Mutagenetix > Incidental Mutation

Incidental Mutation 'R4599:Ankrd13b'

345458

Institutional Source

Beutler Lab

Gene Symbol

Ankrd13b

Ensembl Gene

ENSMUSG00000037907

Gene Name

ankyrin repeat domain 13b

Synonyms

B930093C12Rik

MMRRC Submission

041815-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.527) question?

Stock #

R4599 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

77361311-77380504 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 77362494 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glycine at position 677 (R677G)

Ref Sequence

ENSEMBL: ENSMUSP00000090568 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021190] [ENSMUST00000037593] [ENSMUST00000052515] [ENSMUST00000079770] [ENSMUST00000092892] [ENSMUST00000102493] [ENSMUST00000108391] [ENSMUST00000145934]

AlphaFold

Q5F259

Predicted Effect

probably benign
Transcript: ENSMUST00000021190

SMART Domains

Protein: ENSMUSP00000021190
Gene: ENSMUSG00000020836

Domain	Start	End	E-Value	Type
DUF1899	4	68	7.45e-34	SMART
WD40	67	110	2.1e-7	SMART
WD40	120	160	2.07e-6	SMART
WD40	163	203	2.73e-6	SMART
DUF1900	257	391	1.19e-91	SMART
low complexity region	414	429	N/A	INTRINSIC
coiled coil region	430	463	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000037593
AA Change: E603G

SMART Domains

Protein: ENSMUSP00000073584
Gene: ENSMUSG00000037907
AA Change: E603G

Domain	Start	End	E-Value	Type
ANK	13	43	3.16e2	SMART
ANK	47	76	2.85e-5	SMART
ANK	80	109	1.17e2	SMART
Pfam:GPCR_chapero_1	163	491	5.5e-111	PFAM
UIM	503	522	1.81e-1	SMART
low complexity region	552	580	N/A	INTRINSIC
UIM	585	604	3.15e-1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000052515

SMART Domains

Protein: ENSMUSP00000056862
Gene: ENSMUSG00000020836

Domain	Start	End	E-Value	Type
DUF1899	4	68	7.45e-34	SMART
WD40	67	110	2.1e-7	SMART
WD40	120	160	2.07e-6	SMART
WD40	163	203	2.73e-6	SMART
DUF1900	217	351	1.19e-91	SMART
low complexity region	374	389	N/A	INTRINSIC
coiled coil region	390	424	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000079770

SMART Domains

Protein: ENSMUSP00000078703
Gene: ENSMUSG00000020836

Domain	Start	End	E-Value	Type
DUF1899	4	68	7.45e-34	SMART
WD40	67	110	2.1e-7	SMART
WD40	120	160	2.07e-6	SMART
WD40	163	203	2.73e-6	SMART
DUF1900	217	351	1.19e-91	SMART
low complexity region	374	389	N/A	INTRINSIC
coiled coil region	390	423	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000092892
AA Change: R677G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000090568
Gene: ENSMUSG00000037907
AA Change: R677G

Domain	Start	End	E-Value	Type
ANK	13	43	3.16e2	SMART
ANK	47	76	2.85e-5	SMART
ANK	80	109	1.17e2	SMART
Pfam:GPCR_chapero_1	163	490	3.2e-110	PFAM
UIM	503	522	1.81e-1	SMART
low complexity region	673	686	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000102493

SMART Domains

Protein: ENSMUSP00000099551
Gene: ENSMUSG00000020836

Domain	Start	End	E-Value	Type
DUF1899	4	68	7.45e-34	SMART
WD40	67	110	2.1e-7	SMART
WD40	120	160	2.07e-6	SMART
WD40	163	203	2.73e-6	SMART
DUF1900	257	391	1.19e-91	SMART
low complexity region	414	429	N/A	INTRINSIC
coiled coil region	430	463	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000108391

SMART Domains

Protein: ENSMUSP00000104028
Gene: ENSMUSG00000020836

Domain	Start	End	E-Value	Type
DUF1899	4	68	7.45e-34	SMART
WD40	67	110	2.1e-7	SMART
WD40	120	160	2.07e-6	SMART
WD40	163	203	2.73e-6	SMART
DUF1900	257	391	1.19e-91	SMART
low complexity region	414	429	N/A	INTRINSIC
coiled coil region	430	463	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000143872

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000135227

Predicted Effect

probably benign
Transcript: ENSMUST00000145934

SMART Domains

Protein: ENSMUSP00000119633
Gene: ENSMUSG00000037907

Domain	Start	End	E-Value	Type
Pfam:GPCR_chapero_1	2	276	9.7e-90	PFAM
UIM	288	307	1.81e-1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000127291

SMART Domains

Protein: ENSMUSP00000118247
Gene: ENSMUSG00000037907

Domain	Start	End	E-Value	Type
Pfam:GPCR_chapero_1	1	120	9.7e-31	PFAM
low complexity region	121	133	N/A	INTRINSIC
low complexity region	184	200	N/A	INTRINSIC

