Mutagenetix > Incidental Mutation

Incidental Mutation 'R7057:Htt'

547974

Institutional Source

Beutler Lab

Gene Symbol

Htt

Ensembl Gene

ENSMUSG00000029104

Gene Name

huntingtin

Synonyms

HD, Hdh, htt, huntingtin, IT15

MMRRC Submission

045154-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7057 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

34761740-34912534 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 34821723 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Glycine at position 817 (S817G)

Ref Sequence

ENSEMBL: ENSMUSP00000078945 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080036]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000080036
AA Change: S817G

PolyPhen 2 Score 0.055 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000078945
Gene: ENSMUSG00000029104
AA Change: S817G

Domain	Start	End	E-Value	Type
low complexity region	18	65	N/A	INTRINSIC
SCOP:d1qgra_	92	370	1e-12	SMART
low complexity region	371	388	N/A	INTRINSIC
low complexity region	432	453	N/A	INTRINSIC
low complexity region	1150	1161	N/A	INTRINSIC
low complexity region	1423	1441	N/A	INTRINSIC
Pfam:DUF3652	1494	1534	9.3e-20	PFAM
low complexity region	1812	1822	N/A	INTRINSIC
Blast:GAF	1866	2040	1e-104	BLAST
low complexity region	2461	2472	N/A	INTRINSIC
low complexity region	2611	2621	N/A	INTRINSIC
low complexity region	2622	2635	N/A	INTRINSIC
low complexity region	2857	2872	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Huntingtin is a disease gene linked to Huntington's disease, a neurodegenerative disorder characterized by loss of striatal neurons. This is thought to be caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, which translates as a polyglutamine repeat in the protein product. A fairly broad range of trinucleotide repeats (9-35) has been identified in normal controls, and repeat numbers in excess of 40 have been described as pathological. The huntingtin locus is large, spanning 180 kb and consisting of 67 exons. The huntingtin gene is widely expressed and is required for normal development. It is expressed as 2 alternatively polyadenylated forms displaying different relative abundance in various fetal and adult tissues. The larger transcript is approximately 13.7 kb and is expressed predominantly in adult and fetal brain whereas the smaller transcript of approximately 10.3 kb is more widely expressed. The genetic defect leading to Huntington's disease may not necessarily eliminate transcription, but may confer a new property on the mRNA or alter the function of the protein. One candidate is the huntingtin-associated protein-1, highly expressed in brain, which has increased affinity for huntingtin protein with expanded polyglutamine repeats. This gene contains an upstream open reading frame in the 5' UTR that inhibits expression of the huntingtin gene product through translational repression. [provided by RefSeq, Jul 2016]
PHENOTYPE: Null mutants gastrulate abnormally and die in utero. Conditional mutants are small with progressive neurodegeneration. Knock-ins of 20-150 CAG repeat units variably mimic Huntington's with late-onset motor defects, reactive gliosis and neuronal inclusions. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1810009J06Rik	T	A	6: 40,968,247 (GRCm38)	V220D	probably benign	Het
Ankrd1	T	C	19: 36,118,233 (GRCm38)	E113G	possibly damaging	Het
Aqp12	T	C	1: 93,011,996 (GRCm38)	L249P	probably damaging	Het
Atg4a-ps	A	G	3: 103,645,980 (GRCm38)	F15S	possibly damaging	Het
Bub1	T	A	2: 127,829,527 (GRCm38)	M46L	probably benign	Het
C1ra	G	A	6: 124,517,725 (GRCm38)	E316K	probably benign	Het
C2cd4d	A	G	3: 94,363,493 (GRCm38)	H22R	probably benign	Het
