ZMP
nhp2
Ensembl ID:
ZFIN ID:
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.
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.
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.
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