ZMP
LOC798599
Ensembl ID:
Human Orthologue:
HTR2C
Human Description:
5-hydroxytryptamine (serotonin) receptor 2C [Source:HGNC Symbol;Acc:5295]
Mouse Orthologue:
Htr2c
Mouse Description:
5-hydroxytryptamine (serotonin) receptor 2C Gene [Source:MGI Symbol;Acc:MGI:96281]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa5962 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24033 | Essential Splice Site | Available for shipment | Available now |
sa43720 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12052 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa5962
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 |
---|---|---|---|---|---|
ENSDART00000036537 | Nonsense | 101 | 355 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 42020757)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43619803 |
GRCz11 | 21 | 43614979 |
KASP Assay ID:
554-3868.1 (used for ordering genotyping assays)
KASP Sequence:
TATTGTTGTCTGCTTCCAGATCACACCTGGCCTCTCCCRCAGCYGCTGTG[T/A]CCGCTGTGGATCTTTCTGGACGTGCTTTTCTCCACAGCYTCCATCATGCA
Long Flanking Sequence:
GGATAAGTTGGCGGTTCATTCCACAGTGTTGGCCCCAGAATAATAAAGCAAATAAGCCGAAATGAAAATGAATGAATGAATGAATATCTGAAAATGGTGGCAAAGTGGTTAGCACTGTCACCTCAGAGCAAGAAGGTCGCTGGTTTGAGTCTCGGCTAGGTCAGTTGGCATTTCTGTATAGAGTTTGCATGTTCTCCCTGTCTTAGTATGGGTTTCTTCCGGGTGCTCTGGTTTCCCCCACAATACACAAGCACCATAGGGGAGGTGCATAAGCTAAATTGGTCACAGTGTATGTGTGTGAATGAGTGTGTTTGGGTGTTTCCCGGTGATGGGTTGCAGCTGGAAGGGCATTCGCTGTGTAAAACATATGTTGGATAAGTTGGCGGTTCATTCCGCTGTGGTGACTCCTGATTTATAAAGGGACTAAGCCGAAGAAAAATGAATGATTATTATTGTTGTCTGCTTCCAGATCACACCTGGCCTCTCCCGCAGCTGCTGTG[T/A]CCGCTGTGGATCTTTCTGGACGTGCTTTTCTCCACAGCCTCCATCATGCATCTCTGCGCCATCTCTCTGGACCGCTACATCGGCATCCGCAACCCATTCAGTATCAGTCACACTCAGTCATCTCGCAAGGCCATGATCAAAATAATCACCGTGTGGACCATTTCTATAGGTGAGAGAAGCATTCAGTGGTGAGAGTTACAATAATGGGTAACACTTTACAATAACAGTACATGAATAATGATGTATTAATAAGTAAACTAAACATTACTTTATTATGAATCAATGATTAGTTAAGGTATACACTAATCAAGAATAACTACATCATGAGTTACATGAGTTCATGTGTGAATAACGGCTACCTTAATCACTTGTTAGTACATGTTGTTAATTAATGTATTAATTAACATTTAAGTTTAAGCTAAATGTAACCAACATGAACTCATGAGCTGTTAATGTATAGTTATATCATGACTTTACTTGGAGGGGCACATCACTATTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24033
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000036537 | Essential Splice Site | 158 | 355 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 42020586)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43619632 |
GRCz11 | 21 | 43614808 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCGCAAGGCCATGATCAAAATAATCACCGTGTGGACCATTTCTATAGG[T/A]GAGAGAAGCATTCAGTGGTGAGAGTTACAATAATGGGTAACACTTTACAA
Long Flanking Sequence:
TTCTGTATAGAGTTTGCATGTTCTCCCTGTCTTAGTATGGGTTTCTTCCGGGTGCTCTGGTTTCCCCCACAATACACAAGCACCATAGGGGAGGTGCATAAGCTAAATTGGTCACAGTGTATGTGTGTGAATGAGTGTGTTTGGGTGTTTCCCGGTGATGGGTTGCAGCTGGAAGGGCATTCGCTGTGTAAAACATATGTTGGATAAGTTGGCGGTTCATTCCGCTGTGGTGACTCCTGATTTATAAAGGGACTAAGCCGAAGAAAAATGAATGATTATTATTGTTGTCTGCTTCCAGATCACACCTGGCCTCTCCCGCAGCTGCTGTGTCCGCTGTGGATCTTTCTGGACGTGCTTTTCTCCACAGCCTCCATCATGCATCTCTGCGCCATCTCTCTGGACCGCTACATCGGCATCCGCAACCCATTCAGTATCAGTCACACTCAGTCATCTCGCAAGGCCATGATCAAAATAATCACCGTGTGGACCATTTCTATAGG[T/A]GAGAGAAGCATTCAGTGGTGAGAGTTACAATAATGGGTAACACTTTACAATAACAGTACATGAATAATGATGTATTAATAAGTAAACTAAACATTACTTTATTATGAATCAATGATTAGTTAAGGTATACACTAATCAAGAATAACTACATCATGAGTTACATGAGTTCATGTGTGAATAACGGCTACCTTAATCACTTGTTAGTACATGTTGTTAATTAATGTATTAATTAACATTTAAGTTTAAGCTAAATGTAACCAACATGAACTCATGAGCTGTTAATGTATAGTTATATCATGACTTTACTTGGAGGGGCACATCACTATTAACTCATCCTTAACTACTCATGAACTCCTGTTCATGTTGATGTTGACCAACACTTATCTGGTGTTATTCAGTTTAAACCAAGCGGCAACCTCCCGCTCTCCCTCAGGAAGCCAATACGGAAGTAACTAAAACTGCAATTCATCCGAAATTCCGCTAGTCCTGGCCGCTCCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43720
