ZMP

B0V213_DANRE

Ensembl ID:

ENSDARG00000077310

Description:

Novel protein with a Pentaxin family domain [Source:UniProtKB/TrEMBL;Acc:B0V213]

Human Orthologue:

GPR144

Human Description:

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

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa13107	Nonsense	Available for shipment	Available now
sa34518	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa13107

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109328	Nonsense	401	1066	6	25
ENSDART00000131450	Nonsense	426	614	7	10

Genomic Location (Zv9):

Chromosome 8 (position 54892827)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	52812517
GRCz11	8	52798810

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGAGAGAGTCTCTGAGGTCCAACCCCAGTCCCTTCATGCARAGTCTCATG[C/T]WGTACGGCATGGTAGGAGCTTTTTACCRTTAATATRGCACACACAATTTC

Long Flanking Sequence:

GAAATTTTCCAGAAATTTACCGGTATCACTGTGTGAAAGGGGCTGTTGTGTGTGTGTGTGTATATGTGTGTCTGTCTGTGTCATGTGTGTGTGTGTGTGTGTGTTTGTGTGCGCGCCAGTGTGCGTGCACCTCTGAGAGAGAGTGTCAATATGGGATTGCTCACCCAAAAATTAAATTGTTCAGACATAAAAAAAAACAAGATTTTTAGCTGAGTTTGTGGTGCTTGGTGATGCATAAAATGCAAGTCAGCGATTATTAAGATTAAAATGAAAGCATCTCGTGCTGTAAAATGTTACCAAAAAAGACACTCGCTGTCTTCAATGAGCTGAGTGTGAATAAATTAAGTGTGCGTTTTCAATTTTGGGTGAACTATCCCTTTAATGTCTGTATGTGCAGTTGTGAATGTGTTTATGTCTGGTTCACAGAGCACTATCTGAAGATGAAGGAGCTGAGAGAGTCTCTGAGGTCCAACCCCAGTCCCTTCATGCAGAGTCTCATG[C/T]AGTACGGCATGGTAGGAGCTTTTTACCATTAATATGGCACACACAATTTCATCAGACTATCATGACATATAACCAGAAACAGTAAAGTGATTAATGAAAATCATTAGTAATGCTATTGTGAAATGGCAACATTTTATAATGTATTTCAATAAGTAAACATTTATCATGATAGAGTTCATATTGCAACACCACAAAATAAACAATACTGCAAAATACGAATCTATAGACTTTAATTCATCCTCACTATATATGTAACAGTGCTCAAAGTAATTGAGTACACCCCATTTTGAAAATGAATATTTGTATTTATTTCTCAGGGAATATAGGCAGAGTATTTTGGTGCTTTTAAACAAAACAGATTTATTAAATAGATATAGTAGATATATTTATTAAAATAATATTTTAGTCAACAACTATTTAAAGAAAATGCAATTAGATTCAAGCAAAATAAAATTATAAACTTCAAAATCACAACAAAAAATGTAATTTTTTTGCTTCTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34518

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109328	Essential Splice Site	872	1066	17	25
ENSDART00000131450	None	None	614	None	10

The following genes are also affected by this mutation:

ENSDARG00000094891

Genomic Location (Zv9):

Chromosome 8 (position 54876303)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	52829041
GRCz11	8	52815334

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTCCAGTGTCATTTGGGCTTTTGCAGGGCCGGTGCTCTTTGTTTTGGCT[G/A]TAAGTATGTCTTTTATCTTATTTCAGCTAATAGGATTGTAGAATACTGAT

Long Flanking Sequence:

TCTTTTCGGCTTAGTCCCTTAATTAATCAGGGGTCAACTTATCAGCATATGTTTTACGCTGCGCATACTCTTCCAGCTGCAACCCACCAGTGGGAAACACCCATACACTCCCATTCAAACACACACGCACAACACTACTTACCCTATACCACATGTCTTTAGACTGGGGGGGAAACCGGAGCACCCGGAGGAAACCCACACCAACATGGGGAGAACATGCAAACTCCATACAGAAATGCCAACTGACCCAGCTGATCTTCGAAGCTGTGAGGCGACAGCGCCTCTGTGTGTGTGTGTGTGCATGCATCTCTAGTTTTAATTGATGTTCTGTTTGATTGGTGTTTCTGTCTCTGCTGTGTGTGTAAGGGTTGCCGGTGGTTATAGTGGCTGTGACTTTGGTGGCCACTCTGGACCAGTATAAAGCACAGCAGCACTGCTGGCTGAACCTCCAGTCCAGTGTCATTTGGGCTTTTGCAGGGCCGGTGCTCTTTGTTTTGGCT[G/A]TAAGTATGTCTTTTATCTTATTTCAGCTAATAGGATTGTAGAATACTGATGTGTTGTCCTCTCCCATGCACTGCACTCTGAGTTTACCAACTGATGACTTCTGCTGCAGAGAAACACACACATGTGAAAAGGCTCTATACTCTGCTGAGTGTGTGTGTGTGTGTGTGCGCAGGTGAATGCCGTGGTGTTGTTTCGTGTGGTTCTGGTCACAGTGTCCAGTGCTAGGCGCAGAGCCAAGATGCTGACCCCCAGTTCAGACTCCAAACTGCACACGCTGGACCTCACCTGGTGGGTCACACCTGCAGATACAGCAGCAAACAACCGGCAGACATTAACAATAACACATGCTCGAGTGAGCAGCTGCAGTGTTTCTGTACTGGGTGCAGATGTAAAGTCACTCCAGTTATTCGCTAAATGTACTCAAATGTTTAGAAAGACTTAATCTGTTTTGTTAGATATTTCCTAAATGATGTTGAACAGATTCAGGAATTGTTCACAGT

Associated Phenotype:

Not determined