Mutagenetix > Incidental Mutation

Incidental Mutation 'R7256:Hoxb4'

574568

Institutional Source

Beutler Lab

Gene Symbol

Hoxb4

Ensembl Gene

ENSMUSG00000038692

Gene Name

homeobox B4

Synonyms

Hox-2.6

MMRRC Submission

Accession Numbers

Essential gene?

Probably essential (E-score: 0.904) question?

Stock #

R7256 (G1)

Quality Score

142.008

Status

Not validated

Chromosome

Chromosomal Location

96318267-96321638 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

C to A at 96319896 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000048002 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000049241] [ENSMUST00000093944]

AlphaFold

P10284

Predicted Effect

probably null
Transcript: ENSMUST00000049241

SMART Domains

Protein: ENSMUSP00000048002
Gene: ENSMUSG00000038692

Domain	Start	End	E-Value	Type
low complexity region	71	87	N/A	INTRINSIC
low complexity region	113	120	N/A	INTRINSIC
HOX	161	223	2.83e-26	SMART
low complexity region	230	249	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000093944

SMART Domains

Protein: ENSMUSP00000091476
Gene: ENSMUSG00000048763

Domain	Start	End	E-Value	Type
low complexity region	76	121	N/A	INTRINSIC
low complexity region	154	181	N/A	INTRINSIC
HOX	191	253	5.44e-28	SMART
low complexity region	256	274	N/A	INTRINSIC
Pfam:DUF4074	368	431	1.9e-37	PFAM

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.0%

Validation Efficiency

99% (70/71)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in development. Intracellular or ectopic expression of this protein expands hematopoietic stem and progenitor cells in vivo and in vitro, making it a potential candidate for therapeutic stem cell expansion. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous disruption of this gene causes cervical vertebral transformation and may lead to pre- or neonatal lethality, sternal defects, impaired ventral body wall formation, diaphragm hernias and heart anomalies. Homozygotes for a null allele show a proliferation defect in hematopoietic stem cells. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts5	A	G	16: 85,863,035	Y790H	probably damaging	Het
Bend3	A	C	10: 43,493,671	S7R	probably benign	Het
Ccdc106	A	G	7: 5,060,326	T277A	probably damaging	Het
Ccdc162	G	A	10: 41,556,001	A1832V	probably damaging	Het
Ccser1	A	G	6: 61,311,867	E338G	probably benign	Het
Cd86	CA	CAA	16: 36,606,555		probably null	Het
Cecr2	T	C	6: 120,762,529	S1406P	probably benign	Het
Cep290	A	G	10: 100,546,498	T208A	probably damaging	Het
Cep85l	A	C	10: 53,296,255	C569W	probably damaging	Het
Ces5a	G	A	8: 93,499,526	T527I	probably benign	Het
Clca2	T	A	3: 145,090,847	I200F	probably damaging	Het
Cmas	G	A	6: 142,770,586	D251N	probably damaging	Het
Ctcfl	G	T	2: 173,118,475	A105E	probably benign	Het
Dclk2	C	T	3: 86,793,259	R638H	probably damaging	Het
Dctn6	A	T	8: 34,090,808	I170N	probably damaging	Het
Dnah2	T	C	11: 69,431,094	Y3800C	probably damaging	Het
Dsg2	G	A	18: 20,591,931	V465I	possibly damaging	Het
Dzip1	T	C	14: 118,885,646	T646A	probably benign	Het
Etv4	T	A	11: 101,784,325		probably null	Het
Exoc3l2	T	C	7: 19,484,703	V549A	unknown	Het
Ficd	G	T	5: 113,738,819	A352S	probably damaging	Het
Fry	T	G	5: 150,466,786	I179S		Het
Galntl5	A	G	5: 25,195,300	H109R	probably benign	Het
Garem1	C	A	18: 21,148,754	G182W	probably damaging	Het
Gm10696	T	C	3: 94,176,360	E48G	probably benign	Het
Gm13078	T	A	4: 143,726,279	D93E	probably benign	Het
Gm5916	A	T	9: 36,120,989	Y50N	possibly damaging	Het
Gtf2h2	A	T	13: 100,479,201	F271I	probably benign	Het
Hivep2	G	T	10: 14,129,101	S481I	probably benign	Het
Homez	T	A	14: 54,857,420	Q277L	probably damaging	Het
Igll1	A	G	16: 16,861,093	S118P	probably damaging	Het
Ikzf2	A	C	1: 69,578,053		probably null	Het
Kif5b	A	G	18: 6,225,340	V230A	probably damaging	Het
Ldlr	T	A	9: 21,745,744	V719E	probably benign	Het
Lsm7	G	A	10: 80,853,731	R66W	possibly damaging	Het
Map3k13	T	A	16: 21,892,238	D90E	probably benign	Het
Mmrn1	A	G	6: 60,976,114	K460E	probably damaging	Het
Myh10	A	C	11: 68,790,689	N1061H	probably damaging	Het
Nepn	A	G	10: 52,400,993	Q275R	probably benign	Het
Noc3l	A	T	19: 38,812,356	D227E	probably benign	Het
Nploc4	G	T	11: 120,428,550	S61R	probably benign	Het
Nr4a2	T	C	2: 57,112,369	Y24C	probably damaging	Het
Nup160	T	A	2: 90,723,355	I1143N	probably damaging	Het
Olfr1097	A	G	2: 86,890,612	S188P	probably damaging	Het
Olfr1234	A	T	2: 89,362,494	Y312N	probably benign	Het
Olfr294	G	T	7: 86,615,665	H327N	probably benign	Het
Olfr895	T	A	9: 38,268,708	M57K	probably damaging	Het
Papola	T	A	12: 105,809,345	C204S	probably damaging	Het
Peg10	CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG	CCACATCAGGATCCACATCAGGATGCACATCAG	6: 4,756,398		probably benign	Het
Pgap1	A	T	1: 54,493,207		probably null	Het
Pitrm1	A	G	13: 6,556,597	H229R	probably damaging	Het
Plcl1	A	G	1: 55,698,218	Q906R	probably benign	Het
Ppfia3	T	C	7: 45,341,743	N1018S	probably benign	Het
Prkd1	A	G	12: 50,388,342	V534A	possibly damaging	Het
Pygm	A	T	19: 6,385,896	I126F	probably benign	Het
Rag1	T	C	2: 101,642,070	Y909C	probably damaging	Het
Rasgrf2	G	A	13: 91,884,518	Q560*	probably null	Het
Rbp3	A	T	14: 33,962,583	I1190F	possibly damaging	Het
Reln	T	C	5: 21,978,923	K1693E	probably benign	Het
Rgl2	T	C	17: 33,934,990	F457L	possibly damaging	Het
Rsph3a	A	G	17: 7,946,170	T121A	probably benign	Het
Rufy3	A	G	5: 88,614,947	N112S	possibly damaging	Het
Ryr3	G	A	2: 112,672,246	Q3548*	probably null	Het
Sardh	A	T	2: 27,218,812	V637D	probably benign	Het
Spata16	T	C	3: 26,667,867	V179A	probably benign	Het
Tbc1d30	G	A	10: 121,288,965	T319I	probably damaging	Het
Tlr2	T	A	3: 83,837,606	Q390L	possibly damaging	Het
Tmem53	C	T	4: 117,252,040		probably null	Het
Vmn1r113	T	A	7: 20,787,445	I54N	probably damaging	Het
Vmn1r223	A	C	13: 23,249,866	Y210S	probably damaging	Het
Zbbx	A	T	3: 75,039,898	H670Q	probably benign	Het

