Hhat (hedgehog acyltransferase) - Rat Genome Database

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Gene: Hhat (hedgehog acyltransferase) Mus musculus
Analyze
Symbol: Hhat
Name: hedgehog acyltransferase
RGD ID: 1552712
MGI Page MGI
Description: Enables palmitoyltransferase activity. Involved in N-terminal peptidyl-L-cysteine N-palmitoylation. Acts upstream of or within protein palmitoylation and smoothened signaling pathway. Predicted to be located in Golgi apparatus. Predicted to be active in endoplasmic reticulum. Is expressed in branchial arch; embryo; embryo ectoderm; and limb. Used to study chondrodysplasia-pseudohermaphroditism syndrome. Human ortholog(s) of this gene implicated in chondrodysplasia-pseudohermaphroditism syndrome. Orthologous to human HHAT (hedgehog acyltransferase).
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: 2810432O22Rik; AI462858; AP-2; AP-2CRE; MGC11697; protein-cysteine N-palmitoyltransferase HHAT; S; skinny hedgehog protein; Skn; Tg(TFAP2A-cre)1Will
RGD Orthologs
Human
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: GRCm39 - Mouse Genome Assembly GRCm39
Position:
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391192,195,133 - 192,453,546 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1192,179,019 - 192,453,531 (-)EnsemblGRCm39 Ensembl
GRCm381192,512,825 - 192,771,219 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1192,496,711 - 192,771,223 (-)EnsemblGRCm38mm10GRCm38
MGSCv371194,336,710 - 194,597,413 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361194,213,552 - 194,471,745 (-)NCBIMGSCv36mm8
Celera1199,399,516 - 199,653,201 (-)NCBICelera
Cytogenetic Map1H6NCBI
cM Map197.55NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Mammalian Phenotype
abnormal blood vessel morphology  (IAGP)
abnormal cartilage development  (IAGP)
abnormal cranial ganglia morphology  (IAGP)
abnormal craniofacial morphology  (IAGP)
abnormal cranium morphology  (IAGP)
abnormal eye development  (IAGP)
abnormal fetal Leydig cell differentiation  (IAGP)
abnormal forebrain morphology  (IAGP)
abnormal frontonasal suture morphology  (IAGP)
abnormal mandible morphology  (IAGP)
abnormal mandibular prominence morphology  (IAGP)
abnormal maxillary prominence morphology  (IAGP)
abnormal midbrain morphology  (IAGP)
abnormal nasal bone morphology  (IAGP)
abnormal nasal cartilage morphology  (IAGP)
abnormal nasal cavity morphology  (IAGP)
abnormal nasal septum cartilage morphology  (IAGP)
abnormal neural crest cell morphology  (IAGP)
abnormal neural crest morphology  (IAGP)
abnormal neurocranium morphology  (IAGP)
abnormal optic vesicle formation  (IAGP)
abnormal oral cavity morphology  (IAGP)
abnormal palatal shelf elevation  (IAGP)
abnormal palatal shelf fusion at midline  (IAGP)
abnormal palate development  (IAGP)
abnormal testis cord formation  (IAGP)
abnormal testis development  (IAGP)
abnormal testis morphology  (IAGP)
abnormal trigeminal ganglion morphology  (IAGP)
abnormal ventral interneuron 2 morphology  (IAGP)
abnormal ventral interneuron 3 morphology  (IAGP)
abnormal vertebral column morphology  (IAGP)
absent cornea  (IAGP)
absent floor plate  (IAGP)
absent interparietal bone  (IAGP)
absent mandibular angle  (IAGP)
absent mandibular condyloid process  (IAGP)
absent mandibular coronoid process  (IAGP)
absent nasal septum  (IAGP)
absent parietal bone  (IAGP)
absent supraoccipital bone  (IAGP)
absent tooth placode  (IAGP)
acrania  (IAGP)
agnathia  (IAGP)
arrest of tooth development  (IAGP)
chondrodystrophy  (IAGP)
decreased embryo size  (IAGP)
decreased motor neuron number  (IAGP)
diencephalon hypoplasia  (IAGP)
disproportionate dwarf  (IAGP)
edema  (IAGP)
failure of bone ossification  (IAGP)
hemorrhage  (IAGP)
holoprosencephaly  (IAGP)
malocclusion  (IAGP)
microphthalmia  (IAGP)
nasal cartilage hypoplasia  (IAGP)
neonatal lethality, complete penetrance  (IAGP)
ocular hypertelorism  (IAGP)
oligodactyly  (IAGP)
prenatal lethality, complete penetrance  (IAGP)
short frontal bone  (IAGP)
short nasal bone  (IAGP)
short snout  (IAGP)
small basioccipital bone  (IAGP)
small embryonic telencephalon  (IAGP)
small exoccipital bone  (IAGP)
small frontonasal prominence  (IAGP)
small testis  (IAGP)
small trigeminal ganglion  (IAGP)
tongue hypoplasia  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. MGDs mouse GO annotations MGD data from the GO Consortium
2. MGD IEA MGD IEA
3. Frequent deregulations in the hedgehog signaling network and cross-talks with the epidermal growth factor receptor pathway involved in cancer progression and targeted therapies. Mimeault M and Batra SK, Pharmacol Rev. 2010 Sep;62(3):497-524.
4. Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Okazaki Y, etal., Nature. 2002 Dec 5;420(6915):563-73.
5. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
6. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
7. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10349636   PMID:11042159   PMID:11076861   PMID:11217851   PMID:12477932   PMID:14610273   PMID:14975718   PMID:15075292   PMID:15489334   PMID:15987787   PMID:16141072   PMID:16141073  
PMID:16207751   PMID:18081866   PMID:18272593   PMID:18799693   PMID:21267068   PMID:21873635   PMID:21913308   PMID:22110055   PMID:23055936   PMID:24076664   PMID:24590292   PMID:24784881  
PMID:25799573   PMID:27923152   PMID:28891097   PMID:31875564  


