Mutagenetix > Incidental Mutation

Incidental Mutation 'R0207:Ulk2'

33412

Institutional Source

Beutler Lab

Gene Symbol

Ulk2

Ensembl Gene

ENSMUSG00000004798

Gene Name

unc-51 like kinase 2

Synonyms

A830085I22Rik, Unc51.2

MMRRC Submission

038460-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.219) question?

Stock #

R0207 (G1)

Quality Score

130

Status

Validated

Chromosome

Chromosomal Location

61666475-61745899 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 61668611 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glutamic Acid at position 1037 (V1037E)

Ref Sequence

ENSEMBL: ENSMUSP00000004920 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000004920]

AlphaFold

Q9QY01

Predicted Effect

probably benign
Transcript: ENSMUST00000004920
AA Change: V1037E

PolyPhen 2 Score 0.424 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000004920
Gene: ENSMUSG00000004798
AA Change: V1037E

Domain	Start	End	E-Value	Type
S_TKc	9	271	1.1e-93	SMART
low complexity region	274	309	N/A	INTRINSIC
Blast:S_TKc	310	413	9e-28	BLAST
Blast:S_TKc	433	738	1e-29	BLAST
low complexity region	751	766	N/A	INTRINSIC
low complexity region	771	791	N/A	INTRINSIC
Pfam:DUF3543	821	1032	1.8e-31	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129025

