ZMP
ENSDARG00000060458
Ensembl ID:
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43742 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37396 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44977 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37397 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43742
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
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 |
GRCz11 | 22 | 3078029 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTGGGTTCGGACGCGGATTATTCGAGCGCAGGAAGTGACGAATCCCTG[T/A]GCGCCTTGCCGAAGCGGCGGACACGCACGTCTTTCTAGAGATAAGAAGAT
Long Flanking Sequence:
TGGGTTTCGGCATTCCTCCTCTACGGCCCGGCGATAATCTTCTGGGAGCTGCTGGTGGGCGAAAGCATCGTTCCAGAGGATGAGTGTTTCGCTGAGTTTTACTGCACGTGGTACTTTCTGCTCTCAGCATCCACCTTTGAGTTCTTCTCTCCATTCATCTCAGTGGCCTTCTTCAACTTCAGCATCTATCTCAACATCCAGCGCAGAAACCGCAGTCGGATGGCGCACGTGGAGGCGGAGAAAGAGGACGGCTGGAGGGTTATCGACGGACAAACTTCGTCAGTGTTTTTCGTTAAAACACGTAAAGTGTCGTCGAGTGAACCGGCGGCGGTTTCTGCCGTAATCGAAGACGACGAAGAAGTTTCGCCATCATCCAGTGGTGATCCCAGCAGCACACATTCGGTTTCTTTAACGATGAAGACTACGATTAAAAAACGAGGGTTGTTCGGGGGTTGGGTTCGGACGCGGATTATTCGAGCGCAGGAAGTGACGAATCCCTG[T/A]GCGCCTTGCCGAAGCGGCGGACACGCACGTCTTTCTAGAGATAAGAAGATTGCAAAGTCGTTGGCGGTTATTGTGTGTGTTTTCGGGGTGTGTTGGGCACCGTACACACTCCTGATGATCATAAGGGCAGCCTGCAGTGGTAGCTGTGTGGAGCATCATTGGTATGAAGTCACATTTTGGCTTCTTTGGCTTAATTCGGCCATCAATCCCTTCCTGTATCCACTGTGCCACAGCAGCTTTCGGCGAGCGTTCGCTAAGATCCTGTGCCCAAAACGGCAGTCTGTTCAACCGCACGAGGAAAGCCCTTCATGCCCATGACAGTCTGACAGGGATTTTAACACTGGATATTGAAGGATCAAGTAAAACGTTGACGCACAAGCGAATGAAAAACCCCAGTTTCATTATTTTAATGGTGTAGCATGTTTTGTTCTTCCTGACATAACTCATAGTTGATCTTTTATTCCAGTTCAGCACATCCACGATGTTGTTAAACATTCGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37396
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
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 |
GRCz11 | 22 | 3078218 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTAGCTGTGTGGAGCATCATTGGTATGAAGTCACATTTTGGCTTCTTTG[G/A]CTTAATTCGGCCATCAATCCCTTCCTGTATCCACTGTGCCACAGCAGCTT
Long Flanking Sequence:
CTCAACATCCAGCGCAGAAACCGCAGTCGGATGGCGCACGTGGAGGCGGAGAAAGAGGACGGCTGGAGGGTTATCGACGGACAAACTTCGTCAGTGTTTTTCGTTAAAACACGTAAAGTGTCGTCGAGTGAACCGGCGGCGGTTTCTGCCGTAATCGAAGACGACGAAGAAGTTTCGCCATCATCCAGTGGTGATCCCAGCAGCACACATTCGGTTTCTTTAACGATGAAGACTACGATTAAAAAACGAGGGTTGTTCGGGGGTTGGGTTCGGACGCGGATTATTCGAGCGCAGGAAGTGACGAATCCCTGTGCGCCTTGCCGAAGCGGCGGACACGCACGTCTTTCTAGAGATAAGAAGATTGCAAAGTCGTTGGCGGTTATTGTGTGTGTTTTCGGGGTGTGTTGGGCACCGTACACACTCCTGATGATCATAAGGGCAGCCTGCAGTGGTAGCTGTGTGGAGCATCATTGGTATGAAGTCACATTTTGGCTTCTTTG[G/A]CTTAATTCGGCCATCAATCCCTTCCTGTATCCACTGTGCCACAGCAGCTTTCGGCGAGCGTTCGCTAAGATCCTGTGCCCAAAACGGCAGTCTGTTCAACCGCACGAGGAAAGCCCTTCATGCCCATGACAGTCTGACAGGGATTTTAACACTGGATATTGAAGGATCAAGTAAAACGTTGACGCACAAGCGAATGAAAAACCCCAGTTTCATTATTTTAATGGTGTAGCATGTTTTGTTCTTCCTGACATAACTCATAGTTGATCTTTTATTCCAGTTCAGCACATCCACGATGTTGTTAAACATTCGCCTTTTGTCTTGACGAAAACGAAGGGATTAGGGCTGTGCAATTTGACAACATACAGTGGTCAACATTTGAAGACAAGAACGGGTGTTGTTCGATAGACAACTTTGATGGTTCACTTTTAATGTTGACTACTATATACAATCGTATTGACCTTATTCTTCACGTACGAGGAGACGCCGCCATTACAATCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44977
