Busch Lab

ZMP

htr2a

Ensembl ID:
ENSDARG00000057029
ZFIN ID:
ZDB-GENE-070912-500
Description:
Novel protein similar to vertebrate 5-hydroxytryptamine (Serotonin) receptor 2A (HTR2A) [Source:UniP
Human Orthologue:
HTR2A
Human Description:
5-hydroxytryptamine (serotonin) receptor 2A [Source:HGNC Symbol;Acc:5293]
Mouse Orthologue:
Htr2a
Mouse Description:
5-hydroxytryptamine (serotonin) receptor 2A Gene [Source:MGI Symbol;Acc:MGI:109521]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa21494 Nonsense Available for shipment Available now
sa9359 Nonsense Mutation detected in F1 DNA Not yet available
sa18946 Nonsense Mutation detected in F1 DNA Not yet available
sa27407 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa2517 Nonsense F2 line generated Not yet available

Mutation Details

Allele Name:
sa21494
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079621 Nonsense 25 357 1 2
ENSDART00000141502 Nonsense 70 402 2 3
Genomic Location (Zv9):
Chromosome 9 (position 26244111)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 25399897
GRCz11 9 25210766
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTCATTCAATCTGATTCTCTGCATGTGTATCTCCTCTTCAGGTTACT[C/A]ATGGCCTTTCCCTGCATCACTGTGTCCCATGTGGATCTACCTAGATGTGC
Long Flanking Sequence:
GGTCTAGCTCAGGGCTCTCTCCTGGGACAGCATGCCAAATTTTTATCAATCATCAGCTAAGGGTGAACTCTTGAAATAGACATTTAAAAATTGAATGCATGAATGTATAGGAAATACCAAAAAAATACATATTATATGAATAGATGAAGGACAGTCAGATTAAATTATTCTTAGATAGACGGGTGGAAGGACAGAAATAGAAGAGACACAGACAGACAGTTACGTATAGTAGTGGCTGATACATATAATAGTGTAATGATGAAAGTGTTTTTCTCCTGTGTGTTAAATGAGTGCACTGTCAGTGATTGTTAAGCTCTTGTTCTGTTTTCAAGAGCTCATCACATTCATGCCTTCCCGTGAAATCCCTCACTTGTGGATGAAGCACGTTAAATAATCTCACTGGGTCCATTAGCAAGAAAGTCAGTGTTTCTGTGCCTTTTGTTGTCAGTTTTATTCATTCAATCTGATTCTCTGCATGTGTATCTCCTCTTCAGGTTACT[C/A]ATGGCCTTTCCCTGCATCACTGTGTCCCATGTGGATCTACCTAGATGTGCTCTTCTCCACCGCCTCCATCATGCACCTGTGTGCAATTTCTCTTGACCGCTATGTGGCCATTCGTAACCCCATCCGACACAATCGGTCAAATTCCCGCTCCCGAGCCCGGGCCAAGATTACGGCAGTCTGGACCATCTCTGCAGGTACACCTGATGCCATCAACACATGAGCACAACTCCGTGCTGTAGAGAGATATGATGACAAAAAGATGCCCAATGAGTCATGATTAAGTCATGTAAAGTGGAGATATAAATTAGAAAACAGTAAATGAACACTGGCGGTTCATTCCACTGTGGGGAACCCTTGTAAATCAGGGGAAATAAGCTAAAGAAAAGCGAGTGAGGCAGTGAGTGAATGAACATTGTTTTAGGTTTTACAGAAATAGTGTAATTTTCATTGTTTAGGATTTGAGGGGATTTTAGTTTTCTGTTTATAACATGTCCGTTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9359
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079621 Nonsense 31 357 1 2
ENSDART00000141502 Nonsense 76 402 2 3
ENSDART00000079621 Nonsense 31 357 1 2
ENSDART00000141502 Nonsense 76 402 2 3
Genomic Location (Zv9):
Chromosome 9 (position 26244093)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 25399879
GRCz11 9 25210748
KASP Assay ID:
2260-1892.1 (used for ordering genotyping assays)
KASP Sequence:
TCTCTGCATGTGTATCTCCTCTTCAGGTTACTCATGGCCTTTCCCWGCAT[C/A]ACTGTGTCCCATGTGGATCTACCTAGATGTGCTCTTCTCCACYGCCTCCA
Long Flanking Sequence:
CTCCTGGGACAGCATGCCAAATTTTTATCAATCATCAGCTAAGGGTGAACTCTTGAAATAGACATTTAAAAATTGAATGCATGAATGTATAGGAAATACCAAAAAAATACATATTATATGAATAGATGAAGGACAGTCAGATTAAATTATTCTTAGATAGACGGGTGGAAGGACAGAAATAGAAGAGACACAGACAGACAGTTACGTATAGTAGTGGCTGATACATATAATAGTGTAATGATGAAAGTGTTTTTCTCCTGTGTGTTAAATGAGTGCACTGTCAGTGATTGTTAAGCTCTTGTTCTGTTTTCAAGAGCTCATCACATTCATGCCTTCCCGTGAAATCCCTCACTTGTGGATGAAGCACGTTAAATAATCTCACTGGGTCCATTAGCAAGAAAGTCAGTGTTTCTGTGCCTTTTGTTGTCAGTTTTATTCATTCAATCTGATTCTCTGCATGTGTATCTCCTCTTCAGGTTACTCATGGCCTTTCCCTGCAT[C/A]ACTGTGTCCCATGTGGATCTACCTAGATGTGCTCTTCTCCACCGCCTCCATCATGCACCTGTGTGCAATTTCTCTTGACCGCTATGTGGCCATTCGTAACCCCATCCGACACAATCGGTCAAATTCCCGCTCCCGAGCCCGGGCCAAGATTACGGCAGTCTGGACCATCTCTGCAGGTACACCTGATGCCATCAACACATGAGCACAACTCCGTGCTGTAGAGAGATATGATGACAAAAAGATGCCCAATGAGTCATGATTAAGTCATGTAAAGTGGAGATATAAATTAGAAAACAGTAAATGAACACTGGCGGTTCATTCCACTGTGGGGAACCCTTGTAAATCAGGGGAAATAAGCTAAAGAAAAGCGAGTGAGGCAGTGAGTGAATGAACATTGTTTTAGGTTTTACAGAAATAGTGTAATTTTCATTGTTTAGGATTTGAGGGGATTTTAGTTTTCTGTTTATAACATGTCCGTTAAAAATACAAAAAAAAAAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18946
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079621 Nonsense 31 357 1 2
ENSDART00000141502 Nonsense 76 402 2 3
ENSDART00000079621 Nonsense 31 357 1 2
ENSDART00000141502 Nonsense 76 402 2 3
Genomic Location (Zv9):
Chromosome 9 (position 26244093)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 25399879
GRCz11 9 25210748
KASP Assay ID:
2260-1892.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTGCATGTGTATCTCCTCTTCAGGTTACTCATGGCCTTTCCCTGCAT[C/A]ACTGTGTCCCATGTGGATCTACCTAGATGTGCTCTTCTCCACCGCCTCCA
Long Flanking Sequence:
CTCCTGGGACAGCATGCCAAATTTTTATCAATCATCAGCTAAGGGTGAACTCTTGAAATAGACATTTAAAAATTGAATGCATGAATGTATAGGAAATACCAAAAAAATACATATTATATGAATAGATGAAGGACAGTCAGATTAAATTATTCTTAGATAGACGGGTGGAAGGACAGAAATAGAAGAGACACAGACAGACAGTTACGTATAGTAGTGGCTGATACATATAATAGTGTAATGATGAAAGTGTTTTTCTCCTGTGTGTTAAATGAGTGCACTGTCAGTGATTGTTAAGCTCTTGTTCTGTTTTCAAGAGCTCATCACATTCATGCCTTCCCGTGAAATCCCTCACTTGTGGATGAAGCACGTTAAATAATCTCACTGGGTCCATTAGCAAGAAAGTCAGTGTTTCTGTGCCTTTTGTTGTCAGTTTTATTCATTCAATCTGATTCTCTGCATGTGTATCTCCTCTTCAGGTTACTCATGGCCTTTCCCTGCAT[C/A]ACTGTGTCCCATGTGGATCTACCTAGATGTGCTCTTCTCCACCGCCTCCATCATGCACCTGTGTGCAATTTCTCTTGACCGCTATGTGGCCATTCGTAACCCCATCCGACACAATCGGTCAAATTCCCGCTCCCGAGCCCGGGCCAAGATTACGGCAGTCTGGACCATCTCTGCAGGTACACCTGATGCCATCAACACATGAGCACAACTCCGTGCTGTAGAGAGATATGATGACAAAAAGATGCCCAATGAGTCATGATTAAGTCATGTAAAGTGGAGATATAAATTAGAAAACAGTAAATGAACACTGGCGGTTCATTCCACTGTGGGGAACCCTTGTAAATCAGGGGAAATAAGCTAAAGAAAAGCGAGTGAGGCAGTGAGTGAATGAACATTGTTTTAGGTTTTACAGAAATAGTGTAATTTTCATTGTTTAGGATTTGAGGGGATTTTAGTTTTCTGTTTATAACATGTCCGTTAAAAATACAAAAAAAAAAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27407
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079621 Essential Splice Site 90 357 None 2
ENSDART00000141502 Essential Splice Site 135 402 None 3
Genomic Location (Zv9):
Chromosome 9 (position 26232401)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 25388187