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 |
---|---|---|---|---|---|
ENSDART00000036537 | Nonsense | 312 | 355 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 42015362)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43614408 |
GRCz11 | 21 | 43609584 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATCACCAATGTGCTGAACGCCATCTGTCGGGACAACTGTAGCGAGTA[T/A]GTTCATAAACTCCTCGATATTTTCGTCTGGGTGGGATACGTCTCGTCTGG
Long Flanking Sequence:
GTACTTCACATTTGTTGTTGTTTTTTCTGTCTTCCAGTGTTGTCCCTGCCCATTCCAGTGATGGGTTTGCAGGATGAGCAGAAGGTGTTTATAGACTGCGCGTGTGTCCTGAACGAGCCTCGCTTTATCCTCGTTGGCTCCATCGTGGCCTTCTTCGTTCCTCTGGTCATCATGGTGGTCTGCTATTACCTCACTCTCCATCATCTCCAGAAACACAGCAAGTCCTTCCCGCACGACAGCAAGAGCTCCTGCATGCATTCGTCCATCGAAACAAGTGACACAAGCTTCCTAAACAGCAAGTCCTCCTCCAAAATGTCAGCGTTTCCGGTTATCAAACGCTCGCCGCTCAAAAGCAGACAAGGCATGAATCGAGCTTTGGAAAATGAACGGCGAGCCTCCAAAGTCTTGGGGATCGTCTTCTTTCTGTTCCTGATCATGTGGTGTCCGTTTTTCATCACCAATGTGCTGAACGCCATCTGTCGGGACAACTGTAGCGAGTA[T/A]GTTCATAAACTCCTCGATATTTTCGTCTGGGTGGGATACGTCTCGTCTGGAGTGAACCCCCTGATTTACACCCTTTTCAACAAGACGTACCGCCAAGCCTTCGCTCGATACCTTCGCTGTAAATTTCACTAGGAAACACCACAGGAGAAGTCTGAGGTCAGCGGACATCATGGCAGTCTAAGTGCTAAATGACTATCACAAACACTGTCAATGTTTTTTTTTTATTTCCTATCAACATTTACATTTAGCAGACGCGTTTGTCCAATGCAACTTACAATTACGGAGGCATTCTGCGACTAGACAAGAAGAGGCAATACAAACAAGAAGTGCTGCTTATACACATGAACTGTCAGTGCTCTGGGAATTAAATGCTGGAGTAAAGAGCGGGGAGTGTTTTTATAGTGTTTCTACAGGTGGTTTGTCAAGCCCACTCACCTGTGTGAAGCACACTTCCAAATGCAGACATGAAGGCTGCGTCCGAAACCGCCTACTACTCAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12052
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000036537 | Nonsense | 348 | 355 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 42015256)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43614302 |
GRCz11 | 21 | 43609478 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCCCCTGATTTACACCCTTTTCAACAAGACKTACCGCCAAGCCTTCGCT[C/T]GATACCTTCGCTGTAAATTTCACTAGGAAACACCACAGGAGAAGTCTGWG
Long Flanking Sequence:
TCCTGAACGAGCCTCGCTTTATCCTCGTTGGCTCCATCGTGGCCTTCTTCGTTCCTCTGGTCATCATGGTGGTCTGCTATTACCTCACTCTCCATCATCTCCAGAAACACAGCAAGTCCTTCCCGCACGACAGCAAGAGCTCCTGCATGCATTCGTCCATCGAAACAAGTGACACAAGCTTCCTAAACAGCAAGTCCTCCTCCAAAATGTCAGCGTTTCCGGTTATCAAACGCTCGCCGCTCAAAAGCAGACAAGGCATGAATCGAGCTTTGGAAAATGAACGGCGAGCCTCCAAAGTCTTGGGGATCGTCTTCTTTCTGTTCCTGATCATGTGGTGTCCGTTTTTCATCACCAATGTGCTGAACGCCATCTGTCGGGACAACTGTAGCGAGTATGTTCATAAACTCCTCGATATTTTCGTCTGGGTGGGATACGTCTCGTCTGGAGTGAACCCCCTGATTTACACCCTTTTCAACAAGACGTACCGCCAAGCCTTCGCT[C/T]GATACCTTCGCTGTAAATTTCACTAGGAAACACCACAGGAGAAGTCTGAGGTCAGCGGACATCATGGCAGTCTAAGTGCTAAATGACTATCACAAACACTGTCAATGTTTTTTTTTTATTTCCTATCAACATTTACATTTAGCAGACGCGTTTGTCCAATGCAACTTACAATTACGGAGGCATTCTGCGACTAGACAAGAAGAGGCAATACAAACAAGAAGTGCTGCTTATACACATGAACTGTCAGTGCTCTGGGAATTAAATGCTGGAGTAAAGAGCGGGGAGTGTTTTTATAGTGTTTCTACAGGTGGTTTGTCAAGCCCACTCACCTGTGTGAAGCACACTTCCAAATGCAGACATGAAGGCTGCGTCCGAAACCGCCTACTACTCAGTAGGTACTGCATTTGAATTTAAACGTACTACTCGGCCGTTAGAAAAGTATGTTCTATACAGTATGAATGTGAAAAGTATGAATGGAATTCGGACATACTACATCCGCC
Associated Phenotype:
Not determined