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085196 | Nonsense | 387 | 398 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 22 (position 1145117)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 3060891 |
GRCz11 | 22 | 3078306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCACAGCAGCTTTCGGCGAGCGTTCGCTAAGATCCTGTGCCCAAAACGG[C/T]AGTCTGTTCAACCGCACGAGGAAAGCCCTTCATGCCCATGACAGTCTGAC
Long Flanking Sequence:
CGTCAGTGTTTTTCGTTAAAACACGTAAAGTGTCGTCGAGTGAACCGGCGGCGGTTTCTGCCGTAATCGAAGACGACGAAGAAGTTTCGCCATCATCCAGTGGTGATCCCAGCAGCACACATTCGGTTTCTTTAACGATGAAGACTACGATTAAAAAACGAGGGTTGTTCGGGGGTTGGGTTCGGACGCGGATTATTCGAGCGCAGGAAGTGACGAATCCCTGTGCGCCTTGCCGAAGCGGCGGACACGCACGTCTTTCTAGAGATAAGAAGATTGCAAAGTCGTTGGCGGTTATTGTGTGTGTTTTCGGGGTGTGTTGGGCACCGTACACACTCCTGATGATCATAAGGGCAGCCTGCAGTGGTAGCTGTGTGGAGCATCATTGGTATGAAGTCACATTTTGGCTTCTTTGGCTTAATTCGGCCATCAATCCCTTCCTGTATCCACTGTGCCACAGCAGCTTTCGGCGAGCGTTCGCTAAGATCCTGTGCCCAAAACGG[C/T]AGTCTGTTCAACCGCACGAGGAAAGCCCTTCATGCCCATGACAGTCTGACAGGGATTTTAACACTGGATATTGAAGGATCAAGTAAAACGTTGACGCACAAGCGAATGAAAAACCCCAGTTTCATTATTTTAATGGTGTAGCATGTTTTGTTCTTCCTGACATAACTCATAGTTGATCTTTTATTCCAGTTCAGCACATCCACGATGTTGTTAAACATTCGCCTTTTGTCTTGACGAAAACGAAGGGATTAGGGCTGTGCAATTTGACAACATACAGTGGTCAACATTTGAAGACAAGAACGGGTGTTGTTCGATAGACAACTTTGATGGTTCACTTTTAATGTTGACTACTATATACAATCGTATTGACCTTATTCTTCACGTACGAGGAGACGCCGCCATTACAATCTTTTTGGCTCGAGACTTCCGCTCTCCTTCACTTCCATGGTTTTTAGACGTTAAAGGCAGCTCGTTGTTGCAAACTGATATTTTCTTCTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37397
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
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 |
GRCz11 | 22 | 3078324 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCGTTCGCTAAGATCCTGTGCCCAAAACGGCAGTCTGTTCAACCGCAC[G/T]AGGAAAGCCCTTCATGCCCATGACAGTCTGACAGGGATTTTAACACTGGA
Long Flanking Sequence:
AAACACGTAAAGTGTCGTCGAGTGAACCGGCGGCGGTTTCTGCCGTAATCGAAGACGACGAAGAAGTTTCGCCATCATCCAGTGGTGATCCCAGCAGCACACATTCGGTTTCTTTAACGATGAAGACTACGATTAAAAAACGAGGGTTGTTCGGGGGTTGGGTTCGGACGCGGATTATTCGAGCGCAGGAAGTGACGAATCCCTGTGCGCCTTGCCGAAGCGGCGGACACGCACGTCTTTCTAGAGATAAGAAGATTGCAAAGTCGTTGGCGGTTATTGTGTGTGTTTTCGGGGTGTGTTGGGCACCGTACACACTCCTGATGATCATAAGGGCAGCCTGCAGTGGTAGCTGTGTGGAGCATCATTGGTATGAAGTCACATTTTGGCTTCTTTGGCTTAATTCGGCCATCAATCCCTTCCTGTATCCACTGTGCCACAGCAGCTTTCGGCGAGCGTTCGCTAAGATCCTGTGCCCAAAACGGCAGTCTGTTCAACCGCAC[G/T]AGGAAAGCCCTTCATGCCCATGACAGTCTGACAGGGATTTTAACACTGGATATTGAAGGATCAAGTAAAACGTTGACGCACAAGCGAATGAAAAACCCCAGTTTCATTATTTTAATGGTGTAGCATGTTTTGTTCTTCCTGACATAACTCATAGTTGATCTTTTATTCCAGTTCAGCACATCCACGATGTTGTTAAACATTCGCCTTTTGTCTTGACGAAAACGAAGGGATTAGGGCTGTGCAATTTGACAACATACAGTGGTCAACATTTGAAGACAAGAACGGGTGTTGTTCGATAGACAACTTTGATGGTTCACTTTTAATGTTGACTACTATATACAATCGTATTGACCTTATTCTTCACGTACGAGGAGACGCCGCCATTACAATCTTTTTGGCTCGAGACTTCCGCTCTCCTTCACTTCCATGGTTTTTAGACGTTAAAGGCAGCTCGTTGTTGCAAACTGATATTTTCTTCTTATATTATTTTAATTTTATGT
Associated Phenotype:
Not determined