ZMP
socs5b
Ensembl ID:
ZFIN ID:
Description:
suppressor of cytokine signaling 5b [Source:RefSeq peptide;Acc:NP_001107269]
Human Orthologue:
SOCS5
Human Description:
suppressor of cytokine signaling 5 [Source:HGNC Symbol;Acc:16852]
Mouse Orthologue:
Socs5
Mouse Description:
suppressor of cytokine signaling 5 Gene [Source:MGI Symbol;Acc:MGI:2385459]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9767 | Nonsense | Available for shipment | Available now |
sa35423 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11807 | Nonsense | Available for shipment | Available now |
sa38920 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6285 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42137 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9767
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 |
---|---|---|---|---|---|
ENSDART00000091097 | Nonsense | 172 | 557 | 2 | 2 |
ENSDART00000125735 | Nonsense | 213 | 598 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 7985218)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 8289738 |
GRCz11 | 13 | 8621761 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGAAGTTGGCAGCAGCGGGCGYAGCCTTAGCAGCCGTTCTCTGCGACAA[C/T]GACTTCGAGACACCGTGGGCTTGTGCCTTCCTCTCCCCACACACCGSCGC
Long Flanking Sequence:
TTAGAAGCCGATGCCAAGCTCTCTTCCACAGTGACGGCTCAGAGTCCCATCTGTGTAGTCAAGACTTAGATTGTGCTCACTGTGTGCTGGATTTGGACAGGGGAGCACATGCAGAACCCTATGAAACCAGGTCTTCCACACCTTCACGCAACTTGTCACCTCTTCCATTGGCTACTGGTGGACGCAGAAGCCATAATTGTGTGGCGGATATTCCTCAAATAGTAGAAATCTCCATTGACAAAGAGAGTGAAGATGCACGGAGAGGCCCACTTGTTCGCAGGGACTCCTATTCACGTCATGCTCCCTGGGGAGGTAAAAAGAAGCATTCTTGCTCAACTAAAACACAAAGTTCTCTTGAGGCTGACAGGCGAACAGGACGCTCAAGAGGAAGTACAGCCAGAAGGGAGCGTCGTTATGCCGTCAGCTCCATTCAAGAAATTAATGATTCTGTAGAAGTTGGCAGCAGCGGGCGTAGCCTTAGCAGCCGTTCTCTGCGACAA[C/T]GACTTCGAGACACCGTGGGCTTGTGCCTTCCTCTCCCCACACACCGCCGCTCTCAGTCAGCCAAAGGTCAAGTATCCTCAAAACGTAAGATCCACCTGACAGAACTGATGCTCGAAACATGCCCTTTTCCTCCAGGTTCTGATCTGGCCAACAAGTGGCACCTAATTAAGCAACATACAGCACCAGTCAGCCCTCATTCCTCTTCTGCTCTTTTTGATGCTTTTGATTCAGCCCATTCTTCACCTGAGGACGAGGAGGAGAGGCTGCGTGAACGACGTAGACTTAGCATCGAGGAAGGAGTAGACCCACCTCCAAATGCGCAAATCCATACATTGGAGGCAACTTCAAAGAGCTCTTCCCTCTATAAACTAGGACCAAAGATGGCTCCTGGTGTTGGGGAAACACTTGGGGAGGGCAGGAGCCTAGGAACAGTCTCCTCCATTTCTGGGGGATTATCAGGGATCGCCGCACAGGTTCCAACAAGTATGGCAGTGCCATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35423
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091097 | Nonsense | 263 | 557 | 2 | 2 |
ENSDART00000125735 | Nonsense | 304 | 598 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 7985491)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 8290011 |
