ZMP
si:ch211-155k24.6
Ensembl ID:
ZFIN ID:
Human Orthologue:
GPNMB
Human Description:
glycoprotein (transmembrane) nmb [Source:HGNC Symbol;Acc:4462]
Mouse Orthologue:
Gpnmb
Mouse Description:
glycoprotein (transmembrane) nmb Gene [Source:MGI Symbol;Acc:MGI:1934765]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11355 | Essential Splice Site | Available for shipment | Available now |
sa30711 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13099 | Nonsense | Available for shipment | Available now |
sa13185 | Nonsense | Available for shipment | Available now |
sa23503 | Essential Splice Site, Missense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11355
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090883 | Essential Splice Site | 116 | 621 | None | 12 |
ENSDART00000144891 | Essential Splice Site | 55 | 499 | None | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 20750424)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 20683804 |
GRCz11 | 19 | 20268127 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGAGGACAGCAATGGCAACCTGGTGTATGATGAACACTGTGATGACGG[T/C]ACGATGGACACCTCAGGTGCTTCATACCACTGTAATCTCTAAACAAAGCA
Long Flanking Sequence:
AATAATAATAATAATAATAATAATAATAATAATAAATATTTTGTAGTTAAATAAAAATAAAAACTATAAATAGCTTAAAATAATGAACTATCCTATACATAAAGTACAAAATATATACGTTTTTAAGATGTTTTAAAGTCAATAGTTTTTTCCATTATAGGCTATCAATGCTTTAAAATTTTGACAAAAAAGACAGAATCTTCAGTTTTGAGTGAATTATCCCTTTAAAGTTGTTCAGAATAGCAATATAAGACAGTTTTTCTTGTCTGGGGTCACAGATTTTTTACAAATTAATTTCCATCTTCAAAGACGATGACTGAAATGACATTAATCCCTCAGTCCTCTCTCATGACAGAAAAACCACCAAAGGTGCGTCTAACGAGTGACAGTCCTGCGATGAATGGCTCGTGCATCTCTTTCACTGCTGCTCTGGAGTTTCCTCCATGTCAGAAGGAGGACAGCAATGGCAACCTGGTGTATGATGAACACTGTGATGACGG[T/C]ACGATGGACACCTCAGGTGCTTCATACCACTGTAATCTCTAAACAAAGCAGTATTGTTAAGGGAGAAATGAGCTGTGTTTTAAAAGGTTGTAATTAAGCACACTGTAAAAATGCAGGGCTCCACACAATTCGATAAGGTTATCTTAACAAATTTAAGTGGATTGAACATAAAACAATAATGTTGACCAAAACAAATCTCGATAATTGAGTCGTTTCAGCTCATTTTAAATAAGTAGTTTGAAAAAGCATCAAAACCTTTTATTTTTATTTTTTATTTTTTTATTTTTATTTTTTTGTGCAGGTCATGTGTTGGGTCAATTAATCTGAAAAGTTTCAATTACTCAATAATTTATTTCATACTTGACTCCATACTACATAAAATTCCTACAAATCTCAATGGATCACAAAGAAATTAACCCCTTTTAATTGTTTAAATTTGTCAAACTGGGCCATTTAGTTTTTTATGTAATAAACATTTTCTTAAATGTTATTTAAATTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30711
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090883 | Essential Splice Site | 228 | 621 | 6 | 12 |
ENSDART00000144891 | Essential Splice Site | 167 | 499 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 20744415)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 20677795 |
GRCz11 | 19 | 20262118 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAAACCATTTACATTATTAGATTTTTATTCCATGTGTTTCTTTCATCT[A/G]GATAAGATTCCACTCTCCGTCAACATTTCCCAGAAGGAAGCAGCCAGCAG
Long Flanking Sequence:
ATGTTAATCAAAAGATTTTATTTCAAGTAAATGTAAATAAAAATGTATTACTGTTTCTATTTGAAAAATTCCAACATTGTTCCAATTAAAACTGAAAAGTTATTTTAAGAGGCAACATTGTGGCTCAGTGGTAAGCACTGTCACTTCACAGCAAGAAGGTTGCTGGTTTGAGTCCTGGCTGGACCAGTTTGCATTTTTGTGGGAAGTTTGCATGTTCTCCTCATGTTTACATGGGTTTCTTCTGGGTCCTCCAGTTTGCCCCACAGTCCAAAGACATGCACTATAGGGGAATTGAATAAACTAAATTGGCTGTAGTGTATGTGTGTGAACAAGTGTGTATGGGTGTTTCCCAGAACTAGGTTGCAGCTGGAAGGGCATTTGCTGGTTCATATACTTCATATATGAATTGTTAGATTAAAGGTGGATGGATGGAGGGATGAATGGATGGATGGAAAACCATTTACATTATTAGATTTTTATTCCATGTGTTTCTTTCATCT[A/G]GATAAGATTCCACTCTCCGTCAACATTTCCCAGAAGGAAGCAGCCAGCAGAGCGGACAGAAACATCTTTGTCAGAGGGTCTGATGTTATTTTCAACGTCCAGCTCCACGACCCCAGTAACTATCTGAAAACAGCTGATGCGGTGGACTTCATTTGGGACTTTCGGGATGGCAACCAGTTGGTGACACACAGCAGCGTGGCAACTCATGCATATGACATGCTTGGAAATGTTACAGTCAAGCTCCTGGTAGAGGCAGCATTTCGTGTTCCCTGCCCTCCACCGACTCCAACACCAGTGCACTTTACACAAGCTCACACCACAGGTAATCTCATAAACACAGGCACTTTACGCTCCCAGACAGGAGAGATGCTCTACTGCCAGACATTATCCATCACAATCAAAATGCATCCATTGACAGGGAATGCTGGCATGTTCAGCCCAAGCTTATCATAGTTTATTGTCTTTAAATCAGTTTTATATTTAGTACCATTTTAAAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13099
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 |
---|---|---|---|---|---|
ENSDART00000090883 | Nonsense | 261 | 621 | 6 | 12 |
ENSDART00000144891 | Nonsense | 200 | 499 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 20744315)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 20677695 |
GRCz11 | 19 | 20262018 |
KASP Assay ID:
2261-3216.1 (used for ordering genotyping assays)
KASP Sequence:
GAGCGGACAGRAACATCTTTGTCAGAGGGTCTGATGTTATTTTCAACGTC[C/T]AGCTCCACGACCCCAGTAACTATCTGAAAACWGCTGATGCGGTGGACTWC
Long Flanking Sequence:
TATTTTAAGAGGCAACATTGTGGCTCAGTGGTAAGCACTGTCACTTCACAGCAAGAAGGTTGCTGGTTTGAGTCCTGGCTGGACCAGTTTGCATTTTTGTGGGAAGTTTGCATGTTCTCCTCATGTTTACATGGGTTTCTTCTGGGTCCTCCAGTTTGCCCCACAGTCCAAAGACATGCACTATAGGGGAATTGAATAAACTAAATTGGCTGTAGTGTATGTGTGTGAACAAGTGTGTATGGGTGTTTCCCAGAACTAGGTTGCAGCTGGAAGGGCATTTGCTGGTTCATATACTTCATATATGAATTGTTAGATTAAAGGTGGATGGATGGAGGGATGAATGGATGGATGGAAAACCATTTACATTATTAGATTTTTATTCCATGTGTTTCTTTCATCTAGATAAGATTCCACTCTCCGTCAACATTTCCCAGAAGGAAGCAGCCAGCAGAGCGGACAGAAACATCTTTGTCAGAGGGTCTGATGTTATTTTCAACGTC[C/T]AGCTCCACGACCCCAGTAACTATCTGAAAACAGCTGATGCGGTGGACTTCATTTGGGACTTTCGGGATGGCAACCAGTTGGTGACACACAGCAGCGTGGCAACTCATGCATATGACATGCTTGGAAATGTTACAGTCAAGCTCCTGGTAGAGGCAGCATTTCGTGTTCCCTGCCCTCCACCGACTCCAACACCAGTGCACTTTACACAAGCTCACACCACAGGTAATCTCATAAACACAGGCACTTTACGCTCCCAGACAGGAGAGATGCTCTACTGCCAGACATTATCCATCACAATCAAAATGCATCCATTGACAGGGAATGCTGGCATGTTCAGCCCAAGCTTATCATAGTTTATTGTCTTTAAATCAGTTTTATATTTAGTACCATTTTAAAAATTGCCGTACATGTCAGTTTAGTTTTACACAAAAAAATACAGGGTTTCACACAATAGATTTGGGTTGGGACAACATAAAGGAATTAAGTTAACTTAATAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13185
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090883 | Nonsense | 279 | 621 | 6 | 12 |
ENSDART00000144891 | Nonsense | 218 | 499 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 20744260)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 20677640 |
GRCz11 | 19 | 20261963 |
KASP Assay ID:
2261-3215.1 (used for ordering genotyping assays)
KASP Sequence:
CCACGACCCCAGTAACTATCTGAAAACWGCTGATGCGGTGGACTWCATTT[G/A]GGACTTTCGGGAYGGCAACCAGYTGGTGACACACAGCAGCGTGGCAACTC
Long Flanking Sequence:
AAGGTTGCTGGTTTGAGTCCTGGCTGGACCAGTTTGCATTTTTGTGGGAAGTTTGCATGTTCTCCTCATGTTTACATGGGTTTCTTCTGGGTCCTCCAGTTTGCCCCACAGTCCAAAGACATGCACTATAGGGGAATTGAATAAACTAAATTGGCTGTAGTGTATGTGTGTGAACAAGTGTGTATGGGTGTTTCCCAGAACTAGGTTGCAGCTGGAAGGGCATTTGCTGGTTCATATACTTCATATATGAATTGTTAGATTAAAGGTGGATGGATGGAGGGATGAATGGATGGATGGAAAACCATTTACATTATTAGATTTTTATTCCATGTGTTTCTTTCATCTAGATAAGATTCCACTCTCCGTCAACATTTCCCAGAAGGAAGCAGCCAGCAGAGCGGACAGAAACATCTTTGTCAGAGGGTCTGATGTTATTTTCAACGTCCAGCTCCACGACCCCAGTAACTATCTGAAAACAGCTGATGCGGTGGACTTCATTT[G/A]GGACTTTCGGGATGGCAACCAGTTGGTGACACACAGCAGCGTGGCAACTCATGCATATGACATGCTTGGAAATGTTACAGTCAAGCTCCTGGTAGAGGCAGCATTTCGTGTTCCCTGCCCTCCACCGACTCCAACACCAGTGCACTTTACACAAGCTCACACCACAGGTAATCTCATAAACACAGGCACTTTACGCTCCCAGACAGGAGAGATGCTCTACTGCCAGACATTATCCATCACAATCAAAATGCATCCATTGACAGGGAATGCTGGCATGTTCAGCCCAAGCTTATCATAGTTTATTGTCTTTAAATCAGTTTTATATTTAGTACCATTTTAAAAATTGCCGTACATGTCAGTTTAGTTTTACACAAAAAAATACAGGGTTTCACACAATAGATTTGGGTTGGGACAACATAAAGGAATTAAGTTAACTTAATAGTTTTTACTAAGTTTAAGGATTTTGTTGTCTCAGCTCAAGGTTTAATATTTGCACAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23503
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:
G > T
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090883 | Missense | 603 | 621 | 12 | 12 |
ENSDART00000144891 | Essential Splice Site | 481 | 499 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 20734216)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 20667596 |
GRCz11 | 19 | 20251919 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGAGGATGCAGAGAGGAATACTGATAGCTGGGGCTTAGGCAAACTTAGA[G/T]CAGTTCTGTTCTCAGTGGATGAGGAAAGAAGCTGTTTATTGACCGAAAAG
Long Flanking Sequence:
AACCTAATCAATCTGTGTTGGGACAAAATAAATTGTTAATCCATTTGTAAAACATATTGTCCCAACACAAATCCATTGAGTTAATATCGTTTTTACAAATTTAAGTGGACTGAACATAAACCAATCAAGTTGTTCCCAAAAGAAACTCAAGAATTGTGCTGTTTCAGCCCATTTTAAATAAGTAGTTTGAACAAAGATCTTTTTTGAGTGCCGTGCATTAACCAAACTGATTTCTATTTAAAAAATATGATACTACACTGTAAAACAAACTGGGTTGCTTCAACTCAAATTTAATATGGACAAACCCAACAATTGGGATAAAATTTCGTATACATATCCCATTATCTTTACTTATTTTTAAGGTTTATGTTTATACATCAATTGATTTATTTATTTTTACATTTTTTTCCAGGCGCTACAAGGTGTATCGTCCGGTCAGACGCTCAATGCTAGAGGATGCAGAGAGGAATACTGATAGCTGGGGCTTAGGCAAACTTAGA[G/T]CAGTTCTGTTCTCAGTGGATGAGGAAAGAAGCTGTTTATTGACCGAAAAGCCACAATAGGCTGACCTGAGCTGTCGTAGTCACCAGTTTCTACGGGTGCTACTTATTTAATACATCACCTTAGCTGTAAAACTATAAAAAATACAAGTGATAGGTGAGTGCAAGGGCGTAGAATTGAAATAAATAAAGGGGACATTTGTCCTCACCAATATCCACCAATTACTGACATGTCCCTGCCAATTATTGAATCGACTTCGAAATAAAATAATGCTCTGTCAACCCTTAGTAACCTACTTGTGCACAAAGGGTCAAGTTTGCTATAAGTTTACTATAATACTATTTACCAAGGCTATGCAAATACTCAAAAATCAGTTTGGATTTTGGCCTCCATGATTATGACAAACAATAATCAGAATAAAACAGTAAAATTGCATCACACACCTCTCTAAATTTCTCTACATTCATGTATATTGAAACCTGATTATTTACAACATGTAAGTG
Associated Phenotype:
Not determined