ZMP

ENSDARG00000086566

Ensembl ID:

ENSDARG00000086566

Human Orthologue:

GPR144

Human Description:

G protein-coupled receptor 144 [Source:HGNC Symbol;Acc:18651]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa18623	Essential Splice Site	Available for shipment	Available now
sa3168	Nonsense	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa18623

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
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Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124937	Essential Splice Site	78	210	3	6

Genomic Location (Zv9):

Chromosome 22 (position 22853815)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	22465451
GRCz11	22	22490429

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CRTCTCTCTGTGCACTGCTGGTGACCTTGATGCTGTTTACYGTGTTGGAG[T/C]AAGTGCTTTTYACCCATAYACCGCATCATTCACCGTCTTTATCATGTCTG

Long Flanking Sequence:

TTTTTAAAGTTATAACATTCCCTGTATAATAATGTTCATATACATTTTTGAAGCCTTGAATATAAGATAATGTTTCCTAAAAATAATTATTCCTTATAAAATGTTTTGTAATGAAATGAAAAATGATTGTGTTTTTAAATGTTACATTGAATATCTGTTTTAACACAATCTGTCCAGTAGAGGTCACTGTTAGCTTACAATTGTCCTAAATAAAGCCTTAGTGAATTAGCATCCAGCGTTATATGTATATGTTCTCTGTAAAACTTTATAAACAGCAAATATGATTTTACTTTAATCCTAAACAGGCATTACATTACTAAAACATATATATCTCTCATATCAGTATATGAGCATAATGGCTCCACAATTGTGTTTTGATGGCGTTTTCTCCACAGTGGAGCGCTACAGAGGAGAGTGTTCTGACGAAGCTGACGTTTATCGGGTCTGGAGCGTCTCTCTGTGCACTGCTGGTGACCTTGATGCTGTTTACTGTGTTGGAG[T/C]AAGTGCTTTTCACCCATACACCGCATCATTCACCGTCTTTATCATGTCTGACTTCTAGTGTTGGCTTCCTGAGGACTGTAATGGGGGTCAAAAGTGCCACCAATACGCCTAAAATTATTATATTTTTTTCAACTGGTGCTAAATTATTTTTTAGTAGCTATAAAGATTTATATACATTATTTTATTAAAAAACTGAAGAAATAAGCTCTTAATCAAATGGTTTTGCATTATTTATTTTGTGAACGTTGTGTTATTTAAATTAGCTTTTGTTTTTCATTAATTTTATTTACATTTTTGTAATTTTTTTGCACTGTTTTTAGTACTAACATTTTTATTATATGCAAAATTTTTTAAATAGTTATTCTCATTCATTCATTTTCTTTTCGGCTTAGTCAGTTTAATAATCTGGGGTCGCCACAGCAGAATGAACCACCAACTTATCCAGCATATGTTTAATGCAGTGGATGCACTTCCAACTGCAACCCATCACTGGGAAACAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa3168

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124937	Nonsense	181	210	6	6

Genomic Location (Zv9):

Chromosome 22 (position 22861111)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	22472747
GRCz11	22	22497725

KASP Assay ID:

554-2798.1 (used for ordering genotyping assays)

KASP Sequence:

CTGCCAGTGCTGATCGTCACCATCACACTGGCCTCWGCCTCTGGGAAATA[C/A]ACTGCTGAYGGTCACTGCTGGCTCAGTGTTCAGAAYGGCGTCATATGGGG

Long Flanking Sequence:

ATCAGAGGAGGAAAGCCCCGCCCATTAGTGACGATCTCACTAAAGCACAGGCATTTGTAGCTCCACCCTTTGGCTGCGAGCATTTGAATTTAAAGTGACAGTCACCAAAAGGCACAATTATGATGAAAGCTATTACGGGCAGTTTCTAGGAGTTTTAAAAAATGATCTGTGGTGTATTTTGAGCTGAAATTTCACATAAACACTTTAGTAACATCAGAAACCTCTTTTAAAAAGATTTTGCCTCGTTTAAAAAGTGCAATAACAGGTCCTTAGTAAAGGAAAAGCAGATATACTGATCATAATAAAGACCAAAATGATCAAACTAGTTAAACAATGGCTCTGAAAACTGCTGTGTCACTCGTTTCCAAATGCAGTTTGGTTTATTTGTATAATTTATTCCCCGTCACTGTCAGTCATGTGTATTATAGAAATGTGTGTTGTTTGACAGGTCTGCCAGTGCTGATCGTCACCATCACACTGGCCTCTGCCTCTGGGAAATA[C/A]ACTGCTGACGGTCACTGCTGGCTCAGTGTTCAGAATGGCGTCATATGGGGCTTCGCAGGACCTGTCATCTTCATTATTATGGTGTGCCCTTACTTCTATTATTACTGTTTCACACTTTAAAATACAAATGCTAAATGAATTATTTAGTTATTTAACCATATCCAAAATAAAGTGTGTTTGGAGTGTATTTTTTATTATATAAATACACACATTCATGTACAGTGTATATATTTGTTTTCAATTCATATTTATATATAAATATTCATATGTACAGTTAAAGGCAAATGTATTATTGTGAACGTTTTATTCTTTTTCAAATATTTCCTAAGTGATGTTTAACGGAGCAAGGAAAATTTTTCACAGTATTTATTATCATGTTTTTATCACAGTATATATTAATATTTAAGTATAAGTATATTAAATATATAAGTGTATTTTTTTCTTATGGAAAAAGTCTTATTTTTAATTTTTAAAGCAATTTATTATTTGCTCCATTCAAT

Associated Phenotype:

Not determined