Mutagenetix > Incidental Mutation

Incidental Mutation 'R7195:Hnrnpul1'

559855

Institutional Source

Beutler Lab

Gene Symbol

Hnrnpul1

Ensembl Gene

ENSMUSG00000040725

Gene Name

heterogeneous nuclear ribonucleoprotein U-like 1

Synonyms

E130317O14Rik, Hnrpul1, Hnrnpul, E1B-AP5, E1BAP5

MMRRC Submission

045336-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.621) question?

Stock #

R7195 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

25420590-25454182 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 25424203 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 683 (N683S)

Ref Sequence

ENSEMBL: ENSMUSP00000146263 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000043765] [ENSMUST00000206832]

AlphaFold

Q8VDM6

Predicted Effect

unknown
Transcript: ENSMUST00000043765
AA Change: N583S

SMART Domains

Protein: ENSMUSP00000037268
Gene: ENSMUSG00000040725
AA Change: N583S

Domain	Start	End	E-Value	Type
SAP	3	37	2.86e-10	SMART
low complexity region	62	74	N/A	INTRINSIC
low complexity region	78	91	N/A	INTRINSIC
low complexity region	201	209	N/A	INTRINSIC
SPRY	255	388	8.49e-41	SMART
Pfam:AAA_33	424	569	1.4e-29	PFAM
low complexity region	613	626	N/A	INTRINSIC
low complexity region	631	693	N/A	INTRINSIC
low complexity region	695	718	N/A	INTRINSIC
low complexity region	745	765	N/A	INTRINSIC
low complexity region	768	859	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000206832
AA Change: N683S

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.8%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a nuclear RNA-binding protein of the heterogeneous nuclear ribonucleoprotein (hnRNP) family. This protein binds specifically to adenovirus early-1B-55kDa oncoprotein. It may play an important role in nucleocytoplasmic RNA transport, and its function is modulated by early-1B-55kDa in adenovirus-infected cells. [provided by RefSeq, Mar 2016]