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.4%
20x: 95.4%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca14	T	C	7: 119,854,626 (GRCm39)	V930A	probably benign	Het
Apc	T	A	18: 34,451,040 (GRCm39)	Y2611*	probably null	Het
Apold1	A	G	6: 134,961,032 (GRCm39)	Y162C	probably damaging	Het
Atp6v0a4	T	C	6: 38,055,737 (GRCm39)	I325V	probably benign	Het
Cab39	A	G	1: 85,776,050 (GRCm39)	Y249C	probably damaging	Het
Cd22	T	A	7: 30,575,325 (GRCm39)	H239L	probably damaging	Het
Chrna7	A	G	7: 62,753,538 (GRCm39)	M327T	probably damaging	Het
Cimip2b	T	C	4: 43,427,574 (GRCm39)	H250R	possibly damaging	Het
Clock	T	C	5: 76,383,657 (GRCm39)	M499V	probably benign	Het
Clspn	A	G	4: 126,475,253 (GRCm39)	E1002G	probably benign	Het
Clta	C	T	4: 44,012,819 (GRCm39)	P10S	probably damaging	Het
Col5a3	A	G	9: 20,685,855 (GRCm39)		probably null	Het
Coq6	T	C	12: 84,408,913 (GRCm39)	V30A	probably benign	Het
Csmd2	G	T	4: 127,881,921 (GRCm39)	R20L	probably benign	Het
D430041D05Rik	A	T	2: 104,038,528 (GRCm39)	V1547D	probably damaging	Het
Dapk1	C	T	13: 60,865,861 (GRCm39)	P153S	probably benign	Het
Dock2	T	A	11: 34,189,536 (GRCm39)	Y1545F	probably damaging	Het
Dpp6	G	T	5: 27,839,546 (GRCm39)	G354C	probably damaging	Het
Dyrk1b	T	C	7: 27,881,856 (GRCm39)	L105P	probably damaging	Het
Epor	A	G	9: 21,873,155 (GRCm39)	S86P	probably benign	Het
Gale	C	A	4: 135,695,148 (GRCm39)	S341*	probably null	Het
Galnt4	T	A	10: 98,945,355 (GRCm39)	V360E	probably damaging	Het
Gart	A	T	16: 91,419,833 (GRCm39)	C24*	probably null	Het
Gcnt2	G	T	13: 41,040,966 (GRCm39)	V42L	probably benign	Het
Herc6	A	G	6: 57,636,698 (GRCm39)	I805V	probably benign	Het
Ints12	T	A	3: 132,804,214 (GRCm39)	I67N	probably benign	Het
Irx1	C	A	13: 72,108,232 (GRCm39)	R150L	probably damaging	Het
Kif26b	A	G	1: 178,358,024 (GRCm39)	Y45C	unknown	Het
Krt35	T	C	11: 99,984,834 (GRCm39)	T275A	probably damaging	Het
Laptm5	G	T	4: 130,643,316 (GRCm39)		probably benign	Het
Lin7a	T	C	10: 107,248,027 (GRCm39)	S111P	unknown	Het
Med27	A	G	2: 29,414,470 (GRCm39)	D159G	probably damaging	Het
Msh2	A	G	17: 88,016,006 (GRCm39)	K546R	probably damaging	Het
Myo1a	A	T	10: 127,556,020 (GRCm39)		probably null	Het
Myo1c	T	C	11: 75,559,019 (GRCm39)	F604L	probably damaging	Het
Myrip	A	G	9: 120,293,850 (GRCm39)	K782E	probably damaging	Het
Ndc80	T	C	17: 71,828,063 (GRCm39)	D88G	probably damaging	Het
Nrxn2	A	G	19: 6,505,282 (GRCm39)	D375G	probably damaging	Het
Or2y10	T	C	11: 49,455,545 (GRCm39)	S266P	probably damaging	Het
Or52e7	A	G	7: 104,685,280 (GRCm39)	I292V	probably benign	Het
Padi3	T	C	4: 140,525,422 (GRCm39)	H187R	probably damaging	Het
Pcdhgb1	A	T	18: 37,814,610 (GRCm39)	N367I	probably damaging	Het
Pdrg1	T	C	2: 152,854,310 (GRCm39)	I77V	probably benign	Het
Pfas	T	C	11: 68,881,895 (GRCm39)	E930G	probably benign	Het
Pik3cb	C	T	9: 98,943,817 (GRCm39)	R662Q	probably benign	Het
Pla2g4e	T	G	2: 120,016,863 (GRCm39)	H226P	possibly damaging	Het
Plxnd1	A	T	6: 115,971,237 (GRCm39)	V177E	probably damaging	Het
Prmt7	A	G	8: 106,976,961 (GRCm39)	S558G	possibly damaging	Het
Pspc1	A	C	14: 57,015,246 (GRCm39)		probably null	Het
Rilp	T	C	11: 75,403,586 (GRCm39)	S343P	probably benign	Het
Ror1	A	G	4: 100,265,107 (GRCm39)	M194V	probably damaging	Het
Rsu1	T	C	2: 13,174,815 (GRCm39)	Y225C	probably damaging	Het
Rundc1	A	G	11: 101,324,752 (GRCm39)	N486S	probably damaging	Het
Sema6d	T	A	2: 124,496,151 (GRCm39)	I65N	probably damaging	Het
Slc5a11	A	G	7: 122,857,601 (GRCm39)	E230G	probably benign	Het
Spint1	T	C	2: 119,076,941 (GRCm39)	S342P	probably damaging	Het
Stard3nl	A	G	13: 19,551,923 (GRCm39)	S214P	probably damaging	Het
Tcp10a	A	C	17: 7,604,323 (GRCm39)	T271P	probably damaging	Het
Tie1	A	G	4: 118,329,831 (GRCm39)	Y1091H	probably benign	Het
Tlr12	T	C	4: 128,511,125 (GRCm39)	Y375C	probably benign	Het
Tmem107	T	A	11: 68,962,274 (GRCm39)	M77K	probably damaging	Het
Tns2	C	T	15: 102,017,369 (GRCm39)	R281C	probably damaging	Het
Tns3	T	C	11: 8,481,747 (GRCm39)	K202E	probably damaging	Het
Tspoap1	C	T	11: 87,670,347 (GRCm39)	P1634L	probably damaging	Het
Ttc7b	G	A	12: 100,466,376 (GRCm39)	R79C	probably damaging	Het
Ush2a	A	G	1: 188,643,844 (GRCm39)	N4402S	probably benign	Het
Vmn2r13	A	T	5: 109,304,322 (GRCm39)	I703N	probably damaging	Het
Xrcc4	A	G	13: 90,210,126 (GRCm39)		probably null	Het
Zp3	A	T	5: 136,013,089 (GRCm39)	K168*	probably null	Het