Ccdc157	A	G	11: 4,144,586 (GRCm38)	V480A	probably benign	Het
Cdc42ep3	G	A	17: 79,335,523 (GRCm38)		probably benign	Het
Cela1	T	A	15: 100,682,893 (GRCm38)	T161S	possibly damaging	Het
Chtf18	G	T	17: 25,721,126 (GRCm38)	A697E	possibly damaging	Het
Cr2	T	C	1: 195,151,610 (GRCm38)	D957G	possibly damaging	Het
Cyp2c40	A	G	19: 39,807,619 (GRCm38)	V60A	probably damaging	Het
Dazl	CCATGATGGCGGC	CC	17: 50,293,406 (GRCm38)		probably null	Het
Dock2	T	C	11: 34,695,217 (GRCm38)	Y546C	probably benign	Het
Dock2	A	T	11: 34,227,684 (GRCm38)	L1824Q	probably benign	Het
Fam208a	A	T	14: 27,461,651 (GRCm38)	N689I	probably damaging	Het
Focad	G	A	4: 88,274,105 (GRCm38)	C557Y	unknown	Het
Ftmt	T	A	18: 52,332,108 (GRCm38)	N165K	probably benign	Het
Gen1	A	C	12: 11,242,418 (GRCm38)	S457A	probably benign	Het
Gja1	T	G	10: 56,388,033 (GRCm38)	S163A	probably benign	Het
Gm8267	T	C	14: 44,722,024 (GRCm38)	I194M	probably damaging	Het
Golga3	T	A	5: 110,188,663 (GRCm38)	S389R	probably damaging	Het
Gpc5	C	A	14: 115,133,242 (GRCm38)	Q87K	possibly damaging	Het
Hmcn2	G	A	2: 31,422,649 (GRCm38)	A3420T	probably damaging	Het
Hus1b	C	T	13: 30,947,550 (GRCm38)	C42Y	possibly damaging	Het
Iars2	A	G	1: 185,289,367 (GRCm38)	F913L	probably benign	Het
Kcna4	A	G	2: 107,295,320 (GRCm38)	E133G	probably damaging	Het
Klhl36	T	C	8: 119,876,797 (GRCm38)	L597P	probably benign	Het
Ltv1	T	C	10: 13,180,902 (GRCm38)	E299G	possibly damaging	Het
Mmp12	A	G	9: 7,357,840 (GRCm38)	Y348C	probably damaging	Het
Mmp12	G	A	9: 7,369,173 (GRCm38)	V270I	probably benign	Het
Mmp2	A	G	8: 92,831,705 (GRCm38)	D134G	probably damaging	Het
Mrpl15	A	T	1: 4,776,642 (GRCm38)	M237K	probably benign	Het
Ms4a6b	G	T	19: 11,526,889 (GRCm38)	V177F	possibly damaging	Het
Muc16	A	G	9: 18,646,079 (GRCm38)	S2973P	unknown	Het
Olfr1219	A	C	2: 89,074,464 (GRCm38)	I209S	possibly damaging	Het
Olfr1445	A	T	19: 12,884,642 (GRCm38)	I254F	probably damaging	Het
Olfr1477	G	T	19: 13,502,879 (GRCm38)	D179Y	probably damaging	Het
Olfr390	A	C	11: 73,787,148 (GRCm38)	D70A	possibly damaging	Het
Olfr912	A	T	9: 38,581,754 (GRCm38)	H159L	probably damaging	Het
Pikfyve	T	A	1: 65,247,205 (GRCm38)	I1201K	probably benign	Het
Plekhn1	T	G	4: 156,233,917 (GRCm38)	M83L	probably damaging	Het
Pnlip	G	T	19: 58,676,263 (GRCm38)	D212Y	probably damaging	Het
Pomt2	T	C	12: 87,127,378 (GRCm38)	N417S	probably damaging	Het
Pxylp1	T	A	9: 96,825,050 (GRCm38)	M360L	probably benign	Het
Rbak	G	A	5: 143,173,927 (GRCm38)	T457I	possibly damaging	Het
Runx2	A	T	17: 44,814,537 (GRCm38)	W31R	probably null	Het
Sec16a	T	A	2: 26,425,265 (GRCm38)	I1795F	probably damaging	Het
Sik2	A	T	9: 50,998,561 (GRCm38)	I64N	probably damaging	Het
Slc26a8	T	C	17: 28,638,397 (GRCm38)	E924G	possibly damaging	Het
Slc30a2	G	A	4: 134,347,415 (GRCm38)	R161Q	probably damaging	Het
Slc45a4	C	A	15: 73,587,638 (GRCm38)	D174Y	probably damaging	Het
Slc6a6	A	C	6: 91,741,267 (GRCm38)	E354A	probably damaging	Het
Slc8a1	A	T	17: 81,649,095 (GRCm38)	S171R	probably damaging	Het
Srgap1	T	C	10: 121,804,953 (GRCm38)	I669M	probably benign	Het
Stk39	C	A	2: 68,410,127 (GRCm38)	A87S	possibly damaging	Het
Tbx18	C	A	9: 87,705,264 (GRCm38)	S600I	possibly damaging	Het
Tesc	A	C	5: 118,054,960 (GRCm38)	K114Q	probably damaging	Het
Tll1	T	C	8: 64,101,881 (GRCm38)	D256G	probably damaging	Het
Tmem35b	T	A	4: 127,127,886 (GRCm38)	I45K	probably benign	Het
Tnks	T	C	8: 34,840,014 (GRCm38)	D1127G	probably damaging	Het
Trpm8	A	T	1: 88,362,080 (GRCm38)	D920V	probably null	Het
U2af1	A	T	17: 31,648,857 (GRCm38)	D79E	probably benign	Het
Zfp704	T	C	3: 9,470,917 (GRCm38)	D331G	probably damaging	Het
Znrf3	G	T	11: 5,282,442 (GRCm38)	P261Q	probably benign	Het
Zscan4b	A	T	7: 10,901,709 (GRCm38)	C202*	probably null	Het