Meta Mutation Damage Score

0.0937

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.2%
20x: 95.5%

Validation Efficiency

95% (76/80)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that is similar to a serine/threonine kinase in C. elegans which is involved in axonal elongation. The structure of this protein is similar to the C. elegans protein in that both proteins have an N-terminal kinase domain, a central proline/serine rich (PS) domain, and a C-terminal (C) domain. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Dec 2008]
PHENOTYPE: Homozygous mutation of this gene results in an increased anxiety-like response in males. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca1	A	G	4: 53,086,039 (GRCm39)	F488S	probably damaging	Het
Acap3	C	T	4: 155,983,881 (GRCm39)	R116W	probably damaging	Het
Adamts10	C	A	17: 33,764,364 (GRCm39)	P663T	possibly damaging	Het
Akap12	G	A	10: 4,303,333 (GRCm39)	G48S	probably damaging	Het
Ankrd7	T	A	6: 18,870,030 (GRCm39)	M261K	probably benign	Het
Ankzf1	C	A	1: 75,174,948 (GRCm39)	D599E	possibly damaging	Het
Aox1	T	C	1: 58,144,173 (GRCm39)	I1278T	possibly damaging	Het
Apcdd1	T	C	18: 63,083,150 (GRCm39)	Y327H	probably benign	Het
Asxl3	T	A	18: 22,544,553 (GRCm39)		probably benign	Het
Birc6	C	A	17: 74,969,827 (GRCm39)		probably benign	Het
Btaf1	T	A	19: 36,987,048 (GRCm39)	L1714*	probably null	Het
Cacng6	T	A	7: 3,473,520 (GRCm39)		probably benign	Het
Cdc20b	A	G	13: 113,215,146 (GRCm39)	D238G	probably damaging	Het
Celf5	T	A	10: 81,306,532 (GRCm39)	R113W	probably null	Het
Cfap251	T	C	5: 123,421,510 (GRCm39)	V182A	probably damaging	Het
Cfap70	C	A	14: 20,462,415 (GRCm39)	E659D	probably damaging	Het
Clspn	T	A	4: 126,484,391 (GRCm39)	M1183K	possibly damaging	Het
Dpy19l1	G	A	9: 24,365,187 (GRCm39)	R275C	probably damaging	Het
Dst	C	T	1: 34,226,016 (GRCm39)	S1721L	probably benign	Het
Faap100	T	C	11: 120,265,191 (GRCm39)	T562A	probably damaging	Het
Fam168b	T	C	1: 34,858,769 (GRCm39)	M133V	probably damaging	Het
Farp2	T	C	1: 93,496,809 (GRCm39)	I172T	probably damaging	Het
Fer	T	G	17: 64,203,273 (GRCm39)	S68A	probably damaging	Het
Fmo5	A	G	3: 97,552,997 (GRCm39)	E315G	probably damaging	Het
Gpr89	A	T	3: 96,778,796 (GRCm39)	F426I	probably damaging	Het
Hinfp	T	C	9: 44,207,624 (GRCm39)	I461V	possibly damaging	Het
Hsd11b1	A	T	1: 192,922,556 (GRCm39)	V167D	probably damaging	Het
Htt	A	G	5: 35,054,252 (GRCm39)	K2574E	probably benign	Het
I830077J02Rik	A	G	3: 105,833,821 (GRCm39)	S112P	probably benign	Het
Igf2bp3	T	A	6: 49,082,551 (GRCm39)	M344L	probably benign	Het
Itch	A	T	2: 155,044,177 (GRCm39)	Q494L	probably benign	Het
Itga9	T	C	9: 118,598,321 (GRCm39)		probably benign	Het
Jaml	T	A	9: 45,005,065 (GRCm39)	D152E	probably benign	Het
Kif22	A	C	7: 126,641,572 (GRCm39)	M1R	probably null	Het
Kifap3	T	C	1: 163,710,955 (GRCm39)	Y663H	probably benign	Het
Letm2	T	A	8: 26,068,786 (GRCm39)	N472I	probably damaging	Het
Mthfr	T	G	4: 148,136,681 (GRCm39)	V446G	probably damaging	Het
Myh11	T	C	16: 14,029,124 (GRCm39)	E1206G	possibly damaging	Het
Myo6	G	A	9: 80,195,338 (GRCm39)	V903I	probably damaging	Het
Myo9b	C	T	8: 71,807,869 (GRCm39)		probably benign	Het
Nr2f2	G	C	7: 70,009,923 (GRCm39)	P52R	probably damaging	Het
Nsd3	A	G	8: 26,173,273 (GRCm39)	N859S	probably benign	Het
Nucb2	C	A	7: 116,135,245 (GRCm39)	A384E	probably damaging	Het
Ogdhl	C	A	14: 32,063,994 (GRCm39)		probably null	Het
Or10al3	C	A	17: 38,011,949 (GRCm39)	C129*	probably null	Het
Or1e22	A	T	11: 73,377,401 (GRCm39)	L83Q	probably benign	Het
Or1i2	T	C	10: 78,447,705 (GRCm39)	T257A	probably benign	Het
Or4a74	G	A	2: 89,440,207 (GRCm39)	L80F	probably damaging	Het
Or5b105	G	A	19: 13,080,642 (GRCm39)	R3C	possibly damaging	Het
Parp10	C	T	15: 76,126,833 (GRCm39)	S145N	probably benign	Het
Pigh	A	G	12: 79,130,483 (GRCm39)		probably benign	Het
Pigo	A	G	4: 43,023,824 (GRCm39)		probably benign	Het
Pkp4	T	A	2: 59,135,832 (GRCm39)	V199D	possibly damaging	Het
Polr1e	C	A	4: 45,025,143 (GRCm39)		probably null	Het
Ppfia3	C	A	7: 44,997,958 (GRCm39)	R723L	probably damaging	Het
Prex1	C	A	2: 166,427,818 (GRCm39)	A945S	possibly damaging	Het
Prrt3	A	T	6: 113,472,801 (GRCm39)	V457E	probably damaging	Het
Rab39	A	G	9: 53,617,271 (GRCm39)	F49L	possibly damaging	Het
Rrs1	C	A	1: 9,615,987 (GRCm39)		probably null	Het
Rrs1	G	A	1: 9,615,992 (GRCm39)	E82K	probably damaging	Het
Serpinb3c	T	C	1: 107,204,722 (GRCm39)	D8G	probably benign	Het
Slc17a6	A	G	7: 51,295,928 (GRCm39)		probably benign	Het
Slc24a4	T	A	12: 102,195,210 (GRCm39)		probably null	Het
Smc1b	C	T	15: 85,007,960 (GRCm39)	M272I	probably benign	Het
Smc6	T	C	12: 11,333,179 (GRCm39)		probably benign	Het
Tcf20	T	C	15: 82,739,286 (GRCm39)	T722A	probably benign	Het
Tesmin	A	T	19: 3,454,088 (GRCm39)	M141L	probably benign	Het
Tmprss5	T	A	9: 49,024,460 (GRCm39)	H274Q	possibly damaging	Het
Tns1	C	T	1: 73,976,477 (GRCm39)		probably null	Het
Tpr	T	C	1: 150,293,178 (GRCm39)	S868P	possibly damaging	Het
Trank1	C	T	9: 111,195,321 (GRCm39)	T1115I	probably damaging	Het
Trmt44	A	T	5: 35,730,261 (GRCm39)	I203K	possibly damaging	Het
Usp43	A	G	11: 67,767,325 (GRCm39)	Y682H	probably damaging	Het
Vipr2	A	T	12: 116,106,502 (GRCm39)	Q366L	probably damaging	Het
Vmn1r185	C	A	7: 26,311,014 (GRCm39)	V164L	possibly damaging	Het
Vmn2r120	C	T	17: 57,832,052 (GRCm39)	V246I	probably benign	Het
Wiz	C	T	17: 32,576,007 (GRCm39)	G790R	probably damaging	Het
Wnk1	A	T	6: 119,929,694 (GRCm39)	S1016R	probably damaging	Het
Zc3hav1	A	G	6: 38,288,109 (GRCm39)	L909S	probably benign	Het
Zfp236	T	A	18: 82,658,352 (GRCm39)	I637F	probably damaging	Het
Zfp788	G	A	7: 41,299,020 (GRCm39)	G532D	probably damaging	Het
Zranb1	T	C	7: 132,552,114 (GRCm39)	I255T	probably damaging	Het

