Busch Lab

ZMP

fam120c

Ensembl ID:
ENSDARG00000019205
ZFIN ID:
ZDB-GENE-090313-228
Human Orthologues:
FAM120A, FAM120C
Human Descriptions:
family with sequence similarity 120A [Source:HGNC Symbol;Acc:13247]
family with sequence similarity 120C [Source:HGNC Symbol;Acc:16949]
Mouse Orthologues:
Fam120a, Fam120c
Mouse Descriptions:
family with sequence similarity 120, member A Gene [Source:MGI Symbol;Acc:MGI:2446163]
family with sequence similarity 120, member C Gene [Source:MGI Symbol;Acc:MGI:2387687]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa37663 Nonsense Mutation detected in F1 DNA Not yet available
sa24291 Essential Splice Site Available for shipment Available now
sa959 Essential Splice Site F2 line generated Not yet available
sa1353 Essential Splice Site Confirmed mutation in F2 line Not yet available
sa24290 Nonsense Available for shipment Available now
sa37662 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa37663
Status:
Mutation detected in F1 DNA
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
ENSDART00000065881 Nonsense 135 1051 1 17
ENSDART00000135430 Nonsense 135 1047 1 16
Genomic Location (Zv9):
Chromosome 23 (position 18585343)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 18488282
GRCz11 23 18414625
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCGCTGGCCGGAGTGGGCGCGGCGGGCGCAGGGGCAGCGGCAGACCGCA[C/T]AGCTCATCGTCAACCACGTCGGAAGCAAGGCCACGCCCCCTCCGCGGGCC
Long Flanking Sequence:
CTAACTACAACCGGTCAGATCGAGATCTGAGCACATAACCTACAATTCAACTTGTTATCAAGGTTCATCCATCTCACGCGCTTAGACACACATTCAGTATGGGAGTTCAAGGGTTTCAGGAGTATTTGGAGAAGCGCTGCCCCGGGGCGGCAGTTCCAGTAGATCTCCTCAAGCTCGCCCGCACGGCAGGCCGACAGCCCCCACACCACCATCCACACCACCACCACCATCCCCATCATCCCAGCTCGCTGCCTCCGCCTCCCCCGCCAGCTCGCATTCTGGTTGACGCAGACTCCGGCCTTCAGCGACTCTACGGGGGCTACCAGACCGACTGGGTTTGTGGAGGCGAGTGGAATGCAATGCTCGGCTATCTGGCGGCCCTCTCCCAGGCCTGTTTGTACCAGGGCGGACTGGAGCTTGTGGTGGTTTTTAACGGCACGCTTGGGAAGGATCGCTGGCCGGAGTGGGCGCGGCGGGCGCAGGGGCAGCGGCAGACCGCA[C/T]AGCTCATCGTCAACCACGTCGGAAGCAAGGCCACGCCCCCTCCGCGGGCCTGGTTCCTGCCCCCGGCCTGCCTGAGCCACTGTGTCCGCCTCGCCATGTTCCGATTCCGCGTGCGGGTGAGTGGCCTGATGCCCTCCTCGAGAGGAATTGTTATTAAACCAGTATGTGCTGCAAATGCTTTACCTGCTTTAACTAATTGTCTTATTGTAATGTAAATATGTGCCAAAGTTCATATGCCTTAGTTTAATATTTGATTAATAAAATGTTTAAAAACGATTGATGGTTTAAAATTATGATTCCAGTCCAATAAGTAGCTCTTAAAATCTGTTATTGAGCAGGTCTCCTCATCAGAACTGGTGTGATATTACATGACCAGTCGAATAATTAAATTTGCTATAATTTATTACAAGTTTTTTTTTATGAATTTCGAAGTTGTATTTTCAGCGTCAGGTATGTCAGGTGGCAATGCACATTTTTACATAAAAATGTGTACTATTTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24291
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065881 Essential Splice Site 256 1051 2 17
