Mutagenetix > Incidental Mutation

Incidental Mutation 'R1994:Hdc'

224087

Institutional Source

Beutler Lab

Gene Symbol

Hdc

Ensembl Gene

ENSMUSG00000027360

Gene Name

histidine decarboxylase

Synonyms

Hdc-s, Hdc-a, Hdc-c, Hdc-e, L-histidine decarboxylase

Accession Numbers

Essential gene?

Probably essential (E-score: 0.862) question?

Stock #

R1994 (G1)

Quality Score

223

Status

Not validated

Chromosome

Chromosomal Location

126593667-126619299 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 126616187 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Phenylalanine at position 72 (I72F)

Ref Sequence

ENSEMBL: ENSMUSP00000028838 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000028838]

AlphaFold

P23738

Predicted Effect

probably damaging
Transcript: ENSMUST00000028838
AA Change: I72F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000028838
Gene: ENSMUSG00000027360
AA Change: I72F

Domain	Start	End	E-Value	Type
low complexity region	6	15	N/A	INTRINSIC
Pfam:Pyridoxal_deC	43	421	2.2e-173	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000138752

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000148591

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.9%
20x: 94.1%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the group II decarboxylase family and forms a homodimer that converts L-histidine to histamine in a pyridoxal phosphate dependent manner. Histamine regulates several physiologic processes, including neurotransmission, gastric acid secretion,inflamation, and smooth muscle tone.[provided by RefSeq, Aug 2010]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit abnormal mast cells, altered anxiety-related and nociceptive behavior, altered cognitive function, increased weight gain, visceral adiposity, increased amount of brown adipose tissue, impaired glucose tolerance, hyperinsulinemia, and hyperleptinemia. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 91 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb11	A	T	2: 69,282,670		probably null	Het
Abcc8	T	G	7: 46,157,119	R388S	probably benign	Het
Abhd18	C	T	3: 40,934,926	R414*	probably null	Het
Acap1	C	T	11: 69,889,498	V40I	probably benign	Het
Actn1	C	A	12: 80,204,971	G111*	probably null	Het
Adam26b	T	C	8: 43,520,639	Q442R	probably benign	Het
Adamts19	T	C	18: 58,972,831		probably null	Het
Agtpbp1	T	G	13: 59,531,058	K145N	probably damaging	Het
AI661453	A	G	17: 47,467,034		probably benign	Het
Ap4e1	T	C	2: 127,061,547	S790P	probably benign	Het
Asmt	A	G	X: 170,675,789	E168G	possibly damaging	Het
Atp2a3	T	A	11: 72,975,414	S287T	probably damaging	Het
AY358078	T	A	14: 51,826,062	D388E	probably damaging	Het
Bicd1	A	T	6: 149,513,552	T588S	probably benign	Het
Birc6	T	G	17: 74,598,062	N1283K	probably benign	Het
Cacna1e	T	A	1: 154,477,817	Q423L	probably damaging	Het
Capn3	T	A	2: 120,495,937	Y537N	probably damaging	Het
Cep295	C	T	9: 15,340,883	E397K	probably damaging	Het
Chgb	T	C	2: 132,786,498	S48P	possibly damaging	Het
Cidec	T	A	6: 113,428,232	Y159F	probably damaging	Het
Clec18a	T	C	8: 111,081,602	S66G	possibly damaging	Het
Cpsf1	G	A	15: 76,603,160	T138M	probably benign	Het
Dclre1c	C	T	2: 3,437,985	R61W	probably damaging	Het
Eef1akmt1	A	C	14: 57,550,454	V149G	probably benign	Het
Fam131b	T	C	6: 42,320,884	T112A	possibly damaging	Het
Fbln2	A	G	6: 91,234,301	E409G	probably damaging	Het