Genomics

Comparative Map Data
Hhat
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391192,195,133 - 192,453,546 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1192,179,019 - 192,453,531 (-)EnsemblGRCm39 Ensembl
GRCm381192,512,825 - 192,771,219 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1192,496,711 - 192,771,223 (-)EnsemblGRCm38mm10GRCm38
MGSCv371194,336,710 - 194,597,413 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361194,213,552 - 194,471,745 (-)NCBIMGSCv36mm8
Celera1199,399,516 - 199,653,201 (-)NCBICelera
Cytogenetic Map1H6NCBI
cM Map197.55NCBI
HHAT
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381210,327,328 - 210,676,290 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1210,328,252 - 210,676,296 (+)EnsemblGRCh38hg38GRCh38
GRCh371210,501,596 - 210,849,632 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361208,568,920 - 208,916,261 (+)NCBINCBI36Build 36hg18NCBI36
Build 341206,890,691 - 207,238,033NCBI
Celera1183,724,968 - 184,075,988 (+)NCBICelera
Cytogenetic Map1q32.2NCBI
HuRef1181,175,198 - 181,526,335 (+)NCBIHuRef
CHM1_11211,773,949 - 212,122,400 (+)NCBICHM1_1
T2T-CHM13v2.01209,566,001 - 209,918,121 (+)NCBIT2T-CHM13v2.0
Hhat
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr813106,558,635 - 106,814,723 (-)NCBIGRCr8
mRatBN7.213104,024,507 - 104,283,580 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl13104,010,916 - 104,282,893 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx13106,547,576 - 106,800,518 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.013107,931,425 - 108,184,358 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.013105,146,543 - 105,402,299 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.013111,235,325 - 111,489,075 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl13111,236,466 - 111,474,411 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.013115,830,447 - 115,993,319 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.413108,411,459 - 108,651,307 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.113108,601,112 - 108,830,328 (-)NCBI
Celera13103,464,906 - 103,714,179 (-)NCBICelera
Cytogenetic Map13q27NCBI
Hhat
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554891,553,568 - 1,855,166 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554891,553,580 - 1,868,088 (-)NCBIChiLan1.0ChiLan1.0
HHAT
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2138,737,342 - 39,085,749 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1138,703,765 - 39,051,986 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01185,885,604 - 186,231,857 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11190,755,249 - 191,100,284 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1190,755,249 - 191,100,284 (+)Ensemblpanpan1.1panPan2
HHAT
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.178,949,743 - 9,244,746 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl78,949,743 - 9,275,101 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha78,517,759 - 8,857,806 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.078,637,341 - 8,946,880 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl78,637,216 - 8,946,328 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.178,566,494 - 8,909,599 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.078,661,372 - 9,001,712 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.078,798,783 - 9,139,113 (+)NCBIUU_Cfam_GSD_1.0
Hhat
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934465,256,523 - 65,571,907 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365572,497,710 - 2,793,441 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365572,677,630 - 2,793,478 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
HHAT