Other mutations in Htt

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00230:Htt	APN	5	34,799,408 (GRCm38)	missense	probably benign	0.00
IGL00233:Htt	APN	5	34,896,026 (GRCm38)	splice site	probably null
IGL00559:Htt	APN	5	34,849,104 (GRCm38)	splice site	probably benign
IGL00765:Htt	APN	5	34,877,425 (GRCm38)	splice site	probably benign
IGL00950:Htt	APN	5	34,891,441 (GRCm38)	missense	probably benign
IGL00953:Htt	APN	5	34,818,677 (GRCm38)	missense	probably benign	0.04
IGL00957:Htt	APN	5	34,806,724 (GRCm38)	missense	probably benign
IGL01314:Htt	APN	5	34,878,856 (GRCm38)	missense	probably benign
IGL01412:Htt	APN	5	34,898,572 (GRCm38)	missense	probably damaging	0.98
IGL01510:Htt	APN	5	34,907,512 (GRCm38)	missense	probably damaging	1.00
IGL01617:Htt	APN	5	34,876,755 (GRCm38)	missense	possibly damaging	0.67
IGL01893:Htt	APN	5	34,876,830 (GRCm38)	missense	probably damaging	1.00
IGL01914:Htt	APN	5	34,829,709 (GRCm38)	missense	probably benign
IGL01994:Htt	APN	5	34,832,604 (GRCm38)	missense	possibly damaging	0.83
IGL02102:Htt	APN	5	34,891,481 (GRCm38)	splice site	probably benign
IGL02381:Htt	APN	5	34,829,760 (GRCm38)	missense	probably benign	0.03
IGL02529:Htt	APN	5	34,819,043 (GRCm38)	splice site	probably benign
IGL02678:Htt	APN	5	34,899,902 (GRCm38)	missense	probably damaging	1.00
IGL02707:Htt	APN	5	34,829,881 (GRCm38)	critical splice donor site	probably null
IGL02731:Htt	APN	5	34,803,793 (GRCm38)	missense	probably benign	0.41
IGL02931:Htt	APN	5	34,876,753 (GRCm38)	missense	probably damaging	1.00
IGL03167:Htt	APN	5	34,818,986 (GRCm38)	missense	probably damaging	0.98
IGL03343:Htt	APN	5	34,826,041 (GRCm38)	missense	probably benign
IGL03344:Htt	APN	5	34,879,828 (GRCm38)	missense	probably benign	0.39
IGL03344:Htt	APN	5	34,907,466 (GRCm38)	missense	probably benign	0.02
IGL03366:Htt	APN	5	34,907,580 (GRCm38)	missense	probably damaging	1.00
IGL03410:Htt	APN	5	34,799,445 (GRCm38)	missense	probably damaging	0.99
Chalk	UTSW	5	34,907,086 (GRCm38)	missense	possibly damaging	0.86
IGL02796:Htt	UTSW	5	34,877,482 (GRCm38)	missense	probably benign	0.43
PIT4377001:Htt	UTSW	5	34,875,965 (GRCm38)	missense	probably benign	0.10
R0013:Htt	UTSW	5	34,820,104 (GRCm38)	missense	probably benign	0.25
R0049:Htt	UTSW	5	34,908,662 (GRCm38)	missense	probably damaging	0.97
R0049:Htt	UTSW	5	34,908,662 (GRCm38)	missense	probably damaging	0.97
R0056:Htt	UTSW	5	34,826,078 (GRCm38)	splice site	probably benign
R0207:Htt	UTSW	5	34,896,908 (GRCm38)	missense	probably benign	0.11
R0329:Htt	UTSW	5	34,817,134 (GRCm38)	splice site	probably benign
R0494:Htt	UTSW	5	34,821,844 (GRCm38)	missense	possibly damaging	0.73