Fkbp15	G	A	4: 62,304,381	P1094S	probably benign	Het
Fpr1	A	G	17: 17,877,617	S37P	probably benign	Het
Fryl	G	T	5: 73,108,493	T495K	probably damaging	Het
Gja6	A	T	X: 160,903,378	I186N	possibly damaging	Het
Gm4922	T	C	10: 18,783,640	T445A	probably benign	Het
Gria2	G	A	3: 80,802,357	L10F	probably benign	Het
Gspt2	A	G	X: 94,637,419	D388G	possibly damaging	Het
Igf2r	T	C	17: 12,692,738	K1905E	probably benign	Het
Il33	A	G	19: 29,956,904	D155G	possibly damaging	Het
Klk1b9	C	T	7: 43,979,555	T161I	probably benign	Het
Mfsd12	C	A	10: 81,357,681	H28Q	probably damaging	Het
Mgat5	A	T	1: 127,459,959	I551F	possibly damaging	Het
Miga2	A	T	2: 30,381,988	D25V	probably damaging	Het
Mlc1	T	C	15: 88,974,579	N122S	possibly damaging	Het
Mmp20	T	A	9: 7,645,292	M281K	probably benign	Het
Muc5ac	C	A	7: 141,813,152	P2232T	possibly damaging	Het
N4bp2l2	A	G	5: 150,661,283	S411P	possibly damaging	Het
Ngef	G	A	1: 87,487,904	S346L	probably damaging	Het
Nov	T	A	15: 54,749,354	V253E	probably benign	Het
Olfr1217	T	A	2: 89,023,143	T287S	probably damaging	Het
Olfr1309	T	A	2: 111,984,084	M5L	probably benign	Het
Olfr1408	C	T	1: 173,130,851	R122H	possibly damaging	Het
Olfr553	C	T	7: 102,614,540	V150M	probably damaging	Het
Olfr612	T	C	7: 103,538,359	I292V	possibly damaging	Het
Olfr661	T	C	7: 104,688,483	I156T	probably benign	Het
Olfr720	A	G	14: 14,175,854	I76T	probably benign	Het
Olfr782	T	A	10: 129,350,692	I43N	probably damaging	Het
Olfr811	T	C	10: 129,801,661	Y288C	probably damaging	Het
Papd5	C	T	8: 88,246,484	T277M	probably damaging	Het
Pecam1	G	T	11: 106,695,937	H150N	possibly damaging	Het
Polr3c	A	T	3: 96,714,373		probably null	Het
Pop1	A	C	15: 34,530,471	Q1005P	probably damaging	Het
Prss22	G	A	17: 23,996,314	P163S	probably damaging	Het
Prss33	G	A	17: 23,834,198	A223V	probably damaging	Het
Prss53	C	T	7: 127,887,393	V354I	probably benign	Het
Rab3gap2	C	T	1: 185,236,024	T191I	probably damaging	Het
Rictor	T	C	15: 6,776,156	F608L	probably benign	Het
Ryr3	T	A	2: 112,654,492	E3884V	probably null	Het
Scaf11	G	A	15: 96,418,840	R948*	probably null	Het
Sec61g	A	T	11: 16,506,444	V40E	probably damaging	Het
Serpinb3d	A	T	1: 107,080,788	F116I	possibly damaging	Het
Sipa1l3	T	C	7: 29,399,611	D411G	probably benign	Het
Slc13a3	T	C	2: 165,434,064	N254S	possibly damaging	Het
Slc35a2	T	A	X: 7,892,825	L110Q	probably damaging	Het
Spata31d1b	G	C	13: 59,716,380	L447F	probably benign	Het
Spsb2	T	C	6: 124,809,366		probably null	Het
Tmcc3	T	C	10: 94,578,606	S57P	possibly damaging	Het
Traf7	A	G	17: 24,510,502	V445A	probably damaging	Het
Trib1	A	G	15: 59,649,343	S61G	possibly damaging	Het
Trip12	A	T	1: 84,749,172	F36I	probably damaging	Het
Tshz3	T	C	7: 36,769,822	I412T	probably damaging	Het
Tsku	T	C	7: 98,352,146	Y326C	probably damaging	Het
Ttc30b	A	G	2: 75,938,058	L117P	probably damaging	Het
Ttn	T	G	2: 76,881,694		probably benign	Het
Ugt1a6a	G	A	1: 88,138,748	R92H	probably benign	Het
Vmn1r63	A	G	7: 5,803,255	V126A	probably benign	Het
Vmn2r84	T	A	10: 130,386,009	S781C	probably damaging	Het
Wdr91	T	A	6: 34,892,362	H409L	probably damaging	Het
Wnt7a	T	A	6: 91,365,956	T315S	possibly damaging	Het
Zdhhc25	A	G	15: 88,600,824	T121A	probably benign	Het
Zfp109	T	C	7: 24,229,318	H222R	probably benign	Het
Zfp286	A	G	11: 62,779,820	S476P	probably damaging	Het
Zfp605	T	C	5: 110,127,552	Y179H	probably damaging	Het
Zfp955a	T	C	17: 33,241,646	H504R	probably damaging	Het
Zswim2	T	A	2: 83,915,663	N477I	possibly damaging	Het

