ZMP

mtnr1c

Ensembl ID:

ENSDARG00000035609

ZFIN ID:

ZDB-GENE-990415-158

Description:

Melatonin receptor type 1C [Source:UniProtKB/Swiss-Prot;Acc:P51052]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa20390	Nonsense	Available for shipment	Available now
sa9234	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa20390

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

Mutation:

T > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000051622	Nonsense	191	361	2	2
ENSDART00000121608	Nonsense	142	304	3	3
ENSDART00000128781	Nonsense	191	361	2	2

Genomic Location (Zv9):

Chromosome 5 (position 24448671)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	22161543
GRCz11	5	22665343

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GACCCGCGGGTTTTCTCCTGCACCTTCACCCAGACAGCGAGCTCTTCTTA[T/G]ACAGTCTGTGTTGTTCTGATCCACTTCCTTGTCCCGTTGGGTGTGGTTTC

Long Flanking Sequence:

ATTCAGTAGCATAAAATATATCACAACAATTTCACAACAAAATCATAACAGGCCTTTACACCATAACAAACAGCAGCTTGTGATTTTTCTTATAAAAACTAATCTGTTTTTCAATCTCTCATAGGTAACATCTTTGTGGTGAGTCTTTCTGTGGCTGACCTGGTGGTGGCGCTATACCCCTACCCGTTAGCTCTGATCGCCATCTTTCACAATGACTGGACGATGGGCTCCCTGCACTGCCAGCTGAGTGGCTTTATAATGGGTCTGAGTGTGATCGGCTCAGTCTTCAACATCACAGCTATCGCCATCAACCGCTACTGCTACATCTGCCACAGTCTTCGCTACGACCGACTGTATTCACGCCGAAACACCTGCCTGTACCTGCTGCTCACCTGGATGCTCACTGCTTTAGCCACCGTCCCGAACTTCCTCGTAGGATCCTTAAAATATGACCCGCGGGTTTTCTCCTGCACCTTCACCCAGACAGCGAGCTCTTCTTA[T/G]ACAGTCTGTGTTGTTCTGATCCACTTCCTTGTCCCGTTGGGTGTGGTTTCTTTCTGCTATCTGCGCATCTGGACGTTGGTGATCAGGGTTAAAGGACGCGTGCGGCCCAATCCAAAAGTCAGAGCGGCTGATTTGAGGAATTTCCTGACAATGTTTGTGGTGTTTGTGCTATTCGCCGTGTGCTGGGCACCTCTAAACTTCATTGGACTAGCGGTGGCCATTAACCCCGCAAAAGTGGCGCCCAATATCCCGGAGTGGTTGTTCGTTACCAGCTACTTCATGGCGTATTTCAACAGTTGTCTGAATGCTGTGGTTTACGGATTACTCAATCAGAACTTCAGACAAGAGTACAAACTAATTCTTCGTGCTCTTTGCACACCGAGAGCGCTGTTTACAGACAGTTCCAGGTATAACACTGAAGCCATTAAGAGTAAACAGTCGCCAGCGGGAACGAATAACAATGTGAAAGAAGCCAATGCGTATAAAGGCGGAGTGACACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa9234

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000051622	Nonsense	236	361	2	2
ENSDART00000121608	Nonsense	187	304	3	3
ENSDART00000128781	Nonsense	236	361	2	2

Genomic Location (Zv9):

Chromosome 5 (position 24448805)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	22161677
GRCz11	5	22665477

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

YAGGGTTAAAGGACGCGTGCGGCCCAATCCAAAAGTCAGAGCGGCTGATT[T/A]GAGGAATTTCCTGACAATGTTTGTGGTGTTTGTGCTATTCGCYGTGTGCT

Long Flanking Sequence:

TGTGGTGAGTCTTTCTGTGGCTGACCTGGTGGTGGCGCTATACCCCTACCCGTTAGCTCTGATCGCCATCTTTCACAATGACTGGACGATGGGCTCCCTGCACTGCCAGCTGAGTGGCTTTATAATGGGTCTGAGTGTGATCGGCTCAGTCTTCAACATCACAGCTATCGCCATCAACCGCTACTGCTACATCTGCCACAGTCTTCGCTACGACCGACTGTATTCACGCCGAAACACCTGCCTGTACCTGCTGCTCACCTGGATGCTCACTGCTTTAGCCACCGTCCCGAACTTCCTCGTAGGATCCTTAAAATATGACCCGCGGGTTTTCTCCTGCACCTTCACCCAGACAGCGAGCTCTTCTTATACAGTCTGTGTTGTTCTGATCCACTTCCTTGTCCCGTTGGGTGTGGTTTCTTTCTGCTATCTGCGCATCTGGACGTTGGTGATCAGGGTTAAAGGACGCGTGCGGCCCAATCCAAAAGTCAGAGCGGCTGATT[T/A]GAGGAATTTCCTGACAATGTTTGTGGTGTTTGTGCTATTCGCCGTGTGCTGGGCACCTCTAAACTTCATTGGACTAGCGGTGGCCATTAACCCCGCAAAAGTGGCGCCCAATATCCCGGAGTGGTTGTTCGTTACCAGCTACTTCATGGCGTATTTCAACAGTTGTCTGAATGCTGTGGTTTACGGATTACTCAATCAGAACTTCAGACAAGAGTACAAACTAATTCTTCGTGCTCTTTGCACACCGAGAGCGCTGTTTACAGACAGTTCCAGGTATAACACTGAAGCCATTAAGAGTAAACAGTCGCCAGCGGGAACGAATAACAATGTGAAAGAAGCCAATGCGTATAAAGGCGGAGTGACACACACTCTATTCTAGTAGATCGCTTCTTGTTTACCGAACAACCATAATATTATGGTGCAAGGGGGCTAAAGGTGCACAAGGTAAAATAAATTTACATATATTTACATATAACATTACATTTCCAAACAACATACAC

Associated Phenotype:

Not determined