ZMP
htr1aa
Ensembl ID:
ZFIN ID:
Description:
5-hydroxytryptamine receptor 1A [Source:RefSeq peptide;Acc:NP_001116793]
Human Orthologue:
HTR1A
Human Description:
5-hydroxytryptamine (serotonin) receptor 1A [Source:HGNC Symbol;Acc:5286]
Mouse Orthologue:
Htr1a
Mouse Description:
5-hydroxytryptamine (serotonin) receptor 1A Gene [Source:MGI Symbol;Acc:MGI:96273]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31665 | Nonsense | Available for shipment | Available now |
sa41249 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31665
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 |
---|---|---|---|---|---|
ENSDART00000138217 | Nonsense | 96 | 398 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 8 (position 32790080)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 31932806 |
GRCz11 | 8 | 31942038 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGTGCTCCCCATGGCAGCCCTGTATCAGGTTTTGAATAAATGGACTT[T/A]GGGACAGGAGATGTGCGATATTTTCATCTCTCTAGACGTGCTGTGCTGCA
Long Flanking Sequence:
GTCTGTTTTAAAGCTTGCACGGCTTCTCTGCAAAGTGCACGCGCCTCACTCCGCCATCTCTGACGCACTTAGCACGACTCGTATAAATGAATTGACTTCGTCACTGAGCGCCAATGATCGCAGCTCGAGCGCGCGGCACTTCCTGAGCCCGGAGCCCGCCATGCGTCTTCAGAGCAGCGAGGTGACCGGCGCGAGGAGCTGCTTCTGACTCACCATGGAGAGCTACAACAACACCACAGAAAGCCAAGATTGGAGCGGGAACGCGACGAGTGTCAGCGAAGTTGCTCTGAGTTACCAAATCATCGGCTCGCTTTTCCTGGCCGCGTTAATTCTGTTTGCCATTTTGGGAAACGCGTGTGTCATCGCTGCTATCGCCTTGGAGAGATCGCTTCAGAATGTGGCCAACTATCTCATCGGCTCCCTGGCCGTTACAGACCTTATGGTGTCGGTGCTGGTGCTCCCCATGGCAGCCCTGTATCAGGTTTTGAATAAATGGACTT[T/A]GGGACAGGAGATGTGCGATATTTTCATCTCTCTAGACGTGCTGTGCTGCACTTCTTCCATCCTGCACCTGTGCGCAATCGCTTTGGATAGGTACTGGGCCATCACCGATCCCATAGACTACGTGAATAAAAGGACGCCCAGACGAGCTGCTATCTTGATCAGTCTCACTTGGCTAATAGGATTTTCCATTTCCATTCCGCCCATGTTGGGTTGGAGGAAACCGGAGGACCGGGCAGATCCCGACGCGTGCACAATCAGCCAGGACCACGGGTACACCATCTACTCAACTTTCGGGGCGTTCTACATCCCGCTCATCCTCATGCTGGTCCTTTACGGACGGATATTCCGAGCGGCGAGGTTTCGCATAAGGAAAACGGTAAAGAAAACGGAGAAAGCGAAAATCGCGGATAAATGCTTGGCGGTGTCTCCAGCGCTCTTCCCGAGGAAAGCGAACGGAGAGGTGGGTAAAACTTGGAGGCGAAGCGTGGAGCCGTGCGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41249
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000138217 | Nonsense | 267 | 398 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 8 (position 32790592)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 31933318 |
GRCz11 | 8 | 31942550 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGTAAAACTTGGAGGCGAAGCGTGGAGCCGTGCGCAAACGGCGCGCTG[A/T]AAAACTCGGACGACGGAGAGTCGTTCGAGATTACAGAAGTTCAAAGCATC
Long Flanking Sequence:
TGTGCGATATTTTCATCTCTCTAGACGTGCTGTGCTGCACTTCTTCCATCCTGCACCTGTGCGCAATCGCTTTGGATAGGTACTGGGCCATCACCGATCCCATAGACTACGTGAATAAAAGGACGCCCAGACGAGCTGCTATCTTGATCAGTCTCACTTGGCTAATAGGATTTTCCATTTCCATTCCGCCCATGTTGGGTTGGAGGAAACCGGAGGACCGGGCAGATCCCGACGCGTGCACAATCAGCCAGGACCACGGGTACACCATCTACTCAACTTTCGGGGCGTTCTACATCCCGCTCATCCTCATGCTGGTCCTTTACGGACGGATATTCCGAGCGGCGAGGTTTCGCATAAGGAAAACGGTAAAGAAAACGGAGAAAGCGAAAATCGCGGATAAATGCTTGGCGGTGTCTCCAGCGCTCTTCCCGAGGAAAGCGAACGGAGAGGTGGGTAAAACTTGGAGGCGAAGCGTGGAGCCGTGCGCAAACGGCGCGCTG[A/T]AAAACTCGGACGACGGAGAGTCGTTCGAGATTACAGAAGTTCAAAGCATCTCCAAAAATCACCTGAGCCTGCCAAACAACCCTCAGCCGTGCTTCGAGAACCGAAATGAGAAAAACACGGAAGCGAAGCGCAAAGTGGCTCTGGCCAGAGAACGCAAAACAGTCAAGACTCTGGGAATAATCATGGGCACGTTTATTTTCTGCTGGCTGCCCTTCTTCATCGTAGCGCTCGTGTTGCCTTTTTGTCAGGACTGTTTTATGCCCGAATGGTTGGGCGCTGTCATAAACTGGCTCGGATACTCCAACTCACTTTTGAATCCTGTCATATATGCGTACTTCAATAAAGACTTTCAGAACGCATTCAAGAAGATTTTGAAATGCAAATGTATTAGACAGTGAACCAAGTCAATCAGCGGGTGTTCATGTGCAGATATTGATTGTTAAAGATTGCTCTAAAGGCATTTACAAAGATGGGACTCAGAGCAGAGCAGAGCAGCACAA
Associated Phenotype:
Not determined