ZMP
si:dkey-29d8.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vasoactive intestinal peptide receptor 1 (Vipr1) [Source:UniProtKB/TrEMBL;A
Human Orthologues:
GHRHR, SCTR
Human Descriptions:
growth hormone releasing hormone receptor [Source:HGNC Symbol;Acc:4266]
secretin receptor [Source:HGNC Symbol;Acc:10608]
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]
secretin receptor Gene [Source:MGI Symbol;Acc:MGI:2441720]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32895 | Nonsense | Available for shipment | Available now |
sa8766 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32895
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046127 | Nonsense | 58 | 440 | 3 | 13 |
ENSDART00000135288 | Nonsense | 35 | 417 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 21039040)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 21584978 |
GRCz11 | 2 | 21243040 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCCATTTCTTTGCTAAGGTTGCACAGGTGAATGGGATCTGGCGTGTTG[G/A]CCATCAGCTCGCATTGGAGAAGTAGTCACCATCCCCTGTCCAAACTACTT
Long Flanking Sequence:
TGGCTGCAGTGTATGATTCTGTATGTGAATGTTTTTTTCTAGCTTGGTGCTGGATTGTGATTGGAAGGGCATCCCCTGCGTGACAAACGGCGGTTCATTCCACTGTGACAATAAATCAGGGACTAAGCTGAAGGAAAATGAATGAATGAATTTACCTATATGTGGGAAATAATAACAAATGCAAAAACTGTCAAATTGCTTTCTTTATATGCACGTGTTTATGACTTTAAATCAAAATAATATAATATGAATGCCAGTTTGCAACATCAAACAGCAAAACAAGCTGTATTTTATATCCAAAAATCAGTGGAAGTGTATGACTTAAAGTGAAGTCTTGATACAAAAAAGGTCCCAATAGTTTGGCCACTGTTACCTGAAAAAATACTTGTTAAGTTTATCTGCTTATGATTATTAAAATTAAAGTATGTTTCTATTATCTGTAATAATTTGTTCCCATTTCTTTGCTAAGGTTGCACAGGTGAATGGGATCTGGCGTGTTG[G/A]CCATCAGCTCGCATTGGAGAAGTAGTCACCATCCCCTGTCCAAACTACTTCAGCCATGTCAGTGATCAAATAGGTATGGACACATATTTTCTAATATGTTTTTGTTTTTAACTATTCTGCAATGTCTTTGAAGGATATTTCAGAGAATGTCCTGGTTGTGACTGAATTAGCATCATAACCGCTGTCAGATCTTTTTCACTTTTTTCTGATTAGTCTTTGATGACTACAGACAAGGGAAATATTGTCTATGCAACTGGGATCTGCTGCGTGATATTTGGCAGATACACTGACAAATAAACCGTATTCTTGGGACTTTCTCTAAGGAGAACCTGGTGGGCCAATTATTTGTTGAGATTTGTTGAGTGATGCAATTTATTCAAAGGAAGAAAGCCATGGCTAACTTTTAATGCTGTTTGGTAAGCCTTTTGTAGTTGCGTTGGGCTAATCAGGATTAGCTGTGGATTCGGCAACTAAACAGAACATCAAACGTGCCTGTGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8766
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046127 | Nonsense | 256 | 440 | 8 | 13 |
ENSDART00000135288 | Nonsense | 233 | 417 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 21082241)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 21628179 |
GRCz11 | 2 | 21286241 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGTGTGTGTGTGNNNNGCAGGAGTTCMAGGTGTCTTCATCACAATCT[G/A]GAGCATCACAAAAGCCTAWTTACATGATATCGGGTGAGGGAATGCAGCTT
Long Flanking Sequence:
GCAAACTAAAGTTTAATAAAAGATTATTTTTGTTAGCTAAGATTTATTTTTATTTTTTGGTGTTCAATACAGTAATTTTGTATGTAATAAATATGTTTCACTCCTAAAGTGATGGTAGCAATTCCCTTCCATTTTTTTGGAACCACCAAACATCACAGTTTCAGGTAAAATCAATTTCTGTAGTGTTCTAAATGATGAAAATATAATCTATGTACATGATGGATGGCCTTAATGAGCAAACAGACAGCAACTTTTCATTTTTGAGTAAACTATCTCTAAACTATCCCAATGAATCCCTGCAAACATAGAAACTCCAATGTCAACATGCCTGTAAAGCTGTATGTAATCAAATATTGACAGTATTCATAGTCAACATGTGTGTTTGTGTGTCTGTTTGTGTGTGTGTGTGTGTGTGCGTGCGTGCGTGCGTGCGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGCAGGAGTTCCAGGTGTCTTCATCACAATCT[G/A]GAGCATCACAAAAGCCTATTTACATGATATCGGGTGAGGGAATGCAGCTTGTTTGCCACTTTGCAATTTTTGTTTTATATCTGCTTTTATGGGAGCCGTAAAACCCCTTCTGCCACTGTTATGTAAGACTACCAATTAAAATGAGTGAAGATGTCAGTATTTTTTTATGAGTTTATAGAGTTTATGAGTTTAGATTAATCTTTTTTGCCGATGTCAAAAGTAAAGCTGACACTGTGAAATCAATTCGAATCACTTCCTTAATGATAAATGGCATCCCTTCATGGAGGTCAGATGTCTATATTTAGATGCAGCTCGTATAGAGAATACATCTGAACAGATTTCCTGTGTATATTTTCATTTTCATTGCCATCAAATCTGCACATGAACAGTAGAGAGCAACATTAATTCAAAAGCAACTAACCATTATTATCAGCACTCTTAGTTCTGGAAATATTTTGAAATATTTGAGTAAAATTAAATACATGGGGTGGGGGGGGTGG
Associated Phenotype:
Not determined