Other mutations in Ankrd13b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00929:Ankrd13b	APN	11	77,363,578 (GRCm39)	missense	probably damaging	1.00
IGL01396:Ankrd13b	APN	11	77,363,198 (GRCm39)	splice site	probably null
IGL02731:Ankrd13b	APN	11	77,367,045 (GRCm39)	missense	probably damaging	0.99
R0310:Ankrd13b	UTSW	11	77,363,571 (GRCm39)	missense	possibly damaging	0.71
R0496:Ankrd13b	UTSW	11	77,363,867 (GRCm39)	missense	probably damaging	1.00
R0511:Ankrd13b	UTSW	11	77,364,114 (GRCm39)	missense	possibly damaging	0.89
R0831:Ankrd13b	UTSW	11	77,363,585 (GRCm39)	missense	probably damaging	0.99
R1156:Ankrd13b	UTSW	11	77,363,687 (GRCm39)	missense	probably damaging	1.00
R1237:Ankrd13b	UTSW	11	77,365,400 (GRCm39)	missense	probably damaging	1.00
R2259:Ankrd13b	UTSW	11	77,367,168 (GRCm39)	missense	probably damaging	1.00
R3110:Ankrd13b	UTSW	11	77,368,331 (GRCm39)	missense	possibly damaging	0.67
R3112:Ankrd13b	UTSW	11	77,368,331 (GRCm39)	missense	possibly damaging	0.67
R4190:Ankrd13b	UTSW	11	77,367,201 (GRCm39)	missense	probably damaging	1.00
R4471:Ankrd13b	UTSW	11	77,367,040 (GRCm39)	missense	probably damaging	1.00
R5253:Ankrd13b	UTSW	11	77,364,061 (GRCm39)	intron	probably benign
R5677:Ankrd13b	UTSW	11	77,368,370 (GRCm39)	missense	probably damaging	0.99
R7073:Ankrd13b	UTSW	11	77,363,335 (GRCm39)	missense	probably benign	0.39
R7388:Ankrd13b	UTSW	11	77,363,583 (GRCm39)	missense	probably benign	0.02
R7417:Ankrd13b	UTSW	11	77,367,020 (GRCm39)	missense	probably damaging	0.97
R7592:Ankrd13b	UTSW	11	77,367,327 (GRCm39)	missense	probably benign	0.45
R7596:Ankrd13b	UTSW	11	77,363,140 (GRCm39)	missense	probably benign	0.18
R7643:Ankrd13b	UTSW	11	77,363,911 (GRCm39)	missense	probably benign	0.01
R8434:Ankrd13b	UTSW	11	77,368,552 (GRCm39)	missense	probably benign	0.01
R8959:Ankrd13b	UTSW	11	77,367,452 (GRCm39)	missense	probably damaging	1.00
R9668:Ankrd13b	UTSW	11	77,368,594 (GRCm39)	missense	possibly damaging	0.79

Predicted Primers

PCR Primer
(F):5'- CTGTATCAAACCCCTGGCATC -3'
(R):5'- TGGACCTTCAGACCCTCAAC -3'

Sequencing Primer
(F):5'- TGGCATCTCAAGCCTGATG -3'
(R):5'- ACCTGGGATCTGCCATCACTG -3'

Posted On

2015-09-25