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl9132,347,037 - 132,666,873 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.19132,346,407 - 132,668,067 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.29145,380,415 - 145,703,027 (-)NCBISscrofa10.2Sscrofa10.2susScr3
HHAT
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12518,790,060 - 19,140,455 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2518,792,527 - 19,119,818 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605519,342,001 - 19,704,344 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Hhat
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248071,392,620 - 1,672,286 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248071,392,618 - 1,677,631 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in Hhat
9723 total Variants
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1547
Count of miRNA genes:726
Interacting mature miRNAs:928
Transcripts:ENSMUST00000044190, ENSMUST00000123721, ENSMUST00000128619, ENSMUST00000154203, ENSMUST00000154755
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


QTLs in Region (GRCm39)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
11039528Ccc3_mcolitis susceptibility in the Collaborative Cross 3 (mouse)13680142195051546Mouse
1301202Yaa4_mY-linked autoimmune acceleration 4 (mouse)Not determined1158468817192468938Mouse
1300823Ath9_matherosclerosis 9 (mouse)Not determined1160112768194112883Mouse
1558802Skmw6_mskeletal muscle weight 6 (mouse)Not determined1167954584195154279Mouse
1301652Cpfd2_mcerebellum pattern fissures (mouse)Not determined1172303451195154279Mouse
12790987Tgl5_mtriglyceride 5 (mouse)1160097157194097157Mouse
1301339Hdlq15_mHDL QTL 15 (mouse)Not determined1165873675195154279Mouse
11059556Lmr20b_mleishmaniasis resistance 20b (mouse)1158468817192468938Mouse
11059557Lmr20a_mleishmaniasis resistance 20a (mouse)1158468817192468938Mouse
11059558Lmr20c_mleishmaniasis resistance 20c (mouse)1158468817192468938Mouse
10043863Swrl5_mSWR lupus locus 5 (mouse)Not determined1172303451195154279Mouse
12790988Phdlc5_mplasma HDL cholesterol 5 (mouse)9160097157194097157Mouse
1301596Elnt_mescape latencies during navigation task (mouse)Not determined1162145207194111528Mouse
11049575Lmr8b_mleishmaniasis resistance 8b (mouse)1172303451195154279Mouse
1301251Scc3_mcolon tumor susceptibility 3 (mouse)Not determined1168213823195154279Mouse
1301632Bw8q1_mbody weight at 8 weeks QTL 1 (mouse)Not determined1161201261195154279Mouse
4141483Femwf7_mfemur work to failure 7 (mouse)Not determined167462514195154279Mouse
1302023Orch4_mautoimmune orchitis resistance 4 (mouse)Not determined1175211318195154279Mouse
10402498Lmr20_mleishmaniasis resistance 20 (mouse)Not determined1158468817192468938Mouse
1302158Fembrs5_mfemur breaking strength 5 (mouse)Not determined1167462514195154279Mouse
14700797Mencq2_mmeniscus calcification QTL 2 (mouse)1191583112192212308Mouse
1301132Mors1_mmodifier of obesity related sterility 1 (mouse)Not determined1170379500195154279Mouse
1301431Pcho1_mplasma cholesterol 1 (mouse)Not determined1159262573193262693Mouse
1300727Mptp1_mMPTP sensitivity 1 (mouse)Not determined1171632048192681050Mouse
1559024Zit1_mzinc induced tolerance 1 (mouse)Not determined1167462514195154279Mouse
12880429V25Dq1_mvitamin D inactive form serum level QTL 1 (mouse)1172632197195154279Mouse
12880426V25Dq2_mvitamin D inactive form serum level QTL 2 (mouse)1172532197195154279Mouse
1357732Tbbmd1_mtotal body bone mineral density 1 (mouse)Not determined1171983110195154279Mouse
1300842Sle9_msystematic lupus erythematosus susceptibility 9 (mouse)Not determined1158468817192468938Mouse
11532690Sluc37_msusceptibility to lung cancer 37 (mouse)1175468817194111528Mouse

