ZMP

si:dkeyp-4h4.1

Ensembl ID:

ENSDARG00000021186

ZFIN ID:

ZDB-GENE-050208-334

Description:

Novel protein similar to vertebrate parathyroid hormone receptor 2 (PTHR2) [Source:UniProtKB/TrEMBL;

Human Orthologue:

PTH2R

Human Description:

parathyroid hormone 2 receptor [Source:HGNC Symbol;Acc:9609]

Mouse Orthologue:

Pth2r

Mouse Description:

parathyroid hormone 2 receptor Gene [Source:MGI Symbol;Acc:MGI:2180917]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa1706	Essential Splice Site	F2 line generated	Not yet available
sa1961	Nonsense	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa1706

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000004389	Essential Splice Site	171	487	5	11
ENSDART00000131611	Essential Splice Site	198	509	6	12

Genomic Location (Zv9):

Chromosome 22 (position 12035085)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	11895253
GRCz11	22	11924935

KASP Assay ID:

554-1652.1 (used for ordering genotyping assays)

KASP Sequence:

TTGGCTGGATTCAAACGGCTAGAGGATCCTGATTGGCTGTTTGTATTTTC[A/T]GTTTGGCTGCAAGATCACAGTCCTGTTCTTCATTTATTTCCTGGCGACGA

Long Flanking Sequence:

TATTAGTCTTGGTGTACAAACTAGTGCATAGTTGGCATAACGTTTAGTTGCTGCAGTTTTGTTCCTTGCAGAAACACGGTGTTGAGAAGCCTTTACGATTAATTAACCGTGACGAATTAAATCGCGGTTAATAGTGAAACCGGTTAATCGCATCCCTAGATGTAGAACACCCGAATTTCGTTCATACTCACATTCACACTGTATAGACCGTACTTTTCTAGCGGTCGTGTAGTTCAAATTCAAATATAGCATATACTAGAGTAGTAGGTTATTTAAAATGGAGTCTACAGCTGCGTCCGAAACCGCATTCATCCATACTATATAGTACGCTAAAATCCGTATGCGAGTTGAGTAGTATGTCCGAATTCATAGAATTCGAAAATCAGTATGCGAGAAGTACACGCAGCCGATGACTTAAAAGCTACATAAGAGCAAACTGTTGTCCTCTGATTGGCTGGATTCAAACGGCTAGAGGATCCTGATTGGCTGTTTGTATTTTC[A/T]GTTTGGCTGCAAGATCACAGTCCTGTTCTTCATTTATTTCCTGGCGACGAACTACTACTGGATTCTTGTGGAGGGCCTGTACCTTCACAGCCTCATCTTCATGGCGTTCTTCTCCGACTCCAAATATCTTTGGGGTTTCACCCTCATAGGATGGGGTAAGAGCGCATGATTTTTGTCTCTAAACATTATTGATTCGTCCTACCCAGATGTAACCTCACCAATTCTACAGCTTGTGTGACGGCTTTTGTTGTATCTGCTCATAGGAACGGCAGTGGAAGCATTCTGCTGTGCTTTGAGGCGGCAAACACTTACTTAAAGCCAGATTTATTCATACATTAAGTTTGATGCAAAATACTCCACAGGCAAGCCGGGCAGACATCTTTGAAGTGCAAATTCTTCTGGGAAGGTTGCTGCGTTTTTGGACACTTTGTTAAAATCCCAGTGACAGAGATGTTGGTTTTAAGTTATACAAACCCACAGTGACACAGGGTCCACGTCTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa1961

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
ENSDART00000004389	Nonsense	425	487	11	11
ENSDART00000131611	Nonsense	452	509	12	12

Genomic Location (Zv9):

Chromosome 22 (position 12009175)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	11869343
GRCz11	22	11899025

KASP Assay ID:

554-1949.1 (used for ordering genotyping assays)

KASP Sequence:

CCTCCTCACCAGCAGGRTATACCGTTGCACTAGTCGACCTAGTGTTGGAT[C/A]GCTAACACACACCTCACACATACACACGTCGCTACCAGGGTACGTTTTCA

Long Flanking Sequence:

CACAGTTGTAGCTATTATATGCATCATGCACTGTTTCTTGTGCAATAAAACCTCAAATAAATTAAATTAAATAGAGAGTCCAAAACAAGTAGCATGTTTGGCAAGAAACCCTCTTCCATTTGTACTGTGGTCTCATTTCTACTTGTCATTTACAACCACATTTTTGCTCTCTTTCAGGGATTTTTTGTGTCTATTATCTACTGCTTCTGCAACGGAGAGGTACGTCAAGCTGAAATAGAATTCATATTCATACTCTTTCACAAAGTTCACAGTTTTAATGTTGTCATTATCCCAGGTCCAGGCTGAAATCCGCAAGACCTGGCTCCGCTGGACGCTAGCGTTTGACTGGAAAGGCCCAGTGGTTTTGGCTAACTACCGCTACGGGTCAGTACTAAACAACAGTGGCGCTAGCAATCAATCCCAGCTCACGTCTGTGACCCGAAGCTCTGCCCTCCTCACCAGCAGGATATACCGTTGCACTAGTCGACCTAGTGTTGGAT[C/A]GCTAACACACACCTCACACATACACACGTCGCTACCAGGGTACGTTTTCAGCAACTCAGACATTGAAAGCCTCCCGCCTTCAATTCCGGAGGAATTAGAAGAGGAGGCCAAGCATATTGATGACATCACGCTGAAAGAAAATGCGAAAATTGCTAGCGCCGTCACTGTGCGACAGGAAGCTCTTGGCATCTGTTTTGAGGAGAGTACGCAAAACTCGACATGCATGGATTCCGATGATGTCTCAAAGAGGCATGATGATGTCACCCCTGTGGAAATCGCCAAATTTGCTGATGACATCATGCTGAAGGATTCTTTATCGGTGAGGTACAACAATTTGGATCGGGAGAACGAGGAAGTACTTTAAAAAAACCTGACCATTTTAATGCAAACTAACACTGTCAAACCAAAATTAATTGGATACGTTCATGATTGAAACTGGATATTTGGAGCGAAAACATTGTATTTACAATTGAAAACGGATACAGTCAATTTAGGTTAAT

Associated Phenotype:

Not determined