ZMP
nhsl1a
Ensembl ID:
ZFIN ID:
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 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa36448 | Nonsense | Available for shipment | Available now |
| sa28880 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa803 | Nonsense | F2 line generated | Not yet available |
| sa28881 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa32160 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36448
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 |
|---|---|---|---|---|---|
| ENSDART00000076739 | Nonsense | 82 | 1535 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 30633189)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 30557116 |
| GRCz11 | 17 | 30574079 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTACACAGCCCCCTGGCACCACCAAGAGAACGTCTTCCTGCCTGGGTCC[A/T]GACCAGCATGTGTTGAGGATCTTCACCGTCAGGCCAAAGTCAACCTGAAA
Long Flanking Sequence:
ACTCTAAAAAATTTTTTTAAAAACAACAATGTTTCTAATCTCAGGTTGAGAGCTATATTCCAACCACAAAAGTATGTGTTATGCTGTTTGCGAATAATTGTAGGATTCATAGATCATATTGATCATCAACACTGAATCATTAAACTGAAATGCTCAAAATGATAAAAATTGCACTGATAGTTGGTTAAAGATGCTGTTTTGGAAATAAATCATACCATCTTAGAGGTTCACTCTGGTCAAAACTGGTAGTAATTAACTGGTAGTAATTACTTGGCAGTAATTAAGGAAAAAGCCACTATAAATCTCTTCATGCATTCTTTTTTTTAGTTGCAATACATTTTTACACAAACCACTAACCTTATTTCTTAAACATGTTAAATTTTAATGTGTTCTGGTTTATTTTCCTTATAGCGGTGTCCAGTCTTGATGAGGAGAGCAAATGGTCGGTGCACTACACAGCCCCCTGGCACCACCAAGAGAACGTCTTCCTGCCTGGGTCC[A/T]GACCAGCATGTGTTGAGGATCTTCACCGTCAGGCCAAAGTCAACCTGAAAACAGTCCTCAGAGGTCAGAAACAAAAATACAAACAGAAATAGATTTCAAGTAAAACAAAAAACACAGGTCTAACAATATTCTAATTCTGAACAGAGCAAAATACTGACTAGAAATTTCTATACAAATCACATATGAGATTAAGCATAATTGTTTTAATCAGCAAATTCAAATTACCTTGTAGAAGATTTTTTTTCAGTAACAGACCATTGCTTGTAATGAAGATTACTTTACCACTCTGCAGAAAGTATGTAAAAATATAGATGGGAATAAAAACTAATATTAAGGCTTAATGTTAAGTGTCTTCTATAAAAATAACAAAAATCTGTATAGGAACTTTCTGTTAATGTCCCAAATGTACTTTATAATATCATTGTGACCAAAGAATAACAAAAAACAAAAAACTTTATATTTGTAATATTCTCATATGGCCATAAAATAATTTGGAAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28880
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000076739 | Essential Splice Site | 144 | 1535 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 30640108)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 30564035 |
| GRCz11 | 17 | 30580998 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTTTGTGAAAGTGTACATCTGGATGAAGAGAAGACAAAGAAAAAGAAG[G/A]TTGATACACATTACAATCCGTTCCTCTAAATTCAAATGCACGCAATGGAT
Long Flanking Sequence:
CTGCTATCTATCAGTCAGTTATTGTCCTTTCTCTGCACTGAGGGCAAAAGGACACTGTGTCTCCGCAGTAGTACAGTAATATGCTGAGTGGGATGCAAGTCATCAGTATGTGTAACTTAAATCTGTTCTTTGCAGGGTGCTTAGTCTATGCTTGGCTGTGGTAGTCGGCTCTTTTTTCCATCCAATTAAAAACAATATGTACTGCAATTTTTCATTTCAATATTTTGACAGTATATTTGTGTTCTTAAATTATGGGACAGGACAAAATTTATATTTACCTTTATCCATGTGTAAATGCTTTCTATAGGTTTTTGTGATCTGCATTAACTTATTCGCAATCTGTTTATAATAAGATGGTTATTCTTGCCTTTCCAGAGTGTGACAAGCTCAGAAAAGATGGCTTTCGCAGTTCTCAGTATTACTCCCAAAGCCCAGCATTCTCTGCAACCAGCCTTTGTGAAAGTGTACATCTGGATGAAGAGAAGACAAAGAAAAAGAAG[G/A]TTGATACACATTACAATCCGTTCCTCTAAATTCAAATGCACGCAATGGATAGAAAATAAAACTAGTTTTGCTTGTCTGTGCAATATGTGATGTACTCTCTAAACAATTGCCTAATATTGTATATTAAAACATGATTTTTAAATAAGTAGCGTGTAAGAAAAATGTAAGATATTCAAGAAAAAAATTTTTAAAGCTACTTTTTGCTTAAACATTCTTTTTAAGACTCTTTTTAAGACTGTTGCTTTTATCGCATAAAACAGACAGATTCCTAAATACTCGATCACAACAGAACAGATGGGTCTGTTGTTTTGCATCGCCCCCTTGTGGATGTATGTATGCTAGCGGTGTAGTTTAGTTTCCACTTCAATGAATGAGTCAATGAAGTAGAAACTATTTGTTCCACATTCTGTCATCCCAAAGAAAGGTAATGTCTCACTTCACTTTTGTTCCTTTATTTTATTTTTCTTTCCTCTCATCAAGCGGTTTAAAGTCCTAGACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa803
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000076739 | Nonsense | 737 | 1535 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 30644014)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 30567941 |
| GRCz11 | 17 | 30584904 |
KASP Assay ID:
554-0708.1 (used for ordering genotyping assays)
KASP Sequence:
CCAACACACAGTGACWGCAGCAGTCAGCGCTCAGACTATGCAGAGTCATG[G/A]GACTTCTACATGGATTGCCCATGTMCACGGTCTGACCAGAGTCTTTCCTC
Long Flanking Sequence:
TACTACACCTCCATGCGCCTAGACTCTGGTTTGAAGTCACACAGTCACGGCTGCATCAATAAAGCAGGAGAACAAAAGCACAGTTTGTATGAGTGCAAAGACCACCACAGTCAAAGTGATACTGCAAGTCTGCATAGCAACCGCTCCCTGACTCGTAGCATCTCTCTGCGAAAAGCCAGGAAGCCCCCACTCCCTCCAGAAAGAACCGACTCTTTAAGGCGTAAACCCCAGAGGAAGAGTCGCCACAGTGGTTCAGTCCTTAATGAGCAGTTAATCTCTAGTCTCCAGCAGTCCTTACAACTTAACCTAAATACTCAAACTACATCTTGCTCTGAACAGTCACCCTGTGGTAGGTTTGAAGACCCTTGGGTCCTCCGACCGAGAAGTCAGAGTATCATAAGTGCAGCTAGCAGTGGGGTATCTGCACCAGCTGCTGTATGTCCGGTCACACCAACACACAGTGACAGCAGCAGTCAGCGCTCAGACTATGCAGAGTCATG[G/A]GACTTCTACATGGATTGCCCATGTACACGGTCTGACCAGAGTCTTTCCTCACAAATCACAAGGTCTGCAAGTGCTGAGGAGAATCATGGAGTCATAGGTAATGCATCCTACAACAGTGAATTCCCATCATCCCCCTTCAGCAGTAGTCAGTCAAAATTGACCTCATCTCCTGACAAAGTCCATCGACTCACGTCACCATCAAGTGGCTACTCAAGTCAGTCTAACACTCCAACTGCAGGCACTCCAGTTACGTCTCTAATAAGAGCAAAGTCTCCTGCGGGGAGACCGAAACCAAAAGTGCCAGAAAGAAAGTCCTCTCTACGATCTTCTATATCATCCTCTTCTACATCCCTGTCCTCCAACACCTCAGATTCCATCAGGAACATTCCTCCACCTCCACCTTTACCTGACATGACAACTGCATTATGTGGGTCGCCCAGTTCTGCTTCTTTCTCTCCAACAGCGGCTAAAATAGACCCAATACCCTCTTTTACATCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28881
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 |
|---|---|---|---|---|---|
| ENSDART00000076739 | Nonsense | 1484 | 1535 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 30648648)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 30572575 |