Markers in Region
D1Mit210  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm381192,529,010 - 192,529,115UniSTSGRCm38
MGSCv371194,352,892 - 194,352,997UniSTSGRCm37
Celera1199,415,828 - 199,415,928UniSTS
Cytogenetic Map1H6UniSTS
cM Map1109.0UniSTS
Whitehead Genetic1113.7UniSTS
Whitehead/MRC_RH12440.83UniSTS
Whitehead_YAC1 UniSTS
UniSTS:234314  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm381192,512,977 - 192,513,196UniSTSGRCm38
MGSCv371194,336,859 - 194,337,078UniSTSGRCm37
Celera1199,399,664 - 199,399,883UniSTS
Cytogenetic Map1H6UniSTS


Sequence


Ensembl Acc Id: ENSMUST00000044190   ⟹   ENSMUSP00000046686
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl1192,195,136 - 192,453,531 (-)Ensembl
GRCm38.p6 Ensembl1192,512,828 - 192,771,223 (-)Ensembl
Ensembl Acc Id: ENSMUST00000123721
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl1192,337,268 - 192,370,014 (-)Ensembl
GRCm38.p6 Ensembl1192,654,960 - 192,687,706 (-)Ensembl
Ensembl Acc Id: ENSMUST00000128619   ⟹   ENSMUSP00000120479
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl1192,179,019 - 192,453,521 (-)Ensembl
GRCm38.p6 Ensembl1192,496,711 - 192,771,213 (-)Ensembl
Ensembl Acc Id: ENSMUST00000154203
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl1192,408,505 - 192,419,588 (-)Ensembl
GRCm38.p6 Ensembl1192,726,197 - 192,737,280 (-)Ensembl
Ensembl Acc Id: ENSMUST00000154755
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl1192,309,754 - 192,408,516 (-)Ensembl
GRCm38.p6 Ensembl1192,627,446 - 192,726,208 (-)Ensembl
Ensembl Acc Id: ENSMUST00000192585   ⟹   ENSMUSP00000141575
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl1192,225,456 - 192,453,526 (-)Ensembl
GRCm38.p6 Ensembl1192,543,148 - 192,771,218 (-)Ensembl
Ensembl Acc Id: ENSMUST00000192946
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl1192,418,719 - 192,453,300 (-)Ensembl
GRCm38.p6 Ensembl1192,736,411 - 192,770,992 (-)Ensembl
RefSeq Acc Id: NM_144881   ⟹   NP_659130
RefSeq Status: VALIDATED
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm391192,195,133 - 192,453,546 (-)NCBI
GRCm381192,512,828 - 192,771,219 (-)NCBI
MGSCv371194,336,710 - 194,597,413 (-)RGD
Celera1199,399,516 - 199,653,201 (-)RGD
cM Map1 ENTREZGENE
Sequence:
RefSeq Acc Id: XM_011238934   ⟹   XP_011237236
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm391192,195,133 - 192,419,663 (-)NCBI
GRCm381192,512,825 - 192,737,357 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017320220   ⟹   XP_017175709
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm391192,195,133 - 192,417,751 (-)NCBI
GRCm381192,512,825 - 192,735,449 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017320221   ⟹   XP_017175710
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm391192,195,133 - 192,400,533 (-)NCBI
GRCm381192,512,825 - 192,718,230 (-)NCBI
Sequence:
RefSeq Acc Id: NP_659130   ⟸   NM_144881
- Peptide Label: precursor
- UniProtKB: Q3TA33 (UniProtKB/Swiss-Prot),   B1ANS0 (UniProtKB/Swiss-Prot),   Q922G3 (UniProtKB/Swiss-Prot),   Q8BMT9 (UniProtKB/Swiss-Prot),   A0A0A6YWJ4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011237236   ⟸   XM_011238934
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_017175709   ⟸   XM_017320220
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_017175710   ⟸   XM_017320221
- Peptide Label: isoform X3
- Sequence:
Ensembl Acc Id: ENSMUSP00000141575   ⟸   ENSMUST00000192585
Ensembl Acc Id: ENSMUSP00000120479   ⟸   ENSMUST00000128619
Ensembl Acc Id: ENSMUSP00000046686   ⟸   ENSMUST00000044190

