Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01327:Ctsr'

74349

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: 0.082) question?

Stock #

IGL01327

Quality Score

Status

Chromosome

Chromosomal Location

61307029-61312002 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to G at 61310489 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000021889 (fasta)

Gene Model

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

AlphaFold

Q9JIA9

Predicted Effect

probably benign
Transcript: ENSMUST00000021889

SMART Domains

Protein: ENSMUSP00000021889
Gene: ENSMUSG00000055679

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: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2510039O18Rik	T	A	4: 148,029,521 (GRCm39)	V497E	probably damaging	Het
Adcy7	T	G	8: 89,045,418 (GRCm39)		probably benign	Het
Aldh1a2	T	A	9: 71,193,248 (GRCm39)	F486I	possibly damaging	Het
Alox12	T	A	11: 70,145,375 (GRCm39)	H66L	probably benign	Het
Apoh	T	G	11: 108,288,187 (GRCm39)	Y102D	probably damaging	Het
Arl9	T	C	5: 77,154,401 (GRCm39)	V43A	possibly damaging	Het
Atf6	A	G	1: 170,616,175 (GRCm39)		probably null	Het
Atp4a	T	A	7: 30,412,675 (GRCm39)	I127N	possibly damaging	Het
AY358078	T	A	14: 52,043,166 (GRCm39)		probably benign	Het
Baat	T	G	4: 49,490,338 (GRCm39)	K249Q	probably damaging	Het
Brat1	C	T	5: 140,703,963 (GRCm39)	Q739*	probably null	Het
C8g	A	G	2: 25,389,089 (GRCm39)	F165L	probably damaging	Het
Cel	T	G	2: 28,447,967 (GRCm39)	D353A	possibly damaging	Het
Col6a1	G	T	10: 76,546,813 (GRCm39)	T803K	unknown	Het
Cpxm1	A	G	2: 130,238,277 (GRCm39)	L95P	probably benign	Het
Cyth1	A	G	11: 118,084,439 (GRCm39)		probably null	Het
Dync1h1	A	T	12: 110,583,126 (GRCm39)		probably benign	Het
Ezh1	C	T	11: 101,094,262 (GRCm39)	C407Y	probably damaging	Het
Fam243	T	C	16: 92,117,661 (GRCm39)	Y209C	probably benign	Het
Gm3696	A	T	14: 18,435,903 (GRCm39)	W38R	probably benign	Het
Gm9611	T	C	14: 42,116,622 (GRCm39)	T39A	possibly damaging	Het
Gnpat	T	A	8: 125,605,372 (GRCm39)	L287H	probably damaging	Het
Golm1	G	T	13: 59,792,958 (GRCm39)	N182K	possibly damaging	Het
Hdac6	T	C	X: 7,798,013 (GRCm39)	M899V	probably benign	Het
Hsf3	T	A	X: 95,358,578 (GRCm39)	M272L	probably benign	Het
Kif19a	C	T	11: 114,672,625 (GRCm39)		probably benign	Het
Lcn2	T	G	2: 32,276,030 (GRCm39)	Y100S	possibly damaging	Het
Lrrc8d	T	A	5: 105,960,131 (GRCm39)	S180R	probably damaging	Het
Ly6h	A	G	15: 75,436,948 (GRCm39)		probably benign	Het
Macf1	T	C	4: 123,403,705 (GRCm39)	N705D	probably benign	Het
Mst1r	C	T	9: 107,785,043 (GRCm39)	P234S	probably benign	Het
Msto1	T	A	3: 88,817,939 (GRCm39)		probably null	Het
Myo5a	T	A	9: 75,094,820 (GRCm39)		probably benign	Het
Nipa1	T	C	7: 55,629,409 (GRCm39)	I235V	probably benign	Het
Nlgn3	T	C	X: 100,362,228 (GRCm39)	V399A	probably benign	Het
Or1d2	T	A	11: 74,255,738 (GRCm39)	M81K	possibly damaging	Het
Or2b28	A	G	13: 21,531,377 (GRCm39)	N93S	probably benign	Het
Pih1d1	T	C	7: 44,809,399 (GRCm39)	S289P	probably benign	Het
Ppl	T	C	16: 4,905,508 (GRCm39)	N1596D	probably benign	Het
Psmb6	T	A	11: 70,417,412 (GRCm39)	S114R	possibly damaging	Het
Pum1	C	A	4: 130,457,854 (GRCm39)	Q289K	probably damaging	Het
Shkbp1	T	C	7: 27,054,676 (GRCm39)	I75V	probably benign	Het
Slc24a3	T	A	2: 145,444,478 (GRCm39)	I284N	probably benign	Het
Slc44a3	C	T	3: 121,320,842 (GRCm39)	G53D	probably damaging	Het
Slc9a4	A	C	1: 40,668,565 (GRCm39)	D736A	probably benign	Het
Stra6	A	G	9: 58,059,854 (GRCm39)	D605G	probably benign	Het
Tas2r126	T	A	6: 42,411,684 (GRCm39)	H72Q	probably benign	Het
Tbrg1	C	T	9: 37,564,408 (GRCm39)	R166Q	probably benign	Het
Thumpd1	C	T	7: 119,319,925 (GRCm39)	G14R	probably benign	Het
Ticrr	C	T	7: 79,344,209 (GRCm39)	T1358I	probably benign	Het
Tmtc2	A	T	10: 105,184,340 (GRCm39)	N518K	probably benign	Het
Trpm4	C	A	7: 44,964,497 (GRCm39)	W533C	probably damaging	Het
Tsen54	T	C	11: 115,712,538 (GRCm39)	Y119H	possibly damaging	Het
Tulp3	G	A	6: 128,304,597 (GRCm39)	T219M	probably damaging	Het
Usp19	T	C	9: 108,376,160 (GRCm39)	L1000S	possibly damaging	Het
Vps16	A	T	2: 130,279,616 (GRCm39)	Y43F	probably benign	Het
Vsig1	T	A	X: 139,838,429 (GRCm39)	V283E	possibly damaging	Het

