Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02739:Ctsr'

305804

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Ctsr

Ensembl Gene

ENSMUSG00000055679

Gene Name

cathepsin R

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.106) question?

Stock #

IGL02739

Quality Score

Status

Chromosome

Chromosomal Location

61159204-61164256 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 61161844 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 184 (T184A)

Ref Sequence

ENSEMBL: ENSMUSP00000021889 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021889]

AlphaFold

Q9JIA9

Predicted Effect

probably benign
Transcript: ENSMUST00000021889
AA Change: T184A

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000021889
Gene: ENSMUSG00000055679
AA Change: T184A

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC
Inhibitor_I29	29	88	1.68e-21	SMART
Pept_C1	115	333	1.59e-111	SMART

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 40 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aasdh	A	T	5: 76,878,517 (GRCm38)	C887S	possibly damaging	Het
Adamdec1	C	A	14: 68,570,156 (GRCm38)	E352*	probably null	Het
Bglap2	A	T	3: 88,378,012 (GRCm38)		probably null	Het
Bsn	A	T	9: 108,112,546 (GRCm38)	H2002Q	probably benign	Het
Chtop	T	A	3: 90,502,250 (GRCm38)	Q165L	possibly damaging	Het
Clcn1	A	T	6: 42,286,780 (GRCm38)		probably null	Het
Defb36	T	C	2: 152,604,519 (GRCm38)	L11P	unknown	Het
Dock8	A	G	19: 25,188,488 (GRCm38)	E1912G	probably damaging	Het
Dpp3	A	G	19: 4,923,728 (GRCm38)	Y106H	probably damaging	Het
Epas1	A	G	17: 86,805,282 (GRCm38)	T103A	probably damaging	Het
Epcam	A	T	17: 87,640,494 (GRCm38)	T131S	probably benign	Het
Fam169a	A	G	13: 97,094,055 (GRCm38)		probably benign	Het
Gh	T	A	11: 106,301,733 (GRCm38)		probably benign	Het
Kif20a	A	T	18: 34,628,943 (GRCm38)	K399*	probably null	Het
Lrp1b	A	G	2: 41,498,215 (GRCm38)	I466T	probably damaging	Het
Nlk	A	G	11: 78,574,851 (GRCm38)	V409A	probably benign	Het
Nomo1	A	G	7: 46,044,307 (GRCm38)		probably null	Het
Nr2c1	T	A	10: 94,156,972 (GRCm38)	M16K	probably damaging	Het
Nxph2	A	T	2: 23,399,900 (GRCm38)	Q88L	probably benign	Het
Olfr33	A	G	7: 102,714,314 (GRCm38)	I33T	possibly damaging	Het
Pkdrej	T	A	15: 85,819,694 (GRCm38)	R680S	probably benign	Het
Pkhd1l1	A	T	15: 44,540,950 (GRCm38)	N2325I	probably benign	Het
Pnliprp2	T	C	19: 58,760,509 (GRCm38)		probably null	Het
Ppp1r42	T	A	1: 9,968,853 (GRCm38)	K347N	probably benign	Het
Prtg	T	C	9: 72,851,585 (GRCm38)	V407A	possibly damaging	Het
Psmb8	C	A	17: 34,200,754 (GRCm38)	S194*	probably null	Het
Rnf214	T	C	9: 45,869,474 (GRCm38)	I406V	probably benign	Het
Rreb1	C	T	13: 37,893,821 (GRCm38)	S3L	probably damaging	Het
Sdad1	C	T	5: 92,290,072 (GRCm38)	A539T	probably benign	Het
Sema3a	A	G	5: 13,451,161 (GRCm38)	Y57C	probably damaging	Het
Susd5	A	G	9: 114,096,033 (GRCm38)	E328G	possibly damaging	Het
Syngr3	T	C	17: 24,686,398 (GRCm38)	T175A	probably damaging	Het
Tcf20	T	A	15: 82,856,080 (GRCm38)	Q390L	probably damaging	Het
Tex15	A	G	8: 33,581,693 (GRCm38)	T2423A	possibly damaging	Het
Tlr1	T	C	5: 64,927,126 (GRCm38)	N36S	probably benign	Het
Uchl4	C	T	9: 64,235,537 (GRCm38)	T100M	probably damaging	Het
Uhrf1	A	G	17: 56,305,129 (GRCm38)	K11R	probably benign	Het
Vps13b	T	A	15: 35,879,900 (GRCm38)	D3040E	probably damaging	Het
Wdr62	A	T	7: 30,242,460 (GRCm38)	Y640*	probably null	Het
Zkscan17	T	G	11: 59,503,526 (GRCm38)	E83A	probably damaging	Het

Other mutations in Ctsr

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00647:Ctsr	APN	13	61,162,742 (GRCm38)	missense	probably damaging	1.00
IGL01327:Ctsr	APN	13	61,162,675 (GRCm38)	splice site	probably benign
IGL02169:Ctsr	APN	13	61,163,240 (GRCm38)	splice site	probably benign
IGL02516:Ctsr	APN	13	61,163,178 (GRCm38)	missense	probably benign
PIT4687001:Ctsr	UTSW	13	61,160,532 (GRCm38)	missense	possibly damaging	0.52
R0180:Ctsr	UTSW	13	61,162,745 (GRCm38)	missense	probably damaging	1.00
R1938:Ctsr	UTSW	13	61,162,445 (GRCm38)	missense	probably benign	0.00
R2362:Ctsr	UTSW	13	61,162,796 (GRCm38)	missense	probably damaging	1.00
R3856:Ctsr	UTSW	13	61,161,936 (GRCm38)	missense	possibly damaging	0.75
R4125:Ctsr	UTSW	13	61,161,845 (GRCm38)	missense	probably benign	0.17
R4135:Ctsr	UTSW	13	61,161,270 (GRCm38)	missense	probably benign	0.15
R4903:Ctsr	UTSW	13	61,163,131 (GRCm38)	missense	probably benign	0.01
R5551:Ctsr	UTSW	13	61,159,543 (GRCm38)	missense	probably damaging	1.00
R5705:Ctsr	UTSW	13	61,161,264 (GRCm38)	missense	probably damaging	1.00
R5721:Ctsr	UTSW	13	61,161,853 (GRCm38)	missense	possibly damaging	0.84
R6132:Ctsr	UTSW	13	61,161,768 (GRCm38)	critical splice donor site	probably null
R6196:Ctsr	UTSW	13	61,160,531 (GRCm38)	missense	probably benign	0.09
R6719:Ctsr	UTSW	13	61,160,451 (GRCm38)	missense	possibly damaging	0.60
R7530:Ctsr	UTSW	13	61,163,117 (GRCm38)	missense	probably damaging	1.00
R7698:Ctsr	UTSW	13	61,162,567 (GRCm38)	missense	probably benign	0.01
R7963:Ctsr	UTSW	13	61,162,462 (GRCm38)	missense	probably damaging	1.00
R8251:Ctsr	UTSW	13	61,162,778 (GRCm38)	missense	probably damaging	1.00
R8431:Ctsr	UTSW	13	61,160,490 (GRCm38)	missense	probably damaging	1.00
R8810:Ctsr	UTSW	13	61,161,825 (GRCm38)	missense	probably damaging	1.00
R9464:Ctsr	UTSW	13	61,159,481 (GRCm38)	missense	possibly damaging	0.46
R9572:Ctsr	UTSW	13	61,163,164 (GRCm38)	missense	probably benign

Posted On

2015-04-16