ZMP
mtnr1al
Ensembl ID:
ZFIN ID:
Description:
Melatonin receptor type 1A-like [Source:UniProtKB/Swiss-Prot;Acc:P51047]
Human Orthologue:
MTNR1A
Human Description:
melatonin receptor 1A [Source:HGNC Symbol;Acc:7463]
Mouse Orthologue:
Mtnr1a
Mouse Description:
melatonin receptor 1A Gene [Source:MGI Symbol;Acc:MGI:102967]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10503 | Nonsense | Available for shipment | Available now |
sa38998 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10002 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10503
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 |
---|---|---|---|---|---|
ENSDART00000131008 | Nonsense | 25 | 344 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 27103644)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 25796846 |
GRCz11 | 14 | 26094091 |
KASP Assay ID:
2260-7572.1 (used for ordering genotyping assays)
KASP Sequence:
CGCGTGGCACGGAGGACCGGACCCCTCGCCGCTGTCCTGTTAYGATGAAT[T/A]GAGGATGGTGGAGGGAACAGACGCCCCATTGAAGAWCATTTCGACAGGAA
Long Flanking Sequence:
AAGACAGCTCCATGGATCTCCCGCTGCGTTTCACGGTGGTAACCAACTGAGAACTTTTTAACTTTGGGAGGCGCTTATCCAGCCTTTATCCGCCGGCGACTTCTTGGAGTGAATGAAAGACGCGAGGCAAAGAAATGAGTGAATGGACATGACTTTTTTATTTCATGTGCACATGAATCACCCGTGTGAATGGGCGTTTTGTCAAGAACAGCGCGCTTCACAAGTTCTCATGATCGCAGGATTACAAACGTCCCTCCAGTTATCAGGATTTTATGTCAGCAAATGAGTTTGAATTGCAGCAGTTTTATTTAACACGCTACTTACATTAAAGCAGTCATTATTTTTATATCGCATCCAATTCCTCCAATGGCAGCTGTAAGAGCGCACGGCTGAACTGGAGCTCTACCCGCCGCTGCTAGGTGTCTGGATGCGCCCGTTGCGCGGTAGATGCGCGTGGCACGGAGGACCGGACCCCTCGCCGCTGTCCTGTTATGATGAAT[T/A]GAGGATGGTGGAGGGAACAGACGCCCCATTGAAGAACATTTCGACAGGAAATCGCGATATCAAGTACCTCTCCTTCCCCTGGGTGGTGACTTTACTCTCCAGCGTTCTGATCACTACCATTGTAGTAGATGTTCTGGGCAACCTGTTGGTCATTGTGTCAGTCTTCAGAAACAGAAAGCTCAGGAAGGCAGGTAAATGTCTTCATCTCTTTAATGCATCTTGCTGACGGTGATTTATTCGTGATTTATTTGTCCAGGACTCTGTGCATCACGTTATTAGAGATATCTCTGAATGAGCCACAACAGAGCATCTTGATTTTATTTGTGTTTTATCGACAGAGCAGTGACTAAATAATTAGTTTGCAACAATTACATTAATTAAGAGCATTTATTTCTAGTATTATTTGTCTTGGTAACCTTGAGATGAACTGAACAATGTGCAAACCTTCCTCCAAAACCAGTAGAGTCTAAATTAATTAAAAAGCTGATCAGTCTGACTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38998
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 |
---|---|---|---|---|---|
ENSDART00000131008 | Nonsense | 81 | 344 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 27103477)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 25796679 |
GRCz11 | 14 | 26093924 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATTGTAGTAGATGTTCTGGGCAACCTGTTGGTCATTGTGTCAGTCTTC[A/T]GAAACAGAAAGCTCAGGAAGGCAGGTAAATGTCTTCATCTCTTTAATGCA
