ZMP
atrnl1
Ensembl ID:
ZFIN ID:
Human Orthologue:
ATRNL1
Human Description:
attractin-like 1 [Source:HGNC Symbol;Acc:29063]
Mouse Orthologue:
Atrnl1
Mouse Description:
attractin like 1 Gene [Source:MGI Symbol;Acc:MGI:2147749]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6257 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22125 | Nonsense | Available for shipment | Available now |
sa18278 | Nonsense | Available for shipment | Available now |
sa8730 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7363 | Missense | Mutation detected in F1 DNA | Not yet available |
sa31883 | Nonsense | Available for shipment | Available now |
sa35315 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6257
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
Founder:
SL4-42
KASP Assay Location:
Project 554.35, Plate 11, Well A08
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042514 | Nonsense | 202 | 1364 | 5 | 29 |
Genomic Location (Zv9):
Chromosome 12 (position 31549636)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 29858979 |
GRCz11 | 12 | 29973881 |
KASP Assay ID:
554-4925.1 (used for ordering genotyping assays)
KASP Sequence:
CTCAACAGAATCAACTCATGTCCAAATAACTGCTCTGGCCACGGGAAGTG[T/A]TCCTCGGGGAACTCGAYAGCGAGTCGTGTGTATTGTGACTGTGAGAACTT
Long Flanking Sequence:
CACCGTCACATAGAAATGGCCGTAAACAAAACAGCAGCTCGATGACGCAAGCGTACCGGGGTTCAGAAGGAAAAAAGACAGTATGAACACAAACTAACCGATGAGGTGGCAGGGGGAGAAAATCGAACTTGGGTATGGTCCAGGCAAATGAACCAAGTGTGAAAGCACCCTAAGTGTGTTTTCCTTTCCAATTGTGCATAGGATGTTGTGCATGTTAAGGGAAAACTGGAAAAAAGCCAATTTTTACTGAATATCTATGACATTTCAAAGGCTAATGCCATGCTGCAGACCAGATGTACATGCAAGCTGAGACCGCATGCCTGCTTTATTATGTTTACCCTTAACCTTAAGTGCATGTGTCTGCAGCCAGATATATTGCACATTATACCAACCCTTTTATTAATGGACTTTCCCCCTCTTTGCTTAACAATCTTGTTTCTTTATCTCTCCCTCAACAGAATCAACTCATGTCCAAATAACTGCTCTGGCCACGGGAAGTG[T/A]TCCTCGGGGAACTCGATAGCGAGTCGTGTGTATTGTGACTGTGAGAACTTCTGGAAGGGTGAGGCCTGTGACATCCCGTACTGCAGAAACAACTGTGGCAGCCCTGATCATGGCTACTGCGACTTCTCCGGAGAGAAACTCTGCGTGTGCAACGACAGCTGGCAAGGTACTGCTCTTTTCCACTCTCGTTTCCTCCCCCTCCACAGGACGCTTGAAAATCTGAGACCTTTCCAGACCTTCCCAACAGAGCATTGCGTCTTAGGTAGTTTTGGTCATTTATGTAGGTTGTCTCCCTCTGGTGTTGATTGTGTGATAGTGGATTTGTCACCTCTGCATCACTTTAGCATCCTTATTATCAGGCTTTTTATACAGTGTCACAAAGTGTCAAAGCACAATTGACACTGACAGCTTCTCATGCCAGGAGAGAAAGGAAATATACTGATATAATGATAACTATAGGAAGCTTGCAGATTCTCTTTTTAATGTCTGCATGAACTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22125
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:
Founder:
SL6_01_D6
KASP Assay Location:
Unknown
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042514 | Nonsense | 207 | 1364 | 5 | 29 |
Genomic Location (Zv9):
Chromosome 12 (position 31549622)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 29858965 |
GRCz11 | 12 | 29973867 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCATGTCCAAATAACTGCTCTGGCCACGGGAAGTGTTCCTCGGGGAACT[C/A]GATAGCGAGTCGTGTGTATTGTGACTGTGAGAACTTCTGGAAGGGTGAGG
Long Flanking Sequence:
AATGGCCGTAAACAAAACAGCAGCTCGATGACGCAAGCGTACCGGGGTTCAGAAGGAAAAAAGACAGTATGAACACAAACTAACCGATGAGGTGGCAGGGGGAGAAAATCGAACTTGGGTATGGTCCAGGCAAATGAACCAAGTGTGAAAGCACCCTAAGTGTGTTTTCCTTTCCAATTGTGCATAGGATGTTGTGCATGTTAAGGGAAAACTGGAAAAAAGCCAATTTTTACTGAATATCTATGACATTTCAAAGGCTAATGCCATGCTGCAGACCAGATGTACATGCAAGCTGAGACCGCATGCCTGCTTTATTATGTTTACCCTTAACCTTAAGTGCATGTGTCTGCAGCCAGATATATTGCACATTATACCAACCCTTTTATTAATGGACTTTCCCCCTCTTTGCTTAACAATCTTGTTTCTTTATCTCTCCCTCAACAGAATCAACTCATGTCCAAATAACTGCTCTGGCCACGGGAAGTGTTCCTCGGGGAACT[C/A]GATAGCGAGTCGTGTGTATTGTGACTGTGAGAACTTCTGGAAGGGTGAGGCCTGTGACATCCCGTACTGCAGAAACAACTGTGGCAGCCCTGATCATGGCTACTGCGACTTCTCCGGAGAGAAACTCTGCGTGTGCAACGACAGCTGGCAAGGTACTGCTCTTTTCCACTCTCGTTTCCTCCCCCTCCACAGGACGCTTGAAAATCTGAGACCTTTCCAGACCTTCCCAACAGAGCATTGCGTCTTAGGTAGTTTTGGTCATTTATGTAGGTTGTCTCCCTCTGGTGTTGATTGTGTGATAGTGGATTTGTCACCTCTGCATCACTTTAGCATCCTTATTATCAGGCTTTTTATACAGTGTCACAAAGTGTCAAAGCACAATTGACACTGACAGCTTCTCATGCCAGGAGAGAAAGGAAATATACTGATATAATGATAACTATAGGAAGCTTGCAGATTCTCTTTTTAATGTCTGCATGAACTGGAAGTTGCGACCATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18278
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:
Founder:
SL4_10_F11
KASP Assay Location:
Unknown
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042514 | Nonsense | 468 | 1364 | 9 | 29 |
Genomic Location (Zv9):
Chromosome 12 (position 31541713)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 29851056 |
GRCz11 | 12 | 29965958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGTGTGTATGATAGAGGCAGCAAAAGTGTGTACGTCCAYGRGGGTTA[C/A]AGAWCTCTTCCAGCAAACAAATATGGCCTGGTGGATGAWCTTTACCGCTA
Long Flanking Sequence:
ATCCTGTTGGAATTAGGTAACTCATTGCTATTCAGCTCTTTATGCAGAAACGCGCTTAAAGGCATAGTTCACAATAAAAAAAATTGTAATATCCTTCACCTGTTACAAATGAGTTTTTTTCCTTCTGCTGAACACAAAAGAAGATATTTTGAAGGAATGCTGGAAACCGGTAGCCAGAATTCCAAACACTTATTTTCCTCCTATGAATGTCAATGGCTGCCAATTTCCAACATTCTTCAAGATATCTTCTTTTATGTTCAACAGAATCACTTGAGGCTGAGCAAATGTTGAGTAAATGTTTTGGGAGAACTATGTCAATATCGGGGGAAAAATCCTAAATGTGCCATTTTTTATTTTACAGTAATTGTGATTTTGTTTCTGTGTACAGGGACAAACACGTGGCTGGTGCCAGAGACCAGAGGAGCGATCGCTCAGGGTGGATATGGCCACAGCAGTGTGTATGATAGAGGCAGCAAAAGTGTGTACGTCCACGGGGGTTA[C/A]AGATCTCTTCCAGCAAACAAATATGGCCTGGTGGATGATCTTTACCGCTATGAGGTTCAGACCCGCACATGGTAAGAGCGTGCAGATGTATTTAGGGAACAAAAAAAGGCTTGTTGATCTCAGATATAATACAACAACTCGATGATGTTTGATGGGTGTTGCAGGACGATTCTGAGAGAAAGTGGTTACCCACGGTACCTGCATTCATCTGTGCTGCTGGGAGGAACTCTGCTCATCTTTGGAGGAAATACCCATAATGACACCTCTCTTAGCAATGGAGCCAAGTGCTTTTCTGCTGACTTCCTTGCTTATGACATAGGTTTGTACTTTGCACTTTTGACATGCAATACCATTTAAAAATGTAGGATTTATGAATATTTGTATAGAAATTCCTAATGCTTCCTTTGATGAAAAGGACATTTACTCACTCTTTAACATCCAAAACATTGTTTTGTTTTGTTTTTGCTCTTAAGAACTGAATGCACTTAGCATTCTGTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8730
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
Founder:
SL4_01_D4
KASP Assay Location:
Project 2261.03, Plate 9, Well D04
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042514 | Nonsense | 961 | 1364 | 18 | 29 |
Genomic Location (Zv9):
Chromosome 12 (position 31522848)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 29832173 |
GRCz11 | 12 | 29947075 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGGAGACCCCAGTAACACCGGCCGAGGGCAGTGCATGGAGGGTTCGTA[T/G]CGCGGACCCATGAAGAGCCCCTCCAGACACAGTCAAGACATGGTGCTGGA
Long Flanking Sequence:
AGATTATAAGTAATGCATATTTAATACCAGCACAGCTACTATGTTTACATCATTAAAACTAAACACATGCTGTAATTCCTGCTGTTCTATAATCACCACCTACCGGCAGAGATTGAAGTGGCTTTTAATCCACACTCTTTGTTATTTTTGATATGTACAAGTATGTATATGTAACATCATTTCACAAAGCTGAAGTGAAACCATTACGTTGTATTTTTCTGGATGTATACAGATAATAAATTCTAATTCTGTTTTTTATTTATTTATTTATTTTTATCAAAAAAGAGAGTTAAATCAACTTAAATGCTTGTCATTCAGAGATACTTTCAACCAAGATTATTTCATCACTACCTTTTTCCTCATCTGTGTTTACTGTATGTCTTTGCAGCTCAGAATTGCTCTGGTTTGCGTACATGCGGCCTGTGTCTGGAACAGCCTGACTGTGGATGGTGTGGAGACCCCAGTAACACCGGCCGAGGGCAGTGCATGGAGGGTTCGTA[T/G]CGCGGACCCATGAAGAGCCCCTCCAGACACAGTCAAGACATGGTGCTGGAGACGGGGCTCTGTCCAAAAGAGAGAGGCTTTGAGTGGGCCTTCATCCAGTGTCCTGGTAAAAACTTTTACAGTCAAACAATCACTTGCAAACTTGACCTTTAAAGAGCACGGTTTTGTTTTGCCAGGGGTTTTCAAACTGCTGTTCAGGGATGTCCGGGGGGCACAACATGGTGCTACTTGTTCTGAAAACAAATATTTAAATTTGTTATATAAATTATATATTATATTTTCTTTTTAGGACTGTTATTGGTAATGCTTTATTTAAAGAAATTGCCGTTGTATTATTTATTGATTCAAATAGACCTAAGTCATTCTGTTATCTCAGCAGTAGGTCTTCAACTAAAGAAAGAGAAACAAAGTTGTTTAGATTTGTAGCCAAATTAGAGTGAGATAAATGATTTTATACAGATGGCAGCATAATTGTTTCATTAAAATCATGCTAAAATCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7363
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
