Busch Lab

ZMP

nhp2

Ensembl ID:
ENSDARG00000069422
ZFIN ID:
ZDB-GENE-030131-533
Description:
H/ACA ribonucleoprotein complex subunit 2-like protein [Source:UniProtKB/Swiss-Prot;Acc:Q6PBV6]
Human Orthologue:
NHP2
Human Description:
NHP2 ribonucleoprotein homolog (yeast) [Source:HGNC Symbol;Acc:14377]
Mouse Orthologue:
Nhp2
Mouse Description:
NHP2 ribonucleoprotein homolog (yeast) Gene [Source:MGI Symbol;Acc:MGI:1098547]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa37343 Nonsense Mutation detected in F1 DNA Not yet available
sa39337 Nonsense Mutation detected in F1 DNA Not yet available
sa1137 Nonsense F2 line generated Not yet available

Mutation Details

Allele Name:
sa37343
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101037 Nonsense 20 150 1 4

The following transcripts of ENSDARG00000069422 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 21 (position 29152633)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 30371877
GRCz11 21 30408572
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTAAAGAAGGAGAAAGCCGGGGAAGAGGAAACCGGAGGGACGGAAAAAT[C/A]ATATCAAGAGTTGATTGCTAATATTAACCCAATCGCAAACCCGCTAGCAT
Long Flanking Sequence:
TTTATTAAGTTTCCTATTTATTGTATTTTATTAGCGTCTACCTAAAGCCAGCTTATACAGTGATGTAAAAACGGCCGATTTGCCGCATTTGTTATTTATTATAAATAAATAAATGGTATTTCATTAACGTCTACCCCTAAACTCAACCGTCACAATACTGTAAAATATTATTGTTATACAGTGTTATACAATATATTAAAAATATTATATTAATAATAAAATATTGTTATACAAAAATGATCCGCAGCTGTATCTAGACTTCACCGTCGAGAGCGGCATCTATGTATTATTCGACTCTATGGAGGAAATACTGCAGTGTTCGAAAAACACCGGAAATACGTTTATAGTCATCGCACGTGTGTTGTGCCTTGCATCCTGTGCCTGCAACACTATCAGCCTTAAGTTAATCGCTAAAGTATATTTGTGTACATTTTAACGAAAGATGACAAAGGTAAAGAAGGAGAAAGCCGGGGAAGAGGAAACCGGAGGGACGGAAAAAT[C/A]ATATCAAGAGTTGATTGCTAATATTAACCCAATCGCAAACCCGCTAGCATCGCGAAAACTTAGCAAAAAGCTCTACAAATGCGTCAAGAAAGGTAAATACGTGTTCAGAACTTGTTTTTAACATTCATAAAGAGTAACGTTATTGCCTGCGAGTGTGAATGAAAATATACTAAATATCGCTGTCTGTAGGTTTAGTATGTTGCAGACACGTGGTTGCAGTCATTTGTTCATTGGTTATGAGTGTTATTCATTATTATATTTATATTTTCTTAGCGGCTAAAGTTAAACAGATCCGACGAGGAGTCAAAGAAGTACAGAAGTTTATCAACAAAGGAGAGACTGGGTAAGATTAAGGTTTTTTCAGGTATTTGTTAAGGCCATTGGTTGATCAGTCCAGGGTTTAACCCATATTAGCCTTTTAAAAAGTTCATTCTAGTTTCAAATTGACTACACTACTAGACAAAAAATAATACTAATTTTTAATTTAACACGAAGAAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39337
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
ENSDART00000101037 Nonsense 21 150 1 4

