Busch Lab

ZMP

mtnr1al

Ensembl ID:
ENSDARG00000012057
ZFIN ID:
ZDB-GENE-990415-154
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
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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:
sa10002
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:
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