| GRCz11 | 17 | 30589538 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAAATATGGGCGCTCGCGCACACCACCTTCCGCAGCCAGCAGCCGGTA[T/A]AACAGCCGCAGCCGGATTACCAGTAGGCCAATGACTGCCATCTGTGAACG
Long Flanking Sequence:
GTCAAGACATGCAGTAACCATGCCAAAGGCTTACCTAACAAAATGTCCTGCTGTCTTTTAATCCCCAGGTCAAAAAGGAAGGTCCTGGGCCGTGGCGATTCTGAAGATGAACGCTGCCGTAACCTCCTTCCTTCCCCACCTGTCACTCCAACTGGCTCCTGCCCCAGCTTGCCACGTCAGACCAGCTCCATCCAGCGGAACCTACGTCGCTCCACCACAAGCAATGACAGTTTTAAAGCTTTGCTACTCAAGAAGGGCAGCCGCTCAGAGTCCAGCTTTCGCATGTCAGCCGCTGAGATTCTCAAATGCACAGACCCCCGTTTCCAAAGGGCTAATTCAGAAAATGCACTAGCTGACGGACTGTCCTCTCCGACAAGCAGCAGGAGAGCACATGAAGAGTGGGCACGGACGGAGGGAGCTTTGCCTCGCTTTACCACTGGACAAACTATCCCAAAATATGGGCGCTCGCGCACACCACCTTCCGCAGCCAGCAGCCGGTA[T/A]AACAGCCGCAGCCGGATTACCAGTAGGCCAATGACTGCCATCTGTGAACGAGATGGAGAGGTGGCTGAATCTACAGACTGCTACTTAAGTAGCGAGAATCATTTTGTCTTGGCTTTATCCTCCAGCAGCATGGTCTGCGCTCAAGGCAGCACTTAGAGCTCTTGACACAACTCTAACAGCTAGTTGTCCATTCGATATAAAGGTCTGAACTCTAGCTGGAAGGCCATGATTGTGCTGGCTGACAAAATTCCCCAAGGAATAAAGAAGAAGAGGCAATGGGGGAACTTTCTGTAATTCTGTAACTCTAGTTTTGCTCTGTTCCATCAGTGAGAGTTTTATCTTTCAGAAGACATTAGTATTCTCTAAAGAAAGTGATATTAACAGAGGGTTACTGGTTTTGTTTAATCAAATGTTCCTAGCTTTCTGTATGCAGTTTAGGAGAACATGGAAATGTACATTTATCTTGGCTGGTAAGTTGAGGAAAGAATGAACGTAAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32160
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000076739 | Nonsense | 1501 | 1535 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 30648697)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 30572624 |
| GRCz11 | 17 | 30589587 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAACAGCCGCAGCCGGATTACCAGTAGGCCAATGACTGCCATCTGTGAA[C/T]GAGATGGAGAGGTGGCTGAATCTACAGACTGCTACTTAAGTAGCGAGAAT
Long Flanking Sequence:
GCTGTCTTTTAATCCCCAGGTCAAAAAGGAAGGTCCTGGGCCGTGGCGATTCTGAAGATGAACGCTGCCGTAACCTCCTTCCTTCCCCACCTGTCACTCCAACTGGCTCCTGCCCCAGCTTGCCACGTCAGACCAGCTCCATCCAGCGGAACCTACGTCGCTCCACCACAAGCAATGACAGTTTTAAAGCTTTGCTACTCAAGAAGGGCAGCCGCTCAGAGTCCAGCTTTCGCATGTCAGCCGCTGAGATTCTCAAATGCACAGACCCCCGTTTCCAAAGGGCTAATTCAGAAAATGCACTAGCTGACGGACTGTCCTCTCCGACAAGCAGCAGGAGAGCACATGAAGAGTGGGCACGGACGGAGGGAGCTTTGCCTCGCTTTACCACTGGACAAACTATCCCAAAATATGGGCGCTCGCGCACACCACCTTCCGCAGCCAGCAGCCGGTATAACAGCCGCAGCCGGATTACCAGTAGGCCAATGACTGCCATCTGTGAA[C/T]GAGATGGAGAGGTGGCTGAATCTACAGACTGCTACTTAAGTAGCGAGAATCATTTTGTCTTGGCTTTATCCTCCAGCAGCATGGTCTGCGCTCAAGGCAGCACTTAGAGCTCTTGACACAACTCTAACAGCTAGTTGTCCATTCGATATAAAGGTCTGAACTCTAGCTGGAAGGCCATGATTGTGCTGGCTGACAAAATTCCCCAAGGAATAAAGAAGAAGAGGCAATGGGGGAACTTTCTGTAATTCTGTAACTCTAGTTTTGCTCTGTTCCATCAGTGAGAGTTTTATCTTTCAGAAGACATTAGTATTCTCTAAAGAAAGTGATATTAACAGAGGGTTACTGGTTTTGTTTAATCAAATGTTCCTAGCTTTCTGTATGCAGTTTAGGAGAACATGGAAATGTACATTTATCTTGGCTGGTAAGTTGAGGAAAGAATGAACGTAAGCAGAACGTTATTGAGGGATTTTGTTTTGAATGCTCCATGATGATGGAAAGTA
Associated Phenotype:
Not determined