GRCz11 | 13 | 8622034 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGATTCAGCCCATTCTTCACCTGAGGACGAGGAGGAGAGGCTGCGTGAA[C/T]GACGTAGACTTAGCATCGAGGAAGGAGTAGACCCACCTCCAAATGCGCAA
Long Flanking Sequence:
TTCGCAGGGACTCCTATTCACGTCATGCTCCCTGGGGAGGTAAAAAGAAGCATTCTTGCTCAACTAAAACACAAAGTTCTCTTGAGGCTGACAGGCGAACAGGACGCTCAAGAGGAAGTACAGCCAGAAGGGAGCGTCGTTATGCCGTCAGCTCCATTCAAGAAATTAATGATTCTGTAGAAGTTGGCAGCAGCGGGCGTAGCCTTAGCAGCCGTTCTCTGCGACAACGACTTCGAGACACCGTGGGCTTGTGCCTTCCTCTCCCCACACACCGCCGCTCTCAGTCAGCCAAAGGTCAAGTATCCTCAAAACGTAAGATCCACCTGACAGAACTGATGCTCGAAACATGCCCTTTTCCTCCAGGTTCTGATCTGGCCAACAAGTGGCACCTAATTAAGCAACATACAGCACCAGTCAGCCCTCATTCCTCTTCTGCTCTTTTTGATGCTTTTGATTCAGCCCATTCTTCACCTGAGGACGAGGAGGAGAGGCTGCGTGAA[C/T]GACGTAGACTTAGCATCGAGGAAGGAGTAGACCCACCTCCAAATGCGCAAATCCATACATTGGAGGCAACTTCAAAGAGCTCTTCCCTCTATAAACTAGGACCAAAGATGGCTCCTGGTGTTGGGGAAACACTTGGGGAGGGCAGGAGCCTAGGAACAGTCTCCTCCATTTCTGGGGGATTATCAGGGATCGCCGCACAGGTTCCAACAAGTATGGCAGTGCCATCCCACACGGTTGACTGTGACTCTGAGGAGGACTCAACTACCCTTTGCTTACAGACACGAAGGCCCAAGCAGAGGCATGCCTCTGGAGACACTCACTGCTCCAGACAGCCAGGGCCTTGGAAGGTCCACACACAGATTGACTACATCCATTGTTTAGTACCTGACCTACAGGCCATAACTGCACTTCCTTGTTATTGGGGAGTGATGGACCGGTACCAAGCTGAAGCCCTGCTGGATGGACGGCCAGAAGGCACCTTCCTTCTACGCGACTCCGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11807
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 |
---|---|---|---|---|---|
ENSDART00000091097 | Nonsense | 283 | 557 | 2 | 2 |
ENSDART00000125735 | Nonsense | 324 | 598 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 7985552)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 8290072 |
GRCz11 | 13 | 8622095 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGCATCGAGGAAGGAGTAGACCCACCTCCAAATGCGCARATCCATACAT[T/A]GGAGGCAACTTCAAAGAGCTCTTCCCTCWATAAACTAGGACCAAAGATGG
Long Flanking Sequence:
AACTAAAACACAAAGTTCTCTTGAGGCTGACAGGCGAACAGGACGCTCAAGAGGAAGTACAGCCAGAAGGGAGCGTCGTTATGCCGTCAGCTCCATTCAAGAAATTAATGATTCTGTAGAAGTTGGCAGCAGCGGGCGTAGCCTTAGCAGCCGTTCTCTGCGACAACGACTTCGAGACACCGTGGGCTTGTGCCTTCCTCTCCCCACACACCGCCGCTCTCAGTCAGCCAAAGGTCAAGTATCCTCAAAACGTAAGATCCACCTGACAGAACTGATGCTCGAAACATGCCCTTTTCCTCCAGGTTCTGATCTGGCCAACAAGTGGCACCTAATTAAGCAACATACAGCACCAGTCAGCCCTCATTCCTCTTCTGCTCTTTTTGATGCTTTTGATTCAGCCCATTCTTCACCTGAGGACGAGGAGGAGAGGCTGCGTGAACGACGTAGACTTAGCATCGAGGAAGGAGTAGACCCACCTCCAAATGCGCAAATCCATACAT[T/A]GGAGGCAACTTCAAAGAGCTCTTCCCTCTATAAACTAGGACCAAAGATGGCTCCTGGTGTTGGGGAAACACTTGGGGAGGGCAGGAGCCTAGGAACAGTCTCCTCCATTTCTGGGGGATTATCAGGGATCGCCGCACAGGTTCCAACAAGTATGGCAGTGCCATCCCACACGGTTGACTGTGACTCTGAGGAGGACTCAACTACCCTTTGCTTACAGACACGAAGGCCCAAGCAGAGGCATGCCTCTGGAGACACTCACTGCTCCAGACAGCCAGGGCCTTGGAAGGTCCACACACAGATTGACTACATCCATTGTTTAGTACCTGACCTACAGGCCATAACTGCACTTCCTTGTTATTGGGGAGTGATGGACCGGTACCAAGCTGAAGCCCTGCTGGATGGACGGCCAGAAGGCACCTTCCTTCTACGCGACTCCGCACAGGAGGACTACTTGTTCTCTGTTAGTTTTCGACGTTACAATCGGTCACTGCATGCACGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38920