Other mutations in Hdc

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00572:Hdc	APN	2	126601872	missense	probably benign	0.00
IGL01024:Hdc	APN	2	126603846	missense	probably benign	0.32
IGL01393:Hdc	APN	2	126594661	missense	probably benign	0.28
IGL01802:Hdc	APN	2	126603894	missense	probably benign	0.04
IGL01958:Hdc	APN	2	126594532	missense	possibly damaging	0.87
IGL02193:Hdc	APN	2	126601780	splice site	probably benign
IGL02494:Hdc	APN	2	126594121	missense	probably benign
IGL02696:Hdc	APN	2	126594300	missense	probably damaging	1.00
IGL02874:Hdc	APN	2	126601676	missense	probably benign	0.21
R0453:Hdc	UTSW	2	126594951	splice site	probably benign
R0528:Hdc	UTSW	2	126616232	missense	probably benign	0.00
R1337:Hdc	UTSW	2	126616276	missense	probably benign
R1862:Hdc	UTSW	2	126597933	missense	probably benign	0.36
R1938:Hdc	UTSW	2	126606397	missense	possibly damaging	0.86
R2230:Hdc	UTSW	2	126594018	missense	possibly damaging	0.65
R2257:Hdc	UTSW	2	126616080	splice site	probably null
R2921:Hdc	UTSW	2	126593990	missense	probably damaging	1.00
R2923:Hdc	UTSW	2	126593990	missense	probably damaging	1.00
R3620:Hdc	UTSW	2	126616267	missense	possibly damaging	0.86
R3621:Hdc	UTSW	2	126616267	missense	possibly damaging	0.86
R3914:Hdc	UTSW	2	126603006	missense	probably damaging	1.00
R4076:Hdc	UTSW	2	126616261	missense	possibly damaging	0.92
R4114:Hdc	UTSW	2	126601818	missense	probably benign	0.16
R4213:Hdc	UTSW	2	126597866	splice site	probably null
R4827:Hdc	UTSW	2	126594313	missense	probably benign
R4889:Hdc	UTSW	2	126594133	missense	probably benign	0.00
R5013:Hdc	UTSW	2	126604300	missense	probably benign	0.33
R5593:Hdc	UTSW	2	126618584	utr 5 prime	probably benign
R5604:Hdc	UTSW	2	126594663	missense	probably benign
R5637:Hdc	UTSW	2	126616189	missense	probably benign	0.02
R6211:Hdc	UTSW	2	126593977	missense	probably damaging	0.98
R6312:Hdc	UTSW	2	126607406	missense	possibly damaging	0.65
R7730:Hdc	UTSW	2	126594082	missense	possibly damaging	0.51
R7889:Hdc	UTSW	2	126616210	missense	probably damaging	1.00
R8328:Hdc	UTSW	2	126601883	missense	probably damaging	1.00
R8482:Hdc	UTSW	2	126594205	missense	probably benign
R8517:Hdc	UTSW	2	126597970	critical splice acceptor site	probably null
R9136:Hdc	UTSW	2	126597866	splice site	probably null
R9139:Hdc	UTSW	2	126597917	missense	probably damaging	1.00
R9208:Hdc	UTSW	2	126594680	missense	probably benign	0.32
R9515:Hdc	UTSW	2	126616229	missense	probably damaging	0.96

Predicted Primers

PCR Primer
(F):5'- AGCACTACAGGTCAGCACTG -3'
(R):5'- AATGTGACCCGGTTCCTCTG -3'

Sequencing Primer
(F):5'- TACAGGTCAGCACTGGCACAAG -3'
(R):5'- CTCTGCTTCTGTCCAGGGAAAGAG -3'

Posted On

2014-08-25