	probably benign	0.01
R9371:S100a7l2	UTSW	3	90,997,698 (GRCm39)	missense	unknown
Z1177:S100a7l2	UTSW	3	90,995,663 (GRCm39)	missense	probably benign	0.01

Posted On

2013-10-07