R0548:Htt	UTSW	5	34,870,746 (GRCm38)	missense	probably damaging	1.00
R0601:Htt	UTSW	5	34,846,003 (GRCm38)	missense	probably benign	0.08
R0799:Htt	UTSW	5	34,817,753 (GRCm38)	missense	probably benign	0.00
R0947:Htt	UTSW	5	34,898,924 (GRCm38)	missense	probably damaging	1.00
R1053:Htt	UTSW	5	34,851,217 (GRCm38)	critical splice acceptor site	probably null
R1147:Htt	UTSW	5	34,851,252 (GRCm38)	missense	probably damaging	0.98
R1147:Htt	UTSW	5	34,851,252 (GRCm38)	missense	probably damaging	0.98
R1478:Htt	UTSW	5	34,803,827 (GRCm38)	missense	probably damaging	0.99
R1573:Htt	UTSW	5	34,864,374 (GRCm38)	splice site	probably benign
R1677:Htt	UTSW	5	34,828,574 (GRCm38)	missense	probably damaging	1.00
R1792:Htt	UTSW	5	34,907,199 (GRCm38)	missense	probably damaging	1.00
R1816:Htt	UTSW	5	34,803,740 (GRCm38)	missense	probably benign	0.01
R1833:Htt	UTSW	5	34,905,748 (GRCm38)	splice site	probably benign
R1837:Htt	UTSW	5	34,819,023 (GRCm38)	missense	probably benign	0.00
R1846:Htt	UTSW	5	34,848,944 (GRCm38)	missense	probably damaging	0.98
R1875:Htt	UTSW	5	34,794,112 (GRCm38)	missense	probably benign	0.05
R1899:Htt	UTSW	5	34,907,085 (GRCm38)	missense	probably benign	0.01
R2013:Htt	UTSW	5	34,852,871 (GRCm38)	missense	probably damaging	0.99
R2062:Htt	UTSW	5	34,825,982 (GRCm38)	missense	probably benign	0.00
R2064:Htt	UTSW	5	34,825,982 (GRCm38)	missense	probably benign	0.00
R2067:Htt	UTSW	5	34,825,982 (GRCm38)	missense	probably benign	0.00
R2068:Htt	UTSW	5	34,825,982 (GRCm38)	missense	probably benign	0.00
R2131:Htt	UTSW	5	34,877,109 (GRCm38)	missense	possibly damaging	0.50
R2162:Htt	UTSW	5	34,821,718 (GRCm38)	missense	probably benign	0.44
R2169:Htt	UTSW	5	34,877,475 (GRCm38)	missense	probably benign	0.08
R2345:Htt	UTSW	5	34,826,004 (GRCm38)	missense	possibly damaging	0.80
R2433:Htt	UTSW	5	34,907,541 (GRCm38)	missense	possibly damaging	0.65
R3027:Htt	UTSW	5	34,820,095 (GRCm38)	missense	possibly damaging	0.85
R3123:Htt	UTSW	5	34,804,531 (GRCm38)	missense	probably benign
R3125:Htt	UTSW	5	34,804,531 (GRCm38)	missense	probably benign
R3717:Htt	UTSW	5	34,811,522 (GRCm38)	splice site	probably benign
R3758:Htt	UTSW	5	34,895,970 (GRCm38)	missense	probably damaging	0.97
R3805:Htt	UTSW	5	34,877,204 (GRCm38)	splice site	probably null
R3833:Htt	UTSW	5	34,821,718 (GRCm38)	missense	probably benign	0.44
R4066:Htt	UTSW	5	34,878,847 (GRCm38)	missense	probably benign
R4272:Htt	UTSW	5	34,849,069 (GRCm38)	missense	possibly damaging	0.96
R4625:Htt	UTSW	5	34,829,785 (GRCm38)	missense	probably damaging	0.99
R4634:Htt	UTSW	5	34,875,948 (GRCm38)	missense	probably benign	0.06
R4655:Htt	UTSW	5	34,906,132 (GRCm38)	missense	probably benign	0.06
R4679:Htt	UTSW	5	34,820,080 (GRCm38)	missense	probably benign