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930438A08Rik	T	C	11: 58,179,242 (GRCm39)		probably null	Het
Abca2	A	G	2: 25,332,088 (GRCm39)	D1400G	probably benign	Het
Actl11	A	T	9: 107,806,069 (GRCm39)	K131*	probably null	Het
Adam39	A	T	8: 41,277,812 (GRCm39)	R68*	probably null	Het
Akap7	A	T	10: 25,147,405 (GRCm39)	N108K	probably damaging	Het
Arhgef10l	C	A	4: 140,338,721 (GRCm39)	A14S	probably benign	Het
Ccdc141	T	G	2: 76,879,927 (GRCm39)	N632T	probably benign	Het
Ccm2	T	C	11: 6,546,302 (GRCm39)	S435P	probably damaging	Het
Cd36	A	G	5: 18,019,187 (GRCm39)	L178P	probably damaging	Het
Cd7	T	C	11: 120,929,075 (GRCm39)	I59V	probably benign	Het
Cds2	T	A	2: 132,135,204 (GRCm39)	S32T	probably benign	Het
Cep19	A	G	16: 31,925,904 (GRCm39)	D104G	probably damaging	Het
Col1a2	C	T	6: 4,510,753 (GRCm39)	P68S	unknown	Het
Col20a1	A	G	2: 180,649,024 (GRCm39)	H1011R	probably damaging	Het
Cspg4b	A	T	13: 113,504,463 (GRCm39)	D1864V		Het
D7Ertd443e	A	G	7: 133,896,851 (GRCm39)	V513A	probably damaging	Het
Egfr	C	T	11: 16,818,162 (GRCm39)	P228L	probably damaging	Het
Fam243	C	T	16: 92,118,037 (GRCm39)	V84M	probably damaging	Het
Fam78b	A	G	1: 166,906,131 (GRCm39)	R97G	probably damaging	Het
Flt1	C	T	5: 147,540,386 (GRCm39)	V768M	probably damaging	Het
Gdap1l1	A	T	2: 163,288,050 (GRCm39)	N96Y	probably damaging	Het
Gm7168	T	A	17: 14,169,622 (GRCm39)	Y330N	probably benign	Het
Ice2	C	T	9: 69,335,782 (GRCm39)	P922S	possibly damaging	Het
Iglv2	A	G	16: 19,079,260 (GRCm39)	V81A	not run	Het
Irs1	A	G	1: 82,265,177 (GRCm39)	I1013T	probably benign	Het
Itih4	T	C	14: 30,621,432 (GRCm39)	S832P	probably damaging	Het
Klhl1	A	T	14: 96,517,513 (GRCm39)	Y388N	probably benign	Het
Lrrc37a	G	A	11: 103,348,601 (GRCm39)	S2698L	unknown	Het
Map4k4	T	C	1: 40,058,829 (GRCm39)	Y1008H	possibly damaging	Het
Mdn1	G	T	4: 32,701,823 (GRCm39)	G1519W	probably damaging	Het
Mga	T	A	2: 119,747,809 (GRCm39)	D653E	probably damaging	Het
Npas1	T	C	7: 16,208,733 (GRCm39)	E48G	probably damaging	Het
Nup188	G	A	2: 30,231,842 (GRCm39)		probably null	Het
Or1p1b	G	T	11: 74,130,394 (GRCm39)	M1I	probably null	Het
Or3a4	T	A	11: 73,945,223 (GRCm39)	M121L	probably damaging	Het
Or4c110	G	A	2: 88,832,075 (GRCm39)	L186F		Het
Or51a39	A	G	7: 102,362,873 (GRCm39)	V249A	possibly damaging	Het
Or55b4	A	T	7: 102,133,574 (GRCm39)	V251D	probably damaging	Het
Or7h8	A	G	9: 20,123,840 (GRCm39)	N65S	probably damaging	Het
Oxct1	T	C	15: 4,158,383 (GRCm39)	V439A	probably damaging	Het
Pcdhb22	G	T	18: 37,652,341 (GRCm39)	G13W	probably damaging	Het
Pex11g	A	G	8: 3,509,237 (GRCm39)	V230A	probably benign	Het
Pop1	C	T	15: 34,510,525 (GRCm39)	S439L	probably damaging	Het
Ptpn9	T	A	9: 56,929,533 (GRCm39)	H83Q	probably benign	Het
Qrfp	C	T	2: 31,698,704 (GRCm39)	R76H	probably benign	Het
Slc30a3	A	G	5: 31,246,139 (GRCm39)	V197A	probably benign	Het
Slc8a3	T	C	12: 81,361,047 (GRCm39)	N591D	possibly damaging	Het
Sp4	G	T	12: 118,263,807 (GRCm39)	Q80K	possibly damaging	Het
Spock1	C	T	13: 58,055,316 (GRCm39)	G29D	possibly damaging	Het
Sprr1a	G	T	3: 92,391,674 (GRCm39)	P109Q	probably damaging	Het
Suz12	T	A	11: 79,904,309 (GRCm39)	F239L	probably damaging	Het
Tbx3	A	G	5: 119,813,648 (GRCm39)	Y248C	probably damaging	Het
Trabd2b	T	C	4: 114,266,637 (GRCm39)	L217P	probably damaging	Het
Ubxn11	A	C	4: 133,853,726 (GRCm39)	I398L	possibly damaging	Het
Vmn1r173	T	A	7: 23,401,884 (GRCm39)	S40T	probably damaging	Het
Vmn2r2	T	C	3: 64,023,900 (GRCm39)	S894G	probably benign	Het
Vmn2r65	A	G	7: 84,592,347 (GRCm39)		probably null	Het
Vps13c	G	A	9: 67,853,107 (GRCm39)	G2400D	possibly damaging	Het
Vps8	T	C	16: 21,275,032 (GRCm39)	Y197H	probably damaging	Het
Wdr91	T	C	6: 34,866,209 (GRCm39)	N486D	possibly damaging	Het
Wwp1	A	G	4: 19,627,908 (GRCm39)	I695T	possibly damaging	Het
Zc3hc1	T	C	6: 30,382,547 (GRCm39)	D133G	probably benign	Het
Zcchc14	T	C	8: 122,335,200 (GRCm39)	I307V	unknown	Het
Zfp933	G	A	4: 147,910,636 (GRCm39)	T320I	probably benign	Het