Other mutations in Hoxb4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01634:Hoxb4	APN	11	96318900	missense	probably damaging	1.00
IGL02642:Hoxb4	APN	11	96320224	missense	probably damaging	1.00
R0586:Hoxb4	UTSW	11	96318887	missense	probably damaging	0.99
R1548:Hoxb4	UTSW	11	96318899	nonsense	probably null
R1634:Hoxb4	UTSW	11	96320273	unclassified	probably benign
R1932:Hoxb4	UTSW	11	96320041	missense	probably damaging	1.00
R4571:Hoxb4	UTSW	11	96319166	missense	possibly damaging	0.95
R4879:Hoxb4	UTSW	11	96320188	missense	probably damaging	1.00
R4930:Hoxb4	UTSW	11	96318836	missense	probably damaging	1.00
R5502:Hoxb4	UTSW	11	96320231	missense	probably damaging	1.00
R6082:Hoxb4	UTSW	11	96318533	unclassified	probably benign
R6375:Hoxb4	UTSW	11	96320327	makesense	probably null
R6823:Hoxb4	UTSW	11	96318654	unclassified	probably benign
R7217:Hoxb4	UTSW	11	96319080	missense	probably benign	0.02

Predicted Primers

PCR Primer
(F):5'- GAAAGGTCTAGGGCAACACC -3'
(R):5'- TGTAGTGAAACTCCTTCTCCAACTC -3'

Sequencing Primer
(F):5'- GGCAACACCCCCTCCCAC -3'
(R):5'- TCCAACTCCAGGACCTGCTG -3'

Posted On

2019-09-18