ZMP
nhsl1b
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5SPA0]
Human Orthologue:
NHSL1
Human Description:
NHS-like 1 [Source:HGNC Symbol;Acc:21021]
Mouse Orthologue:
Nhsl1
Mouse Description:
NHS-like 1 Gene [Source:MGI Symbol;Acc:MGI:106390]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43469 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43470 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32298 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43469
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062532 | Nonsense | 591 | 1571 | 6 | 8 |
ENSDART00000145066 | Nonsense | 475 | 1455 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 30903919)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 30975132 |
GRCz11 | 20 | 30878011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAGAAGGACAATGACTTCCAGCTGCTCAACACCCATAAATCATCTATA[T/G]AGTAGCCTTGAACGCTCCTCAAAAGGCACAGACTCTAGTTCACTGTACTC
Long Flanking Sequence:
GCAGTGCACATGAGGAATGCCCCCAGGGTGTGTACTCAAGCCCGCCCAAAATCTCAGGAGGTGCGAGGATCTCAAAGGGAGTGGGGTTCTGTCTCGGGTCCAGCCTGTGTAGTTTCTCCACATGCAGCCTACTCAACCTCCCTTATACCTAATGCTACTCTGTCATGTTCTGCTGAGGTTTTTGCTCTTCACAGCAAATCAAGTCCTGGCCAGAGCCCACTTTCTGGGTCACCATACACTAAAGCTAGACCTCTTAGCATGGTCTCAGTTGTCAACAGTGGGAGTACAAGTAGTGTGGGCACAGGATCTCACACCCCAGATGCAGGCATGAAAGATACCTGCAGTGAGACTGGCCAATCTGATAGCAGTTTGCACAGCCACAGTACCATTGCCGCAGGAACATTGTCTTCAGATGAGCAGTGGATTTACGATACTCCTGATAATGCCTTGCCCAGAAGGACAATGACTTCCAGCTGCTCAACACCCATAAATCATCTATA[T/G]AGTAGCCTTGAACGCTCCTCAAAAGGCACAGACTCTAGTTCACTGTACTCTATGGACAATGATGGCTACTACACTTCCATGCATCTGGATTCAGGCCTTAGGTCAAGAAGCCATGGTAGCGGCCATGGTCATGGCATAGGAGGAAGAGCAGTAAGACACAGTATGTACGAGTGCTTGGGTGAGCAAGAGGATCGAAATAGCTTGTGCAGCGACCACTCGCTATCTCGTTCCATTTCTCTACGCAAGCCTAAGAAACCACCCCTTCCACCTGCACGCACAGACTCTCTACGGAGAAAGCCTGGGAAAAACAGCTCTCCCTCTGCCAATATTGGGCAGTCAAATATTAGGAATGGTTCTCTTCTCAATGAATCATTGATTGCCACTCTCCAACAGTCACTTCAGAATGGGCTTAAAGGCAAAGGATCCTCCACGTCACCATCTCATAGCCCTTGTAGTGACTATGAGGACCCCTGGATGCTTCGTCCAAGGAGCCAGAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43470
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 |
---|---|---|---|---|---|
ENSDART00000062532 | Nonsense | 1012 | 1571 | 6 | 8 |
ENSDART00000145066 | Nonsense | 896 | 1455 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 30905181)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 30976394 |
GRCz11 | 20 | 30879273 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAACAATTCCTCCCCTGAATTTCCACCCCCTCCACCTCCAGAAGTGT[T/A]GACCGACCCTGCCTGTTCAGGCTTTAATAGTTCCTTCAGCCCTCCACCAC
Long Flanking Sequence:
TCAGGAAGGAAGTGACATGTCTGCTAAGCCCAGGACAGGCACCTCTTCACCGGACAGGGTACATCGGTTGACTTCTCCATCAAGTGGATACTCAAGTCAGTCAAACACTCCAACTGCTGGTACTCCCGTTCCCTCCTTCATGAGATGCATGTCCCCATCAGGCAAGCCCAAACCAAGAGTGCCTGAAAGAAAGTCATCCTTGCTTTCATCTGTATCTATATCCTCCTCTTCCACCTCTCTTTCATCCAACACCTCTGATTCTAATAGGAGCAATATTCCACCTCCTCCTCCTCTTCCAGCTGCCCCTGTGGTACTTGTACCTCTTAATCCTCCATCCTTTCCTCCTCCCCTTCCACCCCCAAGCCCTGTGTGCACTGAAGACCAGAAATTTCCACCTCCGCCACCTCCTTTACCCACAACTCCCCATCAGCAAGCATCCATGAACCCTCTTCAAAACAATTCCTCCCCTGAATTTCCACCCCCTCCACCTCCAGAAGTGT[T/A]GACCGACCCTGCCTGTTCAGGCTTTAATAGTTCCTTCAGCCCTCCACCACCTCCCCCTCCACCACCACTGCCTACTTATTCTCCATCCCAAAATCAACATTTACCCCACATGACGCCACAAACACCTTCTTCTGCCTCCTTGAAAGAAATTAAGGGCTGTCTTAAACCAGTGAACTTAGAAGGAAGACCAGTGTTGCCTCAATCTGAGGAACCTAATAAGGTTAGCATGCCTTTGATTACCCCATTTGCACTGCAGAGTGTGCAGCTTCGGCCAGCAAAACGTCCAGAAAACAATGAAGTTAGCAGGACAGACAGACCCCAAACACCAGAAAAAACTCACCCCACAGTTCCTCAGATTTCTTGTATATCTCCAAATGTAAGCCTTTCATCTACAGAGGAAAAACCCTCAATCCAGCATAGCCAGGATGGCCTTGTTGAAGCACAAACTGACTATAGTGTAAAATCCAATTCTGATCCAACATCCTTCCTTACAAATGGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32298
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062532 | Nonsense | 1255 | 1571 | 6 | 8 |
ENSDART00000145066 | Nonsense | 1139 | 1455 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 30905909)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 30977122 |
GRCz11 | 20 | 30880001 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTTCTGGACCCCATACCTGTGCTGGAAAAAGAGGAAGAGACAACTGAG[A/T]AAAGTAGCTTTGACATTTCCGTACCTCCTGTAGAGATAAGAGACATTTCT
Long Flanking Sequence:
TGCCTTTGATTACCCCATTTGCACTGCAGAGTGTGCAGCTTCGGCCAGCAAAACGTCCAGAAAACAATGAAGTTAGCAGGACAGACAGACCCCAAACACCAGAAAAAACTCACCCCACAGTTCCTCAGATTTCTTGTATATCTCCAAATGTAAGCCTTTCATCTACAGAGGAAAAACCCTCAATCCAGCATAGCCAGGATGGCCTTGTTGAAGCACAAACTGACTATAGTGTAAAATCCAATTCTGATCCAACATCCTTCCTTACAAATGGGCCCATAGATCTTGGTGAGGCCACAGATGAAGTAGATGGTTTAAAGACTTTCCTCTCAACACAAGTGGAAAAGTCACTAAACTCTACACCCAAGAAAAAGCCTCCAATGATTTCCAAAAAGCCCAAGTTTTCTCTTACTTTCTCCTCTGTGGATCATGTAAGGGATTTTGTGAGTGCTGAAGTTCTGGACCCCATACCTGTGCTGGAAAAAGAGGAAGAGACAACTGAG[A/T]AAAGTAGCTTTGACATTTCCGTACCTCCTGTAGAGATAAGAGACATTTCTCCCACAAATGGTGAATCTCAGGAGTTCTCACAATCCTCTGGTACCACTATTCTTGATGTAGACAAGAGCACCTCTGAAGCAGAGGATGAGGAAGAAAGAGATGACGAAGATGTAACCAGCAGCACAGGATCGTTCAGTTCTAAAGATGATGAAAATGGTGAGTTAGATTTTTCCTAATTTTACTCTGTGGGAATGGAGATCATTTATTACACTCAATGACACAAAGTCATACAATTTTAAATACCCAGGCCTTTTTAAAGAGTCACAGACAATGTTGTATAGCATGTGATCCCAAGGTTTAAATAAAAATTCCAGGGAGAAATTAAAGGAAAAAGAGAATGCACATTTGCACTTCAGCTCGCAATTAAACAGCTGTGTAAAGAAAAAGAAAAACATGCATTAAAGGCAAGGCAGGTTTTACTCACCTCACTCACATTCACAACCCATCTC
Associated Phenotype:
Not determined