ZMP
si:ch211-107m4.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
HNRNPUL2
Human Description:
heterogeneous nuclear ribonucleoprotein U-like 2 [Source:HGNC Symbol;Acc:25451]
Mouse Orthologue:
Hnrnpul2
Mouse Description:
heterogeneous nuclear ribonucleoprotein U-like 2 Gene [Source:MGI Symbol;Acc:MGI:1915943]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35688 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11936 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35688
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 |
---|---|---|---|---|---|
ENSDART00000079385 | Nonsense | 18 | 716 | 1 | 14 |
ENSDART00000137167 | Nonsense | 18 | 662 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 14 (position 23498374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 22198164 |
GRCz11 | 14 | 22495409 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGCGGGAGGAAGTGAAAAAGCTGAAAGTGACGGAGTTGCGGGCCATGT[T/A]GAAAGAGCGAGGACTTGAAGCGAAGGGCCTGAAGGCCGAGCTTGTGGTTC
Long Flanking Sequence:
AACCAATTTCTATCTTAATCTCCATTTTTTTGTTAATAAACAATTCCAAATCTTTCCAAATATTCTTGAGTAAATACAGTGAAAAAAGATGTAAAATGTCTCTTTTTCTTAACCACAAAATTCAAACATATATGAAATATTGAGTTTAAATCTTTCCAAAACATGTTTAGCTTGTTCAAGAGAATCGATTCACAAATATGAATCTCGCTTACGTCACCGCTGGTAACCAATCAACGATTATCTCTCTCAGCAGCCAATCAGCTCTCAGTCAACGCTCTTGAATCCTCTACAGCGGGTTGTTGTGTATGTTTTGGTAACGTTAGTTGAGGAAGAAAATTCCCAAAAAGTTTTAAGAGTAAAGCTTAACTCGGCGACCTTTTCCTTACAATTGGATCCCATATGTGTTAGTTTTTAAGTCTTAATGTGTAACTGACAATTATTTTTAAAAATGCTGCGGGAGGAAGTGAAAAAGCTGAAAGTGACGGAGTTGCGGGCCATGT[T/A]GAAAGAGCGAGGACTTGAAGCGAAGGGCCTGAAGGCCGAGCTTGTGGTTCGGCTAATCTCTGCGATTGAAGCTGAAAATGAACCCGTCAAACGTGGAGATACAGTGGAAAATGTGTGTGAAGAGACTATCACAGAACCTCCAGAAGATTCGTCAGCGTTTCTCTCTGATGAACATAAGCCGTGTGTTAGGACGCAGTCTCCAGTGTGCGCTAGTTCTTCAAACACCAGCATGAAAGATTTTGCTGATCAAAGTACACAGACTGAACCACAGCAGCTCTGTTCATGTCGCCTCATCGATGCTAGTGCCATCGCAGAGCCGCTGACCACGAGTACTTTACAGGCTATTGAGAAGAGGTTACAGCAGACTAACGTTGATCCACAGCCGTCAGTCCTGAGAGACGCTGAAGAAAATGCATTGTCAGGAGGCTCATTATCAGCCTTGGGTATTTCTAAAGAACCACAGGAGCAAGAACAGGGTAAGTCTCAGACCTCTGTTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11936
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079385 | Nonsense | 111 | 716 | 1 | 14 |
ENSDART00000137167 | Nonsense | 111 | 662 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 14 (position 23498094)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 22197884 |
GRCz11 | 14 | 22495129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATRAAAGATTTTGCTGATCAAARTACACAGACTGARCCACAGCAGCTCTG[T/A]TCATGTCGCCTCRTCGATGYTAGTGCCATCGCAGAGCCGCTGACCACGAG
Long Flanking Sequence:
AATCCTCTACAGCGGGTTGTTGTGTATGTTTTGGTAACGTTAGTTGAGGAAGAAAATTCCCAAAAAGTTTTAAGAGTAAAGCTTAACTCGGCGACCTTTTCCTTACAATTGGATCCCATATGTGTTAGTTTTTAAGTCTTAATGTGTAACTGACAATTATTTTTAAAAATGCTGCGGGAGGAAGTGAAAAAGCTGAAAGTGACGGAGTTGCGGGCCATGTTGAAAGAGCGAGGACTTGAAGCGAAGGGCCTGAAGGCCGAGCTTGTGGTTCGGCTAATCTCTGCGATTGAAGCTGAAAATGAACCCGTCAAACGTGGAGATACAGTGGAAAATGTGTGTGAAGAGACTATCACAGAACCTCCAGAAGATTCGTCAGCGTTTCTCTCTGATGAACATAAGCCGTGTGTTAGGACGCAGTCTCCAGTGTGCGCTAGTTCTTCAAACACCAGCATGAAAGATTTTGCTGATCAAAGTACACAGACTGAACCACAGCAGCTCTG[T/A]TCATGTCGCCTCATCGATGCTAGTGCCATCGCAGAGCCGCTGACCACGAGTACTTTACAGGCTATTGAGAAGAGGTTACAGCAGACTAACGTTGATCCACAGCCGTCAGTCCTGAGAGACGCTGAAGAAAATGCATTGTCAGGAGGCTCATTATCAGCCTTGGGTATTTCTAAAGAACCACAGGAGCAAGAACAGGGTAAGTCTCAGACCTCTGTTAAAAACTAATCATTATATTGAAAAGAAATGTTGATGATGCTGTCTGTTTCTTGCAGAGCTCTATAATCCGTCAGATGGACATGAGACCGTGGACTCCACACCAGAGGATAGCAGAGAACCGGAGAAGCCTTATGAGGAGAGGGGGAGAGATTATTATGAGTTCAAAGAGGACATTCTTTACAATAGGTACTGATATTGTTATGTAGACATTGCAATAATTGGTAGTTAAAGAGCCCCTCTTATGCATTAAAAAGGGTCGTATTTCTGGTTTGGGGGTCTCCAAC
Associated Phenotype:
Not determined