The following transcripts of ENSDARG00000069422 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 21 (position 29152629)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 30371873
GRCz11 21 30408568
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAGGAGAAAGCCGGGGAAGAGGAAACCGGAGGGACGGAAAAATCATA[T/A]CAAGAGTTGATTGCTAATATTAACCCAATCGCAAACCCGCTAGCATCGCG
Long Flanking Sequence:
TTAAGTTTCCTATTTATTGTATTTTATTAGCGTCTACCTAAAGCCAGCTTATACAGTGATGTAAAAACGGCCGATTTGCCGCATTTGTTATTTATTATAAATAAATAAATGGTATTTCATTAACGTCTACCCCTAAACTCAACCGTCACAATACTGTAAAATATTATTGTTATACAGTGTTATACAATATATTAAAAATATTATATTAATAATAAAATATTGTTATACAAAAATGATCCGCAGCTGTATCTAGACTTCACCGTCGAGAGCGGCATCTATGTATTATTCGACTCTATGGAGGAAATACTGCAGTGTTCGAAAAACACCGGAAATACGTTTATAGTCATCGCACGTGTGTTGTGCCTTGCATCCTGTGCCTGCAACACTATCAGCCTTAAGTTAATCGCTAAAGTATATTTGTGTACATTTTAACGAAAGATGACAAAGGTAAAGAAGGAGAAAGCCGGGGAAGAGGAAACCGGAGGGACGGAAAAATCATA[T/A]CAAGAGTTGATTGCTAATATTAACCCAATCGCAAACCCGCTAGCATCGCGAAAACTTAGCAAAAAGCTCTACAAATGCGTCAAGAAAGGTAAATACGTGTTCAGAACTTGTTTTTAACATTCATAAAGAGTAACGTTATTGCCTGCGAGTGTGAATGAAAATATACTAAATATCGCTGTCTGTAGGTTTAGTATGTTGCAGACACGTGGTTGCAGTCATTTGTTCATTGGTTATGAGTGTTATTCATTATTATATTTATATTTTCTTAGCGGCTAAAGTTAAACAGATCCGACGAGGAGTCAAAGAAGTACAGAAGTTTATCAACAAAGGAGAGACTGGGTAAGATTAAGGTTTTTTCAGGTATTTGTTAAGGCCATTGGTTGATCAGTCCAGGGTTTAACCCATATTAGCCTTTTAAAAAGTTCATTCTAGTTTCAAATTGACTACACTACTAGACAAAAAATAATACTAATTTTTAATTTAACACGAAGAAATGCACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1137
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101037 Nonsense 102 150 3 4

The following transcripts of ENSDARG00000069422 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 21 (position 29146439)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 30365683
GRCz11 21 30402378
KASP Assay ID:
554-1048.1 (used for ordering genotyping assays)
KASP Sequence:
GACGTCTACTGTCACCTACCAATCATGTGTGAAGACAGAAGCCTGCCGTA[T/A]GCTTATGTGCCGTCCAAAGTCGTAAGTTAATCAGAAGCGTATACAATAGA
Long Flanking Sequence:
AAATAGTTTTTTGACGTGCCTTTACATTAATTTTACATTTGAATAGCCAAAATTACAAGTTTCAGTCTTTTAAATGTGATTAATCGCGATTAATAATAAAAAAAAAACTGTGATTAATTAGTTAAATGTTTTTTTTCTCGATTGACAGCACTAATTGTATTACAATAAACAATTACATATTATATAAACTATTTAGAATTGTTGTCATTCATTTGTCAATAAATACCCCAAAAGTATTAATATGAAGGCCAGAAAAAAATGTGACCATTTAAAAACGAGATATTTCTGTCATGTTTAAAATATTGTTTATCATAGCCTAAATTGCATCTTTATTCTTGAAATGACCTGTGGGATGTGGCTCTCTGTCGTCTAATATATTGAAAACCCCTAATGTTTCTTATTTTCTGTCCTCTCAGTATTGTAGTGTTTGCTGGGGATACTCTTCCCATCGACGTCTACTGTCACCTACCAATCATGTGTGAAGACAGAAGCCTGCCGTA[T/A]GCTTATGTGCCGTCCAAAGTCGTAAGTTAATCAGAAGCGTATACAATAGATCTCTAATACACCTTTGTGAAAGCTATATTCAGAGATGCTCATGTGTTTGTGCAGGATTTGGGCTCGTCAGCCGGATCTAAGCGTCCCACGTGCGTCATAATGATCAAACCTCATGATGAGTATAAAGAAGCGTATGATGAGTGTGTGGAGGAGGTCACATCTCTGCCGAAACCAATCTGAACACACTTCACTTGTATTTTTTTTTTTTAAGTACAATGACTATATATATCACATCAGATTAGGATGGTGTGATGTTTATCAGCACAAGACTCGCCCTGGTTTTTGTCTTTGTGGACTTTTTCATCTGAAGGAGGAGGAACAAATGTATGATGGCGGTTAATGATCTTGTGTAAAGAAAGCTTTAGTTCATTTCACTGTGCGGTGAATGTTCAGCCTGTTGATTTACTGAATATTTGACGCTGGTGATCTCTAATGATTTATGTATTGGT
Associated Phenotype:
Not determined