Other mutations in Hnrnpul1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00095:Hnrnpul1	APN	7	25,425,579 (GRCm39)	missense	possibly damaging	0.74
IGL01287:Hnrnpul1	APN	7	25,426,323 (GRCm39)	missense	probably damaging	1.00
IGL01409:Hnrnpul1	APN	7	25,424,077 (GRCm39)	missense	unknown
IGL02026:Hnrnpul1	APN	7	25,444,587 (GRCm39)	missense	probably damaging	0.99
IGL02073:Hnrnpul1	APN	7	25,421,766 (GRCm39)	unclassified	probably benign
IGL02474:Hnrnpul1	APN	7	25,426,182 (GRCm39)	missense	probably benign	0.02
IGL02839:Hnrnpul1	APN	7	25,432,667 (GRCm39)	critical splice donor site	probably null
IGL02894:Hnrnpul1	APN	7	25,450,329 (GRCm39)	missense	possibly damaging	0.70
IGL03382:Hnrnpul1	APN	7	25,450,409 (GRCm39)	start codon destroyed	probably null	0.53
R0011:Hnrnpul1	UTSW	7	25,442,340 (GRCm39)	splice site	probably benign
R0525:Hnrnpul1	UTSW	7	25,440,308 (GRCm39)	missense	possibly damaging	0.72
R0587:Hnrnpul1	UTSW	7	25,444,657 (GRCm39)	missense	possibly damaging	0.70
R1121:Hnrnpul1	UTSW	7	25,440,332 (GRCm39)	missense	possibly damaging	0.68
R1313:Hnrnpul1	UTSW	7	25,422,341 (GRCm39)	unclassified	probably benign
R1313:Hnrnpul1	UTSW	7	25,422,341 (GRCm39)	unclassified	probably benign
R1880:Hnrnpul1	UTSW	7	25,432,523 (GRCm39)	missense	possibly damaging	0.95
R1892:Hnrnpul1	UTSW	7	25,426,191 (GRCm39)	missense	probably benign	0.11
R2113:Hnrnpul1	UTSW	7	25,432,694 (GRCm39)	missense	possibly damaging	0.47
R2194:Hnrnpul1	UTSW	7	25,425,347 (GRCm39)	critical splice donor site	probably null
R2269:Hnrnpul1	UTSW	7	25,450,299 (GRCm39)	missense	probably damaging	0.98
R2679:Hnrnpul1	UTSW	7	25,426,300 (GRCm39)	missense	probably damaging	1.00
R3079:Hnrnpul1	UTSW	7	25,432,540 (GRCm39)	nonsense	probably null
R3917:Hnrnpul1	UTSW	7	25,426,300 (GRCm39)	missense	probably damaging	1.00
R4077:Hnrnpul1	UTSW	7	25,426,300 (GRCm39)	missense	probably damaging	1.00
R4079:Hnrnpul1	UTSW	7	25,426,300 (GRCm39)	missense	probably damaging	1.00
R4181:Hnrnpul1	UTSW	7	25,426,237 (GRCm39)	missense	probably damaging	0.98
R4449:Hnrnpul1	UTSW	7	25,421,709 (GRCm39)	unclassified	probably benign
R4707:Hnrnpul1	UTSW	7	25,426,258 (GRCm39)	missense	probably damaging	1.00
R4764:Hnrnpul1	UTSW	7	25,442,436 (GRCm39)	missense	probably benign	0.00
R5040:Hnrnpul1	UTSW	7	25,442,414 (GRCm39)	missense	possibly damaging	0.86
R5131:Hnrnpul1	UTSW	7	25,426,219 (GRCm39)	missense	probably benign	0.08
R5224:Hnrnpul1	UTSW	7	25,444,600 (GRCm39)	missense	probably damaging	0.98
R5599:Hnrnpul1	UTSW	7	25,454,097 (GRCm39)	start gained	probably benign
R5975:Hnrnpul1	UTSW	7	25,453,784 (GRCm39)	missense	possibly damaging	0.93
R7032:Hnrnpul1	UTSW	7	25,450,319 (GRCm39)	missense	probably benign	0.11
R7231:Hnrnpul1	UTSW	7	25,447,842 (GRCm39)	nonsense	probably null
R7667:Hnrnpul1	UTSW	7	25,453,846 (GRCm39)	missense	probably damaging	0.99
R8017:Hnrnpul1	UTSW	7	25,447,889 (GRCm39)	missense	probably benign	0.03
R8060:Hnrnpul1	UTSW	7	25,447,768 (GRCm39)	missense	possibly damaging	0.54
R8319:Hnrnpul1	UTSW	7	25,453,902 (GRCm39)	missense	probably benign
R8356:Hnrnpul1	UTSW	7	25,422,247 (GRCm39)	unclassified	probably benign
Z1176:Hnrnpul1	UTSW	7	25,424,123 (GRCm39)	missense	unknown
Z1176:Hnrnpul1	UTSW	7	25,424,089 (GRCm39)	missense	probably benign	0.23

Predicted Primers

PCR Primer
(F):5'- TGTAGCTGCTCACTGTAGGG -3'
(R):5'- TGTTGTGTCAGGGCAAGAAC -3'

Sequencing Primer
(F):5'- CTGCTCACTGTAGGGGTGCTG -3'
(R):5'- GAAGTGTGCTGAGGGCC -3'

Posted On

2019-06-26