R4684:Htt	UTSW	5	34,852,765 (GRCm38)	missense	probably damaging	1.00
R4832:Htt	UTSW	5	34,824,840 (GRCm38)	missense	probably benign	0.01
R4833:Htt	UTSW	5	34,852,225 (GRCm38)	missense	probably damaging	0.98
R4973:Htt	UTSW	5	34,813,023 (GRCm38)	missense	probably damaging	0.99
R5095:Htt	UTSW	5	34,824,395 (GRCm38)	missense	possibly damaging	0.89
R5132:Htt	UTSW	5	34,905,679 (GRCm38)	missense	possibly damaging	0.89
R5351:Htt	UTSW	5	34,803,833 (GRCm38)	missense	probably damaging	0.99
R5361:Htt	UTSW	5	34,907,584 (GRCm38)	missense	possibly damaging	0.47
R5399:Htt	UTSW	5	34,877,151 (GRCm38)	missense	probably damaging	0.98
R5462:Htt	UTSW	5	34,885,507 (GRCm38)	nonsense	probably null
R5552:Htt	UTSW	5	34,821,774 (GRCm38)	missense	probably benign
R5566:Htt	UTSW	5	34,849,075 (GRCm38)	missense	probably damaging	1.00
R5595:Htt	UTSW	5	34,905,397 (GRCm38)	missense	probably damaging	0.96
R5617:Htt	UTSW	5	34,870,806 (GRCm38)	missense	possibly damaging	0.77
R5835:Htt	UTSW	5	34,813,190 (GRCm38)	missense	probably benign	0.16
R5891:Htt	UTSW	5	34,870,823 (GRCm38)	missense	possibly damaging	0.62
R6158:Htt	UTSW	5	34,907,086 (GRCm38)	missense	possibly damaging	0.86
R6159:Htt	UTSW	5	34,804,676 (GRCm38)	missense	probably benign	0.08
R6169:Htt	UTSW	5	34,907,473 (GRCm38)	missense	probably damaging	1.00
R6242:Htt	UTSW	5	34,846,012 (GRCm38)	missense	probably damaging	1.00
R6274:Htt	UTSW	5	34,852,087 (GRCm38)	missense	possibly damaging	0.81
R6280:Htt	UTSW	5	34,870,759 (GRCm38)	missense	probably benign	0.00
R6294:Htt	UTSW	5	34,821,826 (GRCm38)	missense	probably benign
R6331:Htt	UTSW	5	34,895,887 (GRCm38)	missense	possibly damaging	0.89
R6448:Htt	UTSW	5	34,875,992 (GRCm38)	missense	probably benign	0.05
R6474:Htt	UTSW	5	34,824,895 (GRCm38)	missense	probably benign	0.06
R6592:Htt	UTSW	5	34,877,044 (GRCm38)	missense	possibly damaging	0.92
R6818:Htt	UTSW	5	34,782,767 (GRCm38)	missense	probably damaging	0.99
R6830:Htt	UTSW	5	34,834,326 (GRCm38)	missense	possibly damaging	0.82
R6920:Htt	UTSW	5	34,877,100 (GRCm38)	missense	probably null	1.00
R6962:Htt	UTSW	5	34,899,771 (GRCm38)	critical splice acceptor site	probably null
R7144:Htt	UTSW	5	34,846,006 (GRCm38)	missense	probably damaging	1.00
R7166:Htt	UTSW	5	34,852,894 (GRCm38)	missense	probably benign	0.42
R7329:Htt	UTSW	5	34,829,755 (GRCm38)	missense	probably benign	0.03
R7378:Htt	UTSW	5	34,803,799 (GRCm38)	missense	probably benign	0.04
R7418:Htt	UTSW	5	34,790,353 (GRCm38)	missense	possibly damaging	0.55
R7495:Htt	UTSW	5	34,811,477 (GRCm38)	missense	probably benign	0.00
R7554:Htt	UTSW	5	34,864,740 (GRCm38)	missense	probably damaging	0.97
R7575:Htt	UTSW	5	34,905,643 (GRCm38)	missense	probably damaging	1.00