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8BMT9-F1-model_v2 AlphaFold Q8BMT9 1-499 view protein structure

Promoters
RGD ID:6876144
Promoter ID:EPDNEW_M1523
Type:multiple initiation site
Name:Hhat_1
Description:Mus musculus hedgehog acyltransferase , mRNA.
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm381192,771,238 - 192,771,298EPDNEW
RGD ID:6817882
Promoter ID:MM_KWN:3336
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:3T3L1_Day0,   3T3L1_Day2,   3T3L1_Day3,   3T3L1_Day4,   BoneMarrow_0Hour,   BoneMarrow_4Hour,   Lung,   MEF_B4,   MEF_B6,   Spleen
Transcripts:ENSMUST00000085565,   ENSMUST00000097435,   NM_144881,   OTTMUST00000067020
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv361194,596,931 - 194,598,147 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene MGI:2444681 AgrOrtholog
Ensembl Genes ENSMUSG00000037375 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENSMUST00000044190 ENTREZGENE
  ENSMUST00000044190.12 UniProtKB/Swiss-Prot
  ENSMUST00000128619.8 UniProtKB/Swiss-Prot
  ENSMUST00000192585.2 UniProtKB/TrEMBL
InterPro MB_O-acyltransferase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MBOAT_fam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report mmu:226861 UniProtKB/Swiss-Prot
MGD MGI:2444681 ENTREZGENE
NCBI Gene 226861 ENTREZGENE
PANTHER ACYLTRANSFERASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR13285:SF20 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam MBOAT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PhenoGen Hhat PhenoGen
UniProt A0A0A6YWJ4 ENTREZGENE, UniProtKB/TrEMBL
  B1ANS0 ENTREZGENE
  HHAT_MOUSE UniProtKB/Swiss-Prot
  Q3TA33 ENTREZGENE
  Q3TQW5_MOUSE UniProtKB/TrEMBL
  Q8BMT9 ENTREZGENE
  Q8BWF5_MOUSE UniProtKB/TrEMBL
  Q922G3 ENTREZGENE
UniProt Secondary B1ANS0 UniProtKB/Swiss-Prot
  Q3TA33 UniProtKB/Swiss-Prot
  Q922G3 UniProtKB/Swiss-Prot