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 |
---|---|---|---|---|---|
ENSDART00000091097 | Nonsense | 287 | 557 | 2 | 2 |
ENSDART00000125735 | Nonsense | 328 | 598 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 7985564)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 8290084 |
GRCz11 | 13 | 8622107 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGTAGACCCACCTCCAAATGCGCAAATCCATACATTGGAGGCAACTT[C/A]AAAGAGCTCTTCCCTCTATAAACTAGGACCAAAGATGGCTCCTGGTGTTG
Long Flanking Sequence:
AAGTTCTCTTGAGGCTGACAGGCGAACAGGACGCTCAAGAGGAAGTACAGCCAGAAGGGAGCGTCGTTATGCCGTCAGCTCCATTCAAGAAATTAATGATTCTGTAGAAGTTGGCAGCAGCGGGCGTAGCCTTAGCAGCCGTTCTCTGCGACAACGACTTCGAGACACCGTGGGCTTGTGCCTTCCTCTCCCCACACACCGCCGCTCTCAGTCAGCCAAAGGTCAAGTATCCTCAAAACGTAAGATCCACCTGACAGAACTGATGCTCGAAACATGCCCTTTTCCTCCAGGTTCTGATCTGGCCAACAAGTGGCACCTAATTAAGCAACATACAGCACCAGTCAGCCCTCATTCCTCTTCTGCTCTTTTTGATGCTTTTGATTCAGCCCATTCTTCACCTGAGGACGAGGAGGAGAGGCTGCGTGAACGACGTAGACTTAGCATCGAGGAAGGAGTAGACCCACCTCCAAATGCGCAAATCCATACATTGGAGGCAACTT[C/A]AAAGAGCTCTTCCCTCTATAAACTAGGACCAAAGATGGCTCCTGGTGTTGGGGAAACACTTGGGGAGGGCAGGAGCCTAGGAACAGTCTCCTCCATTTCTGGGGGATTATCAGGGATCGCCGCACAGGTTCCAACAAGTATGGCAGTGCCATCCCACACGGTTGACTGTGACTCTGAGGAGGACTCAACTACCCTTTGCTTACAGACACGAAGGCCCAAGCAGAGGCATGCCTCTGGAGACACTCACTGCTCCAGACAGCCAGGGCCTTGGAAGGTCCACACACAGATTGACTACATCCATTGTTTAGTACCTGACCTACAGGCCATAACTGCACTTCCTTGTTATTGGGGAGTGATGGACCGGTACCAAGCTGAAGCCCTGCTGGATGGACGGCCAGAAGGCACCTTCCTTCTACGCGACTCCGCACAGGAGGACTACTTGTTCTCTGTTAGTTTTCGACGTTACAATCGGTCACTGCATGCACGCATTGAACAATGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6285
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 |
---|---|---|---|---|---|
ENSDART00000091097 | Nonsense | 385 | 557 | 2 | 2 |
ENSDART00000125735 | Nonsense | 426 | 598 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 7985859)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 8290379 |
GRCz11 | 13 | 8622402 |
KASP Assay ID:
554-5421.1 (used for ordering genotyping assays)
KASP Sequence:
CACTGCTCCAGACAGCCAGGGCCTTGGAAGRTCCACACACAGATTGACTA[C/A]ATCCATTGTTTAGTACCTGACCTACAGGCCATAACTGCACTTCCTTGTTA
Long Flanking Sequence:
