ENSDARG00000060458

Ensembl ID:
ENSDARG00000060458
Human Orthologue:
HRH3
Human Description:
histamine receptor H3 [Source:HGNC Symbol;Acc:5184]
Mouse Orthologue:
Hrh3
Mouse Description:
histamine receptor H3 Gene [Source:MGI Symbol;Acc:MGI:2139279]

Alleles

There are 3 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa43742 Nonsense Mutation detected in F1 DNA During 2016
sa37396 Nonsense Mutation detected in F1 DNA During 2016
sa37397 Nonsense Mutation detected in F1 DNA During 2016

Mutation Details

Allele Name:
sa43742
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085196 Nonsense 294 398 3 3
Genomic Location (Zv9):
Chromosome 22 (position 1144840)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 3060614
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GGTTGGGTTCGGACGCGGATTATTCGAGCGCAGGAAGTGACGAATCCCTG[T/A]GCGCCTTGCCGAAGCGGCGGACACGCACGTCTTTCTAGAGATAAGAAGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37396
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
G > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085196 Nonsense 357 398 3 3
Genomic Location (Zv9):
Chromosome 22 (position 1145029)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 3060803
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GGTAGCTGTGTGGAGCATCATTGGTATGAAGTCACATTTTGGCTTCTTTG[G/A]CTTAATTCGGCCATCAATCCCTTCCTGTATCCACTGTGCCACAGCAGCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37397
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
G > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085196 Nonsense 393 398 3 3
Genomic Location (Zv9):
Chromosome 22 (position 1145135)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 3060909
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GAGCGTTCGCTAAGATCCTGTGCCCAAAACGGCAGTCTGTTCAACCGCAC[G/T]AGGAAAGCCCTTCATGCCCATGACAGTCTGACAGGGATTTTAACACTGGA
Associated Phenotype:
Not determined

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