ZMP

npffr2.2

Ensembl ID:

ENSDARG00000060702

ZFIN ID:

ZDB-GENE-070705-159

Description:

Novel protein similar to human and mouse neuropeptide FF receptor 2 (NPFFR2) [Source:UniProtKB/TrEMB

Human Orthologue:

NPFFR2

Human Description:

neuropeptide FF receptor 2 [Source:HGNC Symbol;Acc:4525]

Mouse Orthologue:

Npffr2

Mouse Description:

neuropeptide FF receptor 2 Gene [Source:MGI Symbol;Acc:MGI:1860130]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa478	Nonsense	Confirmed mutation in F2 line	Not yet available
sa26511	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa5304	Essential Splice Site	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa478

Status:

Confirmed mutation in F2 line
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000085821	Nonsense	118	438	2	6
ENSDART00000135063	Nonsense	89	336	2	3

Genomic Location (Zv9):

Chromosome 5 (position 34717352)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	32499301
GRCz11	5	33099454

KASP Assay ID:

554-0210.1 (used for ordering genotyping assays)

KASP Sequence:

TAATTTTTCATGTTTCTCCTGCAGGCTGGCCTTTTGGCAGTTTGGTGTGT[A/T]AGCTGAGTGGGATGGTGCAAGGAATATCAGTATCCGCATCAGTATTTACA

Long Flanking Sequence:

TCCTTCACTGACACTTAGTTCTCATGATGTATTTATATAAGAATGAGAAGTGACACATGTCCCCATGTTAATTATGATTAAGATGAGCAGAGCTTTTGGAGATGTTATTCTTTTTGCTATAAAACAAAACCATTTTATCTGTAATCTTTATAAAGCCTTGAGAGCTTGAGGTATGAACAATCAGCAGTTTTGATCTTAAAACTACAAGGGGTTATTTTTCTTACCCTTAAAAATGTGTATGTGTGTGTGTTCACATAGCCATCATCCCATTCTACTAAAGCAATAATTTCAACATTTAAAAAAGTAAATCTATTTTTTTATCTATCGGTAAATTCTGACTGAAGAGGCCCAAACAGTTGATGTCAGTACAAAGAGTCGTAAAAGATTTGGGAAAGGGTCTTTTTCGAAAAAGTAGTTTGTGTGTGCATATGATTGTGTGCATTTCATGAATAATTTTTCATGTTTCTCCTGCAGGCTGGCCTTTTGGCAGTTTGGTGTGT[A/T]AGCTGAGTGGGATGGTGCAAGGAATATCAGTATCCGCATCAGTATTTACACTAGTGGCCATTGCTGTGGACAGGTGAGCCAAATATTAGTGTGCTCAAGACATTTTATTTCAATAAATCTCAAGAGTCAATACCACCCACATAATCACTGTATTTGCACTACTGTTAACATGTTTTGGTTTTTCTGTAAGATGTCTGTTGTGCTACAATTATTAATTATATTATTATTCTTTAAATAAGCCATTCTTTTTAAATATAATTTTAGGGTATAAATCAGGGGTGCCCAATTTTTTTTCATATAAAGGGCCAAAAAGCAAACTTGAGTGAGGGGTGTAGGCTGAATATATACCAAACCGTATACATTACATTTTCCATGGGTCATTTTCTAATTTATTCTGTAATATTTAAAATGAACTAGAAAACACTGCTTTAAATCATATTGACTAATGCAGTATTATTTTAATCATTGTATAATGAACATATTATAGTAAAACATAAACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa26511

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000085821	Essential Splice Site	423	438	3	6
ENSDART00000135063	None	None	336	None	3

Genomic Location (Zv9):

Chromosome 5 (position 34722117)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	32504066
GRCz11	5	33104219

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAAGGACTCATCCAGGGGCTGGTGTCTGTGAGCAATGGGAAGGGTTTGGG[T/G]GAAAGAAGCCAGTCTTCAGGGAAAGAGAACATGAAAGAACAGGATCTGAT

Long Flanking Sequence:

GTTGGCACCTCAGGCTCCGGTTCTGGCTCGGGGAAACAGTGCAGATATGAAAGTCGCCAACTGGTGTCCCGGAAGAAGAAGCGGGTGATTAAAATGTTGCTGGTGGTCGCCCTGCTCTTCATCCTGTCTTGGCTGCCATTGTGGGCACTCATGATGCTGAGCGACTATGCGAGTTTGAGCGAGCGCCAGCATCGGGTCATTAATATCTATTTTTATCCTCTGGCCCACTGGCTGGCATTCTGTAATAGCAGCGTCAATCCTATAATATATGGCTTTTTCAATGAGAACTTTCGCAAAGGTTTCAAGGCAGCTTTTAAACTGCAGCTGTGCTCAGGGCATTCAGGCAATAGGAGGACTTACTCGCACCGACTGCAGGGCAATGCTGTTTTACCAGCCAATTTACCACTAACCAAGCAAACAGCACTGGAGACTGGAGCTCCCAGACCAGGACAAGGACTCATCCAGGGGCTGGTGTCTGTGAGCAATGGGAAGGGTTTGGG[T/G]GAAAGAAGCCAGTCTTCAGGGAAAGAGAACATGAAAGAACAGGATCTGATCATGGAAGATTTGGAGAAGGTATGTGTGTATGCCTGTGTGTGTGTGTGCGTGCGTGCGTGCGTGCGTGCTTGCGTGCGTGCGTGTGTGTGTGTTTAGGGATGTTTACACCAGGTCACTTCATCCGTTTTTCTTTTTTTAGATCAGAAAGCTATCTCAATCAAGAAATGTGCAGTTGTAAATACCCTCTGACACACATTTGAGATATAAATCCAATCGAGGGAGAAGGAGATGGTTTCTAGGCCAAACTAAACATGTCTAAATGCATCTGGTTATTAAACCACACATTTAAATTTTACTCCTCCTGTTTTTGTTTTGTTTTATTCTTGACCATGAAATTCTGAAATTAAATTGTTAAATAATATCAGATGGTGGAATTAACAACAGAGATACCACCAGTATCTTCTGTAAAAAGAGAAGAATAAAAATACAGGGCGATTCAAAAAGAATAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa5304

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000085821	Essential Splice Site	428	438	5	6
ENSDART00000135063	None	None	336	None	3

Genomic Location (Zv9):

Chromosome 5 (position 34723130)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	32505079
GRCz11	5	33105232

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGGAACAAGTTTRGTRATYCCTGCTTTACAGCATGCACATAAAATAATTT[G/A]AATGCCAAACAASATATATACAGCTGAAGTCAGAATGATTAGCCCCCCTG

Long Flanking Sequence:

ACGCATTTACTTTTTTGTTAAGTACTCATCACATTGATTAATTACTCAAGTTTCCATTATGTTTCTTTGATTAAATGCAGATTTTCAAAGTTCAAAAGCGGTATAGTGCTGCGTTCATTTACAATGTCATGTTGTTGTTTTTATTTTTGGGAGAGTGTGTTATACACTAGATTTGAATGATGTCTTGCACATATCTATATGACAAAAATAGATGTTTCTTTTAGCCTATACTAAAAGTAATCACAGAGTCTGCCTTGTGCACTTGTAATGATGCTTTACAGCAAGGGTCACCAATCTCGTTTCTGGAGGTCCGGTGCCCTGCAGGGTTTAGCTACAACTTACCTCAACACACCTGCCTGGGTGTTTCAAATATACTGAGTAAGACCTTGATTAGCTTGTTCAGGTGTTTGATTAGGGTTGGAGCTAAAATGTGCAGGACACCAGCTCTCTAGGAACAAGTTTAGTGATCCCTGCTTTACAGCATGCACATAAAATAATTT[G/A]AATGCCAAACAACATATATACAGCTGAAGTCAGAATGATTAGCCCCCCTGTTCATTTTTTTTCCCTTAATTTCTATTTAATGAAGGGAAAAAAATTTTCAACACATTTCTAAATATGATAGTTGTAATAACTCATTTCTAAAAGCTAATTAATTTTTATTTTCGCCATGATGACAGTACATAATATTTTACTAAATATTATTATAGACATTTCTACACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTTATTAGGTTAACTAGGCAGATTAGGGCAAGTAGGCAAGTCATTGTGTAATGATGGTTTGTTCTGTAGATTATACAAAAATATATACCTTAAAGGGGTAAATAATTTTGGACTTAAAATGTTTATTAAAAATATAAAACTTTCCTTGCTCTGTTAAACATCATTTGGGAAATATTAAAAAATAAATAAATAAATAAAATGGGGGCTAATAATTCTGACTTAAACTGTAGTTTACTTTTCTGTAAATAGT

Associated Phenotype:

Not determined