R7763:Htt	UTSW	5	34,852,190 (GRCm38)	missense	probably damaging	1.00
R7782:Htt	UTSW	5	34,882,992 (GRCm38)	missense	probably benign	0.03
R7850:Htt	UTSW	5	34,852,287 (GRCm38)	splice site	probably null
R7870:Htt	UTSW	5	34,898,547 (GRCm38)	missense	possibly damaging	0.77
R7871:Htt	UTSW	5	34,864,649 (GRCm38)	missense	probably benign	0.00
R7879:Htt	UTSW	5	34,823,908 (GRCm38)	missense	probably benign
R7992:Htt	UTSW	5	34,829,881 (GRCm38)	critical splice donor site	probably null
R8058:Htt	UTSW	5	34,820,100 (GRCm38)	missense	probably benign
R8168:Htt	UTSW	5	34,882,956 (GRCm38)	missense	probably benign	0.00
R8188:Htt	UTSW	5	34,761,943 (GRCm38)	missense	probably benign	0.03
R8262:Htt	UTSW	5	34,895,960 (GRCm38)	missense	probably benign
R8343:Htt	UTSW	5	34,905,724 (GRCm38)	missense	probably damaging	1.00
R8353:Htt	UTSW	5	34,877,155 (GRCm38)	missense	possibly damaging	0.49
R8769:Htt	UTSW	5	34,820,289 (GRCm38)	missense	probably benign	0.05
R8808:Htt	UTSW	5	34,889,447 (GRCm38)	missense	probably benign	0.10
R8825:Htt	UTSW	5	34,825,960 (GRCm38)	missense	probably benign	0.24
R8843:Htt	UTSW	5	34,889,465 (GRCm38)	missense	possibly damaging	0.92
R8856:Htt	UTSW	5	34,903,331 (GRCm38)	missense	probably benign	0.44
R8882:Htt	UTSW	5	34,821,717 (GRCm38)	missense	probably benign
R8898:Htt	UTSW	5	34,819,032 (GRCm38)	missense	probably benign	0.01
R8964:Htt	UTSW	5	34,905,376 (GRCm38)	missense	probably benign	0.09
R8987:Htt	UTSW	5	34,820,024 (GRCm38)	missense	probably benign	0.18
R8991:Htt	UTSW	5	34,905,718 (GRCm38)	missense	probably damaging	1.00
R9005:Htt	UTSW	5	34,817,751 (GRCm38)	missense	possibly damaging	0.92
R9019:Htt	UTSW	5	34,866,576 (GRCm38)	missense	probably damaging	1.00
R9057:Htt	UTSW	5	34,852,110 (GRCm38)	missense	possibly damaging	0.86
R9157:Htt	UTSW	5	34,829,827 (GRCm38)	missense	probably null	0.89
R9205:Htt	UTSW	5	34,819,023 (GRCm38)	missense	probably benign	0.00
R9223:Htt	UTSW	5	34,905,348 (GRCm38)	missense	probably benign	0.01
R9243:Htt	UTSW	5	34,898,932 (GRCm38)	splice site	probably benign
R9329:Htt	UTSW	5	34,832,613 (GRCm38)	missense	possibly damaging	0.69
R9355:Htt	UTSW	5	34,895,903 (GRCm38)	missense	probably benign
R9402:Htt	UTSW	5	34,848,980 (GRCm38)	missense	probably damaging	1.00
R9446:Htt	UTSW	5	34,761,928 (GRCm38)	missense	probably benign
R9716:Htt	UTSW	5	34,854,675 (GRCm38)	missense	probably damaging	1.00
Z1177:Htt	UTSW	5	34,852,231 (GRCm38)	missense	probably null	0.87

Predicted Primers

PCR Primer
(F):5'- TTGAGGCTCAAGAGTCAAGGC -3'
(R):5'- AACTGCAGAGACCTCAGGAC -3'

Sequencing Primer
(F):5'- CTCAAGAGTCAAGGCAAGTAATC -3'
(R):5'- AGTCAATCTCTGCCAGAG -3'

Posted On

2019-05-13