ENSDART00000135430 Essential Splice Site 256 1047 2 16
Genomic Location (Zv9):
Chromosome 23 (position 18579873)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 18482812
GRCz11 23 18409155
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTTGGCCTCAAGACACAGCACCTGCCCATTTTTGCTGCTCTTCTTGG[T/A]AAGCGAAGCTAACATGAACATGACTTTATCTTTAAAGAACATTATTTAGT
Long Flanking Sequence:
TGCGAAGGCTTTCTCTCCTCTAATTAAATTACAGCTTAATATCTAAGAGAGTTAAGAAGTACAAGTGATATCAGTGTATTGAAAATATGCAGAAAATAAGTATTGAAATTATTTTTAAAAATCTGTGTTATTTTCATATTAATCCAAGATTATTGTCAGCAAATGTAGTATTTTCAGTTCAGATCAGTTGTAGCTTGTTGCTTAGTAAGTCACAAGAACACGTGATCACCTTCCACCCTGCTTGTGTTGTAGGTGGTGCAGACCCTGGAGGACCATCATCAGGAGGTGCTATCCCTGTACAGAGACTATGGTTTTCAGGGTCTGATTGCACAGGACTCAGAGTTTGCGCTATGCAACGTTCCGGCCTATTTCAGCTCCCACGCTCTCAAGCTCTCCTGGAATGGCAAGAATCTGACCACTCACCAGTACCTGCTATCAGAGGCGGCTCGCCAGCTTGGCCTCAAGACACAGCACCTGCCCATTTTTGCTGCTCTTCTTGG[T/A]AAGCGAAGCTAACATGAACATGACTTTATCTTTAAAGAACATTATTTAGTTCTAAATGTGGCCCTTCAAAAAAACAAACAGGTAACCACATTCTGCCAGATGAAGACTTGGCTGCCTTTCATTGGAGTCTTCTAGGCCCAGAACACCCTCTTGCCTCCCTCAAGGTGCTAAAATGATTTGTCAGTTCACACACTTTATGATATTCTCTTTTTTTTGTAGTTGTAATGGATGAGATATTTAAGCATCCTTGTGCTTTACACTTATTAGCACAACCCATACTTTATTTGTTGCTCTTTGCTTCATTATTTGTTTGTTTTTTTTTCTGCTCAGGTAAGGGCTCATCAGTTAGTCCTCCCTCCATGTGAGGTTGTTATCAAGGCTGTTTCTGAGTATGTGGCATCCATCAAAGATCTTGGGAATTTAGATTCGGTGGCCAAGGATGTTTTCAAGCAGTCACAGGTGAAGCATGCCGTGTTTACACATTTATTTGCATGTGAGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa959
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065881 Essential Splice Site 385 1051 6 17
ENSDART00000135430 Essential Splice Site 385 1047 6 16
Genomic Location (Zv9):
Chromosome 23 (position 18577504)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 18480443
GRCz11 23 18406786
KASP Assay ID:
554-0864.1 (used for ordering genotyping assays)
KASP Sequence:
TGCTGGACCTCCAGGCCATGTGGGGGCAGTACAGCCATTAAAAGCTCAGG[T/A]AATGTTTTTTTAAACTATAAAAGTTTGGTGATTTTTTTGTGTNNATTTTA
Long Flanking Sequence:
TATATATATATATATATATATATATATATATATATATATATATATATATATGTGTATGTGTATATATATATATATATATATATATATATATATATATATATATAATTTTTTTTTTATAAATTAACACTTTTTATTCATGACAGAATCCACATGTTAAACAGTTTTTGACTTAGTTTTTTCTTGAGCACCAATTTGTCTTATTAGAATCAAGAATCTGAAGTAATGTTGCTGAAACTGAATAGTTTCATGATTTAATTATATGGTAAAGGTATTAAAAACAGTTATTTTCAATTGTAATTGTATTAAAATATCTTAGTAGTTTTGTGACAAACAAGTGATAAAAAAAAGTGGTAGTTTGCAAGACAAACTCTGACACCAGTTTGTACTCAGTATTTATCTGTTGTTGTTACTTTGACTTATCTCAGTTCCAGGCTTTGGGCCTAGTCCATTTGCTGGACCTCCAGGCCATGTGGGGGCAGTACAGCCATTAAAAGCTCAGG[T/A]AATGTTTTTTTAAACTATAAAAGTTTGGTGATTTTTTTGTGTGTATTTTACAGAAACTAATGGCATCTAAATATCTTTTTGCTTGTTTTTGGGTCTCTGCAGTTTGGTCCACCCCAGGTGTCAGGTGTTAAGGTGCCTTATCCAGGTGGGCTCTATGGACCCGGTCCTGCCACTGGTCCAGCCCTTTTATGCCAGAACCCAACACAGCCACTGCAGGACTGTAACGATTCACTTGTTGGGAAAATGGGCTTTGCTGATTGGTCTGCTCCATATGATTCCTCTCAAGGTGGCAGCCGACAGCCCAATCACCACACTGCTGCTCCCACAGGCCCCTCCCCCTCGTCATCTTCGTCTTCAGATGGGGAGGAGCAAAATGACACCAGCGCTAAGTGAGTTCACCAGTTGCTAGTTGCTAAATACAACAGAAAAACAAACACAATAATGTGAATATTAAGCATAACGTTGTAAATTTAGTTTATGTTTTCATAGTTTCTTTCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1353
Status:
Confirmed mutation in F2 line
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065881 Essential Splice Site 563 1051 8 17
ENSDART00000135430 Essential Splice Site 563 1047 8 16
Genomic Location (Zv9):
Chromosome 23 (position 18576335)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 18479274
GRCz11 23 18405617
KASP Assay ID:
554-1267.1 (used for ordering genotyping assays)
KASP Sequence:
ACACAGAAGAGGACTCATGTATCCACAGATCTACCACATCCTGACCAAGG[T/C]ACTGCAATCACATAGCATGTGCATAAACCATCAGCAATTTTCTTCACTAA
Long Flanking Sequence:
CTCCTTGAATGAAGATGCTTTTAAATGACGCTAAAGGAATCAAGGATGTATCATTTTTTTCATTCAATTCCTCTGGCCTCCCATCTATTTTTTGGGCCCTCCACTCACATCCTCCATGGGTGTCGAGCTAAGACTTGAAAAGAAGAAACGAGGATGCACAAATAAGAATTGAAAAGCCCCCAATATGTAGCGAGCCTCTTTTAATAATAAACTTGTGTTTAGAGCAGGTTGAATATTTCTTTTCTTCCATAGTCATTTGGCTGACAAGTCCACGAGATGGGAAGATCCCAGTGGACGGAGTGGCAGTGGCTCTGGGGATGGCCACCATGGCAACGGAAGTGGGCCGTCCATCCCATCATTGCTTTCCATGCCAACTCGGAGTCACATGGACATCACAACGCCACCCCTTCCCCAGGTCAGTGCAGAGGTGCTGAGAGTGGCCGAGCACAGACACAGAAGAGGACTCATGTATCCACAGATCTACCACATCCTGACCAAGG[T/C]ACTGCAATCACATAGCATGTGCATAAACCATCAGCAATTTTCTTCACTAAATTATCTGACTGAATCTGCTGTGTTTATAAAATTGACATATGACTCATTTTTCCTTTACGTCAAATCTGACTAGAAATGGAAACTTTTTGTTTACCTCAAAGCAGCATCATTGCTTATGCTTTTATTATAAGCTGTTATACTTTATTACAAAAAAATACACAATGTTTTCATTAAAACAATGCTAAAATGATATAGTTTTATTATAGCATTAGTTTTCCATTTATGGTGGCAGATGTTTAAACAATCCTTGAAGTCTCACATAAAATAATGAAGTAATAAAGAATGAAGTAAAATAACTTATATCTTCATTACTGTGTGTACTCAATTATTTTTATTATTTCAACAAATTCCATTTAAAGTTTTAAACAGCAGGCAATAATTAGTTTACATTTATTGTGATTAATTCCCTGAAAACCCATTTAATATTCAGAAAGCATATATTGTAATAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24290
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065881 Nonsense 896 1051 14 17
ENSDART00000135430 Nonsense 896 1047 14 16
Genomic Location (Zv9):
Chromosome 23 (position 18564921)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 18467860
GRCz11 23 18394203
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGCTTAGTGTTTTTGCTCTCTCCTTTAGGAATCCAGTCTATACCTCCC[C/T]AGGGCGGCAAACTGGAAATAGCTGGCATGGTTGTTGGTCAGTGGGCTGGA
Long Flanking Sequence:
TTCTATAATAGGAAAAATGCAATGGAAGTCAATGTTGACCATTAACCAGAAATGGTAGTCATTGGTGACCAATCATTCTGGAAATACTATTAATAATGTAATATTTACTGTAATATTTACGTGTTTTCGGAATTTTTTATATTTTTGAAACTCTGTCCCTAAAGGAGGAACTGGTTTCAAGGGTGGAGAAGATGCGTCAGGCCATTCTGGAAGGCATCAACCTGTCCCGGCCACCACCTCCACCTCCACCACTGCCACCCCCTGCATTCCTCCCACCTGCTATGGTGCCACCTTTCTACCCCATGCATCCTCTGTACCCTCCTCGCCCATTGGGCTCTATGCCTCCTCCTCCCCCTCACCATCACCACCAGCACCGACCCAGGGCCTTTCCAGGTTAGACAGTTCTGTTGTTTAGTACATTTAGTTCAGTTTCTTTACTGCACTTTCAGTGTTGCTTAGTGTTTTTGCTCTCTCCTTTAGGAATCCAGTCTATACCTCCC[C/T]AGGGCGGCAAACTGGAAATAGCTGGCATGGTTGTTGGTCAGTGGGCTGGAAACAAGCCAATTCGTGGCAAAGGGGGGTTCAACATGCAGGTGGTGTCAGTAGGAGGGAAAGGGTGAGTTTATTCAGTCTTAAAACACTTAAAACTTATTTTTGGAGGTATGGAATGCGCTTCACTACAAATGTTTTTGTTTTCCATTTGTCAATATTAACTCTTGATTGCACCACCTGCTGGTGGAGAATACCAGTAGTAGGTCGAAATCATGTTCAGCAAACTATTCAGGCTGACTGCACTGTATTTCCACTAAAATATTAGTGCTTTGACTTTCAGATGTAGTTTTCTCCCATAGAAAATTGTAGTAATATCAAACTCTGCAATGTGTCTAGTAAATATGTAGTTTAATATTTGCTAAATGTTACAATATAATATTTTCTCTGCAATGCAAAATATAATGAGCTAAATTTGAGCTGTTACAAAGATCATAAATACAGTGCATACCAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37662
Status:
Mutation detected in F1 DNA
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
ENSDART00000065881 Nonsense 1041 1051 17 17
ENSDART00000135430 None None 1047 None 16
Genomic Location (Zv9):
Chromosome 23 (position 18553241)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 18456180
GRCz11 23 18382523
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTGCAGGGTAGCAGGCATTGGGGGCTGTGGAATGAGGTAGTAGTTTG[T/A]ATAGTTTGGGATCACACCAGATCTGGGAGATAACTATACAGCCTACTGTC
Long Flanking Sequence:
GTAGTGATTCAGAGAACTCTGTGACATATACTTCTGCTGTAAGACATGTACTTTATCATAAATCACTATTTAATAAAAAGTGGTCATGTTTATTTCACCATCGCTTTCTAAGCTTTTCACTGATCCTAAAACGGCAATACATTTATTACATCAAACACTGCAAAGCAGCAGATCCTCATCCATCTCTTTGTTGTTGGTGGTATATCATGACTCATATTTCAAAAGATGAGATGCATTGCCAGAAACCTGCCCACACTCTGTGGCGTGGATGTTTGATCAAGGTTAATACTGGGTTAAAGGATGATGACGACAGCCTTTCACTGTGGGATTTATGAAAATCAAATTAGCAATTGCAAGGGTGGTTCATTATATTTTGAATAAAAATAGCACAAACAAGCAAACATGTTTATGGTGCTGCTGCTGCTGACACGTCTGTTTGCCTCTTGTCTCCTCTTGCAGGGTAGCAGGCATTGGGGGCTGTGGAATGAGGTAGTAGTTTG[T/A]ATAGTTTGGGATCACACCAGATCTGGGAGATAACTATACAGCCTACTGTCTTTCTCACAGCTGCTCCTTCACATCAGACCCTCCAATGACGGACCTTGGCACAGACAGGGCTTTTGTGGAGAGCTGAATTTGTGCATCTTTGTACTGTGTGTTCTTTCTAAGAGTACAAATTGTAGAGACATTGTGAACTAAAGTTTAATAAATAAAACATTGATGTCAGAACTCGTATTCATGACTCGTCTTTAGTTGATGGATAAAAGGATTGTTCAACAAAACATGAAAATGTACTCACCCTCAAGTGGGCACAAATGATAATGTTTTAACTGATATTAGAAACAATTGACATCCTCAGTGGAAAAATATATATATTTCTGCTTTTATCTTCTTTTGGTTCAAAAGAAGAATGAAACCCAAACACTGTGACAAGTAAAGCGTGAGTAAATGATGGCAGAATTTTCGGGTTTGGGTAAACTCATTTATTAATTTTCTTTCGGCTTAGT
Associated Phenotype:
Not determined