GATCTGGCCAACAAGTGGCACCTAATTAAGCAACATACAGCACCAGTCAGCCCTCATTCCTCTTCTGCTCTTTTTGATGCTTTTGATTCAGCCCATTCTTCACCTGAGGACGAGGAGGAGAGGCTGCGTGAACGACGTAGACTTAGCATCGAGGAAGGAGTAGACCCACCTCCAAATGCGCAAATCCATACATTGGAGGCAACTTCAAAGAGCTCTTCCCTCTATAAACTAGGACCAAAGATGGCTCCTGGTGTTGGGGAAACACTTGGGGAGGGCAGGAGCCTAGGAACAGTCTCCTCCATTTCTGGGGGATTATCAGGGATCGCCGCACAGGTTCCAACAAGTATGGCAGTGCCATCCCACACGGTTGACTGTGACTCTGAGGAGGACTCAACTACCCTTTGCTTACAGACACGAAGGCCCAAGCAGAGGCATGCCTCTGGAGACACTCACTGCTCCAGACAGCCAGGGCCTTGGAAGGTCCACACACAGATTGACTA[C/A]ATCCATTGTTTAGTACCTGACCTACAGGCCATAACTGCACTTCCTTGTTATTGGGGAGTGATGGACCGGTACCAAGCTGAAGCCCTGCTGGATGGACGGCCAGAAGGCACCTTCCTTCTACGCGACTCCGCACAGGAGGACTACTTGTTCTCTGTTAGTTTTCGACGTTACAATCGGTCACTGCATGCACGCATTGAACAATGGAATCACAACTTCAGCTTTGATGCACATGACCCATGTGTCTTCCACTCCTCCACAGTAACAGGTTTACTGGAGCATTATAAAGACCCCAGTGCTTGTATGTTCTTTGAACCCCTGCTCACTGCTCCCTTACACCGGACCTTCCCTTTCAGCCTTCAGCACCTGGCACGATCCTCCATCTGTAGACACACCACCTATGATGGCATTGGTGCCCTGCCACTGCCTCCAACCATGCAGGACTTCCTCAAGGAGTATCACTACAAACAAAAAGTTCGTGTGCGCTGGTTAGAGAGAGAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42137
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091097 | Nonsense | 440 | 557 | 2 | 2 |
ENSDART00000125735 | Nonsense | 481 | 598 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 7986022)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 8290542 |
GRCz11 | 13 | 8622565 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTCTACGCGACTCCGCACAGGAGGACTACTTGTTCTCTGTTAGTTTT[C/T]GACGTTACAATCGGTCACTGCATGCACGCATTGAACAATGGAATCACAAC
Long Flanking Sequence:
ACCCACCTCCAAATGCGCAAATCCATACATTGGAGGCAACTTCAAAGAGCTCTTCCCTCTATAAACTAGGACCAAAGATGGCTCCTGGTGTTGGGGAAACACTTGGGGAGGGCAGGAGCCTAGGAACAGTCTCCTCCATTTCTGGGGGATTATCAGGGATCGCCGCACAGGTTCCAACAAGTATGGCAGTGCCATCCCACACGGTTGACTGTGACTCTGAGGAGGACTCAACTACCCTTTGCTTACAGACACGAAGGCCCAAGCAGAGGCATGCCTCTGGAGACACTCACTGCTCCAGACAGCCAGGGCCTTGGAAGGTCCACACACAGATTGACTACATCCATTGTTTAGTACCTGACCTACAGGCCATAACTGCACTTCCTTGTTATTGGGGAGTGATGGACCGGTACCAAGCTGAAGCCCTGCTGGATGGACGGCCAGAAGGCACCTTCCTTCTACGCGACTCCGCACAGGAGGACTACTTGTTCTCTGTTAGTTTT[C/T]GACGTTACAATCGGTCACTGCATGCACGCATTGAACAATGGAATCACAACTTCAGCTTTGATGCACATGACCCATGTGTCTTCCACTCCTCCACAGTAACAGGTTTACTGGAGCATTATAAAGACCCCAGTGCTTGTATGTTCTTTGAACCCCTGCTCACTGCTCCCTTACACCGGACCTTCCCTTTCAGCCTTCAGCACCTGGCACGATCCTCCATCTGTAGACACACCACCTATGATGGCATTGGTGCCCTGCCACTGCCTCCAACCATGCAGGACTTCCTCAAGGAGTATCACTACAAACAAAAAGTTCGTGTGCGCTGGTTAGAGAGAGAGCCACCATTCAAGGTCAAATGAGGTCTGGCTCTGTGCCTGAGTAAACCTGGGGTGTGAGCTTACCTTCTCATATTATTATGTGCTTCAGACACATGGCAATAGAGGATGTTTTGAACTTCCGGCAGTTTTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Associated Phenotype:
Not determined