ZMP

vipr1

Ensembl ID:

ENSDARG00000059058

ZFIN ID:

ZDB-GENE-050311-6

Description:

vasoactive intestinal peptide receptor 1 [Source:RefSeq peptide;Acc:NP_001013371]

Human Orthologues:

GHRHR, SCTR

Human Descriptions:

growth hormone releasing hormone receptor [Source:HGNC Symbol;Acc:4266]
secretin receptor [Source:HGNC Symbol;Acc:10608]

Mouse Orthologues:

Ghrhr, Sctr

Mouse Descriptions:

growth hormone releasing hormone receptor Gene [Source:MGI Symbol;Acc:MGI:95710]
secretin receptor Gene [Source:MGI Symbol;Acc:MGI:2441720]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39446	Nonsense	Mutation detected in F1 DNA	Not yet available
sa45828	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39446

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
ENSDART00000082062	None	None	422	1	13
ENSDART00000143759	Nonsense	9	446	1	13

Genomic Location (Zv9):

Chromosome 24 (position 21416461)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	20663590
GRCz11	24	20808009

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAAAATTAACAAAGAAAACGCAACGATGGACGCCTCAAAAGTGGTTTTAT[T/A]GGCTTCAGCGTTTGGCTTCGTGTTTTCTCCGGTAAGTGTTTGTTTTGGTA

Long Flanking Sequence:

CAGAAAGCAATAATAACGGAAAAGAAAAAAAAACTCCCACCTGAGTCATTTTCTACGGCCAGGTGTTCACAAAGAGCACAGACCTTGAAATTTAACCCACTGCTTTCGCACTAACGCAACAAAGGCATTCGTAAGCCGATGACGAACACTAGTGATGCAGTCTTCAGTGTATTGTCAACATCTTGCAAGTAGTGAAGCTGTGAAGCTCTTCTCGCGCTCTGCCTGTGATTCTCTCATTGGTCGCTGAACTGTCAGCAGCTCGAGCCGCGATATGAGCCACTCACCCGGAGGACAGTTCACTCACGGCTCTAGTGATGCTCACACATATAAACTTGCTATGTTTTACTCGTCTGCCAGCGCCGCGTCCGATAACATTTGACTGAGGTTGCTTTTACGCGCTTGTAAAGCAGGATAAACTTTATGGACTTTTAAGTTTCTACACGATAAACAAAAAATTAACAAAGAAAACGCAACGATGGACGCCTCAAAAGTGGTTTTAT[T/A]GGCTTCAGCGTTTGGCTTCGTGTTTTCTCCGGTAAGTGTTTGTTTTGGTATTTTAAATAGCTCTGTGTTTGATTGCGGTCGATGAGGTAATGTGGATGTTTGCATGTATTTAATCCATTTAGTGGGAATGACACGCAATTTGTGTAAAGATATAATATTATTTACCTCATATCTTTAGTAAAACCAGCAATTCTTACTAGAAAGCCACTAAAAAGTTGGATGCTGATTCAACAGACCGAAAGCAGAAGTGCGCGCGCATGGCACGGTCCATCGAAGAAGCGTTTTTTACTTTATAAAGGCATAATTTGGGCTAAGGAAGTCATTAATGATGTTTCGAACACCTGATATACAGGCGTAGTTTTCTTTTCTTTTTTTTTTTTTAAATATAACGCATGCATGTTGCCTGTTTAACCATGCAGATGCGCGCGCCCTATACCAGAGAGCAAGGAATTTTATCATTGCTAGCAATTGAAGTCATTTAAACATGTTTACTCATGTTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa45828

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
ENSDART00000082062	Essential Splice Site	25	422	2	13
ENSDART00000143759	Essential Splice Site	49	446	2	13

Genomic Location (Zv9):

Chromosome 24 (position 21387223)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	20634352
GRCz11	24	20778771

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCTGGCAAGAGCGAGGTGTGAGAATAAAACAGCAGGAAATGTCACATCAG[G/A]TAATTTTCAAGAAACAATGTTGCTTTGTGCCATTTTCATAGTCATTAAAC

Long Flanking Sequence:

GGAAGCACCTATTTGTCTGCTTTCCCTGTTAAATAATAACTAAAAAAGAACAAAATTATAGGAAAATCTATGTAAAAAAAACCTCTGTAAAAGACCTCCAAAACAAATGTAGGCAGCTTTAAATTAGCATAATATGGACAATTTAAGTTTGTGGCTATTTTAAGCAGTGGATGAGCTAATGCTGTAAATGTTTATCCAAAATAAGCCCCTGTGAGGCTCTGCTACAATCCATAAATATGCATATGAAATGAAAGCCTTACAAGATGAAAGCTGACACCTTAAAGTAATAGACTACCCGGAGAGTATTATTGTAGTGAATCACTGAGATGAACAAGATTGAAGCTTTGAAGGCTGTGCTGTGTTTTAACAACTCAATTTTTTTTCTCTCTCTTCACTGTGTCTATTACAGGTTGCCGCTGTTCAGATGTGTGACGTGGTAAATGAGATTGAGCTGGCAAGAGCGAGGTGTGAGAATAAAACAGCAGGAAATGTCACATCAG[G/A]TAATTTTCAAGAAACAATGTTGCTTTGTGCCATTTTCATAGTCATTAAACAATTTTGCATTGATGAGGAAAAATGGATGTTAACTGTAGATCACAGAGATATGAGATTTGGTGCAGAAACAGGATATTTTGTTGCAGTTCTAAATAAAAAAAAAAAAACAGAGTAAAAAAATAGCAAAAATGTACTGTATATACTGTAAACGTGTTTTTTATGTTGTGCATCTATTGCACAAAGTCTTTTGCATAATTCTATTTTCCCTATTTATTTTTAGTAATTAATATTTACATAACAAATTACATGGGCGATGCAGTGGCAGAGTTTGTAGTGCTGTTGCCACGCAGCAAGAAGGTCACTGATTCGAGTCTCTGCTGGGTCAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGTGTTCGCGTGGGTTTCCTCCGGGTGCTCTGGTTTCCCCCACAGTCCAAAGACATGCGGTACAGGTGAATTGGGTAGGCTAAATTGTC

Associated Phenotype:

Not determined