Other mutations in Ctsr

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00647:Ctsr	APN	13	61,310,556 (GRCm39)	missense	probably damaging	1.00
IGL02169:Ctsr	APN	13	61,311,054 (GRCm39)	splice site	probably benign
IGL02516:Ctsr	APN	13	61,310,992 (GRCm39)	missense	probably benign
IGL02739:Ctsr	APN	13	61,309,658 (GRCm39)	missense	probably benign	0.01
PIT4687001:Ctsr	UTSW	13	61,308,346 (GRCm39)	missense	possibly damaging	0.52
R0180:Ctsr	UTSW	13	61,310,559 (GRCm39)	missense	probably damaging	1.00
R1938:Ctsr	UTSW	13	61,310,259 (GRCm39)	missense	probably benign	0.00
R2362:Ctsr	UTSW	13	61,310,610 (GRCm39)	missense	probably damaging	1.00
R3856:Ctsr	UTSW	13	61,309,750 (GRCm39)	missense	possibly damaging	0.75
R4125:Ctsr	UTSW	13	61,309,659 (GRCm39)	missense	probably benign	0.17
R4135:Ctsr	UTSW	13	61,309,084 (GRCm39)	missense	probably benign	0.15
R4903:Ctsr	UTSW	13	61,310,945 (GRCm39)	missense	probably benign	0.01
R5551:Ctsr	UTSW	13	61,307,357 (GRCm39)	missense	probably damaging	1.00
R5705:Ctsr	UTSW	13	61,309,078 (GRCm39)	missense	probably damaging	1.00
R5721:Ctsr	UTSW	13	61,309,667 (GRCm39)	missense	possibly damaging	0.84
R6132:Ctsr	UTSW	13	61,309,582 (GRCm39)	critical splice donor site	probably null
R6196:Ctsr	UTSW	13	61,308,345 (GRCm39)	missense	probably benign	0.09
R6719:Ctsr	UTSW	13	61,308,265 (GRCm39)	missense	possibly damaging	0.60
R7530:Ctsr	UTSW	13	61,310,931 (GRCm39)	missense	probably damaging	1.00
R7698:Ctsr	UTSW	13	61,310,381 (GRCm39)	missense	probably benign	0.01
R7963:Ctsr	UTSW	13	61,310,276 (GRCm39)	missense	probably damaging	1.00
R8251:Ctsr	UTSW	13	61,310,592 (GRCm39)	missense	probably damaging	1.00
R8431:Ctsr	UTSW	13	61,308,304 (GRCm39)	missense	probably damaging	1.00
R8810:Ctsr	UTSW	13	61,309,639 (GRCm39)	missense	probably damaging	1.00
R9464:Ctsr	UTSW	13	61,307,295 (GRCm39)	missense	possibly damaging	0.46
R9572:Ctsr	UTSW	13	61,310,978 (GRCm39)	missense	probably benign

Posted On

2013-10-07