ZMP
zgc:194119
Ensembl ID:
ZFIN ID:
Description:
5-hydroxytryptamine receptor 2B [Source:RefSeq peptide;Acc:NP_001038208]
Human Orthologue:
HTR2B
Human Description:
5-hydroxytryptamine (serotonin) receptor 2B [Source:HGNC Symbol;Acc:5294]
Mouse Orthologue:
Htr2b
Mouse Description:
5-hydroxytryptamine (serotonin) receptor 2B Gene [Source:MGI Symbol;Acc:MGI:109323]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16649 | Nonsense | Available for shipment | Available now |
sa32414 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16649
Status:
Available for shipment
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:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104569 | Nonsense | 233 | 443 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 22 (position 40657209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 37737124 |
GRCz11 | 22 | 37672132 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCGAGAGCTGCGAGGCCCTCCATTTCCACGGTCTTCCAGCAGGAACTCT[C/A]AGTTCTTGCTTCACCAGAGAAAATGGTCATATCGAATGGAATAAAAAGAG
Long Flanking Sequence:
CAGTAATTACAGTCCTTTGCTGTTCGTTTGGTGTGTTCAAAGGTTTTGGACCGGATGCGGCTGACAAGTTCAAGTTCTTAGGAGTCAGCTTTGCGTGTCCCAGATTTTAGCTAAACACTGTAGGACAGTGAATCTCCAAGAAAAAGACTCAACACTTCCAACTTAGTCAATGAATGTCAATGTTTTATTTAAGTCCTGTTCTCTGCTCAATTTAACGATTGGTCTTTCTCCAACAGGCATTGCGATACCGATTCCAATCAAAGGGCTTCAATTCTTTGATCATCCGAACATCACCTTCAACAAAAACCACACCTGCTTGTTGTCGCCGGAGGGCTTCAGGGACTTCAAGGTGTACGGGTCTTTGGTGGCTTTCTTCATACCCCTCGCAATCATGATGATCATTTACTTGCTGACAATCCAAGTACTGCGGAAAAAGGCCTATCTTTTAAGATCGAGAGCTGCGAGGCCCTCCATTTCCACGGTCTTCCAGCAGGAACTCT[C/A]AGTTCTTGCTTCACCAGAGAAAATGGTCATATCGAATGGAATAAAAAGAGACCGAACACTGAACCCCGTCAATCCCATCACAGGAGATGAGGTCCCTCTGCGCAGGATGTCCACCATAGGAAAGAGGTCCATGCAAAACTTGACCAATGAACAAAGGGCCTCGAAGGTTCTGGGGATCGTATTCATGCTGTTCGTTGTGATGTGGTGTCCTTTCTTCATTACTAACGTGACTTCTGTGCTCTGTGAAAGGTGCAACGGTAATCTAGTGGACCAGCTGCTGGATATCTTTCAGTGGGTGGGCTATGTTTCGTCAGGCATCAACCCGCTGGTCTATACTCTGTTCAATAGGACGTTCAGACTGGCCTTCAGGCGCTACATCACCTGTAACTACAAGAGCGTGAGGACTCCGAAACTGCAACGGAGAAGCAAAATCTCCTTTCGTTCATCAGTGACCGAAAACTCAAAGCGGTTTATGAAACACGGTATGAAGAATGGCATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32414
Status:
Available for shipment
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:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104569 | Nonsense | 344 | 443 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 22 (position 40656875)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 37736790 |
GRCz11 | 22 | 37671798 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTTTCAGTGGGTGGGCTATGTTTCGTCAGGCATCAACCCGCTGGTCTA[T/A]ACTCTGTTCAATAGGACGTTCAGACTGGCCTTCAGGCGCTACATCACCTG
Long Flanking Sequence:
TTCAGGGACTTCAAGGTGTACGGGTCTTTGGTGGCTTTCTTCATACCCCTCGCAATCATGATGATCATTTACTTGCTGACAATCCAAGTACTGCGGAAAAAGGCCTATCTTTTAAGATCGAGAGCTGCGAGGCCCTCCATTTCCACGGTCTTCCAGCAGGAACTCTCAGTTCTTGCTTCACCAGAGAAAATGGTCATATCGAATGGAATAAAAAGAGACCGAACACTGAACCCCGTCAATCCCATCACAGGAGATGAGGTCCCTCTGCGCAGGATGTCCACCATAGGAAAGAGGTCCATGCAAAACTTGACCAATGAACAAAGGGCCTCGAAGGTTCTGGGGATCGTATTCATGCTGTTCGTTGTGATGTGGTGTCCTTTCTTCATTACTAACGTGACTTCTGTGCTCTGTGAAAGGTGCAACGGTAATCTAGTGGACCAGCTGCTGGATATCTTTCAGTGGGTGGGCTATGTTTCGTCAGGCATCAACCCGCTGGTCTA[T/A]ACTCTGTTCAATAGGACGTTCAGACTGGCCTTCAGGCGCTACATCACCTGTAACTACAAGAGCGTGAGGACTCCGAAACTGCAACGGAGAAGCAAAATCTCCTTTCGTTCATCAGTGACCGAAAACTCAAAGCGGTTTATGAAACACGGTATGAAGAATGGCATCAGCCCTGTAGGTTATCAGAGTCCGATCAGGCATCGATCAACGCAGCTGCAGACGTCTGCAAATATCATGTTAGACACGTTGCTGTTGACAGACAATGAAGACTGCAAACCTGATGAACACGTAAGCCACGTGTAGAAGATCTCATGAAAAGCCAAGAAAGAGATGTGCGATAGTCTTTTAGTGGCCACAAAGCTCATGTGAGGCAATGAAATATGGCAACACTAGGATATTGCACCCAATGTATGAACGTTTCCATAGTTCCTATAACTATTGGTGGAAGTGCACTTTTTTTGGCACGTTTGTGCATTACAGGAACTGAGAATATTTTTAGCTTT
Associated Phenotype:
Not determined