Long Flanking Sequence:
TGCACATGAATCACCCGTGTGAATGGGCGTTTTGTCAAGAACAGCGCGCTTCACAAGTTCTCATGATCGCAGGATTACAAACGTCCCTCCAGTTATCAGGATTTTATGTCAGCAAATGAGTTTGAATTGCAGCAGTTTTATTTAACACGCTACTTACATTAAAGCAGTCATTATTTTTATATCGCATCCAATTCCTCCAATGGCAGCTGTAAGAGCGCACGGCTGAACTGGAGCTCTACCCGCCGCTGCTAGGTGTCTGGATGCGCCCGTTGCGCGGTAGATGCGCGTGGCACGGAGGACCGGACCCCTCGCCGCTGTCCTGTTATGATGAATTGAGGATGGTGGAGGGAACAGACGCCCCATTGAAGAACATTTCGACAGGAAATCGCGATATCAAGTACCTCTCCTTCCCCTGGGTGGTGACTTTACTCTCCAGCGTTCTGATCACTACCATTGTAGTAGATGTTCTGGGCAACCTGTTGGTCATTGTGTCAGTCTTC[A/T]GAAACAGAAAGCTCAGGAAGGCAGGTAAATGTCTTCATCTCTTTAATGCATCTTGCTGACGGTGATTTATTCGTGATTTATTTGTCCAGGACTCTGTGCATCACGTTATTAGAGATATCTCTGAATGAGCCACAACAGAGCATCTTGATTTTATTTGTGTTTTATCGACAGAGCAGTGACTAAATAATTAGTTTGCAACAATTACATTAATTAAGAGCATTTATTTCTAGTATTATTTGTCTTGGTAACCTTGAGATGAACTGAACAATGTGCAAACCTTCCTCCAAAACCAGTAGAGTCTAAATTAATTAAAAAGCTGATCAGTCTGACTAAGACCACCACATTAGTCAAGACAGGTTTAATTTGTTCTTCTTCAGTATAGTGTGTTCAACATTTATATTTGTATTTTTGAACTTTTTCTTTATACTTTATATAATGAAATGTATAAAACGATACAATTCACCAGGTTTATTATTATTAATAATCAATTTAATCTTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10002
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000131008 | Nonsense | 102 | 344 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 27086140)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 25779342 |
GRCz11 | 14 | 26076587 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCTTTACAGGAAATGCCTTTGTGGTGAGTTTGGCTATAGCAGATCTGW[T/G]AGTGGCCATCTACCCCTACCCGCTTGTCCTGACCGCCATCTTCCACGACC
Long Flanking Sequence:
AAACCAAATGAAATGTTTTTATAATATAAAGCATTTACATACATTCATTAGACTTGGATCAAATGGCTTGATTCAGAAAGATTTATTAAATTATATAAAGATTTAAAGGAACCTTAGAGGGAAAGAAATCCCTCACAAATCTTTAAAGATGTATTAACTTGTGATCCAAACATGAGCAGGACTTTTTGGTGTTTTTAATGACATGAACGTGAATAATTGATACAAATTTAAGGGTAAAACAAACTCAGTAAATAATCCTAAAAAACAATAATGTTGCTAATGTTGACATACATTTGAATGCACATTTGAGCATTCATTTTGAACACATTTGCAATGTTGTGTCTATACTCTTTCTTCCATGCTTGTAATATGTTTGAGAGCCTATTTCTGATATTGAAAATGCCATTTTTATTGCTTCTCTACACTAAGCACTTAAATAGTTTTTTCTCTCTTCTTTACAGGAAATGCCTTTGTGGTGAGTTTGGCTATAGCAGATCTGT[T/G]AGTGGCCATCTACCCCTACCCGCTTGTCCTGACCGCCATCTTCCACGACCGCTGGATCGCTGGTGATATTCACTGCCAGATCAGTGGCTTCCTGATGGGGCTCAGTGTGATCGGCTCCATTTTCAACATTACAGGCATCGCCATCAACCGCTACTGTTACATCTGTCACAGCCTTAAGTACGACAAGCTCTTCTCCAACAAGAACACGGTATGCTACGTAATCCTGGTCTGGGCGCTGACTGTATTGGCAATCGTCCCGAACTGGTTTGTGGAGTCTCTGCAGTACGACCCACGTGTTTTCTCATGCACTTTCGCCCAGTCGGTGAGTTCACTTTATACCATCATGGTGGTGGTGGTGCATTTTATTGTGCCCATCGGCATCGTCACCTACTGCTACCTGCGAATTTGGATCCTCGTCATTCAGGTCCGCAGACGAGTCAAGCCTGACAGTCGGCCTAAAATCAAGCCTCACGACTTCCGGAACTTTCTGACTATGTTTG
Associated Phenotype:
Not determined