Other mutations in Ulk2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01599:Ulk2	APN	11	61,682,262 (GRCm39)	nonsense	probably null
IGL02044:Ulk2	APN	11	61,672,465 (GRCm39)	missense	probably damaging	1.00
IGL02185:Ulk2	APN	11	61,672,886 (GRCm39)	missense	probably damaging	1.00
IGL03036:Ulk2	APN	11	61,725,660 (GRCm39)	missense	probably damaging	1.00
BB007:Ulk2	UTSW	11	61,682,258 (GRCm39)	critical splice donor site	probably null
BB009:Ulk2	UTSW	11	61,698,916 (GRCm39)	missense	probably benign
BB017:Ulk2	UTSW	11	61,682,258 (GRCm39)	critical splice donor site	probably null
BB019:Ulk2	UTSW	11	61,698,916 (GRCm39)	missense	probably benign
R0362:Ulk2	UTSW	11	61,678,412 (GRCm39)	missense	probably benign
R0657:Ulk2	UTSW	11	61,698,880 (GRCm39)	splice site	probably benign
R1076:Ulk2	UTSW	11	61,710,135 (GRCm39)	missense	probably damaging	1.00
R1144:Ulk2	UTSW	11	61,690,886 (GRCm39)	missense	possibly damaging	0.80
R1573:Ulk2	UTSW	11	61,670,581 (GRCm39)	missense	probably damaging	1.00
R1583:Ulk2	UTSW	11	61,674,371 (GRCm39)	missense	possibly damaging	0.95
R1619:Ulk2	UTSW	11	61,672,572 (GRCm39)	missense	probably damaging	1.00
R1757:Ulk2	UTSW	11	61,732,165 (GRCm39)	splice site	probably benign
R1845:Ulk2	UTSW	11	61,703,564 (GRCm39)	missense	probably benign	0.04
R1883:Ulk2	UTSW	11	61,721,438 (GRCm39)	missense	probably damaging	1.00
R1966:Ulk2	UTSW	11	61,710,297 (GRCm39)	splice site	probably null
R2177:Ulk2	UTSW	11	61,682,335 (GRCm39)	missense	probably benign	0.01
R2416:Ulk2	UTSW	11	61,672,865 (GRCm39)	missense	probably damaging	1.00
R2509:Ulk2	UTSW	11	61,678,340 (GRCm39)	missense	probably benign	0.00
R2847:Ulk2	UTSW	11	61,715,555 (GRCm39)	critical splice acceptor site	probably null
R4736:Ulk2	UTSW	11	61,724,261 (GRCm39)	missense	probably damaging	1.00
R4997:Ulk2	UTSW	11	61,689,982 (GRCm39)	missense	probably benign	0.00
R5081:Ulk2	UTSW	11	61,694,488 (GRCm39)	missense	probably damaging	1.00
R5190:Ulk2	UTSW	11	61,672,537 (GRCm39)	missense	probably benign
R5346:Ulk2	UTSW	11	61,725,740 (GRCm39)	missense	probably damaging	1.00
R5348:Ulk2	UTSW	11	61,674,439 (GRCm39)	missense	probably benign
R5520:Ulk2	UTSW	11	61,698,970 (GRCm39)	missense	probably damaging	1.00
R5954:Ulk2	UTSW	11	61,694,622 (GRCm39)	splice site	probably benign
R6153:Ulk2	UTSW	11	61,672,572 (GRCm39)	missense	probably damaging	1.00
R6223:Ulk2	UTSW	11	61,678,330 (GRCm39)	nonsense	probably null
R7204:Ulk2	UTSW	11	61,674,457 (GRCm39)	missense	probably benign	0.11
R7205:Ulk2	UTSW	11	61,725,657 (GRCm39)	missense	possibly damaging	0.84
R7259:Ulk2	UTSW	11	61,672,909 (GRCm39)	missense	probably damaging	1.00
R7353:Ulk2	UTSW	11	61,710,174 (GRCm39)	missense	probably damaging	1.00
R7734:Ulk2	UTSW	11	61,744,127 (GRCm39)	nonsense	probably null
R7797:Ulk2	UTSW	11	61,672,928 (GRCm39)	missense	probably benign	0.06
R7808:Ulk2	UTSW	11	61,745,378 (GRCm39)	missense	probably damaging	1.00
R7930:Ulk2	UTSW	11	61,682,258 (GRCm39)	critical splice donor site	probably null
R7932:Ulk2	UTSW	11	61,698,916 (GRCm39)	missense	probably benign
R8882:Ulk2	UTSW	11	61,698,887 (GRCm39)	critical splice donor site	probably null
R8909:Ulk2	UTSW	11	61,690,380 (GRCm39)	missense	probably benign
R9704:Ulk2	UTSW	11	61,716,694 (GRCm39)	missense	probably damaging	1.00
X0028:Ulk2	UTSW	11	61,690,394 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- CAGAGAGCTGAATGAAGCCACTCAC -3'
(R):5'- CCACTACAGCATTAAGCTCCTGGTC -3'

Sequencing Primer
(F):5'- TGACTTCTCCAATAAGGCAGG -3'
(R):5'- AAGCTCCTGGTCATATCTGAACTG -3'

Posted On

2013-05-09