Founder:
SL4-37
KASP Assay Location:
Project 554.35, Plate 4, Well C04
Mutation:
C > G
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042514 | Missense | 1198 | 1364 | 24 | 29 |
Genomic Location (Zv9):
Chromosome 12 (position 31494817)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 29806181 |
GRCz11 | 12 | 29921083 |
KASP Assay ID:
554-4317.1 (used for ordering genotyping assays)
KASP Sequence:
ACAGYAACCCAAACATCACMTTCTATGTGTATGTCAGCAACTTCTCATGG[C/G]CAATCAAAATACAGGTAAGGACTCTTTTCCTCTGGTTTGTCAGCTATTGA
Long Flanking Sequence:
AAGTAGCATTTAGTCTTGAACTCTTGTAAGCCCACCAGTCCAAGCAGGGGCGAACCTGTGAATTTTTTTCCAAACTTTTAGGATACTGGTGATCAGATTTGCACAATCCATATGCACAACGCTTTGGCTTGTTTCCCTCATTCAAAAGCTTGACAGACCTCTAGCGCATAGCTATGGTTGCTAAGTCACGATAGGTGTACGGTGGTTTTCGGGTGTGATTTAGCAAAGAGTCAGTTGATTGATTAAGTTGTGTCAAATGGTATTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATTTGCATTCATCTATTCATTTTTGATTTCTTCCTACAGCTGGGACCATCTCTGGAGAAGAGATTCCTATTGTGTCCAAGACCAACATCAAAGAGTACAGAGACAGTTTCTCTTGTGAAAAGTTCAGTTTTCACAGTAACCCAAACATCACATTCTATGTGTATGTCAGCAACTTCTCATGG[C/G]CAATCAAAATACAGGTAAGGACTCTTTTCCTCTGGTTTGTCAGCTATTGAGACTTCAAAATGCTTCTTTTTTACTTTTGGGTGACACGTGAATCATCCATCTCCTTTGTGAAATGGAAATCTACAAAAACAAATGTTTCTAAAACAGTGATACAGCGATATGAAAATCAATTATTCAGTTATGCACTGGGACAAGGGTGCATCTTATGGTCCATAAAATTGAATCAGCTCTTAAGTGGCAATGTGTTACATTGCCAGATGCCTAGACGACGAACATGAAATGACATTGCTGGAGTAATGTGTAGACTGATGCTATCTATCATGGAAAAACATTTACGTTGAATCTCCAAGGTGGAACATCACTCTTATTATGAACGATGGTTGCCGTCTTTATTGCCTGCAATCAAACAGAATAAGACAAATGCATTCGATTGCACAGGTAGTTTGGTTTTAGAAGGGAAAAAAAAACTTGTCTGGATGAAACCTCTAACCTATTTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31883
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:
Founder:
SL6_05_B6
KASP Assay Location:
Unknown
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042514 | Nonsense | 1312 | 1364 | 28 | 29 |
Genomic Location (Zv9):
Chromosome 12 (position 31424819)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 29737924 |
GRCz11 | 12 | 29852826 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGTTCAGGGGGTAAAGCTGCAGTGCTTACGGTGCTAATGTGCCTCCCA[C/T]GAGTGGCATCTGGTGTCCCTCCACCCGGCCAGTCAGGTCAGTAATTTACC
Long Flanking Sequence:
GTAGCTGAAAAATCCATAATGTGACTTAAAAGATGACATTTTAAGATCACTGCGATCGCCTGTGGGTTCTTCCCTCCTCATTCCACTGTTTCATCTGATGCACGCTTCTAACCAGAGCAGCGTTTATAGGGACAGAGAGGGAGTGCTACAACACGACCCGAGCTGGTAGTCGACAACCTCAAATGTCACAGATTTTCTCCGCCTCTGCGTGCCTGATGTGAACTTTGAAAGTGGCTCGCTTTGAGTTTCACAGAGGTGATTTGTTACTGAGATTATCACAATGTGAATTTTCCTTTTCTGGCGATGTGCGAGAGACATCCTACAATGTCATCTCACACTGTGACATTTGTGACTGATGGTGATGTGTTAGGGAGAAGGCTTGTTATAGATGACACATTTCCTCTCTTCTGATCTCTCTGCAGGGGCCGCCCAAGCCAGTTGCTGTGGAACCCTGTTCAGGGGGTAAAGCTGCAGTGCTTACGGTGCTAATGTGCCTCCCA[C/T]GAGTGGCATCTGGTGTCCCTCCACCCGGCCAGTCAGGTCAGTAATTTACCAACATATCCTAATACTGGATGTGTGCATGCTTTAAATTGATCTTGTTTTATATGTAGCCTAAAACTGTGTGTGCGTGTATATATATATATATACACACACACGCAAACACACATACCGTTGTAGTCAGAATTATTAGCCCCCCTTAATTATTAACCCAACTATGTTTATATATATTTTATCAAATGTATAGCTTTAAAATTAATAGATTGAATAAACGAAATATGAATGCTTTAATGGTTGATATTAACAACCCTGTTTTGTGACAGATTATGAGAACATCAAGGTAGATTTTTAGAGAAGGGCTGCACAATATATATTTTCAGCATCAATATCGCAATGTGCACTTCCACAATAGTCACCAGTGGTTTAAAGTAACAAATTAAAAATGCTCAGATTACTGTAATTGAGTAGTTCTACTCAGAAATTGTTATTTACTATGTAGTTTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35315
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
Founder:
SL6_08_B10
KASP Assay Location:
Unknown
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042514 | Nonsense | 1363 | 1364 | 29 | 29 |
Genomic Location (Zv9):
Chromosome 12 (position 31416851)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 29729956 |
GRCz11 | 12 | 29844858 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGGATTGAAGAACCGCAAAGCTCTGCCTCCTGCTCACCAGGGCACCTG[C/A]GTTTGAATCGTCTGTGGCCTCGGTGGGCTGTCCTTTTTTCCAGAGCGACC
Long Flanking Sequence:
TTTGGGGTTGTGGCCATGGTTTTGGCTACAGCAGCCCATGACAGAATTCTGGCGAAAGCATATAGGGCACTGGGAGTCAAATTCACTTCAAACCCCTATCCTAGAATAAAGGATGCGCCTTAAAACTGATGACCTTGACATTTAATAAGAAGTTTTTCAAAGCTCCCAACTCTCTCTCTTTTTTTAATACATACACTCTGTCTTTAAAAATGAATGAGCTGATAGTTGTTCTTTTGACAGAGATAGCTTTAAGTAACCATTGTCCCTTTTTAAATAACTTTGCTTTGACATGTAAATGAAGCGTTTTTGCTTTTGAATGCTCTCGGTGAAGTCTACGCTGCTCTTCTCTGACCCTCGGCTTGCTTTGTTGTGTTGTCTGCAGGTATAGCTATCGCCAGCGCTCTTATCGACACGTCCCAGCAGAAGCCCATGGACTTCAAAGAGAAAAGCCAAGGATTGAAGAACCGCAAAGCTCTGCCTCCTGCTCACCAGGGCACCTG[C/A]GTTTGAATCGTCTGTGGCCTCGGTGGGCTGTCCTTTTTTCCAGAGCGACCTCCTCTCTTGTGCTGTTCCAGGCAGACGACGGTGGCCTCATGCGGCTCCATATGAGGGGATTATTTAGGTGACAGAGTGCCCTCTATTTCCACTCAAACATTCACTTTATCTTTCCATGTCAACTGAACATCGTAAATAGATCTCGTCCATCACAAACGACCTGCTCCGGCTCAAGAATCACTTTACCAGTCCCTAACCCTAACCTCAGCTTAAATCATCCTTCCTCTAGAGCCATTTCAAGACCTTTTGAACTTCCAGTCGTCTCGCCATCAGCTTCTTACCAAGCACAGATGTGCCTCTAGCATGGTTTGTATTTAAATTATGGACCAGAGTGTCTTGCTAAGCCAGAAATAGCATTCTGGTAGTTCAAGTACGGGTTGAACAGCTCACCTTATTTGTATGCTTGCCAACTGAACTTAGATTTTTGCTCTTTTTTTTCTTTTTATTTA
Associated Phenotype:
Not determined