GRCz11 9 25199056
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCTGCAGACCTATACTATTAACACACTTTCTTCCCTCTGTCTGTCTGC[A/T]GGCATCTCTATGCCAATCCCAGTGCTGGGTTTGCGTGATCACACCAAAGT
Long Flanking Sequence:
GCAATGTATTTTCAAAAGTAACTTTCCCCAACACTGTCTAGCAAGCATTAGGGTTGTAATGAAGTATTTGTCAACTGCAAAATCATGATTAGTAATAAGTTGACAATAACACAGAATCTTTAAGATAACAGACAGCAGACCGTCTACAAATACTCTAACAACTGTGAGTCTTACAGTCAAAAGGTATTACCAAAAAGAATAATATCAACATGTTGTGTTATGTATGAAAGCACTGTTATTATATTTATTTCTATGTACTATTATTCATCCGTGTCAGCTTGTACAAATGGACTGTGAAAAGAACACTAGCAGAACAGCAGCATACAGTATGTCACTGACAAACTGCAGGTCACACAACCTCGCCTTTGTGTTTTGCATGAAATAACCGACTGTCATCATTTATTTTGTTCCGTTTGGTTTCTCAGCCACCTTTTTTTTAGCCTGTCTTAAATTCTGCAGACCTATACTATTAACACACTTTCTTCCCTCTGTCTGTCTGC[A/T]GGCATCTCTATGCCAATCCCAGTGCTGGGTTTGCGTGATCACACCAAAGTTTTCAAGGACGGCAGCTGCCTATTGACTGACAACTCTTTTGTATTGATTGGGTCCTTTGTGGCATTCTTTGTGCCATTGACTATTATGGTGGTGACCTACTTTTTGACTATCAGCGCTCTGCAGAGTGAAGCCACGCTCTGCCTTGACCAACTGGTGCCCAGGCCCAAATGGAGCACAGGTTTAACTCTTAACTTTCTACCAGGACCCTCGTTTTCGCCGTCAGAGAAAAAACTCTTCCTGAGGCGTTCATTGAGCCGGGAGCCAGGAGCAGATTCAGGAGTTGTCACACCTCCTTTTGGACGGCATAACATGCAGTCTATCAGCAATGAACAGAAGGCCTCTAAAGTTCTGGGGGTAGTTTTCTTTCTCTTTGTGGTCATGTGGTGCCCCTTTTTTATAACCAATGTTTTGGCAGTGGTTTGTGAACCGAATGCGTGCAATGCTAATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2517
Status:
F2 line generated
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
ENSDART00000079621 Nonsense 234 357 2 2
ENSDART00000141502 Nonsense 279 402 3 3
ENSDART00000079621 Nonsense 234 357 2 2
ENSDART00000141502 Nonsense 279 402 3 3
Genomic Location (Zv9):
Chromosome 9 (position 26231967)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 25387753
GRCz11 9 25198622
KASP Assay ID:
554-3255.1 (used for ordering genotyping assays)
KASP Sequence:
GAAGGCCTCTAAAGTTCTGGGGGTAGTTTTCTTTCTCTTTGTGGTCATGT[G/A]GTGCCCCTTTTTTATMACCAATGTTTTGGCAGTGGTTTGTGAACCRAATG
Long Flanking Sequence:
TTTTAGCCTGTCTTAAATTCTGCAGACCTATACTATTAACACACTTTCTTCCCTCTGTCTGTCTGCAGGCATCTCTATGCCAATCCCAGTGCTGGGTTTGCGTGATCACACCAAAGTTTTCAAGGACGGCAGCTGCCTATTGACTGACAACTCTTTTGTATTGATTGGGTCCTTTGTGGCATTCTTTGTGCCATTGACTATTATGGTGGTGACCTACTTTTTGACTATCAGCGCTCTGCAGAGTGAAGCCACGCTCTGCCTTGACCAACTGGTGCCCAGGCCCAAATGGAGCACAGGTTTAACTCTTAACTTTCTACCAGGACCCTCGTTTTCGCCGTCAGAGAAAAAACTCTTCCTGAGGCGTTCATTGAGCCGGGAGCCAGGAGCAGATTCAGGAGTTGTCACACCTCCTTTTGGACGGCATAACATGCAGTCTATCAGCAATGAACAGAAGGCCTCTAAAGTTCTGGGGGTAGTTTTCTTTCTCTTTGTGGTCATGT[G/A]GTGCCCCTTTTTTATAACCAATGTTTTGGCAGTGGTTTGTGAACCGAATGCGTGCAATGCTAATATAATGAACAGACTGTTGAATGTTTTTGTATGGGTTGGTTACCTGTCCTCCGCCGTTAACCCATTGGTTTACACACTCTTCAACAAGACTTATCGCTCAGCCTTCGCGAGATACATCCGATGCCAGTTTCATGAAGAAAAGAAACCGTTACAGTTAATTCTGGTCAACACAATCCCACCGATGGCCTATCAGTCCACACACCTGCCACTCACTGGATCAATAGGCAATGGGGATTTCTCTCTACCCCTTCCTAATAAAAACCACCATCTGTCCAAAAGCGGCAAAAATGAGAGTGTCAGCTGCTTGTGAATTCACTCTACGAAAGTAGGATTTTCTTCTGGGTTCTTGTTTGGCATTAAATCCTTCTTACCTCTACAGAGATTGGTTCTGAATGGTCTAAAGTATTAGTATTCAAAGCTCAATCGTATCTGTGAAT
Associated Phenotype:
Not determined